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重症肌无力患者肌内注射新斯的明的动力学与代谢

Kinetics and metabolism of intramuscular neostigmine in myasthenia gravis.

作者信息

Somani S M, Chan K, Dehghan A, Calvey T N

出版信息

Clin Pharmacol Ther. 1980 Jul;28(1):64-8. doi: 10.1038/clpt.1980.132.

Abstract

Neostigmine kinetics and metabolism were studied after intracellular administration to 8 patients with myasthenia gravis. The plasma neostigmine level declined monoexponentially from 21 +/- 2 to 9 +/- 1 ng/ml between 30 and 120 min. The data were interpreted in terms of a 1-compartment model. Estimates of plasma half-life (t1/2) ranged from 51.1 to 90.5 min; apparent volume of distribution varied from 32.0 to 60.6 1; and total body clearance from 434 to 549 ml/min. Approximately 80% of the drug was eliminated in urine within 24 hr either as unchanged neostigmine or its metabolites. Approximately 50% of the dose was eliminated as the unchanged drug, 15% as 3-hydroxyphenyltrimethylammonium, and 15% as other unidentified metabolites. The neostigmine t1/2, based on the urinary excretion of the unchanged drug, ranged from 90.2 to 118.7 min. It was concluded that neostigmine was eliminated by renal and extrarenal mechanisms.

摘要

对8例重症肌无力患者进行细胞内给药后,研究了新斯的明的动力学和代谢情况。在30至120分钟之间,血浆新斯的明水平从21±2 ng/ml呈单指数下降至9±1 ng/ml。数据按照一室模型进行解释。血浆半衰期(t1/2)估计值在51.1至90.5分钟之间;表观分布容积在32.0至60.6升之间;全身清除率在434至549毫升/分钟之间。约80%的药物在24小时内以原形新斯的明或其代谢产物的形式经尿液排出。约50%的剂量以原形药物排出,15%以3-羟基苯基三甲基铵排出,15%以其他未鉴定的代谢产物排出。基于原形药物的尿排泄情况,新斯的明的t1/2在90.2至118.7分钟之间。得出的结论是,新斯的明通过肾脏和肾外机制被清除。

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