[0001] The present invention relates to flexible, hollow devices, particularly microneedles
or hollow cantilevers with complex tip shape and integrated force sensor, and methods
of manufacture and uses thereof.
[0002] Micropipette-based technologies represent still today the simplest approach for cell
injections and manipulations in general. Most techniques for the fabrication of micopipettes
are low throughput and rely on heating and pulling principles. They are limited to
tubular and straight tips and are therefore not compatible with the realization of
tips with complex geometries such as comers, high curvature and several cm in length.
Furthermore, conventional micropipettes are usually fabricated of brittle materials
(e.g. glass).
[0003] A further technology targeting single-cell applications evolved from the Atomic Force
Microscopy (AFM) technology. Integrating a microchannel into an AFM cantilever allowed
broadening the spectrum of AFM applications in liquid towards a force-controlled nanopipette
enabling novel range of applications such as controlled spatial manipulation, local
injection and dispensing, selective and massive force spectroscopy, and serial perturbation
experiments.
[0004] AFM cantilevers are usually made of silicon or silicon nitride, which exhibit high
Young's moduli (190 and 385 GPa, respectively). For biological applications, cantilevers
are mostly operating in liquid environment with contact mode where a low spring constant
is desirable to be less invasive on fragile biomaterials. Replacing silicon by soft
polymeric material would allow higher sensitivity for the same considered channel
and cantilever thicknesses. On the other hand, thicker channel and cantilever dimensions
could potentially enable a larger range of microfluidic applications with similar
force detection sensitivity to conventional silicon-based AFM cantilevers.
[0005] SU-8 (IBM) is known as the negative-tone photoresist with the highest available epoxide
functionality for its eight epoxy sites per monomer component. Thanks to the strongly
cross-linked nature of this photoplastic material, SU-8 exhibits important mechanical
stability as well as chemical resistance to a multitude of solutions, which makes
it a good candidate for robust microfluidic systems. SU-8 does not only present advantages
in terms of surface chemistry with the possibility of multiple surface functionalisations
but also, physical surface modification by laser or plasma treatment among others.
[0006] Furthermore, the SU-8 presents other interesting features: low Young's modulus of
4.5 GPa, transparent material, ease to tailor the thickness down to 500 nm simply
by spin-coating, and high aspect-ratio structuring (> 18). Finally, SU-8 can be also
directly photo patterned allowing complex designs and potential mass fabrication.
After optimization of a working fabrication process, it is rather simple to adapt
the design of the device directly by changing the photolithography masks. If one takes
into account the formula for the spring constant of a cantilever, geometrical dimensions
of the cantilever contribute more to the final stiffness in the case of SU-8 because
of its lower Young's Modulus compared to silicon. This provides the possibility for
the fabrication of devices with a wider spectrum of spring constants on the same wafer.
[0007] First polymer-based AFM cantilevers were fabricated in 1999 by means of a simple
batch process where the integrated tip and the lever were obtained in one photolithography
step (IBM). They showed a resolution comparable to that of standard silicon cantilevers.
Later on, polymer-based cantilevers were used as highly sensitive stress sensors.
[0008] In addition, for a gentle single-cell patterning by a micropipette or a hollow cantilever,
the use of a force sensor within or at the micropipette or the hollow cantilever is
advantageous to avoid the application of too excessice forces on the single cell.
Similarly for single-cell injection, a force sensor can help to rupture gently the
membrane, maximizing therefore the rate of cell recovery. However, most force sensors
are based on laser reflective methods, which are therefore invasive and non-usable
in surgical environment.
[0009] Based on this background it is the objective of the present invention to provide
flexible hollow micropipettes or cantilevers that are particularly suitable for manipulating
microscopic objects, particularly single cells, in the submicrometer range, as well
as methods for making those.
[0010] The objective is attained by the subject matter of the independent claims. Preferred
embodiments of the invention are further specified in the dependent claims and described
below.
[0011] The present invention is particularly based on the on the novel concept that metal
may be used as sacrifial filling material in a photolithographic process using photoresists
for the manufacturing of devices in the micrometer scale with microfludic channels.
Furthermore, the concept of fabricating a thick hollow needle layer-by-layer, from
a side to another, is newly introduced. Thereby, it is possible to provide new designs
of flexible hollow needles that particularly overcome the limitations of glass micropipettes
in terms of tip geometry, fluidic robustness and fabrication throughput.
[0012] According to a first aspect of the invention, a method for manufacturing a device
comprising a flexible shank is provided, wherein the shank comprises a microfluidic
channel and an aperture, which is in fluid communication with microfluidic channel.
[0013] The method comprises the steps of:
- providing a support covered by a sacrificial release layer;
- depositing a bottom layer of a first photoresist onto said sacrificial release layer;
- partially curing the bottom layer within a first defined pattern, thereby yielding
a bottomside or a first sidewall of the device comprising the flexible shank, wherein
the bottomside optionally comprises the aperture;
- depositing a metal seed layer onto the bottom layer, and particularly onto the sacrificial
layer not covered by the bottom layer;
- depositing a mould layer of a second photoresist onto the metal seed layer,
- curing the mould layer within a second defined pattern, thereby yielding a cured mould
layer, wherein a part of the metal seed layer covering the bottom layer is not covered
by the cured mould layer, and the cured mould layer forms the mould that later defines
the microfluidic channel and optionally the aperture and/or a reservoir in fluid communication
with the microfluidic channel;
- depositing an additional metal layer onto the part of the metal seed layer not covered
by the cured mould layer, whereby particularly the additional metal layer defines
the space of the microfluidic channel, and optionally of the aperture and/or of the
reservoir in fluid communication to the microfluidic channel;
- dissolving the second photoresist or the mould layer, and the metal seed layer;
- depositing a cover layer of the first photoresist onto the bottom layer and the additional
copper layer;
- completely curing the first photoresist comprised within the cover layer and the bottom
layer within a third defined pattern, thereby forming sidewalls and a topside of the
device or a bottomside, a second sidewall opposite to the first sidewall and a topside
of the device, whereby the topside or the second sidewall opionally comprises an opening,
the cover layer merge with the bottom layer such that at least one part of the first
photoresist delimiting the microfluidic channel is integrally formed in one piece,
and the bottomside, the sidewalls and the topside embrace the additional metal layer
optionally with the exception of the opening or the aperture;
- dissolving the additional metal layer yielding the microfluidic channel and optionally
the aperture and/or the reservoir, wherein optionally the opening comprised within
the topside or the second sidewall of the device is in fluid communication with the
microfluidic channel, or optionally with the reservoir; and
- dissolving the sacrificial release layer releasing the device from the support.
[0014] Advantageously, the method of the invention enables the access to new designs of
flexible hollow needles, whose tip can be made of a complex shape by mass production.
By the method of the invention, a high throughput fabrication of needles with complex
tip shape (corners or high curvature) is enabled, on the contrary of individually
made glass micropipettes. The fabrication relies on a layer-by-layer photolithography
process where bottom or side layer, channel and top or second side layer are accordingly
patterned in a three-step protocol.
[0015] Advantageously, the device of the invention may be produced with the method of the
invention from bottom to top or it may be fabricated sideways from a side to another.
The sideways fabrication offers more possibilities to get a sharp tip with high curvature,
e.g. for single-cell injection or for biopsy-like applications.
[0016] The term "shank" in the context of the present specification particularly refers
to a structural element that houses a microfluidic channel and an aperture being in
fluidic communication with the microfluidic channel. The shank may be designed as
a beam of a hollow cantilever or a shank of a micropipette.
[0017] The term "photoresists" in the context of the present specification particularly
refers to a viscous composition essentially consisting of, or comprising, a species
of photoreactively polymerisable or depolymerisable compounds, and optionally comprising
a solvent, wherein particularly the viscous composition is characterized by a viscosity
of at least 100 cSt (centi Stokes), for example in range of 100 cSt to 500 cSt or
10,000 cSt to 60,000 cSt.
[0018] Such photoreactive compounds may polymerise or be cross-linked upon light expore,
such as the monomers comprised within a negative photoresists. Such photoreactive
compound may also depolymerise upon light exposure, for example by cleavage of cross-link
bondings, such as compounds comprised within a positive photoresist.
[0019] The term "curing" is used in the context of the present specification in the meaning
known to the skilled person. It particularly refers to the process of solidifying
of the above-mentioned photoresists or the above-mentioned visous composition by means
of light exposure (triggering cross-linking reactions) and/or heat (for evaporating
a solvent optionally present in the photoresists or the viscous composition). Curing
may also comprise the post-exposure bake, developing by contacting the cured photoresists
with a solvent such as propylene glycol monomethyl ether acetate, and rising with
an organic solvent such as isopropanol or acetone, thereby removing unpolymerised
photoresists. In case of a negative photoresist, a post exposure bake may be important
to complete the photo-activation process.
[0020] Furthermore, "curing within a defined pattern" means in the context of the present
specification that the photoresist layer is exposed to light (particularly light in
the ultraviolet region) within the defined pattern resulting in polymerization of
the photoresist within the pattern, in case of a negative photoresist, or in case
of a positive photoresist in depolymerisation of the photoresist within the pattern
and curing of the photoresist outside of the pattern.
[0021] The term "partly curing" in the context of the present specification particularly
means that the respective photoresist layer is cured in such a manner that only a
fraction of the photoresist is cured, or in other words, that part of the photoresist
monomers remains reactive for further polymerisation. Avantageously, a partly cured
photoresists layer may be connected with another photoresist layer such that both
layer are integrally formed in one piece.
[0022] Particularly, such partly curing of the bottom layer may be achieved by limited light
exposure and/ or reduced baking time of the bottom layer.
[0023] By forming the part of the device of the invention delimiting the microfluidic channel
intergrally in one piece, the microfluidic channel is characterized by complete tightness
or perfect sealing while applying pressure to the channel, particularly up to 6 bar.
Additionally, the integrally one-piece design of the device avoids problems such as
delamination of the device or adhesion issues.
[0024] In certain embodiments, the first photoresist comprised within the partly cured bottom
layer and the cover layer is completely cured such that at least a part of the cured
photoresist delimiting the microfluidic channel exhibits a homogenous structure.
[0025] The above-mentioned metal seed layer has the advantage that the metal seed layer
effectively separates the partly cured bottom layer of the device from the mould layer,
thereby avoiding undesired interaction between the aforementioned layers. Additionally,
in case of the bottom layer in made of a negative photoresist and the mould layer
is made of a positive photoresist, the bottom layer is shielded by the metal seed
layer from light exposure during the curing of the mould layer, thereby avoiding complete
curing of the bottom layer.
[0026] An advantage of using the metal layer as sacrifical filing body that later defines
the microfluidic channel and optionally the aperture and/or the reservoir is that
the deposition of the additionally metal layer can be performed under conditions,
under which a complete curing of the bottom layer can be avoided, in contrast to the
use of, for example, expoxy or polydimethylglutaridimide as sacrifical filing material,
wherein the high temperatures being applied to evaporate the solubilizing solvent
can lead to an undesired complete curing of the bottom layer. Additionally, the additional
metal layer does not exhibit any undesired interactions with the first photoresist
and is furthermore easily removable. Particularly, the metal doesn't dissolve into
the freshly spin-coated cover photoresist, which may comprise a solvent, particularly
when the photoresist layer hasn't undergone baking until complete solvent evaporation.
Without the additional metal layer, the freshly spin-coated mould layer may directly
dissolve the patterned and only partly cured bottom layer.
[0027] Alternatively, instead of metal any material, for example a viscous ink or a liquid
plastic, may be used as sacricial filling body that does not interact with the first
photoresist and optionally can be cured under condition that avoids complete curing
of the bottom layer and/or shields the bottom layer form light exposure during curing
of the mould layer and/or is easily removable.
[0028] Particularly, the mould layer is cured such under such conditions that a complete
curing of the bottom layer is avoided, e.g. by reducing the baking time of the mould
layer.
[0029] Particularly, the second defined pattern defines the shape of mould that later defines
the shape and space of the microfluidic channel and optionally of the aperture and/or
of the reservoir.
