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新型抗疟化合物:咯萘啶的研究。

Studies on a new antimalarial compound: pyronaridine.

作者信息

Chang C, Lin-Hua T, Jantanavivat C

机构信息

Institute of Parasitic Diseases, Chinese Academy of Preventive Medicine, Shanghai.

出版信息

Trans R Soc Trop Med Hyg. 1992 Jan-Feb;86(1):7-10. doi: 10.1016/0035-9203(92)90414-8.

Abstract

Pyronaridine, a hydroxyanilino-benzonaphthyridine derivative synthesized in 1970, is a new antimalarial compound which has been in use in China for more than 10 years. The drug is highly effective against Plasmodium falciparum and P. vivax. Furthermore, it is efficacious in combatting chloroquine-resistant strains of falciparum malaria both in vitro and in vivo, in human patients. Extensive field studies involving several thousand cases have shown that pyronaridine has promising therapeutic value in the treatment of malarial infection, including chloroquine-resistant infections. Pyronaridine given orally, intramuscularly or by intravenous drip is not only effective against malaria but also has low toxicity.

摘要

咯萘啶是1970年合成的一种羟基苯胺基苯并萘啶衍生物,是一种新型抗疟化合物,在中国已使用10多年。该药对恶性疟原虫和间日疟原虫高度有效。此外,它在体外和体内对恶性疟原虫的氯喹抗性菌株均有疗效,适用于人类患者。涉及数千例的广泛现场研究表明,咯萘啶在治疗疟疾感染,包括氯喹抗性感染方面具有有前景的治疗价值。口服、肌肉注射或静脉滴注咯萘啶不仅对疟疾有效,而且毒性低。

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