Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China; Laboratory for the Analysis of Medicines, Department of Pharmaceutical Sciences, CIRM, University of Liege, Avenue Hippocrate 15, 4000 Liege, Belgium.
J Pharm Biomed Anal. 2018 Aug 5;157:217-225. doi: 10.1016/j.jpba.2018.05.025. Epub 2018 May 18.
Phenolic acids represent one third of the total phenolic compounds in extra virgin olive oil (EVOO) and contribute greatly to the biological and sensory properties of EVOO. In the present research, an analytical method based on supercritical fluid chromatography coupled with single quadrupole mass spectrometry (SFC-MS) was developed for the analysis of phenolic acids in EVOOs. The chromatographic and MS conditions were optimized in terms of selectivity, peak shape and sensitivity. Satisfactory separation of 12 phenolic acids was achieved within 20 min on a Platisil CN column (250 mm × 4.6 mm, 5 μm) using 7% (v/v) water and 0.5% (v/v) formic acid in MeOH as mobile phase additives at the backpressure of 140 bar and temperature of 60 °C. The developed method was validated by evaluating the linearity, sensitivity, repeatability, intermediate precision and accuracy. The limits of detection (LODs) and limits of quantification (LOQs) of the SFC-MS method for phenolic acids ranged from 0.03 to 5.00 μg/mL and 0.08 to 15.0 μg/mL, respectively. The relative standard deviations (RSDs) for intraday and interday precision were lower than 9.91% and the recoveries ranged from 80.2 to 117% and 80.9 to 118% for low-level and high-level concentrations of standards spiked in olive oil, respectively. Compared to an HPLC method, the SFC method was about three times faster and provided better selectivity. Finally, the SFC-MS method was successfully employed for the quantitative analysis of phenolic acids in EVOOs. Differences in individual and total phenolic acid contents were observed between six varieties.
酚酸是特级初榨橄榄油(EVOO)中总酚类化合物的三分之一,对 EVOO 的生物和感官特性有很大贡献。本研究建立了一种基于超临界流体色谱-单四极杆质谱(SFC-MS)联用的分析方法,用于 EVOO 中酚酸的分析。从选择性、峰形和灵敏度等方面对色谱和 MS 条件进行了优化。在 Platisil CN 柱(250mm×4.6mm,5μm)上,以 7%(v/v)水和 0.5%(v/v)甲酸在 MeOH 中为流动相添加剂,在 140bar 的背压和 60°C 的温度下,可在 20min 内实现 12 种酚酸的良好分离。通过评价线性、灵敏度、重复性、中间精密度和准确度对所建立的方法进行了验证。SFC-MS 法测定酚酸的检出限(LOD)和定量限(LOQ)范围分别为 0.03-5.00μg/mL 和 0.08-15.0μg/mL。日内和日间精密度的相对标准偏差(RSD)均低于 9.91%,低浓度和高浓度标准加标橄榄油的回收率分别为 80.2-117%和 80.9-118%。与 HPLC 方法相比,SFC 方法的速度约快三倍,选择性更好。最后,成功地将 SFC-MS 法用于 EVOO 中酚酸的定量分析。六种不同品种的橄榄油中个体和总酚酸含量存在差异。