In Vitro and In Vivo Evaluation of 28DAP010, a Novel Diamidine for Treatment of Second-Stage African Sleeping Sickness

被引:17
作者
Wenzler, Tanja [1 ,2 ]
Yang, Sihyung [3 ]
Patrick, Donald A. [4 ]
Braissant, Olivier [2 ,5 ]
Ismail, Mohamed A. [6 ]
Tidwell, Richard R. [4 ]
Boykin, David W. [6 ]
Wang, Michael Zhuo [3 ]
Brun, Reto [1 ,2 ]
机构
[1] Swiss Trop & Publ Hlth Inst, Basel, Switzerland
[2] Univ Basel, Basel, Switzerland
[3] Univ Kansas, Sch Pharm, Dept Pharmaceut Chem, Lawrence, KS 66045 USA
[4] Univ N Carolina, Sch Med, Dept Pathol & Lab Med, Chapel Hill, NC USA
[5] Univ Basel Hosp, Dept Urol, CH-4031 Basel, Switzerland
[6] Georgia State Univ, Dept Chem, Atlanta, GA 30303 USA
关键词
TRYPANOSOMA-BRUCEI-GAMBIENSE; DRUG-RESISTANCE; AZA-ANALOGS; ISOTHERMAL MICROCALORIMETRY; ANTIPROTOZOAL ACTIVITY; PRODRUG DB289; CYP4F ENZYMES; PENTAMIDINE; MELARSOPROL; BINDING;
D O I
10.1128/AAC.02309-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
African sleeping sickness is a neglected tropical disease transmitted by tsetse flies. New and better drugs are still needed especially for its second stage, which is fatal if untreated. 28DAP010, a dipyridylbenzene analogue of DB829, is the second simple diamidine found to cure mice with central nervous system infections by a parenteral route of administration. 28DAP010 showed efficacy similar to that of DB829 in dose-response studies in mouse models of first-and second-stage African sleeping sickness. The in vitro time to kill, determined by microcalorimetry, and the parasite clearance time in mice were shorter for 28DAP010 than for DB829. No cross-resistance was observed between 28DAP010 and pentamidine on the tested Trypanosoma brucei gambiense isolates from melarsoprol-refractory patients. 28DAP010 is the second promising preclinical candidate among the diamidines for the treatment of second-stage African sleeping sickness.
引用
收藏
页码:4452 / 4463
页数:12
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