[0001] This invention relates to the flow of liquid through an aperture leading from a surface,
the liquid having arrived on the surface in the form of a drop.
[0002] In U.S. Patent Specification No. 3,690,836 there is disclosed a device for use in
the study of chemical and biological reactions and method of making same. One embodiment
therein disclosed includes an exterior surface having an aperture extending from the
exterior surface to a zone within the device. This zone is a capillary tube or chamber.
The tube or chamber is filled with liquid introduced through the aperture. In this
known device the ingress aperture for introduction of liquid has a smooth, cylindrical
sidewall. Such an aperture has the disadvantage that a drop of liquid which is not
accurately placed on the exterior surface, that is, it is placed with its centre outside
the sidewall of the aperture, tends to stay outside the aperture rather than move
into it. It is only when the centre of the drop is deposited well within the aperture
that the surface tension of the liquid drop forces.the drop into the aperture in full
contact with the sidewall. In particular this has been a problem when the exterior
surface is formed of material which tends to be hydrophobic, that is, that forms with
the liquid a liquid-vapour contact angle that is greater than 90°. For example certain
plastics materials are sufficiently hydrophobic that drops of liquid such as blood
serum are more likely to remain on the exterior surface than to flow into the aperture.
[0003] In accordance with the present invention there is provided a liquid transport device
having an exterior surface, an aperture extending from the exterior surface to a zone
within the device, said zone having means for transporting the liquid through a zone,
characterized in that at least the intersection of said exterior surface and the bounding
surface of the aperture includes, at a predetermined location, means for substantially
urging a portion of a drop of liquid deposited thereon to move into contact with the
bounding surface of the aperture.
[0004] Such a device is particularly useful in introducing liquid into a transport zone
between two opposed transport surfaces spaced apart a distance effective to induce
capillary flow of the liquid between the transport surfaces.
[0005] Embodiments of the present invention will now be described, by way of example, with
reference to the accompanying drawings in which:
Fig. 1 is an enlarged perspective view of a device in accordance with the invention;
Fig. 2 is an elevational view in section taken on the line II-II in Fig. 1, demonstrating
the operation of the device;
Fig. 3 is a fragmentary, diagrammatic plan view illustrating an effect achieved in
a device in accordance with the invention;
Fig. 4 is a plan view of a second embodiment of the invention; and
Fig. 5 is a sectional view taken generally along the plane of line V-V in Fig. 4.
[0006] The device and method of this invention is described in connection with embodiments
featuring the capillary transport of biological liquids and particularly blood serum,
between two opposed surfaces. In addition, the device and method can be applied to
any liquid a drop of which is to be carried through an ingress aperture from an exterior
surface to a transport means for transporting the liquid for any purpose. For example,
industrial liquids can be so transported.
[0007] A device 10 constructed in accordance with one embodiment of the invention comprises
(see Fig. 1) two members 12 and 14 having respective exterior surfaces 16 and 18,
and respective interior, opposed surfaces 20 and 22. The members 12, 14 have
boundary edge surfaces 24. Surfaces 20 and 22 are spaced apart a distance "x" (see
Fig. 2) such that capillary flow of liquid is induced between the surfaces. In this
manner the spaced-apart surfaces 20 and 22 define a transport zone 26 and act as means
for transporting introduced liquid between the surfaces. As will be readily apparent,
a range of values for "x" is permissible, and the exact value depends upon the liquid
being transported.
[0008] Surfaces 20 and 22 can each be smooth, as illustrated in Figs. 1 and 2, or provided
with a variety of surface configurations such as parallel grooves, the grooves of
one surface being aligned, or at a positive angle, with respect to the grooves of
the other.
[0009] A preferred means for introducing a drop of liquid into zone 26 is an aperture 30
extending from surface 16 to surface 20, through member 12. The aperture 30 comprises
a sidewall 32 extending between the surfaces 16 and 20. The preferred largest dimension
of aperture 30 in plan (for example the diameter of the smallest circle which entirely
encompasses the plan form of the aperture), is one which is about equal to the greatest
diameter of the drop expected to be received by the aperture 30. The drop diameter
is dictated by the volume and surface tension of the drop. The volume of the drop
should be adequate to fill transport zone 26 to the extent desired. For uses such
as clinical analysis as herein described, a convenient drop volume is about 10 µl.
