Design, synthesis, and in vivo evaluation of oxamniquine methacrylate and acrylamide prodrugs

被引:27
作者
Parise Filho, Roberto
de Souza Menezes, Carla Maria
Silva Pinto, Pedro Luiz
Paula, Gilberto Alvarenga
Brandt, Carlos Alberto
Barata da Silveira, Maria Amelia
机构
[1] Univ Sao Paulo, Fac Pharmaceut Sci, Dept Pharm, BR-05508900 Sao Paulo, Brazil
[2] Adolfo Lutz Inst, Schistosomiais Sector, BR-01246902 Sao Paulo, Brazil
[3] Butantan Inst, BR-05503900 Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Math & Stat, Dept Stat, BR-05508900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
oxamniquine; schistosomicide; polymeric prodrug; molecular modeling;
D O I
10.1016/j.bmc.2006.11.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxamniquine is an antiparasitic agent commonly used in therapeutics against Schistosoma mansoni. Although it is well tolerated, some adverse effects justify the search for new compounds with prolonged biological action, so that monomeric and polymeric oxamniquine prodrugs were designed. Synthetic results assisted by molecular modeling study showed the possibility to obtain the corresponding monomeric forms of the oxamniquine methacrylate (1) and oxamniquine acrylamide (2). Successful copolymerization procedure only occurred on the methacrylic compound, generating the oxamniquine methacrylate copolymer (3). Submitted to a preliminary in vivo biological evaluation, a similar oxamniquine profile was observed to the monomeric forms although an inadequate drug release may be responsible for the methacrylic copolymer failure. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1229 / 1236
页数:8
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