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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >DEVELOPMENT, FORMULATION AND EVALUATION OF A BILAYER GASTRIC RETENTIVE FLOATING TABLETS OF RANITIDINE HCL AND CLARITHROMYCIN USING NATURAL POLYMERS
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DEVELOPMENT, FORMULATION AND EVALUATION OF A BILAYER GASTRIC RETENTIVE FLOATING TABLETS OF RANITIDINE HCL AND CLARITHROMYCIN USING NATURAL POLYMERS

机译:天然聚合物对盐酸拉尼替丁盐酸盐和克拉霉素的双层胃液漂浮片剂的开发,配方和评价

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Objective: Bilayer gastric retentive floating tablets (BGRFT) with ranitidine HCl and clarithromycin using natural gums have been developed to prolong the gastric residence time and increase drug bioavailability. Literature review revealed no published studies on the present study. Methods: Immediate release (IR) layer prepared by using different diluents and super disintegrants like sodium starch glycolate, crosscarmellose sodium and crospovidone. Controlled released (CR) layer prepared by using neem gum, damar gum and copal gum. Prepared tablets were evaluated for in vivo and in vitro buoyancy, in vitro dissolution studies and fourier transformation-infrared spectroscopy (FTIR). Drug release was evaluated with zero and first order for release kinetics, Higuchi , Hixson-Crowell erosion models for release mechanism. Results: Prepared IR layer followed first order rate kinetics and CR layer followed zero order rate kinetics with non-Fickian diffusion mechanism. BGRFT also showed similar results as that of the individual layer. Optimized formulations were characterized by FTIR studies and found no interactions between drug and polymer. Conclusion: The results demonstrate the feasibility of the model in the development of BGRFT. BGRFT enhanced the drug release and finally the bioavailability of clarithromycin when compared with commercial tablet (Biomycin 250). The present study could establish the suitability of neem gum as CR polymer in the design of BGRFT.
机译:目的:已开发出使用天然树胶与盐酸雷尼替丁和克拉霉素联用的双​​层胃滞留漂浮片(BGRFT),可延长胃的停留时间并增加药物的生物利用度。文献综述显示,本研究尚无已发表的研究。方法:通过使用不同的稀释剂和超级崩解剂(如乙醇酸淀粉钠,交叉羧甲基纤维素钠和交聚维酮)制备速释层。通过使用印em胶,达玛胶和椰棕胶制备的控释(CR)层。评价制备的片剂的体内和体外浮力,体外溶出度研究和傅里叶变换红外光谱(FTIR)。用零和一阶释放动力学评价药物释放,Higuchi,Hixson-Crowell腐蚀模型用于释放机理。结果:制备的IR层遵循一级速率动力学,CR层遵循零级速率动力学,且具有非Fickian扩散机理。 BGRFT还显示出与各个层相似的结果。通过FTIR研究对优化配方进行了表征,发现药物与聚合物之间没有相互作用。结论:结果证明了该模型在BGRFT开发中的可行性。与商用片剂(Biomycin 250)相比,BGRFT增强了克拉霉素的药物释放并最终提高了其生物利用度。本研究可以确定印em胶作为CR聚合物在BGRFT设计中的适用性。

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