首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >DEVELOPMENT AND VALIDATION OF HPLC METHOD FOR SOME AZOLES IN PHARMACEUTICAL PREPARATION
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DEVELOPMENT AND VALIDATION OF HPLC METHOD FOR SOME AZOLES IN PHARMACEUTICAL PREPARATION

机译:药学制备中某些偶氮化合物HPLC方法的建立与验证。

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A new, simple and rapid reversed-phase high-performance liquid chromatography (HPLC) method was developed and validated for the determination of some azoles drug (Ketoconazole, Isoconazole and Miconazole) in pharmaceutical dosage forms in Jordan market. The HPLC separation was achieved on a C18?BDS column (100?mm?×?4.6?mm) using a mobile phase of acetonitrile and 0.05 M Ammonium Acetate buffer (70:30,?v/v) that adjusted to pH 6 using phosphoric acid at a flow rate of 1?mL?min?1 and using UV absorbance detection at 254?nm. The method was validated for specificity, linearity, precision, accuracy, robustness. The separation was completed within 11.77 minutes and the assay was linear over the concentration range of 50% to 150%?(r2?=?0.9999), the percent recovery for test and reference formulation was (98.14%-101.12%).
机译:开发了一种新颖,简单,快速的反相高效液相色谱(HPLC)方法,并已验证该方法可用于测定约旦市场中药物剂型中的某些唑类药物(酮康唑,异康唑和咪康唑)。使用乙腈和0.05 M乙酸铵缓冲液(70:30,?v / v)在C 18? BDS色谱柱(100?mm××4.6?mm)上进行HPLC分离。 v)用磷酸以1?mL?min ?1 的流速和254?nm的紫外吸收检测将pH调节至6。验证了该方法的特异性,线性,精密度,准确性,鲁棒性。分离在11.77分钟内完成,并且在50%至150%?(r 2 ?=?0.9999)的浓度范围内呈线性分析,测试和参考配方为(98.14%-101.12%)。

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