Automated methods, kits, and systems for clarifying obfuscating pigments in histology samples

Patent metadata

Field	Value
Publication number	US-9869617-B2
Application number	US-201314432962-A
Country	US
Kind code	B2
Filing date	Oct 7, 2013
Priority date	Oct 8, 2012
Publication date	Jan 16, 2018
Grant date	Jan 16, 2018

Abstract

Methods, kits, and systems for clarifying obfuscating pigments in histology samples such as an automated method of treating a histology sample with a clarifying reagent so that the clarifying reagent, contacts the sample and the pigments within the sample are decolorized , thus alleviating staining obfuscations associated with pigments. Decolorizing the pigments within the sample enables the histology sample to be interpretable by a qualified reader. An antigen retrieval step is performed after the clarification step.

First claim

The invention claimed is:

1. An automated method of treating a sample mounted on a substrate to alleviate staining obfuscations associated with pigments within the sample, the method comprising the following steps in the following order:
(a) applying a clarifying reagent in an amount sufficient to contact the sample and decolorize the pigments in said sample, wherein application of the clarifying reagent includes mixing to agitate the clarifying reagent while in contact with the sample;
(b) applying a rinsing reagent so that the clarifying reagent is substantially removed from contacting the sample,
(c) applying a cell conditioning reagent for antigen retrieval subsequent to applying the clarifying reagent, the cell conditioning reagent contacts the sample; and
(d) applying a chromogenic reagent subsequent to applying the cell conditioning reagent, the chromogenic reagent is applied so that the sample is specifically stained;
wherein the pigments within the sample are decolorized so that the specifically stained sample is interpretable by a qualified reader.

2. The method of claim 1 further comprising applying heat to the substrate so that the sample and the clarifying reagent are maintained at a predetermined temperature while in contact.

3. The method of claim 2 , wherein the predetermined temperature is between about 35° C. and about 100° C., between about 40° C. and about 90° C., between about 45° C. and about 80° C., or between about 50° C. and about 70° C.

4. The method of claim 2 , wherein the substrate is a glass slide and a heated slide platform is used for applying heat to the glass slide.

5. The method of claim 4 , wherein the heated slide platform has a uniformity in temperature across the slide of less than about plus or minus 2° C. at 37° C. and less than about plus or minus about 4° C. at 100° C. or the uniformity in temperature across the slide is less than about plus or minus 2° C. at 37° C. and less than about plus or minus about 3° C. at 100° C.

6. The method of claim 4 , wherein the sample can be increased in temperature from 37° C. to 100° C. within eight (8) minutes and cooled from 100° C. to 50° C. within eight (8) minutes or the sample can be increased in temperature from 37° C. to 100° C. within four (4) minutes and cooled from 100° C. to 37° C. within eight (8) minutes.

7. The method of claim 1 , wherein the automated method is devoid of steps requiring a user to handle the substrate between placing the substrate upon which the sample is mounted on the automated instrument and contacting the sample with the chromogenic reagent such that the sample is specifically stained.

8. The method of claim 1 , wherein the step of applying the clarifying reagent, the step of applying the rinsing reagent, and the step applying the chromogenic reagent are walk-away fully-automated functions of the automated instrument.

9. The method of claim 1 , wherein the step of applying the clarifying reagent includes the clarifying reagent contacting the sample for a time between about 2 minutes and about 2 hours, between about 4 minutes and about 1.5 hours, between about 6 minutes and about 1 hour, or between about 8 minutes and about 0.5 hours.

10. The method of claim 1 , wherein the step of applying the clarifying reagent does not include submersing the substrate in a bath.

11. The method of claim 1 , wherein the step of applying the clarifying reagent includes an amount of the clarifying reagent of between about 0.05 mL and about 3 mL, between about 0.1 mL and about 1.5 mL, between about 0.2 mL and about 1 mL, or between about 0.3 mL and about 0.5 mL.

12. The method of claim 1 , further comprising applying an immunohistochemical binding reagent or an in situ hybridization binding reagent so that the immunohistochemical binding reagent or the in situ hybridization binding reagent contact the sample.

13. The method of claim 12 , wherein the applying the immunohistochemical binding reagent or the in situ hybridization binding reagent occurs subsequently to the step of applying the cell condition reagent and prior to the step of applying the chromogenic reagent.

14. The method of claim 1 further comprising applying a buffered preparatory solution so that the buffered preparatory solution contacts the sample prior to applying the clarifying reagent.

15. The method of claim 1 , wherein the clarifying reagent includes about 1% to about 12% hydrogen peroxide (v/v), about 2% to about 10% hydrogen peroxide (v/v), or about 3% to about 9% hydrogen peroxide (v/v).

16. The method of claim 1 , wherein the clarifying reagent includes a phosphate buffer at a concentration of about 0.001 M to about 0.5 M, about 0.01 M to about 0.1 M, or about 0.05 M.

17. The method of claim 1 , wherein the clarifying reagent is buffered at a pH of between about 3 to about 11, between about 4 to about 10, between about 5 to about 9, between about 6 to about 8, or about 7.

18. The method claim 1 , wherein the clarifying reagent includes a Sorensen's buffer at a concentration of about 0.001 M to about 0.5 M, about 0.01 M to about 0.1 M, or about 0.05 and a pH of between about 4 to about 10, between about 5 to about 9, between about 6 to about 8, or about 7.

19. The method of claim 1 , wherein interpretable by the qualified reader includes the sample exhibiting morphological characteristics consistent with those of the sample prior to the applying the clarifying reagent.

20. The method of claim 1 , wherein interpretable by the qualified reader includes the sample exhibiting antigenic and genetic characteristics consistent with or improved with respect to those of the sample prior to applying the clarifying reagent.

21. The method of claim 1 further comprising applying a protease reagent so that the protease reagent contacts the sample.

22. The method of claim 1 , wherein applying the clarifying reagent includes applying drops of the clarifying reagent onto the sample or applying drops of the clarifying reagent in the vicinity of the sample and forcing the drops to contact with the sample in a turbulent flow regime.

23. The method of claim 22 , wherein the drops of the clarifying reagent have a volume of between about 0.05 mL and about 3 mL, between about 0.1 mL and about 1.5 mL, between about 0.2 mL and about 1 mL, or between about 0.3 mL and about 0.5 mL.

24. The method of claim 1 , further comprising applying a second clarifying reagent so that the second clarifying reagent contacts the sample subsequent to applying the clarifying reagent and prior to applying the chromogenic reagent.

Assignees

• Ventana Med Syst Inc

Inventors

• Carrigan Patricia
• Grille James
• Martin Greg
• Robida Mark
• Roche Patrick C

Classifications

• G01N1/312

  for samples mounted on planar substrates · CPC title

• 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

• G01N2001/302

  Stain compositions · CPC title

• G01N2035/00138

  Slides · CPC title

• G01N35/00029

  provided with flat sample substrates, e.g. slides (G01N35/028 takes precedence) · CPC title