[0030] In certain embodiments, the first defined pattern defines the shape of the bottomside
of the device of the invention and optionally the position and size of the aperture.
In certain embodiments, the first defined pattern defines the shape of a first sidewall
of the device of the invention.
[0031] In certain embodiments, the third defined pattern defines the shape of the topside
of the device of the invention and optionally the position and size of an opening
in the topside. In certain embodiments, the third defined pattern defines the shape
of a second sidewall opposite to the first sidewall of the device of the invention
and optionally the position and size of an opening in the second sidewall.
[0032] In certain embodiments, the third defined pattern is identical to the first defined
pattern, optionally with the exception of the opening comprised within the topside
or second sidewall of the device of the invention.
[0033] In certain embodiments, the first photoresist is a negative photoresist. Non-limiting
examples for negative photoresists include SU-8 and phenol formaldehyde resins (CAS
Nr. 9003-35-4) such as Novolac.
[0034] In certain embodiment, the second photoresist is a positive photoresist. Non-limiting
examples for positive photoresists include AZ 4620 AZ 4533, AZ 4562, and PMMA.
[0035] In certain embodiments, a handling block layer or a handling block is attached onto
the cover layer, the topside or the second sidewall of the device of the invention,
wherein the handling block layer or the handling block comprises a through hole that
is in fluid communication with the microchannel. Particularly, the handling block
layer or the handling block is attached to a part of the topside or second sidewall
of the device that does not comprise the flexible shank. In certain embodiments, the
through hole in the handling block layer or the handling block has the same diameter
as the opening in the topside or the second sidewall. In certain embodiments, the
handling block layer or the handling block is characterized by a thickness in the
range of 100 µm to 300 µm. In some embodiments, the handling block layer is characterized
by a thickness of 250 µm.
[0036] In certain embodiments, the handling block layer consists of or comprises the first
photoresist, is deposited onto the top layer, and the handling block layer is cured.
In this case, the cover layer may be only partly cured before deposition of the handling
block layer, and after deposition of the handling block layer, the first photoresit
comprised within bottom layer, the cover layer and the handling block layer is completely
cured such the device is integrally formed in one piece.
[0037] In certain embodiments, the bottom layer is characterized by a thickness in the range
of 0.5 µm to 100 µm. In certain embodiments, the bottom layer is characterized by
a thickness in the range of 4 µm to 10 µm. In certain embodiments, the bottom layer
is characterized by a thickness in the range of 5 µm.
[0038] In certain embodiments, the cover layer is characterized by a thickness in the range
of 0.5 µm to 100 µm. In certain embodiments, the cover layer is characterized by a
thickness in the range of 5 µm to 12 µm. In certain embodiments, the cover layer is
characterized by a thickness of 7 µm. The aforementioned thickness of the cover layer
particularly refers to the thickness of the part of the coverlayer covering the additional
metal layer.
[0039] In certain embodiments, the additional metal layer is characterized by a thickness
in the range of 0.1 µm to 50 µm. In certain embodiments, the additional metal layer
is characterized by a thickness in the range of 0.5 µm to 23 µm. In certain embodiments,
the additional metal layer is characterized by a thickness of 3 µm.
[0040] Alternatively, thicker channels may be manufactured using the method of the invention
for a different range of applications e.g. 3D printing, dispensing of micro-objects
such as single cells, or robust patch clamping.
[0041] In certain embodiments, the sacrificial release layer characterized by a thickness
in the range of 5 nm to 500 nm. In certain embodiments, the sacrificial release layer
characterized by a thickness in the range of 5 nm to 150 nm. In certain embodiments,
the metal seed layer is characterized by a thickness of 150 nm.
[0042] In certain embodiments, the metal seed layer consisits of or comprises a metal selected
from the group comprised of copper, aluminium, chromium, gold, silver, platinum, and
zinc. In certain embodiments, the additional metal layer consists of or comprises
a metal selected from the group comprised of copper, aluminium, chromium, gold, silver,
platinum, and zinc.
[0043] In certain embodiments, the support is formed by a silicon wafer.
[0044] In certain embodiments, the sacrificial layer comprises a bottom sacrificial layer,
a top sacrificial layer and optionally a sacrificial interlayer, wherein the top sacrificial
layer is removed within the first defined pattern, particularly by etching, before
the bottom layer is deposited onto the sacrifical layer. In certain embodiments, areas
of the sacrificial layer lying outside of the first defined pattern are coated with
a protective layer, particularly a cured photoresist, areas not coated by the protective
layer are contacted with an etchant solution, and the protective layer is removed
after etching. In certain embodiments, the top sacrifical layer and/or the bottom
consit of or comprise chromium. In certain embodiments, the sacrifical interlayer
consists of or comprises gold.
[0045] In certain embodiments, the bottom layer is deposited by spin coating. In certain
embodiments, the mould layer is deposited by spin coating. In certain embodiments,
the cover layer is deposited by spin coating.
[0046] In certain embodiments, the metal seed layer is deposited by thermal evaporation,
particularly at low current for low UV radiation. In certain embodiments, the metal
seed layer is deposited with an emission current of below 5 A, particulary below 1
A, more particular at 0.5 A.
[0047] In certain embodiments, the additional metal layer is electrochemically deposited
in a bath comprising a solution with the respective metal ions, such as, for example,
copper sulphate in case of the additional metal layer consist or comprises copper,
accompanied by the application of a current.
[0048] In certain embodiments, the bottom layer and the cover layer are cured such with
the first defined pattern and the third defines pattern, respectively, that the shaft
of the device comprises a tip that extends along a first direction. In certain embodiments,
the angle between the first direction a longitudinal axis of the shank or the microfluidic
channel is in the range of 180° to 90°. In certain embodiments, the tip comprises
a plurality of segments extending from the shank, wherein each segment is characterized
by a tapered shape, and between each segment a portion of the tip is arranged, and
wherein at least one of the portions arranged between the segments is designed as
predetermined breaking point. Advantageously, the tip curvature, shape and/or length
can directly be patterned with the method of the invention, e.g. by patterning with
a respective photomask. Provided that the tip defines the bottomside of the device,
the device is in this case manufactured sideways, meaning particulary that the bottom
layer becomes the first sidewall of the device and the cover layer becomes the bottomside,
the topside and the second sidewall of the device.
[0049] In certain embodiments, the bottom layer and the coverlayer are cured such with the
first defined pattern and the third defined pattern, respectively, that the shaft
exhibits a curved shape, a jagged shape, a zigzag shape or a shape comprising a step,
or in other words, the shank comprises one or more corners.
[0050] The term "a shape comprising a step" particularly refers to the shape of a shank
that comprises two parts each of them extending along a direction, respectively, wherein
one of the two directions is arragned with respect to the other direction at an angle
in the range of - 30° to 30°C, particularly in the range of -10°C to 10°C, more particular
0°, and the two parts are connected to each other by a intermediate part extending
along a direction, which parallel to none of the aforementioned two direction.
[0051] In certain embodiments, the bottom layer and the cover layer are cured such with
the first defined pattern and the third defines pattern, respectively, that the shaft
of the device comprises a tip that extends along a first direction, the angle between
the first direction a longitudinal axis of the shank or the microfluidic channel is
in the range of 180° to 90, and the shaft exhibits a curved shape, a jagged shape,
a zigzag shape or a shape comprising a step, wherein the curved shape, the jagged
shape, the zigzag shape or the shape comprising a step extends within a plane being
parallel to the first direction. Also in this embodiment, the device of the invention
is manufactured sideways as described above. Advantageously, the production of devices,
particularly of cantilevers with complex shapes of the shank and the tip may be performed
with the method of the invention, which additionally suitable for mass production.
[0052] According to a further aspect of the invention, a device is provided. The device
has
- a flexible shank comprising a microfluidic channel and an aperture that is in fluid
communication with the microfluidic channel, wherein the microfluidic channel extends
through the shank along the longitudinal axis of the shank and is delimited by at
least one surface being formed by a polymer
- a reservoir in fluid communication to the microfluidic channel, whereby the aperture
is oriented at the end of the flexible shank opposite to the reservoir, and
- optionally a means for measuring a mechanical force acting on the flexible shank arranged
on or within the flexible shank.
[0053] In certain embodiments, the polymer forming the at least one surface delimiting the
microfluidic channel is integrally formed in one piece. In certain embodiments, the
polymer forming the at least one surface delimiting the microfluidic channel is characterized
by an elasticity in the range of 0.5 GPa to 20 Gpa, preferably in the range of 1 GPa
to 10 GPa, more preferable in the range of 4 GPa to 5 GPa, even more preferable 4.5
GPa.
[0054] In certain embodiments, the microfluidc channel is configured to pass a fluid stream
with pressure of up to 6 bar, and and particularly is fluid tight up a pressure of
6 bar(a).
[0055] In certain embodiments, the flexible shank is characterized by a spring constant
in the range of 0.01 N*m
-1 to 1,000 N*m
-1, preferably in the range of 0.5 N*m
-1 to 80 N*m
-1.
[0056] Advantageously, by the one-piece design of the polymer, the microfluidic channel
is completely fluid tight up to a pressure of 6 bar(a), when applied to the microfluidic
channel.
[0057] In certain embodiments, the device of the invention is manufactured by a method according
to the first aspect of the invention or any embodiment thereof.
[0058] In certain embodiments, the polymer forming the at least one surface delimiting the
microfluidic channel exhibits a homogenous structure.
[0059] In certain embodiments, the device of the invention is integrally formed in piece,
and particularly exhibits a homogenous structure.
[0060] In certain embodiments, the device further comprises a handling means with a through
hole in fluid communication with the reservoir, wherein particularly the handling
means is arranged above the reservoir such that the shank is deformable without be
obstructed by the handling means. Particularly, the reservoir extends to the through
hole.
[0061] In certain embodiments, the polymer is cured photosensitive polymer, in other words
a polymer formed by curing, wherein oligomers are cross-linked upon exposure of light.
In certain embodiments, the polymer is SU-8.
[0062] In certain embodiments, the polymer is a blend of at least two photosensitive polymers
that are cured such that the blend is integrally formed in one piece.
[0063] In certain embodiments, the microfluidic channel has a length in the range of 0.05
mm to 50 mm. In certain embodiments, the microfluidic channel has a length in the
range of 0.1 mm to 0.5 mm. In certain embodiments, the microfluidic channel has a
length in the range of 1 mm to 5 mm. In certain embodiments, the microfluidic channel
has a width in the range of 1 µm to 50 µm, particulary from 1 µm to 30 µm. In certain
embodiments, the microfluidic channel has height in the range of 0.1 µm to 30 µm.
[0064] In certain embodiments, the shank has a thickness in the range of 10 µm to 50 µm.
In certain embodiments, the shank has a thickness of 12 µm. In certain embodiments,
the shank has a width in the range of 20 µm to 80 µm.
[0065] In certain embodiments, the aperture is characterized by a diameter in the range
of 1 µm to 50 µm, particularly in range of 5 µm to 35 µm, more particular in the range
of 20 µm to 30 µm.
[0066] In certain embodiments, the handling means is characterized by a height in the range
of 100 µm to 300 µm, particularly 250 µm.
[0067] In certain embodiments, the through hole comprised within the handling means is characterized
by a diameter in the range of 100 µm to 500 µm.
[0068] In certain embodiments, the means for measuring a mechanical force acting on the
flexible shank is formed by a metal layer consisting of at least one noble, non-toxic
metal, whereby the metal layer is able to changes its resistance in dependence of
a mechanical force acting on the metal layer and thereby on the shanks. In certain
embodiments, the noble, non-toxic metal is gold.
[0069] In certain embodiments, the means for measuring a mechanical force acting on the
flexible shank is formed by a sensing layer comprising a plurality of nanowires made
of metal, wherein the nanowires are partially coated with an isolator such that at
least a part of the nanowires are in conductive contact to each other when no mechanical
force is acting on the shank, and the at least one part of the nanowires in conductive
contact to each other decreases with increase of the mechnical forces acting on the
shank. Such means is particularly suitable to detect mechanical forces in the range
of pN to nN. In certain embodiments, the nanowires are characterized by a thickness
in the range of 40 nm to 60 nm and/or a length in the range of 5 µm to 20 µm. In certain
embodiments, the nanowires consist of or comprise silver. In certain embodiments,
the isolator is aluminium oxide. In certain embodiments, the sensing layer is characterized
by a thickness in the range of 2 µm to 3 µm, wherein the nanowires comprised within
the sensing layer are characterized by a length of 5 µm to 10 µm and a diameter of
approx. 60 nm. The above described means is also disclosed in the patent application
EP 15171419.3.
