High-throughput liquid chromatography/mass spectrometry method for the determination of the chromatographic hydrophobicity index

Citation
G. Camurri et A. Zaramella, High-throughput liquid chromatography/mass spectrometry method for the determination of the chromatographic hydrophobicity index, ANALYT CHEM, 73(15), 2001, pp. 3716-3722
Citations number
31
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYTICAL CHEMISTRY
ISSN journal
00032700 → ACNP
Volume
73
Issue
15
Year of publication
2001
Pages
3716 - 3722
Database
ISI
SICI code
0003-2700(20010801)73:15<3716:HLCSMF>2.0.ZU;2-Y
Abstract
A fast gradient reversed-phase liquid chromatography (LC) method, using an acetonitrile gradient was developed to determine the chromatographic hydrop hobicity index (CHI), as reported by Valco et al. (Anal. Chem. 1997, 69, 20 22-2029). The analytical method provides retention times, based on UV detec tion at two different wavelengths, which then are converted into CHI values after calibration with a set of test compounds. The CHI of each compound i s measured at three different pH values, 2.0, 7.4. and 10.5; so using an 8- min gradient at each pH value one compound can be analyzed in similar to 24 min. The aim of this work is to improve the throughput of the CHI screenin g using a LC/MS approach, so the application of the LC/MS technique is an e xtension of the LC/UV approach previously reported by Valco et al. This app roach allows contemporary injection of N compounds into the LC/MS system, t he retention time of each compound can be then extracted from the selected ion recording chromatograms. The throughput of the existing screening metho d could be increased by N times, where N is the number of compounds injecte d, so only three runs are needed to determine the CHI at three different pH values for a set of N compounds. The highest value of N depends on the tot al number of channels that can be monitored simultaneously; in the present work, 32 channels were used. This LC/MS method has been tested for a number of commercial products analyzed as mixtures, and data obtained were compar ed with those coming from the classical LC/UV approach. In the same way, th e method was tested for a number of compounds associated with two GlaxoWell come projects in the antibacterial area. Data reported show that the LC/MS method can be successfully applied for analyzing compounds in mixtures and for compounds with poor UV absorption, which cannot be analyzed with the st andard LC/UV method.