克拉霉素-甲硝唑胃原位凝胶的制备、评价与优化

R. Patel, B. Dadhani, R. Ladani, A. Baria, J. Patel
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引用次数: 42

摘要

本文研究了海藻酸钠基克拉霉素-甲硝唑原位凝胶的制备、优化和性能评价。以海藻酸钠为聚合物,碳酸钙为交联剂。原位制剂具有良好的粘度、药物含量和缓释性能;本研究报道,口服含有海藻酸钠的水溶液会导致原位凝胶的形成,这种配方在口服时是均匀的液体,在接触部位变成凝胶。32全因子设计结果显示,海藻酸钠浓度和CaCO3浓度显著影响因变量Q1、Q12和T80。因此,这些原位凝胶适用于口服缓释克拉霉素和甲硝唑苯甲酸酯。关键词:原位凝胶;胃具体;胃停留时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation, evaluation and optimization of stomach specific in situ gel of clarithromycin and metronidazole benzoate
The present investigation deals with the formulation, optimization and evaluation of sodium alginate based In situ gel of Clarithromycin and Metronidazole Benzoate. Sodium alginate used as a polymer and CaCO3 was used as a cross-linking agent. The In situ formulation exhibited well, viscosity, drug content and sustained drug release; this study reports that oral administration of aqueous solutions containing sodium alginate results in formation of In situ gel, such formulations are homogenous liquid when administered orally and become gel at the contact site. The results of a 32 full factorial design revealed that the concentration of sodium alginate and concentration of CaCO3 significantly affected the dependent variables Q1, Q12 and T80. These In situ gels are, thus, suitable for oral sustained release of Clarithromycin and Metronidazole Benzoate. Keywords: In situ gel; Stomach specific; Gastric residence time.
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