TECHNICAL FIELD
[0001] The present invention relates generally to microneedle arrays and is particularly
directed to a method for manufacturing microneedle structures using soft lithography
and photolithography. The invention is specifically disclosed as a method of manufacturing
microneedles by creating micromold structures made of a photoresist material or PDMS,
and in some cases using a sacrificial layer for ease of separation from a substrate
layer.
BACKGROUND OF THE INVENTION
[0002] Topical delivery of drugs is a very useful method for achieving systemic or localized
pharmacological effects, although there is a main challenge involved in providing
sufficient drug penetration across the skin. Skin consists of multiple layers, in
which the stratum corneum layer is the outermost layer, then a viable epidermal layer,
and finally a dermal tissue layer. The thin layer of stratum corneum represents a
major barrier for chemical penetration through the skin. The stratum corneum is responsible
for 50%-90% of the skin barrier property, depending upon the drug material's water
solubility and molecular weight.
[0003] An alternative to the use of hypodermic needles for drug delivery by injection is
disclosed in
U.S. Patent No. 3,964,482 (by Gerstel), in which an array of either solid or hollow microneedles is used to penetrate through
the stratum corneum and into the epidermal layer. Fluid is dispensed either through
the hollow microneedles or through permeable solid projections, or perhaps around
non-permeable solid projections that are surrounded by a permeable material or an
aperture. A membrane material is used to control the rate of drug release, and the
drug transfer mechanism is absorption.
[0005] The use of microneedles has one great advantage in that intracutaneous drug delivery
or drug sampling can be accomplished without pain and without bleeding. As used herein,
the term"microneedles"refers to a plurality of elongated structures that are sufficiently
long to penetrate through the stratum corneum skin layer and into the epidermal layer.
In general, the microneedles are not to be so long as to penetrate into the dermal
layer, although there are circumstances where that would be desirable. Since microneedles
are relatively difficult to manufacture, it would be an advantage to provide methodologies
for constructing microneedles that are made from various types ofmicromolds that can
be manufactured relatively quickly. The use of metallic molds or semiconductor molds
is possible, but such structures usually take a relatively long period of time for
construction. On the other hand, if the molds are made of a polymer or other type
of plastic (or other moldable) material, then such mold structures can be made relatively
quickly and with much less expense.
WO-A-00/74763 discloses a device for transport of a material across or into a biological barrier
which comprises
inter alia a plurality of hollow microneedles. A number of microfabrication processes that may
be used in making the microneedles are disclosed including lithography; etching techniques,
such as wet chemical, dry, and photoresist removal; thermal oxidation of silicon;
electroplating and electroless plating; diffusion processes, such as boron, phosphorus,
arsenic and antimony diffusion; ion implantation; film deposition, such as evaporation
(filament, electron beam, flash and shadowing and step coverage), sputtering, chemical
vapor deposition (CVD), epitaxy (vapor phase, liquid phase, and molecular beam), electroplating,
screen printing, lamination, stereolithography, laser machining, and laser ablation
(including projection ablation).
[0006] US-A-6 106 751 discloses a method of fabricating a needle via conformal deposition in a two-piece
mold, said method comprising the steps of:
attaching a top mold member to a bottom mold member such that said top mold member
and said bottom mold member define an enclosed, elongate needle trench with a deposition
aperture;
passing a conformal substance through said deposition aperture such that said conformal
substance is deposited via vapor deposition within said enclosed, elongated needle
trench;
stopping said passing step before said elongated needle trench is filled with said
conformal substance; and
removing said top mold member and said bottom mold member to expose a needle.
[0007] WO-A-00/05166 discloses a method of providing a micro-projection on the surface of a first material,
the micro-projection having a base portion adjacent the first material and a remote,
or a tip portion, and a duct at least in a region of the tip portion and the method
comprising micro-machining the first material to provide the micro-projection and
duct.
[0008] US-A-6 107 210 discloses a method of fabricating an epidermal abrasion device, said method comprising
the steps of:
providing a semiconductor substrate with a planar surface;
defining a mask configuration on said semiconductor substrate to facilitate the formation
of an epidermal abrasion device; and
exposing said mask configuration on said semiconductor substrate to an isotropic etchant,
said isotropic etchant forming a matrix of isotropically etched structures on said
semiconductor substrate adapted for epidermal abrasion, said isotropically etched
structures having isotropically etched sidewalls positioned between wide bases and
narrow tips;
wherein said exposing step includes forming a matrix of isotropically etched pyramids
on said semiconductor substrate.
SUMMARY OF THE INVENTION
[0009] Accordingly, it is an advantage of the present invention to provide a method for
fabricating microneedles using photolithography and soft lithography techniques, which
allow for quick manufacturing of both micromolds and usable microneedle structures.
[0010] It is another advantage of the present invention to provide a method for fabricating
microneedles in which a photoresist material is applied in a single layer, or in multiple
layers, and patterned via photolithography, thereby either creating a microneedle
structure that can be directly used, or creating micromold structure that can be used
with moldable material such as polymers to manufacture the microneedle structures.
[0011] It is a further advantage of the present invention to provide a method for fabricating
microneedles in which soft lithography is used to create microneedle structures that
can be directly used, or to create micromold structures that can be used with moldable
material such as polymers to manufacture the microneedle structures, in which a moldable
material has its shape formed, at least in part, by another relatively "soft" material—e.g.,
something other than a metal.
[0012] It is still another advantage of the present invention to provide a method for fabricating
microneedles in which soft lithography is used to create microneedle structures that
can be used to create flexible micromold structures that can be used with moldable
material such as polymers to manufacture the microneedle structures, in which the
resulting microneedle array is either concave or convex in overall shape.
[0013] It is yet a further advantage of the present invention to provide a method for fabricating
microneedles in which photolithography and/or soft lithography is used to create micromold
structures, and in which a sacrificial layer of material is dissolved or decomposed
to separate the micromold structures from a substrate.
[0014] It is still a further advantage of the present invention to provide a method for
fabricating microneedles in which photolithography and/or soft lithography is used
to create microneedle structures, and further coating a surface of the microneedle
structures using a vapor deposition process, and/or another coating process such as:
electroplating, electrodeposition, electroless plating, sputtering, or plasma deposition.
[0015] It is yet another advantage of the present invention to provide a method for fabricating
microneedles in which photolithography and/or soft lithography is used to create master
structures, and further using a microembossing or molding process to manufacture microneedle
structures.
[0016] It is still another advantage of the present invention to provide a method for fabricating
microneedles in which photolithography and/or soft lithography is used to create microneedle
structures, and further creating electrodes on the microneedle structures, either
in "bands" of electrically conductive material that each encompass multiple microneedles,
or in individual small electrically conductive structures that run inside a single
hollow microneedle.
[0017] It is a further advantage of the present invention to provide a method for fabricating
microneedles in which photolithography and/or soft lithography is used to create microneedle
structures, in which the tips of the microneedles are either hardened or made more
flexible, or in which the base (or substrate) of the microneedle array is made more
flexible, or in which the microneedles break away from the base (substrate) of the
array after application to skin, thereby leaving behind hollow microtubes that protrude
through the stratum corneum.
[0018] Additional advantages and other novel features of the invention will be set forth
in part in the description that follows and in part will become apparent to those
skilled in the art upon examination of the following or may be learned with the practice
of the invention.
[0019] To achieve the foregoing and other advantages, and in accordance with one aspect
of the present invention, a method for fabricating microneedles is provided including
steps of: (a) providing a substrate that includes multiple microstructures; (b) coating
the substrate with a layer of a first moldable material that takes the negative form
of the microstructures, and hardening the first moldable material; (c) separating
the hardened first moldable material from the substrate, and creating a micromold
from the hardened first moldable material containing the microstructures; and (d)
applying a second moldable material onto the micromold, allowing the second moldable
material to harden using a soft lithography procedure, then separating the hardened
second moldable material from the micromold, thereby creating a microneedle structure
from the hardened second moldable material having the three-dimensional negative form
of the microstructures of the patterned micromold.
[0020] Still other advantages of the present invention will become apparent to those skilled
in this art from the following description and drawings wherein there is described
and shown a preferred embodiment of this invention in one of the best modes contemplated
for carrying out the invention. As will be realized, the invention is capable of other
different embodiments, and its several details are capable of modification in various,
obvious aspects all without departing from the invention. Accordingly, the drawings
and descriptions will be regarded as illustrative in nature and not as restrictive.
BRIEF DESCRIPTION OF THE DRAWINGS
[0021] The accompanying drawings incorporated in and forming a part of the specification
illustrate several aspects of the present invention, and together with the description
and claims serve to explain the principles of the invention. In the drawings:
Figures 1A-1F are diagrammatic views in cross-section that illustrate some of the
process steps for manufacturing polymeric microneedles by replica molding, in which
PDMS molds are prepared by employing a photoresist master,
Figures 2A-2E are diagrammatic views in cross-section that illustrate some of the
process steps for manufacturing polymeric microneedles by replica molding, in which
PDMS molds are made utilizing a silicon specimen that was fabricated by deep reactive
ion etching (DRIE).
Figures 3A-3E are diagrammatic views in cross-section showing the steps employed to
construct microneedle arrays made of a photoresist maternal, in which photolithography
is used on a substrate that is coated with silicon oxide.
Figures 4A-4E are diagrammatic views in cross-section showing the steps employed to
construct microneedle arrays made of a photoresist material, in which photolithography
is used on a substrate that is coated with PDMS.
Figures 5A-5F are diagrammatic views in cross-section showing the various steps employed
to fabricate hollow microneedles using deposition techniques, in which metallic hollow
microneedles are made by electroplating on a PDMS structure.
Figures 6A-6E are diagrammatic views in cross-section showing the various steps employed
to fabricate hollow microneedles using deposition techniques, in which polymeric hollow
microneedles are constructed by electrodeposition on PDMS posts.
Figures 7A-7B, 7X-7Z are diagrammatic views in cross-section showing some of the structural
steps used in fabricating arrays of detachable microtubes, in which photolithography
is used on a wafer coated with PDMS.
Figures 8A-8D, 8X-8Z are diagrammatic views in cross-section showing some of the structural
steps used in fabricating arrays of detachable microtubes, in which photolithography
on an oxidized silicon wafer.
Figures 9A-9G are diagrammatic views in cross-section illustrating some of the structural
steps employed to fabricate hollow microneedles using deposition techniques, in which
metallic hollow microneedles are made by electroplating on a PDMS structure.
Figures 10A-10G are diagrammatic views in cross-section illustrating some of the structural
steps employed to fabricate hollow microneedles using deposition techniques, in which
polymeric hollow microneedles are constructed by electrodeposition on PDMS posts.
Figures 11A-11K are diagrammatic views in cross-section showing the structural steps
utilized to manufacture hollow microneedles using complimentary PDMS molds.
Figures 12A-12G are diagrammatic views in cross-section of some of the structural
steps employed to fabricate polymeric hollow microneedles by replica molding of multilayer
patterns.
Figure 12H is a perspective view of a PDMS replica molding, as seen in Figure 12E.
Figures 12I-12J are further diagrammatic views in cross-section of some of the structural
steps employed to fabricate polymeric hollow microneedles by replica molding of multilayer
patterns.
Figures 13A-13C, 13F-13I, are perspective views of some of the structural steps used
to construct electrodes inside hollow microneedles.
Figures 13D-13E are magnified plan views of the individual electrode patterns used
in the photolithography steps of Figures 13B and 13C.
Figure 13J is a perspective view in partial cross-section and magnified of a single
hollow microneedle having an internal electrode, as seen in Figure 13I.
Figure 14 is a plan view of a microneedle array that contains electrode bands.
Figures 15A-15L are diagrammatic cross-sectional views of structural steps used to
fabricate sharp tipped microneedles.
Figures 16A-16E are perspective views showing the structural steps utilized to manufacture
convex or concave microneedles using flexible molds.
Figure 17 is a perspective view of a solid microneedle having an external channel
along its elongated side wall.
Figure 18 is a top, elevational view of multiple solid microneedles each having two
external channels along their elongated side wall.
DETAILED DESCRIPTION OF THE INVENTION
[0022] Reference will now be made in detail to the present preferred embodiment of the invention,
an example of which is illustrated in the accompanying drawings, wherein like numerals
indicate the same elements throughout the views.
[0023] Using the principles of the present invention, polymeric microneedles can be fabricated
by replica molding in which PDMS molds are prepared using a photoresist master. Alternatively,
polymeric microneedles can be made by replica molding in which PDMS molds are made
utilizing a silicon wafer that is fabricated by deep reactive ion etching or any other
etching technique known by those skilled in the art. In both cases, the PDMS material
becomes a negative replica which is used as a mold that can be later filled with a
prepolymer material that will itself become an array of microneedles. Both solid and
hollow microneedles can be made by the techniques of the present invention.
[0024] Although the term "PDMS" is used throughout this patent document in very many places,
it will be understood that other materials could instead be used with the present
invention in lieu of PDMS, depending upon the microfabrication process of choice.
In a replication molding procedure, one could use any moldable material having low
surface energy, and the consequent poor adhesion with most substrates. For sacrificial
layers, highly reactive polymers or other materials that are soluble in organic or
inorganic solvents could replace PDMS. Furthermore, silanization will not generally
be necessary if totally inert elastomers are used for replication (e.g., fluorinated
polymers). PDMS
™ is manufactured by Dow Corning Corporation of Midland, Michigan.
[0025] In the situation where a photoresist material is used, this material is patterned
by use of photolithography techniques, and the patterned structure is used to create
the PDMS negative replica. The precise design for the transparency mask used in the
photolithography procedures utilizes a microfabrication method that is based on a
rapid prototyping technique which uses design software and a high resolution printer;
however, masks prepared using the traditional methodologies known by those skilled
in the art can also be implemented using this process. The present invention makes
good use of photolithography, generally using SU-8 photoresist materials, and a combination
of replica molding using soft lithography, electroplating or microembossing processes.
Such processes are less expensive and have quicker turnaround time (e.g., less than
twenty-four hours) than those previously known in the art for the fabrication of microneedles.
[0026] Although the term "SU-8" is used throughout this patent document in very many places
as an example of photoresist material, it will be understood that other materials
could instead be used in lieu of SU-8, which is a particular brand of photoresist
manufactured by MicroChem Corporation of Newton, Massachusetts. SU-8
™ has some particularly desirable characteristics, in that as a photoresist it can
produce a film thickness greater than or equal to thirty (30) microns. Of course,
if the designer wishes to produce a photoresist film having a thickness less than
30 microns, then certainly other photoresist materials could be used. Moreover, photoresist
materials other than SU-8 that produce film thicknesses greater than 30 microns may
be available, or may become available, and those could perhaps be advantageously used
in the present invention.
