Determination of ceftazidime in plasma using high-performance liquid chromatography and electrochemical detection - Application for individualizing dosage regimens in elderly patients

被引:22
作者
Guitton, J
Laffont, A
Bruzeau, J
Rochet-Mingret, L
Bonnefoy, M
Bureau, J
机构
[1] Ctr Hosp Lyon Sud, Serv Pharmaceut, F-69495 Pierre Benite, France
[2] Ctr Hosp Lyon Sud, Serv Med Interne Diabetol, F-69495 Pierre Benite, France
[3] Ctr Hosp Lyon Sud, Serv Med Geriatr, F-69495 Pierre Benite, France
[4] Inst Sci Pharmaceut & Biol Lyon, Lab Pharmacocinet, F-69373 Lyon 08, France
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 1998年 / 719卷 / 1-2期
关键词
ceftazidime;
D O I
10.1016/S0378-4347(98)00333-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This study describes a sensitive HPLC-electrochemical detection method for the analysis of ceftazidime, a third-generation cephalosporin, in human plasma. The extraction procedure involved protein precipitation with 30% trichloroacetic acid. The separation was achieved on a reversed-phase column (250X4.6 mm I.D., 5 mu m) packed with C-18 Kromasil with isocratic elution and a mobile phase consisting of acetonitrile-25 mM KH2PO4-Na2HPO4 buffer, pH 7.4 (10:90, v/v). The proposed analytical method is selective, reproducible and reliable. The assay has a precision of 0.2-15.1% (C.V.) in the range of 5-200 mu g ml(-1) (corresponding to 0.5 to 20 ng of ceftazidime injected onto the column), and is optimised for assaying 50 mu l of plasma. The extraction recovery from plasma was approximately 100%. The method was highly specific for ceftazidime and there was no interference from either commonly administered drugs or endogenous compounds. This assay was used to measure ceftazidime in elderly patients for therapeutic drug monitoring. (C) 1998 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:151 / 157
页数:7
相关论文
共 27 条
[21]   ELECTROCHEMICAL ANALYSIS OF CEPHALOSPORIN ANTIBIOTICS [J].
OGOREVC, B ;
GOMISCEK, S .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1991, 9 (03) :225-236
[22]   COMPARATIVE-STUDY OF PHARMACOKINETICS AND SERUM BACTERICIDAL ACTIVITIES OF CEFPIROME, CEFTAZIDIME, CEFTRIAXONE, IMIPENEM, AND CIPROFLOXACIN [J].
PARADIS, D ;
VALLEE, F ;
ALLARD, S ;
BISSON, C ;
DAVIAU, N ;
DRAPEAU, C ;
AUGER, F ;
LEBEL, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (10) :2085-2092
[23]   THE MICROBIOLOGICAL ASSAY OF CEFTAZIDIME [J].
THORNTON, JE .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1981, 8 :225-226
[24]   DETERMINATION OF CEFTAZIDIME IN DOLPHIN SERUM BY LIQUID-CHROMATOGRAPHY WITH ULTRAVIOLET VISIBLE DETECTION AND CONFIRMATION BY THERMOSPRAY LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
TYCZKOWSKA, KL ;
SEAY, SS ;
STOSKOPF, MK ;
STOSKOPF, MK ;
AUCOIN, DP .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1992, 576 (02) :305-313
[25]   Population pharmacokinetics of ceftazidime in cystic fibrosis patients analyzed by using a nonparametric algorithm and optimal sampling strategy [J].
Vinks, AATMM ;
Mouton, JW ;
Touw, DJ ;
Heijerman, HGM ;
Danhof, M ;
Bakker, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (05) :1091-1097
[26]   Intermittent bolus dosing of ceftazidime in critically ill patients [J].
Young, RJ ;
Lipman, J ;
Gin, T ;
Gomersall, CD ;
Joynt, GM ;
Oh, TE .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (02) :269-273
[27]   INFLUENCE OF PH, TEMPERATURE, AND BUFFERS ON THE KINETICS OF CEFTAZIDIME DEGRADATION IN AQUEOUS-SOLUTIONS [J].
ZHOU, MX ;
NOTARI, RE .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (05) :534-538