Method for tissue sample fixation

Patent metadata

Field	Value
Publication number	US-11624684-B2
Application number	US-201815877277-A
Country	US
Kind code	B2
Filing date	Jan 22, 2018
Priority date	Feb 17, 2011
Publication date	Apr 11, 2023
Grant date	Apr 11, 2023

Abstract

An aldehyde fixative solution at a first temperature is caused to contact a tissue sample for a first time period, additionally an aldehyde fixative solution is caused to contact the tissue sample at a second temperature higher than the first temperature for a second time period. The first time period typically ranges from about 15 minutes up to about 4 hours, and the first temperature typically is from greater than 0° C. to at least 15° C. The second temperature typically is from greater than about 22° C. to about 55° C., and the second time period ranges from about 1 hour to about 4 hours. Using this process, improved tissue morphology and IHC staining as well as superior preservation of post-translation modification signals have been accomplished in approximately 4 hours compared to 24 hours for room temperature protocols, and more even morphology and antigen preservation are observed.

First claim

We claim:

1. A method for processing a tissue sample, the method comprising:
immersing the tissue sample in a first aldehyde solution at a first temperature for a first time period to diffuse the first aldehyde solution into an interior region of the tissue sample, wherein the first temperature ranges from between 0° C. to 10° C.; and
heating the sample by immersing the tissue sample in a second aldehyde solution pre-heated to a second temperature ranging from between 22° C. to 55° C. for a second time period, the second time period being sufficient to fix the tissue sample,
wherein the tissue sample is not exposed to ultrasonic or electromagnetic irradiation during diffusion of the first aldehyde solution into the interior region of the tissue sample or during fixation of the tissue sample in the second aldehyde solution,
wherein the first and second aldehyde solutions are the same or different; and
wherein at least one of the first or second time periods is a fixation time of a tissue processing protocol derived from a time of flight curve for one or more of: (i) a tissue type that is about the same type as the tissue sample; (ii) a tissue shape that is about the same shape as the tissue sample; or (iii) a tissue size that is about the same size as the tissue sample.

2. The method of claim 1 , wherein the first time period is at least 1 hour.

3. The method of claim 1 , wherein the first time period is at least 2 hours.

4. The method of claim 1 , wherein the first aldehyde solution is a formalin solution.

5. The method of claim 4 , wherein the formalin solution is a neutral buffered formalin (NBF).

6. The method of claim 5 , wherein the first aldehyde solution is 10% NBF.

7. The method of claim 1 , wherein the second aldehyde solution is a formalin solution.

8. The method of claim 7 , wherein the formalin solution is a neutral buffered formalin (NBF).

9. The method of claim 1 , wherein the first aldehyde solution is a formalin solution and the second aldehyde solution is a formalin solution.

10. The method of claim 9 , wherein the formalin solution is a neutral buffered formalin (NBF).

11. The method according to claim 1 , where the temperature of the second temperature range is from 35° C. to 45° C.

12. A method comprising:
immersing a tissue sample in a first aldehyde solution at a first temperature for a first time period to diffuse the first aldehyde solution into an interior region of the tissue sample, wherein the first temperature is less than 10° C., and wherein the tissue sample is not exposed to ultrasonic or electromagnetic irradiation during the first time period;
heating the tissue sample in a second aldehyde solution to a second temperature ranging from between 22° C. to 50° C. for a second time period ranging from between 1 hours to 4 hours to fix the tissue sample, wherein the first and second aldehyde solutions are the same or different and wherein the tissue sample is not exposed to ultrasonic or electromagnetic irradiation during the second time period, and;
wherein at least one of the first or second time periods is a fixation time of a tissue processing protocol derived from a datatime of flight curve for at least one of (i) a tissue type that is about the same type as the tissue sample; and (ii) a tissue size that is about the same size as the tissue sample.

13. The method of claim 12 , wherein the first temperature range is from 0° C. to 10° C.

14. The method of claim 12 , wherein the first aldehyde solution is a formalin solution.

15. The method of claim 14 , wherein the formalin solution is a neutral buffered formalin (NBF).

16. The method of claim 15 , wherein the first aldehyde solution is 10% NBF.

17. The method of claim 12 , wherein the second aldehyde solution is a formalin solution.

18. The method of claim 17 , wherein the formalin solution is a neutral buffered formalin (NBF).

19. The method of claim 18 , wherein the second aldehyde solution is 10% NBF.

20. The method of claim 12 , wherein the first aldehyde solution is a formalin solution and the second aldehyde solution is a formalin solution.

21. The method of claim 20 , wherein the formalin solution is a neutral buffered formalin (NBF).

22. The method of claim 21 , wherein the first aldehyde solution is 10% NBF and the second aldehyde solution is 10% NBF.

23. The method according to claim 12 , where the temperature of the second temperature range is from 35° C. to 45° C.

24. The method of claim 12 , further comprising:
subjecting the fixed tissue sample to a series of alcohol immersions to obtain a dehydrated fixed tissue sample.

25. The method of claim 24 , further comprising:
subjecting the dehydrated tissue sample to an immersion in a clearing solution.

26. The method of claim 25 , further comprising:
embedding the dehydrated tissue sample in a wax block after the immersion in the clearing solution.

27. The method of claim 26 , further comprising:
sectioning the wax block to obtain the tissue section; and
applying a histochemical stain to the tissue section.

28. The method of claim 27 , wherein the histochemical stain comprises a chromogen.

29. The method of claim 27 , wherein the histochemical stain is a hematoxylin and eosin stain.

30. The method of claim 27 , wherein the histological stain is applied via an immunohistochemical process.

31. The method of claim 30 , wherein the immunohistochemical process is specific for a protein.

32. The method of claim 30 , wherein the immunohistochemical process is specific for a post-translationally modified protein.

33. The method of claim 32 , wherein the post-translational modification is a phosphorylation.

34. The method of claim 27 , wherein the histological stain is applied via an in situ hybridization process.

35. The method of claim 34 , wherein the in situ hybridization process targets an RNA.

36. The method of claim 1 , wherein the first and second aldehyde solutions are the same.

37. The method of claim 12 , wherein the first and second aldehyde solutions are the same.

38. The method of claim 37 , wherein the tissue sample is immersed in the second aldehyde solution for 2 hours.

39. A method comprising:
immersing a tissue sample in an aldehyde solution at a first temperature for a first time period ranging from between 1 hour to 4 hours to diffuse the aldehyde solution into an interior region of the tissue sample, wherein the first temperature is maintained at less than 10° C. throughout the duration of the first time period, and wherein the tissue sample is not exposed to ultrasonic irradiation during the first time period; and
allowing the tissue sample immersed in the aldehyde solution to warm to a second temperature for a second time period ranging from between 1 hour to 4 hours to fix the tissue sample, wherein the tissue sample is allowed to warm to the second temperature without an application of ultrasonic irradiation, and
wherein at least one of the first or second time periods is a fixation time of a tissue processing protocol predetermined time period that is derived from a time of flight data curve for (i) a tissue type that is about a same type as the tissue sample,

Assignees

• Ventana Med Syst Inc

Inventors

• Chafin David
• Pierson Theiss Abbey
• Otter Michael
• Roberts Esteban

Classifications

• G01N1/30 Primary

  Staining; Impregnating {; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis} · CPC title

• G01N1/31

  Apparatus therefor · CPC title