采用熔融制粒技术配制和评估酒石酸唑吡坦控释片剂。

ISRN Pharmaceutics Pub Date : 2011-01-01 Epub Date: 2011-06-27 DOI:10.5402/2011/208394
Shailesh T Prajapati, Amit N Patel, Chhagan N Patel
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引用次数: 0

摘要

本研究采用 3(2) 全因子设计法研究了 PEG 6000 作为熔融粘合剂的浓度和 HPMC K4M 与 PVP 的比例对盐酸唑吡坦控释片剂的影响:PVP 对酒石酸唑吡坦控释片剂的影响。选择 HPMC K4M 和 PVP K30 的比例(X(1))和熔融粘合剂的浓度(X(2))为自变量,1 小时(Q(1))、4 小时(Q(4))、8 小时(Q(8))的药物释放量、扩散系数(n)和释放速率常数(K)为因变量。采用熔融造粒技术制备了片剂,并对各种评价参数进行了评估。结果表明,熔融粘合剂的浓度对 Q(1)、Q(4)、n 和 K 有显著影响。优化配方(F(7))与药物的理论曲线非常相似。X(2) 变量对因变量有显著影响,而 X(1) 变量对因变量没有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Formulation and evaluation of controlled-release tablet of zolpidem tartrate by melt granulation technique.

The present investigation describes the influence of the concentration of PEG 6000 as a melt binder and ratio of HPMC K4M : PVP on Zolpidem tartrate controlled-release tablet formulations using 3(2) full factorial design. The ratio of HPMC K4M and PVP K30 (X(1)) and the concentration of melt binder (X(2)) were selected as independent variables, and drug release at 1 hr (Q(1)), 4 hr (Q(4)), 8 hr (Q(8)), diffusion coefficient (n), and release rate constant (K) were selected as a dependent variable. Tablets were prepared by melt granulation technique and evaluated for various evaluation parameters. It was observed that concentration of melt binder had significant effect on Q(1), Q(4), n, and K Binder concentration 25% w/w was found optimum. Optimized formulation (F(7)) showed good similarity with theoretical profile of drug. The X(2) variable had a significant effect on dependent variables, and the X(1) variable had no significant effect on dependent variables.

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