[0027] The present invention not only uses photolithography for patterning certain structures,
but also uses "soft lithography" for creating structures in three dimensions using
molds made of a polymer material or similar non-metallic material. The soft lithography
is a methodology in which all members involved share a common feature in that they
use a patterned elastomer as the mask, stamp, or mold. (See, "
Soft Lithography," by Younan Xia and George M. Whitesides," Angew. Chem. Int. Ed.
1998.37.550-575.) This elastomeric stamp or mold transfers its pattern to the "moldable material"
which can comprise flexible organic molecules or other materials, rather than rigid
inorganic materials now commonly used in the fabrication of microelectronic systems.
In the present invention, such soft lithography processes are utilized in almost every
methodology for creating an array of microneedles.
[0028] Professor George Whitesides and colleagues have used soft lithography in numerous
microfabrication processes, including: fabrication of carbon microstructures utilizing
elastomeric molds (see
published patent application, WO 98/34886 A1), etching of articles via microcontact printing (see
WO 98/34886 A1), microcontact printing of catalytic colloids (see
WO 97/34025), fabrication of small coils and bands by patterning cylindrical objects with patterns
of self-assembled monolayers (see
WO 97/44692 and
WO 97/07429), formation of articles via capillary micromolding (see
WO 97/33737), and the utilization of elastomeric masks to fabricate electroluminescent displays
(see
WO 99/54786).
[0029] Silicon masters fabricated using conventional silicon micromachining technologies
such as deep reaction ion etching, or structures prepared using LIGA processes, also
can be employed for replica molding of microneedles. Such silicon masters will generally
require more time in creating the replica molds as compared to the microfabrication
methods of the present invention that create mold replicas using photoresist or PDMS
(or similar) materials.
[0030] The methodologies described below can be used to manufacture solid, partially hollow,
or totally hollow microneedles, and such microneedles can be made of electrodepositable
metals, thermoplastics, or polymers that cure using heat energy, light energy, or
by the addition of an initiator under normal conditions. When photolithography techniques
are used, then the light energy is generally used for both patterning and curing the
materials, although the curing methodologies can certainly involve other types of
energy sources than light.
[0031] As noted above, the fabrication techniques described in this document have quicker
turnarounds than many others that have been described in the prior art for the fabrication
of microneedles. The replica mold can often be made of PDMS material, which is formed
into the appropriate shapes by use of a silicon or metallic structure that has been
entirely formed to the proper shape, or a silicon wafer structure that has predetermined
protrusions that are made of a photoresist material, in which the photoresist was
patterned using photolithography techniques. Once the PDMS mold negative replica has
been formed, it can be filled with a prepolymer or other type of moldable material,
in which the prepolymer or other material becomes the actual array of microneedles.
The prepolymer is then cured in a soft lithography process step.
[0032] An alternative fabrication technique is to begin with a layer of photoresist material
that is separated from a silicon wafer or other substrate material by a "sacrificial
layer," made of a material such as PDMS or silicon oxide. One fabrication technique
is to place a first layer of photoresist that is cured without using a mask, and then
placing a second layer of photoresist that is patterned using photolithography or
other patterning techniques. The first photoresist layer later becomes the substrate
or base of a microneedle array, while the second layer of photoresist material later
becomes the actual protrusions that create the microneedle structures, either solid
or hollow. Once the photoresist layers are completely patterned and cured, the sacrificial
layer is then dissolved or otherwise decomposed, thereby separating the silicon wafer
initial substrate from the microneedle array.
[0033] As noted above, the fabrication procedures can be used to make either solid or hollow
microneedles. If hollow microtubes are to be created from a silicon wafer having a
photoresist top layer, then the top layer of photoresist is patterned as an array
of hollow microtubes using photolithography techniques. After that has occurred, the
"wafer/patterned photoresist" is silanized and coated with a PDMS material that is
cured in a soft lithography process. Once the PDMS has been cured, it is separated
from the original silicon wafer/substrate and patterned photoresist combination, thereby
producing a negative replica comprising PDMS. The negative replica is then filled
with a prepolymer material that is cured with electromagnetic energy or heat energy
in a soft lithography process, and once cured the prepolymer is detached from the
PDMS mold replica, thereby forming an array of hollow microneedles. At this point,
the microneedles may not be completely hollow, as the through-holes only go so far
into the photoresist material. Of course, these "microcups" can be opened by laser
ablation, or some other type of microfabrication technique.
[0034] An alternative methodology for creating hollow microneedles or "microtubes" is to
begin with a silicon wafer or other substrate material, place a sacrificial layer
on its top, and further place a layer of photoresist above that sacrificial layer.
This first layer of photoresist is cured without using a mask, and then it is covered
with a second layer of photoresist that is baked to dryness. An array of microneedles
or "microtubes" is then formed in the second layer of photoresist by photolithography
techniques. Once this has occurred, the sacrificial layer is dissolved or otherwise
decomposed, thereby leaving behind an array of microneedles made of the photoresist
material. At this point, the microneedles may not be completely hollow, as the through-holes
only go so far into the photoresist material. Of course, these "microcups" can be
opened by laser ablation, or some other type of microfabrication technique.
[0035] Once hollow microtubes or microcups have been formed on a silicon wafer or other
substrate, they can be made more detachable in skin by an application of an acid along
the base of the outer walls of the microneedles, to thereby etch away a small portion
of the material at the base. This will make it more likely that the microneedles can
easily detach from the main base or substrate of the microneedle array. This is useful
in situations where the microneedles are used to penetrate the stratum corneum of
skin, and then have the array base or substrate removed from the skin surface. The
microneedles will break away from that substrate/base at that time, thereby leaving
hollow microneedles within the stratum corneum. Such microneedles will stay embedded
in the stratum corneum until the stratum corneum is renewed, thereby providing a location
on the skin where liquids temporarily can be introduced or extracted.
[0036] Break-away microneedles can also be made by use of PDMS materials or other coatings
that have poor adhesion with photopolymers as the substrate and a photoresist material
that makes up the actual microneedles. Such photoresist hollow microneedles would
likely break away from the PDMS substrate/base of the microneedle array upon application
into the stratum corneum of skin. This would then leave behind multiple such hollow
microneedles in the stratum corneum once the array's base/substrate is removed.
[0037] The present invention also provides procedures that can fabricate hollow microneedles
using deposition techniques. Both metallic hollow microneedles and polymeric hollow
microneedles can be constructed in such a manner. The metallic hollow microneedles
are made by creating a PDMS negative replica that is then electroplated onto the microneedle
structure. This would typically produce "closed" microneedles, which could have their
own usefulness, although in many cases the microneedles will be opened to create microtubes
with through-holes by use of some type of polishing operation.
[0038] Polymeric hollow microneedles can be constructed using deposition techniques by creating
a negative PDMS replica and electrodepositing a polymer on "posts" or other microneedle-type
structures that are constructed from the PDMS. Once the polymer has been plated on
the PDMS, the plated polymer is separated from the PDMS mold, thereby leaving behind
multiple microneedle structures that have the form of "closed" microneedles. Such
microneedles can be opened to create completely through-hole hollow microneedles by
a polishing operation.
[0039] The principles of the present invention can also be used to manufacture hollow microneedles
using complimentary molds made of PDMS. In this situation, two separate silicon wafers,
for example, can be used as starting points in which each are coated with a layer
of photoresist material. Using photolithography techniques, each of these wafers has
its photoresist layer patterned; in the first case holes are formed in the photoresist
layer, and in the second case posts or other similar structures are formed in the
photoresist. These patterns will be complimentary, as will be seen below. Both wafers
are now silanized and coated with PDMS. The PDMS is cured, and once cured, the PDMS
forms a negative replica that can be removed or detached from their respective silicon
wafers. The photolithography stage forms both holes and "posts" that are complimentary
to one another, and therefore, the two negative replicas made of PDMS are also complimentary.
One of these negative replicas is turned upside down, a layer of prepolymer is then
placed on top of that "turned-around" PDMS negative replica, and then the second negative
replica is placed on top of the prepolymer, thereby sandwiching the prepolymer in
place. The prepolymer is now cured and the two PDMS molds are detached, thereby leaving
behind a separate polymer structure. If the shape formed "closed" hollow microneedles,
then the closed end of these microneedles can be opened by use of some type of finishing
or polishing procedure.
[0040] Multiple layers of patterns can also be used with the principles of the present invention
to create polymeric microneedles, either solid or hollow, as desired. A first layer
of photoresist is placed on a silicon wafer or other substrate structure, and holes
or other similar patterns are formed in the photoresist by photolithography techniques.
A second layer of photoresist is then coated onto this structure, and using a second
photolithography procedure, microneedle forms can be made, including hollow tube microneedles.
This structure is now silanized, and a PDMS negative replica is formed based upon
this pattern. The PDMS now becomes a mold itself, and a polymer material can be placed
onto the PDMS negative replica and cured or embossed, thereby forming an array of
microneedle structures. If the microneedles form "closed" hollow microneedles, then
the closed ends can be removed by polishing or other type of finishing procedure.
This would leave behind an array of hollow microneedles having through-holes. Polishing
can be avoided by pressing a PDMS flat against the mold filled with prepolymer.
[0041] The principles of the present invention can also be used to create microneedles having
internal electrodes. Two different initial structures are used to create the electrode-microneedle
combinations. On one hand, a polymer microneedle array is constructed according to
one of the processes described above, in which the microneedles are hollow with through-holes.
The other structure consists of a silicon (or other material) substrate that has a
layer of photoresist material applied and patterned using photolithography. This structure
is then silanized and coated with PDMS, which is then cured. The cured PDMS layer
is then separated from the photoresist-substrate structure, thereby becoming a mask
that will be aligned with the hollow microneedles of the first structure. Once the
patterned PDMS mask is aligned with the hollow microneedles, metal is vapor deposited
on the inside of the microneedles in a pattern that will run through a portion of
the length of the hollow microneedles along their inner cylindrical surfaces. Similar
masks could also be prepared using electroplating, electroless plating, electrochemical
micromachining, silicon or polymer etching.
[0042] The electrode-microneedle combination can be constructed so that each hollow microneedle
has an electrode that is electrically isolated from each other such hollow microneedle.
Alternatively, groups of microneedles can be electrically connected together by use
of electrode "bands" in which a first group of multiple microneedles are electrically
connected to a "working electrode," a second group of multiple microneedles are connected
to a "reference electrode," and finally a third group of multiple microneedles are
electrically connected to a "counter electrode."
[0043] A reference electrode is not needed in a two-electrode system and, depending upon
the electrochemical cell design, microneedle arrays could be used on structures that
consist of only one electrode type, such as a working electrode, counter electrode,
or reference electrode. These unitary-type electrode structures could be combined
in a two-electrode or a three-electrode device. Microneedles are so small in size,
that the "electrode bands" might be more useful in certain applications, and the microneedles
could be either solid or hollow.
[0044] The principles of the present invention can also be used to construct microneedles
having a very sharp tip. This could be done by having multiple layers that are patterned
one after the other, in which each pattern creates a cylindrical or elliptical opening
such that each lower opening is smaller in size than the next adjacent higher opening.
This will create a series of photoresist layers, for example, that taper down to a
very small opening. When these photoresist structures are finished, they can be separated
from a substrate (such as silicon), and this separation could be facilitated by use
of a sacrificial layer of material, such as silicon oxide. Once the mold has been
separated from the substrate, a polymer or prepolymer material to be placed on top
of the mold and forced into the openings that taper down to the smallest opening.
Each one of these tapered-down structures, when cured, will become a sharpened tip
microneedle. After curing, the array of sharp-tip microneedles is separated from the
photoresist mold.
[0045] Other types of alternative structures are available when using the principles of
the present invention. For example, the base material of the microneedle array can
be made from a first structural material, while the microneedles themselves can be
made of a second structural material. This allows design freedom to create hydrophobic-hydrophilic
combinations and controlled adhesion of the needles to the base. Another alternative
structure is to chemically modify the microneedles to change their properties, such
as treatment of silicon microneedles with silanizing reagents to derivatize the surfaces.
A further alternative structural treatment is the use of a plasma treatment of epoxy
or other polymeric microneedles that impart different surface properties (that would
affect the hydrophobic or hydrophilic properties). The use of plasma treatment, or
chemically modifying the microneedles, can occur at the molecular level, and such
processes are commonly referred to as "surface modification" of structures.
[0046] Another alternative construction is to incorporate carbon fibers or other composite
materials into epoxy microneedles or polymeric microneedles, as well as their substrates,
in order to make the substrates and/or microneedles more rigid. Certainly the use
of composite materials or carbon fibers could reinforce the microneedles themselves
to make them more rigid. Alternatively, such substrates could be made more flexible,
including the use of micro channels and grooves in the substrate. It may be likely
that the microneedles themselves are to remain rigid in such a structure.
[0047] A further alternative construction of microneedles is to make them more flexible,
in which the microneedles are rigid enough to break skin, but still have a certain
amount of flexibility. This could be used in situations where the microneedles are
to penetrate the skin and be held in place for a relatively long period of time. This
could be used for continuous monitoring and/or dispensing systems. It would be an
advantage to provide such flexible microneedles that would be virtually unbreakable
while being used in such circumstances.
[0048] Another alternative construction is to place a metal coating over the microneedles
as a final outer layer. Several different processes can be used to coat microstructures
with metal layers, including electroplating (or electrodeposition), electroless plating,
sputtering, vapor deposition, and plasma deposition. It is possible to electroplate
some alloys, metal oxides, polymers, and composite materials. Depending on the material
that is electroplated, the plating solution can be aqueous or organic.
[0049] Electroless plating can be used to deposit metal, oxides, or polymers on virtually
any kind of substrates. Sputtering can only be used to deposit thin metal films (from
angstroms to nanometers), although sputtering is a fast and inexpensive technique
that is convenient to coat non-conductive samples with seed metal layers for a later
step of electroplating.
[0050] Vapor deposition is preferred over sputtering in the cases where microsmooth metal
and oxide films are desired or when common metals do not adhere strongly to the substrates.
For vapor deposition, the sample are placed in a vacuum chamber where the metals are
evaporated using resistive heating or an electron beam. The metal vapors deposit on
the cold areas of the vacuum chamber, including the sample surface. Usually, the specimens
are coated with a few angstroms of a metal adhesion layer prior to the deposition
of the metal or oxide or interest.
