The activity of artemisinin in combination with mefloquine was tested in vitro against a chloroquine-sensitive (F32) strain of Plasmodium falciparum. A method of repetitive dosing and extending the culture observation period to 28-30 days was used to mimic the in vivo pharmacokinetic situation. Plasmodium falciparum was exposed to artemisinin from 10(-8) to 10(-5) M, mefloquine from 3 x 10(-9) to 10(-5) M and their combinations. The exposure time for artemisinin was 3 hours twice daily and for mefloquine 24 hours. The drug-dosing duration was 3 days. Neither artemisinin nor mefloquine alone provided radical clearance of P. falciparum, even when maximum concentrations (10(-5) M) were applied. The antiparasitic activity of artemisinin and mefloquine were significantly higher when dosed alone. Effective concentrations for different degrees of inhibition (EC 50, 90 and 99) of both artemisinin and mefloquine respectively were significantly lower when used in combination. At concentrations normally reached in vivo, this effect was clearly synergistic (P = 0.016) Our in vitro model of intermittent dosing of artemisinin and mefloquine combinations for 3 days provides significant evidence of positive interaction between the two compounds. Lower combination concentrations around the MIC-values for the individual compounds showed synergistic effect, and high concentrations showed additive effect. This indicates that such drug combinations may provide radical clearance at concentrations lower than those required for single-drug treatment.

译文

在体外测试了青蒿素与甲氟喹对恶性疟原虫氯喹敏感 (F32) 菌株的活性。使用重复给药并将培养观察期延长至28-30天的方法来模拟体内药代动力学情况。恶性疟原虫暴露于青蒿素从10(-8) 到10(-5) M,甲氟喹从3x10(-9) 到10(-5) M及其组合。青蒿素的暴露时间为3小时,每天两次,甲氟喹24小时。给药时间为3天。即使施加最大浓度 (10(-5) M),青蒿素和甲氟喹都不能提供恶性疟原虫的自由基清除。单独给药时,青蒿素和甲氟喹的抗寄生虫活性明显更高。青蒿素和甲氟喹的不同抑制程度 (EC 50、90和99) 的有效浓度在联合使用时均显着降低。在体内通常达到的浓度下,这种作用显然是协同的 (P = 0.016)。我们的青蒿素和甲氟喹组合间歇给药3天的体外模型提供了两种化合物之间正相互作用的重要证据。单个化合物的MIC值附近的较低组合浓度显示出协同作用,而高浓度显示出累加作用。这表明此类药物组合可能以低于单药治疗所需的浓度提供自由基清除。

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