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抗疟药物 Fansimef(乙胺嘧啶+磺胺多辛+甲氟喹)在健康受试者中的多剂量药代动力学。

Multiple-dose pharmacokinetics of the antimalarial drug Fansimef (pyrimethamine + sulfadoxine + mefloquine) in healthy subjects.

作者信息

Schwartz D E, Weidekamm E, Mimica I, Heizmann P, Portmann R

出版信息

Chemotherapy. 1987;33(1):1-8. doi: 10.1159/000238468.

Abstract

Fansimef is a new antimalarial combination containing pyrimethamine, sulfadoxine and mefloquine in the weight proportions 1 + 20 + 10. It has been designed to fight plasmodia resistant to the presently used antimalarial drugs and to counter the development of new resistant forms of the parasites. In the present study tablets containing 25 mg pyrimethamine, 500 mg sulfadoxine and 250 mg mefloquine were used. Six Brazilian volunteers received a loading dose of 2 tablets followed by 20 maintenance doses of 1 tablet at a dosage interval of 7 days. The pharmacokinetic evaluation of each of the three components was based on the assumption of an open linear two-compartment model. After the last maintenance dose the following kinetic parameters were determined for pyrimethamine, sulfadoxine and mefloquine, respectively: elimination half-life = 123, 179 and 550 h; volume of distribution in the postdistributive phase = 2.5, 0.15 and 18.6 1 X kg-1, and total systemic clearance = 14.0, 0.64 and 24.0 ml X h-1 X kg-1. All these values agree fairly well with those measured in previous single-dose kinetic studies. At steady state, Cmin values of each of the three components generally showed small variations. No unexpected accumulation of any of the three components was observed, indicating that induction or inhibition of metabolic enzymes did not occur during the trial.

摘要

法西姆(Fansimef)是一种新型抗疟复方制剂,含有乙胺嘧啶、磺胺多辛和甲氟喹,其重量比例为1 + 20 + 10。它的设计目的是对抗对目前使用的抗疟药物耐药的疟原虫,并对抗寄生虫新耐药形式的发展。在本研究中,使用了含有25毫克乙胺嘧啶、500毫克磺胺多辛和250毫克甲氟喹的片剂。六名巴西志愿者接受了2片的负荷剂量,随后以7天的给药间隔服用20次维持剂量,每次1片。对这三种成分中每一种的药代动力学评估基于开放线性二室模型的假设。在最后一次维持剂量后,分别测定了乙胺嘧啶、磺胺多辛和甲氟喹的以下动力学参数:消除半衰期分别为123、179和550小时;分布后相的分布容积分别为2.5、0.15和18.6升×千克⁻¹,总全身清除率分别为14.0、0.64和24.0毫升×小时⁻¹×千克⁻¹。所有这些值与先前单剂量动力学研究中测得的值相当吻合。在稳态时,这三种成分中每一种的Cmin值通常显示出较小的变化。未观察到这三种成分中的任何一种有意外的蓄积,表明在试验期间未发生代谢酶的诱导或抑制。

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