[0051] Plasma deposition is a technique that can be employed to deposit very thin films
(having a thickness in the order of angstroms) of several kinds of materials on conductive
or non-conductive substrates. However, this process typically is slow and expensive.
It is normally utilized to prepare films of materials that cannot be handled using
the methodologies mentioned above.
[0052] One methodology utilizing the principles of the present invention involves fabrication
of solid polymeric microneedles using photolithography and replica molding. Two different
fabrication schemes are described below, and these are illustrated in Figures 1 and
2. "Figure 1" consists of Figures 1A-1F, and illustrates a process that can produce
polydimethylsiloxane (PDMS) molds used in the fabrication of solid microneedles that
are made of thermally light, or self-curable polymers or by embossing thermoplastics.
The first step in the microfabrication method of the present invention is to spin-coat
a layer that is about 20-200 microns in thickness of a photoresist compound (e.g.,
SU-8) on a silicon wafer, and baking to dryness at 90°C. The silicon wafer is at reference
numeral 10, and the photoresist is at reference numeral 12 on Figure 1A.
[0053] The photoresist film is then patterned with posts 14 having a diameter in the range
of 10-100 microns, using photolithography, as illustrated in Figure 1B. The wafer
is then silanized with an alkyl chlorosiloxane compound, then covered with PDMS and
cured in an oven at about 60-70°C for about two hours. This soft lithography step
is illustrated in Figure 1C, where the layer of PDMS is at reference numeral 16.
[0054] The PDMS negative replica is detached manually from the silicon/SU-8 master, as illustrated
by the negative replica 16 of Figure 1D. Naturally, this detachment operation can
be automated.
[0055] The PDMS structure is then filled under a vacuum with a photocurable polymer or a
prepolymer material, such as epoxy known as UVO-110 under a vacuum. This structure
is irradiated with ultraviolet light for two hours using a mercury lamp, or other
ultraviolet light source to cure the prepolymer 18, in a soft lithography process
step. This is illustrated in Figure 1E, in which the prepolymer is at reference numeral
18. Finally, the microneedle structure is separated from the mold, leaving a microneedle
array 18 made of polymer as seen in figure 1F.
[0056] As an alternative methodology, silicon microstructure array masters prepared using
deep reactive ion etching (DRIE), or metallic microstructure array masters (prepared
using, e.g., LIGA techniques) could be employed instead of the SU-8 photoresist masters
to manufacture polymeric microneedles as shown in Figure 1. This alternative methodology
is illustrated in "Figure 2," which consists of Figures 2A-2E. In Figure 2A, the silicon
microstructure array master is illustrated at the reference numeral 20. As noted above,
instead of a silicon structure, the microstructure could be made of a metallic substance.
[0057] The silicon structure 20 is then silanized and covered with PDMS at 22, as seen in
Figure 2B. After being covered with the PDMS material, the structure is cured in an
oven at about 60-70°C for about two hours.
[0058] The PDMS negative replica is detached from the silicon or metallic master 20, leaving
the negative replica structure 22, as viewed in Figure 2C. The PDMS structure 22 is
then filled with a photocurable polymer at 24, as seen in Figure 2D. This photocurable
polymer is then exposed to a light source, such as an ultraviolet light source from
a mercury lamp. This cures the polymer, and the microneedle apparatus is then separated,
leaving the microneedle array 24, as viewed in Figure 2E. An example of an ultraviolet-curable
polymer is a compound known as UV-114, manufactured by Epoxy Technologies Inc.
[0059] The process described in Figure 1 can be modified to generate freestanding photoresist
microneedle devices, examples of which are illustrated in Figures 3 and 4 with respect
to their construction techniques. "Figure 3" consists of Figures 3A-3E. An oxidized
silicon wafer at 30 includes a top layer of PDMS at 32, which is coated with a layer
of photoresist material at 34, as viewed in Figure 3A. This structure is baked to
dryness and cured with ultraviolet light to obtain a solid film of the cured photoresist
material at 36 (see Figure 3B). An example of this photoresist material is SU-8. The
structure of Figure 3B is coated again with photoresist, in this case a layer 38 in
the range of 20-200 microns thick. This structure is baked to dryness at approximately
90°C, providing the structure of Figure 3C in which the second layer of photoresist
is illustrated at the reference numeral 38.
[0060] Microneedles are formed in the second layer of photoresist 38 by a photolithography
technique using a transparency mask patterned with dots having a diameter in the range
of 20-100 microns. This provides the structure of Figure 3D, in which solid microneedles
at 40 are formed in an array-type structure.
[0061] The microneedle structure is separated from the wafer by dissolving a "sacrificial
layer" with an appropriate reagent, in which the PDMS layer 32 is decomposed with
tetrabutylammonium fluoride (TBAF) and tetrahydrofuran, leaving behind the microneedle
array structure 40 of Figure 3E.
[0062] An alternative methodology for generating a freestanding photoresist material microneedle
array is described in connection with "Figure 4," which consists of Figures 4A-4E.
In Figure 4A, an oxidized silicon wafer 30 which includes a layer of silicon oxide
at 42, is coated with a layer of photoresist material 34 and baked to dryness. The
photoresist layer 34 is exposed without using a mask and cured, which is illustrated
at the reference numeral 36 in Figure 4B. The wafer structure is then coated with
a second layer of photoresist material at 38 and baked to dryness at about 90°C, which
is illustrated in Figure 4C.
[0063] Microneedle-like structures are formed in the second photoresist layer by a photolithography
procedure using a transparency mask that is patterned with dots having a general diameter
in the range of 20-100 microns. This is the structure illustrated in Figure 4D, in
which the top layer 44 is the second photoresist layer that has microneedle structures
protruding upwards in the figure. The wafer structure is then immersed in hydrofluoric
acid (e.g., 10% solution) to detach the polymeric structure from the silicon substrate.
This provides the separate microneedle (polymeric) structure at 44, as illustrated
in Figure 4E. The silicon oxide layer 42 acts as a sacrificial layer by dissolving
or otherwise decomposing in the hydrofluoric acid.
[0064] The array of solid microneedles in Figures 3E at 40 and 4E at 44 can be converted
into "hollow" microneedles by various techniques. One well known technique is laser
ablation, which would essentially burn holes through the centerline (or approximately
near the centerline) of each of the cylindrical microneedle structures.
[0065] One aspect of the present invention is to create microneedle arrays that include
individual microneedles that exhibit a "high aspect ratio." The overall length of
a microneedle divided by its overall width is equal to the aspect ratio. If a microneedle
is 200 microns in length, and its width (or diameter if it is circular) is 50 microns,
then its aspect ratio is 4.0. It is desirable to use a relatively high aspect ratio
of at least 3:1, although creating such structures can be difficult.
[0066] The microneedles are so tiny in actual size (especially in the smaller widths or
diameters) that it is not an easy task to make them sufficiently strong to penetrate
the stratum corneum of skin without breaking. So there is a trade-off; one cannot
merely make the microneedles "thicker" (or wider), because there needs to be some
open area between each of the microneedles in the array to allow the tips of the microneedles
to actually penetrate the outer skin layer. This aspect of the use of microneedles
is described in detail in a patent application that is assigned to The Procter & Gamble
Company, under Serial No.
09/328,947 which was filed on June 9, 1999, and titled "Intracutaneous Microneedle Array Apparatus."
This patent application is incorporated herein by reference in its entirety.
[0067] At the same time, one cannot merely make the microneedles shorter to decrease the
chance of their being broken upon insertion into skin. The individual microneedles
should be longer than the thickness of the stratum corneum, or they will not sufficiently
increase the permeability of the skin to the fluid of interest. These constraints
call for a structure that is relatively high in aspect ratio in most instances (such
as 3:1, noted above).
[0068] Two different methodologies for fabricating hollow microneedles are illustrated in
Figures 5 and 6, and are described immediately below. "Figure 5" (which comprises
Figures 5A-5F) starts with a silicon wafer at 50 with a top layer of photoresist at
52 (see Figure 5A). One preferred methodology for creating this structure is to use
a spin-coating procedure to apply a layer of photoresist material that is in the range
of 20-200 microns thick on the silicon wafer 50. This structure is baked to dryness
at approximately 90°C, and then the photoresist 52 is patterned with hollow cylinders
by use of a photolithography procedure, which results in the structure of Figure 5B.
In Figure 5B, the photoresist material has been formed into multiple hollow tubes
at 54, in which each of these hollow tubes comprises a hollow cylinder having a wall
58 and an open hollow space at 56 within these walls 58.
[0069] The structure is then silanized with an alkyl chlorosiloxane compound, then covered
with PDMS under a vacuum, and cured in an oven in the range of 60-70°C for approximately
two hours in a soft lithography process step. This provides the structure seen in
Figure 5C, in which the PDMS layer is designated by the reference numeral 60.
[0070] The PDMS mold is separated from the photoresist master, thereby providing the structure
60 by itself, as seen in Figure 5D. This structure 60 will be used to obtain plastic
"microcups."
[0071] In Figure 5E, the PDMS mold 60 has been inverted with respect to Figure 5D. This
PDMS mold 60 is now filled with a prepolymer material 62, and this prepolymer is cured
with some type of heat energy or with electromagnetic radiation, such as ultraviolet
light in another soft lithography process step. Once cured, the prepolymer material
62 is detached from the mold 60, thereby leaving behind the structure 62 as seen in
Figure 5F. As can be seen in Figure 5F, polymeric microneedles are formed as part
of the structure 62, in which each of these microneedles has the form of a "microcup"
64. These microcups include an outer cylindrical wall 68 and a center open volume
66. Of course, these microcups could be made into "microtubes" or other type of hollow
microneedle by use of laser ablation, or by some other technique, if desired.
[0072] In the procedure illustrated in "Figure 5," the hollow microneedles or microcups
were formed using PDMS molds. As an alternative methodology for fabrication, photolithography
of a photoresist mounted on a substrate covered with a sacrificial film could be utilized,
as will now be discussed in reference to "Figure 6," which consists of Figures 6A-6E.
[0073] Starting with a silicon wafer 70, having a layer of either PDMS or silicon dioxide
material at 72, a layer of photoresist material 74 is applied, preferably by spin-coating.
This is the structure illustrated in Figure 6A. This structure is then baked to dryness
at approximately 90°C. If PDMS is used for layer 72, it could have a thickness of
approximately 100 microns, or if silicon oxide is used, its thickness could be much
smaller, on the order of 500 nm.
[0074] After being baked, the structure has the appearance as illustrated in Figure 6B,
in which the silicon wafer 70 and intermediate layer 72 is topped by a cured or "baked"
layer of photoresist at 76.
[0075] This structure is then coated again with a further layer of photoresist at 78, as
viewed in Figure 6C. This structure is then baked, and patterned with a transparency
mask using photolithography techniques. This provides the structure as viewed in Figure
6D, in which multiple hollow structures 82 are formed as part of an overall photoresist
layer 80. These hollow structures 82 are also in the form of "microcups," similar
to those disclosed in reference to Figure 5F.
[0076] The microcups 82 each have a cylindrical wall 86, as well as a hollow volumetric
space at 84 within the cylindrical walls 86. This microneedle or microcup array structure
80 can be readily detached from the substrate, thereby leaving behind the array structure
as viewed in Figure 6E. This could involve dissolving the sacrificial layer 72, which
if the sacrificial layer consisted of PDMS would involve TBAF (tetrabutylammonium
fluoride) in THF (tetrahydrofuran); if the sacrificial layer consisted of silicon
dioxide, then the dissolving fluid would be 10% hydrofluoric acid.
[0077] Wafers that have been coated with sacrificial layers can also be used to fabricate
hollow microtubes that can be easily detached from the base structure or substrate
of the microneedle array, upon the application of small forces. Such detachable hollow
microneedles or microtubes can be used to open momentary cavities across the stratum
corneum of the skin. These cavities are not permanent, due to the natural shedding
process of the stratum corneum. One methodology for constructing such detachable hollow
microtubes is illustrated in "Figure 7." "Figure 7" consists of Figures 7A-7B and
7X-7Z, but it will be understood that the first three steps of this procedure in Figures
7X-7Z involve the structures illustrated in Figures 3A, 3B, and 3C.
[0078] The structure illustrated in Figure 3C involves a silicon wafer 30, a layer 38 of
PDMS material that is baked to dryness. In Figure 3D, solid microneedles were formed
using a photolithography process. In Figure 7A, instead of solid microneedles, hollow
microtubes will be formed, and these structures are indicated at the reference numeral
90.
[0079] After the silicon wafer has been covered with PDMS and baked to dryness, photolithography
is used to make the hollow tubes 90. Each of these hollow microtubes consist of a
cylindrical wall portion 94, which encompasses an open volume 92. The microneedles
fabricated on the PDMS film (i.e., layer 32) do not need any type of treatment prior
to skin penetration, because the adhesion between PDMS and most polymers is relatively
weak. Therefore, the microneedles will fairly easily detach upon penetration into
the stratum corneum. This is illustrated on Figure 7B, in which the microtubes 90
are shown in place in the stratum corneum layer 100. The epidermis layer 102 and the
dermis layer 104 are also illustrated in Figure 7B, which of course lie beneath the
stratum corneum layer 100.
[0080] An alternative fabrication methodology would be to use a silicon wafer that has a
silicon oxide layer 42, such as that provided by the structure illustrated in Figure
4C. This alternative fabrication methodology is illustrated in "Figure 8," which consists
of Figures 8A-8D and 8X-8Z. It will be understood that the first three process steps
in Figures 8X-8Z involve structures having the appearance of Figures 4A, 4B, and 4C.
[0081] The structure of Figure 4C included a silicon wafer 30, a layer of silicon oxide
42, an upper layer of cured photoresist 36, and a second layer of photoresist at 38
that was baked to dryness. In Figure 4D, the photolithography process was used to
form solid microneedles. However, in Figure 8A, the transparency mask is used to create
hollow microneedles or "microtubes" by the same type of photolithography process.
[0082] In Figure 8A, the microtubes 90 are very similar in appearance to those illustrated
in Figure 7A. Each of the microtubes has a cylindrical outer wall 94 that encompasses
a hollow volumetric space 92.
[0083] In Figure 8B, an additional procedure of treating the "sacrificial layer" 42 with
hydrogen fluoride (at 10%) for approximately two (2) to five (5) minutes will weaken
the needle/substrate interface, as seen at the portion designated by the reference
numeral 96. In other words, the hydrogen fluoride treatment will tend to etch away
a certain portion of the silicon oxide layer, and leave behind "break away" portions
of the cylindrical walls that will facilitate the detachment of the hollow microtubes
upon skin penetration. A magnified view of the resulting microtube 98 having the "weakened"
(or "break-away") area 96 is provided on Figure 8D.
