Device and method for collecting, transporting and recovering low molecular weight analytes in saliva

• US 20040254500A1
• Filed: 08/16/2004
• Published: 12/16/2004
• Est. Priority Date: 07/18/2001
• Status: Abandoned Application

• Current Assignee: Agilex Biosciences Incorporated
• Original Assignee: Agilex Biosciences Incorporated
• Inventors: Pronovost, Allan D
• Application Number:
  US10/484,315
• Publication Number:
  US 20040254500A1
• Time in Patent Office: Days
• US Class Current: 600/584
• CPC Class Codes: A61B 10/0051 for taking saliva or sputum samples devices for receiving spittle A61J9/00
• CPC Class Codes: B01D 15/34 Size selective separation, e.g. size exclusion chromatography, gel filtration, permeation
• CPC Class Codes: B01J 20/18 Synthetic zeolitic molecular sieves
• CPC Class Codes: B01J 20/20 comprising free carbon; comprising carbon obtained by carbonising processes
• CPC Class Codes: B01J 20/24 Naturally occurring macromolecular compounds, e.g. humic acids or their derivatives
• CPC Class Codes: B01J 20/26 Synthetic macromolecular compounds
• CPC Class Codes: B01J 2220/64 In a syringe, pipette, e.g. tip or in a tube, e.g. test-tube or u-shape tube in columns B01J2220/58
• CPC Class Codes: G01N 1/405 by adsorption or absorption
• CPC Class Codes: G01N 30/02 Column chromatography

Abstract

This invention relates to low molecular weight analyte sequestration, storage, transport and recovery device and methods for its use with saliva samples in the detection of glucose and other low molecular weight analytes. A stimulated or non-stimulated saliva sample is contacted with a matrix (16) disposed within a container (12) that adsorbs glucose, absorbs water and excludes molecules above a certain size when hydrated. After hydration of the matrix by the saliva sample, the glucose is both adsorbed to the matrix, and migrates into the cavities within the matrix, whereas microbes such as bacteria and larger molecules such as proteins cannot. A membrane (18) keeps the matrix (16) in the bottom of the container (12). The sample is then transported to a location where the glucose will be eluted from the matrix and assayed.

Claims

1. A device for sequestering a low molecular weight analyte from a saliva sample and storing the low molecular weight analyte until detection, comprising:

(a) a matrix, said matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva, and

(b) a container, into which the saliva sample and the matrix may be placed.

2. The device of claim 1 wherein the low molecular weight analyte is glucose.

3. The device of claim 1 further comprising a preservative in the container.

4. The device of claim 1 wherein the matrix is affixed to a solid support.

5. The device of claim 1 further comprising a membrane, said membrane providing a low molecular weight analyte-permeable barrier between the sample and the matrix.

6. The device of claim 1 further comprising a means for sealing the container.

7. The device of claim 1 wherein the container contains a marking that indicates the level to which the sample must be collected.

8. The device of claim 1 further comprising a plastic dropper, for transfer of saliva into the container.

9. The device of claim 1 wherein the container is comprised of plastic or glass.

10. The device of claim 1 wherein the matrix is cross-linked agarose.

11. The device of claim 1 wherein the matrix is a zeolite.

12. The device of claim 1 wherein the matrix is one of:

(a) a cross-linked anionic polyamine flocculent material, or (b) a cross-linked anionic polyacrylamide flocculent material.

13. The device of claim 1 wherein the matrix is selected from a group consisting of:

cross-linked aluminosilicate, clinoptilolite, gel alumina, alumino-silicate adsorbant sieves, activated carbon, activated charcoal, cross-linked cationic polyamine flocculent material, and cross-linked cationic polyacrylamide flocculent material.

14. The device of claim 3 wherein the preservative is one of:

(a) 2-methyl-4-isothiazolin-3-one, or (b) 5-chloro-2-methyl-4-isothiazolin-3-one.

15. The device of claim 3 wherein the preservative is selected from a group consisting of:

sodium azide, benzoic acid, sorbic acid, salts of sorbic acid, thimerosal, phenyl mercuric acetate, phenyl mercuric nitrate, ethyl alcohol, chlorhexidine gluconate and benzalkonium chloride.

