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An integrated Taguchi and response surface methodological approach for the optimization of an HPLC method to determine glimepiride in a supersaturatable self-nanoemulsifying formulation

机译:集成的Taguchi和响应面方法学方法,用于优化HPLC方法以确定过饱和自纳米乳化配方中的格列美脲

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We studied the application of Taguchi orthogonal array (TOA) design during the development of an isocratic stability indicating HPLC method for glimepiride as per TOA design; twenty-seven experiments were conducted by varying six chromatographic factors. Percentage of organic phase was the most significant (p0.001) on retention time, while buffer pH had the most significant (p0.001) effect on tailing factor and theoretical plates. TOA design has shortcoming, which identifies the only linear effect, while ignoring the quadratic and interaction effects. Hence, a response surface model for each response was created including the linear, quadratic and interaction terms. The developed models for each response found to be well predictive bearing an acceptable adjusted correlation coefficient (0.9152 for retention time, 0.8985 for tailing factor and 0.8679 for theoretical plates). The models were found to be significant (p0.001) having a high F value for each response (15.76 for retention time, 13.12 for tailing factor and 9.99 for theoretical plates). The optimal chromatographic condition uses acetonitrile - potassium dihydrogen phosphate (pH 4.0; 30mM) (50:50, v/v) as the mobile phase. The temperature, flow rate and injection volume were selected as 35+/-2^oC, 1.0mLmin^-^1 and 20@mL respectively. The method was validated as per ICH guidelines and was found to be specific for analyzing glimepiride from a novel supersaturatable self-nanoemulsifying formulation.
机译:我们研究了Taguchi正交阵列(TOA)设计在等度稳定性开发过程中的应用,该方法表明按照TOA设计进行格列美脲的HPLC方法;通过改变六个色谱因子进行了二十七个实验。有机相百分比对保留时间的影响最大(p <0.001),而缓冲液pH对拖尾因子和理论塔板的影响最大(p <0.001)。 TOA设计有一个缺点,即仅识别线性效应,而忽略了二次效应和交互效应。因此,创建了每个响应的响应表面模型,包括线性,二次和交互作用项。针对每种响应开发的模型具有良好的预测性,并具有可接受的调整后相关系数(保留时间0.9152,拖尾因子0.8985和理论塔板0.8679)。发现该模型是有意义的(p <0.001),其每个响应的F值都很高(保留时间为15.76,拖尾因子为13.12,理论塔板为9.99)。最佳色谱条件为使用乙腈-磷酸二氢钾(pH 4.0; 30mM)(50:50,v / v)作为流动相。温度,流速和注射量分别选择为35 +/- 2℃,1.0mLmin-1和20mL。该方法已按照ICH指南进行了验证,并被发现可用于分析新型过饱和自纳米乳化配方中的格列美脲。

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