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首页> 外文期刊>RSC Advances >Preparation of magnetic pH-sensitive microcapsules with an alginate base as colon specific drug delivery systems through an entirely green route
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Preparation of magnetic pH-sensitive microcapsules with an alginate base as colon specific drug delivery systems through an entirely green route

机译:以藻酸盐为基质的磁性pH敏感微囊通过完全绿色的途径制备为结肠特异性药物递送系统

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The aim of this work was to prepare pH-sensitive drug carriers for colon specific drug delivery through a completely green and environmentally friendly route (without using any organic solvents, hazardous chemicals and even a harsh procedure). To achieve this, natural biopolymers (sodium alginate, chitosan and carboxymethylcellulose sodium) were used. Naproxen (as a model drug) and magnetic nanoparticles were encapsulated into the alginate microcapsules by formation of an alginate-Ca2+ complex. To overcome the drawbacks of the alginate microcapsules like porosity and burst drug release, they were coated with chitosan and carboxymethylcellulose sodium by a layer-by-layer technique that led to the formation of polyelectrolyte complexes through inter-ionic interactions between oppositely charged biopolymers. After coating with these natural polymers, porosity was reduced and burst drug releases were modified. The prepared magnetic microcapsules were characterized by FT-IR, DSC and SEM to study their structures and the roles that each polymeric layer plays. The swelling ratios and in vitro drug release profiles of the microcapsules were studied in both enzyme-free simulated gastric (SGF, pH 1) and simulated colonic fluids (SCF, pH 7.4). These microcapsules could be driven by means of an external magnet and also the results show that these coated microcapsules are completely pH-sensitive and potentially can be used as stimuli responsive carriers for colon specific drug delivery.
机译:这项工作的目的是通过完全绿色和环境友好的途径(不使用任何有机溶剂,危险化学品甚至是苛刻的程序)来制备用于结肠特异性药物输送的pH敏感药物载体。为此,使用了天然生物聚合物(海藻酸钠,壳聚糖和羧甲基纤维素钠)。通过形成藻酸盐-Ca 2+复合物,将萘普生(作为模型药物)和磁性纳米颗粒封装到藻酸盐微胶囊中。为了克服藻酸盐微胶囊的缺点,如孔隙率和药物释放,它们通过一层一层的技术用壳聚糖和羧甲基纤维素钠包被,从而通过带相反电荷的生物聚合物之间的离子间相互作用形成聚电解质复合物。用这些天然聚合物包衣后,孔隙率降低,药物释放的释放得到改善。通过FT-IR,DSC和SEM对制备的磁性微胶囊进行了表征,以研究其结构以及每个聚合物层所起的作用。在无酶模拟胃(SGF,pH 1)和模拟结肠液(SCF,pH 7.4)中研究了微囊的溶胀率和体外药物释放曲线。这些微胶囊可以通过外部磁体来驱动,并且结果还表明,这些包衣的微胶囊对pH值完全敏感,并且有可能被用作刺激响应载体,用于结肠特异性药物递送。

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