Thus, since a 10 µl drop of serum having 70 dynes/cm surface tension has a diameter
of about 0.26 cm, the largest flow- through dimension, measured as described above
is preferably about 0.26 cm.
[0010] The intersection of surface 16 and sidewall 32 is provided with means that encourage
the selected drop of liquid deposited or received in the plane of surface 16 generally
at aperture 30, to move into contact with the entire perimeter of sidewall 32. More
specifically, sidewall 32 is shaped so as to comprise a plurality of surfaces that
intersect, at least at and adjacent surface 16, at predetermined locations to form
a plurality of interior corners 34. As used herein, "predetermined location" or "locations"
means locations deliberately chosen, and distinguishes the present invention from
cylindrical apertures which inadvertently or accidentally have imperfections, such
as microscopic corners, in the sidewall. Such accidental constructs are not capable
of providing the substantial urging of the drop into the aperture which the present
invention provides. As shown in Fig. 1, sidewall 32 comprises throughout its perimeter,
six sidewall surfaces and six such predetermined corners 34. In this embodiment equal
angles of such corners 34 and equal lengths of the intersecting surfaces (measured
in the direction of the perimeter of the sidewall 32) are selected to provide a shape,
when viewed in plan, i.e. perpendicular to the surface l6, that is a regular hexagon,
the preferred configuration.
[0011] In operation (see Fig. 2) device 10 is placed in a drop-displacing zone adjacent
to a source of drops. A drop A of liquid such as blood serum, or whole blood, is dropped
onto the device as a free- form drop or is touched off from a pendant surface onto
surface 16 generally at aperture 30. The surface l6 preferably is maintained in a
generally horizontal orientation during this step. Corners 34 act to centre the drop
and urge it into contact with the surfaces of sidewall 32. It then moves down into
zone 26 and into contact with surface 22, where capillary attraction further causes
the liquid to spread throughout zone 26, (see the arrows 36), so that the bounding
meniscus arrives at the position shown in broken lines. Assuming sufficient volume
in the drop, the spreading ceases at edge surfaces 24 which define an energy barrier
to further capillary flow. Once the drop of liquid is so distributed, a variety of
processing can be done to or with the liquid.
[0012] In order to ensure effective filling of the aperture the drop should be applied to
aperture 30 so as to contact one of the corners. The effect is most pronounced when
the centre of gravity of the drop is positioned over the aperture 30, rather than
over the solid surface 16.
[0013] To vent air as the liquid advances within zone 26, means are provided within the
device, such as the open space between members 12 and 14 along all or a portion of
any one of edge surfaces 24. Alternatively, a second aperture (not shown) can be formed
in either member 12 or 14.
[0014] The corners of the aperture 30, at the surface 16 where the drop is first applied,
seem to act as centres of force which induce the drop to move into contact with sidewall
32 along its entire perimeter or circumference. That is, referring to Fig. 3, it is
believed that the centring force F
3 of a drop A applied at one of the corners 34 is significantly greater than the corresponding
centring force F
1 or F
2 that exists for a drop A' placed at any adjacent location 38 or 39 spaced away from
a corner 34. At least one corner
34 is needed for the.effect. However, at least three corners 34 are preferred, as in
Fig. 3, to ensure a greater likelihood that the drop A will be is contact with a corner
34 when it contacts surface 16,
[0015] For a predetermined largest dimension of the aperture 30 calculated as described
above, the greater the number of corners that are created by the use of a corresponding
number of intersecting surfaces, then the greater is the likelihood that the drop
will contact a corner. However, as the number of corners is increased, so is the value
of the interior angle of each corner, until eventually the sidewall 32 approaches
a smooth, curved surface in shape wherein all the centring forces are equal, and the
effect is lost. It has been found, therefore, that a preferred number of corners is
between three and about ten. Highly preferred is six corners in a regular hexagon.
[0016] As a matter of practicality, the corners 34 will have a slight radius of curvature.
For the corners to be effective, they each should have a radius of curvature that
is no larger than about 0.4 mm.