[0070] In certain embodiments, the means for measuring a mechanical force acting on the
flexible shank is formed by a sensing layer comprising a plurality of nanowires made
of metal, wherein the nanowires are arranged such within the sensing layer that at
least a part of the nanowires are in conductive contact to each other when no mechanical
force acts on the shank, and the at least one part of the nanowires in conductive
contact to each other decreases with increase of an mechnical forces acting on the
shank. Such means is particularly suitable to detect mechanical forces in the range
of 100 nN and higher. In certain embodiments, the nanowires are characterized by a
thickness in the range of 40 nm to 60 nm and/or a length in the range of 5 µm to 50
µm. In certain embodiments, the nanowires consitst of or comprise silver.
[0071] In certain embodiments, the means for measuring a mechanical force acting on said
flexible shank is formed by a part of the shank being optically transparent, wherein
the part of the shank is configured to change its optical properties, particularly
its refractive or diffractive properties, in dependence of a mechanical force acting
on the part of the shank.
[0072] In certain embodiments, the aperture is comprised within a tip of the shank. In certain
embodiment, the tip extends along a first direction from the shank, wherein the angle
between the first direction and the longitudinal axis of the shank is in the range
of 180° to 90°C. In certain embodiments, the tip is characterized by a cylindrical
shape or a tapered shape, particularly a conical or pyramidal shape. Such device may
advantageously be used as cantilever for single-cell injections or imaging of soft
tissues with high sensitivity.
[0073] In certain embodiments, the shank is characterized by a curved shape, a jagged shape,
a zigzag shape or a shape comprising a step, wherein particularly the curved shape,
the jagged shape, the zigzag shape or the shape comprising a step extends within a
plane being parallel to the first direction along which the tip extends from the shank.
[0074] In certain embodiments, a tip comprising a plurality of segments extends from the
shank, each segment is characterized by a tapered shape, and between each segment
a portion of the tip is arranged, and wherein at least one of the portions arranged
between the segments is designed as predetermined breaking point. Advantageously,
clogging possibly occuring within the tip can be overcome by removing the clogged
segment, e.g. by breaking off the clogged segment with a tweezer.
[0075] In certain embodiments, the device is designed as a cantilever or a micropipette.
In certain embodiments, the micropipette comprises a re-usable tip such as a tip comprising
a plurality of segments extends from the shank, each segment is characterized by a
tapered shape, and between each segment a portion of the tip is arranged, and wherein
at least one of the portions arranged between the segments is designed as predetermined
breaking point.
[0076] Advantageously, the device of the invention is particularly suitable for for fine
surgical applications.
[0077] According to a further aspect of the invention, a method for spatially manipulating
a microscopic object, particularly a single cell, is provided. The method comprises
the steps of:
- providing a device having a flexible shank with a microfluidic channel and an aperture
in fluidic communication with said microfluidic channel according to any one of the
above aspects or embodiments of the invention, and
- capture the microscopic object at or within the microfluidic channel or release the
microscopic object from or out of the microfludic channel by applying or altering
a fluidic current within the microfluidic channel.
[0078] In certain embodiments, the microscopic object is located at first postion and captured,
and the captured microscopic object is released at a second position, wherein particularly
- a) the device of the of the invention is positioned such that the microscopic object
is capturable at the first position,
- b) the microscopic object is captured at the first position,
- c) the device of the invention comprising the captured microscopic object is positioned
such that the captured microscopic object is releasable at the second position, and
- d) the captured microscopic object is released at the second position.
[0079] In certain embodiments, the microscopic object is captured by attaching the microscopic
object at the aperture. In certain embodiments, the microscopic is released by detaching
the microscopic object from the aperture.
[0080] In certain embodiments, the microscopic object is captured by sucking the microscopic
object into the microfluidic channel. In certain embodiments, the microscopic object
is released by pumping the microscopic object out of the microfluidic channel.
[0081] In certain embodiments, the microscopic object is capture by sucking the microscopic
object through the microfluidc channel into a reservoir in fluid communictation with
the microfluid channel and released by pumping the microscopic object out of the reservoir
through the microscopic channel.
[0082] The invention is further illustrated by the following examples and figures, from
which further embodiments and advantages can be drawn. These examples are meant to
illustrate the invention but not to limit its scope.
Description of the figures
[0083]
- Fig. 1
- shows the microfabrication process for producing micro-channeled SU-8 cantilevers
with A) deposited Cr/ Au/ Cr release layer on a silicon wafer and patterned SU-8 bottom
layer with definition of a circular aperture, B) deposited copper seed layer, C) patterned
positive AZ sacrificial photoresist, D) electroplated copper growth layer, E) dissolved
positive photoresist and copper seed layer, F) patterned SU-8 top layer with definition
of an inlet, G) patterned SU-8 chip layer for handling and H) etching of the channel
sacrificial layer and release from the wafer.
- Fig. 2
- shows the characterization of the SU-8 devices with A) optical picture of a cantilever
after copper plating, B) and C) SEM views of a cantilever of 12 µm thickness for channel
thickness of 3 µm (flipped upside down compared to Figure 1), D) fluorescent microscopy
top view with fluorescent liquid coming out at the aperture, E) apparent liquid meniscus
reaching the transparent cantilever and F) flow rate as a function of pressure applied
on the chip with linear fit in red dash line. Uncertainty measured in the flow rate
was at most 4% for the same applied pressure. It is not represented on the graph for
more clarity.
- Fig. 3
- shows the force adhesion measurements of S. cerevisiae. The yeast cells were measured on bare glass and PDA-coated glass substrates with
A) an optical picture of a cantilever with a 6 µm diameter aperture before and B)
during force spectroscopy of single targeted yeast. In C), a typical force spectroscopy
curve of a yeast cell on glass substrate showed adhesion forces of 15.8 nN (distance
of detachment of 240 nm) as a difference between approach curve in blue and retract
curve in red. In D), adhesion forces on the 2 substrates were compared exhibiting
forces of 15 ± 7.6 nN on glass and 33 nN ± 11.9 nN on PDA, averaged respectively,
over 21 and 26 force curves for 10 and 12 different yeasts and performed with the
same cantilever. On the graph, the mean is represented as a square, the median as
a line separating two boxes with each box determined by the 25th and 75th percentiles and whiskers determined by the 5th and 95th percentiles.
- Fig. 4
- shows examples of forces curves obtained with a SU-8 cantilever in A) air and B) liquid
environment on glass substrate. In this configuration, only the end of the cantilever
was touching the substrate.
- Fig. 5
- shows schematics illustrating the main approaches developed for single-cell patterning
using a hollow cantilever. A) A micropipette-like configuration for a best cell placement
resolution of 250 µm (configuration 1). B) Controlled direct deposition by mechanical
squeezing and physical confinement of individual cells (configuration 2). C) The same
cantilever was used for fine negative or subtractive patterning with the possibility
of single-cell detachment if cell sitting on an adhesive substrate (configuration
3) or coarse negative patterning if cell on a repulsive substrate (configuration 4).
- Fig. 6
- shows the precise deposition of single C2C12 cells using configuration 2 with A) a
grid pattern of 4 single cells deposited frame after frame from top left to bottom
right and B) a grid pattern of six spots with varying number of cells per spot. Green
circles represent the aperture of the cantilever during deposition, while the numbers
of the bottom panel correspond to the order of deposition.
- Fig. 7
- shows the negative patterning of C2C12 mammalian myoblast cells using configurations
3 and 4, corresponding respectively to top and bottom panels. In the configuration
3, where C2C12 were seeded on a PDL-coated adhesive surface, the cantilever was approached
A) on the cell of interest. A large underpressure of -800 mbar was applied to the
cantilever for 10 sec to detach the cell in B). In the configuration 4, where cells
were seeded on a PLL-g-PEG coated repulsive surface, the cantilever was brought 10
µm away from the surface-level C). Low underpressure of-10 mbarwas applied for 1 sec
D), thus removing the cells roughly contained within a perimeter of 300 µm diameter
around the aperture.
- Fig. 8
- shows the subtractive patterning of primary hippocampal neurons on a fully PDL-coated
adhesive surface (configuration 3). Optical pictures of the area of interest are displayed
before patterning in A), after patterning in B) and after 5 DIV in C). After longer
time in vitro, the pattern became less obvious due to cell migration.
- Fig. 9
- shows the subtractive patterning of primary hippocampal neurons using configurations
3 (A to D) and 3-4 (E and F). A PDL pattern was locally dispensed in the form of a
smiley before backfilling the remainder with PLL-g-PEG for a better adhesive to non-adhesive
contrast. A) Neurons seeded on the surface before patterning, B) Neurons on the surface
after removal of those sitting on the repulsive surface. Neurons viability was tracked
by transfecting the culture visible in bright field in C), with adeno-associated virus
(AAV) after 6 DIV, showing in D) spontaneous calcium activity expressed in GFP after
12 DIV and neurite outgrowth activity. Similarly, neurons were removed from PLL-g-PEG
surface on a second pattern as well as the half-right of the PDL pattern shown by
a bright field image of healthy neurons population with no apparent neuron adhering
again on the half-right of the PDL-coated smiley in E) and in F) calcium activity
expressed after 12 DIV in GFP.
- Fig. 10
- shows the in situ modifications of an existing pattern of neurons. In A), the pattern realized in Fig.
9C) is illustrated after 14 DIV in fluorescence light microscopy. The two white encircled
areas were subject to removal in B) as well as an eye of the smiley in C), by applying
with the cantilever high and constant suction for 10 sec onto each spot (pressure
inferior to -800mbar). Another existing pattern is shown in bright field microscopy
after 14 DIV before patterning in D), and additional deposition of 3 fresh primary
neurons forming a second eye to the smiley, as pointed out in E).
- Fig. 11
- shows the upside down SEM images of A) a cantilever used in the micropipette-like
configuration with the aperture defined in the front plane for a channel thickness
of 22 µm (configuration 1) and B) a cantilever with the aperture designed at the bottom
plane with same channel thickness for an aperture diameter varying from 20 to 35 µm
(configurations 2 to 4).
- Fig. 12
- shows in A), B) and C) a layer-by-layer photolithography process, wherein bottom layer,
channel and top layer are patterned in a three-step protocol; in D) a global view
of the sketched device and in E) an optical image of the finalized device.
- Fig. 13
- shows optical pictures of four different designs of cantilevers microfabricated sideways,
scalebar being identical for all. A) shows a curved tip, whereas B) and C) depict
a triangle-like tip and D) a rectangle-like tip.
- Fig. 14
- shows optical pictures of five different micropipette designs. A) and B) depict a
geometry of probe, which could act as an diffractometer upon mechanical force, C)
and D) have a high and long tip to reach inaccessible locations, E) and F) a sliceable
tip for several uses. G) and H) display a long tip with an additional corner.
- Fig. 15
- shows corresponding SEM images of figure 14.
- Fig. 16
- shows SEM images of the sliceable tip before in A) and after cutting in B) at the
location represented by a dashed green line. C) depicts a close-up view of B) where
the aperture is electrically charging because of the non-existing conductive coating
while SEM imaging. Despite the charging effect, the dark hollow channel is apparent.
- Fig. 17
- shows SEM images of two different thick cantilevers (respectively at bottom and top
panels) demonstrating a pillar-like structure at the aperture-level.
- Fig. 18
- shows the process flow for tube-like tips with in A) patterning of SU-8 bottom layer,
B) copper seed layer deposition, C) AZ sacrificial patterning for channel definition,
D) copper plating for thickness of 10 µm, E) etching of AZ and copper seed layer and
patterning of SU-8 top layer and F) release of the probe.
- Fig. 19
- shows a scheme of the mode of action of one possible force sensor.
