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Flavonoid Profiling Analysis by Liquid Chromatography–Tandem Mass Spectrometry

机译:通过液相色谱 - 串联质谱法进行黄酮类化分析分析

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摘要

Flavonoids are secondary metabolites with antioxidant, anticancer, and anti‐inflammatory properties. However, no method has yet been reported for the simultaneous profiling analysis for flavonoids of various types. Thus, simultaneous profiling analysis of various flavonoids was performed in this study. Under optimal conditions, the developed method showed good linearity (r ≥?0.9973) in the range 25–1000?ng/μL with a limit of detection (LOD) of 0.9–12.1 pg. and a limit of quantification (LOQ) of 2.6–36.5 pg., respectively. The repeatability as a percentage of relative standard deviation (% RSD) varied from 0.5 to 5.9 (% RSD). And accuracy as a percentage of relative error (% RE) was from ?11.8 to 10.5 (% RE). The validated method was applied to a solid phase extraction fraction of Orostachys japonicus (Maxim.) A. Berger. Six flavonoids of catechin, rutin, quercitrin, quercetin, luteolin, and kaempferol were positively identified and quantified. Therefore, the present method will be useful for the monitoring and screening of flavonoids in natural products.
机译:黄酮类化合物是具有抗氧化剂,抗癌和抗炎性质的次生代谢物。然而,尚未涉及同时分析各种类型的类黄酮的分析分析。因此,在本研究中进行了各种黄酮的同时分析分析。在最佳条件下,开发方法显示出良好的线性度(r≥≤0.9973),其范围为25-1000μg/μl,其检测限为0.9-12.1pg。分别为2.6-36.5 pg的量化(LOQ)限制。可重复性为相对标准偏差(%RSD)的百分比范围为0.5至5.9(%RSD)。和准确性作为相对误差(%RE)的百分比来自?11.8至10.5(%RE)。将验证的方法应用于Orostachys japonicus(maxim。)A. Berger的固相提取分数。六种儿茶素,芦丁,槲皮素,槲皮素,葡萄黄素和Kaempferol六种类黄酮类化合物呈正鉴定和定量。因此,本方法将用于监测和筛选天然产物中的黄酮类化合物。

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