配方和特征:琥珀酸美托洛尔控释基质片剂

Alagusundaram M, Priyanka Keshri, Pratibha Sharma, Nem Kumar Jain, China Babu Dara
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引用次数: 0

摘要

琥珀酸美托洛尔控释基质片采用湿法制粒工艺与不同比例的羟丙基甲基纤维素(HPMC K4M)制成。异丙醇用作聚维酮(PVP K30)溶液的造粒剂。除了用作提高片剂重量的稀释剂外,还添加了硬脂酸镁和滑石粉,以增强颗粒在压片过程中的流动能力。对压碎的片剂进行了理化特性、体外试验和动力学试验,并对生成颗粒的微粒特性进行了评估。每种配方的结果都基本令人满意,其中 M4 的效果最好。所有配方都显示出良好的相关性。基质片剂的药物扩散动力学似乎为零阶,释放机制为扩散调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and characterization: Metoprolol succinate controlled release matrix tablets
Metoprolol succinate-controlled release matrix tablets were made utilizing the wet granulation process with various ratio of Hydroxypropyl methyl cellulose (HPMC K4M). Isopropyl alcohol is used as a granulating agent in the Povidone (PVP K30) solution. In addition to being utilised as diluents to raise the weight of the tablets, magnesium stearate and talc were added to enhance the granules' flow ability during tablet compression. The crushed tablets underwent physicochemical characteristics, in-vitro and kinetic tests, and the micromeritic properties of the generated granules were evaluated. In every formulation, results were nearly satisfactory, with M4 being the best among the others. All of the formulations showed good correlation. The drug diffusion kinetics from matrix tablets appeared to be zero order, and the release mechanism was diffusion regulated.
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