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金刚烷胺与经典抗疟药物在恶性疟原虫感染中的体外药物相互作用。

In vitro drug interaction between amantadine and classical antimalarial drugs in Plasmodium falciparum infections.

作者信息

Evans S G, Havlik I

机构信息

Department of Experimental and Clinical Pharmacology, University of the Witwatersrand Medical School, Parktown, South Africa.

出版信息

Trans R Soc Trop Med Hyg. 1994 Nov-Dec;88(6):683-6. doi: 10.1016/0035-9203(94)90229-1.

Abstract

The interactions of amantadine with classical antimalarial drugs were evaluated against a chloriquine-resistant and a chloroquine-sensitive strain of Plasmodium falciparum in vitro. Amantadine potentiated the effect of chloroquine and quinine in both strains; it also potentiated the effect of mefloquine, halofantrine and primaquine in the chloroquine-resistant strain but had no effect in the chloroquine-sensitive strain. Amantadine had no effect on the response to pyrimethamine of either strain. Amantadine does not interfere with the activity of these compounds and may possibly enhance it.

摘要

在体外,针对氯喹抗性和氯喹敏感的恶性疟原虫株,评估了金刚烷胺与经典抗疟药物的相互作用。金刚烷胺增强了两种菌株中氯喹和奎宁的作用;它还增强了氯喹抗性菌株中甲氟喹、卤泛群和伯氨喹的作用,但对氯喹敏感菌株没有影响。金刚烷胺对两种菌株中乙胺嘧啶的反应均无影响。金刚烷胺不干扰这些化合物的活性,并且可能会增强其活性。

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