16. The device of claim 5 wherein the membrane is selected from a group consisting of:

glass fiber, filter paper, PVC membrane filters, polypropylene, polyethersulfone prefilters, RW prefilters;

nylon membranes, supported PTFE, unsupported PTFE, hydrophilized PTFE, quartz fiber filters, mixed cellulose esters filters, polyvinylidene fluoride membrane, dacron membranes, rayon membranes, polyethelene membranes, cellulose acetate membranes, cellulose nitrate membranes, and nitrocellulose membranes.

34. The device of claim 1 wherein the matrix is a first matrix and said first matrix is in the bottom of the container, further comprising a second matrix in the container, said second matrix being layered on the top surface of the first matrix, and separated from said first matrix by a membrane, and said second matrix being able to absorb water from the sample, and said second matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva.

35. The device of claim 34 wherein the low molecular weight analyte is glucose.

17. A method of sequestering a low molecular weight analyte from a saliva sample, comprising:

(b) providing;

(i) a matrix, said matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva, and

(ii) a saliva sample, and

(b) contacting the matrix with the saliva sample.

18. A method of sequestering a low molecular weight analyte from a saliva sample and storing the low molecular weight analyte until detection, comprising:

(b) providing;

(i) a matrix, said matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva, and

(ii) a preservative;

(b) contacting the matrix with the sample and preservative, such that the matrix becomes hydrated by the sample.

19. The method of claim 18 wherein, at step (b), the sample and the preservative are placed into a container.

20. The method of claim 18 wherein the low molecular weight analyte is glucose.

21. The method of claim 19 wherein at step (b), the sample is introduced into the container by expectoration into the container.

22. The method of claim 19 wherein at step (b), the matrix is placed into the container before the sample, and further comprising the step of placing a membrane on the top surface of the matrix before the sample is added, said membrane providing a low molecular weight analyte-permeable barrier between the sample and the matrix.

23. The method of claim 19 further comprising the step of sealing the container, after the sample has been added in step (b).

24. A method of transporting a low molecular weight analyte in a saliva sample from a location of collection to a location of detection comprising:

(a) sequestering and storing the low molecular weight analyte according to the method of claim 23, and

(b) transporting the sample to a location where it will be analysed.

25. The method of claim 24 wherein the low molecular weight analyte is glucose.

28. A method of assaying for a low molecular weight analyte in a saliva sample comprising:

(a) sequestering and storing the low molecular weight analyte according to the method of claim 23;

(b) transporting the sample to a location where it will be analysed;

(c) removing liquid that is not absorbed into the matrix;

(d) releasing the low molecular weight analyte that is sequestered within the cavities of the matrix; and

(k) detecting the released low molecular weight analyte.

29. The method of claim 28 wherein the low molecular weight analyte is glucose.

30. The method of claim 18 further comprising the step of stimulating salivary gland secretion before step (b).

26. A method of assaying for a low molecular weight analyte in a saliva sample comprising:

(f) providing a matrix, said matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva;

(g) contacting the matrix with the sample;

(h) removing liquid that is not absorbed into the matrix;

(i) releasing the low molecular weight analyte that is sequestered within the cavities of the matrix, and

(j) detecting the released low molecular weight analyte.

27. The method of claim 26 wherein the low molecular weight analyte is glucose.

31. A kit for sequestering a low molecular weight analyte from a saliva sample and storing the low molecular weight analyte until detection, comprising:

(a) a matrix, said matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva, and

(b) a container into which the matrix and the saliva sample may be placed.

32. The kit of claim 31 further comprising a preservative.

33. The kit of claim 32 further comprising a lid for sealing the container.

36. A method of sequestering a low molecular weight analyte from a saliva sample and storing the low molecular weight analyte until detection, comprising:

(a) providing;

(i) a first matrix, said first matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said first matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva;

(ii) a second matrix, and said second matrix being able to absorb water from the sample and said second matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva, and

(iii) a preservative;

(b) placing said first matrix at the bottom of a container, and layering said second matrix on the top surface of the first matrix,

(c) introducing the sample into the container by applying the sample to the top surface of second matrix; and

(d) allowing the sample to hydrate the second matrix and then the first matrix.

