de Jager Lowri S, Perfetti Gracia A, Diachenko Gregory W
U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, 5100 Paint Branch Pkwy, College Park, MD 20740, USA.
J AOAC Int. 2004 Sep-Oct;87(5):1042-8.
A method was developed for determination of St. John's wort marker compounds hypericin, pseudohypericin, hyperforin, and adhyperforin in functional foods. Solid-phase extraction provided analyte extraction and significant sample cleanup prior to analysis using liquid chromatography (LC) with UV and fluorescence detection. In addition to quantification using LC-UV, confirmation was made with electrospray ionization LC mass spectrometry (LC/MS). Several commercially available tea and drink products claiming to contain St. John's wort were tested. Recoveries ranged from 51 to 98% for the liquid samples. Comparison of the concentrations in 4 St. John's wort teas showed a variation in analyte concentration (1044-10 ng/mL marker compounds in brewed tea) and composition. No marker compounds were found in the beverages, indicating possible decomposition of the marker compounds caused by low pH and/or exposure to light. A solvent extraction procedure was developed for analysis of the marker compounds from solid samples. Analytes were detected at low parts per million, with an average recovery of 75%. No St. John's wort components were found in the 2 solid functional food samples analyzed.
开发了一种用于测定功能性食品中圣约翰草标记化合物金丝桃素、假金丝桃素、贯叶连翘素和去甲贯叶连翘素的方法。在使用液相色谱(LC)和紫外及荧光检测进行分析之前,固相萃取可实现分析物的萃取和显著的样品净化。除了使用LC-UV进行定量分析外,还通过电喷雾电离LC质谱(LC/MS)进行确证。对几种声称含有圣约翰草的市售茶和饮品进行了检测。液体样品的回收率在51%至98%之间。对4种圣约翰草茶中的浓度进行比较,结果显示分析物浓度(冲泡茶中标记化合物的浓度为1044 - 10 ng/mL)和成分存在差异。在饮品中未发现标记化合物,这表明标记化合物可能因低pH值和/或光照而分解。开发了一种溶剂萃取程序用于分析固体样品中的标记化合物。分析物的检测限为百万分之几,平均回收率为75%。在所分析的2个固体功能性食品样品中未发现圣约翰草成分。