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Sulfasalazine release from alginate-N,O-carboxymethyl chitosan gel beads coated by chitosan

机译:磺胺嘧啶从壳聚糖包被的藻酸盐-N,O-羧甲基壳聚糖凝胶珠中释放

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摘要

In the present study, spherical beads were prepared from a water-soluble chitosan (N,O-carboxymethyl chitosan, NOCC) and alginate with ionic gelation method. Then, swollen calcium-alginate-NOCC beads were coated with chitosan. To prepare drug loaded beads, sulfasalazine (SA) was added to the initial aqueous polymer solution. The effect of coating, as well as drying procedure, on the swelling behavior of unloaded beads and SA release of drug loaded ones were evaluated in simulated gastrointestinal tract fluid. The rate of swelling and drug release were decreased for air-dried and coated beads in comparison with freeze-dried and uncoated ones, respectively. No burst release of drug was observed from whole tested beads. Chitosan coated beads released approximately 40% of encapsulated drug in simulated gastric and small intestine tract fluid. Based on these results, the chitosan coated alginate-NOCC hydrogel may be used as potential polymeric carrier for colon-specific delivery of sulfasalazine.
机译:在本研究中,球形珠是由水溶性壳聚糖(N,O-羧甲基壳聚糖,NOCC)和藻酸盐通过离子凝胶法制备的。然后,用壳聚糖包被溶胀的海藻酸钙-NOCC珠。为了制备载药珠,将柳氮磺吡啶(SA)添加到初始聚合物水溶液中。在模拟胃肠道液中,评估了包衣以及干燥程序对未载药珠的溶胀行为和载药珠SA释放的影响。与冷冻干燥和未涂布的珠相比,风干和涂布的珠的溶胀和药物释放速率分别降低。从整个测试珠未观察到药物的突发释放。壳聚糖包被的珠粒在模拟的胃和小肠液体中释放约40%的封装药物。基于这些结果,壳聚糖包被的藻酸盐-NOCC水凝胶可以用作潜在的聚合物载体,用于柳氮磺吡啶类药物的结肠特异性递送。

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