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本文报告了用药理方法研究口服蝮蛇抗栓酶的生物利用度。结果表明,口服蝮蛇抗栓酶的最大效应强度(E_(max))较静注低,E_(max)出现时间(T_(max))较静注慢,与静注比较,其绝对生物利用度为11%。
This article reports the pharmacological approach to study the bioavailability of oral viperns antithrombotics. The results showed that the maximum effect intensity (E max) of oral viper snake antithrombin was lower than that of intravenous injection and the time of emergence of E max (T max) was slower than that of intravenous injection. Compared with intravenous injection, the absolute bioavailability The degree is 11%.