[0084] One structure that has been successfully tested involves a silicon oxide layer that
is approximately 500 nm in thickness, and covered with a photoresist material (e.g.,
SU-8) of about 20-200 microns that have been baked to dryness at 90°C. This will produce
hollow microtubes or microneedles that have a length in the range of about 20-200
microns.
[0085] Figure 8C shows the final result, in which the "break-away" hollow microneedles or
microtubes at 98 are embedded in the stratum corneum 100.
[0086] Metallic hollow microneedles can also be constructed using photolithography techniques.
Figures 9 and 10 illustrate some of the steps for two different methodologies of fabricating
metallic hollow microneedles. "Figure 9" consists of Figures 9A-9G while "Figure 10"
consists of Figures 10A-10G.
[0087] Figure 9A illustrates a silicon wafer 110 that has had a photoresist layer spin-coated
at 112. An example of photoresist material is SU-8, and the thickness of this material
could be in the range of 20-200 microns. The photoresist is then patterned with cylindrical
holes 116 using a photolithography process, thereby providing the structure in Figure
9B in which the silicon wafer 110 is now topped by a photoresist layer 114 that has
a plurality of such cylindrical holes 116. These holes could have a diameter in the
range of 20-100 microns, or virtually any other size, as desired for a particular
application.
[0088] This structure is now silanized and then covered with PDMS material that is cured
for about two hours at approximately 60-70°C in a soft lithography process step. The
resulting structure is illustrated in Figure 9C, in which the silicon wafer 110 and
photoresist layer 114 are topped by the cured PDMS 118.
[0089] The PDMS negative replica 118 is now removed or detached from the photoresist master,
leaving behind the unitary structure 118 that is illustrated in Figure 9D.
[0090] The PDMS mold negative replica 118 is now coated with a metallic substance using
sputtering or vapor deposition. This is illustrated in Figure 9E, in which the PDMS
material 118 is coated or plated with a metal layer at 120. One example of this metal
coating could be a layer of gold that is approximately 50 angstroms in thickness.
[0091] Another example is to use a layer of nickel, copper, gold, platinum, or silver having
a thickness in the range of 10-30 microns, by use of an electroplating procedure on
the previously coated gold/PDMS structure. This will form an array of metallic needles
that can be isolated by dissolving the PDMS layer in a 1 M solution of TBAF in THF,
thereby leaving the unitary structure 120 that is illustrated in Figure 9F.
[0092] The structure 120 is the separate metal layer that has been detached from the PDMS
mold. This structure 120 includes an array of protrusions at 122, each of which will
become the basis for a hollow microneedle or microtube. At this point in the process,
the microneedles 122 are essentially "closed" and have the form of "microcups" in
essence, when viewed from above. Of course, when viewed from below, these closed microneedles
122 essentially act as liquid tight microneedles that have the appearance of solid
microneedles.
[0093] These tubular microneedles 122 are now "opened" by polishing the closed ends by one
of several possible techniques, thereby leaving behind an array of hollow microneedles
in a unitary array structure 124 that is illustrated in Figure 9G. Each of the hollow
microneedles or "microtubes" 122 includes a cylindrical wall 128 that surrounds a
hollow volumetric space 126 that, in this illustrated embodiment, supplies a tubular
passageway or through-hole from one surface of the unitary structure 124 to the opposite
side of that same structure. The polishing technique described above could be as simple
as using sandpaper on the surface where the closed end 122 existed in Figure 9F, or
it could be some type of milling or grinding operation, or finally some non-mechanical
technique could be used, such as a laser beam to burn away or vaporize the closed
end by laser ablation.
[0094] The microneedle arrays could be separated by hand from the PDMS molds and the metallic
structures could be synthesized using electroless plating techniques. The molds could
be reused if the structures are disconnected by hand. Moreover, the polishing step
could be avoided if the tips of the PDMS/gold posts (at 122) were earlier stamped
with a non-conductive material such as thiol monolayer or a polymer, or were peeled
off using adhesive tape.
[0095] An alternative technique for creating metallic microneedles is illustrated in Figure
10. Starting at Figure 10A, a silicon wafer 110 that has had a photoresist layer spin-coated
at 112 is illustrated (similar to Figure 9A). An example of photoresist material is
SU-8, and the thickness of this material could be in the range of 20-200 microns.
The photoresist is then patterned with cylindrical holes 116 using a photolithography
process, thereby providing the structure in Figure 10B in which the silicon wafer
110 is now topped by a photoresist layer 114 that has a plurality of such cylindrical
holes 116. These holes could have a diameter in the range of 20-100 microns, or virtually
any other size, as desired for a particular application.
[0096] This structure is now silanized and then covered with PDMS material that is cured
for about two hours at approximately 60-70°C in a soft lithography process step. The
resulting structure is illustrated in Figure 10C, in which the silicon wafer 110 and
photoresist layer 114 are topped by the cured PDMS 118.
[0097] The PDMS negative replica 118 is now removed or detached from the photoresist master,
leaving behind the unitary structure 118 that is illustrated in Figure 10D. The PDMS
negative replica 118 of Figure 10D is now used in a vapor deposition procedure, and
then a procedure where polymer is electroplated. The vapor deposition could involve
chromium or gold, for example. This would lead to the structure 118 of Figure 10E,
in which the plated polymer layer is at 130.
[0098] This particular procedure could also be modified to construct tapered microneedles
by overexposing the photoresist master and then fabricate plastic hollow microneedles
by electrodepositing the polymers, such as the layer 130 of plated polymer material.
Such polymer materials that can be electroplated include POWECRON
Ⓡ acrylic epoxies (manufactured by PPG Industrial Coatings of Pittsburgh, Pennsylvania),
and EAGLE 2100
Ⓡ (manufactured by The Shipley Company of Marlboro, Massachusetts.
[0099] The polymer microneedles are separated from the PDMS mold, thereby leaving behind
the unitary structure 130 of Figure 10F. At this point, the projections that will
eventually become tubular microneedles are "closed," as viewed at 132 on Figure 10F.
Therefore, a procedure is performed to "open" the microneedles, by use of some type
of polishing technique, similar to that described above in reference to Figure 9G.
This provides the structure 134 illustrated in Figure 10G. The microneedle array structure
134 includes hollow microneedles or "microtubes," each of which consists of a cylindrical
wall 138 that encompasses an open volumetric space 136 that expends from one surface
to the other of the microneedle array 134.
[0100] "Figure 11" illustrates a fabrication technique by which microneedles are constructed
by curing polymers that are sandwiched between complimentary PDMS structures. "Figure
11" consists of Figures 11A-11K, and beginning at Figure 11A a silicon wafer 140 is
spin-coated with a photoresist material 142, such as SU-8. A second wafer 150 is also
spin-coated with a photoresist compound 152, as illustrated in Figure 11E. The photoresist
layer 142 thickness is approximately 175 microns for the wafer 140 of Figure 11A,
while the thickness of the photoresist layer 152 is approximately 200 microns on Figure
11E.
[0101] These structures are now patterned using a photolithography process, and an array
of holes are formed in the photoresist layer 142, which is illustrated on Figure 11B
by the holes 146, which are bounded by the remaining portions of the photoresist at
144. The separation of these holes is approximately 300 microns, and these cylindrical
holes have a height of about 175 microns, and a diameter of about 50 microns.
[0102] An array of posts 154 are formed from the photoresist 152 by use of patterning and
photolithography techniques, and these posts have a separation of approximately 300
microns with a height of approximately 200 microns and a diameter somewhat less than
50 microns. See Figure 11F. After the post 154 and holes 146 are formed on their respective
structures, both wafers are silanized, covered with PDMS or an equivalent material,
and cured at approximately 60°C for about two hours using soft lithography. This provides
the structures illustrated in Figures 11C and 11G, in which the PDMS layer 148 protrudes
into the "hole" spaces 146 that are between the photoresist structures 144, and the
PDMS layer 156 on Figure 11G, which surrounds the post 154.
[0103] The specimens are now cooled to room temperature, and the PDMS replicas are detached
from the wafers, thereby providing the structures 148 and 156, as illustrated in Figures
11D and 11H, respectively. One of these replica structures (preferably the structure
156 having the "holes") is now coated with a relatively thin layer of a prepolymer
material, such as polyurethane (PU), epoxy, polymethyl methacrylate (PMMA), bone suturing
materials, dental polymers, or other similar prepolymer compound. The two structures
148 and 156 are now aligned, in which the posts now resident in the structure 148
are aligned with the "holes" resident in the structure 156. The result is illustrated
in Figure 11I, in which the replica structure having "posts" 148 is fitted atop the
replica structure having the "holes" at 156, and in which the above prepolymer material
160 is placed between these two replica structures 148 and 156. Once they are aligned,
they are pressed, or held together, and cured as appropriate, using heat energy or
perhaps electromagnetic energy, such as ultraviolet light or visible light.
[0104] The two PDMS mold replicas 148 and 156 are now separated and the now cured polymer
material 160 is separated from both of these mold replicas. This provides the structure
illustrated in Figure 11J, in which the cured polymer array 160 consists of multiple
posts or protrusions at 162. These posts/protrusions 162 are not solid, but are hollow,
and have a form somewhat similar to a "microcup" as described above. As viewed from
above in Figure 11J, these protrusions would have the appearance of microcups, although
when viewed from below, they would have the appearance of solid posts or microneedles.
[0105] The purpose of this structure is not necessarily to create solid microneedles or
microcups, and therefore, the closed ends at 162 of these protrusions are opened by
some type of polishing procedure, thereby forming hollow microneedles or microtubes.
These microneedles/microtubes have cylindrical walls at 168 (see Figure 11K), and
the walls 168 surround an empty volumetric space, as illustrated at 166. The polishing
procedure could be simply the use of sandpaper, or a more sophisticated or automated
procedure using a milling machine or a grinder, for example.
CONVEX OR CONCAVE MICRONEEDLE ARRAYS
[0106] If desired, the mold material 156 of Figure 11G can be made of a material that has
flexibility characteristics. Such a flexible mold can then be used to form microneedle
arrays that are convex or concave in overall shape (i.e., the shape of their substrate).
Referring now to "Figure 16" (which comprises Figures 16A-16E), the original rectangular
shape of the mold 156 is illustrated in Figure 16A, along with a top mold plate 500
that is convex and a bottom mold plate 502 that is concave.
[0107] In Figure 16B, the two mold plates 500 and 502 are pressed against the flexible mold
156, which itself takes the overall shape of a concave structure (as seen from above
in this view). An open chamber at 504 is thereby created between the top microstructure
portions of the mold and the bottom surface of the top mold plate 500. A hole 506
in the top mold plate 500 can be used to place fluidic material (such as a molten
plastic or a prepolymer material) into this chamber 504.
[0108] The chamber 504 is now filled with a prepolymer material, such as polyurethane (PU),
epoxy, polymethyl methacrylate (PMMA), bone suturing materials, dental polymers, or
other similar prepolymer compound. Once the prepolymer material is in place, it is
cured as appropriate, using heat energy or perhaps electromagnetic energy, such as
ultraviolet light or visible light (one of the mold halves would have to be transparent
to the particular wavelength if curing via light). This is the configuration viewed
in Figure 16C.
[0109] Once cured, the mold plates 500 and 502 are separated to release the cured polymer
material, which has now become a convex microneedle array 510. The individual microneedles
are designated by the reference numeral 512, while the semi-circular substrate surface
between microneedles is designated by the reference number 514. The "inner" surface
516 of the substrate is essentially concave, and could be used to form a reservoir
to hold a liquid, if desired.
[0110] If the mold plates 500 and 502 are made in the opposite shapes—i.e., if the top mold
plate 500 was made in a concave shape and the bottom mold plate was made in a convex
shape—then the resulting microneedle array would also be in the opposite shape, i.e.,
an overall concave shape. This results in a microneedle array 520 that has the appearance
as illustrated in Figure 16E. The individual microneedles are designated by the reference
numeral 522, while the semi-circular substrate surface between microneedles is designated
by the reference number 524. The "outer" surface 526 of the substrate is essentially
convex.
[0111] The use of the above flexible mold has many advantages: a single microstructure mold
156 can be used to manufacture microneedle arrays that are of various circular arcuate
aspects. For example, two different convex shapes can be manufactured from the single
flexible mold 156, simply by using two different angled plates for the top and bottom
plates 500 and 502. Of course, concave shaped microneedles can also be made from the
same flexible mold 156, by use of two opposite shaped top and bottom plates (not shown).
POLYMERIC HOLLOW MICRONEEDLES
[0112] Polymeric hollow microneedles can be fabricated using multilayer photoresist masters,
as illustrated in "Figure 12," which consists of Figures 12A-12G. Starting at Figure
12A, a film 172 of a photoresist material such as SU-8 is spin-coated on a silicon
wafer 170, then baked to dryness at about 90°C. The thickness of the photoresist could
be in the range of 10-100 microns. This photoresist film 172 is then patterned with
cylindrical holes by use of photolithography, thereby resulting in an array of holes
having a diameter of about 10-100 microns, as illustrated in Figure 12B. The holes
are represented at the reference numerals 176, while the remaining photoresist film
is represented at 174, which bounds these holes 176.
[0113] This patterned wafer structure is now coated again with a second layer of photoresist
176, having a thickness of about 10-200 microns, or perhaps thicker if desired, resulting
in the structure illustrated in Figure 12C. The photoresist layer 176 is now patterned
with hollow cylinders that are centered on the holes of the bottom layer (originally
the film layer 172) using photolithography techniques.
[0114] This photoresist structure is now silanized, covered with polydimethylsiloxane (PDMS)
under a vacuum, and cured for about two hours in the range of 60-70°C. The resulting
structure is illustrated in Figure 12D, in which the final photoresist material has
the form of an array of hollow microneedles, and given the overall designation 180.
Each of the microneedles has an outer cylindrical wall at 184, which encompasses a
hollow cylindrical volume 182.
[0115] The PDMS material 180 is detached from the silicon/photoresist master at room temperature,
and now becomes a mold itself, which is filled with a prepolymer such as polyurethane
(PU), epoxy, polymethyl methacrylate (PMMA), bone suturing materials, or dental polymers.
This now has the form of the structure 190 on Figure 12E. As can be seen in Figure
12E, cylindrical "posts" at 192 are formed, which are surrounded by open areas 194,
which become a mold replica for forming microneedles that are hollow and cylindrical.
