Bartlett M S, Queener S F, Tidwell R R, Milhous W K, Berman J D, Ellis W Y, Smith J W
Indiana University School of Medicine, Indianapolis 46202-5120.
Antimicrob Agents Chemother. 1991 Feb;35(2):277-82. doi: 10.1128/AAC.35.2.277.
Three 8-aminoquinolines from the Walter Reed Army Institute for Research (WRAIR), WR6026, WR238605, and WR242511, strongly inhibited Pneumocystis carinii growth in vitro at 1 microgram/ml. This activity was similar to that of primaquine. In rat therapy models, the WRAIR compounds affected Pneumocystis pneumonia at doses as low as 0.25 mg/kg (WR242511) or 0.5 mg/kg (WR6026 and WR238605). At these doses, primaquine alone was ineffective as therapy. In a rat prophylaxis model, all three WRAIR 8-aminoquinolines were extremely effective at daily doses of 0.57 mg/kg, showing activity greater than that of primaquine at this dosage and comparable to that of trimethoprim-sulfamethoxazole at 50/250 mg/kg.
来自沃尔特·里德陆军研究所(WRAIR)的三种8-氨基喹啉,即WR6026、WR238605和WR242511,在1微克/毫升的浓度下能强烈抑制体外卡氏肺孢子虫的生长。这种活性与伯氨喹相似。在大鼠治疗模型中,WRAIR化合物在低至0.25毫克/千克(WR242511)或0.5毫克/千克(WR6026和WR238605)的剂量下对卡氏肺孢子虫肺炎有影响。在这些剂量下,单独使用伯氨喹作为治疗无效。在大鼠预防模型中,所有三种WRAIR 8-氨基喹啉在每日剂量为0.57毫克/千克时都极其有效,在此剂量下显示出比伯氨喹更强的活性,且与50/250毫克/千克的甲氧苄啶-磺胺甲恶唑相当。