FIELD: medicine.
SUBSTANCE: invention is a method for production of biological implants, characterized in that surgically purified and mechanically fragmented initial bone tissue biomaterial is subjected to two to three freeze-thawing cycles, cleaned in the ultrasonic bath by a solution of 0.1 M ethylenediaminetetraacetic acid and 0.01 M sodium hydroxide, then with a solution of 1M hydrochloric acid and 1M sodium chloride, then treated with a solution of 1M sodium chloride and 0.1 M phosphate buffer with washing by a solution of 0.1 M phosphate buffer to pH 7-8, then with a solution of 0.1% Triton x-100 and 1% sodium dodecyl sulfate, followed by a solution of 0.1-1% trypsin and 0.125-0.3% papain at a ration of 1:1 ratio, after that the biomaterial is processed in an ultrasonic bath in 3% hydrogen peroxide, and then treated with a mixture of ethanol or isopropanol and diethyl ether or chloroform at a ratio of 1:2, then treatment is carried out in supercritical carbon dioxide in an autoclave at a pressure of 75-700 atm and a temperature of 32-50°C at periodic pressure drop below the critical point, at the second stage, distilled water and carbon dioxide are introduced into the autoclave at a ratio of 1:(1-3) at a pressure of 150-350 atm and a temperature of 15-25°C, and after autoclave decompression, the biomaterial is subjected to lyophilization and sterilisation.
EFFECT: obtaining of biomaterials for bone tissue regeneration with a high degree of biocompatibility.
6 cl, 3 ex
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Authors
Dates
2017-05-18—Published
2016-03-31—Filed