The PDMS mold replica also has relatively flat surfaces at 196 that will become the
substrate substantially flat surfaces between microneedle positions, and also has
a final "bottom" surface (as viewed on Figure 12E) at 198 that represents the deepest
portion of the cylindrical open areas 194.
[0116] Figure 12H provides a perspective view of this structure 190, in which the relatively
flat surface 196 represents the largest surface area as seen in this view. The cylindrical
posts that protrude the farthest are designated at the reference numerals 192, which
have the cylindrical outer channels 194 with a bottom surface at 198.
[0117] An embossing polymer is now placed on top of this surface, which will become the
actual microneedle structure after the embossing procedure has been completed. In
general, the embossing polymer would be squeezed against the PDMS mold replica 190,
although that may not be necessary in certain applications or by use of certain materials.
This results in a microneedle array structure 200, as illustrated in Figure 12F.
[0118] As an alternative to embossing, a prepolymer material could be placed against the
replica mold structure 190 and cured as appropriate (e.g., by use of heat energy or
electromagnetic energy, such as visible light or ultraviolet light) in a soft lithography
process; and after curing the microneedle array is separated from the mold 190. This
also results in a microneedle array structure 200, as illustrated in Figure 12F.
[0119] The microneedle array structure 200 consists of multiple microneedle structures 202,
each having a cylindrical wall at 206, which encompasses a cylindrical volumetric
space at 204. These microneedles are "closed" at this point, and take the overall
form of "microcups." The closed end portion of the microneedles is formed by the surface
208 of the array structure 200.
[0120] Since it may be desired to create hollow microneedles that have through-holes, the
closed portion 208 can be removed from the array structure, which then provides the
structure 210 illustrated on Figure 12G. These hollow microneedles or microtubes are
indicated at the reference numeral 212, and have outer cylindrical walls 216 which
encompass a through-hole of an open cylindrical shape at 214.
[0121] If the embossing procedure is to be used with a PDMS mold, such as that described
above, then the softening point of the polymer to be embossed should be less than
about 400°C to avoid any significant deformation of the PDMS microstructures of the
mold piece 190. Of course, if the mold was instead made of a metallic material, then
a much higher temperature embossing procedure and material could be used.
[0122] The mold structure 190 on Figure 12E can also be used to directly create hollow microneedles
without the need for a milling or grinding procedure to remove the closed portion
208, as seen on Figure 12F. Referring now to Figure 12I, the surface of the mold structure
190 is covered with an embossing polymer material at 220, and is squeezed under pressure
by a top plate (or top mold half) 230. The embossing polymer material is allowed to
harden or cure before the top mold half 230 is removed. Hollow cylindrical structures
are thereby formed in the embossing polymer material 220, in which the walls of the
cylinders are indicated at 222, and the internal openings at 224.
[0123] Figure 12J illustrates the molded material after the top mold half 230 is removed.
The new structure 220 continues to exhibit cylindrical openings which are now through-holes
at 224, each such hole having a cylindrical wall structure at 222. The holes 224 were
directly formed during the molding process because the top mold half 230 removed all
excess embossable material from the top of the posts 192 of the mold structure 190
(see Figure 12I).
[0124] It will be understood that the through-holes and associated wall structures could
have a shape other than cylindrical without departing from the principles of the present
invention. Certainly these hollow microneedles formed in the microneedle array structure
220 instead could be elliptical, square, rectangular, or edged in form.
ELECTROCHEMICAL SENSORS INSIDE MICRONEEDLES:
[0125] Macroscale glucose electrochemical sensors consisting of two electrodes immersed
in a conducting media composed of glucose oxidase, electrolytes, and hydrogel are
among the most reliable sugar detectors available. In such systems, glucose oxidase
converts sugar to carbon dioxide and hydrogen, and an electrical signal is generated
by the catalytic oxidation of hydrogen on the surface of a platinum electrode. Microneedle
devices that include electrodes can be used as electrochemical sensors, and also they
can be used for iontophoretic or electrophoretic delivery of drugs in interstitial
fluids. Fabrication techniques to create electrodes that are integrated with the microneedle
devices is described in detail below. Procedures for the construction of such microelectrodes
on the surface of metallic or polymeric microneedles is disclosed using vapor deposition
techniques.
[0126] "Figure 13" illustrates the fabrication processes and structural designs of such
microelectrodes in microneedle structures, and consists of Figures 13A-13J. In Figure
13A, a silicon wafer 300 has a spin-coating of photoresist 302, which could be SU-8
photoresist having a thickness of approximately 50 microns. The photoresist is patterned
with a structure illustrated in Figure 13D. One specific design is illustrated in
Figure 13D, in which the photoresist at 304 has dimensions provided on Figure 13,
and which appears on Figure 13B as an array of such patterned designs.
[0127] This patterning procedure preferably involves photolithography, after which the structure
is silanized. After that has occurred, the patterned wafer is covered with PDMS, pressed
against a flat surface such as a glass slide, then cured at about 60°C in a soft lithography
process step. The PDMS membrane is illustrated in Figure 13C after it has been removed
from the wafer, and is designated generally by the reference numeral 306. A single
structure having this shape is illustrated in Figure 13E, in which the PDMS membrane
306 has an open area of a shape as illustrated at 308.
[0128] The structure 306 represents holes or openings 308 in the PDMS membrane that will
be used as a mask during a metal vapor deposition procedure. The longitudinal portion
316 of this opening 308, in the relative center area of the pattern, is designed to
form two microelectrodes inside each microneedle. The larger rectangular segments
318 of the pattern 308 are utilized to construct electrically conductive pads 304
that will connect the microelectrodes to leads of an electrochemical analyzer. When
using the dimensions illustrated on Figure 13D, each of the pads 304 will have dimensions
of about 300 microns x 700 microns, and the longitudinal portion is represented by
a rectangular shape 316 having dimensions of about 25 microns by 300 microns.
[0129] An array 310 of polymeric or metallic microneedles is prepared, and forms a structure
as illustrated in Figure 13F, by which microneedles 312 protrude from one surface
of the array structure or substrate 310. If the microneedles are metallic, they can
be prepared using the fabrication techniques as described in reference to either Figures
9 or 10. If metallic microneedles are utilized, a thin film (of approximately 5-10
microns in thickness) of an insulating polymer is electroplated on the surfaces of
this array 310, thereby providing a structure as illustrated in Figure 13G which is
coated by an insulative layer of material. This will lead to a layer of insulative
coating at 314 on the microneedles themselves. Of course, if the microneedle array
structure 310 consists of an insulative material, then no additional polymer layer
is required.
[0130] The cured PDMS pattern 306 is now placed upon the planar face of the microneedle
structure 310 and the linear or longitudinal center portions 316 of each of the patterns
308 are aligned with each of the microneedle structures 314. This involves the PDMS
layer 306 being placed against the top surface of the microneedle array 310, as viewed
in Figure 13H. Once that has occurred, a metal vapor deposition procedure can commence,
while the structures are held in place by some type of clamp, tape, or temporary adhesive.
[0131] A layer of metal, such as gold or platinum, is then vapor deposited on the membrane/microneedle
structure in a thermal evaporator, after which the PDMS mask 306 is detached from
the microneedles, thereby forming a microneedle array structure 330, as illustrated
in Figure 13I. While in the thermal evaporator, the samples are held at about 30-45°C
with respect to the metal source to ensure the deposition of metal inside the microneedles.
The needles are filled with the conducting media described above (e.g., hydrogel,
electrolytes, or glucose oxidase) before they are used as glucose sensors. Each of
the resulting microneedles 314 protrudes from the planar substrate 310, and each of
these hollow microneedles 314 includes an electrode structure 320 that runs at least
part way down the inside cylindrical wall surface 322 of the microneedles 314. The
electrode structure 320 is electrically connected to a pad 306, as illustrated in
Figure 13I.
[0132] A more detailed view of this structure 330 is provided in Figure 13J, by which the
microneedle array 330 includes an upper planar surface or substrate 310, an electrically
conductive pad 306, an electrode 320 that is both connected to the pad 306 and runs
down the inside surface of the cylindrical wall 322 that forms the inner hollow surface
of the microneedle itself.
[0133] The fabrication of a PDMS mask and the vapor deposition of metallic material is not
necessary if the polymer to be electroplated is a photoresist. In this situation,
the electrodes and pads can be constructed by use of photolithography techniques.
Not only are very small electrode structures able to be constructed by photolithography,
but in addition larger electrode structures can be formed, also using photolithography.
Such an example is illustrated in Figure 14.
[0134] In Figure 14, electrode "bands" are formed on a microneedle array structure, rather
than using independent electrode systems for each microneedle as illustrated in Figure
13I. In Figure 14, a large number of microneedles 352 are formed on a microneedle
array 350. The top planar surface 354 shows that different materials can be applied
thereto. For example, a "working electrode" 360 can be formed on one portion of this
structure 350, and can encompass a number of the microneedles 352, including the inner
cylindrical hollow surfaces of these microneedles 352. A "counter electrode" 364 can
be formed in a different area, and can also encompass many such microneedle structures
352. Finally, a "reference electrode" 362 can be formed using a third set of microneedles
352. Each electrode area is electrically conductive between each of its individual
microneedles 352 by an electrically conductive metallic surface along the top of the
substrate at 354. Such electrode bands could alternatively be formed on the opposite
side of the microneedle array. In other words, electrode bands could be formed on
either the top or the bottom of the microneedle array 350 when hollow microneedles
are used.
[0135] On the other hand, solid microneedles could be used at 352, if desired. In that circumstance,
the solid structure 352 could have the form of cylindrical posts that are coated by
electrically conductive metal within the various bands 360, 362, or 364. If the microneedles
started as hollow structures, their inner diameters could be filled (or at least plugged)
by the metal of the electrode bands 360, 362, or 364.
[0136] Glucose sensors could also be formed using polymeric microneedles, as mentioned above.
The polymeric microneedles can be formed in the same manner as metallic microneedles,
in which the initial specimen is covered with a PDMS mask prepared as described in
reference to Figures 13A-13C. The electrodes can then be formed by metal vapor deposition
in a thermal evaporator, or perhaps in a sputtering machine.
[0137] Using the principles of the present invention, it is also possible to make a mold
insert that can create a microneedle having a sharp tip using photolithography techniques.
"Figure 15" illustrates some of the fabrication steps in such a procedure, in which
"Figure 15" consists of Figures 15A-15L. Starting with a silicon wafer 400 that has
a top layer 402 of either PDMS material or silicon oxide material, the wafer structure
is coated with a layer of photoresist 404. This layer 404 is baked to dryness and
then patterned using a transparency mask and an electromagnetic light source (such
as an ultraviolet light source) so as to create locally a relatively small cylindrical
hole, as seen at 410 in Figure 15B. In Figure 15B, the photoresist layer 404 is now
shown as two halves, at 406 and 408.
[0138] After this first photolithography step, a second layer of photoresist material 420
is now placed atop the structure, as viewed in Figure 15C. After this photoresist
420 has been baked to dryness, it is patterned using ultraviolet light and a transparency
mask to create locally another cylindrical opening that is somewhat larger than the
first one 410. This second cylindrical opening is designated by the reference numeral
426 on Figure 15D, and it can be seen as separating the photoresist material 420 into
two halves, 422 and 424. It will be understood that this Figure 15D is a cut-away
view, and the opening 426 is actually the further half (from the observer) of a cylindrical
inner wall, and therefore, the two "halves" 422 and 424 still make up a single layer
of photoresist material that has certain openings, such as the one at 426.
[0139] The next step after this second photolithography step is to again place a further
layer of photoresist material 430 atop the structure, thereby arriving at the structure
illustrated on Figure 15E. After this new layer of photoresist at 430 has been baked
to dryness, it is patterned using a light source and a transparency mask to create
locally a somewhat larger cylindrical hole, as seen at 436 on Figure 15F. The photoresist
layer 430 is now illustrated as consisting of two halves at 432 and 434, which are
indeed a single layer.
[0140] After this third photolithography step, still another layer of photoresist material
440 is placed atop this structure, as viewed in Figure 15G. In this example, the photoresist
layer 440 is much thicker than any of the earlier photoresist layers 404, 420, or
430.
[0141] After the photoresist layer 440 has been baked to dryness, it is patterned using
ultraviolet light and a transparency mask to create locally a still larger cylindrical
hole, as seen at 446 on Figure 15H. The photoresist layer 440 is now shown in two
halves at 442 and 444. It will be understood that certainly more than three intermediate
layers of photoresist material could be used to create a mold form, as compared to
that shown in Figure 15H.
[0142] In Figure 15I, the mold structure, generally designated by the reference numeral
450, has been separated from the silicon wafer 400 by dissolving or otherwise decomposing
the sacrificial layer 402 with an appropriate reagent. As noted above, PDMS can be
decomposed with TBAF, and silicon oxide or silicon dioxide can be immersed in hydrofluoric
acid to cause the detachment.
[0143] Figure 15J shows several of the holes 446 as part of an array of such holes in the
total mold structure 450. Certainly, for any practical microneedle array mold, there
would be dozens if not hundreds or thousands of such holes 446 as part of the mold
structure 450 in its entirety.
[0144] Now that the mold 450 has been fabricated, microneedles can be formed by use of injection
molding, embossing, or some other type of microfabrication technique, even including
microcasting if it is desirable to create metallic microneedles (although different
materials would have to be used). Figure 15K shows an arrangement where a plastic
structure generally designated at the reference numeral 460 is placed between two
mold halves 470 and 472, which act as pressure bases, and also retain the plastic
material 460 within the mold cavities that are available in contact with the patterned
mold 450. As can be seen in Figure 15K, the plastic material 460 will flow into the
shaped holes 446 that were created in this mold structure 450. Once detached from
the mold, an array of microneedles is formed, generally designated by the reference
numeral 460. Array 460 includes multiple "sharp" microneedles 462, as viewed in Figure
15L. As noted above, these "sharp tip" microneedles could be of various sizes and
shapes, and certainly could be created from more than three stages of photoresist
layers being patterned by use of photolithography techniques, without departing from
the principles of the present invention.
[0145] One optional variant in the microneedles described above is to create a structure
in which the base material is different from the microneedle structure material, which
allows the designer freedom to create hydrophobic-hydrophilic combinations. Examples
of such different types of materials are as follows: glass, mica, Teflon®, and metalized
surfaces.
