首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, kinetic studies and pharmacological evaluation of mutual azo prodrugs of 5-aminosalicylic acid for colon-specific drug delivery in inflammatory bowel disease.
【24h】

Synthesis, kinetic studies and pharmacological evaluation of mutual azo prodrugs of 5-aminosalicylic acid for colon-specific drug delivery in inflammatory bowel disease.

机译:5-氨基水杨酸互偶氮前药在炎性肠病中结肠特异性药物递送的合成,动力学研究和药理学评价。

获取原文
获取原文并翻译 | 示例
           

摘要

Colon-specific mutual azo prodrugs of 5-aminosalicylic acid with essential amino acids were synthesized for the management of inflammatory bowel disease. The structures were confirmed by elemental and spectral analyses. 85-88% release of 5-aminosalicylic acid was achieved in rat fecal matter with half-lives ranging from 140 to 160 min, following first order kinetics. The prodrugs exhibited comparable ameliorating effect as that of sulfasalazine on trinitrobenzenesulfonic acid-induced experimental colitis in rats with a better safety profile.
机译:合成了5-氨基水杨酸与必需氨基酸的结肠特异性互偶氮前药,用于治疗炎症性肠病。通过元素分析和光谱分析确认了结构。遵循一级动力学,在大鼠粪便中实现了5-氨基水杨酸的85-88%释放,半衰期为140至160分钟。前药显示出与柳氮磺吡啶类似的改善作用,对大鼠三硝基苯磺酸诱发的实验性结肠炎具有较好的安全性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号