Voltammetric behavior and square-wave voltammetric determination of cefotaxime in urine

Abstract The voltammetric behavior of cefotaxime (CFX) is investigated by cyclic and square-wave voltammetry in BR buffers (pH 1.80–12.0). Based on the cathodic reduction peak at approximately −0.5 V in BR buffer (pH 2.8 and 9.25), a robust, highly reliable square-wave voltammetric method (SW) was developed for determination of CFX. The linearity was achieved by SW voltammetry in 7.5 × 10−9  M (3.52 ng ml−1) to 1.0 × 10−7 M (47 ng ml−1) and from 1.2 × 10−7 M (56.4 ng ml−1) to 1.2 × 10−6 M (568.8 ng ml−1) range at pH 2.8 with detection and quantification limits of 0.813 ng ml−1 and 2.71 ng ml−1, and 12.6 ng ml−1 and 42.2 ng ml−1, respectively. At pH 9.25 linear range was obtained from 4 × 10−8 M (18.8 ng ml−1) to 1.6 × 10−7 M (75.2 ng ml−1) with detection and quantification limits of 2.947 ng ml−1 and 9.82 ng ml−1. The method was applied for CFX determination in spiked humane urine sample. A detection and quantification limits of 7.2 ng ml−1 and 23.9 ng ml−1 were achieved for determination of CFX in urine at pH 2.8 and 13.6 ng ml−1 and 45.1 ng ml−1 at pH 9.25. The comparative reference method was DPV. The proposed method was checked for determination of CFX in real human urine, and selectivity of the method over the metabolites was found to be quite satisfactory.

[1]  M. Aleksić,et al.  Recent Developments in Electroanalytical Chemistry of Cephalosporins and Cefamycins , 2000 .

[2]  M. Aleksić,et al.  Two-step reduction of the O-methyloxime group in the antibiotic cefetamet , 2001 .

[3]  B. Ogorevc,et al.  Adsorptive stripping voltammetry of selected cephalosporin antibiotics and their direct determination in urine , 1991 .

[4]  I. Al-Momani Spectrophotometric determination of selected cephalosporins in drug formulations using flow injection analysis. , 2001, Journal of pharmaceutical and biomedical analysis.

[5]  Luisa Gallo Martinez,et al.  Comparison of several methods used for the determination of cephalosporins. Analysis of cephalexin in pharmaceutical samples. , 2002 .

[6]  D. Sužnjević,et al.  Study of Cephalexin and Cefaclor Adsorption at the Mercury/Solution Interface by AC Polarography , 1997 .

[7]  M. Aleksić,et al.  Adsorptive properties of cefpodoxime proxetil as a tool for a new method of its determination in urine. , 2004, Journal of pharmaceutical and biomedical analysis.

[8]  I. Biryol,et al.  Anodic voltammetry of cefotaxime. , 1998, Journal of pharmaceutical and biomedical analysis.

[9]  A. Alwarthan,et al.  Flow-injection spectrophotometric determination of certain cephalosporins based on the formation of dyes. , 2001, Farmaco.

[10]  K. Yuen,et al.  Simple liquid chromatographic method for the determination of cefotaxime in human and rat plasma. , 2003, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[11]  M. Aleksić,et al.  Adsorptive stripping voltammetric determination of cefetamet in human urine. , 2003, Journal of pharmaceutical and biomedical analysis.

[12]  M. Aleksić,et al.  Polarographic and Voltammetric Behavior of the Antibiotic Cefetamet; Reduction of the Methoxyimino Group , 2004 .

[13]  B. Ogorevc,et al.  Polarographic analysis of some cephalosporin antibiotics , 1988 .

[14]  M. Aleksić,et al.  Acidity constants of cefetamet, cefotaxime and ceftriaxone; the effect of the substituent at C3 position. , 2005, Journal of pharmaceutical and biomedical analysis.

[15]  D. D. Perrin,et al.  Buffers for pH and metal ion control , 1974 .