Capillary ultrahigh-pressure liquid chromatography-mass spectrometry for fast and high resolution metabolomics separations

被引:16
|
作者
Sorensen, Matthew J. [1 ]
Kennedy, Robert T. [1 ,2 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
ultrahigh-pressure liquid chromatography; mass spectrometry; metabolomics; peak capacity; sub-2 micron particles; PEAK-CAPACITY; SLURRY CONCENTRATION; HIGH-EFFICIENCY; MICRODIALYSIS SAMPLES; RPLC SEPARATIONS; SLIP-FLOW; UPLC-MS; PARTICLES; COLUMNS; PERFORMANCE;
D O I
10.1016/j.chroma.2020.461706
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
LC-MS is an important tool for metabolomics due its high sensitivity and broad metabolite coverage. The goal of improving resolution and decreasing analysis time in HPLC has led to the use of 5 - 15 cm long columns packed with 1.7 - 1.9 mu m particles requiring pressures of 8 - 12 kpsi. We report on the potential for capillary LC-MS based metabolomics utilizing porous C18 particles down to 1.1 mu m diameter and columns up to 50 cm long with an operating pressure of 35 kpsi. Our experiments show that it is possible to pack columns with 1.1 mu m porous particles to provide predicted improvements in separation time and efficiency. Using kinetic plots to guide the choice of column length and particle size, we packed 50 cm long columns with 1.7 mu m particles and 20 cm long columns with 1.1 mu m particles, which should produce equivalent performance in shorter times. Columns were tested by performing isocratic and gradient LC-MS analyses of small molecule metabolites and extracts from plasma. These columns provided approximately 100,000 theoretical plates for metabolite standards and peak capacities over 500 in 100 min for a complex plasma extract with robust interfacing to MS. To generate a given peak capacity, the 1.1 mu m particles in 20 cm columns required roughly 75% of the time as 1.7 mu m particles in 50 cm columns with both operated at 35 kpsi. The 1.1 mu m particle packed columns generated a given peak capacity nearly 3 times faster than 1.7 mu m particles in 15 cm columns operated at similar to 10 kpsi. This latter condition represents commercial state of the art for capillary LC. To consider practical benefits for metabolomics, the effect of different LC-MS variables on mass spectral feature detection was evaluated. Lower flow rates (down to 700 nL/min) and larger injection volumes (up to 1 mu L) increased the features detected with modest loss in separation performance. The results demonstrate the potential for fast and high resolution separations for metabolomics using 1.1 mu m particles operated at 35 kpsi for capillary LC-MS. (C) 2020 Elsevier B.V. All rights reserved.
引用
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页数:10
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