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甲氟喹作为抗疟药物的研发。联合国开发计划署/世界银行/世界卫生组织最新情况

Development of mefloquine as an antimalarial drug. UNDP/World Bank/WHO update.

出版信息

Bull World Health Organ. 1983;61(2):169-78.

Abstract

The spread of multiresistant strains of Plasmodium falciparum in south-east Asia and South America and the appearance of chloroquine resistance in Africa indicates the urgent need for alternative drugs against these parasites. Mefloquine, a 4-quinoline methanol, is the only new drug that is currently at an advanced stage of development.Studies in animal models and in the clinic have shown that it is highly active as a blood schizontocide against strains that are resistant to many established antimalarials, e.g., chloroquine and pyrimethamine. It is not, however, effective as a causal prophylactic agent. Preclinical toxicological, teratological, and carcinogenicity studies do not indicate any major contraindications to its use.Intensive clinical studies have been carried out in Africa, North and South America, south-east Asia, and Europe. These studies have indicated that the compound is generally well tolerated, safe, and effective in the treatment of malaria, particularly infections with chloroquine-resistant parasites.In order to protect this new and promising drug against the development of resistance to it in endemic areas, it is important that its introduction should be accomplished in a rational and deliberate manner. Appropriate precautionary measures include the development of mefloquine combinations (a combination of mefloquine with pyrimethamine-sulfadoxine is presently under investigation), its use with primaquine as a gametocytocidal drug to prevent transmission, and its deployment primarily for treatment, being used for prophylaxis only in special risk groups.

摘要

恶性疟原虫多重耐药菌株在东南亚和南美洲的传播以及非洲出现的氯喹耐药性表明,迫切需要研发针对这些寄生虫的替代药物。甲氟喹,一种4-喹啉甲醇,是目前处于研发后期的唯一新药。动物模型和临床研究表明,它作为一种血内裂殖体杀灭剂,对许多已有的抗疟药(如氯喹和乙胺嘧啶)耐药的菌株具有高度活性。然而,它作为病因性预防药物无效。临床前毒理学、致畸学和致癌性研究未表明其使用有任何重大禁忌。在非洲、南北美洲、东南亚和欧洲都进行了深入的临床研究。这些研究表明,该化合物在治疗疟疾,特别是氯喹耐药寄生虫感染方面,通常耐受性良好、安全且有效。为了保护这种新的有前景的药物在流行地区不产生耐药性,重要的是应以合理和审慎的方式引入它。适当的预防措施包括研发甲氟喹复方制剂(目前正在研究甲氟喹与乙胺嘧啶-磺胺多辛的复方制剂),将其与伯氨喹作为配子体杀灭药物联合使用以防止传播,以及主要将其用于治疗,仅在特殊风险群体中用于预防。

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