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游离苯丁酸氮芥及其泼尼松龙酯(泼尼莫司汀,Leo 1031)给药后在人体内的药代动力学。

Pharmacokinetics of chlorambucil in man after administration of the free drug and its prednisolone ester (prednimustine, Leo 1031).

作者信息

Ehrsson H, Wallin I, Nilsson S O, Johansson B

出版信息

Eur J Clin Pharmacol. 1983;24(2):251-3. doi: 10.1007/BF00613827.

Abstract

The pharmacokinetics of chlorambucil has been investigated in a cross over study after oral administration of the free drug (10 mg) and its prednisolone ester (prednimustine, 100 mg). The bioavailability of chlorambucil was about five times lower when given as prednimustine as compared to administration of the free drug. The peak plasma concentration was about twice as high and it was obtained more rapidly when the free drug was given. No intact prednimustine could be detected in plasma.

摘要

在一项交叉研究中,对口服游离苯丁酸氮芥(10毫克)及其泼尼松龙酯(泼尼松苯丁酸氮芥,100毫克)后的药代动力学进行了研究。与游离药物给药相比,以泼尼松苯丁酸氮芥给药时,苯丁酸氮芥的生物利用度约低五倍。游离药物给药时,血浆峰浓度约高两倍,且达到更快。血浆中未检测到完整的泼尼松苯丁酸氮芥。

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