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Formulation and statistical optimization of controlled release pellets of Cetrizine Dihydrochloride

机译:盐酸西替利嗪控释微丸的研制及统计学优化

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The objective of this study was to formulate controlled release pellets of cetrizine dihydrochloride and optimize the effect of formulation variables i.e. concentration of Eudragit RLPO and ethyl cellulose. The experimental design selected was 32 full factorial design using these two variables. Drug release after 24 hr and t50% were evaluated as response parameters. Polymers were coated onto the drug loaded pellets using pan coater. It was observed that the concentrations of polymers directly affected the drug release profile. Eudragit RLPO and ethyl cellulose showed effects opposite to each other on drug release. Mathematical models were generated for each response parameters to predict their values at selected levels of formulation variables. The effect of the variables and behavior of the system was studied using response surface plots. The optimized formulation showed drug release of 96.22% in 24 hr and t50% of 11hr 54 min. The results of this study revealed that the pellets of cetrizine dihydrochloride coated with 1:5 ratio of Eudragit RLPO: Ethyl cellulose showed optimum controlled release.
机译:这项研究的目的是配制西替利嗪二盐酸盐的控释药丸,并优化配方变量的效果,即Eudragit RLPO和乙基纤维素的浓度。选择的实验设计是使用这两个变量的32个全因子设计。将24小时和t50%后的药物释放评估为响应参数。使用锅包衣机将聚合物包衣到载有药物的药丸上。观察到聚合物的浓度直接影响药物释放曲线。 Eudragit RLPO和乙基纤维素在药物释放方面显示出彼此相反的作用。为每个响应参数生成数学模型,以预测其在所选配方变量水平上的值。使用响应曲面图研究了变量和系统行为的影响。优化的配方在24小时内显示96.22%的药物释放,在11小时54分钟内显示50%的药物释放。这项研究的结果表明,用Eudragit RLPO:乙基纤维素以1:5的比例包被的西替利嗪盐酸盐小丸显示出最佳的控制释放。

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