Corrigendum to "Development of a lipid profiling system using reverse-phase liquid chromatography coupled to high-resolution mass spectrometry with rapid polarity switching and an automated lipid identification software" [J. Chromatogr. A 1292, (2013) 211-218]

Please cite this article in press as: T. Yamada, et al., J. Chromatogr. A (2013), http://dx.doi.org/10.1016/j.chroma.2013.12.040 ormate (1 mol/L), and formic acid. However, in the published manuscript, we did not take into consideration the volume of water resent in the aqueous solution of ammonium formate. Please note the revised preparation for the two solvents. Solvent A should be n acetonitrile–methanol–water mixture (19:19:2.8, v/v) with 19.6 mmol/L ammonium formate and 0.02% (v/v) formic acid, and solvent should be a 2-propanol–water mixture (50:1) with 19.6 mmol/L ammonium formate and 0.02% (v/v) formic acid.