Lin Yu-Ting, Wu Shihn-Sheng, Wu Hsin-Lung
Graduate Institute of Pharmaceutical Sciences, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
J Chromatogr A. 2007 Jul 13;1156(1-2):280-7. doi: 10.1016/j.chroma.2007.01.091. Epub 2007 Feb 1.
A simple and sensitive method is described for the quantitative analysis of important animal and plant sterols (cholesterol and sitosterol) by liquid chromatography with fluorimetric detection. The method is based on the derivatization of cholesterol and sitosterol with a fluorescent reagent (naproxen acyl chloride) in toluene. The resulting derivatives were isocratically separated on a C(8) column with a mixed solvent of methanol-isopropanol-water (90:5:5, v/v) as a mobile phase and monitored with a fluorimetric detector (excitation 231 nm and emission 352 nm). The linear range for the quantitation of cholesterol or sitosterol was 0.1-2.0 microM with a detection limit (S/N=3 with 10 microl injected) of about 25 nM. Recoveries of cholesterol spiked in milk (n=5) ranged over 99-104% with relative standard deviations (RSD) less than 6.0%. Application of the method to the analysis of cholesterol or sitosterol in milk, saliva and urine proved simple and feasible.
描述了一种通过液相色谱荧光检测法定量分析重要动植物甾醇(胆固醇和谷甾醇)的简单灵敏方法。该方法基于胆固醇和谷甾醇在甲苯中与荧光试剂(萘普生酰氯)进行衍生化反应。所得衍生物在C(8)柱上以甲醇 - 异丙醇 - 水(90:5:5,v/v)的混合溶剂作为流动相进行等度分离,并用荧光检测器监测(激发波长231nm,发射波长352nm)。胆固醇或谷甾醇定量的线性范围为0.1 - 2.0 microM,检测限(进样10微升,S/N = 3)约为25 nM。加标于牛奶中的胆固醇回收率(n = 5)在99 - 104%之间,相对标准偏差(RSD)小于6.0%。该方法应用于牛奶、唾液和尿液中胆固醇或谷甾醇的分析,证明简单可行。