首页> 外文期刊>Journal of food and drug analysis >An ecofriendly green liquid chromatographic method for simultaneous determination of nicotinamide and clindamycin phosphate in pharmaceutical gel for acne treatment
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An ecofriendly green liquid chromatographic method for simultaneous determination of nicotinamide and clindamycin phosphate in pharmaceutical gel for acne treatment

机译:同时测定痤疮药物凝胶中烟酰胺和磷酸克林霉素的绿色环保液相色谱方法

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Abstract A new green micellar liquid chromatographic method was developed and validated for the quantitative estimation of nicotinamide (NICO) and clindamycin phosphate (CLD) in bulk and pharmaceutical gel formulation. The analytes are well resolved in less than 6.0 minutes using micellar mobile phase consisting of 0.10M sodium dodecyl sulfate (SDS), 0.3% triethylamine, and 10% 2-propanol in 0.02M orthophosphoric acid at pH 3.0, running through an Eclipse XDB-C8 column (150?mm × 4.6?mm, 5?μm particle size) with flow rate 1.0?mL/min. The effluent was monitored with diode array detection at 210?nm. The retention times of {NICO} and {CLD} were 3.8 minutes and 5.6 minutes, respectively. The method was validated according to the International Conference on Harmonisation (ICH) guidelines in terms of linearity, limit of detection, limit of quantification, accuracy, precision, robustness, and specificity to prove its reliability. Linear correlation was achieved by plotting the peak area of each drug against its concentration. It was found to be rectilinear in the ranges of 1.0–40.0?μg/mL and 0.5–15.0?μg/mL with limits of detection of 0.06?μg/mL and 0.03?μg/mL and limits of quantification of 0.19?μg/mL and 0.09?μg/mL for {NICO} and CLD, respectively. The method was successfully implemented for the simultaneous determination of the analytes in their bulk powder and combined gel formulation with high % recoveries. The ease of sample treatment facilitates and greatly expedites the treatment with reduced cost and improved accuracy of the procedure.
机译:摘要提出了一种新的绿色胶束液相色谱方法,并已用于定量测定批量和药物凝胶制剂中的烟酰胺(NICO)和磷酸克林霉素(CLD)的定量。使用胶束流动相,在Eclipse XDB-X上运行,胶束流动相由0.02M正磷酸中的0.10M十二烷基硫酸钠(SDS),0.3%三乙胺和10%2-丙醇在0.02M正磷酸中组成,在不到6.0分钟的时间内即可完成分离。 C8色谱柱(150?mm×4.6?mm,粒径5?μm),流速1.0?mL / min。用二极管阵列检测器在210?nm处监测废水。 {NICO}和{CLD}的保留时间分别为3.8分钟和5.6分钟。该方法已根据国际协调会议(ICH)指南在线性,检测限,定量限,准确性,精密度,鲁棒性和特异性方面进行了验证,以证明其可靠性。通过将每种药物的峰面积相对于其浓度作图来实现线性相关。发现在1.0–40.0?μg/ mL和0.5–15.0?μg/ mL范围内是直线的,检出限为0.06?μg/ mL和0.03?μg/ mL,定量限为0.19?μg/ mL {NICO}和CLD分别为mL和0.09?g / mL。该方法已成功用于同时测定散装粉末中的分析物和回收率高的组合凝胶制剂。样品处理的简便性以降低的成本和提高的程序准确性促进并大大加快了处理速度。

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