Ionspray ionization mass spectrometric separation and determination of heptafluorobutyryl derivatives of polyamines

Citation
N. Furuumi et al., Ionspray ionization mass spectrometric separation and determination of heptafluorobutyryl derivatives of polyamines, ANALYT BIOC, 265(2), 1998, pp. 253-259
Citations number
20
Categorie Soggetti
Biochemistry & Biophysics
Journal title
ANALYTICAL BIOCHEMISTRY
ISSN journal
00032697 → ACNP
Volume
265
Issue
2
Year of publication
1998
Pages
253 - 259
Database
ISI
SICI code
0003-2697(199812)265:2<253:IIMSSA>2.0.ZU;2-C
Abstract
We describe here an application of ionspray ionization-mass spectrometry (I S-MS) for simultaneous determination of putrescine, spermidine, and spermin e without the need for coupling with other separation techniques such as hi gh-performance liquid chromatography or capillary electrophoresis. Because it was essential to increase the mass of these compounds to eliminate conta minated low-mass ions, heptafluorobutyryl (HFB) derivatives were chosen. It was found that each HFB-polyamine appeared as a single major cation carryi ng an ammonium ion in a solution of 50% acetonitrile-water containing 0.5% ammonium acetate at an orifice potential of 20 V. Under these conditions, t he three polyamines after addition of N-15-labeled polyamines as internal s tandards, followed by heptafluorobutylation, were determined simultaneously . It was shown, using a sample injection bulb set between the syringe drive and ionspray probe, that the analysis time for data acquisition was about 3 min and the sensitivity was about 10 fmol. In addition, polyamines in rat liver were determined by this method after simple fractionation with a sma ll column of CM-cellulose with reasonable accuracy and precision. Behaviors of acetylated polyamines were also described, and the results showed that the acetylated polyamines would become additional target compounds in the p resent method. (C) 1998 Academic Press.