- Fig. 20
- schematically shows an embodiment of the force sensor comprised within shank (cantilever
beam) of the device of the invention (here designed as cantilever), wherein the force
sensor is formed by a composite structure in the shape of a cantilever beam.
- Fig. 21
- schematically shows a method for producing the composite structure depicted in fig.
20.
- Figs. 22 to 23
- show optical images of a cantilever equipped with the force sensor depicted in Figs.
20 and 21.
- Fig. 24
- shows an embodiment of the device of the invention characterized by a needle-like
design made by sideways fabrication; (A) global view from different perspectives and
(B) a section of the shank with the tip (upper panel) and a cross section thereof.
- Fig. 25
- shows an embodiment of the device of the invention characterized by a biopsy tool-like
design; (A) global view from different perspectives and (B) a section of the shank
with the tip (upper panel) and a cross section thereof.
- Fig. 26
- shows an embodiment of the device of the invention characterized by a biopsy tool-like
design with light sensor; (A) global view from different perspectives and (B) a section
of the shank with the tip (upper panel) and a cross section thereof.
- Fig. 27
- shows an embodiment of the device of the invention being a sealed and reusable micropipette
with sliceable tips; (A) global view from different perspectives and (B) a section
of the shank with the tip (upper panel) and a cross section thereof.
- Fig. 28
- shows an embodiment of the device of the invention characterized by a micropipette
design with force sensor; (A) global view from different perspectives and (B) a section
of the shank with the tip (upper panel) and a cross section thereof.
- Fig. 29
- shows an embodiment of the device of the invention characterized by a blunt (tipless)
cantilever design; (A) global view from different perspectives and (B) a section of
the shank with the aperture (upper panel) and a cross section thereof.
- Fig. 30
- shows an embodiment of the device of the invention characterized by a cantilever design
with a triangle tip; (A) global view from different perspectives and (B) a section
of the shank with the triangle tip (upper panel) and a cross section thereof.
- Fig. 31
- shows an embodiment of the device of the invention characterized by a cantilever design
with a rectangle tip; (A) global view from different perspectives and (B) a section
of the shank with the rectangle tip (upper panel) and a cross section thereof.
- Fig. 32
- shows an embodiment of the device of the invention characterized by a cantilever design
with two sharp tips; (A) global view from different perspectives and (B) a section
of the shank with the rectangle tip (upper panel) and a cross section thereof.
- Fig. 33
- shows an embodiment of the device of the invention characterized by a micropipette
design for patch-clamp; (A) global view from different perspectives and (B) a section
of the shank with the tip (upper panel) and a cross section thereof.
Examples
[0084] A novel fabrication method was established to produce flexible, transparent and robust
tipless hollow atomic force microscopy (AFM) cantilevers made entirely from SU-8.
Channels of 3 µm thickness and several millimeters length were integrated into 12
µm thick and 40 µm wide cantilevers. Connected to a pressure controller, the devices
showed robust sealing performance with no leakage up to 6 bars. Changing the cantilevers
length from 100 µm to 500 µm among the same wafer allowed targeting various spring
constants range from 0.5 to 80 N/m within a single fabrication run. Such hollow polymeric
AFM cantilevers were operated using optical beam deflection method (OBD). To demonstrate
the performance of the device, single-cell force spectroscopy (SCFS) experiments were
carried out with a single probe detaching in a serial protocol more than 100
Saccharomyces cerevisiae yeast cells from glass and glass-coated with polydopamine measuring adhesion forces
in the sub-nanoNewton range.
[0085] SU-8 now offers a new alternative to conventional silicon-based hollow cantilevers
with more flexibility in terms of complex geometric design and surface chemistry modification.
[0086] As scope of this work, SU-8 hollow AFM tipless cantilevers were developed. The process
for the realization of robust embedded microchannel is presented together with the
corresponding integration into the final device, i.e. an AFM chip. Serial single-cell
force spectroscopy (SCFS) with forces recorded in the sub-nanoNewton range validated
the AFM feasibility and functionality of those flexible cantilevers.
[0087] As SU-8 has been standardly used in microfluidic applications, several processes
have been developed in order to realize hollow structures. Nonetheless, it still remains
challenging to fabricate entire SU-8 fluidic devices because SU-8 is a negative-tone
resist: oligomers from bottom SU-8 of the microchannel must always be present in sufficient
quantity to polymerize with top SU-8 covering the channel in order to ensure a watertight
sealing at the interface.
[0088] Herein, a promising process for fabrication of 1 to 5 mm long and sub-µm to 10 µm
thick hollow channels that show high fluidic robustness with resistance over 6 bars
of pressure is provided.
Microfabrication Process for Tipless SU-8 Hollow AFM Cantilevers:
[0089] Figure 1 illustrates the process flow that was established for this fabrication.
A novel "sacrificial-filling-material" approach based on electrochemical deposition
was investigated. For easy handling of the devices as well as to limit their initial
bending, 12-µm thick cantilevers were designed on a wafer- scale.
[0090] In the process, the first step consisted in depositing a sacrificial release layer
21 made of 5 nm chromium/ 50 nm gold/50 nm chromium on a silicon carrier substrate,
known as enhanced sacrificial layer, to ensure a fast release of the probes from the
wafer. Then, a 5-µm thick SU-8 bottom layer 22 was photolithographically patterned
with the formation of a circular outlet aperture 13 having a diameter down to 4 µm
(Fig. 1A). After development of the first layer 21, a copper seed layer 23 of 150
nm thickness was deposited on the wafer surface using thermally resistive evaporation
for low UV radiation (Fig. 1 B). This layer 23 was consequently thick to support uniform
electrical conductivity over the surface. As depicted in Fig. 1C, a positive photoresist
24 such as AZ4562 was then patterned to define the shape of the future hollow channel
12 as well as to guarantee straight walls during the sacrificial metal growth 25.
Here, the use of a positive photoresist 24 was advantageously so that SU-8 areas 22
on the bottom plane supposed to polymerize subsequently with the cover layer 26 were
spared from UV exposure while patterning the positive resist. Reduced baking time
was also advantageous to prevent complete polymerization. Then, a sacrificial copper
layer 25 was electrochemically deposited in a bath of copper sulfate for a thickness
of 3 µm (Fig. 1 D). Prior to electroplating, the wafer was quickly plasma treated
and dipped in sulfuric acid to ensure a better wetting. Next, the positive photoresist
24 was dissolved by immersing the wafer for 5 s in acetone followed by a quick dipping
of 3-4 s in a hydrogen peroxide based etchant until the thin copper seed layer 23
disappeared, as seen in Fig. 1 E. Then, a 7 µm thick SU-8 top layer 26 of the probe
was spin-coated over the existing structures and patterned accordingly as seen in
Fig. 1 F. To improve mechanical stability of the assembly, a 250-µm thick block layer
28 of SU-8 was patterned to form the handling chip part 15 of the probe 100 making
a cylindrical reservoir 14, 16 directly connected to the channel 12 (Fig. 1 G). The
sacrificial layer 25 forming the channel 12 was then dissolved in a copper etching
solution for several days depending on agitation (2-mm long channels). This versatile
approach allowed fabricating several millimeter long channels 12 for thicknesses ranging
from 100 nm to tens of micrometers. A ferric chloric based copper etchant was preferred
over hydrogen peroxide based etchant because the latter one formed oxygen bubbles
that stayed confined at the inlet's surface because of SU-8's hydrophobicity. Then,
the fabricated probe 100 was released from the carrier wafer by using a chromium etching
solution to dissolve the release layer 21 in two hours as shown in Fig. 1 H. Cantilevers
showed maximal initial bending of 5° because of their consequently high thickness
(> 10 µm). Therefore, there was no need to use a more complex dry release technique
to further minimize such bending. Finally, probes 100 were squeezed on top of hydrophobic
parafilm substrate for easy handling before gold deposition. A 10-nm thin layer was
deposited onto the entire device to ensure a satisfactory laser reflection on top
of the cantilever and by doing so, enabling optical beam deflection (OBD) method for
force detection. Depending on the use, this thickness may be increased or decreased
if one wanted to privilege AFM laser force signal or better visibility of surface
objects through the transparent microlever. Finally, probes 100 could be gently peeled
off with tweezers from the parafilm substrate.
[0091] A specific holder with many more conductive pins could also be designed to guarantee
even better copper growth uniformity.
Cantilever-like designs with tip
[0092] Most of current biological applications require a tip. This protrusion allows for
sharper AFM imaging but also diverse fluidic applications such as single-cell injection
and extraction, patchclamp or chemical stimulation. One of the biggest limitations
commonly observed with silicon-based hollow cantilevers is the need for milling an
aperture outlet individually for each probe. This is mostly done using the tedious
focused ion beam (FIB), which cannot be multiplexed. Therefore, a human incertitude
and an increase of the cost are necessarily introduced. Only one type of geometry
with an aperture at the end of the pyramidal tip can be directly defined through photolithography
processing. This important drawback can be circumvented by slightly adapting the process
initially developed for blunt hollow probes described above. In the original version
of the process, the layer-by-layer fabrication consisted in the sequential assembly
of bottom 22, channel 25 and top layers 26. For the version of cantilevers equipped
with tips, the process has been modified to fabricate the devices sideways with the
sequential assembly of one side, channel and opposite side layers, as displayed in
the corresponding schematics in Figure 12 A), B) and C). In Fig 12D) a global view
of the device can be observed, which was slightly changed for the final version as
shown on the optical image of the finalized device in E).
[0093] Using silicon-based technology, this was not developed mostly because of the necessary
important thickness of all different layers. Indeed, it means for devices fabricated
sideways that each layer is at least couple of microns thick to, once the device is
tilted back, get any laser signal focused on the top of the cantilever. Despite the
difficulties in term of fabrication, silicon-based cantilevers would be much stiffer.
By considering Young's Modulus of silicon or silicon nitride, a nominal width of 4
µm for each layer (giving a total width of 12 µm) and conventional cantilever dimensions
such as 400 µm in length and 15 µm in thickness, one can estimate the spring constant
in the range of 10 N*m
-1. Since the device is tilted, width and thickness in this configuration are respectively
equivalent to usual thickness and width. In comparison, the spring constant would
be 40 times lower for identical dimensions using SU-8 polymer. Another significant
advantage with this process is the possibility to give various shapes and lengths
to the tips instead of a single pyramidal geometry in the case of a silicon-based
hollow cantilever. The natural disadvantage with the following process is the unavoidable
"fake" 3D of the tip since it is only a projection of a 2D design in the third dimension.
This aspect can be minimized by adding some photolithography steps to obtain different
step heights which could be rendered then probably smoother using high hard baking
temperature. As depicted in Figure 13, cantilevers 100 with curved, triangle-like
and rectangle-like tips 17 could be fabricated. All tips were "cut" following an angle
of 10 degrees with the substrate in order to be compatible with the JPK AFM setup
for monitoring force-deflection.
Micropipette-like designs
[0094] By the method of the invention, micropipettes with complex shapes can be manufactured,
particularly in a high-through-put manner. In addition, SU-8 offers some advantages
in terms of electrical isolation in the case of piezoresistive force sensing in comparison
with force sensors known in the art. This latter electrical-based sensing only comes
with 2 electrical wires to contact the sensing film (described below), limiting de
facto the intrusion for surgical applications. Prototypes of SU-8 micropipettes with
various designs were realized. Figure 14 depicts in A) and B) possible geometries
of a pipette tip, which upon applied force will change the periodicity between the
triangles. Thus, by passing light through the periodically arranged triangles, one
could modulate the diffracted or refracted light depending on mechanical strain exerted
at the tip-level. Also depicted in C) is a curved tip, in D) a straight tip, in E)
and F) a sliceable tip (see further below) and in G) and H) a mm-long tip with an
additional comer for sensing deflection within two axes if the sensor is coating the
total surface of the probe. Figure 15 depict the SEM images of the same designs in
B), D), E) and F) and others in A) and C).
[0095] Another common issue in micro- or nano-fluidics is the channel or aperture clogging.
