Kaminsky R, Chuma F, Wasike R P
International Laboratory for Research on Animal Diseases (ILRAD), Nairobi, Kenya.
Vet Parasitol. 1994 Apr;52(3-4):235-42. doi: 10.1016/0304-4017(94)90115-5.
Trypanosoma congolense bloodstream forms were propagated in vitro axenically in a simplified cultivation medium at 34 degrees C. Viability of a drug-sensitive and a drug-resistant clone were examined for 10 days following exposure to 0.1, 1.0 and 10.0 micrograms ml-1 of diminazene aceturate and 0.1, 1.0 and 10.0 ng ml-1 of isometamidium chloride for various time intervals. Drug-sensitive T. congolense were irreversibly damaged after incubation with 10 micrograms ml-1 or 1 microgram ml-1 diminazene aceturate for 30 min or 2 h, respectively, while drug-resistant trypanosomes were not affected. Exposure to 10 ng ml-1 isometamidium chloride eliminated drug-sensitive trypanosomes after 24 h and drug-resistant trypanosomes after 96 h. The data obtained on in vitro time-dose responses of T. congolense were related to pharmacokinetic data of diminazene and isometamidium in cattle plasma.
刚果锥虫血流型在34摄氏度的简化培养基中进行体外无菌培养。在不同时间间隔暴露于0.1、1.0和10.0微克/毫升的乙酰氨基阿维菌素以及0.1、1.0和10.0纳克/毫升的氯异喹胍后,对一个药物敏感克隆和一个耐药克隆的活力进行了10天的检测。药物敏感的刚果锥虫在分别与10微克/毫升或1微克/毫升的乙酰氨基阿维菌素孵育30分钟或2小时后受到不可逆损伤,而耐药锥虫则未受影响。暴露于10纳克/毫升的氯异喹胍24小时后消除了药物敏感锥虫,96小时后消除了耐药锥虫。关于刚果锥虫体外时间-剂量反应的数据与牛血浆中乙酰氨基阿维菌素和氯异喹胍的药代动力学数据相关。