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高剂量甲苯咪唑在治疗囊尾蚴病患者中的临床药代动力学

Clinical pharmacokinetics of high dose mebendazole in patients treated for cystic hydatid disease.

作者信息

Braithwaite P A, Roberts M S, Allan R J, Watson T R

出版信息

Eur J Clin Pharmacol. 1982;22(2):161-9. doi: 10.1007/BF00542462.

Abstract

The plasma concentrations of mebendazole and its metabolites have been monitored in twelve patients after receiving a 10 mg/kg dose for cystic hydatid disease. The mebendazole plasma concentration-time profiles differed considerably between patients; elimination half-lives ranged from 2.8-9.0 h, time to peak plasma concentration after dosing ranged from 1.5-7.25 h and peak plasma concentrations ranged from 17.5 to 500 ng/ml. The mean peak plasma concentration of mebendazole after an initial dose (69.5 ng/ml) was lower than found in patients during chronic therapy (137.4 ng/ml). The plasma AUCTS for the major metabolites of mebendazole (methyl 5-(alpha-hydroxybenzyl)-2-benzimidazole carbamate and 2-amino-5 benzoylbenzimidazole) were about five times the plasma AUCT found for mebendazole in patients on chronic therapy. It is suggested that the slower clearance of these polar metabolites relative to mebendazole results from enterohepatic recycling. Since mebendazole is also highly plasma protein bound, caution should be observed in administering mebendazole to patients with liver disease. Concentrations of mebendazole found in the tissue and cyst material collected from two patients during surgery ranged from 59.5 to 206.6 ng/g wet weight.

摘要

在12名接受10mg/kg剂量甲苯咪唑治疗囊型包虫病的患者中监测了甲苯咪唑及其代谢物的血浆浓度。患者之间甲苯咪唑的血浆浓度-时间曲线差异很大;消除半衰期为2.8 - 9.0小时,给药后达到血浆峰浓度的时间为1.5 - 7.25小时,血浆峰浓度为17.5至500ng/ml。初始剂量后甲苯咪唑的平均血浆峰浓度(69.5ng/ml)低于慢性治疗患者中的浓度(137.4ng/ml)。甲苯咪唑主要代谢物(5-(α-羟基苄基)-2-苯并咪唑氨基甲酸甲酯和2-氨基-5-苯甲酰基苯并咪唑)的血浆药时曲线下面积约为慢性治疗患者中甲苯咪唑血浆药时曲线下面积的五倍。提示这些极性代谢物相对于甲苯咪唑清除较慢是由于肝肠循环所致。由于甲苯咪唑也与血浆蛋白高度结合,因此对肝病患者使用甲苯咪唑时应谨慎。手术中从两名患者收集的组织和囊肿材料中甲苯咪唑的浓度为59.5至206.6ng/g湿重。

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