Because of particles, dust, cell residues or other unexpected events related to experiments,
it is generally easy to obstruct such a small and hollow surface area. To overcome
this problem, a prototype of sliceable tip has been developed. It consists in having
several tips mounted together in series with higher mechanical weakening for the last
tip. In our configuration, the latter tip is more susceptible to break off while touching
it with tweezers. A worn-out tip could be broken and replaced by a new one in the
middle of an experiment without many adjustments. The proof of concept is demonstrated
in figure 18 depicting a sliceabletip before (A) and after breaking (B) a tip, wherein
thereby created new tip exhibits an apparent channel (C). The tip may be breaken of
by simply touching the last tip with tweezers. Figure 16 depicts the breakage of the
last 3 tips.
Thick cantilevers
[0096] Thick cantilevers with integrated microchannels of 22 µm height were fabricated as
well for single-cell patterning purposes. It is a very similar process to the one
described above with the difference that the AZ4562 sacrificial photoresist is spin-coated
and patterned at a higher thickness of 27 µm for control over the copper growth within
the channel. Cantilevers show a total thickness of 50 µm. Interesstingly, some cantilevers
randomly selected for SEM imaging showed a perfectly cylindrical pillar formed in
the center of the circular aperture, as for example, depicted in Fig. 19. This necessarily
has to do with the copper growth during the electroplating process. One hypothesis
to explain this phenomenon might result from the fact that the channel thickness is
below expected. From the measurements on the profilometer before spin-coating of the
top SU-8 layer, a few devices among the wafer show a channel thickness below 15 µm.
As depicted by Figure 18, the hollow cylinder formed by the bottom SU-8layer gets
filled during plating starting from the vertical walls and the horizontal bottom surface
with a uniform thickness of about 10 µm thick copper (Figure 18 D). Considering the
aperture is 30 µm wide, the hollow cylinder is not completely filled after deposition.
A pillar structure can be left empty and subsequently formed by the spin-coating of
the top SU-8 layer (Figure 17A and Figure 18 F). Figure 17 A) and B) show a 10 µm
wide pillar structure, whereas width in C) and D) the pillar sturcture is 5 µm wide.
Force sensors
[0097] Depending on the design of the device of the invention and the application, for which
it serves, mechanical strain can cause bending, compression or elongation on the surface
of the device. This strain can be measured within 2 configurations based on piezoresistive
sensing. The sensing layer is always located on the surface, as far as possible from
the neutral axis of the cantilever or pipette for higher force sensitivity.
[0098] The different configurations can be classified as following (from low to higher strain):
- 1. A composite film of metallic nanowires coated with an insulator at the interface
for force detection between pN and nN.
Here, a large network of silver nanowires 31 (AgNWs) is first deposited on a surface.
A thin aluminum oxide coating (from few angstroms to few nm) is conformally deposited
on the surface of the nanowires 31. The AgNWs network 31 with Al2O3 is then embedded in the SU8 polymer (Fig. 21). The Al2O3 coating does not alter the initial resistance R0 of the network; at rest, R0 is low since all wires are in contact (Fig. 19). However, upon bending of the cantilever
the AgNW network is displaced and the single AgNWs slide along each other's insulator
coating, causing a proportion of the wires not to be in contact with other wires anymore,
but with the insulating Al2O3 layer. The latter results in a significant increase in resistance (ΔR) resulting
in a higher GF and thus higher sensitivity. Once back at rest the wires have returned
to their initial positions again where they contact each other at initial location,
showing low resistance. The increase in ΔR during bending is appointed to the tunneling
resistance which arises at the contact interface of two metal wires, as well as to
the ratio of wires in contact/out of contact. The only place where the Al2O3 layer is not deposited is on the AgNWs pads as they form the electrical contact points
for piezoresistive readout.
- 2. A film of bare metallic nanowires for force higher than 100 nN.
[0099] A system less sensitive using a thick network of nanowires is ideal for such an application.
Method of manufacture a composite structured force sensor
[0100] As depicted in Fig. 20, conductive elements 31, particularly nanowires made of silver,
are arranged in or on a cantilever beam 11 in a specific pattern. When the cantilever
beam 11 is bent, some sections of the beam 11 are compressed and other sections are
stretched. Depending on their location and arrangement relative to one another, conductive
elements 31 will remain in contact, lose contact or come into contact physically and/or
electrically. The conductivity function of the trail for the described bending is
a step function: at first zero (or almost zero), then constant (or almost constant)
at a higher level, and then again zero (or almost zero). By superimposing several
step functions every conductivity function of practical interest can be approximated.
In practice the superimposition can be realized e.g. by connecting various trails
or tracks (virtually) in parallel.
[0101] Additionally, the amount of bending can thereby be measured by measuring the (change
in) conductivity in one or more tracks of the composite structure.
[0102] Fig. 21 illustrates a process scheme for manufacturing the above described force
sensor.
Step a) A sacrificial layer 21 is deposited.
Step b) Metallic pads 30 for better subsequent electric contact are created, e.g.
by vapour deposition. An example for a suitable metal is gold.
Step c) A percolation structure 31, e.g. a silver nanowire (AgNW) network, is deposited
using centrifugation, drop-casting or vacuum filtration on the sacrificial layer 21
and the pads 30. Optionally, a deposition of shell material, in particular layer deposition,
e.g. atomic layer deposition of aluminium oxide, can be performed. For example, the
layer thickness can range from 2-3 angstroms to 50 nm.
Step d) A polymer 22, e.g. SU-8 polymer photoresist, is used as the constituent material
of the cantilever beam 11. Optionally, it can be photolithographically patterned in
the shape of a beam attached to a handling block 15, which makes the handling easier.
Step e) Optionally, the thickness of the handling block 15 is further increased by
additional patterning of thick SU-8 26. The increased thickness of the handling block
15 can improve the handling of the cantilever beam.
Step f) Optionally, after etching of the sacrificial layer 21, a passivation layer
(such as parylene) can be deposited thermally to isolate the cantilever beam 11. The
pads' 30 contact area on the hanling block 15 can be protected from the passivation
layer e.g. by some cover (because it can have a rather big area, e.g. several mm2). The figure f) shows the cantilever beam 11 from the bottom side (turned over as
compared to the figures d) and e)) after etching and after deposition of the passivation
layer. Therefore only the pads' 30 contact areas are visible. The percolation structure
31 is hidden under the passivation layer and the pads' 30 contact areas, respectively.
[0103] When the cantilever beam 11 is bent, the conductive elements 31, e.g. the AgNW, move
relative to each other, thereby physically connecting or disconnecting and/or sliding
relative to each other. Note that in the case of an aluminium oxide coating at the
interface between two conductive elements 31, the elements do not physically touch
but are physically close. They can therefore exchange electric charges, this phenomenon
is known as the tunnel-effect.
[0104] In an embodiment, it can be the case that conductive elements 31 initially physically
touch. In conventional Atomic Force Microscopy (AFM) applications the strain is typically
low, e.g. 5% or smaller. Therefore for such an application the shell's thickness can
be tailored with a steep function (resistance dependant on tunnelling effect dependant
on shell's thickness).
[0105] An optical image of the resulting device is displayed in figure 22. The process only
differs from figure 23 in the sense that there are no metallic pads, instead the NW
network 31 is patterned and etched using a sacrificial photoresist. Holes 32 were
created to minimize the gap between filled structures in order to accelerate the release.
As seen in figure 23, silver nanowire pads 31 are glued together with a conductive
silver epoxy 35 to gold flexible wires 34 for electrical contact.
Optical and Fluidic Performances
[0106] The developed process was highly successful for the realization of hollow AFM cantilevers
100 made entirely of SU-8, integrating mm-long and µm thick robust channels 12. As
shown in Figure 2A, the positive resist 24 could truly help to confine the copper
growth and define sharp channel walls. Channels 12 were generally defined, starting
5 µm away from the edges of the SU-8 cantilevers. In Fig. 2B and 2C, SEM pictures
reveal the cross-section of the microchannel 12 using an open cantilever design; bottom
22 and SU-8 layers 26 were specifically shorter than the copper layer itself at the
end of the cantilever for channel imaging. One can observe in Fig. 2C that the bottom
of the channel (corresponding to top copper layer of Figure 1) is not completely straight
because of the granular copper growth. Its curved profile follows the topography of
a trench after copper electroplating fill process. Thicknesses of bottom 22 and top
SU-8 layers 26 were 5 and 7 µm respectively. Channel 12 dimensions from inlet to outlet
were: 1800 µm long, 10-50 µm wide and 3 µm thick.
[0107] Each probe was then fixed and glued on a probeholder to assess its watertightness:
a FITC-based fluorescent solution did fill the microchannel and came out only from
the micro aperture after plasma treatment (Fig. 2D).
[0108] Fluidic robustness was obtained as the optimized result of several interdependent
parameters :
- Reduced UV exposure and baking time of the SU-8 bottom layer 22,
- Deposition of the copper seed layer 23 using thermal evaporation at minimal current
for low UV radiation,
- Use of a positive photoresist 24 for the copper plating to avoid direct UV exposure
onto the channel walls surface,
- Important overexposure of the top 26 and chip SU-8 layers 28.
[0109] One important point was to save sufficient amount of oligomers in the bottom SU-8
22 before the patterning of the SU-8 top layer 26. Polymerization was only completed
once top layer 26 was patterned accordingly. The hydrostatic strength or fluidic robustness
was proved by applying repeated times high continuous overpressure of 1 bar to release
yeasts from the cantilever. Furthermore, using a FITC dye within the channel, no leakage
was optically detected for an overpressure higher than 6 bars showing extremely high
resistance.
[0110] Native SU-8 is highly hydrophobic. However, the possibility to enhance its hydrophilic
surface properties by using oxygen plasma or ceric ammonium nitrate etchant has already
been demonstrated. This leads to the increase of C=O and COO groups at the surface.
By performing several oxygen plasma steps as well as prolonged chromium etching in
ceric ammonium nitrate solution, SU-8 channel surface was made hydrophilic. It facilitated
the filling of the cantilever, as pointed out in Fig. 2E by the low contact angle
of the liquid meniscus. The cantilevers presented laminar flow showing linear relation
of flow rate at the aperture for pressure range applied onto the device (Fig. 2F).
[0111] Showing the versatility of the technology, different cantilever designs could be
fabricated on the same wafer with a thickness ranging from 10 µm to 50 µm thickness,
lengths varying from 100 mM to 50 mm, widths from 1 µm to 50 µm, apertures from 4
to 20 µm diameter corresponding to channel volumes from 10 to 50 pL. Those different
geometries allow targeting wide spring constants range of 0.01 to 1,000 N/m calibrated
via Sader's method for resonance frequencies measured from 10 to 5 MHz. These soft
cantilevers are considered to have a range of spring constants relevant for biological
applications, such as imaging of biological samples or single-molecule force spectroscopy
applications.
[0112] Fig. 11 depicts the two types of cantilevers used for the proof of concept experiments
described below. The micropipette-like cantilever of Fig. 11A was realized by patterning
the positive photoresist 24 in a way that the SU-8 became shorter in length than the
sacrificial copper layer 25, opening the cantilever on the front plane. The second
design of Fig. 11 B used for the physical confinement of single-cell patterning applications
was simply defined by patterning the 6 µm thick bottom SU-8 layer 22 with a circular
aperture ranging from 20 to 35 µm in diameter. The typical spring constant of such
cantilevers was calculated to range from 150 to 500 N/m according to the different
lengths and widths of the cantilevers, with an average of 300 N/m. Based on calculations,
the difference in the spring constants of plain and hollow cantilevers is less the
10%, due to the small channel size as compared to the full cross section of the cantilevers.
Cell Adhesion Studies using Force Spectroscopy
[0113] The microfabricated devices can potentially be used as micropipettes with or without
force-feedback. To prove their functionality in AFM conditions, the SU-8 cantilevers
were mounted on an AFM controller and connected to a fluidic system.
