Faraz Ina, Ali Arslan, Ul Haq Faraz, Tchamgoue Joseph, Kouam Simeon F, Miana Ghulam Abbas, Musharraf Syed Ghulam
HEJ Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, University Road, Karachi-75270, Sindh, Pakistan.
Department of Chemistry, Higher Teachers Training College, University of Yaoundé I, P.O. Box 47, Yaoundé, Cameroon.
J Chromatogr Sci. 2020 Jan 17;57(10):944-949. doi: 10.1093/chromsci/bmz072.
One of the major problems with the formulation of herbal medicines is the quality control of plant material to ensure its efficacy and safety. Quality control of medicinal plants requires analysis of many bioactive compounds present in the plant. C-alkylated flavonoids are an important bioactive subclass of flavonoids. A simple, rapid, sensitive and selective method is presented here for the quantification of bioactive C-alkylated flavonoids. This is the first quantitative method for analysis of C-alkylated flavonoids based on the multiple reaction monitoring (MRM) approach so far. This study focuses on method development for quantification of bioactive C-alkylated flavonoids. Quantification of a total of five C-alkylated flavonoids was done employing the MRM approach on an HPLC-QqQ-MS instrument. LODs and LOQs for quantified flavonoids were in the range of 0.41-1.32 and 1.23-3.96 ng/mL, respectively. Linear calibration curves between 25 and 1500 ng/mL were obtained with the regression coefficients of ≥0.996. Accuracy (% bias) and precision (% RSD) of the analyses were found to be less than 5%. Developed HPLC-ESI-MS/MS can be employed as a quality control method of plant raw materials.
草药配方的主要问题之一是植物材料的质量控制,以确保其有效性和安全性。药用植物的质量控制需要分析植物中存在的许多生物活性化合物。C - 烷基化黄酮类化合物是黄酮类化合物的一个重要生物活性亚类。本文提出了一种简单、快速、灵敏且选择性好的方法,用于定量生物活性C - 烷基化黄酮类化合物。这是迄今为止基于多反应监测(MRM)方法分析C - 烷基化黄酮类化合物的首个定量方法。本研究聚焦于生物活性C - 烷基化黄酮类化合物定量分析方法的开发。在HPLC - QqQ - MS仪器上采用MRM方法对总共五种C - 烷基化黄酮类化合物进行了定量分析。定量黄酮类化合物的检测限和定量限分别在0.41 - 1.32 ng/mL和1.23 - 3.96 ng/mL范围内。在25至1500 ng/mL之间获得了线性校准曲线,回归系数≥0.996。分析的准确度(偏差百分比)和精密度(相对标准偏差百分比)均小于5%。所开发的HPLC - ESI - MS/MS可作为植物原材料的质量控制方法。