Integrated patch and assay device with visual detection means

• US 20070179373A1
• Filed: 12/22/2006
• Published: 08/02/2007
• Est. Priority Date: 12/22/2005
• Status: Abandoned Application

• Current Assignee: Promdx Technology Incorporated
• Original Assignee: Promdx Technology Incorporated
• Inventors: Pronovost, Allan
• Application Number:
  US11/644,496
• Publication Number:
  US 20070179373A1
• Time in Patent Office: Days
• US Class Current: 600/362
• CPC Class Codes: A61B 2560/0412 Low-profile patch shaped housings
• CPC Class Codes: A61B 5/1486 using enzyme electrodes, e.g. with immobilised oxidase
• CPC Class Codes: A61B 5/6833 Adhesive patches
• CPC Class Codes: B01L 2300/0681 Filter
• CPC Class Codes: B01L 2300/0887 Laminated structure
• CPC Class Codes: B01L 2400/0406 capillary forces
• CPC Class Codes: B01L 2400/084 Passive control of flow resistance
• CPC Class Codes: B01L 3/5023 with a sample being transported to, and subsequently stored in an absorbent for analysis
• CPC Class Codes: G01N 21/01 Arrangements or apparatus for facilitating the optical investigation
• CPC Class Codes: G01N 21/78 producing a change of colour
• CPC Class Codes: G01N 31/22 using chemical indicators G01N31/02 takes precedence

Abstract

Methods and apparatus for collecting a fluid sample using an integrated collection device are disclosed. The integrated collection device includes an analyte detector and a gradient means to actively and rapidly drive the transport of a sample fluid from the point of contact to the point of detection and reading. The analyte detector can include a visually-read colorimetric detector using a chemical or enzymatic detection process. The gradient means can include physical and/or chemical processes as described in more detail herein. In some embodiments, the device is provided as an occlusive patch. Preferably, the test device provides a reading immediately upon fluid contact with the analyte detector. Consequently, the time-to-result is sample volume and transport time dependent. By providing immediate or nearly immediate reading of results, the device is particularly useful in those applications in which immediate results are advantageous.

Claims

1. An integral fluid collection device for collecting a fluid sample from a sample surface comprising:

at least three internal layers of which a first layer includes a hydrophilic nanofiltration material adhered to a second layer;

the second layer includes absorbent material adhered to a third layer;

the third layer includes an assay detection zone having integrated direct chemical calorimetric or enzymatic-based calorimetric detection suitable for detecting an analyte, the third layer adhered to a fourth layer; and

a fourth layer including a visually-clear occlusive material, and being external to the first, second and third layers, the fourth layer also having an area greater than the at least three internal layers so as to overlap the three internal layers at an area of contact with the sample surface.

2. The apparatus of claim 1, wherein the fourth layer comprises an adhesive zone peripheral to the three internal layers.

3. The apparatus of claim 2, wherein non-aqueous permeable double-stick adhesive layer is provided along the adhesive zone to promote containment of fluid within the device, when adhered to the sample surface.

4. The apparatus of claim 3, wherein the adhesive layer is covered by a releasable liner.

5. The apparatus of claim 1, wherein the hydrophilic nanofiltration material comprises a membrane defining substantially straight-through pores acting as a molecular sieve to allow for immediate passage of fluid.

6. The apparatus of claim 5, wherein the maximum pore diameter is not more than about 200 nm.

7. The apparatus of claim 1, further comprising a gradient from the area of contact with the sample surface to the assay detection zone, the gradient selected from the group consisting of:

dryness (moisture) gradient;

a hydrophilic gradient for polar water molecules;

an absorbent polymer gradient;

a chemical equilibrium osmosis gradient;

a physical gradient; and

combinations thereof.

8. A method for detecting a target analyte obtained from a sample surface comprising:

obtaining a patch comprising;

at least three internal layers, the first layer having hydrophilic nanofiltration material adhered to a second layer;

the second layer having absorbent material adhered to a third layer;

the third layer comprising an assay detection zone having integrated direct chemical colorimetric or enzymatic-based colorimetric detection suitable for detecting an analyte, the third layer adhered to a fourth layer;

the fourth layer having a visually-clear occlusive region and being external to the first, second, and third layers and having an area greater than the three internal layers so as to overlap the three internal layers;

applying the patch to the sample surface; and

viewing through the visually-clear occlusive region a calorimetric change in the patch, wherein the colorimetric change indicates the presence of the target analyte.

9. The method of claim 8, further comprising collecting the sample from the sample surface.

10. The method of claim 8, wherein the sample surface comprises a mammalian skin.

11. The method of claim 8, wherein the sample surface comprises a fluid vessel.

12. The method of claim 8, further comprising establishing a gradient from the sample surface to the assay detection zone, the gradient selected from the group consisting of:

dryness (moisture) gradient;

a hydrophilic gradient for polar water molecules;

an absorbent polymer gradient;

a chemical equilibrium osmosis gradient;

a physical gradient; and

combinations thereof.

13. The method of claim 8, wherein the fourth layer has a release liner and an adhesive zone peripheral to the three internal layers.

14. The method of claim 8, further comprising forcing a fluid sample into the patch through application of end-user pressure.

15. A method for producing an analyte detection patch for collecting a sample from a sample surface comprising:

providing a first layer having hydrophilic nanofiltration material;

providing a second layer having absorbent material;

providing a third layer comprising an assay detection capability including integrated direct chemical calorimetric or enzymatic-based colorimetric detection chemistry suitable for detecting an analyte; and

providing a fourth layer comprising a visually-clear occlusive material, the fourth layer being external to the first, second and third layers and having an area greater than these three internal layers, the fourth layer also having a release liner and an adhesive zone peripheral to the three internal layers.

16. The method of claim 15, further comprising adhering the first layer to the second layer, adhering the third layer to the first and second layers and overlapping the three internal layers with the fourth layer.

17. The method of claim 15, further comprising establishing a gradient from the sample surface to the assay detection zone, the gradient selected from the group consisting of:

dryness (moisture) gradient;

a hydrophilic gradient for polar water molecules;

an absorbent polymer gradient;

a chemical equilibrium osmosis gradient;

a physical gradient; and

combinations thereof.

18. The method of claim 15, wherein the hydrophilic nanofiltration material comprises a membrane defining substantially straight-through pores acting as a molecular sieve to allow for immediate passage of fluid.

19. The method of claim 15, wherein the absorbent material comprises at least one of a cellulosic material and a glass fiber material.

20. The method of claim 15, further comprising defining a narrow channel within the fourth layer, the narrow channel containing the first, second, and third layers.