Liu Yue, Hu Jia, Li Yan, Li Xiao-Shuang, Wang Zhong-Liang
Key Laboratory of Inorganic-Organic Hybrid Functional Materials Chemistry (Tianjin Normal University), Ministry of Education, Tianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin, P. R. China.
State Power Economic Research Institute, Beijing, China.
Electrophoresis. 2016 Oct;37(19):2478-2486. doi: 10.1002/elps.201600118. Epub 2016 Aug 15.
A novel method with high sensitivity for the rapid determination of chrysin, apigenin and luteolin in environment water samples was developed by double-pumps controlled on-line solid-phase extraction (SPE) coupled with high-performance liquid chromatography (HPLC). In the developed technique, metal organic framework MIL-101 was synthesized and applied as a sorbent for SPE. The as-synthesized MIL-101 was characterized by scanning electron microscope, X-ray diffraction spectrometry, thermal gravimetric analysis and micropore physisorption analysis. The MIL-101 behaved as a fast kinetics in the adsorption of chrysin, apigenin and luteolin. On-line SPE of chrysin, apigenin and luteolin was processed by loading a sample solution at a flow rate of 1.0 mL/min for 10 min. The extracted analytes were subsequently eluted into a ZORBAX Bonus-RP analytical column (25 cm long × 4.6 mm i.d.) for HPLC separation under isocratic condition with a mobile phase (MeOH: ACN: 0.02 M H PO = 35:35:30) at a flow rate of 1.0 mL/min. Experimental conditions, including ionic strength, sample pH, sample loading rates, sample loading time and desorption analytes time, were further optimized to obtain efficient preconcentration and high-precision determination of the analytes mentioned above. The method achieved the merits of simplicity, rapidity, sensitivity, wide linear range and high sample throughput. The possible mechanism for the adsorption of flavonoids on MIL-101 was proposed. The developed method has been applied to determine trace chrysin, apigenin and luteolin in a variety of environmental water samples.
建立了一种高灵敏度的新方法,用于快速测定环境水样中的白杨素、芹菜素和木犀草素,该方法采用双泵控制在线固相萃取(SPE)与高效液相色谱(HPLC)联用。在所开发的技术中,合成了金属有机框架MIL-101并将其用作SPE的吸附剂。通过扫描电子显微镜、X射线衍射光谱、热重分析和微孔物理吸附分析对合成的MIL-101进行了表征。MIL-101在白杨素、芹菜素和木犀草素的吸附中表现出快速动力学。以1.0 mL/min的流速加载样品溶液10 min,对白杨素、芹菜素和木犀草素进行在线SPE。随后将萃取的分析物洗脱到ZORBAX Bonus-RP分析柱(25 cm长×4.6 mm内径)中,在等度条件下,以1.0 mL/min的流速用流动相(甲醇:乙腈:0.02 M H₃PO₄ = 35:35:30)进行HPLC分离。进一步优化了包括离子强度、样品pH值、样品加载速率、样品加载时间和解吸分析物时间在内的实验条件,以实现上述分析物的高效预浓缩和高精度测定。该方法具有简便、快速、灵敏、线性范围宽和样品通量高的优点。提出了黄酮类化合物在MIL-101上的吸附可能机制。所开发的方法已应用于测定各种环境水样中的痕量白杨素、芹菜素和木犀草素。