Investigating the effect of chromatographic conditions on retention of organic acids in hydrophilic interaction chromatography using a design of experiment

被引:99
作者
Guo, Y.
Srinivasan, S.
Gaiki, S.
机构
[1] Johnson & Johnson Pharmaceut Res & Dev, Analyt Dev Global ChemPharm Dev, LLC, Raritan, NJ 08869 USA
[2] MicroDose Technol, Analyt R&D, Monmouth Jct, NJ 08852 USA
关键词
hydrophilic interaction chromatography; design of experiment; organic acid;
D O I
10.1365/s10337-007-0264-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Small organic acids have shown significant retention on various stationary phases, such as amide, amino, aspartamide, silica and sulfobetaine phase commonly used in hydropkilic interaction chromatography (HILIC). This study investigated the effect of chromatographic conditions on the retention behavior of organic acids in HILIC using the tool of design of experiment (DOE). The results of the DOE study indicated that both the content of organic solvent (i.e., acetonitrile) and salt concentration in the mobile phase had significant effects on the retention of organic acids. Higher content of organic solvent in the mobile phase led to a significant increase in retention on all types of stationary phases. Increasing salt concentration also resulted in a moderate increase in retention; however, the effect of salt concentration varied with the type of stationary phase. The study also revealed that column temperature had less impact on retention than organic solvent content and salt concentration in HILIC.
引用
收藏
页码:223 / 229
页数:7
相关论文
共 26 条
[1]   HYDROPHILIC-INTERACTION CHROMATOGRAPHY FOR THE SEPARATION OF PEPTIDES, NUCLEIC-ACIDS AND OTHER POLAR COMPOUNDS [J].
ALPERT, AJ .
JOURNAL OF CHROMATOGRAPHY, 1990, 499 :177-196
[2]  
APPELBLAD P, 2005, APPL BOOK MARCH 2005, P47
[3]   Separation and quantitation of water soluble cellular metabolites by hydrophilic interaction chromatography-tandem mass spectrometry [J].
Bajad, Sunil U. ;
Lu, Wenyun ;
Kimball, Elizabeth H. ;
Yuan, Jie ;
Peterson, Celeste ;
Rabinowitz, Joshua D. .
JOURNAL OF CHROMATOGRAPHY A, 2006, 1125 (01) :76-88
[4]   A practical approach to optimization and validation of a HPLC assay for analysis of polyribosyl-ribitol phosphate in complex combination vaccines [J].
Belfast, M ;
Lu, R ;
Capen, R ;
Zhong, JL ;
Nguyen, MA ;
Gimenez, J ;
Sitrin, R ;
Mancinelli, R .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2006, 832 (02) :208-215
[5]   Investigation of the toxin profile of Greek mussels Mytilus galloprovincialis by liquid chromatography-mass spectrometry [J].
Ciminiello, P ;
Dell'Aversano, C ;
Fattorusso, E ;
Forino, M ;
Magno, S ;
Santelia, F ;
Tsoukatou, M .
TOXICON, 2006, 47 (02) :174-181
[6]   Improving method capability of a drug substance HPLC assay [J].
Dejaegher, B. ;
Jimidar, M. ;
De Smet, M. ;
Cockaerts, P. ;
Smeyers-Verbeke, J. ;
Vander Heyden, Y. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 42 (02) :155-170
[7]   Analysis of dichloroacetic acid in rat blood and tissues by hydrophilic interaction liquid chromatography with tandem mass spectrometry [J].
Delinsky, AD ;
Delinsky, DC ;
Muralidhara, S ;
Fisher, JW ;
Bruckner, JV ;
Bartlett, MG .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2005, 19 (08) :1075-1083
[8]   Hydrophilic interaction liquid chromatography-mass spectrometry for the analysis of paralytic shellfish poisoning (PSP) toxins [J].
Dell'Aversano, C ;
Hess, P ;
Quilliam, MA .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1081 (02) :190-201
[9]   MultiSimplex and experimental design as chemometric tools to optimize a SPE-HPLC-UV method for the determination of eprosartan in human plasma samples [J].
Ferreirós, N. ;
Iriarte, G. ;
Alonso, R. M. ;
Jiménez, R. M. .
TALANTA, 2006, 69 (03) :747-756
[10]   A quality evaluation strategy for multi-sourced active pharmaceutical ingredient (API) starting materials [J].
Gavin, PF ;
Olsen, BA ;
Wirth, DD ;
Lorenz, KT .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 41 (04) :1251-1259