NUCLEIC ACID ISOLATION IN PRESERVED WHOLE BLOOD

• US 20110300608A1
• Filed: 09/17/2008
• Published: 12/08/2011
• Est. Priority Date: 09/21/2007
• Status: Abandoned Application

• Current Assignee: Streck
• Original Assignee: Streck
• Inventors: Ryan, Wayne L., Chan, Kate Chao-Wei
• Application Number:
  US12/678,190
• Publication Number:
  US 20110300608A1
• Time in Patent Office: Days
• US Class Current: 435/270
• CPC Class Codes: C12N 15/1003 Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor

Abstract

A method for isolating nucleic acids is disclosed, wherein a sample having nucleic acid containing starting material is fixed, lysed, and treated to remove unwanted contaminants. The initial fixing of the sample aids in maintaining the structure and integrity of the isolated DNA and reduces the incidence of end product contaminants and DNA shearing.

Claims

1. A method of isolating DNA comprising:

providing a tube containing an anticoagulant agent and a fixative agent selected from the group consisting of diazolidinyl urea, imidazolidinyl urea and combinations thereof;

suspending a sample in the fixative agent;

contacting the sample with an erythrocyte lysis buffer;

contacting the sample with a nucleus lysis buffer; and

contacting the sample with proteinase K and alcohol.

5. The method of claim 1, wherein the erythrocyte lysis buffer includes ammonium chloride, ammonium bicarbonate, and a chelating agent.

6. The method of claim 5, wherein the chelating agent is EDTA.

7. The method of claim 1, wherein the nucleus lysis buffer includes ingredients selected from the group consisting of a chelating agent, a buffer, an anionic surfactant, a polysorbate surfactant, a non-ionic surfactant, and a chaotrope.

8. The method of claim 1, wherein the nucleus lysis buffer includes a buffer, a chelating agent, a polysorbate surfactant, a non-ionic surfactant and a chaotrope.

9. The method of claim 1, wherein the nucleus lysis buffer includes a buffer, a chelating agent and an anionic surfactant.

10. The method of claim 8, wherein the chelating agent is EDTA.

11. The method of claim 8, wherein the buffer is tris-HCL.

12. The method of claim 8, wherein the chelating agent is EDTA and the anionic surfactant is sodium dodecyl sulfate.

13. The method of claim 1, wherein one or more samples are extracted from one or more patients at a sample extraction site.

14. The method of claim 1, wherein the fixative agent allows for the sample to be transferred to a remote location prior to a cell lysis processing step.

15. The method of claim 14, wherein isolated DNA is analyzed and resulting data is provided to the sample extraction site, the remote location, an additional location, or any combination thereof.

16. The method of claim 1, wherein prior to contact with the sample, the fixative agent is present at a concentration of about 10 to about 200 grams per liter.

17. The method of claim 1, wherein prior to contact with the sample, the fixative concentration is about 1 to about 20 grams per 100 ml of a fixative solution.

18. The method of claim 1, wherein prior to contact with the sample, the fixative concentration is about 4 to about 6 grams per 100 ml of a fixative solution.

19. The method of claim 1, wherein the sample includes RNA.

20. The method of claim 1, wherein the sample includes cell-free DNA.

21. The method of claim 20, wherein the cell-free DNA is fetal DNA.

22. The method of claim 19, wherein the RNA is cell-free RNA.

23. The method of claim 22, wherein the cell-free RNA is mRNA.

24. The method of claim 1, wherein the sample includes cellular DNA.

25. The method of claim 1, wherein the sample includes cellular RNA.

26. The method of claim 1, wherein the fixative agent allows for the sample to be processed up to 3 days after initial contact with the fixative agent.

27. The method of claim 1, wherein:

the sample is contacted by the fixative agent and anticoagulant upon blood draw; and

the sample is contacted by the erythrocyte lysis buffer, nucleus lysis buffer, proteinase K, and ethanol at least 24 hours after blood draw.

28. The method of claim 1, wherein the amount of an active agent used to fix a tissue or blood sample is generally about 10 to about 200 grams per liter.

29. The method of claim 1, wherein the fixative agent comprises about 4 to about 6 grams of imidazolidinyl urea per 100 ml of buffered salt solution.

30. The method of claim 1, wherein the fixative agent comprises about 1 to about 20 grams of diazolidinyl urea per 100 ml of buffered salt solution.

2-4. -4. (canceled)