Studies of signal suppression in liquid chromatography-electrospray ionization mass spectrometry using volatile ion-pairing reagents

被引:150
作者
Gustavsson, SA
Samskog, J
Markides, KE
Långström, B
机构
[1] Uppsala Univ, Inst Chem, Dept Analyt Chem, SE-75121 Uppsala, Sweden
[2] Uppsala Univ, Inst Chem, Dept Organ Chem, SE-75121 Uppsala, Sweden
[3] Uppsala Univ, PET Ctr, SE-75121 Uppsala, Sweden
关键词
electrospray ionization; interfaces; LC-MS; ion-pairing reagents; amines;
D O I
10.1016/S0021-9673(01)01328-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Volatile ion-pairing reagents are useful due to their compatibility with liquid chromatography-electrospray ionization (ESI) mass spectrometry. In this study trifluoroacetic acid, heptafluorobutanoic acid and perfluoroheptanoic acid were used as ion-pairing reagents. The signal intensities of eight amine analytes were measured in the presence of these fluorinated carboxylic acids and compared with the signal intensity when using an ion-pair free formic acid-ammonium formate buffer. It was shown that the ESI signal from most of the studied analytes decreased about 30-80% when the fluorinated carboxylic, acids were added to the mobile phase at useful concentrations. The use of these acids in ion-pair chromatography was also compared to the more conventional sodium heptane sulphonate additive. It was found that the chromatographic performance was comparable. Finally, the long-term performance of the ESI interface and the chemical background caused by these fluorinated reagents were examined. No degradation of the ESI interface performance could be seen for over 24 h of continuous infusion. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:41 / 47
页数:7
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