[0146] It will be understood that all of the microneedle structures described above can
be of any length or width, or any inner diameter for hollow microneedles or microcups,
without departing from the principles of the present invention. Certain exemplary
dimensions have been disclosed above, but these are only examples of prototypical
units. It will also be understood that the microneedles (both solid and hollow) could
be constructed of various shapes other than cylinders, such as elliptical profiles,
or "edged" microneedles, such as disclosed in a patent application that is assigned
to The Procter & Gamble Company, under Serial No.
09/580,780) which was filed on May 26, 2000, and titled "Intracutaneous Edged Microneedle Apparatus."
This patent application is incorporated herein by reference in its entirety.
[0147] It will be further understood that the chemical compounds disclosed above are exemplary
for certain prototypical microneedles, and as such are quite useful, but at the same
time other compounds might easily be employed without departing from the principles
of the present invention. For example, the substrate does not always need to be silicon,
and the sacrificial layer is not always required to be either PDMS or silicon oxide.
Certainly other polymers or plastics could be used than disclosed above, or other
metals.
[0148] Another alternative embodiment of the microneedle structures described above is to
change their properties by a "surface modification" treatment which allows a coating
to occur at the molecular level. To effect this treatment, the silicon needles can
be silanized with reagents to derivatize the surfaces. Typically, such coating would
occur after the microneedles are already formed.
[0149] Yet another alternative embodiment would be a plasma treatment of epoxy or other
types of polymeric microneedles to impart different surface properties. Again, such
treatment would typically occur after the microneedles have been formed. One such
different surface properties could be to impart hydrophobic/hydrophilic properties
to the microneedles.
[0150] Still another alternative embodiment of the microneedles of the present invention
is to incorporate carbon fibers or other composite materials into epoxy or polymeric
needles and perhaps the substrate. The use of harder materials could reinforce the
polymeric needles and make them more rigid. One example would be to add carbon fibers
or composite materials into a photoresist compound, such as that illustrated in Figure
3A at 34. This would lead to the microneedles at the microneedle array 40 in Figure
3D to be more rigid. The entire microneedle structure could be hardened, if desired,
by incorporating carbon fibers or other composite materials into all of the materials
used to manufacture the structure, including the base or substrate.
[0151] As an alternative to the above, the substrate materials utilized in creating the
microneedles of the present invention could be made more flexible, although it normally
would be preferred to keep the microneedles themselves as a rigid structure. One methodology
for creating substrates that are more flexible is to add microchannels and grooves
to the substrate, thereby making the fairly rigid material have some "bendability"
while not being prone to fracture.
[0152] Another alternative "flexible" embodiment is to create more flexible microneedles
themselves, in which the microneedle structures would be sufficiently rigid to break
the skin, but still have some flexibility that would be quite useful for continuous
sensing and dispensing systems. This would be the opposite of the break-away microneedles
disclosed above, for example in Figures 8B and 8C. These flexible microneedles would
be achieved by using materials such as elastomers and polyurethanes that are moldable
or embossable. Examples of such elastomers are silicones.
[0153] Yet another alternative "flexible" embodiment is to create a microneedle structure
in which the entire structure is at least somewhat flexible, although the flexibility
properties of the needles could be different than the flexibility properties of the
base. An example of this is where the needles, or at least their tips, are made of
a first material (having a first flexibility or elasticity property) and the base/substrate
is made of a second material (having a second flexibility or elasticity property).
For example, the base/substrate could be made of nylon while the microneedles are
made of silicone or polyurethane, thereby providing a microneedle array that has a
barely flexible base/substrate but a much more flexible set of needles.
[0154] A further alternative embodiment for the microneedles of the present invention is
to place a final outer layer of a metal coating over the microneedle structures. For
solid microneedles, this would have the appearance as viewed in Figure 9E, which illustrates
plated metal over a PDMS replica that itself could become a microneedle array. Such
a structure has the advantage of fairly quick manufacturing, while remaining accurate
at the microstructure level and while having the surface properties of a structure
formed entirely from metal. The thickness of the outer metal coating can be controlled
by a vapor deposition or electroplating process.
[0155] Several different processes can be used to coat microstructures with metal layers.
The most common techniques are electroplating (or electrodeposition), electroless
plating, sputtering, vapor deposition, and plasma deposition. In an electroplating
process, a conductive sample is used as the cathode (or the anode for electrooxidation
reactions) of an electrochemical system that contains ions of the metal that will
be deposited on the substrate (e.g., Ni, Cu, Ag, Au, Pb, Sn, Al or Pt).
[0156] It is also possible to electroplate some alloys (e.g., Pb/Sn, bronze, or steel),
metal oxides (e.g., titanium or aluminum oxides), and polymers (e.g., polyphenols
or polypyrroles). Depending on the material that is electroplated, the plating solution
can be aqueous (e.g., Ni, Cu, Ag, Au, Pb, Sn, or Pt) or organic (e.g., polymers, Al,
or titanium oxides) and may contain stabilizers, brighteners, and wetting agents.
In many instances, electroplating allows the formation of crystalline films as thick
as 1-2 millimeters. If the sample to be electroplated is not electrically conductive,
it must be coated with a thin film of a conductive material (e.g. metals or conductive
polymers) prior to immersion in the electrochemical cell.
[0157] Electroless plating can be used to deposit metal, oxides, or polymers on virtually
any kind of substrates. In this case, the sample is cleaned using organic solvents
(e.g., acetone or methanol) and/or mineral acids (e.g., hydrofluoric or nitric acid),
activated for metal deposition using a metallization catalyst (e.g., palladium chloride),
and immersed in a solution including electron donor species (e.g., phosphate ions)
and the material that is going to be plated. The thickness of the electroless plated
films can range from a several angstroms to a few millimeters and is affected by the
pH of the plating solution, time of reaction, and concentration of the chemicals involved
in the deposition process.
[0158] Sputtering can only be used to deposit thin metal films (from angstroms to nanometers)
on either conductive or non-conductive substrates. In the sputtering instrument, gas
ions (e.g., Ar) are used to vaporize the atoms of a metal source (e.g., Au, Pt, Cr,
Ag, or Cu) that are then directed towards the sample surface for deposition using
an electric field. Sputtering is a fast (e.g., taking only a few minutes) and inexpensive
technique that is convenient to coat non-conductive samples with seed metal layers
for a later step of electroplating, including the fabrication of microelectrodes (employing
a mask, such as the mask 306 in Figure 13H), provided that there is good adhesion
between the metal film and the substrate.
[0159] Vapor deposition is preferred over sputtering in the cases where microsmooth metal
and oxide films are desired (having a coating thickness on the order of angstroms
or nanometers) or when common metals (e.g., Au, Ag, Al, or Cu) do not adhere strongly
to the substrates. For vapor deposition, the sample are placed in a vacuum chamber
where the metals are evaporated using resistive heating or an electron beam. The metal
vapors deposit on the cold areas of the vacuum chamber, including the sample surface.
Usually, the specimens are coated with a few angstroms of a metal adhesion layer (e.g.,
Cr or Ti) prior to the deposition of the metal or oxide or interest. This process
is generally completed in one or two hours and is employed for the fabrication of
electrodes, seed layers for electroplating processes, and the deposition of thin layers
of metal on three dimensional samples (in which the sample can be rotated at an angle
in the vacuum chamber).
[0160] Plasma deposition is a technique that can be employed to deposit very thin films
(having a thickness in the order of angstroms) of several kinds of materials (e.g.,
organic compounds, polymers, oxides, or metal precursors) on conductive or non-conductive
substrates. This process is slow and expensive. It is normally utilized to prepare
films of materials that cannot be handled using the methodologies mentioned above.
EXTERNAL CHANNEL MICRONEEDLES
[0161] Solid microneedles can be manufactured with external channels running along one or
more sides of the elongated walls. For example, Figure 17 illustrates a solid microneedle
600 that has a elongated side wall 610 and a top surface 612 at its tip. The length
of the microneedle is designated by the dimension line 614, which could be in the
range of 100-500 microns.
[0162] An external channel 620 is formed in one side of the wall 610. The channel 620 is
substantially rectangular in profile in this view, and could have dimensions (at 622
and 624, respectively) of about 10 microns by 10 microns. Of course, the channel 620
could be of other dimensions, if desired. Channels can also be made to taper so as
to increase capillary driving forces.
[0163] The external channel 620 is preferably in communication with another channel 632
that is in the base structure 630 of the microneedle array. This base channel 632
could be used to transport interstitial fluid, for example, to a sensor device 640.
This sensor device could be electrochemical or optical in nature, or perhaps could
use a different principle of operation.
[0164] Groups of solid microneedles having external channels could be formed of a single
microneedle array. On Figure 18, four such solid microneedles are illustrated at the
reference numerals 650, 652, 654, and 656. Their corresponding external channels are
designated by the reference numerals 660, 662, 664, and 666, respectively. Note that
each microneedle has two such external channels on Figure 18.
[0165] Some of the external channels are fluidically joined by channels in the base structure
690. These base channels are designated by the reference numerals 670, 672, 674, and
676, respectively. All four of the base channels 670, 672, 674, and 676 meet at a
"collection port" 680, which could be a through-hole in the microneedle base structure
(or substrate) 690. Such collection ports could be located anywhere on the base 690,
and the illustrated embodiment of Figure 18 is merely an exemplary situation where
four such microneedles are grouped to a single collection port. Moreover, there could
be an individual collection port per microneedle, if desired; such paired microneedles
and collection ports would typically be located proximal to one another.
[0166] The fluid that traverses the base channels 670, 672, 674, and 676 and external microneedle
channels 660, 662, 664, and 666 could be traveling in either direction. If sampling
interstitial fluid, for example, then the collection ports would likely lead to a
chamber or reservoir that will either have an associated sensing apparatus, or will
trap the fluid for later use or measurement. If dispensing a fluid, for example, the
collection ports would be in fluidic communication with a reservoir that contains
the drug or active that is to be placed through the outer skin layer.
[0167] The foregoing description of a preferred embodiment of the invention has been presented
for purposes of illustration and descrippion. It is not intended to be exhaustive
or to limit the invention to the precise form disclosed. Obvious modifications or
variations are possible in light of the above teachings. The embodiment was chosen
and described in order to best illustrate the principles of the invention and its
practical application to thereby enable one of ordinary skill in the art to best utilize
the invention in various embodiments and with various modifications as are suited
to the particular use contemplated. It is intended that the scope of the invention
be defined by the claims appended hereto.
1. A method for fabricating microneedles, said method comprising:
(a) providing a substrate (10, 20, 30) that includes a plurality of microstructures;
(b) coating said substrate with a layer of a first moldable material (16, 22, 32)
that takes the negative form of said plurality of microstructures, and hardening said
first moldable material;
(c) separating said hardened first moldable material from said substrate, thereby
creating a micromold from said hardened first moldable material containing said plurality
of microstructures; and
(d) applying a second moldable material (18, 24) onto said micromold, allowing said
second moldable material to harden using a soft lithography procedure, then separating
said hardened second moldable material from said micromold, thereby creating a microneedle
structure from said hardened second moldable material having the three-dimensional
negative form of said plurality of microstructures of the patterned micromold.
2. The method as recited in claim 1, wherein said microneedle structure comprises one
of: (a) a plurality of solid protrusions, (b) a plurality of hollow protrusions forming
through-holes, (c) a plurality of hollow protrusions forming microcups that do not
extend entirely through said hardened second moldable material, or (d) a plurality
of solid protrusions, each having at least one surface external channel.
3. The method as recited in claim 1, wherein said first moldable material comprises PDMS,
said second moldable material comprises a prepolymer, and said substrate comprises
one of silicon or a metallic substance; and wherein said microneedle structure comprises
a polymeric material.
4. The method as recited in claim 1, wherein said first moldable material is processed
and hardened by a second soft lithography procedure.
5. The method as recited in claim 1, further comprising:
providing a second substrate that includes a second plurality of microstructures,
wherein said second plurality of microstructures is substantially complementary in
shape as compared to said first plurality of microstructures;
coating said second substrate with a layer of a third moldable material that takes
the negative form of said second plurality of microstructures, and hardening said
third moldable material;
separating said hardened third moldable material from said second substrate, thereby
creating a second micromold from said hardened third moldable material containing
said second plurality of microstructures;
applying a fourth moldable material onto said second micromold, allowing said fourth
moldable material to harden using a soft lithography procedure,
then separating said hardened fourth moldable material from said second micromold,
thereby creating a second microneedle structure from said hardened fourth moldable
material having the three-dimensional negative form of said second plurality of microstructures
of the patterned second micromold; and
applying a layer of a fifth moldable material upon one of said first or second microneedle
structures, placing said first and second microneedle structure into a face-to-face
relationship to thereby sandwich said layer of fifth moldable material therebetween,
allowing said layer of fifth moldable material to harden using a soft lithography
procedure, then separating said hardened fifth moldable material from both said first
and second microneedle structures, thereby creating a third microneedle structure
from said hardened fifth moldable material having the three-dimensional negative form
of both said first and second microneedle structures.
6. The method as recited in claim 5, wherein said first and third moldable materials
comprise PDMS, said second and fourth moldable materials comprise a prepolymer, said
substrate comprises one of silicon or a metallic substance, and said fifth moldable
material comprises a prepolymer; and wherein said first, second, and third microneedle
structures each comprises a polymeric material.
7. The method as recited in claim 1, wherein said first moldable material after hardening
exhibits a flexibility characteristic and, therefore, can be deformed to a predetermined
extent without breaking; and further comprising: after creating said micromold from
said hardened, flexible first moldable material, deforming said micromold during the
step of applying the second moldable material onto said micromold, thereby creating
either a concave or convex micromold.
8. The method as recited in claim 1, wherein said substrate that includes a plurality
of microstructures is constructed by a method comprising the steps of:
providing a base substrate material;
coating said base substrate material with at least one layer of a photoresist material,
and patterning said photoresist material with a plurality of microstructures by use
of a photolithography procedure.
9. The method as recited in claim 8, wherein said base substrate material comprises silicon,
said photoresist material comprises SU-8, said first moldable material comprises PDMS,
and said second moldable material comprises a prepolymer; and wherein said microneedle
structure comprises a polymeric material.
10. The method as recited in claim 8, further comprising separating said patterned photoresist
material from said base substrate material, thereby creating a substrate that includes
a plurality of microstructures from said patterned photoresist material containing
said plurality of microstructures.
11. The method as recited in claim 8, wherein said photoresist material comprises a first
layer and a second layer, said first layer being cured before said second layer is
applied, and said second layer being patterned by said photolithography procedure.
12. The method as recited in claim 10, further comprising: applying a layer of acid-dessolvable
material between said base substrate and said photoresist material at the commencement
of said method, and during said step of separating the patterned photoresist material
from the substrate, dissolving said acid-dissolvable material as a sacrificial layer.
