Nielsen S E, Dragsted L O
Institute of Foodsafety and Toxicology, Danish Veterinary and Food Administration, Søborg, Denmark.
J Chromatogr B Biomed Sci Appl. 1998 Aug 25;713(2):379-86. doi: 10.1016/s0378-4347(98)00187-x.
A high-performance liquid chromatographic (HPLC) method is described for the determination of apigenin and the 4'-methylated derivative acacetin in human urine using column-switching and ultraviolet (UV) absorbance detection. Urine samples were enzymatically hydrolysed and solid-phase extracted prior to injection onto the HPLC system. Prior to elution of apigenin and the internal standard, 5,7,8-trihydroxyflavone, from the first column used for sample clean-up, the six-port valve was switched to the second column for analysis with UV detection. Detection of apigenin was precise and reproducible, with a limit of quantification of 10 ng ml(-1) urine. Detection and quantification of acacetin was linear down to 70 ng ml(-1) urine. The method has been successfully applied to determine the level of apigenin in 100 human urine samples from an intervention study with parsley.
描述了一种高效液相色谱(HPLC)方法,用于使用柱切换和紫外(UV)吸光度检测来测定人尿中的芹菜素及其4'-甲基化衍生物刺槐素。尿样在注入HPLC系统之前进行酶促水解和固相萃取。在用于样品净化的第一根柱上洗脱芹菜素和内标5,7,8-三羟基黄酮之前,将六通阀切换到第二根柱上进行紫外检测分析。芹菜素的检测精确且可重复,定量限为10 ng ml(-1)尿液。刺槐素的检测和定量在低至70 ng ml(-1)尿液时呈线性。该方法已成功应用于测定来自一项香菜干预研究的100份人尿样中芹菜素的含量。