Gastro retentive floating drug delivery system of model drug using central composite design

Nidhi Km, K. Uma, Jaya Sing, Amarjeet Singh
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Abstract

The work plans to build up a Gastro retentive floating drug delivery system of Model drug using central composite design. The model drug is a drug which is used in the treatment of antiulcer. Extended-release tablets of model drug provide constant plasma concentration with a less frequent administration and also reduce the side effects to some extent. This could extend its safe administration and improve patient compliance. The present study aims to develop floating tablets of model drug using HPMC K4M, Carbopol 934 and an effervescent agent which can float on gastrointestinal fluid for sustained release and evaluate the model drug tablets in-vitro for their TFT, FLT, and drug release pattern. Gastro retentive drug delivery system (GRDDS) refers to systems in which the drug retained in the stomach for a prolonged period that improves the bioavailability of drug substances. Any delivery system aims to deliver a therapeutic amount of drug to the specific site in the body to obtain rapid and then maintain a requisite amount of drug. The formulated tablets evaluated for both pre-compression and post compression parameters including weight variation, hardness, friability, in vitro drug release and different pharmacokinetic plots. Final formulation was agreeable when assessed for all assessment parameters.
采用中心复合设计的模型药物胃内保留漂浮给药系统
本研究拟采用中心复合设计,建立模型药物的胃潴留漂浮给药系统。模型药是一种用于治疗抗溃疡的药物。模型药缓释片给药次数少,血药浓度稳定,副作用也有所减轻。这可以延长其安全管理并提高患者的依从性。本研究以HPMC K4M、卡波波尔934和一种可在胃肠液上漂浮缓释的泡腾剂为主要成分,制备模型药漂浮片剂,并对模型药片剂的TFT、FLT和药物释放模式进行体外评价。胃保留给药系统(GRDDS)是指药物在胃中保留较长时间以提高原料药生物利用度的系统。任何给药系统的目的都是将治疗量的药物递送到体内的特定部位,以快速获得并保持所需的药物量。对制剂的重量变化、硬度、脆度、体外释药量及药动学等参数进行了评价。当评估所有评估参数时,最终配方是令人满意的。
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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