硝唑昔尼缓释片的研制及体外评价

Lakshminarayana Reddy Golamaru, K. Rajnarayana, K. Jayaveera
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引用次数: 1

摘要

目的:研制硝唑昔尼特缓释片的处方。方法:采用湿法制粒,以亲水性聚合物为缓释剂制备硝唑昔尼特片。溶出度数据还评价了药物释放机制和动力学。并对优化后的配方进行了家兔体内实验。结果:根据体外药物释放研究数据,选择5%w/w的Methocel K100M作为缓释剂。药物释放遵循一级动力学和动力学扩散。结论:该制剂具有缓释作用。
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Development and in vitro- in vivo evaluation of Nitazoxanide sustained release tablets
Objective: The objective of the present investigation was to develop a sustained release (SR) tablet formulation of Nitazoxanide.Methods: Nitazoxanide Tablets were prepared by employing wet granulation methods and hydrophilic polymers used as drug release retardants. The dissolution data also evaluated for the drug release mechanism and kinetics. The optimized formulation was subjected for in vivo studies in rabbits.Results: Based on data obtained from the in vitro drug release studies 5%w/w of Methocel K100M was selected as a release retardant. The drug release followed first order kinetics and fickian diffusion.Conclusion: Present investigation indicates that the developed formulation was able to sustain the drug release.
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