[0114] Cell adhesion forces can be measured with hollow AFM cantilevers, aspiring a single
cell by applying negative pressure at the aperture while overcoming and measuring
the immobilization or adhesion forces of the cell on the substrate. This method presents
significant advantages over the more conventional approach which consists in gluing
irreversibly one cell per cantilever. The latter approach is time-consuming but also
limits through investigation of cell adhesion behavior as a function of time for life
cycle analysis. Furthermore, cell fixation forces on the cantilever are often too
low to detach entire cells from the surface of interest. Therefore, SCFS represents
the right approach to validate the AFM capability of the manufactured hollow tipless
SU-8 cantilevers. In this study, adhesion forces of
Saccharomyces cerevisiae were measured by performing force spectroscopy with a single SU-8 hollow probe on
more than 100 cells without fouling the aperture. No clogging or leaking issue at
the cantilever level was observed highlighting the maturity of the process.
[0115] S.
cerevisiae is a yeast species, which is extensively exploited in baking and brewery fermentation
processes and one of the most investigated eukaryotic model organism. The adhesion
of microbial cells to abiotic or biotic surfaces is mediated by a complex and dynamic
process of interactions affecting cell development and survival. It also plays an
active role in the infection process and is furthermore of relevance in biotechnological
processes, making necessary a deeper understanding of the ongoing cell to substrate
interactions. Here, we performed a proof of concept measuring the yeast adhesion both
on bare glass and on glass coated with polydopamine (PDA). This polymer is inspired
from the 3,4-dihydroxy-L-phenylalanine, which is naturally secreted from mussels and
commonly used for irreversible cell immobilization to the cantilever in conventional
AFM measurements.
[0116] In the present configuration, the modus operandi was rather straightforward. First,
force-approach curves were measured with a hollow cantilever onto a glass surface
in air and liquid environment showing elastic and reversible mechanical behavior of
SU-8 within the range of applied forces. Examples of forces curves obtained with a
SU-8 cantilever in A) air and B) liquid environment on glass substrate (Fig. 4). In
this configuration, only the end of the cantilever was touching the substrate as shown
in Fig 4. Then, the cantilever was positioned optically with the aperture over a single
yeast cell and approached the cantilever on it using systematically the same set point,
as shown in Figure 3A. The approach was followed by a contact pause where the single
yeast was aspired at the aperture before complete retraction of the cantilever (Fig.
3B). For future biological applications targeting mammalian cells, surface modification
with an antifouling layer of SU-8 for enhanced biofunctionality could be considered.
In the current case, mechanical overpressure was shown sufficient for the release
of yeast cells from the aperture.
[0117] Adhesion forces of
S.
cerevisiae to glass and PDA-coated glass surface were compared at room temperature using a soft
cantilever presenting a spring constant of 1.2 N/m. Fig. 4 shows the spring constant
calibration of a SU-8 cantilever (with 500 µm length 40 µm width and 10 µm thickness)
via Sader method in air environment using JPK SPM software. The latter was chosen
to measure the low adhesion force range. Considering the formula for the spring constant
of a cantilever with respective length, width and thickness of 500 µm, 50 µm and 12
µm, the theoretical spring constant is 0.8 N/m. From calculations, the influence of
the hollow channel on the total spring constant is limited to 0.1% because of its
relative ly low thickness. Fig. 4C shows an example of a typical force-distance curve
obtained for single yeast on glass substrate with adhesion forces of 15.8 nN. Averaged
adhesion forces were 15 ± 7.6 nN on glass and 33 nN ± 11.9 nN on PDA showing twofold
higher adhesion of S. cerevisiae on PDA substrate (Fig. 4D). Adhesion on glass was
found similar to other studies [9, 50] whereas adhesion on PDA was quantified hereby
for the first time, showing the expected behavior.
[0118] Cell elasticity and cell adhesion to the substrate could be decoupled: based on our
calculations, elasticity of
S.
cerevisiae is found to be out of range by 3 orders of magnitude and should not interfere with
the range of adhesion forces, if one considers average surface modulus or yeast elasticity
of 11.1 N/m and yeast adhesion measured of 58 mN/m with 14 nN force for a detachment
distance of 240 nm (Fig. 3C). Adhesion studies were also shown to be dependent on
the loading rate (applied force set point and tip speed) but also the contact time.
However, the influence of these parameters was not further investigated.
Controlled single-cell deposition and patterning by the highly flexible hollow cantilevers
of the invention
[0119] Fig. 5 illustrates the different approaches used and developed in order to evaluate
the newly developed hollow SU-8 polymeric cantilevers for the application of single-cell
patterning. In a standard micropipette-like configuration demonstrated in Fig. 5A,
cell deposition from the cantilever is limited by factors like: the lowest reliable
external pressure possibly applied to the system, the drag force acting on the cells,
as well as dynamical properties such as the response time. A first approach was taking
advantage of the highly flexible polymeric cantilever. This technique has not been
investigated so far because most fluidic components in printing technologies are mostly
made of rigid and brittle materials. Originally inclined at 8-10°, the cantilever
was significantly bent so that the cell remained confined at the aperture-level (Fig.
5B). Since the aperture was not perfectly parallel to the surface, the liquid could
flow out allowing continuous fluidic circulation in the cantilever. To be immobilized
and steadily stick to the surface, the cell was mechanically squeezed onto the substrate.
A second approach was used to selectively detach cells originally adhering on a substrate
in order to realize larger and complex patterns (Fig. 5C). This last approach was
also enabled because of the possibility to geometrically confine the flow through
the cylindrical hole.
[0120] Designing the aperture at the bottom of the cantilever opens up new possibilities
for more precise single-cell deposition and patterning. The first approach has been
demonstrated using fluorescently labeled C2C12 cells, as depicted in Fig. 6. On a
PDL-coated surface filled with medium, the cantilever was approached onto the surface
with cells carried in the reservoir. The approach of the cantilever was performed
using fluorescent light microscopy. To this end, overpressure of 20 mbar was constantly
applied to the cantilever, ejecting individual fluorescent cells while the cantilever
was brought closer to the substrate by one-micrometer vertical steps. As soon as cells
stopped flying away and that one cell appeared to be confined within the circular
aperture, the z-position was defined at 0 with the stepper for subsequent patterning
events (Fig. 6A). Pressure was then stopped before lifting up the cantilever and moving
it to the next deposition spot. Same operation was performed again until the next
fluorescent cell appeared. The 0-position, necessary for mechanical confinement of
the cells, was actually reproducibly matching with the position of the cantilever
at which it was bent 5 µm further down after only touching the surface. This specific
configuration where the aperture was inclined with respect to the surface is profitable
for fine patterning.
[0121] Using this configuration, myoblast cells were patterned with high resolution for
the corresponding outcome displayed in Fig. 6B. At most deposition spots, a single
cell was patterned. Compared to the opening contour of the cantilever represented
in green, the cells appeared to be spotted with high resolution of 5 µm. For patterning
of smaller or wider cells, a cantilever with respective smaller or wider aperture
should be accordingly designed. During patterning, cells were mechanically squeezed
and flattened, which was correlated to their apparent large diameter after patterning
(generally above 20 µm). Cells came back to their original size slowly, within the
next 10 min after patterning.
[0122] The main limitation of the present setup is related to cell adhesion and sedimentation.
Initially contained into the reservoir of the cantilever, the cells started adhering
to the surface after 30 min. The pressure required to push them out needed slowly
to be higher. Cell settling within the supply compartment is a common issue observed
in bioprinting techniques, which affects directly the long-term stability of the system.
To prevent this, other antifouling coatings than PII-g-Peg may be used. A fluidic
system may be as well set up on the back of the device to decouple the reservoir from
the cantilever in order to keep a constant flow running for gentle agitation. Embedding
cells in bio-inks may be an additional alternative.
[0123] So far only additive patterning techniques have been presented, however, large and
complex patterns can be created also by selectively removing cells from an initially
homogeneous culture, as schematized in Fig. 5C. The technology developed was successfully
used as well for selective removal of a single cell or several cells simultaneously
depending on the surface functionalization of the substrate, as illustrated in Fig.
7. As shown in the top panel, on a PDL-coated surface, the cantilever is approached
on the cell of interest before applying underpressure of -800 mbar to detach completely
the cell. One can observe that single cells can be targeted and locally removed in
series without causing any disturbance in the surrounding.
[0124] On a PLL-g-PEG coated surface (bottom panel), we observed that little applied underpressure
of -10 mbar to the cantilever was sufficient to remove cells in a proximity of 300
µm to the aperture (Fig. 7C and D). At higher negative pressures, hundreds of cells
could be aspirated at high speeds, providing a powerful technique for systematic cell
adhesion studies, which could be, for example, modulated by different cantilever-to-substrate
gaps and applied pressures.
[0125] Cell patterns of primary hippocampal neurons were entirely realized on adhesive-coated
surfaces. One pattern example is shown in Fig. 8 in the form of a pumpkin-like smiley.
Although it was not measured, adhesion of neurons on PDL surface was relatively lower
compared to myoblasts: -500 mbar of underpressure was high enough to remove neurons
in the 20 µm vicinity of the aperture contour.
[0126] For such large patterns, the cantilever was set at a sufficient height from the surface-level
(∼10 µm) to avoid moving away the cells on the surface by sweeping the cantilever
on the surface. Since neurons easily gather and migrate together, those patterns realized
on PDL-coated surface were difficult to track after more than a week in vitro.
[0127] To overcome this limitation and provide long-term restrictions on the neuronal growth
of the patterned cultures, the removal process has been repeated on pre-patterned
surfaces. First, smileys of 530 µm in diameter were drawn on bare glass surfaces using
fluorescently labeled PDL ink and a linewidth of 15 µm. The dishes were then backfilled
with PLL-g-PEG, and the neurons were seeded and incubated for 20 min. The cantilever
could enable a selective removal of the unwanted cells that were located on the PII-g-Peg
surface, for a better defined pattern of cells (Fig. 9B). More complex patterns, with
gap interval between PDL lines down to 30 µm, could be realized such as a brain-like
pattern. After 12 DIV, the pattern from B) remained intact without any cell migrating
to the repulsive surface although several neurites started to grow and bridge over
the PEG-coated surface. The pattern depicted in bright field D) and GFP D) constituted
a loop, which was 2 mm-long with mostly one or small group up to 3 neurons connecting
to each other along the circle.
[0128] The technique was also proved to be functional to fully remove unwanted neurons from
the repulsive surface as well as those on the half-right of the adhesive smiley (Fig.
9E) and F)). After 12 DIV, it was unexpectedly observed in E) that no neuron appeared
to move to the PDL-coated area from where cells got initially removed. It also seemed
that neurites and axons could grow over one-mm length on the PDL surface without encountering
another neighbour cell. The loop architecture representing the outline of the smiley
would potentially help to track the novelty in the signal transmitted compared to
the previous reference signal in order to assess meaningful information but also perceive
the selective directionality of the given signal. Viability of those primary neural
cultures was tracked by measuring fluorescent calcium activity.
[0129] In addition, the cantilever proved to be a successful tool to modify
in situ an existing pattern of adhering and mature cell cultures. The thick cantilevers were
robust enough to undergo high underpressure (nearly -900 mbar). Up to 10 sec were
necessary to remove portions of the pattern where neurons started to develop a large
carpet of neurites over the PEG-coated surface, as depicted in Fig. 10A), B) and C).
[0130] Similarly, the cantilever was used to dispense fresh neurons on an existing pattern.
As illustrated in Fig. 10D) and E), a smiley pattern was completed by the controlled
deposition of additional cells at the right-eye location. This approach could largely
profit to extensive mechanical studies of neural networks. Besides, it presents a
high potential to study
in situ mechanisms of cell growth, migration and interaction over long-term studies.
Conclusion
[0131] In this work, a working process was developed based on a sacrificial copper layer
deposited by electroplating to produce robust SU-8 hollow AFM cantilevers. Cantilevers
of various shapes and dimensions, e.g. of 12 µm thickness with channels of 3 µm thickness,
could be fabricated with various spring constants ranging from 0.01 to 1,000 N/m.
Also cantilevers of 50 µm thicknesses with channels of 23 µm thickness could be manufactured.
[0132] The AFM capability of these tipless cantilevers was demonstrated in a biologically
relevant application, by performing single-cell force spectroscopy of yeast cells.
