Removal of embedding media from biological samples and cell conditioning on automated staining instruments
The present invention provides reagents for use in an automated environment for removing or etching embedding media by exposing a biological sample to be stained in histochemical or cytochemical procedures without the dependence on organic solvents. The reagents comprise components optimized to facilitate removal or etching of the embedding media from the biological sample. The present invention also provides reagents for use in an automated environment for cell conditioning biological samples wherein the cells are predisposed for access by reagent molecules for histochemical and cytochemical staining procedures. The reagents comprise components optimized to facilitate molecular access to cells and cell constituents within the biological sample.
1. An automated method of simultaneously removing paraffin based embedding medium from a biological sample comprising an epitope and/or target while providing antigen retrieval, the method comprising the steps of:
loading a plurality of biological samples into an automated apparatus wherein the biological samples are embedded with a paraffin based embedding medium that includes infused media;
applying a single deparaffinizing and antigen retrieval reagent that includes a detergent to the biological sample; and
applying heat to the biological sample to raise its temperature above at least about sixty degrees C. while the deparaffinizing and antigen retrieval reagent remains in contact with the biological sample to effectively melt the paraffin based embedding medium including the infused media and to sufficiently expose the epitope and/or target for subsequent detection.
2. The automated method of claim 1 , wherein the at least one cell conditioning reagent is selected from the group consisting of de-ionized water, citrate buffer (pH 6.0-8.0), Tris-HCl buffer (pH 6-10), phosphate buffer (pH 6.0-8.0), sodium chloride-sodium citrate buffer, acidic buffers or solutions (pH 1-6.9), and basic buffers or solutions (pH 7.1-14).
3. The automated method of claim 1 wherein the detergent is at least one ionic or non-ionic surfactants selected from the group consisting of octylphenoxypolyethoxy (5) ethanol, polyoxyethelene(20)sorbitan, polyoxyethelene(23) dodecyl ether, sodium dodecylsulfate and saponin.
4. An automated method of removing paraffin based embedding media from a biological sample comprising an epitope and/or target and subsequently providing ell antigen retriveal, the method comprising the steps of
loading a plurality of biological samples into an automated apparatus wherein the biological samples are embedded with a paraffin based embedding medium that includes infused media;
heating the biological sample containing paraffin based embedding medium to a temperature at or above the paraffin based embedding medium's melting point to liquefy the paraffin based embedding medium including the infused media;
applying an immiscible liquid that includes a detergent to the biological sample to separate the liquified paraffin based embedding medium including the infused media from the biological sample, wherein said immiscible liquid has a density greater than that of the liquefied paraffin based embedding medium,
rinsing away said separated and liquefied paraffin based embedding medium from the biological sample with a rinsing liquid or gas;
applying at least one reagent to the biological sample to facilitate antigen retrieval; and
applying heat to the biological sample to raise its temperature above at least about sixty degrees C. thereby effectively exposing the epitope and/or target for subsequent detection.
5. The method of claim 4 wherein the immiscible liquid comprises water.
6. The method of claim 4 wherein the detergent comprises ionic or non-ionic surfactants.
7. The automated method of claim 6 wherein the ionic or non-ionic surfactants are selected from the group consisting of octylphenoxypolyethoxy (5) ethanol, polyoxyethelene(20)sorbitan, polyoxyethelene(23) dodecyl ether, sodium dodecylsulfate and saponin.
8. The method of claim 4 , wherein the at least one cell conditioning reagent is selected from the group consisting of de-ionized water, citrate buffer (pH 6.0-8.0), Tris-HC1 buffer (pH 6-10), phosphate buffer (pH 6.0-8.0), sodium chloride-sodium citrate buffer, acidic buffers or solutions (pH 1-6.9), and basic buffers or solutions (pH 7.1-14).
9. The automated method of claim 4 , wherein the step of heating the biological sample containing paraffin based embedding medium to a temperature at or above the paraffin based embedding medium's melting point includes conductively heating the biological sample to temperatures above at least about 55° C.
10. The automated method of claim 4 wherein the immiscible liquid is applied once to a biological sample.
11. An automated method of removing embedding media from a biological sample, the method comprising tic steps of:
heating the biological sample containing embedding medium to a temperance at or above the embedding medium's melting point;
applying an immiscible liquid to the biological sample to separate the liquified embedding medium from the biological sample, wherein said immiscible liquid has a density greater than that of the liquefied embedding medium; and
rinsing away said liquefied embedding medium from the biological sample without leaving significant amounts of residual embedding medium.
12. The method of claim 11 wherein said embedding medium is paraffin.
13. The method of claim 11 wherein the immiscible liquid comprises water.
14. The method of claim 11 wherein the immiscible liquid comprises a detergent.
15. The method of claim 14 wherein the detergent comprises ionic or non-ionic surfactants.
16. The automated method of claim 15 wherein the ionic or non-ionic surfactants are selected from the group consisting of octylphenoxypolyethoxy (5) ethanol, polyoxyethelene(20)sorbitan, polyoxyethelene(23) dodecyl ether, sodium dodecylsulfate and saponin.
17. The automated method of claim 11 , wherein the step of heating the biological sample containing embedding medium to a temperature at or above the embedding medium's melting point includes conductively heating the biological sample to temperatures above at least about 55° C.
18. An automated method of removing embedding media from a biological sample, the method comprising the steps of:
heating the biological sample containing embedding medium to a temperature at or above the embedding medium's melting point;
applying an immiscible liquid with a detergent to the biological sample to separate the liquified embedding medium from the biological sample, wherein said immiscible liquid has a density greater than that of the liquefied embedding medium; and
rinsing away said liquefied embedding medium from the biological sample without leaving significant amounts of residual embedding medium.
19. The method of claim 18 wherein said embedding medium is paraffin.
20. The method of claim 18 wherein the immiscible liquid comprises water.
21. The method of claim 18 wherein the detergent comprises ionic or non-ionic surfactants.
22. The automated method of claim 21 wherein the ionic or non-ionic surfactants are selected from the group consisting of octylphenoxypolyethoxy (5) ethanol, polyoxyethelene(20)sorbitan, polyoxyethelene(23) dodecyl ether, sodium dodecyl sulfite and saponin.
23. The automated method of claim 18 , wherein the step of heating the biological sample containing embedding medium to a temperature at or above the embedding medium's melting point includes conductively heating the biological sample to temperatures above at least about 55° C.
24. An automated method of removing embedding media from a biological sing the steps of:
heating the biological sample containing embedding medium to at least about 55° C.;
applying an immiscible liquid and a detergent to the biological sample to separate the liquified embedding medium from the biological sample, wherein said immiscible liquid has a density greater than that of the liquefied embedding medium; and
rinsing away said liquefied embedding medium from the biological sample without leaving significant amounts of residual embedding medium.