4.2 Article

A simple liquid chromatography method for the determination of captopril in urine

Journal

CHROMATOGRAPHIA
Volume 66, Issue 1-2, Pages 71-74

Publisher

SPRINGER HEIDELBERG
DOI: 10.1365/s10337-007-0232-8

Keywords

column liquid chromatography; derivatization; captopril in urine

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A simple and specific method for the determination of total captopril in human urine was developed. 2-Chloro-1-methylquinolinium tetrafluoroborate was used as a thiol precolumn derivatizing reagent after conversion of a disulfide forms to free captopril with tris(2-carboxyethyl)phosphine hydrochloride. The 2-S-quinolinium derivative of captopril was separated on a Zorbax SB C- 18 column using reversed-phase ion-paring chromatography and monitored by spectrophotometric detector at 355 nm. The calibration curve for the derivatized captopril showed linearity in the range 0.1-200 mu mol L-1 of urine with a regression coefficient corresponding to 0.9999. The detection and quantitation limits were 0.05 and 0.1 mu mol L-1, respectively. The intra-day imprecision was from 0.01 to 10.58%. This method can be used for routine clinical monitoring of the thiol-drug. Omission of the reduction step gives result for concentration of the reduced form of captopril.

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