Method for histoprocessing
The invention relates to the processing of a biological sample for histological analysis. In particular, it relates to a rapid automated processing system that can be operated with continuous throughput and that eliminates the use of toxic solvents such as xylene. Provided is a method for processing a biological sample for histological analysis, comprising contacting the sample with a composition comprising a supercritical or near supercritical fluid followed by impregnating the sample under a pressure of more than 1 bar with an embedding medium, preferably paraffin. Also provided is a processor ( 1 ) for preparing at least one sample ( 10 ) for histological analysis, comprising at least one process reactor ( 9 ) for the at least one sample ( 10 ), characterized in that the processor ( 1 ) comprises supplying means ( 4 ) for supplying to the reactor ( 9 ) at least one substance of which at least one is in supercritical phase or near supercritical phase and at least one supplying means ( 7 ) for adding the embedding medium to the reactor ( 9 ) through conduit ( 8 ).
1. A method for processing a biological sample for histological analysis, comprising the steps of:
a) contacting the sample with a dehydrating agent;
b) removing the dehydrating agent with a composition comprising a supercritical or a near supercritical fluid at a temperature in the range of 0.7 to 1.4 times its critical temperature and at a pressure in the range of 0.3 to 7 times its critical pressure; and
c) replacing the supercritical fluid by infiltrating an embedding medium at a pressure of at least 1 bar.
2. A method according to claim 1 , wherein said supercritical or near supercritical fluid is carbon dioxide.
3. A method according to claim 1 , wherein said biological sample is a fresh, frozen, or fixed, or non-fixed tissue sample.
4. A method according to claim 1 , wherein said biological sample comprises an organ or a part thereof.
5. A method according to claim 1 , wherein said sample is dehydrated, defatted and/or decalcified prior to impregnation by using a composition comprising a supercritical fluid.
6. A method according to claim 5 , wherein said composition additionally comprises a dehydrating agent.
7. A method according to claim 5 , wherein said composition additionally comprises a decalcifying agent.
8. The method of claim 7 , wherein the decalcifying agent is an acid.
9. The method of claim 1 , wherein the embedding medium is paraffin.
10. The method of claim 3 , wherein the biological specimen is a fresh, non-fixed sample.
11. The method of claim 6 , wherein the dehydrating agent is an alcohol.