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首页> 外文期刊>International Journal of Pharmaceutics >Preparation of ionic-crosslinked chitosan-based gel beads and effect of reaction conditions on drug release behaviors.
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Preparation of ionic-crosslinked chitosan-based gel beads and effect of reaction conditions on drug release behaviors.

机译:离子交联壳聚糖凝胶凝胶的制备及反应条件对药物释放行为的影响。

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摘要

Drug-loaded chitosan (CS) beads were prepared under simple and mild condition using trisodium citrate as ionic crosslinker. The beads were further coated with poly(methacrylic acid) (PMAA) by dipping the beads in PMAA aqueous solution. The surface and cross-section morphology of these beads were observed by scanning electron microscopy and the observation showed that the coating beads had core-shell structure. In vitro release of model drug from these beads obtained under different reaction conditions was investigated in buffer medium (pH 1.8). The results showed that the rapid drug release was restrained by PMAA coating and the optimum conditions for preparing CS-based drug-loaded beads were decided through the effect of reaction conditions on the drug release behaviors. In addition, the drug release mechanism of CS-based drug-loaded beads was analyzed by Peppa's potential equation. According to this study, the ionic-crosslinked CS beads coated by PMAA could serve as suitable candidate for drug site-specific carrier in stomach.
机译:使用柠檬酸三钠作为离子交联剂,在简单温和的条件下制备了载有药物的壳聚糖(CS)珠。通过将珠子浸入PMAA水溶液中,进一步用聚(甲基丙烯酸)(PMAA)涂覆珠子。通过扫描电子显微镜观察这些珠的表面和横截面形态,并且观察结果表明涂层珠具有核-壳结构。在缓冲液(pH 1.8)中研究了在不同反应条件下从这些磁珠中体外释放模型药物的过程。结果表明,PMAA涂层抑制了药物的快速释放,并通过反应条件对药物释放行为的影响决定了制备CS基载药微球的最佳条件。此外,还通过Peppa势方程分析了CS基载药珠的释药机理。根据这项研究,由PMAA包覆的离子交联的CS珠可以作为胃中药物位点特异性载体的合适候选者。

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