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首页> 外文期刊>Chromatography Research International >Stress Degradation Studies on Flupirtine Maleate Using Stability-Indicating RP-HPLC Method
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Stress Degradation Studies on Flupirtine Maleate Using Stability-Indicating RP-HPLC Method

机译:稳定性指示RP-HPLC法研究马来酸氟吡汀的应力降解

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With the objective of developing an advanced method for rapid separation with shorter runtime, a simple, precise, and accurate stability-indicating isocratic RP-LC method coupled with PDA detector was developed for the quantitative determination of flupirtine maleate in bulk and in capsule dosage form. Good resolution between the peaks for degradation products and the analyte was achieved on a Waters Agilent XDB C18(150×4.6 mm, 5 μm) column using mobile phase containing a mixture of phosphate buffer pH 3.36 and acetonitrile in the ratio of 65 : 35. The eluted compounds were monitored at 344 nm and the flow rate employed for the present investigation was 1 mL/min. The newly developed method was validated as per ICH guidelines with respect to specificity, linearity, limit of detection, limit of quantification, accuracy, precision, and robustness. The method may be employed for the assay determination of flupirtine maleate in pharmaceutical dosage forms.
机译:为了开发一种先进的快速分离方法,更短的运行时间,开发了一种简单,精确,准确的,指示稳定性的等度RP-LC方法和PDA检测器,用于定量测定散装和胶囊剂型马来酸氟吡汀。在Waters Agilent XDB C18(150×4.6 mm,5μm)色谱柱上,使用流动相包含pH = 3.36的磷酸盐缓冲液和乙腈比例为65:35的乙腈的混合物,可以实现降解产物峰与分析物之间的良好分离度。在344 compoundsnm处监测洗脱的化合物,本研究采用的流速为1 mL / min。新开发的方法已根据ICH指南验证了特异性,线性,检测限,定量限,准确性,精密度和鲁棒性。该方法可以用于测定药物剂型中的马来酸氟吡汀的含量。

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