13. The method as recited in claim 12, wherein said substrate comprises one of a silicon
or a metallic substance, said photoresist material comprises SU-8, and said acid-dissolvable
material comprises one of PDMS or silicon oxide.
14. The method as recited in claim 12 or 13, further comprising: creating break-away microneedles
by briefly etching a portion of said plurality of microstructures proximal to a junction
between a base structure and protrusions of the patterned photoresist material containing
said plurality of microstructures, said base structure and said microstructure protrusions
both being constructed of said photoresist material.
15. The method as recited in claim 10, wherein said photoresist material comprises at
least two individual layers, a first of said at least two individual layers being
patterned with a first plurality of openings that are of a first size, a second of
said at least two individual layers being patterned with a second plurality of openings
that are of a second size that is larger than said openings of said first size, said
first and second plurality of openings being substantially in alignment with one another;
and after said separation of the substrate from the patterned photoresist material,
said plurality of microstructures comprises a plurality of microneedles having sharp
tips.
16. The method as recited in claim 1 or 8, wherein said microneedle structure comprises
a plurality of individual microneedles that have an aspect ratio of at least 3:1.
17. The method as recited in claim 1, further comprising: coating said at least one surface
of said substrate that includes a plurality of microstructures, separate hardened
first moldable material, or microneedle structure by use of one of the following procedures:
(a) electroplating, (b) electrodeposition, (c) electroless plating, (d) sputtering,
(e) vapor deposition, or (f) plasma deposition; thereby creating an independent microstructure
layer.
18. The method as recited in claim 17, wherein said independent microstructure layer protects
and strengthens the surface to which it is applied, and wherein said independent microstructure
layer comprises one of: an electroplated metal or an electroplated polymer.
19. The method as recited in claim 17, further comprising: separating said independent
microstructure layer from the surface to which it is applied, thereby creating a microneedle
array structure that entirely comprises said microstructure layer made of at least
one of: an electroplated metal, an electroplated polymer, or an electroplated composite
material.
20. The method as recited in claim 8, wherein said base substrate material comprises silicon,
said photoresist material comprises SU-8, and said first moldable material comprises
PDMS.
21. The method as recited in claim 2, further comprising a polishing or grinding procedure
to open one end of said plurality of microcups, thereby creating a plurality of hollow
protrusions forming through-holes.
22. The method as recited in claim 1, wherein said second moldable material comprises
a polymeric material that softens at a temperature less than the softening temperature
of said first moldable material.
23. The method as recited in claim 1, wherein during the step of applying said second
moldable material onto said micromold, pressure is applied by use of a second mold
half to remove excess uncured material from the furthest extending microstructures,
thereby creating through-holes in said microneedle structure upon separation of said
microneedle structure from said micromold.
24. The method of claim 1, further comprising
positioning a mask proximal to said microneedle structure and applying an electrically
conductive substance through said mask onto a surface of said microneedle array structure,
thereby creating at least one pattern of electrically conductive pathways on said
surface.
25. The method as recited in claim 24, wherein said electrically conductive pathways each
are sized and positioned so as to cover an area upon said surface that is larger than
a spacing between at least two of the microneedles: of said microneedle structure,
thereby creating at least one electrode band.
26. The method as recited in claim 24, wherein said electrically conductive pathways each
are sized and positioned so as to cover an area upon said surface that is smaller
than each of said plurality of individual protrusions, thereby creating a plurality
of electrically isolated electrodes, such that at least one such electrode corresponds
to a single one of the microneedles of said microneedle structure.
27. The method as recited in claim 26, wherein said at least one of the microneedles of
said microneedle structure comprises a hollow microneedle, and said at least one of
the electrically isolated electrodes comprises a pad surface and a longitudinal segment,
said longitudinal segment extending into an inner surface of said hollow microneedle
by way of a vapor deposition procedure.
28. The method as recited in claim 1, further comprising: hardening a tip of a plurality
of microneedles of said microneedle structure.
29. The method as recited in claim 28, wherein said tip is hardened by adding carbon fibers,
or by adding a composite material.
1. Verfahren zur Herstellung von Mikronadeln, wobei das Verfahren aufweist
a) Bereitstellen eines Substrats (10. 20, 30), das eine Mehrzahl von Mikrostrukturen
enthält;
b) Beschichten des Substrats mit einer Schicht aus einem ersten formbaren Material
(16. 22, 32), das die Negativform der Mehrzahl von Mikrostrukturen annimmt, und Härten
des ersten formbaren Materials:
c) Trennen des gehärteten ersten formbaren Materials von dem Substrat unter Erzeugung
einer Mikroform aus dem gehärteten ersten formbaren Material, die die Mehrzahl von
Mikrostrukturen enthält; und
d) Aufbringen eines zweiten formbaren Materials (18, 24) auf die Mikroform, Härten-Lassen
des zweiten formbaren Materials unter Verwendung eines Weichlithografie-Verfahrens,
dann Trennen des gehärteten zweiten formbaren Materials von der Mikroform unter Erzeugung
einer Mikronadelstruktur aus dem gehärteten zweiten formbaren Material mit der dreidimensionalen
Negativform der Mehrzahl von Mikrostrukturen der strukturierten Mikroform.
2. Verfahren wie in Anspruch 1 angegeben, bei dem die Mikronadelstruktur eine der folgenden
Strukturen aufweist: (a) eine Mehrzahl kompakter Vorsprünge, (b) eine Mehrzahl hohler
Vorsprünge, die durchgehende Löcher bilden, (c) eine Mehrzahl hohler Vorsprünge, die
Mikrobecher bilden, die sich nicht völlig durch das gehärtete zweite formbare Material
verstrecken, oder (d) eine Mehrzahl kompakter Vorsprünge, von denen jeder mindestens
einen Außenoberflächenkanal hat.
3. Verfahren wie in Anspruch 1 angegeben, bei dem das erste formbare Material PDMS aufweist,
das zweite formbare Material ein Präpolymer aufweist, und das Substrat Silicium oder
eine metallische Substanz aufweist; und bei dem die Mikronadelstruktur ein polymeres
Material aufweist.
4. Verfahren wie in Anspruch 1 angegeben, bei dem das erste formbare Material mittels
eines zweiten Weichlithografie-Verfahrens bearbeitet und gehärtet wird.
5. Verfahren wie in Anspruch 1 angegeben, bei dem das Basissubstratmaterial Silicium
aufweist, das Fotoresistmaterial SU-8 aufweist, das erste formbare Material PDMS aufweist,
und das zweite formbare Material ein Präpolymer aufweist; und bei dem die Mikronadelstruktur
ein polymeres Material aufweist.
6. Verfahren wie in Anspruch 1 angegeben, außerdem aufweisend:
Bereitstellen eines zweiten Substrats, das eine zweite Mehrzahl von Mikrostrukturen
enthält, wobei die zweite Mehrzahl von Mikrostrukturen im Vergleich zu der ersten
Mehrzahl von Mikrostrukturen hinsichtlich der Form im Wesentlichen komplementär ist.;
Beschichten des zweiten Substrats mit einer Schicht aus einem dritten formbaren Material,
das die Negativform der zweiten Mehrzahl von Mikrostrukturen annimmt, und Härten des
dritten formbaren Materials:
Trennen des gehärteten dritten formbaren Materials von dem zweiten Substrat unter
Erzeugung einer zweiten Mikroform aus dem gehärteten dritten formbaren Material, die
die zweite Mehrzahl von Mikrostrukturen enthält;
Aufbringen eines vierten formbaren Materials auf die zweite Mikroform. Härten-Lassen
des vierten formbaren Materials unter Verwendung eines Weichlithografie-Verfahrens,
dann Trennen des gehärteten vierten formbaren Materials von der zweiten Mikroform
unter Erzeugung einer zweiten Mikronadelstruktur aus dem gehärteten vierten formbaren
Material mit der dreidimensionalen Negativform der zweiten Mehrzahl von Mikrostrukturen
der strukturierten zweiten Mikroform; und
Auftragen einer Schicht aus einem fünften formbaren Material auf die erste oder die
zweite Mikronadelstruktur, Bringen der ersten und der zweiten Mikronadelstruktur in
eine zueinander weisende Beziehung, um dadurch mit der Schicht aus fünftem formbaren Material dazwischen ein Sandwich zu bilden,
Härten-Lassen der Schicht aus fünftem formbaren Material unter Verwendung eines Weichlithografie-Verfahrens,
dann Trennen des gehärteten fünften formbaren Materials sowohl von der ersten als
auch der zweiten Mikronadelstruktur unter Erzeugung einer dritten Mikronadelstruktur
aus dem gehärteten fünften formbaren Material mit der dreidimensionalen Negativform
von sowohl der ersten als auch der zweiten Mikronadelstruktur.
7. Verfahren wie in Anspruch 6 angegeben, bei dem das erste und das dritte formbare Material
PDMS aufweist, das zweite und das vierte formbare Material ein Präpolymer aufweist,
das Substrat Silicium oder eine metallische Substanz aufweist, und das fünfte formbare
Material ein Präpolymer aufweist; und bei dem die erste, zweite und dritte Mikronadelstruktur
jeweils ein polymeres Material aufweist.
8. Verfahren wie in Anspruch 1 angegeben, bei dem das erste formbare Material nach dem
Härten eine Siegsamkeitseigenschaft aufweist und daher in einem vorbestimmten Ausmaß
verformt werden kann, ohne zu brechen; und das au-Lierdem aufweist nach der Erzeugung
der Mikroform aus dem gehärteten, biegsamen ersten formbaren Material, ein Verformen
der Mikroform während des Schritts des Aufbringens des zweiten formbaren Materials
auf die Mikroform unter Erzeugung entweder einer konkaven oder einer konvexen Mikroform.
9. Verfahren wie in Anspruch 1 angegeben, bei dem das Substrat, das eine Mehrzahl von
Mikrostrukturen enthält, durch ein Verfahren aufgebaut wird, das folgende Schritte
aufweist:
Bereitstellen eines Basissubstratmaterials:
Beschichten des Basissubstratmaterials mit mindestens einer Schicht aus einem Fotoresistmaterial,
und Strukturieren des Fotoresistmaterials mit einer Mehrzahl von Mikrostrukturen unter
Verwendung eines Fotollthografie-Verfahrens.
10. Verfahren wie in Anspruch 9 angegeben, außerdem aufweisend das Trennen des strukturierten
Fotoresistmaterials von dem Baslssubstratmaterial unter Erzeugung eines Substrats,
das eine Mehrzahl von Mikrostrukturen enthält, aus dem strukturierten, die Mehrzahl
von Mikrostrukturen enthaltenden Fotoresistmaterial.
11. Verfahren wie in Anspruch 9 angegeben, bei dem das Fotoresistmaterial eine erste Schicht
und eine zweite Schicht aufweist, wobei die erste Schicht vor dem Aufbringen der zweiten
Schicht gehärtet wird, und wobei die zweite Schicht durch das Fotolithografie-Verfahren
strukturiert wird.
12. Verfahren wie in Anspruch 10 angegeben, außerdem aufweisend: Aufbringen einer Schicht
aus säurelöslichem Material zwischen dem Basissubstrat und dem Fotoresistmaterial
zu Beginn des Verfahrens, und Auflösen des säurelöslichen Materials als eine Opferschicht
während des Schritts des Trennens des strukturierten Fotoresistmaterials von dem Substrat.
13. Verfahren wie in Anspruch 12 angegeben, bei dem das Substrat Silicium oder eine metallische
Substanz aufweist, das Fotoresistmaterial SU-8 aufweist, und das säurelösliche Material
PDMS oder Siliciumoxid aufweist
14. Verfahren wie in Anspruch 12 oder 13 angegeben, außerdem aufweisend: Erzeugen von
Wegbrech-Mikronadeln durch kurzes Ätzen eines Bereichs der Mehrzahl von Mikrostrukturen
proximal zu einem Übergang zwischen einer Basisstruktur und Vorsprüngen des strukturierten
Fotoresistmaterials, das die Mehrzahl von Mikrostrukturen enthält, wobei die Basisstruktur
und die Mikrostruktur-Vorsprünge beide aus dem Fotorasistmaterial aufgebaut sind.
15. Verfahren wie in Anspruch 10 angegeben, bei dem das Fotoresistmaterial mindestens
zwei Einzelschichten aufweist, wobei eine erste der mindestens zwei Einzelschichten
mit einer ersten Mehrzahl von Öffnungen, die von einer ersten Größe sind, strukturiert
wird, eine zweite der mindestens zwei Einzelschichten mit einer zweiten Mehrzahl von
Öffnungen, die von einer zweiten Größe sind, die größer als die Öffnungen der ersten
Größe ist, strukturiert wird, wobei die erste und die zweite Mehrzahl von Öffnungen
im Wesentlichen miteinander fluchtend sind; und bei dem die Mehrzahl von Mikrostrukturen
nach der Trennung des Substrats von dem strukturierten Fotoresistmaterial eine Mehrzahl
von Mikronadeln mit scharfen Spitzen aufweist.
16. Verfahren wie in Anspruch 1 oder 9 angegeben, bei dem die Mikronadelstruktur eine
Mehrzahl von Einzel-Mikronadeln aufweist, die ein Höhe-Breite-Verhältnis von mindestens
3:1 haben.
17. Verfahren wie in Anspruch 1 angegeben, außerdem aufweisend: Beschichten der mindestens
einen Oberfläche des Substrats, das eine Mehrzahl von Mikrostrukturen enthält, Abtrennen
des gehärteten ersten formbaren Materials oder der Mikronadelstruktur durch Verwendung
eines der folgenden Verfahren: (a) Elektroplattieren, (b) elektrolytische Abscheidung,
(c) außenstromloses Plattieren, (d) Sputtern, (e) Dampfabscheidung oder (f) Plasmaabscheidung;
unter Erzeugung einer unabhängigen Mikrostrukturschicht.
18. Verfahren wie in Anspruch 17 angegeben, bei dem die unabhängige Mikrostrukturschicht
die Oberfläche, auf die sie aufgebracht wird, schützt und festigt, und bei dem die
unabhängige Mikrostrukturschicht ein elektroplattiertes Metall oder ein elektroplattiertes
Polymer aufweist.
19. Verfahren wie in Anspruch 17 angegeben, außerdem aufweisend: Trennen der unabhängigen
Mikrostrukturschicht von der Oberfläche, auf die sie aufgebracht ist, unter Erzeugung
einer Mikronadelanordnungs-Struktur, die die Mikrostrukturschicht, die aus mindestens
einem der folgenden Materialien hergestellt ist: einem elektroplattierten Metall,
einem elektroplattierten Polymer oder einem elektroplattierten Verbundmaterial, vollständig
enthält.
