Method of collecting, identifying, and quantifying saliva

• US 5,334,502 A
• Filed: 12/24/1991
• Issued: 08/02/1994
• Est. Priority Date: 11/27/1991
• Status: Expired due to Term

• Current Assignee: Labone Incorporated (Quest Diagnostics Incorporated)
• Original Assignee: Osborn Laboratories Incorporated
• Inventors: Sangha, Jangbir S.
• Primary Examiner(s): Scheiner, Toni R.
• Assistant Examiner(s): Chin, Christopher L.
• Application Number:
  US07/814,077
• Time in Patent Office: 952 Days
• Field of Search: 128/760, 128/769, 128/771, 604/1, 604/2, 422/55-58, 435/4, 435/14, 435/22, 435/25, 435/28, 435/805, 435/810, 435/7.21, 435/7.9, 435/7.92, 435/5, 435/974, 435/967, 436/164, 436/165, 436/169, 436/518, 436/528, 436/530, 436/805, 436/810, 436/901
• US Class Current: 435/7.21
• CPC Class Codes: A61B 10/0051 for taking saliva or sputum samples devices for receiving spittle A61J9/00
• CPC Class Codes: A61B 2010/0009 Testing for drug or alcohol abuse
• CPC Class Codes: B01L 2400/0406 capillary forces
• CPC Class Codes: B01L 3/5029 using swabs
• CPC Class Codes: B01L 3/50825 Closing or opening means, corks, bungs closures for containers B65D; means for removing stoppers B67B7/02
• CPC Class Codes: C12Q 1/28 involving peroxidase
• CPC Class Codes: C12Q 1/40 involving amylase
• CPC Class Codes: G01N 2001/007 Devices specially adapted for forensic samples, e.g. tamper-proofing, sample tracking
• CPC Class Codes: G01N 33/523 the element being adapted for a specific analyte
• CPC Class Codes: G01N 33/54386 Analytical elements
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: Y10S 435/805 Test papers
• CPC Class Codes: Y10S 435/967 Standards, controls, materials, e.g. validation studies, buffer systems
• CPC Class Codes: Y10S 435/974 Aids related test
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/81 Tube, bottle, or dipstick

Abstract

A method is provided for rapidly determining during a saliva specimen collection procedure the presence of an amount of saliva, and for verifying that the sample obtained is in fact saliva. Color indication by dye markers and/or enzymatic activation of color indicators provides an indication that at least a predetermined amount of saliva has been applied to an absorbent and the enzymatic reaction indicates that saliva is contained in the sample collected.

Claims

1. A method of collecting and identifying saliva for analysis, said method comprising the steps of:

(a) inserting a first absorbent element into the mouth of a subject for application of a fluid saliva specimen thereto,

(b) providing a second absorbent element which is separate from said first absorbent element and having a zone of application for transfer of saliva thereto, wherein said zone of application comprises an indicator which indicates the presence of said fluid saliva specimen when contacted with said specimen, said indicator is spaced a predetermined distance from said zone of application to require transfer of a predetermined quantity of saliva to said second absorbent element prior to said applied saliva contacting said indicator, said predetermined distance also provides for collection of a sufficient quantity of specimen which is uncontacted by said indicator to permit subsequent analysis of said specimen,

(c) transferring the fluid saliva from said first absorbent element to said zone of application, and

(d) observing said indicator for saliva contact therewith in order to determine that said predetermined quantity of saliva has been transferred to said second absorbent element.

2. The method as claimed in claim 1, further comprising the steps of:

(e) allowing said fluid saliva specimen to dry on said second absorbent element; and

(f) utilizing said dried saliva to test for the presence of agents foreign to saliva and disease states.

3. The method as claimed in claim 1, wherein said indicator comprises:

a peroxide; and

a leuco dye for oxidation by interaction of said peroxide and the saliva such that a colored compound is produced to indicate the presence of saliva.

4. The method as claimed in claim 3, wherein said perioxide is selected from the group consisting of hydrogen peroxide, methyl hydroperoxide, ethyl hydroperoxide, isopropyl hydroperoxide, butyl hydroperoxide, benzoyl hydroperoxide and cumene hydroperoxide.

