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首页> 外文期刊>Drug development and industrial pharmacy >Preparation and in vitro evaluation of controlled release hydrophilic matrix tablets of ketorolac tromethamine using factorial design.
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Preparation and in vitro evaluation of controlled release hydrophilic matrix tablets of ketorolac tromethamine using factorial design.

机译:阶乘设计制备酮咯酸三甲胺控释亲水性基质片剂并进行体外评估。

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摘要

Controlled release matrix tablets of ketorolac tromethamine (KT) were prepared by direct compression technique using cellulose derivatives as hydroxypropylmethyl cellulose (HPMC), hydroxyethyl cellulose (HEC), and carboxymethyl cellulose (CMC) in different concentrations (10-20%). The effect of polymer type and concentration was investigated on drug release by 2(3) factorial design. For the quality control of matrix tablets, weight deviation, hardness, friability, diameter-height ratio, content uniformity of KT, and in vitro dissolution technique were performed. UV Spectrophotometric method was used to detection of KT in matrix tablets. This method was validated. Dissolution profiles of the formulations were plotted and evaluated kinetically. An increase in polymer content resulted with a slow release rate of drug as was expected. According to the dissolution results, tablets prepared with HPMC + HEC + CMC (F1 and F8) were found to be the most suitable formulation for KT. About 99.27% KT was released from F8 in 7 h.
机译:酮咯酸三甲胺(KT)的控释基质片是通过直接压片技术制备的,使用纤维素衍生物的羟丙基甲基纤维素(HPMC),羟乙基纤维素(HEC)和羧甲基纤维素(CMC)的浓度不同(10-20%)。通过2(3)析因设计研究了聚合物类型和浓度对药物释放的影响。为了控制基质片剂的质量,进行了重量偏差,硬度,易碎性,直径高度比,KT含量均匀性和体外溶出技术。紫外分光光度法用于检测基质片剂中的KT。该方法已经过验证。绘制制剂的溶解曲线并进行动力学评估。如预期的那样,聚合物含量的增加导致药物的缓慢释放速率。根据溶出度结果,发现用HPMC + HEC + CMC(F1和F8)制备的片剂是最适合KT的制剂。 F8在7小时内释放了约99.27%的KT。

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