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新型苯二氮䓬类药物的临床药代动力学

Clinical pharmacokinetics of the newer benzodiazepines.

作者信息

Greenblatt D J, Divoll M, Abernethy D R, Ochs H R, Shader R I

出版信息

Clin Pharmacokinet. 1983 May-Jun;8(3):233-52. doi: 10.2165/00003088-198308030-00003.

Abstract

New benzodiazepine derivatives continue to be developed and introduced into clinical use. The pharmacokinetic properties of these newer drugs can best be understood by their categorisation according to range of elimination half-life and pathway of metabolism (oxidation versus conjugation). Clobazam and halazepam are long half-life (and therefore accumulating) anxiolytics metabolised by oxidation. Alprazolam and clotiazepam also are oxidised compounds but have short to intermediate half-life values and therefore produce considerably less accumulation. Temazepam and lormetazepam are hypnotic agents with intermediate half-lives but metabolised by conjugation. The most unique of the newer benzodiazepines are the ultra-short half-life (oxidised) compounds midazolam, triazolam and brotizolam, which are essentially non-accumulating during multiple dosage.

摘要

新型苯二氮䓬衍生物不断被研发并投入临床使用。根据消除半衰期范围和代谢途径(氧化与结合)对这些新药进行分类,能更好地理解它们的药代动力学特性。氯巴占和哈拉西泮是通过氧化代谢的长效(因此会蓄积)抗焦虑药。阿普唑仑和氯噻西泮也是经氧化的化合物,但半衰期短至中等,因此蓄积量要少得多。替马西泮和氯美扎酮是半衰期中等的催眠药,但通过结合代谢。新型苯二氮䓬类药物中最独特的是超短效(氧化型)化合物咪达唑仑、三唑仑和溴替唑仑,多次给药时它们基本不会蓄积。

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