[0017] Although flat or planar surfaces are preferred between the corners, they can also
be continuously curved as is shown, between the two lower corners 34 in Fig. 3.
[0018] Although the centring mechanism of the corners is not fully understood, it is believed
that the effect is due to forces that apply to the compound meniscus when the drop
is located at a corner 34. As is well known, a compound meniscus is one in which the
principal radii of curvature of the drop surface vary, depending on the location taken
on the surface of the drop. If the drop is properly located at a corner, the compound
meniscus forms a drop that extends laterally farther out over the aperture than it
does when not located at a corner, and the weight of this extension causes the drop
to fall or otherwise move into contact with the perimeter of sidewall 32 and then
through the aperture 30. It may also be-that there is at the corner a greater tendency
for the drop to wet the sidewall than would occur in the absence of a corner.
[0019] It will be readily appreciated that the centring force of corners 34 is needed primarily
at the intersection of sidewall 32 and exterior surface 16. Thus, aperture 30 will
function equally as well if sidewall 32 is smoothed out, as it approaches surface
20,to form a cylinder (not shown).
[0020] In addition, it will also be appreciated that the presence of a capillary zone around
the downstream end of aperture 30 assists in drawing the drop through aperture 30
and into the zone.
[0021] Members 12 and 14 can be formed from any suitable material, such as plastics or metal.
[0022] In Figs. 4 and 5, there is illustrated a second embodiment of the device. This second
embodiment is one in which a transport chamber is formed for radiometric analysis
of an analyte of a biological liquid such as blood. Parts similar to those previously
described bear the same reference numeral but with the distinguishing suffix "a" appended.
Device 10a features a support member 14a (see Fig. 5), a cover member 12a, a spacer
member 50 used to adhere members 12a and 14a together, and a radiometrically detectable
test element 60 disposed on support 14a. The test element 60 is spaced away from member
12a so that there is a transport zone 26a between element 60 and member 12a. The spacing
between surface 20a and the test element 60 is such as to produce a capillary effect
to induce the drop that enters through aperture 30a to spread throughout the zone
26a. Preferably, the test element 60 abuts against the spacer member 50, and is held
against member 14a by, for example, adhesive..
[0023] Thus, the members 12a, 14a and 50 define a capillary transport chamber containing
the test element 60 and having any convenient shape, such as a rectangular chamber
when viewed in plan, as in Fig. 4.
[0024] Any suitable joining means can be employed between members 12a and 50, and members
50 and l4a. For example, a variety of adhesives can be used, or if all the members
are thermoplastic, ultrasonic welding or heat-sealing can be used.
[0025] Member 12a is provided with an access aperture 30a extending through the member from
its exterior surface 16a to zone 26a, disposed directly above a portion of test element
60. At least that portion of the aperture's sidewall 32a that intersects with surface
16a is provided with corners 34a, as described above. Preferably sidewall 32a is in
the cross-sectional shape of a regular hexagon. An additional, cylindrically shaped,
aperture 70 in member 12a acts as a vent for expelled air.
[0026] A viewing port 80 is optionally provided in support member l4a, particularly when
the latter member is not itself transparent.
[0027] Test element 60 comprises an optional transparent support 62, formed, for example
of poly (ethylene terephthalate), and at least an absorbent layer 64 disposed on support
62. Such layer can have- a variety of binder compositions, for example, gelatin, cellulose
acetate butyrate, polyvinyl alcohol, agarose and the like, the degree of hydrophilicity
of which depends upon the material selected. Gelatin is particularly preferred as
it acts as a wetting agent to provide for uniform liquid flow through zone 26a. Support
62 can be omitted where adequate support for layer 64 can be obtained from support
member 14a.
[0028] Additional layers such as a layer 66 can be disposed above layer 64 to provide a
variety of chemistries or functions, such as to provide, either in layer 66 alone
or together with layer 64, a reagent composition. Filtering, registration and mordanting
functions can be provided also by such additional layers, such as are described in
U.S. Patent Specification No. 4,042,335. Thus, layer 66 .can comprise a reagent, such
as an enzyme, and a binder of the same type as is used for layer 64.