37. The method of claim 36 wherein the low molecular weight analyte is glucose.

38. The method of claim 36 wherein at step (b) a membrane is placed between the first matrix and the second matrix.

39. The method of claim 36 wherein at step (c), the sample is introduced into the container by expectoration into the container.

40. The method of claim 36 further comprising the step of placing a membrane on the top surface of the second matrix before the sample is added in step (c), said membrane providing a low molecular weight analyte-permeable barrier between the sample and the matrix.

41. The method of claim 36 further comprising the step of sealing the container, after the sample has been added in step (b).

42. A method of transporting a low molecular weight analyte in a saliva sample from a location of collection to a location of detection comprising:

(a) sequestering and storing the low molecular weight analyte according to the method of claim 41, and

(b) transporting the sample to a location where it will be analysed.

45. A method of assaying for a low molecular weight analyte in a saliva sample comprising:

(a) sequestering and storing the low molecular weight analyte according to the method of claim 41;

(b) transporting the sample to a location where it will be analysed;

(c) removing liquid that is not absorbed into the first or the second matrix;

(d) releasing the low molecular weight analyte that is sequestered within the cavities of the first matrix; and

(e) detecting the released low molecular weight analyte.

46. The method of claim 45 wherein the low molecular weight analyte is glucose.

43. A method of assaying for a low molecular weight analyte in a saliva sample comprising:

(a) providing;

(i) a first matrix, said first matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said first matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva;

(ii) a second matrix, and said second matrix being able to absorb water from the sample and said second matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva,

(b) contacting the sample with the second matrix and then with the first matrix;

(c) removing liquid that is not absorbed into the first or the second matrix;

(d) releasing the low molecular weight analyte that is sequestered within the cavities of the first matrix, and

(e) detecting the released low molecular weight analyte.

44. The method of claim 43 wherein the low molecular weight analyte is glucose.

47. A device for sequestering a low molecular weight analyte from a saliva sample and storing the low molecular weight analyte until detection, comprising:

(a) a matrix, said matrix being able to absorb water from the sample and reversibly adsorb the low molecular weight analyte from the sample, and said matrix comprising cavities sized to accommodate the low molecular weight analyte within, and to exclude selected components of saliva, and

(b) a solid support to which said matrix is affixed.

48. The device of claim 47 in which the solid support is selected from the group consisting of:

stick, rod, slide, wick and card.

49. The device of claim 48 further comprising a container, into which one of (a) the sample and (b) the matrix, may be placed.

50. The device of claim 48 further comprising a container into which both the sample and the matrix may be placed.

51. The device of claim 47 wherein the low molecular weight analyte is glucose.

52. The device of claim 47 further comprising a preservative on the support, in the matrix, or both.

53. The device of claim 47 wherein the matrix is cross-linked agarose.

54. The device of claim 47 wherein the matrix is a zeolite.

55. The device of claim 47 wherein the matrix is one of:

(a) a cross-linked anionic polyamine flocculent material, or (b) a cross-linked anionic polyacrylamide flocculent material.

56. The device of claim 47 wherein the matrix is selected from a group consisting of:

cross-linked aluminosilicate, clinoptilolite, gel alumina, alumino-silicate adsorbant sieves, activated carbon, activated charcoal, cross-linked cationic polyamine flocculent material, and cross-linked cationic polyacrylamide flocculent material.

57. The device of claim 52 wherein the preservative is one of:

(a) 2-methyl-4-isothiazolin-3-one, or (b) 5-chloro-2-methyl-4-isothiazolin-3-one.

58. The device of claim 52 wherein the preservative is selected from a group consisting of:

sodium azide, benzoic acid, sorbic acid, salts of sorbic acid, thimerosal, phenyl mercuric acetate, phenyl mercuric nitrate, ethyl alcohol, chlorhexidine gluconate and benzalkonium chloride.