Biocompatible and biodegradable pH-responsive hydrogels based on N-vinyl pyrrolidone (NVP), polyethylene glycol diacrylate (PAC) and chitosan were prepared for controlled drug delivery. These interpolymeric hydrogels were synthesized by a free radical polymerization technique using azobisisobutyronitrile (AIBN) as initiator and N,N'-methylenebisacrylamide (BIS) as crosslinker. These hydrogels were subjected to equilibrium swelling studies in enzyme-free simulated gastric and intestinal fluids (SGF and SIF). These swelling studies clearly indicated that these hydrogels were swollen more in SGF when compared to SIF. Theophylline and 5-fluorouracil (5-FU) were entrapped into these hydrogels and equilibrium-swelling studies were carried out for the drug-entrapped gels in enzyme-free SGF and SIF. The in-vitro release profiles of the drugs were established in enzyme-free SGF. More than 50% of the entrapped drugs were released in the first 2 h at gastric pH and the rest of the drug release was slower.

译文

制备了基于N-乙烯基吡咯烷酮 (NVP),聚乙二醇二丙烯酸酯 (PAC) 和壳聚糖的生物相容性和可生物降解的pH响应水凝胶,用于控制药物递送。这些共聚水凝胶是通过自由基聚合技术合成的,使用偶氮二异丁腈 (AIBN) 作为引发剂,N,N'-亚甲基双丙烯酰胺 (BIS) 作为交联剂。这些水凝胶在无酶的模拟胃液和肠液 (SGF和SIF) 中进行了平衡肿胀研究。这些溶胀研究清楚地表明,与SIF相比,这些水凝胶在SGF中的溶胀更多。将茶碱和5-氟尿嘧啶 (5-FU) 包埋到这些水凝胶中,并对无酶SGF和SIF中的药物包埋凝胶进行了平衡溶胀研究。在无酶SGF中建立了药物的体外释放曲线。在胃pH下的前2小时内释放了超过50% 的截留药物,其余的药物释放较慢。

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