Hu Lihong, Jhoo Jin-Woo, Ang Catharina Y W, Dinovi Michael, Mattia Antonia
U.S. Food and Drug Administration, National Center for Toxicological Research, Division of Chemistry, HFT-230, 3900 NCTR Rd, Jefferson, AR 72079, USA.
J AOAC Int. 2005 Jan-Feb;88(1):16-25.
Kava (Piper methysticum) dietary products have been sold worldwide for treatment of nervous anxiety, tension, and restlessness. Recent reports showed potential association of kava usage and liver injuries. This study was conducted to develop simple and reliable methodologies for the extraction and determination of 6 major kavalactones: (+)-methysticin, (+)-dihydromethysticin, (+)-kavain, (+)-dihydrokavain, yangonin, and desmethoxyyangonin. Ultrasonic extraction techniques and isocratic reversed-phase liquid chromatography (LC) were optimized for different types of samples, including capsules containing kava root extract or root powder, raw root material, tea bags, and snack bar. A suitable internal standard, 5,7-dihydroxyflavone, was used for LC calibration. Kavalactones were completely separated in 30 min using a Luna C18-2 column at 60 degrees C with an isocratic mobile phase consisting of 2-propanol-acetonitrile-water-acetic acid (16 + 16 + 68 + 0.1, v/v/v/v). Within-laboratory, intraday, and interday method variation (% relative standard deviation) for most samples extracted by methanol or methanol-water mixture were <5%. Lower levels of kavalactone contents and higher variations were observed for tea bags from water extraction or infusion as compared to methanol extraction. Labeling information of tea bags based on methanol extraction could be misleading to consumers. Analytical recoveries of snack bar fortified at 10 and 20 microg/g were >84% with RSD values <8%. Methods developed in this study offer a simple and reproducible means for analysis of kavalactones in various matrixes of dietary products.
卡瓦(胡椒科植物卡瓦胡椒)膳食产品在全球范围内销售,用于治疗神经焦虑、紧张和烦躁不安。最近的报告显示,使用卡瓦可能与肝损伤有关。本研究旨在开发简单可靠的方法,用于提取和测定6种主要的卡瓦内酯:(+)-醉椒素、(+)-二氢醉椒素、(+)-卡瓦因、(+)-二氢卡瓦因、杨戈宁和去甲氧基杨戈宁。针对不同类型的样品,包括含有卡瓦根提取物或根粉的胶囊、生原料、茶包和能量棒,对超声提取技术和等度反相液相色谱(LC)进行了优化。使用合适的内标物5,7-二羟基黄酮进行LC校准。使用Luna C18-2色谱柱,在60℃下,采用由异丙醇-乙腈-水-乙酸(16 + 16 + 68 + 0.1,v/v/v/v)组成的等度流动相,30分钟内可完全分离卡瓦内酯。在实验室内部,大多数用甲醇或甲醇-水混合物提取的样品的日内和日间方法变异(相对标准偏差%)<5%。与甲醇提取相比,水提取或冲泡的茶包中卡瓦内酯含量较低且变异较大。基于甲醇提取的茶包标签信息可能会误导消费者。在10和20μg/g加标的能量棒的分析回收率>84%,相对标准偏差值<8%。本研究中开发的方法为分析膳食产品各种基质中的卡瓦内酯提供了一种简单且可重复的手段。