首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Simultaneous determination of econazole nitrate, main impurities and preservatives in cream formulation by high performance liquid chromatography
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Simultaneous determination of econazole nitrate, main impurities and preservatives in cream formulation by high performance liquid chromatography

机译:高效液相色谱法同时测定乳膏剂中的硝酸益康唑,主要杂质和防腐剂

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摘要

A reversed-phase high performance liquid chromatographic (RP-HPLC) method for determination of econazole nitrate, preservatives (methylparaben and propylparaben) and its main impurities (4-chlorobenzl alcohol and alpha-(2,4-dicholorophenyl)-1H-imidazole-1-ethanol) in cream formulations, has been developed and validated. Separation was achieved on a column Bondclone (R) C18 (300 mm x 3.9 mm i.d., 10 mu m) using a gradient method with mobile phase composed of methanol and water. The flow rate was 1.4 mL min(-1), temperature of the column was 25 C and the detection was made at 220 nm. Miconazole nitrate was used as an internal standard. The total run time was less than 15 min, The analytical curves presented coefficient of correlation upper to 0.99 and detection and quantitation limits were calculated for all molecules. Excellent accuracy and precision were obtained for econazole nitrate. Recoveries varied from 97.9 to 102.3% and intra- and inter-day precisions, calculated as relative standard deviation (R.S.D), were lower than 2.2%. Specificity, robustness and assay for econazole nitrate were also determined. The method allowed the quantitative determination of econazole nitrate, its impurities and preservatives and could be applied as a stability-indicating method for econazole nitrate in cream formulations. (C) 2008 Elsevier B.V. All rights reserved.
机译:反相高效液相色谱(RP-HPLC)法测定硝酸益康唑,防腐剂(对羟基苯甲酸甲酯和对羟基苯甲酸丙酯)及其主要杂质(4-氯苯甲醇和α-(2,4-二氯苯并苯基)-1H-咪唑-已开发和验证了乳膏配方中的1-乙醇)。使用具有甲醇和水组成的流动相的梯度法,在C18柱Bondclone(R)C18(300mm x 3.9mm i.d.,10μm)上实现分离。流速为1.4 mL min(-1),柱温为25 C,检测波长为220 nm。硝酸咪康唑用作内标。总运行时间少于15分钟,分析曲线显示相关系数最高为0.99,并计算了所有分子的检测和定量限。硝酸益康唑获得了极好的准确性和精密度。回收率从97.9%到102.3%不等,按相对标准偏差(R.S.D)计算的日内和日间精度低于2.2%。还确定了硝酸益康唑的特异性,稳健性和含量。该方法可定量测定硝酸益康唑,其杂质和防腐剂,可作为乳油配方中硝酸益康唑的稳定性指示方法。 (C)2008 Elsevier B.V.保留所有权利。

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