5. The method as claimed in claim 3, wherein said peroxide is produced by reaction of glucose oxidase with glucose, wherein said glucose oxidase is included in said indicator and said glucose is present in the saliva specimen.

6. The method as claimed in claim 3, wherein said leuco dye is selected from the group consisting of o-phenylenediamine, o-dianisidine, o-tolidine, guaiacol, 4-aminoantipyrine, pyrogallol, benzidine, tetramethyl benzidine, 4-chloro-1-naphthol and 2,2'"'"'-azino-di (3-ethylbenzthiazoline sulphonic acid-6).

7. The method as claimed in claim 1, wherein said second absorbent element comprises a sheet of material having a portion comprising said zone of application and upon which the applied fluid saliva specimen is dried, and wherein said indicator is positioned on said sheet in circumscribing relationship relative to said zone.

8. The method as claimed in claim 1, wherein said indicator comprises:

a substrate reactive with an amylase enzyme of said saliva, said substrate having a portion thereof which upon reaction with said amylase presents visible color.

9. The method as claimed in claim 8, wherein said substrate is a polysaccharide having a chromogen attached thereto.

10. The method as claimed in claim 9, wherein said chromogen-containing polysaccharide is a p-nitrophenyl-containing polysaccharide.

11. The method as claimed in claim 9, wherein said chrmogen-containing polysaccharide is selected from the group consisting of α

-4-nitrophenyl maltoheptaoside, β

-4-nitrophenyl maltoheptaoside, 4,6 ethylidine-blocked-4-nitrophenylmaltoheptaoside, silyl-blocked-4-nitrophenylmaltoheptaoside, and 3-ketobutylidene-beta-2-chloro--4-nitrophenylmaltopentaoside.

12. The method as claimed in claim 9, wherein said chromogen-containing polysaccharide is an indole-containing polysaccharide.

13. The method as claimed in claim 9, wherein said chromogen-containing polysaccharide is selected from the group consisting of indolyl-α

-maltoheptaoside;

indolyl-β

-maltoheptaoside;

4,6 ethylidine-blocked-indolyl maltoheptaoside;

silyl-blocked-indolyl maltoheptaoside;

3-ketobutylidene-beta-2-chloro-indolyl maltopentaoside; and

indolyl-α

-D-maltoheptaoside.

14. A method of collecting for analysis, said method comprising the steps of:

(a) providing an absorbent element having a zone of application thereon for insertion into a subject'"'"'s mouth for absorption of saliva, said absorbent element being sized to extend out of the subject'"'"'s mouth to provide an exterior absorbent element portion, wherein said exterior absorbent portion has an indicating means thereon which indicates the presence of saliva when contacted with saliva, said indicating means is positioned on said exterior absorbent element in sufficient spaced relationship to said zone of application to require application of at least a predetermined amount of said specimen to said absorbent element prior to the presence of the saliva being indicated, said spaced relationship further providing for collection of a sufficient quantity of saliva which is uncontacted by said indicator to permit subsequent analysis of the collected saliva,

(b) inserting said zone of application into the mouth of a subject,

(c) collecting a fluid specimen of saliva on said zone of application,

(d) allowing said saliva to migrate on said absorbent from said zone of application to said exterior portion, and `(e) observing said indicating means for saliva contact therewith for determination that said at least predetermined quantity of saliva has been absorbed.

15. The method as claimed in claim 14, wherein said absorbent element comprises an elongated wick having an end portion comprising said zone of application.

16. The method as claimed in claim 14, wherein said means for indicating comprises a dye at least partially soluble in saliva such that contact therewith solubilizes the dye to indicate the presence of at least said predetermined amount of the specimen on said absorbent element.

17. The method as claimed in claim 16, wherein said indicating means is a vegetable dye.

18. The method as claimed in claim 16, wherein said indicating means is non-toxic to humans.

19. The method as claimed in claim 14, wherein said indicating means comprises saliva-insoluble, dyed or fluorescent micro particles which migrate with the specimen as it diffuses on said element to indicate the presence of at least said predetermined amount of the specimen.

