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
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.