Simultaneous determination of cefotaxime and desacetylcefotaxime in real urine sample using voltammetric and high-performance liquid chromatographic methods

被引:24
作者
Aleksic, Mara M. [1 ]
Kapetanovic, Vera [2 ]
Atanackovic, Jasmina [2 ]
Jocic, Biljana [3 ]
Zecevic, Mira [3 ]
机构
[1] Univ Belgrade, Fac Pharm, Inst Phys Chem, Belgrade 11000, Serbia
[2] Univ Belgrade, Fac Pharm, Inst Analyt Chem, Belgrade 11000, Serbia
[3] Univ Belgrade, Fac Pharm, Inst Pharmaceut Chem, Belgrade 11000, Serbia
关键词
Cefotaxime; Desacetylcefotaxime; Simultaneous determination; Real urine; Voltammetry; RP-HPLC;
D O I
10.1016/j.talanta.2008.05.047
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Two rapid, accurate and sensitive methods are developed and validated for the quantitative simultaneous determination of cefotaxime (CFX) and its active metabolite desacetylcefotaxime (DCFX) in urine. Based on the previous results which showed the four electron reduction of CFX at approximate to -0.5 V, and the new findings that DCFX reduction occurred at more positive potential (-0.23 V), the new adsorptive stripping differential pulse voltammetric (AdSDPV) method was developed for determination of CFX in the presence of DCFX. Linear responses were observed over a wide concentration range (0.07-0.52 mu g/ml for CFX and 0.22-1.3 mu g/ml for DCFX) in urine. The second assay involves subsequent separation on a reversed-phase HPLC column, with ultraviolet detection at 262 nm. Retention times were 4.057 and 1.960 min for CFX and DCFX, respectively. Linear responses were observed over a wide range, 0.55-6.60 mu g/ml for CFX and 1.10-11.00 mu g/ml for DCFX, in urine. The statistical evaluation for both methods was examined by means of within-day repeatability (n=5) and day-to-day precision (n=3) and was found to be satisfactory with high accuracy and precision. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 137
页数:7
相关论文
共 19 条
[1]   Polarographic and voltammetric behavior of the antibiotic cefetamet; Reduction of the methoxyimino group [J].
Aleksic, M ;
Kapetanovic, V ;
Zuman, P .
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 2004, 69 (07) :1429-1442
[2]   Voltammetric behavior and square-wave voltammetric determination of cefotaxime in urine [J].
Aleksic, Mara M. ;
Kapetanovic, Vera .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2006, 593 (1-2) :258-266
[3]   KINETICS AND MECHANISM OF DEGRADATION OF CEFOTAXIME SODIUM IN AQUEOUS-SOLUTION [J].
BERGE, SM ;
HENDERSON, NL ;
FRANK, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (01) :59-63
[4]  
Connors K. A., 1986, CHEM STABILITY PHARM, P302
[5]   First-derivative spectrophotometric and LC determination of cefuroxime and cefadroxil in urine [J].
El-Gindy, A ;
El Walily, AFM ;
Bedair, MF .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2000, 23 (2-3) :341-352
[6]   Study of cephalexin and cefaclor adsorption at the mercury/solution interface by AC polarography [J].
Erceg, M ;
Kapetanovic, V ;
Suznjevic, D ;
Dumanovic, D .
MICROCHEMICAL JOURNAL, 1997, 57 (01) :73-80
[7]   CAPILLARY ELECTROPHORESIS AS AN ALTERNATIVE METHOD FOR THE DETERMINATION OF CEFOTAXIME [J].
FABRE, H ;
PENALVO, GC .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1995, 18 (18-19) :3877-3887
[8]  
Gallo Martinez Luisa, 1998, Journal of Chromatography B, V718, P143, DOI 10.1016/S0378-4347(98)00335-1
[9]   Two-step reduction of the O-methyloxime group in the antibiotic cefetamet [J].
Kapetanovic, V ;
Aleksic, M ;
Zuman, P .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 507 (1-2) :263-269
[10]  
LAVIRON E, 1980, J ELECTROANAL CHEM, V112, P1, DOI 10.1016/S0022-0728(80)80002-7