FIELD: medicine.
SUBSTANCE: what is described is a biointegrated composite containing the following ingredients, wt %: collagen 5%-10%, polyazolidine ammonia modified by halogen hydrate ions 0.5%-4%, water dispersion of sub-micron flavonoid aggregates 0.5%-1%, water - the rest. What is described is a method for the coating formation, which consists in applying the biologically active composite by immersion or deposition followed by lyophilisation. The drying process is single-staged at a temperature of 3-5°C and pressure of 5×10-1 Pa. What is also described is a method for administering the biodegradable composite into a bone cavity by separating a mucoperiosteal flap of the operated portion of the alveolar process by special taps, burs and drills forming a bone bed to be filled with a targeted osteointegration substance, mounting an implant, placing back the flap and closing the wound.
EFFECT: composite has biocompatibility and haemocompatibility, optimal physical-chemical properties, as well as rapid resorbability in vivo with generating no toxic products and negative reactions when in use.
3 cl, 9 dwg, 2 tbl, 4 ex
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Authors
Dates
2014-12-10—Published
2013-08-19—Filed