替米沙坦口腔崩解膜的生物制药和药效学特性

R. Kaza, S. M, K. M, A. A., Nagaraju R
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引用次数: 0

摘要

本研究旨在研制替米沙坦快溶膜。快速溶解膜允许药物在口腔内快速溶解,从而绕过第一关代谢。以天然聚合物虎普胶(HG)、瓜尔胶(GG)和黄原胶(XG)为原料,通过揉制法制备了替米沙坦固体分散体,并将优化后的固体分散体用于速溶膜的研制。采用不同等级的HPMC (E5、50 cps和K4M),采用溶剂铸造法制备替米沙坦薄膜。制备了6种配方(FT1-FT6)的替米沙坦薄膜,并对其厚度、拉伸强度、伸长率、重量变化、折叠耐力、药物含量均匀性和表面pH等物理特性进行了评价,取得了满意的结果。通过红外光谱(FTIR)和差示分光光度(DSC)研究证实了该制剂的配伍性。对制剂进行崩解、体外释放和自发性高血压大鼠的药效学研究。在FT1-FT6的配方中,以含HPMC E5和替米沙坦瓜尔胶固体分散体(质量比为1:2)的FT6为最佳配方,其成膜性能良好,崩解时间为42秒,10 min内释药率为97.98%。优化后的薄膜配方(FT6)在40°C/60% RH条件下保存45天以上,具有优异的稳定性。SHR的药效学研究证明,快速溶解的替米沙坦薄膜产生更快的起效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biopharmaceutical and Pharmacodynamic Characteri-stics of Telmisartan Oral Disintegrating Films
This research work was aimed to develop the telmisartan fast dissolving films. Fast dissolving films allow rapid drug dissolution in the oral cavity and thereby bypass the first pass metabolism. Solid dispersions of telmisartan using natural polymers such as hupu gum (HG), guar gum (GG) and xanthan gum (XG) were prepared by kneading technique and the optimized solid dispersion was exploited in the development of rapidly dissolving film. Telmisartan films were prepared by solvent casting method using different grades of HPMC (E5, 50 cps and K4M). Six formulations (FT1-FT6) of telmisartan films were prepared and evaluated for their physical characteristics such as thickness, tensile strength, percentage elongation, weight variation, folding endurance, drug content uniformity and surface pH and gave satisfactory results. The compatibility of the drug in the formulation was confirmed by FTIR and DSC studies. The formulations were subjected to disintegration, in vitro drug release and pharmacodynamic studies on spontaneous hypertensive rats (SHR). Amongst the formulations of FT1-FT6, FT6 was found as best formulation which contains HPMC E5 and telmisartan solid dispersion with guar gum at weight ratio of 1:2 and showed excellent film forming characteristics such as disintegration time at 42 sec and percentage drug release 97.98% within 10 minutes. The optimized film formulation (FT6) showed excellent stability over 45 days when stored at 40°C/60% RH. The pharmacodynamic study in SHR proved that fast dissolving films of telmisartan produced a faster onset of action.    
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