[0029] As used herein, "reagent" in "reagent composition" means a material that is capable
of interaction with an analyte, a precursor of an analyte, a decomposition product
of an analyte, or an intermediate. Thus, one of the reagents can be a preformed, radiometrically
detectable species that is caused by the analyte of choice to move out of a radiometrically
opaque portion or layer of the element, such as layer 66, into a radiometrically transparent
portion or layer, such as a registration layer.
[0030] The noted interaction between the reagents of the reagent composition and the analyte
is therefore meant to refer to chemical reaction, catalytic activity as in the formation
of an enzyme-substrate complex, or any other form of chemical or physical interaction,
including physical displacement, that can produce ultimately a radiometrically detectable
signal in the element 60. As is well known, radiometric detection includes both colorimetric
and fluorimetric detection, depending upon the indicator reagent selected for the
assay. The assay of the element is designed to produce a signal that is proportional
to the amount of analyte that is present.
[0031] A wide variety of radiometric assays can be provided by element 60. Preferably, the
assays are all oxygen-independent, as the flow of blood or blood serum into zone 26a
tends to seal off element 60 from any additional oxygen. Typical analytes which can
be tested include BUN, total protein, bilirubin and the like. The necessary reagents
and binder or vehicle compositions for the layers of element 60, such as layers 64
and 66, for these analytes can be those described in, respectively, U.S. Patent Specification
Nos. 4,066,403, 4,132,528 and 4,069,016 or 4,069,017.
[0032] Quantitative detection of the change produced in element 60 by reason of the analyte
of the test element is preferably made by scanning the element through port 80 with
a photometer or fluori- meter. A variety of such instruments can be used, for example
the radiometer disclosed in German OLS 2,755,334, or the photometer described in U.S.
Patent Specification No. 4,119,381. '
[0033] The following is an illustrative example of the device shown in Figs. 4 and 5.
Example
[0034] Members 12a and 14a are formed from polystyrene of a thickness 0.127 and 0.254 mm,
respectively. Member 50 is steel of a thickness 0.38 mm. The three members are sealed
together by adhesives such as polybutyl acrylate adhesive obtainable from Franklin
Chemical under the trademark "Covinax". Apertures 30a and 70 in member 12a are about
8 mm apart on centre. The outside diameter of the hexagon form of aperture 30a is
about 2.6 mm. View port 80 is about 5 mm in diameter. The capillary spacing between
test element 60 and member 12a is about 0.05 mm and the width of element 60 is about
11.5 mm.
[0035] For a test element 60 designed to detect total protein in a 10 µl drop of blood serum,
the following sequential layers are used:

1. A liquid transport device having an exterior surface, an aperture extending from
the exterior surface to a zone within the device, said zone having means for transporting
the liquid through a zone, characterized in that at least the intersection of said
exterior surface and the bounding surface of the aperture includes, at a predetermined
location, means for substantially urging a portion of a drop of liquid deposited thereon
to move into contact with the bounding surface of the aperture.
2. A device according to claim 1, characterized in that said urging means comprises
a surface configuration capable of forming a compound meniscus on a contacting liquid
drop.
3. A device according to claim 1 or 2, characterized in that said urging means comprises
at least one interior corner in the bounding surface of the aperture at at least its
intersection with said exterior surface.
4. A device according to claim 3, characterized in that there are from three to ten
similar interior corners at predetermined spaced-apart locations at at least said
intersection.
5. A device according to claim 4, characterized in that there are six of said corners.
6. A device according to claim 5, characterized in that the bounding surface of the
aperture conforms to a regular hexagon at least adjacent the exterior surface.
7. A device according to any one of the preceding claims, characterized in that the
transporting means in said zone includes two opposed surfaces of the zone spaced apart
a distance such as to cause capillarity.
8. A device according to claim 7, characterized in that at least one of said two spaced-apart
opposed surfaces includes an absorbent layer containing at least one reagent capable
of producing a radiometrically detectable signal when contacted by the liquid of the
drop.
9. A device according to claim 3 or any one of claims 4 to 8 when appendant directly
or indirectly to claim 3, characterized in that the corner or each of the corners
extends throughout the length of the bounding surface of the aperture, from the exterior
surface to the zone.