卡马西平的生物利用度。

L M Cotter, G Smith, W D Hooper, J H Tyrer, M J Eadie
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引用次数: 0

摘要

服用卡马西平片的患者血浆卡马西平水平与药物剂量的相关性从两个方面提示了药物从人体消化道吸收不完全和不稳定的可能性。为了研究这种可能性,对6名志愿者进行了药代动力学研究,这些志愿者在适当的间隔时间内服用卡马西平片剂,单次剂量不断增加。这些研究提供了卡马西平吸收缓慢且可能不完全的证据。5例患者经特殊配制的卡马西平溶液给药后,药物吸收迅速,其中4例患者的药物吸收比相同正常剂量给药时更多。结论卡马西平片剂的制剂限制了该药的生物利用度,如果要提高该药的生物利用度,可能会出现问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The bioavailability of carbamazepine.

Two aspects of the correlation of plasma carbamazepine level with drug dose in patients taking carbamazepine tablets indicated the possibility that the drug may be incompletely and variably absorbed from the alimentary tract of man. To investigate this possibility, pharmacokinetic studies were undertaken in six volunteers, who were given increasing single doses of carbamazepine in tablet form at appropriate intervals. These studies gave evidence of slow, and probably incomplete, absorption of carbamazepine. After administration of carbamazepine in a specially-prepared solution to 5 of the subjects, rapid absorption of the drug occurred, and in 4 subjects more drug was absorbed than when the same normal dose was given as tablets. It was concluded that the pharmaceutical formulation of carbamazepine tablets limits the bioavailability of the drug, and that problems may arise if the bioavailability of the drug is to be increased.

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