Comparison of peak shape in hydrophilic interaction chromatography using acidic salt buffers and simple acid solutions

被引:51
|
作者
Heaton, James C. [1 ]
Russell, Joseph J. [1 ]
Underwood, Tim [2 ]
Boughtflower, Robert [2 ]
McCalley, David V. [1 ]
机构
[1] Univ W England, Ctr Res Biosci, Bristol BS16 1QY, Avon, England
[2] GlaxoSmithKline, Analyt Chem, Stevenage, Herts, England
基金
英国工程与自然科学研究理事会;
关键词
HILIC; Buffers; Column efficiency; Hydride phases; INTERACTION LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; STATIONARY PHASES; ACETONITRILE/WATER MIXTURES; SILICA COLUMNS; PERFORMANCE; SELECTIVITY; SEPARATION; IONIZATION; RETENTION;
D O I
10.1016/j.chroma.2014.04.026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The retention and peak shape of neutral, basic and acidic solutes was studied on hydrophilic interaction chromatography (HILIC) stationary phases that showed both strong and weak ionic retention characteristics, using aqueous acetonitrile mobile phases containing either formic acid (FA), ammonium formate (AF) or phosphoric acid (PA). The effect of organic solvent concentration on the results was also studied. Peak shape was good for neutrals under most mobile phase conditions. However, peak shapes for ionised solutes, particularly for basic compounds, were considerably worse in FA than AF. Even neutral compounds showed deterioration in performance with FA when the mobile phase water concentration was reduced. The poor performance in FA cannot be entirely attributed to the negative impact of ionic retention on ionised silanols on the underlying silica base materials, as results using PA at lower pH (where their ionisation is suppressed) were inferior to those in AF. Besides the moderating influence of the salt cation on ionic retention, it is likely that salt buffers improve peak shape due to the increased ionic strength of the mobile phase and its impact on the formation of the water layer on the column surface. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
相关论文
共 35 条
  • [21] Qualitative and quantitative comparison of cyclic phosphatidic acid and its related lipid species in rat serum using hydrophilic interaction liquid chromatography with tandem-mass spectrometry
    Fukasawa, Keiko
    Nakajima, Shingo
    Gotoh, Mari
    Tanaka, Seiya
    Murofushi, Hiromu
    Murakami-Murofushi, Kimiko
    JOURNAL OF CHROMATOGRAPHY A, 2018, 1567 : 177 - 184
  • [22] Determination of Ascorbic Acid, Total Ascorbic Acid, and Dehydroascorbic Acid in Bee Pollen Using Hydrophilic Interaction Liquid Chromatography-Ultraviolet Detection
    Zhu, Meifei
    Tang, Jian
    Tu, Xijuan
    Chen, Wenbin
    MOLECULES, 2020, 25 (23):
  • [23] Accurate and efficient amino acid analysis for protein quantification using hydrophilic interaction chromatography coupled tandem mass spectrometry
    Shrikaar Kambhampati
    Jia Li
    Bradley S. Evans
    Doug K. Allen
    Plant Methods, 15
  • [24] Development of Ultra-Performance Liquid Chromatography Method Using Hydrophilic Interaction Liquid Chromatography for Quantification of Azetidine-2-Carboxylic Acid in Rhizomes of Polygonatum sibiricum F. Delaroche
    Kim, Hyo Seon
    Lee, A. Yeong
    Choi, Goya
    Kang, Young Min
    Kim, Ho Kyoung
    JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2015, 38 (16) : 1515 - 1520
  • [25] On-line comprehensive two-dimensional separations of charged compounds using reversed-phase high performance liquid chromatography and hydrophilic interaction chromatography. Part I: Orthogonality and practical peak capacity considerations
    D'Attoma, Amelie
    Grivel, Candice
    Heinisch, Sabine
    JOURNAL OF CHROMATOGRAPHY A, 2012, 1262 : 148 - 159
  • [26] Analysis of 2-oxothiazolidine-4-carboxylic acid by hydrophilic interaction liquid chromatography: application for ocular delivery using chitosan nanoparticles
    Al-Kinani, Ali Athab
    Naughton, Declan P.
    Calabrese, Gianpiero
    Vangala, Anil
    Smith, James R.
    Pierscionek, Barbara K.
    Alany, Raid G.
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2015, 407 (09) : 2645 - 2650
  • [27] Analysis of 2-oxothiazolidine-4-carboxylic acid by hydrophilic interaction liquid chromatography: application for ocular delivery using chitosan nanoparticles
    Ali Athab Al-Kinani
    Declan P. Naughton
    Gianpiero Calabrese
    Anil Vangala
    James R. Smith
    Barbara K. Pierscionek
    Raid G. Alany
    Analytical and Bioanalytical Chemistry, 2015, 407 : 2645 - 2650
  • [28] Poly(acrylamide-co-N,N′-methylenebisacrylamide) Monoliths for High-Peak-Capacity Hydrophilic-Interaction Chromatography-High-Resolution Mass Spectrometry of Intact Proteins at Low Trifluoroacetic Acid Content
    Passamonti, Marta
    de Roos, Chiem
    Schoenmakers, Peter J.
    Gargano, Andrea F. G.
    ANALYTICAL CHEMISTRY, 2021, 93 (48) : 16000 - 16007
  • [29] Sensitive Analysis of Sialic Acid and Related Compound by Hydrophilic Interaction Liquid Chromatography Using Fluorescence Detection after Derivatization with DBD-PZ
    Kawasaki, Akane
    Yasuda, Makoto
    Mawatari, Ken-ichi
    Fukuuchi, Tomoko
    Yamaoka, Noriko
    Kaneko, Kiyoko
    Iijima, Ryosuke
    Yui, Satoru
    Satoh, Motonobu
    Nakagomi, Kazuya
    ANALYTICAL SCIENCES, 2018, 34 (07) : 841 - 844
  • [30] Sensitive Analysis of Sialic Acid and Related Compound by Hydrophilic Interaction Liquid Chromatography Using Fluorescence Detection after Derivatization with DBD-PZ
    Akane Kawasaki
    Makoto Yasuda
    Ken-Ichi Mawatari
    Tomoko Fukuuchi
    Noriko Yamaoka
    Kiyoko Kaneko
    Ryosuke Iijima
    Satoru Yui
    Motonobu Satoh
    Kazuya Nakagomi
    Analytical Sciences, 2018, 34 : 841 - 844