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新型植物胶在控释给药中的基质特性

Matrix properties of a new plant gum in controlled drug delivery.

作者信息

Kalu V D, Odeniyi M A, Jaiyeoba K T

机构信息

Department of Pharmaceutics & Industrial Pharmacy, University of Ibadan, Ibadan, Nigeria.

出版信息

Arch Pharm Res. 2007 Jul;30(7):884-9. doi: 10.1007/BF02978841.

Abstract

A new plant gum, Okra (extracted from the pods of Hibiscus esculentus), has been evaluated as a controlled-release agent in modified release matrices, in comparison with sodium carboxymethyl cellulose (NaCMC) and hydroxypropylmethyl cellulose (HPMC), using Paracetamol as a model drug. Tablets were produced by direct compression and the in-vitro drug release was assessed in conditions mimicking the gastro intestinal system, for 6 h. Okra gum matrices provided a controlled-release of Paracetamol for more than 6 h and the release rates followed time-independent kinetics. The release rates were dependent on the concentration of the drug present in the matrix. The addition of tablet excipients, lactose and Avicel, altered the dissolution profile and the release kinetics. Okra gum compared favourably with NaCMC, and a combination of Okra gum and NaCMC, or on further addition of HPMC resulted in near zeroorder release of paracetamol from the matrix tablet. The results indicate that Okra gum matrices could be useful in the formulation of sustained-release tablets for up to 6 h.

摘要

一种新型植物胶——秋葵胶(从黄秋葵的豆荚中提取),已作为控释剂在缓释基质中进行了评估,以对乙酰氨基酚为模型药物,与羧甲基纤维素钠(NaCMC)和羟丙基甲基纤维素(HPMC)进行比较。通过直接压片制备片剂,并在模拟胃肠系统的条件下评估6小时的体外药物释放情况。秋葵胶基质能使对乙酰氨基酚控释超过6小时,且释放速率遵循非时间依赖性动力学。释放速率取决于基质中药物的浓度。片剂辅料乳糖和微晶纤维素的添加改变了溶出曲线和释放动力学。秋葵胶与NaCMC相比具有优势,秋葵胶与NaCMC的组合,或进一步添加HPMC后,对乙酰氨基酚从基质片剂中的释放接近零级释放。结果表明,秋葵胶基质可用于制备长达6小时的缓释片剂。

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