BIOCHIP STORAGE WELLS
20170348692 · 2017-12-07
Inventors
- Stuart JACKSON (Northern Ireland, GB)
- Ivan MCCONNELL (Northern Ireland, GB)
- John LAMONT (Northern Ireland, GB)
- Peter FITZGERALD (Northern Ireland, GB)
- Marc WHARRY (Northern Ireland, GB)
Cpc classification
B01L2300/045
PERFORMING OPERATIONS; TRANSPORTING
B01L2300/0636
PERFORMING OPERATIONS; TRANSPORTING
B01L2300/047
PERFORMING OPERATIONS; TRANSPORTING
B01L2300/044
PERFORMING OPERATIONS; TRANSPORTING
B01L9/52
PERFORMING OPERATIONS; TRANSPORTING
B01L2300/161
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
The present invention is directed to a cap for a biochip storage well. The cap comprises a resilient sealant layer capable, under the application of pressure, of forming a vapour-proof seal with a line contact interface formation extending around the perimeter of a biochip storage well.
An assay assembly comprising the cap of the invention and a biochip storage is disclosed. Methods of sealing a biochip storage well using a cap of the invention are also disclosed.
Claims
1-11. (canceled)
12. An assay assembly comprising a biochip storage well having a base and one or more side walls, adapted to receive a biochip, with a line contact interface formation facing away from the base and extending along an upwardly facing perimeter of the wall(s) and a cap comprising a resilient sealant layer, wherein a vapour-proof seal can be formed between the resilient sealant layer of the cap and the line contact interface formation of the biochip storage well, when the resilient sealant layer of the cap is applied, under pressure, against the line contact interface formation.
13. The assay assembly according to claim 12, wherein the line contact interface formation is in the form of a knife-edge.
14. The assay assembly according to claim 12, wherein the pressure applied is in the range of 10-50 N.
15-16. (canceled)
17. A method of sealing the assay assembly of claim 12, comprising the steps of: placing the cap onto the biochip storage well wall so that the resilient sealant layer is above the line contact interface formation; applying external force onto the cap so that the cap closes the biochip storage well and the resilient sealant layer is pressed into the line contact interface formation, forming a vapour-proof seal.
18. The method of claim 17, wherein the biochip storage well has a corresponding flange extending along the perimeter of the biochip storage well and wherein the cap slides onto the corresponding flange extending along the perimeter of the biochip storage well so as to form a vapour-proof seal with the line contact interface formation of the biochip storage well.
19. The method according to claim 17, wherein the pressure applied is in the range of 10-50 N
20. The method according to claim 17, wherein the vapour-proof seal provides less than 6% evaporation of the fluid within.
21. The method according to claim 17, wherein the line contact interface formation is in the form of a knife-edge.
22. The assay assembly according to claim 12, wherein the cap further comprises two opposing slide members, each defining a groove to enable the cap to slide onto a corresponding flange extending along the perimeter of the biochip storage well and thereby forming the vapour-proof seal with the line contact interface formation extending around the perimeter of the biochip storage well.
23. The assay assembly according to claim 22, further comprising a support member having a recess in which the biochip well sits, wherein the corresponding flange extending along the perimeter of the biochip storage well is formed by the support member.
24. The assay assembly according to claim 12, wherein the cap further includes a component extending away from the sealant layer to allow the cap to be manipulated.
25. The assay assembly according to claim 24, wherein the component extending away from the sealant layer is a hollow tube through which a pipette can be inserted.
26. The assay assembly according to claim 25, further comprising a pierceable membrane at the base of the hollow tube.
27. The assay assembly according to claim 12, wherein the resilient sealant layer is a polymer sealant.
28. The assay assembly according to claim 27 wherein the resilient sealant layer is polytetrafluoroethylene (PTFE), polychlorotrifluoroethylene (PCTFE) or polyethylene (PE).
29. The assay assembly according to claim 27, wherein the resilient sealant layer is a nitrile layer.
30. The assay assembly according to claim 29, wherein the nitrile sealant layer is 0.1 to 10 mm in thickness.
31. The assay assembly according to claim 12, further comprising a hydrophobic layer, coated onto the resilient sealant layer.
32. The assay assembly according to claim 12, wherein the cap is made from injection moulding.
33. The assay assembly according to claim 12, wherein the cap comprises a plastic flat top section.
Description
[0037] Preferred embodiments of the invention will now be explained with reference to the accompanying drawings, in which;
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[0049] The flat top section 2 is made of a plastic material and is bonded to the resilient sealant layer 3 by adhesive. Optionally, a component 1 extending away from the resilient sealant layer is present. This component 1 is cylindrical in shape. Component 1 is in the shape of a hollow tube, and is made of a plastic material and could be integrally formed by injection moulding, with the flat top section 2. The hollow tube of component 1 may contain a pierceable membrane at its base aligning with a hole in the flat top section 2 and the resilient sealant layer 3 (not shown).
[0050] The cylindrical component 1 is typically 12 mm in height and is hollow with an internal diameter of 5 mm, and is joined to the flat top section 2. The flat top section 2 covers an area of 225 mm.sup.2 and is composed of a square area with an adjoining triangular area, with all corners rounded to 3 mm radii, and is preferably 2 mm thick. The sealant layer 3 covers the same area and dimension as the flat top section 2 and is preferably 1 mm thick.
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EXAMPLES
[0057] The invention will now be described in relation to the following non-limiting examples. The amount of evaporation occurring in an assay assembly comprising a cap according to the first embodiment of the present invention and biochip storage well as illustrated in
[0058] The test method used to determine the % of evaporation was as follows; [0059] Heat wells to 60° C. for 1 hour [0060] Place 550 μl of deionised water into the wells [0061] Weigh the wells before and after test [0062] Well caps should be clamped at 50 N
[0063] Table 1 shows the results for the above method when testing a nitrile sealant layer of 1 mm. The cap according to the present invention, comprising a 1 mm nitrile sealant layer was placed onto the storage well of
TABLE-US-00001 TABLE 1 Weight Weight of Weight Weight Weight without well with of of well of Sample sample Sample after sample Difference before test before test prior test after test Percentage Run (g) (g) (g) (g) (g) (%) 1 2.7735 3.3219 0.5483 3.3021 0.5286 3.59 2 2.6696 3.2700 0.6004 3.2568 0.5872 2.20 3 2.7569 3.3267 0.5698 3.3119 0.5550 2.59 4 2.6716 3.1275 0.4559 3.1151 0.4435 2.72 5 2.7255 3.2823 0.5568 3.2561 0.5306 4.71 6 2.7589 3.3127 0.5538 3.2975 0.5386 2.75 7 2.7849 3.4232 0.6383 3.3719 0.5870 8.01 8 2.8199 3.3003 0.4804 3.2864 0.4665 2.89
[0064] The test method as described above was then repeated for various different polymer sealants, specifically, 0.8 mm thick neoprene, 1 mm thick neoprene, 1.5 mm thick EPDM, 1.5 mm thick natural rubber and 1 mm thick nitrile.
CONCLUSION
[0065] Analysis of