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首页> 外文期刊>American Journal of PharmTech Research >Simultaneous Estimation of Gentamicin and Clobetasol in Bulk and Pharmaceutical Formulations by RP-HPLC Method
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Simultaneous Estimation of Gentamicin and Clobetasol in Bulk and Pharmaceutical Formulations by RP-HPLC Method

机译:RP-HPLC法同时估算散装和药物制剂中庆大霉素和氯倍他索的含量

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ABSTRACT A new simple, precise, accurate and reproducible RP-HPLC method for simultaneous estimation of gentamicin and clobetasol in bulk and pharmaceutical formulations. Separation of gentamicin and clobetasol was successfully achieved on a Zorbax C18 (150 mm x 4.6mm x 5µ ) in an isocratic mode utilizing disodium hydrogen phosphate buffer and methanol (60:40 v/v) at a flow rate of 1.0 mL/min. The method was validated according to ICH guidelines for linearity, sensitivity, accuracy, precision, specificity and robustness. The response was found to be linear in the drug concentration range of 0.1-0.30 mg/mL for gentamicin and 0.05–0.15 mg/mL for clobetasol. The correlation coefficient was found to be 0.9997 for both the drugs. The LOD and LOQ for gentamicin were found to be 0.3525 µg/mL and 1.1751 µg/mL respectively. The LOD and LOQ for clobetasol were found to be 0.1938 µg/mL and 0.6460 µg/mL respectively.  The proposed method was found to be good percentage recovery for gentamicin and clobetasol, which indicates that the proposed method is highly accurate. The specificity of the method shows good correlation between retention times of standard solution with the sample solution. Therefore, the proposed method specifically determines the analyte in the sample without interference from excipients of pharmaceutical dosage forms. Keywords: RP-HPLC, gentamicin, clobetasol, pharmaceutical formulation, analysis.
机译:摘要一种新的简单,精确,准确和可重复的RP-HPLC方法,用于同时估算散装和药物制剂中的庆大霉素和氯倍他索。使用磷酸氢二钠缓冲液和甲醇(60:40 v / v)以1.0 mL / min的流速在等度模式下,在Zorbax C18(150 mm x 4.6mm x 5µ)上成功实现了庆大霉素和氯倍他索的分离。该方法已根据ICH指南验证了线性,灵敏度,准确性,精密度,特异性和鲁棒性。在庆大霉素的药物浓度范围为0.1-0.30 mg / mL,而氯倍他索的药物浓度范围为0.05–0.15 mg / mL时,发现反应是线性的。发现两种药物的相关系数均为0.9997。庆大霉素的LOD和LOQ分别为0.3525 µg / mL和1.1751 µg / mL。氯倍他索的LOD和LOQ分别为0.1938 µg / mL和0.6460 µg / mL。发现该方法对庆大霉素和氯倍他索的回收率良好,这表明该方法非常准确。该方法的特异性表明标准溶液与样品溶液的保留时间之间具有良好的相关性。因此,所提出的方法可以特异性地测定样品中的分析物,而不会受到药物剂型赋形剂的干扰。关键词:RP-HPLC庆大霉素氯倍他索药物制剂分析

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