Automated determination of verapamil and norverapamil in human plasma with on-line coupling of dialysis to high-performance liquid chromatography and fluorometric detection

被引:30
作者
Ceccato, A [1 ]
Chiap, P [1 ]
Hubert, P [1 ]
Toussaint, B [1 ]
Crommen, J [1 ]
机构
[1] UNIV LIEGE,INST PHARM,LAB DRUG ANAL,B-4000 LIEGE,BELGIUM
关键词
dialysis; sample preparation; automation; verapamil; norverapamil; gallopamil;
D O I
10.1016/0021-9673(96)00471-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fully automated method for the simultaneous determination of verapamil and its main metabolite norverapamil in human plasma is described. This method is based on on-line sample preparation using dialysis followed by clean-up and enrichment of the dialysate on a precolumn and subsequent HPLC analysis with fluorometric detection. All sample handling operations were performed automatically by a sample processor equipped with a robotic arm (ASTED system). The plasma samples were dialysed on a cellulose acetate membrane (cut-off: 15 kD) and the dialysate was purified and enriched on a short pre-column filled with cyanopropyl silica. Before starting dialysis, this trace enrichment column (TEC) was first conditioned with the HPLC mobile phase and then with pH 3.0 acetate buffer. 370 mu l of plasma sample spiked with the internal standard (gallopamil) were dialysed in the static-pulsed mode. The solution at the donor side was pH 3.0 acetate buffer containing Triton X-100 while the acceptor solution was made of the same acetate buffer. When dialysis was discontinued, the analytes were desorbed from the TEC by the HPLC mobile phase and transferred to the C-18 analytical column by means of a switching valve. This mobile phase consisted of a mixture of acetonitrile, pH 3.0 acetate buffer and 2-aminoheptane. The influence of different parameters of the dialysis process on the recovery of verapamil and norverapamil has been studied. The effect of the volume, the aspirating and dispensing flow-rates of the dialysis solution has been investigated. The recoveries of verapamil and norverapamil in plasma were close to 75% and the limits of quantification were 5 ng/ml for both analytes. The method was found to be linear in the concentration range from 5 to 500 ng/ml (r(2): 0.9996 for both analytes). The intra-day and inter-day reproducilities at a concentration Of 100 ng/ml were 2.3% and 5.6% for verapamil and 1.7% and 5.1% for norverapamil, respectively.
引用
收藏
页码:351 / 360
页数:10
相关论文
共 25 条
[1]   ONLINE COMBINATION OF DIALYSIS AND COLUMN-SWITCHING LIQUID-CHROMATOGRAPHY AS A FULLY AUTOMATED SAMPLE PREPARATION TECHNIQUE FOR BIOLOGICAL SAMPLES - DETERMINATION OF NITROFURAN RESIDUES IN EDIBLE PRODUCTS [J].
AERTS, MML ;
BEEK, WMJ ;
BRINKMAN, UAT .
JOURNAL OF CHROMATOGRAPHY, 1990, 500 :453-468
[2]   AUTOMATED-ANALYSIS OF OXOLINIC ACID AND FLUMEQUINE IN SALMON WHOLE-BLOOD AND PLASMA USING DIALYSIS COMBINED WITH TRACE ENRICHMENT AS ONLINE SAMPLE PREPARATION FOR HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
AGASOSTER, T ;
RASMUSSEN, KE .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1991, 564 (01) :171-179
[3]   ONLINE DIALYSIS, LIQUID-CHROMATOGRAPHY AND POSTCOLUMN REACTION DETECTION OF OXYTETRACYCLINE IN SALMON MUSCLE EXTRACTS [J].
AGASOSTER, T ;
RASMUSSEN, KE .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1992, 10 (05) :349-354
[4]   FULLY AUTOMATED HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF WHOLE-BLOOD AND PLASMA SAMPLES USING ONLINE DIALYSIS AS SAMPLE PREPARATION - DETERMINATION OF OXYTETRACYCLINE IN BOVINE AND SALMON WHOLE-BLOOD AND PLASMA [J].
AGASOSTER, T ;
RASMUSSEN, KE .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1991, 570 (01) :99-107
[5]   AUTOMATED HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OF IOPENTOL IN HUMAN PLASMA AND WHOLE-BLOOD USING ONLINE DIALYSIS AS SAMPLE PREPARATION [J].
ANDRESEN, AT ;
JACOBSEN, PB ;
RASMUSSEN, KE .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1992, 575 (01) :93-99
[6]   AUTOMATED-DETERMINATION OF FREE PHENYTOIN IN HUMAN PLASMA WITH ONLINE EQUILIBRIUM DIALYSIS AND COLUMN-SWITCHING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
ANDRESEN, AT ;
RASMUSSEN, KE ;
RUGSTAD, HE .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1993, 621 (02) :189-198
[7]   METHOD VALIDATION IN THE BIOANALYTICAL LABORATORY [J].
BUICK, AR ;
DOIG, MV ;
JEAL, SC ;
LAND, GS ;
MCDOWALL, RD .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1990, 8 (8-12) :629-637
[8]   RAPID HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHOD FOR THE MEASUREMENT OF VERAPAMIL AND NORVERAPAMIL IN BLOOD-PLASMA OR SERUM [J].
COLE, SCJ ;
FLANAGAN, RJ ;
JOHNSTON, A ;
HOLT, DW .
JOURNAL OF CHROMATOGRAPHY, 1981, 218 (1-3) :621-629
[9]   AUTOMATED SEQUENTIAL TRACE ENRICHMENT OF DIALYSATES AND ROBOTICS - A TECHNIQUE FOR THE PREPARATION OF BIOLOGICAL SAMPLES PRIOR TO HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
COOPER, JDH ;
TURNELL, DC ;
GREEN, B ;
VERILLON, F .
JOURNAL OF CHROMATOGRAPHY, 1988, 456 (01) :53-69
[10]   ANALYSIS OF CALCIUM BLOCKER DRUGS IN PLASMA, HRGC AND HPLC ANALYTICAL CONDITIONS FOR PHARMACOKINETIC STUDIES [J].
GIACHETTI, C ;
POLETTI, P ;
ZANOLO, G .
JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY & CHROMATOGRAPHY COMMUNICATIONS, 1987, 10 (12) :654-658