Literature DB >> 3307616

Recent analytical methods for cephalosporins in biological fluids.

R D Toothaker, D S Wright, L A Pachla.   

Abstract

Since 1980, RP chromatography has been the principal analytical technique used for cephalosporins. This technology offers selectivity, accuracy, and ease of use. Most of the methods rely on protein precipitation and, to a lesser extent, solid-phase isolation or extraction procedures. The proper selection of a method depends on the analytical constraints imposed by the overall objective of the study. For example, pharmacokinetic datum interpretation mandates that the method be validated and provide specific and accurate results. LC is the preferred technique, since it not only meets these specifications but may also distinguish between the drug and metabolites. Those chromatographic methods which quantify several different cephalosporins are not desirable for pharmacokinetic datum interpretation, since accuracy and precision are usually compromised in order that many different drugs may be quantified in a single analysis. The proper selection of sample preparation method is dependent on the presence of potential interferences and the acceptable lower limit of quantitation. Protein precipitation methods offer ease of sample preparation but may suffer from nonselectivity. Solid-phase isolation and extraction procedures may increase selectivity and improve the limit of quantitation. Although LC provides specific and accurate results, clinical laboratories may prefer to use the less specific methods for therapeutic drug monitoring. In this case, microbiological, enzymatic, and fluorimetric methods offer improved sample throughput but less specificity. However, these methods should not be used for drugs that may have a low margin of safety or if the patient is on multiple-antibiotic therapy. Future methods may involve incorporating solid-phase isolation columns to enhance the specificity of chromatographic, microbiological, enzymatic, and fluorescence methods. Advancements in microbore column technology may allow improvements in the selectivity and sensitivity of LC methods. Many investigators prefer to use simple protein precipitation procedures for sample preparation because of sample throughput constraints. However, advances in robotic sample preparation may allow the more cumbersome solid-phase isolation or extraction techniques to be used to improved sample throughput and specificity.

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Year:  1987        PMID: 3307616      PMCID: PMC174896          DOI: 10.1128/AAC.31.8.1157

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  59 in total

1.  Quantitative liquid chromatographic determination of cefatrizine in serum and urine by fluorescence detection after post-column derivatization.

Authors:  E Crombez; G Van der Weken; W Van den Bossche; P De Moerloose
Journal:  J Chromatogr       Date:  1979-09-21

2.  Fluorometric determination of cephalexin, cephradine, and cephatrizine in biological fluids.

Authors:  K Miyazaki; O Ogino; T Arita
Journal:  Chem Pharm Bull (Tokyo)       Date:  1979-10       Impact factor: 1.645

3.  [Liquid chromatographic determination of current cephalosporin derivatives in biological fluids].

Authors:  A Csiba; H Gráber
Journal:  Acta Pharm Hung       Date:  1983-11

4.  High-pressure liquid chromatographic analysis of ceftazidime in serum and urine.

Authors:  J S Leeder; M Spino; A M Tesoro; S M MacLeod
Journal:  Antimicrob Agents Chemother       Date:  1983-11       Impact factor: 5.191

5.  Comparison of microbiological and high pressure liquid chromatographic assays of the new cephalosporin cefroxadine.

Authors:  T Bergan; R Solberg
Journal:  Methods Find Exp Clin Pharmacol       Date:  1981 May-Jun

6.  Determination of antibiotic concentrations in bone.

Authors:  V T Rosdahl; T S Sørensen; H Colding
Journal:  J Antimicrob Chemother       Date:  1979-05       Impact factor: 5.790

7.  [Technic for assaying cefotaxime and desacetylcefotaxime in serum by high performance liquid chromatography].

Authors:  M Boyer; J Sirot; R Cluzel
Journal:  Pathol Biol (Paris)       Date:  1984-04

8.  High-performance liquid chromatographic determination of cefoperazone in human serum and urine.

Authors:  J Dokladalova; G T Quercia; J P Stankewich
Journal:  J Chromatogr       Date:  1983-08-12

9.  Determination of cefsulodin in biological fluids by high-pressure liquid chromatography.

Authors:  I M Ackers; C M Myers; J L Blumer
Journal:  Ther Drug Monit       Date:  1984       Impact factor: 3.681

10.  High-performance liquid chromatographic analysis of cefotetan epimers in human plasma and urine.

Authors:  F Kees; H Grobecker; K G Naber
Journal:  J Chromatogr       Date:  1984-02-10
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  2 in total

1.  High pressure liquid chromatographic analysis of the serum concentration of cefuroxime after an intravenous bolus injection of cefuroxime in patients with a coronary artery bypass grafting.

Authors:  M J Koot; F N IJdenberg; R M Stuurman; J Poell; L J Bras; J J Langemeijer; L Lie-A-Huen
Journal:  Pharm Weekbl Sci       Date:  1992-12-11

2.  Cefazolin Concentration in the Mediastinal Adipose Tissue of Patients Undergoing Cardiac Surgery.

Authors:  Rodrigo Mezzalira Tchaick; Michel Pompeu Barros Oliveira Sá; Fernando Ribeiro de Moraes Figueira; Kilma Coelho Paz; Álvaro Antonio Bandeira Ferraz; Fernando Ribeiro de Moraes
Journal:  Braz J Cardiovasc Surg       Date:  2017 Jul-Aug
  2 in total

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