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Quantification of cefuroxime and flucloxacillin in synovial tissue and bone using ultra-performance convergence chromatography-tandem mass spectrometry.
- Source :
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences [J Chromatogr B Analyt Technol Biomed Life Sci] 2024 Jul 01; Vol. 1241, pp. 124169. Date of Electronic Publication: 2024 May 26. - Publication Year :
- 2024
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Abstract
- After a revision surgery, approximately 1-2 % of patients will develop a periprosthetic joint infection (PJI). During the revision surgery, the infected prosthesis is removed, a debridement is performed and a new or temporary spacer is placed. Additionally, patients are treated with antibiotics during and after the surgery. Adequate exposure of the administered antibiotic to the pathogen is of crucial importance during the treatment of any infection. Inadequately low concentrations are associated with an increase in antibiotic resistance, antibiotic related side effects, treatment failures and prolonged infections. While high concentrations may lead to serious adverse events and potential lasting damage. Despite the importance of optimal dosing, there is a lack of knowledge with respect to the correlation between the plasma concentrations and target site concentrations of the antibiotics. Two of the commonly administered antimicrobial agents during the arthroplasty exchange are cefuroxime and flucloxacillin. Therefore, an accurate, specific, and sensitive quantification method is required in order to assess pharmacokinetics of cefuroxime and flucloxacillin in synovial tissue and bone. The aim of this study is to develop and validate a quantification method for the measurement of cefuroxime and flucloxacillin in human synovial tissue and bone using the UPC <superscript>2</superscript> -MS/MS conform Food and Drug Administration guidelines. The method was found linear for both compounds in both matrices (r <superscript>2</superscript>  > 0.990) from 1 µg/g to 20 µg/g, except for cefuroxime in bone, which was validated from 1 µg/g to 15 µg/g. We developed and validated a quantification method for cefuroxime and flucloxacillin in synovial tissue and bone using a simple sample preparation and a short analysis run time of 5.0 min, which has been already successfully applied in a clinical study. To our knowledge, no methods have been described earlier for the simultaneous quantification of cefuroxime and flucloxacillin in synovial tissue and bone.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Humans
Chromatography, High Pressure Liquid methods
Linear Models
Reproducibility of Results
Anti-Bacterial Agents analysis
Anti-Bacterial Agents blood
Anti-Bacterial Agents pharmacokinetics
Bone and Bones chemistry
Bone and Bones metabolism
Synovial Membrane chemistry
Synovial Membrane metabolism
Limit of Detection
Tandem Mass Spectrometry methods
Cefuroxime analysis
Cefuroxime pharmacokinetics
Cefuroxime blood
Floxacillin analysis
Floxacillin pharmacokinetics
Floxacillin chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1873-376X
- Volume :
- 1241
- Database :
- MEDLINE
- Journal :
- Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
- Publication Type :
- Academic Journal
- Accession number :
- 38815354
- Full Text :
- https://doi.org/10.1016/j.jchromb.2024.124169