20. The method as claimed in claim 14, wherein said means for indicating comprises:

a substrate reactive with an amylase enzyme of said saliva, said substrate having a portion thereof which upon reaction with said amylase presents visible color.

21. The method as claimed in claim 20, wherein said substrate is a polysaccharide having a chromogen attached thereto.

22. The method as claimed in claim 14, wherein said indicating means comprises:

a peroxide; and

a leuco dye for oxidation by interaction of said peroxide and the saliva such that a colored compound is produced to indicate the presence of saliva.

23. The method as claimed in claim 22, wherein said peroxide is produced by reaction of glucose oxidase with glucose, wherein said glucose oxidase is included in said indicating means and said glucose is present in the saliva.

24. A method of collecting and identifying saliva for analysis, said method comprising the steps of:

(a) applying a fluid specimen to an absorbent element having a sample portion and a separable test portion;

(b) providing a means for testing that upon contact with said specimen gives an indication of the presence of saliva in said specimen;

(c) following said step (a), removing said test portion from said sample portion; and

(d) applying said testing means to said test portion to contact the applied specimen, whereby the presence of saliva therein results in said indication and analysis may proceed utilizing said sample portion.

25. The method as claimed in claim 24, wherein said means for testing comprises:

a peroxide; and

a leuco dye for oxidation by interaction of said peroxide and the saliva such that a colored compound is produced to indicate the presence of saliva.

26. The method as claimed in claim 25, wherein said peroxide is selected from the group consisting of hydrogen peroxide, methyl hydroperoxide, ethyl hydroperoxide, isopropyl hydroperoxide, butyl hydroperoxide, benzoyl hydroperoxide and cumene hydroperoxide.

27. The method as claimed in claim 25, wherein said peroxide is produced by reaction of glucose oxidase with glucose, wherein said glucose oxidase is included in said indicator and said glucose is present in the saliva.

28. The method as claimed in claim 25, wherein said leuco dye is selected from the group consisting of o-phenylenediamine, o-dianisidine, o-tolidine, guaiacol, 4-aminoantipyrine, pyrogallol, benzidine, tetramethyl benzidine, 4-chloro-1-naphthol and 2,2'"'"'-azino-di (3-ethylbenzthiazoline sulphonic acid-6).

29. The method as claimed in claim 24, wherein said means for testing comprises:

a substrate reactive with an amylase enzyme of said saliva, said substrate having a portion thereof which upon reaction with said amylase presents visible color.

30. The method as claimed in claim 29, wherein said substrate is a polysaccharide having a chromogen attached thereto.

31. The method as claimed in claim 30, wherein said chromogen-containing polysaccharide is a p-nitrophenyl-containing polysaccharide.

32. The method as claimed in claim 30, wherein said chromogen-containing polysaccharide is selected from the group consisting of α

-4-nitrophenyl maltoheptaoside, β

-4-nitrophenylmaltoheptaoside, 4,6, ethylidine-blocked-4-nitrophenylmaltoheptaoside, silyl-blocked-4-nitrophenylmaltoheptaoside, and 3-ketobutylidene-beta-2 chloro-4-nitrophenylmaltopentaoside.

33. The method as claimed in claim 30, wherein said chromogen-containing polysaccharide is an indole-containing polysaccharide.

34. The method as claimed in claim 30, wherein said chromogen-containing polysaccharide is selected from the group consisting of indoly-α

-maltoheptaoside;

indolyl-β

-maltoheptaoside;

4,6 ethylidine-blocked-indolyl maltoheptaoside;

silyl-blocked-indolyl maltoheptaoside;

3-ketobutylidene-beta-2-chloro-indolyl maltopentaoside; and

indolyl-α

-D-maltoheptaoside.

