In vitro release kinetics study of Esomeprazole Magnesium Trihydrate tablet available in Bangladesh and comparison with the originator brand (Nexium

S. Halder, Madhabi Lata Shuma, A. Kabir, A. S. Rouf
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引用次数: 2

Abstract

The main aim of present investigation was to study the dissolution pattern of most commercially available formulations of Esomeprazole in Bangladesh. Commercially available ten national brands and originator brand of esomeprazole magnesium trihydrate tablets were studied in simulated gastric medium (pH 1.2) for first 15 minutes and simulated intestinal medium (pH 6.8) for next 30 minutes time period using USP reference dissolu-tion apparatus (Type II). No brands met the dissolution pattern like the originator brand (E1). But three brands (E3, E6 and E7) were found to be very close to it in terms of dissolution pattern. One brand E11 was found to be sub-standard compared to originator one. Drug release profiles were analyzed for zero order, first order and Higuchi equation to reveal the release kinetics perspective of Esomeprazole magnesium trihydrate enteric coated tablets. It was found that first order kinetics was predominant for E1 (Originator Brand). Zero order and Higuchi release kinetics was predominant release mechanism than first order release kinetics for E2, E4 and E11. First order release kinetics was predominant for rest of the brands (E3, E5, E6, E7, E8, E9 and E10). It was found that drug release of those brands followed moderately diffusion method and concentration dependant from the dosage form. Among all of these locally manufactured Esomeprazole brands E3, E6 and E7 showed compatible dissolution pattern and release kinetics compared with the originator brand. Key words : In vitro dissolution; Market preparations; Kinetics study; Esomeprazole; National brand; Originator brand. DOI: http://dx.doi.org/10.3329/sjps.v4i1.8875 SJPS 2011; 4(1): 79-83
孟加拉国埃索美拉唑三水合镁片体外释放动力学研究及与原研品牌耐信的比较
本研究的主要目的是研究孟加拉国大多数市售埃索美拉唑制剂的溶出规律。采用USP标准溶出度仪(II型)对市售的10个国家品牌和初始品牌埃索美拉唑三水合物镁片在模拟胃介质(pH 1.2)中前15分钟和模拟肠道介质(pH 6.8)中后30分钟的溶出度进行了研究。没有一个品牌符合初始品牌(E1)的溶出模式。但发现E3、E6和E7三个品牌在溶出模式上非常接近。其中一个品牌E11被发现与原厂产品相比不合格。通过零级、一级和Higuchi方程分析药物释放曲线,揭示三水合埃索美拉唑镁肠溶片的释放动力学视角。发现E1 (Originator Brand)以一级动力学为主。E2、E4和E11的释放机制以零级和Higuchi释放动力学为主。其余品牌(E3、E5、E6、E7、E8、E9和E10)均以一级释放动力学为主。结果表明,各剂型的药物释放均符合适度扩散方式,且具有浓度依赖性。在所有国产埃索美拉唑品牌中,E3、E6和E7与原产品牌相比具有相容的溶出模式和释放动力学。关键词:体外溶出度;市场准备工作;动力学研究;拉唑;国家品牌;发起者的品牌。DOI: http://dx.doi.org/10.3329/sjps.v4i1.8875 SJPS 2011;4 (1): 79 - 83
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