...
首页> 外文期刊>Journal of Applied Polymer Science >Alginate-based biodegradable superabsorbents as candidates for diclofenac sodium delivery systems
【24h】

Alginate-based biodegradable superabsorbents as candidates for diclofenac sodium delivery systems

机译:基于藻酸盐的生物可降解超吸收剂,可作为双氯芬酸钠输送系统的候选物质

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Novel types of highly swelling hydrogels were prepared by grafting crosslinked polyacrylamide-co-poly-2-acrylamido-2-methylpropane sulfonic acid (PAAm-co-PAMPS) chains onto sodium alginate (Na-Alg) through a free radical polymerization method. The superabsorbent formation was confirmed by Fourier transform infrared spectroscopic (FTIR). The controlled release behavior of diclofenac sodium (DS) from superabsorbent polymer was factinvestigated, and shown that the release profiles of DS from superabsorbent polymer were slow in simulated gastric fluid (SGF, pH 1.2) over 3 h, but nearly all of the initial drug content was released in simulated intestinal fluid (SIF, pH 7.4) within 21 h after changing media. Overall the results demonstrated that biodegradable superabsorbent could successfully deliver a drug to the intestine without losing the drug in the stomach, and could be potential candidates as an orally administrated drug delivery system.
机译:通过自由基聚合方法将交联的聚丙烯酰胺-共-聚丙烯-2-丙烯酰胺基-2-甲基丙烷磺酸(PAAm-co-PAMPS)链接枝到藻酸钠(Na-Alg)上,制备了新型的高溶胀水凝胶。通过傅立叶变换红外光谱法(FTIR)证实了超吸收剂的形成。事实研究了双氯芬酸钠(DS)从超吸收性聚合物的控释行为,结果表明,在模拟胃液(SGF,pH 1.2)中,超吸收性聚合物的DS释放曲线在3 h内缓慢,但几乎所有初始药物更换培养基后21小时内,模拟肠液(SIF,pH 7.4)中的蛋白质含量释放。总体而言,结果表明,可生物降解的超吸收剂可以成功地将药物输送到肠道,而不会在胃中流失,并且可以作为口服给药系统的潜在候选药物。

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