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Studies on Rebamipide Loaded Gastroretentive Alginate Based Mucoadhesive Beads: Formulation & In-vitro, In-vivo Evaluation

机译:瑞巴派特负载的胃滞留藻酸盐基粘膜粘附微珠的研究:配方与体外,体内评估

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Introduction: Oral route is the most common and convenient routeto deliver the drug. Many oral drug delivery systems were developed toimprove drug bio availability; gastro retentive drug delivery system is oneof them. Gastroretentive drug delivery system is the system in which adrug can remain in the gastric region for several hours in order to prolongits gastric residence time. The purpose of this work was to develop andevaluate rebamipide loaded gastro retentive alginate based muco adhesivebeads. Materials and Methods: Rebamipide loaded alginate beads wereprepared by ionotropic gelation and polyelectrolyte complexation method.Prepared beads were characterized for IR, DSC, SEM and evaluated fordissolution and stability studies. Results: The FTIR spectra revealed thatthere were no interaction between drug and excipients. The particle sizeanalysis showed that beads with 3% of sodium alginate were spherical inshape. The mucoadhesion study reveals that as concentration of alginateand carbopol 934 increases percentage of mucoadhesion also increases.Conclusion: From in-vivo study it was concluded that the preparedformulation showed better control on ulcer than that of pure rebamipide.Rebamipide was successfully formulated as gastroretentive floating andmucoadhesive alginate beads by using ionotropic gelation and polyelectrolytecomplexation method.
机译:简介:口服途径是最常见,最方便的药物递送途径。开发了许多口服药物递送系统以改善药物的生物利用度。胃保持性药物输送系统就是其中之一。胃滞留药物递送系统是其中药物可以在胃区域中保留数小时以延长胃停留时间的系统。这项工作的目的是开发和评估负载瑞巴派特的胃滞留藻酸盐基粘膜胶珠。材料与方法:采用离子凝胶法和聚电解质络合法制备负载瑞巴派特的藻酸盐微珠,对制备的微珠进行IR,DSC,SEM表征,并评价其溶出度和稳定性。结果:FTIR光谱显示药物与赋形剂之间没有相互作用。粒度分析表明,含3%海藻酸钠的珠粒为球形。粘膜黏附研究表明,随着藻酸盐和卡波姆934浓度的增加,粘膜黏附的百分比也随之增加。结论:体内研究得出的结论是,所制备的制剂对溃疡的控制作用优于纯瑞巴派特。瑞巴派特成功地制成了具有胃滞留性的漂浮和粘膜黏附剂海藻酸盐珠采用离子化凝胶和聚电解质络合方法。

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