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Pharmacokinetics of the CHR compound in blood plasma and its content in the brain after single administration to mice was studied. It was demonstrated that the CHR compound at a dose of 5.0 mg/kg is absorbed from the gastrointestinal tract and penetrates into the brain in a relatively short period. It is assumed that the existing concentration of analgesic in the brain is insufficient for the development of psychotropic effects with normal function of the blood-brain barrier, which is confirmed by the results of the previously conducted "Open Field" test.