Snyder Christopher, Chollet Jacques, Santo-Tomas Josefina, Scheurer Christian, Wittlin Sergio
Swiss Tropical Institute, Socinstrasse 57, CH-4002 Basel, Switzerland.
Exp Parasitol. 2007 Mar;115(3):296-300. doi: 10.1016/j.exppara.2006.09.016. Epub 2006 Nov 7.
RBx11160 (OZ277) is a promising antimalarial drug candidate that Ranbaxy Laboratories Limited and Medicines for Malaria Venture (MMV) are currently developing as a fixed combination with piperaquine. Here, we describe the in vitro (Plasmodium falciparum) and in vivo (Plasmodium berghei) activities of piperaquine in combination with RBx11160 and artemether. In vitro, both combinations demonstrated a slight tendency towards antagonism with mean sums of fractional inhibitory concentrations (mean Sigma FICs) of 1.5. In vivo, piperaquine and artemether were borderline antagonistic (mean Sigma FIC of 1.4). However, an additive in vivo interaction of piperaquine and RBx11160 (mean Sigma FIC of 1.1) was identified, suggesting that a RBx11160-piperaquine combination therapy in humans should allow each molecule to exert its full antimalarial effect.
RBx11160(OZ277)是一种很有前景的抗疟候选药物,兰伯西实验室有限公司和疟疾药物事业机构(MMV)目前正在将其开发成与哌喹的固定复方制剂。在此,我们描述了哌喹与RBx11160及蒿甲醚联合使用时的体外(恶性疟原虫)和体内(伯氏疟原虫)活性。在体外,两种联合用药均表现出轻微的拮抗倾向,平均分数抑制浓度总和(平均∑FICs)为1.5。在体内,哌喹和蒿甲醚表现为临界拮抗(平均∑FIC为1.4)。然而,已确定哌喹和RBx11160在体内具有相加相互作用(平均∑FIC为1.1),这表明在人类中使用RBx11160-哌喹联合疗法应能使每个分子充分发挥其抗疟作用。