采用23因子设计对抗糖尿病药黏附含片的处方及评价

P. Nagaveni, Sirisha. S, C. A. Rao
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引用次数: 0

摘要

本研究旨在探讨抗糖尿病药物格列齐特黏附含片的配方及评价,采用直接压缩法制备格列齐特黏附含片。本研究采用23随机全因子设计,分别以黄原胶、carbol -934、HPMC-E15LV为原料制备格列齐特黏附含片,实验模型:目的是考察调整黏附含片中高分子黄原胶、HPMC-E15LV、卡波波-934的浓度对其90%的释药率和黏附特性的影响。2设计3个全因子试验,以确定低、高浓度两个水平下3个自变量的相互作用。测定片剂的重量变化、硬度、表面pH、药物含量均匀性、肿胀指数、黏附强度及体外释药研究、离体黏附时间。从药物释放研究中发现,与其他制剂相比,含有H4的制剂具有较好的药物释放性。
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Formulation and Evaluation of Mucoadhesive Buccal Tablets of Anti-Diabetic Drug using 23 Factorial Design
The aim of the present study involved the formulation and evaluation of mucoadhesive buccal tablets of anti-diabetic drug gliclazide, Mucoadhesive buccal tablets of Gliclazide are prepared by direct compression method In this present investigational research work the mucoadhesive buccal tablets of gliclazide is prepared separately employing 23 randomized full factorial design by using xanthan gum, carbopol-934, HPMC-E15LV, In this experimental model, target is to determine how the t90% of drug release and mucoadhesive characters can be affected by adjusting three parameters, concentration of polymers xanthan gum, HPMC-E15LV, carbopol-934, of the mucoadhesive buccal tablets. 2 3 full factorial studies were designed to determine the interaction of three independent variables at two levels (low and high level concentration) The tablets were tested for weight variation, hardness, surface pH, drug content uniformity, swelling index, mucoadhesion strength and in-vitro drug release study, Ex- vivo mucoadhesion time. From the drug release studies it was found that formulation H4 containing has good drug release when compared to other formulations.
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