IP Library Granted Patent US 9,359,649
Granted Patent B2
US 9,359,649 · App. 14/165,877 · Granted Jun 7, 2016

Methods for collection, storage and transportation of biological specimens

Inventors: Robert M. Lloyd, Jr. (Suwanee, GA); Darrell A. Burns (Dacula, GA); Joe T. Huong (Norcross, GA)
Assignee: VIVEBIO, LLC
C12Q1/70B01L3/50825C12M45/22B01L3/502B01L2200/185B01L2300/042B01L2300/046B01L2300/047B01L2300/069B01L2300/105Y10T436/108331Y10T436/255Y10T436/2575Y10T436/25375Y10T436/25625
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Quick Facts
Patent No.
US 9,359,649
App. No.
14/165,877
Granted
Jun 7, 2016
Kind
B2
Abstract

The present invention provides methods for collecting, storing or transporting liquid suspension of biological specimens containing analytes of interest in a dry state. The dried biological specimens containing analytes of interest are reconstituted and released for subsequent analysis by compressing or centrifuging the matrix. Also provided are method of using kits for collecting, storing, transporting and recovering biological specimens containing analytes of interest.

Claims (40)

1. A method for recovering a dried biological specimen comprising:

(a) providing a dried biological specimen contained on an absorbent three dimensional matrix in a sealed container, wherein the matrix has an absorption capacity of at least 0.1 ml;

(b) exposing the matrix by opening the container;

(c) selecting a fixed volume of a reconstitution buffer;

(d) applying the fixed volume of the reconstitution buffer to the matrix containing the dried biological specimen, thereby forming a reconstituted biological specimen contained on the matrix, wherein the fixed volume of the reconstitution buffer is less than the absorption capacity of the matrix; and

(e) removing the reconstituted biological specimen from the matrix.

2. The method of claim 1 , wherein the absorption capacity of the matrix is at least 0.5 ml.

3. The method of claim 1 , wherein the absorption capacity of the matrix is at least 1.0 ml.

4. The method of claim 1 , wherein the matrix is at least 50% porous.

5. The method of claim 1 , wherein the matrix is at least 75% porous.

6. The method of claim 1 , wherein the container comprises an openable lid, and wherein exposing the matrix by opening the container comprises opening the lid.

7. The method of claim 6 , wherein the lid comprises an internal surface lid extension, and wherein the matrix is removably mounted to the lid via the internal surface lid extension.

8. The method of claim 1 , wherein removing the reconstituted biological specimen from the matrix comprises compressing the matrix.

9. The method of claim 8 , wherein the matrix is compressed by at least 50% of a volume of the matrix.

10. The method of claim 8 , wherein the matrix is compressed by at least 75% of a volume of the matrix.

11. The method of claim 1 , wherein removing the reconstituted biological specimen from the matrix comprises centrifuging the matrix.

12. The method of claim 1 , wherein the fixed volume of the reconstitution buffer is less than or equal to a sample volume of at least 0.1 ml of a biological specimen previously absorbed and dried on the matrix to form the dried biological specimen.

13. The method of claim 1 , wherein the fixed volume of the reconstitution buffer is less than a sample volume of at least 0.1 ml of a biological specimen previously absorbed and dried on the matrix to form the dried biological specimen.

14. The method of claim 1 , wherein the biological specimen contains an analyte of interest selected from the group consisting of nucleic acids, proteins, carbohydrates, lipids, whole cells, cellular fragments, whole virus and viral fragments.

15. The method of claim 1 , wherein the biological specimen contains an analyte of interest selected from the group consisting of DNA and RNA.

16. The method of claim 1 , wherein the biological specimen is selected from the group consisting of whole blood, plasma, serum, lymph, synovial fluid, urine, saliva, sputum, semen, vaginal lavage, bone marrow, cerebrospinal cord fluid, physiological body liquids, pathological body liquids, and combinations thereof.

17. A method for recovering a dried biological specimen comprising:

(a) providing a dried biological specimen contained on an absorbent three dimensional matrix, wherein the matrix has an absorption capacity of at least 0.1 ml;

(b) selecting a fixed volume of a reconstitution buffer;

(c) reconstituting the dried biological specimen on the matrix with the fixed volume of the reconstitution buffer, thereby forming a reconstituted biological specimen contained on the matrix, wherein the fixed volume of the reconstitution buffer is less than the absorption capacity of the matrix; and

(d) removing the reconstituted biological specimen from the matrix.

18. The method of claim 17 , wherein the fixed volume of the reconstitution buffer is less than or equal to a sample volume of at least 0.1 ml of a biological specimen previously absorbed and dried on the matrix to form the dried biological specimen.

19. The method of claim 17 , wherein the fixed volume of the reconstitution buffer is less than a sample volume of at least 0.1 ml of a biological specimen previously absorbed and dried on the matrix to form the dried biological specimen.

20. The method of claim 17 , wherein the biological specimen contains an analyte of interest selected from the group consisting of nucleic acids, proteins, carbohydrates, lipids, whole cells, cellular fragments, whole virus and viral fragments.

21. The method of claim 17 , wherein the biological specimen contains an analyte of interest selected from the group consisting of DNA and RNA.

22. A method for recovering a dried biological specimen comprising:

(a) providing a dried biological specimen contained on an absorbent three dimensional matrix sealed in a container, wherein the matrix has an absorption capacity of at least 0.1 ml;

(b) exposing the matrix by opening the container;

(c) selecting a fixed volume of a reconstitution buffer;

(d) applying the fixed volume of the reconstitution buffer to the matrix containing the dried biological specimen, thereby forming a reconstituted biological specimen contained on the matrix, wherein the fixed volume of the reconstitution buffer is less than or equal to a sample volume of at least 0.1 ml of a biological specimen previously absorbed and dried on the matrix to form the dried biological specimen; and

(e) removing the reconstituted biological specimen from the matrix.

23. The method of claim 22 , wherein the fixed volume of the reconstitution buffer is less than the sample volume of the biological specimen.

24. The method of claim 22 , wherein the fixed volume of the reconstitution buffer is less than the absorption capacity of the matrix.

25. The method of claim 22 , wherein the biological specimen contains an analyte of interest selected from the group consisting of nucleic acids, proteins, carbohydrates, lipids, whole cells, cellular fragments, whole virus and viral fragments.

26. The method of claim 22 , wherein the biological specimen contains an analyte of interest selected from the group consisting of DNA and RNA.

Continuity (4)
Continuation 12482907 · Jun 11, 2009
Division 11061698 · Feb 18, 2005
Provisional Application 60561037 · Apr 9, 2004
Related Publication 20140141411A1 · May 22, 2014