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首页> 外文期刊>International Scholarly Research Notices >Formulation and Evaluation of Controlled-Release Tablet of Zolpidem Tartrate by Melt Granulation Technique
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Formulation and Evaluation of Controlled-Release Tablet of Zolpidem Tartrate by Melt Granulation Technique

机译:熔融制粒技术制备酒石酸唑吡坦控释片及其评价

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摘要

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 32full factorial design. The ratio of HPMC K4M and PVP K30 (X1) and the concentration of melt binder (X2) were selected as independent variables, and drug release at 1 hr (Q1), 4 hr (Q4), 8 hr (Q8), 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 onQ1,Q4,n, andKBinder concentration 25% w/w was found optimum. Optimized formulation (F7) showed good similarity with theoretical profile of drug. TheX2variable had a significant effect on dependent variables, and theX1variable had no significant effect on dependent variables.
机译:本研究使用32全因子设计描述了作为熔融粘合剂的PEG 6000的浓​​度和HPMC K4M:VPPVP的比例对酒石酸唑吡坦控释片剂的影响。选择HPMC K4M和PVP K30的比例(X1)和熔融粘合剂的浓度(X2)作为自变量,分别在1?hr(Q1),4?hr(Q4),8?hr(Q8)时释放药物,扩散系数(n)和释放速率常数(K)作为因变量。通过熔融造粒技术制备片剂,并评价各种评价参数。观察到熔融粘合剂的浓度对Q1,Q4,n有显着影响,KBinder浓度25%w / w最佳。优化的配方(F7)与药物的理论特征具有良好的相似性。 X2变量对因变量有显着影响,X1变量对因变量没有显着影响。

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