Determination of captopril in biological samples by highperformance liquidchromatography with ThioGlo(TM)3 derivatization

Citation
N. Aykin et al., Determination of captopril in biological samples by highperformance liquidchromatography with ThioGlo(TM)3 derivatization, BIOMED CHRO, 15(7), 2001, pp. 427-432
Citations number
21
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOMEDICAL CHROMATOGRAPHY
ISSN journal
02693879 → ACNP
Volume
15
Issue
7
Year of publication
2001
Pages
427 - 432
Database
ISI
SICI code
0269-3879(200111)15:7<427:DOCIBS>2.0.ZU;2-P
Abstract
Captopril, a well-known angiotensin converting enzyme (ACE) inhibitor, is w idely used for treatment of arterial hypertension. Recent studies suggest t hat it may also act as a scavenger of free radicals because of its thiol gr oup. Therefore, the present study describes a rapid, sensitive and relative ly simple method for the detection of captopril in biological tissues with reverse-phase HPLC. Captopril was first derivatized with ThioGlo (TM)3 [3H- Naphto[2,1-b]pyran,9-acetoxy-2-(4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)phe nyl-3-oxo-)]. It was then detected by fluorescence-HPLC using an Astec C-18 column as the stationary phase and a water: acetonitrile:acetic acid:phosp horic acid mixture (50:50; 1 mL/L acids) as the mobile phase (excitation wa velength, 365 nm; emission wavelength, 445 nm). The calibration curve for c aptopril was linear over a range of 10-2500 nm and the coefficient of varia tion acquired for the within- and between-run precision for captopril was 0 .5 and 3.8%, respectively. The detection limit of captopril with this metho d was found to be 200 fmol/20 muL injection volume. Its relative recovery f rom biological samples was determined to the range from 93.3 to 105.3%. Bas ed on these results, we believe that our method is advantageous for captopr il determination. Copyright (C) 2001 John Wiley & Sons, Ltd.