Development and validation of a UPLC-MS/MS method for simultaneous quantification of levofloxacin, ciprofloxacin, moxifloxacin and rifampicin in human plasma: Application to the therapeutic drug monitoring in osteoarticular infections.


Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
10 May 2020
Historique:
received: 08 10 2019
revised: 06 01 2020
accepted: 29 01 2020
pubmed: 23 2 2020
medline: 15 12 2020
entrez: 23 2 2020
Statut: ppublish

Résumé

Fluoroquinolones and rifampicin are antibiotics frequently used for the treatment of osteoarticular infections, and their therapeutic drug monitoring is recommended. The aim of this study was to develop and validate a rapid and selective method of simultaneous quantification of levofloxacin, ciprofloxacin, moxifloxacin and rifampicin with short pretreatment and run times in order to be easily used in clinical practice. After a simple protein precipitation of plasma samples, the chromatographic separation was performed using an ultra-performance liquid chromatography system coupled with mass tandem spectrometry in a positive ionization mode. The mobile phase consisted of a gradient elution of water-formic acid (100:0.1, v/v)-ammonium acetate 2 mM (A) and methanol-formic acid (100:0.1, v/v)-ammonium acetate 2 mM (B) at a flow rate at 0.3 mL/min. Analysis time was 5 min per run, and all analytes and internal standards eluted within 0.85-1.69 minutes. The calibration curves were linear over the range from 0.5-30 μg/mL for levofloxacin, ciprofloxacin, moxifloxacin and rifampicin with linear regression coefficients above 0.995 for all analytes. The intra-day and inter-day coefficients of variation were below 10 % for lower and higher concentration. This method was successfully applied to drug monitoring in patients with an osteoarticular infection. A simple, rapid, and selective liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous quantification of levofloxacin, ciprofloxacin, moxifloxacin and rifampicin in human plasma.

Sections du résumé

BACKGROUND BACKGROUND
Fluoroquinolones and rifampicin are antibiotics frequently used for the treatment of osteoarticular infections, and their therapeutic drug monitoring is recommended. The aim of this study was to develop and validate a rapid and selective method of simultaneous quantification of levofloxacin, ciprofloxacin, moxifloxacin and rifampicin with short pretreatment and run times in order to be easily used in clinical practice.
METHODS METHODS
After a simple protein precipitation of plasma samples, the chromatographic separation was performed using an ultra-performance liquid chromatography system coupled with mass tandem spectrometry in a positive ionization mode. The mobile phase consisted of a gradient elution of water-formic acid (100:0.1, v/v)-ammonium acetate 2 mM (A) and methanol-formic acid (100:0.1, v/v)-ammonium acetate 2 mM (B) at a flow rate at 0.3 mL/min.
RESULTS RESULTS
Analysis time was 5 min per run, and all analytes and internal standards eluted within 0.85-1.69 minutes. The calibration curves were linear over the range from 0.5-30 μg/mL for levofloxacin, ciprofloxacin, moxifloxacin and rifampicin with linear regression coefficients above 0.995 for all analytes. The intra-day and inter-day coefficients of variation were below 10 % for lower and higher concentration. This method was successfully applied to drug monitoring in patients with an osteoarticular infection.
CONCLUSION CONCLUSIONS
A simple, rapid, and selective liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous quantification of levofloxacin, ciprofloxacin, moxifloxacin and rifampicin in human plasma.

Identifiants

pubmed: 32086125
pii: S0731-7085(19)32455-0
doi: 10.1016/j.jpba.2020.113137
pii:
doi:

Substances chimiques

Ciprofloxacin 5E8K9I0O4U
Levofloxacin 6GNT3Y5LMF
Moxifloxacin U188XYD42P
Rifampin VJT6J7R4TR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113137

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

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.

Auteurs

Benoit LLopis (B)

AP-HP, Pitié-Salpêtrière Hospital, Department of Pharmacology, CIC-1421, F-75013 Paris, France.

Christian Funck-Brentano (C)

AP-HP, Pitié-Salpêtrière Hospital, Department of Pharmacology, CIC-1421, F-75013 Paris, France; Sorbonne Université Médecine, INSERM CIC Paris-Est, AP-HP, ICAN, Pitié-Salpêtrière Hospital, Department of Pharmacology, F-75013 Paris, France.

Nadine Tissot (N)

AP-HP, Pitié-Salpêtrière Hospital, Department of Pharmacology, CIC-1421, F-75013 Paris, France.

Alexandre Bleibtreu (A)

AP-HP, Hôpital Pitié-Salpêtrière, Service des maladies infectieuses et médecine tropicale, Centre d'Immunologie et des Maladies Infectieuses de Paris, Centre National de Référence du Paludisme-site Pitié Salpetrière, Paris, F-75013, France.

Stéphane Jaureguiberry (S)

AP-HP, Hôpital Pitié-Salpêtrière, Service des maladies infectieuses et médecine tropicale, Centre d'Immunologie et des Maladies Infectieuses de Paris, Centre National de Référence du Paludisme-site Pitié Salpetrière, Paris, F-75013, France.

Eric Fourniols (E)

AP-HP, Pitié-Salpêtrière Hospital, Department of Orthopedia, Paris, France.

Alexandra Aubry (A)

Sorbonne Université, Centre d'Immunologie et des Maladies Infectieuses-Paris, Cimi-Paris, INSERM U1135, National Reference Center for Mycobacteria, Laboratoire de Bactériologie-Hygiène, AP-HP, Pitié-Salpêtrière, Paris, France.

Noël Zahr (N)

AP-HP, Pitié-Salpêtrière Hospital, Department of Pharmacology, CIC-1421, F-75013 Paris, France. Electronic address: noel.zahr@aphp.fr.

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Classifications MeSH