One main advantage of this invention is the provision of micropipette that overcome
the limitation of glass micropipettes limited in terms of throughput and geometry.
[0133] Furthermore, the present work introduces a novel technology based on highly flexible
hollow cantilevers for cell patterning via controlled deposition and selective removal
of single cells. The flexibility of the method has been demonstrated using yeast and
C2C12 cells, as well as primary hippocampal neurons. Several patterning strategies
have been tested in liquid environment with the use of fully cell adhesive and patterned
adhesive/repulsive flat surfaces. The key principle behind the method resulting in
single-cell patterning with an accuracy of 5 µm relies on the physical cell confinement
enabled by the high flexibility of the polymeric cantilevers.
[0134] It has been shown that large engineered neuron patterns can be realized with the
presented method, however, for high throughput and large patterns, subtractive patterning
was found to be more promising with an average removal speed of one targeted cell
per second. Additive patterning is limited by an order of magnitude slower speed and
the consequently smaller patterns.
[0135] Combined with surface patterning methods, the developed precise cell-patterning techniques
can become essential tools for studies related to signal processing and computation
in neuroscience. Providing single neuron-based networks with arbitrary topology can
lead to a better understanding of the relationships between connectivity and function.
[0136] The versatility of the cantilever was proved by modifying
in situ patterns previously realized. Additional cells could be indeed removed or deposited
thanks to the robust hollow cantilever. This latter technique allows deeper studies
for mechanical and cell interactions of cell networks.
[0137] In summary, the developed highly flexible hollow cantilevers represent a promising
new tool for single-cell manipulations and patterning. Compared to other techniques
requiring complex setups and feedback, the presented method works with simple components
and does not require laser feedback. This makes it possible to parallelize the process,
and to operate in complex, highly scattering samples in liquid environment.
Photolithography process
[0138] The microfabrication process was entirely carried out in the BRNC cleanroom facilities
(IBM Zurich Laboratories and ETH Zurich, CH).
[0139] First, a sacrificial release layer 21 of 5 nm chromium/ 50 nm gold/ 50 nm chromium
was deposited onto a silicon wafer used as a carrier substrate (100 mm outside diameter
× 500 µm thickness, SILTRONIX Silicon Technologies, France) by e-beam deposition (BAK501,
Evatec, CH). Wafers were cleaned in 5 min acetone and 5 min isopropanol in ultrasonic
bath (Wet bench, Ramgraber, Germany) before dehydration bake at 200 °C for 5 min (M-HP
200 Hotplate, Ramgraber). Alignment marks, for proper alignment of the different SU-8
layers, were patterned by etching away the chromium top layer only at the mark spots
using MaN 1405 negative photoresist. MaN photoresist was spun at 3000 rpm for 30 s
(OPTIspin SB20, Sigmatek, CH) before being baked at 120 °C for 1 min. Samples were
exposed for 200 mJ/cm
2 at λ = 365 nm (MA6, Suss, Germany) followed by 30 s of development in ma-D533S solution.
Alignment marks could be etched within 10 s in a chromium etchant solution (Chromium
etchant, Sigma Aldrich, USA). Removal of the exposed photoresist and cleaning of the
wafers were carried out by immersion in acetone and isopropanol for 5 min each before
another dehydration bake at 200 °C for 5 min.
[0140] (Fig. 1A): The bottom SU-8 layer 22 was patterned with spin-coating at 3000 rpm (SU-8
2005, Microchem, USA), soft bake for 1 min at 65 °C and 2 min at 95 °C. Systematically,
wafers were cooled down to 50 °C on a hot plate avoiding any thermal shock. UV exposure
was performed using 160 mJ/cm
2 exposure dose at λ = 365 nm in vacuum contact mode (for a better definition of the
aperture). Post-exposure bake was performed for 1 min at 65 °C and 3 min at 95 °C
before development for 2 min (PGMEA, Sigma Aldrich) and rinsing with fresh isopropanol.
[0141] (Fig. 1 B): The copper seed layer 23 was deposited by thermal evaporation for a thickness
of 150 nm in two steps with 75 nm each using a tilted plate at 35 degrees, an emission
current of 3.6 A, a pressure of 5x10
-7 bar and a deposition rate of 0.45 nm/s (PLS 500, Pfeiffer, CH).
[0142] (Fig. 1 C): Positive AZ4562 photoresist 24 was used to confine the growth according
to the following parameters: spin-coating at 4000 rpm for 40 s, soft bake for 1 min
at 65 °C and 1 min at 95 °C, exposure for 160 mJ/cm
2 at λ = 365 nm, post-exposure bake for 1 min at 65 °C and 1 min at 95 °C before development
for 2 min in AZ 400K 1:3 diluted solution (MicroChemicals, Germany). Prior to electroplating,
samples were plasma treated at 200 W for 1 min (GIGAbatch 310 M, PVA TePla, Germany)
and dipped in sulfuric acid for 20 s at 1:9 diluted solution (99.999 % Sulfuric acid,
Sigma Aldrich).
[0143] (Fig. 1 D): Copper plating 25 was performed using copper sulfate solution (InterVia
Cu 8540, Rohm and Haas, USA) and commercial setup (Luder Technik AG, CH) for current
and voltage applied of respectively 160 mA and 10.2 V during 3 min for copper thickness
growth of 3 µm, after electrically contacting the wafer edges at eight equidistant
locations. Thickness was controlled with a stylus profiler (Dektak 6M, Veeco, USA).
[0144] (Fig. 1 E): AZ4562 24 was stripped within 10 s in an acetone bath before etching
of the seed copper layer 23 for another 5 s (Copper etchant, Sigma Aldrich) and rinsing
for 2 min in DI-water.
[0145] (Fig. 1 F): The top SU-8 layer 26 was patterned with spin-coating at 4000 rpm for
30 s (SU-8 10, Microchem), soft bake for 3 min at 65 °C and 7 min at 95 °C, exposure
for 400 mJ/cm
2 at λ = 365 nm, post-exposure bake for 1 min at 65 °C and 3 min at 95 °C, development
for 3 min and rinsing with fresh isopropanol.
[0146] (Fig. 1 G): The thick block SU-8 layer 28 (SU-8 100, Microchem) was patterned with
spin-coating at 1250 rpm for 40 s, break of few hours to flatten the thick layer,
soft bake for 30 min at 65 °C and 75 min at 95 °C, cooling down on hot plate back
to room temperature, exposure for 1200 mJ/cm
2 at λ = 365 nm, post-exposure bake for 2 min at 65 °C and 18 min at 95 °C, cooling
down on hot plate back to room temperature, development for 40 min and rinsing with
fresh isopropanol.
[0147] Finally, hard bake was performed to enhance adhesion between both bottom 22 and top
layers 26 at 70 °C for 2 h (VT6060M, Thermo Scientific Heraeus). This step was optimized
for better cross-linking and mechanical robustness of the cantilevers but also to
limit their delamination from the substrate. To enhance wetting, wafers were plasma-treated
with air pressure of 0.02 mbar, RF power of 18 W for 2 min (PDC-32G, Harrick Plasma,
USA) before copper etching during 10 days and release from the wafer (Fig. 1 H).
[0148] For AFM applications, SU-8 cantilevers were coated with a thin reflective layer of
2 nm Cr/10 nm Au (E306A Coating System, Edwards, England). Parafilm M substrate (Bemis,
USA) was used to carry the devices (excluding cantilevers bending).
[0149] Hollow SU-8 polymeric cantilevers for controlled single-cell deposition and patterning
decribed above were fabricated following the protocol described above. The process
based on electroplated copper as sacrificial layer was adapted for the cell-related
experiments by producing cantilevers with integrated microchannels of 22 µm in height.
In brief, a positive AZ4562 photoresist was patterned with a thickness of 25 µm to
confine the copper growth within the channel area using the following parameters:
spin-coating at 2 000 rpm for 4 sec with 1 000 rpm/sec acceleration, baking for 1
min at 65 °C and 1 min at 95 °C, exposure in 500 mJ/cm2 at λ = 365 nm, then post-exposure
baking for 1 min at 65 °C and 1 min at 95 °C before development. Applying 500 mA and
10.2 V for 6 min resulted in a growth of a copper layer with a thickness of 22 µm
on the wafer. Further steps of the fabrication process were identical to that of the
original protocol. The resulted cantilevers had a total height of 45 µm, lengths ranging
from 250 to 400 µm, and widths from 50 to 80 µm.
SEM
[0150] Scanning electron microscopic (SEM) images were taken using a Zeiss NVision 40 (Germany)
with an accelerating voltage between 5 and 10 kV.
Fluidic setup
[0151] SU-8 cantilevers were glued on a PMMA clip containing a 25 µL reservoir connected
to a pressure controller (Cytosurge, CH) through a tubing system allowing to apply
a large range of pressure from -800 mbar to + 1000 mbar. Before use, to avoid any
possible contamination of copper residues, copper etchant, or chromium etchant, the
SU-8 device was completely flushed with DI-water for 15 min after plasma activation
for 5 min (PDC-32G, Harrick Plasma).
[0152] The flow rate was calibrated using a digital liquid flow sensor placed close to the
reservoir (LG16- 0025-D, Sensirion, CH).
[0153] Hydrostatic tests were performed using stationary gas supply from the lab connected
to a pressure regulator and a manometer (pressure limited to 6 bars). An FITC dye
was used to fill the cantilever and to detect any potential leaks.
AFM experiments for studying cell adhesion using force spectroscopy
[0154] The AFM experiments were carried at 23 °C with a NanoWizard® I BioAFM from JPK Instruments
(Germany) mounted on an optical microscope (Axiovert 40 MAT, Zeiss). The AFM was operated
with a 15 µm range piezo-stage using the force spectroscopy mode. Before performing
force spectroscopy experiments, all cantilevers were kept at rest in liquid from 30
min to 1 h until voltage- deflection signal became stable. Drift is inevitable with
the use of polymeric SU-8 cantilevers. However, high overexposure and baking time
probably limited the voids rate within the SU-8 matrix, capable of absorbing liquid.
[0155] The SU-8 cantilever spring constant was calibrated using the thermal noise via the
conventional Sader's method in air environment on glass substrate with the SPM Control
Software V4 (JPK). The sensitivity deflection measured with regard to the optical
lever sensitivity (OLS) followed the configuration where only the end of the cantilever
was touching the substrate.
[0156] Force spectroscopy curves were obtained by selecting optically a single yeast and
subsequently approaching the cantilever on top by systematically using a set point
fixed at 50 nN. Approach and retraction curves were both recorded over a length of
10 µm for 5 s each (i.e. speed of 2 µm/s). Approach was followed by a contact pause
of 5 s during which force was kept constant and an underpressure of -500 mbar was
applied to immobilize the yeast cell at the aperture of the cantilever before subsequent
retraction. Finally, every yeast was released by applying an overpressure of 1000
mbar before targeting a new yeast.
Experimental setup for controlled single-cell deposition and patterning by the highly
flexible hollow cantilevers of the invention
[0157] Hollow cantilevers were connected to a pressure controller (Cytosurge, Switzerland)
and mounted on an atomic force microscope (NanoWizard 1 BioScience AFM; JPK Instruments
AG, Germany) for controlling their z-position with sub-µm precision (no laser force
feedback has been used for the experiments). Free-hanging cantilevers had an inclination
angle of 8-10° with respect to the substrate. The AFM stage was placed on an inverted
microscope (Axio Observer.Z1) equipped with a Colibri LED light source system (both
from Carl Zeiss AG, Switzerland), an incubation chamber, and a CCD camera (C9100-13;
Hamamatsu, Japan). The temperature control of the incubation chamber has been used
only for the neuron related experiments keeping the setup at 37 °C, the other experiments
were performed at room temperature.
[0158] Additionally, CLSM images were taken using a LSM 510 mounted on an Axiovert 200 M
motorized microscope (Zeiss), while scanning electron microscope (SEM) images were
taken with the help of an NVision 40 (Zeiss) using accelerating voltages in the range
of 5-10 kV.
