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首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Reverse Phase High Performance Liquid Chromatography for the Quantification of Eurycomanone in Eurycoma longifolia Jack (Simaroubaceae) Extracts and their Commercial Products
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Reverse Phase High Performance Liquid Chromatography for the Quantification of Eurycomanone in Eurycoma longifolia Jack (Simaroubaceae) Extracts and their Commercial Products

机译:反相高效液相色谱法定量长叶杜仲提取物及其商品中的杜仲酮

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Purpose: To develop a reverse phase high performance liquid chromatography (HPLC) method for the determination of eurycomanone in E. longifolia Jack (Simaroubaceae) aqueous root extract and their commercial products. Methods: Analysis was carried out using reverse phase HPLC at 254 nm and a gradient mobile phase that comprised of acetonitrile and 0.1 % formic acid. Flow rate was 1 ml/min and separation was done using Phenomenex, Luna C18 column (150 mm x 4.6 mm, 5 μm). Validation tests were performed in order to demonstrate the linearity, precision, accuracy, limit of detection (LOD) and limit of quantification (LOQ) of the method. Results: Linearity was in the range 0.1 – 50.0 μg/ml ( R2 = 0.9999). Precision, as relative standard deviation of retention time and peak area of reference compound was E. longifolia extracts and commercial products was 0.89 – 3.28, and 0.07 – 0.16 %, respectively. Analysis of the ethanol extract and chloroform sub-extract showed high resolution of > 10 peaks, which indicate the suitability of the method for the analysis of extracts prepared in organic solvents as well. Conclusion: The proposed method shows good linearity, precision, accuracy and high sensitivity. The method can be applied in the routine quantification of eurycomanone for quality control of E. longifolia extracts and commercial products.
机译:目的:建立一种反相高效液相色谱法(HPLC),用于测定长叶艾草(E. longifolia Jack)(Simaroubaceae)水根提取物及其市售产品中的杜仲酮。方法:使用反相HPLC在254 nm和由乙腈和0.1%甲酸组成的梯度流动相中进行分析。流速为1 ml / min,并使用Phenomenex Luna C18色谱柱(150 mm x 4.6 mm,5μm)进行分离。进行验证测试以证明该方法的线性,精密度,准确度,检测限(LOD)和定量限(LOQ)。结果:线性度在0.1 – 50.0μg/ ml的范围内(R 2 = 0.9999)。精密度,因为保留时间和参比化合物的峰面积的相对标准偏差为长叶提取物和商业产品分别为0.89 – 3.28和0.07 – 0.16%。乙醇提取物和氯仿提取物的​​分析显示> 10个峰的高分辨率,这表明该方法也适用于分析在有机溶剂中制备的提取物。结论:该方法具有良好的线性度,精密度,准确性和高灵敏度。该方法可用于常规定量的杜仲酮,以控制长叶E提取物和市售产品的质量。

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