20. Verfahren wie in Anspruch 9 angegeben, bei dem das Basissubstratmaterial silicium
aufweist, das Fotoresistmaterial SU-8 aufweist und das erste formbare Material PDMS
aufweist.
21. Verfahren wie in Anspruch 2 angegeben, außerdem aufweisend ein Polierverfahren oder
Schleifverfahren zur Öffnung eines Endes der Mehrzahl von Mikrobechern unter Erzeugung
einer Mehrzahl von hohlen Vorsprüngen, die durchgehende Löcher bilden.
22. Verfahren wie in Anspruch 1 angegeben, bei dem das zweite formbare Material ein polymeres
Material aufweist, das bei einer geringeren Temperatur als der Erweichungstemperatur
des ersten formbaren Materials erweicht.
23. Verfahren wie in Anspruch 1 angegeben, bei dem während des Schritts des Aufbringens
des zweiten formbaren Materials auf die Mikroform durch Verwendung einer zweiten Formhälfte
Druck angewendet wird, um überschüssiges ungehärtetes Material von den sich am weitesten
erstreckenden Mikrostrukturen zu entfernen, wodurch beim Trennen der Mikronadelstruktur
von der Mikroform durchgehende Löcher in der Mikronadelstruktur erzeugt werden.
24. Verfahren nach Anspruch 1, außerdem aufweisend
Anbringen einer Maske proximal zu der Mikronadelstruktur, und Aufbringen einer elektrisch
leitfähigen Substanz durch die Maske auf eine Oberfläche der Mikronadelanordnungs-Struktur
unter Erzeugung mindestens einer Struktur elektrisch leitfähiger Wege auf der Oberfläche.
25. Verfahren wie in Anspruch 24 angegeben, bei dem die elektrisch leitfähigen Wege jeweils
so bemessen und angebracht sind, dass sie einen Bereich auf der Oberfläche bedecken,
der größer ist als ein Abstand zwischen mindestens zwei der Mikronadeln der Mikronadelstruktur,
wodurch mindestens ein Elektrodenband erzeugt wird.
26. Verfahren wie in Anspruch 24 angegeben, bei dem die elektrisch leitfähigen Wege jeweils
so bemessen und angebracht sind, dass sie einen Bereich auf der Oberfläche bedecken,
der kleiner ist als jeder der Mehrzahl von Einzel-Vorsprüngen, wodurch eine Mehrzahl
elektrisch isolierter Elektrode dergestalt erzeugt wird, dass einer einzigen der Mikronadeln
der Mikronadelstruktur mindestens eine derartige Elektrode entspricht.
27. Verfahren wie in Anspruch 26 angegeben, bei dem die mindestens eine der Mikronadeln
der Mikronadelstruktur eine hohle Mikronadel aufweist, und die mindestens eine der
elektrisch isolierten Elektroden eine Auflageoberfläche und ein längliches Segment
aufweist, wobei sich das längliche Segment mittels eines Dampfabscheidungsverfahrens
in eine Innenoberfäche der hohlen Mikronadel erstreckt.
28. Verfahren wie in Anspruch 1 angegeben, außerdem aufweisend: Härten einer Spitze einer
Mehrzahl von Mikronadeln der Mikronadelstruktur.
29. Verfahren wie In Anspruch 28 angegeben, bei dem die Spitze durch Zugabe von Kohlenstofffasern
oder durch Zugabe eines Verhundmaterials gehärtet wird.
1. Méthode pour fabriquer des microaiguilles, comprenant les étapes qui consistent :
(a) à fournir un substrat (10, 20, 30) qui présente plusieurs microstructures ;
(b) à revêtir le substrat d'une couche d'une première matière moulable (16, 22, 32)
qui prend la forme négative des microstructures, et à faire durcir cette première
matière moulable ;
(c) à séparer la première matière moulable du substrat, une fois durcie, ce qui crée
à partir de cette première matière moulable durcie un micromoule qui contient les
microstructures :
(d) et à appliquer une seconde matière moulable (18, 24) sur le micromoule, à permettre
à cette seconde matière de durcir à l'aide d'une opération de lithographie douce,
puis à séparer ladite seconde matière moulable du micromoule, une fois durcie, ce
qui crée à partir de cette seconde matière moulable durcie une structure de microaiguilles
qui a la forme négative tridimensionnelle des microstructures du micromoule à dessins.
2. Méthode selon la revendication 1, selon laquelle la structure de microaiguilles comprend
:
(a) plusieurs saillies pleines,
(b) ou plusieurs saillies creuses qui forment des trous traversants,
(c) ou plusieurs saillies creuses formant des microgodets qui ne traversent pas entièrement
la seconde matière moulable durcie,
(d) ou plusieurs saillies pleines qui présentent chacune un conduit extérieur de surface.
3. Méthode selon la revendication 1, selon laquelle la première matière moulable comprend
du PDMS, la seconde matière moulable comprend un prépolymère et le substrat comprend
une substance de silicone ou métallique ; et selon laquelle la structure de microaiguilles
comprend une matière polymère.
4. Méthode selon la revendication 1, selon laquelle la première matière moulable est
traitée et durcie grâce à une seconde opération de lithographie douce.
5. Méthode selon la revendication 9, selon laquelle la matière de substrat de base comprend
du silicone, la matière de photorésist comprend du SU-8, la première matière moulable
comprend du PDMS et la seconde matière moulable comprend un prépolymère ; et selon
laquelle la structure de microaiguilles comprend une matière polymère.
6. Méthode selon la revendication 1, comprenant également les étapes qui consistent :
à fournir un second substrat qui présente plusieurs secondes microstructures, ces
secondes microstructures étant globalement complémentaires, par leur forme, par rapport
aux premières ;
à revêtir le second substrat d'une couche d'une troisième matière moulable qui prend
la forme négative des secondes microstructures, et à faire durcir la troisième matière
moulable ;
à séparer la troisième matière moulable du second substrat, une fois durcie, ce qui
crée à partir de ladite troisième matière moulable durcie un second micromoule qui
contient les secondes microstructures ;
à appliquer une quatrième matière moulable sur le second micromoule, à permettre à
cette quatrième matière moulable de durcir à l'aide d'une opération de lithographie
douce, puis à séparer ladite quatrième matière moulable du second micromoule, une
fois durcie, ce qui crée à partir de cette quatrième matière moulable durcie une seconde
structure de microaiguilles qui a la forme négative tridimensionnelle des secondes
microstructures du micromoule à dessins ; et
à appliquer une couche d'une cinquième matière moulable sur la première ou la seconde
structure de microaiguilles, à placer la première et la seconde structure de microaiguilles
face à face, avec entre les deux, en sandwich, la couche de cinquième matière moulable,
à permettre à ladite cinquième couche de matière moulable de durcir à l'aide d'une
opération de lithographie douche, puis à séparer la cinquième matière moulable des
première et seconde structures de microaiguilles, une fois durcie, ce qui crée à partir
de la cinquième matière moulable durcie une troisième structure de microaiguilles
qui présente la forme négative tridimensionnelle à la fois de la première et de la
seconde structure de microaiguilles.
7. Méthode selon la revendication 6, selon laquelle les première et troisième matières
moulables comprennent du PDMS, les deuxième et quatrième matières moulables comprennent
un prépolymère, le substrat comprend une substance de silicone ou métallique, et la
cinquième matière moulable comprend un prépolymère ; et selon laquelle les première,
deuxième et troisième structures de microaiguilles comprennent chacune une matière
polymère.
8. Méthode selon la revendication 1, selon laquelle la première matière moulable, une
fois durcie, présente une caractéristique de flexibilité et peut par conséquent être
déformée jusqu'à un degré prédéterminé, sans se casser ; et qui comprend également
l'étape qui consiste, après la création du micromoule à partir de la première matière
moulable flexible durcie, à déformer ce micromoule pendant l'étape de l'application
de la seconde matière moulable sur le micromoule, ce qui crée un micromoule concave
ou convexe.
9. Méthode selon la revendication 1, selon laquelle le substrat qui comprend plusieurs
microstructures est construit à l'aide d'une méthode comprenant les étapes qui consistent
:
à fournir une matière de substrat de base ;
à revêtir cette matière de substrat de base d'au moins une couche de matière photorésist
et à dessiner sur la matière photorésist plusieurs microstructures à l'aide d'une
opération de photolithographie.
10. Méthode selon la revendication 9, comprenant également l'étape qui consiste à séparer
la matière photorésist à dessins de la matière de substrat de base, ce qui crée un
substrat comprenant plusieurs microstructures à partir de ladite matière photoresist
à dessins contenant plusieurs microstructures.
11. Méthode selon la revendication 9, selon laquelle la matière photorésist comprend une
première et une seconde couche, la première couche étant cuite avant l'application
de la seconde, et la seconde couche étant pourvue d'un dessin à l'aide de l'opération
de photolithographie.
12. Méthode selon la revendication 10, comprenant également les étapes qui consistent
: à appliquer une couche de matière soluble dans l'acide entre le substrat de base
et la matière photorésist, au début de ladite méthode, et pendant l'étape de séparation
de la matière photorésist à dessins du substrat, à dissoudre ladite matière soluble
dans l'acide, comme couche sacrificielle.
13. Méthode selon la revendication 12, selon laquelle le substrat comprend une substance
de silicone ou métallique, la matière photorésist comprend du SU-8 et la matière soluble
dans l'acide comprend du PDMS ou un oxyde de silicium.
14. Méthode selon la revendication 12 ou 13, comprenant également l'étape qui consiste
: à créer des microaiguilles à détacher, en gravant brièvement une partie des microstructures
située près d'une jonction entre une structure de base et les saillies de la matière
photorésist à dessins contenant les mircrostructures, la structure de base et les
saillies des microstructures se compostant de ladite matière photorésist.
15. Méthode selon la revendication 10, selon laquelle la matière photorésist comprend
au moins deux couches individuelles, une première couche portant le dessin de premières
ouvertures qui ont une première taille, une deuxième couche portant le dessin de secondes
ouvertures qui ont une seconde taille plus grande que celle des premières ouvertures,
les premières et secondes ouvertures étant globalement alignées ; et après la séparation
du substrat et de la matière photorésist à dessins, les microstructures comprennent
plusieurs microaiguilles présentant des extrémités pointues.
16. Méthode selon la revendication 1 ou 9, selon laquelle la structure de microaiguilles
comprend plusieurs microaiguilles individuelles qui ont un rapport de forme d'au moins
3:1.
17. Méthode selon la revendication 1, comprenant également l'étape qui consiste : à revêtir
la ou les surfaces du substrat présentant plusieurs microstructures, une première
matière moulable durcie séparée ou une structure de microaiguilles, à l'aide de l'une
des opérations suivantes : (a) galvanoplastie, (b) dépôt électrolytique, (c) dépôt
chimique, (d) pulvérisation cathodique, (e) dépôt en phase vapeur ou (f) dépôt par
plasma ; ce qui crée une couche à microstructure indépendante.
18. Méthode selon la revendication 17, selon laquelle la couche de microstructure indépendante
protège et renforce la surface sur laquelle elle est appliquée, et selon laquelle
la couche de microstructure indépendante comprend : un métal déposé par galvanoplastie
ou un polymère déposé par galvanoplastie.
19. Méthode selon la revendication 17, comprenant également l'étape qui consiste à séparer
la couche de microstructure indépendante de la surface sur laquelle elle est appliquée,
ce qui crée une structure formant un ensemble de microaiguilles qui comprend entièrement
la couche de microstructure composée de l'une au moins des matières suivantes : métal
déposé par galvanoplastie, polymère déposé par galvanoplastie ou matière composite
déposée par galvanoplastie.
20. Méthode selon la revendication 9, selon laquelle la matière de substrat de base comprend
du silicone, la matière de photorésist comprend du SU-8 et la première matière moulable
comprend du PDMS.
21. Méthode selon la revendication 2, comprenant également une opération de polissage
ou de meulage pour ouvrir une extrémité des microgodets, ce qui crée plusieurs saillies
creuses formant des trous traversants.
22. Méthode selon la revendication 1, selon laquelle la seconde matière moulable comprend
une matière polymère qui ramollit à une température inférieure à la température de
ramollissement de la première matière moulable.
23. Méthode selon la revendication 1, selon laquelle pendant l'étape d'application de
la seconde matière moulable sur le micromoule, une pression est appliquée à l'aide
d'une seconde moitié de moule pour débarrasser les microstructures les plus éloignées
de l'excédent de matière non cuite, ce qui crée des trous traversants dans la structure
de microaiguilles, lors de la séparation de la structure de microaiguilles du micromoule.
24. Méthode selon la revendication 1, comprenant également l'étape qui consiste à placer
un masque près de la structure de microaiguilles et à appliquer une substance conductrice
d'électricité, par l'intermédiaire du masque, sur une surface de la structure formant
un ensemble de microaiguilles, ce qui crée sur ladite surface au moins un dessin de
pistes conductrices d'électricité.
25. Méthode selon la revendication 24, selon laquelle chacune des pistes conductrices
d'électricité est dimensionnée et positionnée de manière à couvrir une zone au-dessus
de la surface qui est supérieure à un écartement entre au moins deux des microaiguilles
de la structure de microaiguilles, ce qui crée au moins une bande d'électrode.
26. Méthode selon la revendication 24, selon laquelle chacune des pistes conductrices
d'électricité est dimensionnée et positionnée de manière à couvrir une zone au-dessus
de la surface qui est plus petite que chacune des saillies individuelles, ce qui crée
plusieurs électrodes isolées électriquement, de telle sorte que l'une au moins de
ces électrodes corresponde à une seule microaiguille de la structure de microaiguilles.
27. Méthode selon la revendication 26, selon laquelle la ou les microaiguilles de la structure
de microaiguilles comprennent une microaiguille creuse, et la ou les électrodes isolées
électriquement comprennent une surface formant plaquette et un segment longitudinal,
le segment longitudinal s'étendant dans une surface intérieure de la microaiguille
creuse grâce à une opération de dépôt en phase vapeur.
28. Méthode selon la revendication 1, comprenant également l'étape qui consiste : à durcir
une point de plusieurs microaiguilles de la structure de microaiguilles.
29. Méthode selon la revendication 28, selon laquelle ladite pointe est durcie grâce à
l'adjonction de fibres de carbone ou grâce à l'adjonction d'une matière composite.