Simultaneous determination of eight β-blockers by gradient high-performance liquid chromatography with combined ultraviolet and fluorescence detection in corneal permeability studies in vitro

被引:65
作者
Ranta, VP
Toropainen, E
Talvitie, A
Auriola, S
Urtti, A
机构
[1] Univ Kuopio, Dept Pharmaceut, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Pharmaceut Chem, FIN-70211 Kuopio, Finland
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2002年 / 772卷 / 01期
基金
芬兰科学院;
关键词
beta-blockers;
D O I
10.1016/S1570-0232(02)00059-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A gradient HPLC method with combined ultraviolet and fluorescence detection was developed for the simultaneous determination of eight beta-blockers (alprenolol, atenolol, metoprolol, nadolol, pindolol, propranolol, sotalol and timolol) in corneal permeability studies in vitro. Fluorescence detection with excitation wavelength at 230 nm and emission at 302 nm was selective for six of the compounds, whereas UV detection at 205 nm was able to detect all the compounds. Calibration was performed with fluorescence detection for six compounds from 50 or 200 nM to 3 muM and with UV detection for all the eight compounds from 100 or 200 nM to 30 muM. With optimized fluorescence detection, detection limits between 0.7 and 1.3 nM (0.035-0.065 pmol per 50 mul injection) were obtained for atenolol, metoprolol, nadolol and sotalol. A mixture of eight beta-blockers was used in cassette dosing permeability studies with a cultured corneal epithelium. The HPLC method revealed marked differences in the permeation between hydrophilic and lipophilic beta-blockers through the corneal epithelial cell culture model. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 87
页数:7
相关论文
共 14 条
[1]   DRUG LEVEL MONITORING - CARDIOVASCULAR DRUGS [J].
AHNOFF, M ;
ERVIK, M ;
LAGERSTROM, PO ;
PERSSON, BA ;
VESSMAN, J .
JOURNAL OF CHROMATOGRAPHY, 1985, 340 (MAY) :73-138
[2]  
ARAKISASAKI K, 1995, INVEST OPHTH VIS SCI, V36, P614
[3]   EPITHELIAL TRANSPORT OF DRUGS IN CELL-CULTURE .1. A MODEL FOR STUDYING THE PASSIVE DIFFUSION OF DRUGS OVER INTESTINAL ABSORPTIVE (CACO-2) CELLS [J].
ARTURSSON, P .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (06) :476-482
[4]  
Gergov M, 2000, J MASS SPECTROM, V35, P912, DOI 10.1002/1096-9888(200007)35:7<912::AID-JMS19>3.0.CO
[5]  
2-4
[6]   Small blood volumes from children for quantitative sotalol determination using high-performance liquid chromatography [J].
Läer, S ;
Wauer, I ;
Scholz, H .
JOURNAL OF CHROMATOGRAPHY B, 2001, 753 (02) :421-425
[7]   Enantioselective determination of metoprolol and major metabolites in human urine by capillary electrophoresis [J].
Lim, HK ;
Linh, PT ;
Hong, CH ;
Kim, KH ;
Kang, JS .
JOURNAL OF CHROMATOGRAPHY B, 2001, 755 (1-2) :259-264
[8]   Enantiomeric separation of metoprolol and α-hydroxymetoprolol by liquid chromatography and fluorescence detection using a chiral stationary phase [J].
Mistry, B ;
Leslie, JL ;
Eddington, ND .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2001, 758 (02) :153-161
[9]   A STRATEGY FOR THE DETERMINATION OF BETA-BLOCKERS IN PLASMA USING SOLID-PHASE EXTRACTION IN COMBINATION WITH HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
MUSCH, G ;
BUELENS, Y ;
MASSART, DL .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1989, 7 (04) :483-497
[10]   CORNEAL PENETRATION BEHAVIOR OF BETA-BLOCKING-AGENTS .1. PHYSICOCHEMICAL FACTORS [J].
SCHOENWALD, RD ;
HUANG, HS .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (11) :1266-1272