35. A method of collecting from a subject a desired quantity of saliva sample for analysis comprising the steps of:

(a) providing a saliva collection absorbent comprising a zone for saliva application adapted for insertion into the subject'"'"'s mouth and an absorbent indicator portion sufficiently spaced from said zone to position said indicator portion outside the mouth, said collection absorbent is attached to a handle which allows for uncontaminated manipulation of the absorbent and permits insertion of said zone for saliva application into the subject'"'"'s mouth, said indicator portion has an indicator thereon which signals the presence of saliva on said indicator portion of said absorbent and said indicator spaced a predetermined distance from said zone to permit collection of a predetermined amount of saliva prior to contact of the collected saliva with said indicator, said predetermined distance providing for collection of a sufficient quantity of specimen which is uncontacted by said indicator for subsequent analysis of the collected saliva sample,

(b) inserting said application zone into the subject'"'"'s mouth for saliva collection,

(c) allowing saliva to absorb onto said zone and migrate toward said indicator,

(d) observing said indicator during saliva collection to determine saliva contact with sad indicator, and

(e) withdrawing said zone from the mouth upon indicator reaction with the saliva.

36. The method as claimed in claim 35, wherein said indicator comprises:

a peroxide; and

a leuco dye for oxidation by the interaction of said peroxide and the saliva such that a colored compound is produced to provide said indication.

37. The method as claimed in claim 36, wherein said peroxide is selected from the group consisting of hydrogen peroxide, methyl hydroperoxide, ethyl hydroperoxide, isopropyl hydroperoxide, butyl hydroperoxide, benzoyl hydroperoxide and cumene hydroperoxide.

38. The method as claimed in claim 36, wherein said peroxide is produced by reaction of glucose oxidase with glucose, wherein said glucose oxidase is included in said indicator and said glucose is present in the saliva.

39. The method as claimed in claim 36, wherein said leuco dye is selected from the group consisting of o-phenylenediamine, o-dianisidine, o-tolidine, guaiacol, 4-aminoantipyrine, pyrogallol, benzidine, tetramethyl benzidine, 4-chloro-1-naphthol and 2,2'"'"'-azino-di (3-ethylbenzthiazoline sulphonic acid-6).

40. The method as claimed in claim 35 wherein said handle comprises:

a hollow tube adapted for insertion of said absorbent indicator portion therein, and

means on said tube for allowing observation of saliva contact of said indicator on said absorbent.

41. The method as claimed in claim 40 wherein said means for allowing observation comprises an opening in said tube to permit observation of said indicator containing portion of said absorbent.

42. The method as claimed din claim 35 further comprising the step of:

marking said collected saliva sample to correlate the subject'"'"'s identity with the collected saliva sample.

43. The method as claimed din claim 35, wherein said indicator comprises:

a substrate reactive with an amylase enzyme of said saliva, said substrate having a portion thereof which upon reaction with said amylase presents visible color.

44. The method as claimed in claim 43, wherein said substrate is a polysaccharide having a chromogen attached thereto.

45. The method as claimed in claim 44, wherein said chromogen-containing polysaccharide is a p-nitrophenyl-containing polysaccharide.

46. The method as claimed in claim 44, wherein said chromogen-containing polysaccharide is selected from the group consisting of α

-4-nitrophenyl maltoheptaoside, β

-4-nitropehnyl maltoheptaoside, 4, 6 ethylidine-blocked-4-nitrophenylmaltoheptaoside, silyl-blocked-4-nitrophenylmaltoheptaoside, and 3-ketobutylidine-beta-2-chloro-4-nitrophenylmaltopentaoside.

47. The method as claimed in claim 44, wherein said chromogen-containing polysaccharide is an indole-containing polysaccharide.

48. The method as claimed in claim 44, wherein said chromogen-containing polysaccharide is selected from the group consisting of indolyl-α

-maltoheptaoside;

indolyl-β

-maltoheptaoside;

4, 6 ethylidine-blocked-indolyl maltoheptaoside;

silyl-blocked-indolyl maltoheptaoside;

3-ketobutylidine-beta-2-chloro-indolyl maltopentaoside; and

indolyl-α

-D-maltoheptaoside.