Chemicals
[0159] Purified Milli-Q water was produced by an Elix 5 water purification system (Merck
Millipore, USA). Fluorescent cell-adhesive solution was prepared by mixing 100 µg/ml
Poly-D-lysine (PDL, P6407 70-150kDa; Sigma-Aldrich) with 40 µg/ml fluorescently tagged
secondary antibody (anti-mouse IgG (H+L), CF 555; Sigma-Aldrich) diluted in phosphate-buffered
saline (PBS, pH 7.4; Thermo Fisher Scientific AG, Switzerland). PLL-g-PEG solution
was prepared from powder (PLL(20)-g[3.5]-PEG(2); SuSoS AG, Switzerland) and diluted
in PBS to a final concentration of 100 µg/ml if not indicated otherwise.
Cells culturing and substrate preparation
[0160] Glass substrates (GWSB-5040, WillcoWells, NL) were plasma treated for 30 s.
[0161] PDA-coated substrates were initially plasma treated for 30 s, immersed in a 10 mM
TRIS HCL solution pH 8 containing 4 mg/mL PDA (Sigma Aldrich) for 1 h, then intensively
washed with filtered PBS and dried with N
2.
[0162] Wildtype Saccharomyces cerevisiae (W303) were grown in yeast extractpeptone-dextrose
medium (10 g yeast extract (Oxoid), 20 g bactopeptone (BD) and 20 g glucose (Sigma-Aldrich)
in 1 L ddH
2O, with 15 g Agar (Sigma-Aldrich) for solid media). The yeasts were plated onto YPD
plates and incubated for 2-3 days at 28 °C. Until the force spectroscopies were performed,
colony containing plates were kept for up to three month at 4 °C.
[0163] Prior to the experiments, individual colonies were picked, resuspended in PBS medium
(10010023, Life Technologies, USA) before directly letting them sediment on top of
glass substrates for SCFS experiments at room temperature during 10 min. 20 µL yeasts
colony solution was directly injected on top of the substrates previously filled up
with 3 mL PBS.
[0164] Mouse myoblast C2C12 cells (American Type Cell Collection) were cultured in C2C12
culture medium (DMEM/F-12 supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic;
all from Thermo Fischer) at 37 °C and 5% CO
2. Prior to the patterning experiments, cells were trypsinized (with TrypLE Express;
Thermo Fischer) and fluorescently tagged with a PKH26 Red Fluorescent Cell Linker
Kit (Sigma Aldrich).
[0165] Primary Hippocampal Neurons were prepared from E17 embryos of time-mated pregnant
Wistar rats (Harlan Laboratories, NL), and cultured in neuronal culture medium (neurobasal
medium mixed with 2% B-27 serum-free supplement, 1% penicillin-streptomycin, and 1%
GlutaMAX; all from Thermo Fischer) at 37°C and 5% CO
2.
Cantilever preparation
[0166] Before the experiments, cantilevers were coated with PLL-g-PEG (0.5 mg/ml in PBS)
for 45 min then flushed with fresh PBS to make the surface anti-adhesive. For plating
experiments with yeast, individual colonies were resuspended in PBS and injected into
the reservoir of the cantilevers at a concentration of 100'000 cells/ml. For plating
experiments with C2C12, cells were resuspended at a concentration of 100'000 cells/ml
in HBSS (Hank's Balanced Salt Solution H8264; Thermo Scientific).
Substrate preparation
[0167] Glass bottom dishes (GWSB-5040; WillCo Wells B.V., The Netherlands) were used for
all the experiments. The dishes were oxygen plasma activated for 2 min at 18 W, then
were either filled up with PBS, or incubated with a non-fluorescent PDL solution for
1 h, rinsed 3 times with Milli-Q water, and blow dried with nitrogen gas to create
a fully adhesive surface.
[0168] Before the patterning experiments, dishes were filled with medium corresponding to
the cell type used. For the subtractive patterning experiments, cells were seeded
at a density of 150'000 cells/cm
2 and incubated for 20 min.
Surface patterning
[0169] Patterned cell-adhesive surfaces for neuronal cultures have been prepared with the
help of a hollow cantilever as a probe. In brief, a tipless hollow cantilever was
filled with the fluorescent cell-adhesive solution, connected to the pressure controller,
and then mounted on a standard AFM head (FlexAFM; Nanosurf, Switzerland). Once the
probe was placed on top of the dish and submerged in the PBS, 10 mbar overpressure
was applied from the pressure controller to continuously push the patterning solution
out of the probe. After the patterning, dishes were rinsed with Milli-Q and blow dried
with nitrogen gas, and then PLL-g-PEG solution was added in order to increase the
contrast between patterned and non-patterned surface regions by backfilling. After
1 h of incubation the dishes were rinsed three times with PBS, then were filled up
with cell culture medium and stored in the incubator until cell seeding.
1. A method for manufacturing a device (100) comprising a flexible shank (11), and said
shank (11) comprises a microfluidic channel (12) having an aperture (13), the method
comprises the steps of:
- providing a support covered by a sacrificial release layer (21), wherein particularly
said sacrificial release layer (21) is characterized by a thickness in the range of 5 nm to 500 nm;
- depositing a bottom layer (22) of a first photoresist onto said sacrificial release
layer (21), wherein said bottom layer (22) is characterized by a thickness in the range of 0.5 µm to 100 µm;
- partially curing said bottom layer (22) within a first defined pattern (22), wherein
said bottom layer (22) optionally comprises said aperture (13);
- depositing a metal seed layer (23) onto said bottom layer (22);
- depositing a mould layer (24) of a second photoresist onto said metal seed layer
(23);
- curing said mould layer (24) within a second defined pattern (24), thereby yielding
a cured mould layer (24), wherein a part (23a) of said metal seed layer (23) covering
said bottom layer (22) is not covered by said cured mould layer (24);
- depositing an additional metal layer (25) onto said part (23a) of said metal seed
layer (23) not covered by said cured mould layer (24), wherein said additional metal
layer (25) is characterized by a thickness in the range of 0.1 µm to 30 µm;
- dissolving said cured mould layer (24) and said metal seed layer (23);
- depositing a cover layer (26) of said first photoresist onto said bottom layer (22)
and said additional metal layer (25), wherein said cover layer is characterized by a thickness in the range of 0.5 µm to 100 µm;
- completely curing said first photoresist comprised within said cover layer (26)
and said bottom layer (22) within a third defined pattern (26), thereby forming a
bottomside, sidewalls and a topside of said device (100);
- dissolving said additional metal layer (25); and
- dissolving said sacrificial release layer (21) releasing said device (100) from
said support.
2. The method according to claim 1, characterized in that a handling block layer (28, 15) is attached onto said cover layer (26), wherein said
handling block layer (28, 15) comprises a through hole (16) being in fluid communication
with said microchannel (12), and wherein said handling block layer (28, 15) is characterized by a thickness in the range of 100 µm to 300 µm, preferably 250 µm.
3. The method according to claim 1 or 2, characterized in that said first photoresist is a negative photoresist, particularly SU-8.
4. The method according to any one of the preceding claims, characterized in that said second photoresist is a positive photoresist, particularly AZ4562.
5. The method according to any one of the preceding claims, characterized in that said bottom layer (22), said mould layer (24) and/or said cover layer (26) are deposited
by spin coating.
6. The method according to any one of the preceding claims, characterized in that said bottom layer (22) and said coverlayer (26) are cured such with said first defined
pattern and said third defined pattern, respectively, that said shaft (11) of said
device (100) comprises a tip (17) that extends along a first direction, wherein the
angle between said first direction and the longitudinal axis of said shank (11) or
said microfluidic channel (12) is in the range of 180° to 90°.
7. The method according to any one of the preceding claims, characterized in that said said bottom layer (22) and said coverlayer (26) are cured such with said first
defined pattern and said third defined pattern, respectively, that said shaft (11)
exhibits a curved shape, a jagged shape, a zigzag shape, or a shape comprising a step.
8. A device (100) having:
- a flexible shank (11) comprising a microfluidic channel (12) and an aperture (13)
that is in fluid communication with said microfluidic channel (12), wherein said microfluidic
channel (12) is delimited by at least one surface being formed by a polymer, and
- a reservoir (14) in fluid communication to said microfluidic channel (12), whereby
said aperture (13) is oriented at the end of said flexible shank (12) opposite to
said reservoir (14), and
- a means for measuring a mechanical force acting on said flexible shank (11) arranged
on or within said flexible shank (11), and
- optionally a handling means (15) with a through hole (16) in fluid communication
with said reservoir (14),
characterized in that
- said polymer forming said at least one surface delimiting said microfluidic channel
(12) is integrally formed in one piece, and particularly said polymer is characterized by an elasticity of 1 GPa to 10 GPa, preferably 4 GPa to 5 GPa, more preferable 4.5
GPa, and
- said microfluidc channel (12) is configured to pass a fluid stream with pressure
of up to 6 bar (a), and particularly is fluid tight up a pressure of 6 bar(a), and
- said flexible shank (11) is characterized by spring constant in the range of 0.01 N*m-1 to 1,000 N*m-1.
9. The device according to claim 8, characterized in that said polymer forming at least one surface delimiting said microfluidic channel (12)
exhibits a homogenous structure.
10. The device according to claim 8 or 9, characterized in that said polymer is a cured photosensitive polymer, particularly SU-8.
11. The device according to any one of claims 8 to 10,
characterized in that
- said microfluidic channel (12) has a length in the range of 0.1 mm to 50 mm and/or
a width in the range of 1 µm to 50 µm and/or a height in the range of 0.1 µm to 30
µm; and/or
- said shank (11) has a thickness in the range of 10 µm to 50 µm, and/or a width in
the range of 20 µm to 80 µm.
12. The device according to any one of claims 8 to 11,
characterized in that said means for measuring a mechanical force acting on said flexible shank (11) is
formed by
- a metal layer consisting of at least one noble, non-toxic metal, whereby said metal
layer is able to changes its resistance in dependence of a mechanical force acting
on said metal layer; or
- a sensing layer comprising a plurality of nanowires (31) made of metal, wherein
said nanowires (31) are partially coated with an isolator such that at least a part
of said nanowires (31) are in conductive contact to each other when no mechanical
force is acting on said shank (11), and said at least one part of said nanowires (31)
in conductive contact to each other decreases with increase of an mechnical forces
acting on said shank, wherein particularly said nanowires (31) are characterized by a thickness in the range of 40 nm to 60 nm and/or a length in the range of 5 µm to
50 µm;
- a sensing layer comprising a plurality of nanowires (31) made of metal, wherein
said nanowires (31) are arranged such within the sensing layer that at least a part
of said nanowires (31) are in conductive contact to each other when no mechanical
force acts on said shank (11), and said at least one part of said nanowires (31) in
conducting contact to each other decreases with increase of an mechnical forces acting
on said shank, wherein particularly said nanowires (31) are characterized by a thickness in the range of 40 nm to 60 nm and/or a length in the range of 5 µm to
50 µm;
- a part of said shank (11) being optically transparent, wherein said part of said
shank (11) is configured to change its optical properties, particularly its refractive
or diffractive properties, in dependence of a mechanical force acting on said part
of said shank (11).
13. The device according to any one of claims 8 to 12, characterized in that said aperture (13) is comprised within a tip (17) of said shank (11), wherein said
tip (17) extends along a first direction, and the angle between said first direction
(R) and the longitudinal axis of said shank (11) or said microfluidic channel (12)
is in the range of 180° to 90°, and wherein said tip (17) has a tapered shape or a
cylindrical shape.
14. The device according to any one of claims 8 to 13, characterized in that said shank (11) exhibits a curved shape, a jagged shape, a zigzag shape or a shape
comprising a step, wherein said curved shape, said jagged shape, said zigzag shape
or said shape comprising a step extends within a plane being parallel to said first
direction.
15. The device according to any one of claims 8 to 14, characterized in that said device (100) or said flexible shank (11) is designed as a cantilever or a micropipette,
wherein said micropipette optionally comprises a re-usable tip (17) comprising a plurality
of segments extending from said shank (11), wherein each segment is characterized by a tapered shape, and between each segment a portion of said tip is arranged, and
wherein at least one of said portions arranged between said segments is designed as
predetermined breaking point.