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肠贾第虫对阿奇霉素、强力霉素、甲氟喹、替硝唑和呋喃唑酮二元组合的体外敏感性。

Sensitivity in vitro of Giardia intestinalis to dyadic combinations of azithromycin, doxycycline, mefloquine, tinidazole and furazolidone.

作者信息

Crouch A A, Seow W K, Whitman L M, Thong Y H

机构信息

Department of Child Health, University of Queensland, Mater Children's Hospital, South Brisbane, Australia.

出版信息

Trans R Soc Trop Med Hyg. 1990 Mar-Apr;84(2):246-8. doi: 10.1016/0035-9203(90)90273-h.

Abstract

The new macrolide antibiotic, azithromycin, produced significant growth inhibition of Giardia intestinalis at 100 micrograms/ml, but adherence inhibition was significant at concentrations as low as 1 microgram/ml for the two strains used in these experiments. The dyadic combinations of azithromycin-furazolidone, doxycycline-mefloquine, doxycycline-tinidazole and mefloquine-tinidazole were synergistic for inhibition of adherence. These results suggest that these dyadic combinations may be worthy of consideration for chemotherapy of recalcitrant giardiasis.

摘要

新型大环内酯类抗生素阿奇霉素在浓度为100微克/毫升时对肠道贾第虫有显著的生长抑制作用,但在这些实验中所使用的两个菌株中,浓度低至1微克/毫升时对黏附就有显著抑制作用。阿奇霉素-呋喃唑酮、多西环素-甲氟喹、多西环素-替硝唑以及甲氟喹-替硝唑的二元组合在抑制黏附方面具有协同作用。这些结果表明,这些二元组合可能值得考虑用于顽固性贾第虫病的化疗。

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