Pilařová Veronika, Gottvald Tomáš, Svoboda Pavel, Novák Ondřej, Benešová Karolína, Běláková Sylvie, Nováková Lucie
Department of Analytical Chemistry, Faculty of Pharmacy, Charles University in Prague, Heyrovského 1203, 500 05, Hradec Králové, Czech Republic.
Laboratory of Growth Regulators, Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany CAS & Faculty of Science of Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic.
Anal Chim Acta. 2016 Aug 31;934:252-65. doi: 10.1016/j.aca.2016.06.008. Epub 2016 Jun 9.
The goal of this study was to develop an effective supercritical fluid chromatography method using single quadrupole MS for analysis of all isomeric forms of vitamin E. Finally, two fast and effective methods, the high resolution one and the high speed one, for the determination of 8 vitamin E isomers in human serum were developed. Rapid high-throughput liquid-liquid extraction was selected as a sample preparation step. Sample pretreatment of 100 μL human serum was consisted of protein precipitation with 200 μL ethanol and liquid-liquid extraction by 400 μL hexane/dichloromethane (80/20, v/v). The separation was performed on BEH 2-EP (3.0 × 100 mm, 1.7 μm) stationary phase, using isocratic elution with carbon dioxide and 10 mM ammonium formate in methanol in the ratio 98:2 for high resolution method with run time 4.5 min and in the ratio 95:5 for high speed method, where the run time was 2.5 min. The method development included optimization of key parameters: the choice of the suitable stationary phase and the composition of mobile phase, where an influence of various modifiers, their ratio and additives were tested, and optimization of fine tunning parameters including BPR pressure, flow-rate and column temperature. Quantification of all isomeric forms was performed using SIM (single ion monitoring) experiments in ESI positive ion mode. Both high speed and high resolution chromatographic methods were validated in terms of precision, accuracy, range, linearity, LOD, LOQ and matrix effects using the same LLE procedure. The high resolution method provided more sensitive results (LOD: 0.017-0.083 μg mL(-1)) and better linearity (r(2) > 0.9930) than the high speed one (LOD: 0.083-0.25 μg mL(-1), r(2) > 0.9877) at the cost of double time of analysis.
本研究的目标是开发一种使用单四极杆质谱的高效超临界流体色谱法,用于分析维生素E的所有异构体形式。最终,开发了两种快速有效的方法,即高分辨率法和高速法,用于测定人血清中的8种维生素E异构体。选择快速高通量液液萃取作为样品制备步骤。100μL人血清的样品预处理包括用200μL乙醇进行蛋白质沉淀,以及用400μL己烷/二氯甲烷(80/20,v/v)进行液液萃取。分离在BEH 2-EP(3.0×100mm,1.7μm)固定相上进行,高分辨率法采用等度洗脱,二氧化碳与10mM甲酸铵在甲醇中的比例为98:2,运行时间为4.5分钟;高速法的比例为95:5,运行时间为2.5分钟。方法开发包括关键参数的优化:合适固定相的选择和流动相的组成,测试了各种改性剂、它们的比例和添加剂的影响,以及微调参数的优化,包括背压调节器压力、流速和柱温。使用ESI正离子模式下的SIM(单离子监测)实验对所有异构体形式进行定量。高速和高分辨率色谱方法均使用相同的液液萃取程序在精密度、准确度、范围、线性、检测限、定量限和基质效应方面进行了验证。高分辨率方法提供了比高速方法更灵敏的结果(检测限:0.017 - 0.083μg mL⁻¹)和更好的线性(r² > 0.9930),但分析时间加倍。