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A high-performance liquid chromatography method with pre-column derivatization for the simultaneous determination of reduced glutathione, carnosine and taurine

机译:柱前衍生高效液相色谱法同时测定还原型谷胱甘肽,肌肽和牛磺酸

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A new gradient reversed-phase HPLC method with pre-column derivatization was developed and validated for simultaneous determination of reduced glutathione, carnosine and taurine in new pharmaceutical eye drops. Chromatographic separation was achieved with a fused core analytical column Supelco Ascentis Express C18 (100 mm ?— 4.6 mm, 2.7 ??m). A 30 mM triethylamine in acetonitrile with 30 mM triethylamine aqueous solution (pH 2.5, adjusted with glacial acetic acid) was used in a gradient elution mode at a flow rate of 0.8 mL mina?’1. The column temperature was maintained at 30 ?°C, the injection volume of the derivatized sample was 5 ??L and the detection wavelength was 375 nm. The tested validation parameters included system suitability, accuracy, precision, linearity, LOD, LOQ and sample solution stability. The standard calibration curves showed good linearity with correlation coefficients r 0.997 for all compounds. The mean percentage recoveries obtained for reduced glutathione, carnosine and taurine were 99.61, 99.38 and 99.43%, respectively. Precision was 2% for retention times and peak areas. The applicability of this method was demonstrated by the analysis of a multicomponent eye drop formulation containing reduced glutathione, carnosine and taurine.
机译:开发了一种新的具有柱前衍生化的梯度反相HPLC方法,并经过验证,可同时测定新型药用滴眼液中还原型谷胱甘肽,肌肽和牛磺酸的含量。用熔融核芯分析柱Supelco Ascentis Express C18(100 mmφ-4.6 mm,2.7φm)进行色谱分离。将乙腈中的30 mM三乙胺与30 mM三乙胺水溶液(pH 2.5,用冰醋酸调节)的梯度洗脱模式使用,流速为0.8 mL min-1。柱温保持在30℃,衍生样品的进样量为5ΔL,检测波长为375 nm。测试的验证参数包括系统适用性,准确性,精度,线性,LOD,LOQ和样品溶液稳定性。对于所有化合物,标准校准曲线均显示出良好的线性,相关系数r> 0.997。还原型谷胱甘肽,肌肽和牛磺酸的平均回收率分别为99.61%,99.38%和99.43%。保留时间和峰面积的精密度<2%。该方法的适用性通过分析含有还原型谷胱甘肽,肌肽和牛磺酸的多组分滴眼剂制剂得到了证明。

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