Literature DB >> 21840010

Development and validation of a confirmatory method for the determination of 12 non steroidal anti-inflammatory drugs in milk using liquid chromatography-tandem mass spectrometry.

Estelle Dubreil-Chéneau1, Yvette Pirotais, Mélaine Bessiral, Brigitte Roudaut, Eric Verdon.   

Abstract

A rapid and reliable LC-MS/MS method for the simultaneous confirmation of twelve non steroidal anti-inflammatory drugs (NSAIDs) in bovine milk was developed and fully validated in accordance with the European Commission Decision 2002/657/EC. The validation scheme was built in accordance with the MRLs or target analytical levels (EU-CRL recommended concentrations and detection capabilities) of the analytes, except for diclofenac for which the lower level of validation achieved was 0.5 μg kg(-1) whereas its MRL is 0.1 μg kg(-1). The NSAIDs investigated were as follows: phenylbutazone (PBZ), oxyphenylbutazone (OPB), naproxen (NP), mefenamic acid (MF), vedaprofen (VDP), flunixin (FLU), 5-hydroxyflunixin (FLU-OH), tolfenamic acid (TLF), meloxicam (MLX), diclofenac (DC), carprofen (CPF) and ketoprofen (KTP). Several extraction procedures had been investigated during the development phase. Finally, the best results were obtained with a procedure using only methanol as the extraction solvent, with an evaporation step included and no further purification. Chromatographic separation was achieved on a C18 analytical column and the run was split in 2 segments. Matrix effects were also investigated. Data acquisition implemented for the confirmatory purpose was performed by monitoring 2 MRM transitions per analyte under the negative electrospray mode. Mean relative recoveries ranged from 94.7% to 110.0%, with their coefficients of variation lying between 2.9% and 14.7%. Analytical limits expressed in terms of decision limits (CCα) were evaluated between 0.69 μg kg(-1) (FLU) and 27.54 μg kg(-1) (VDP) for non-MRL compounds, and at 0.10 (DC), 15.37 (MLX), 45.08 (FLU-OH), and 62.96 μg kg(-1) (TLF) for MRL compounds. The validation results proved that the method is suitable for the screening and confirmatory steps as implemented for the French monitoring plan for NSAID residue control in bovine milk.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21840010     DOI: 10.1016/j.chroma.2011.06.006

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  5 in total

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Authors:  N Molina-Fernandez; C Perez-Conde; S Rainieri; J Sanz-Landaluze
Journal:  Environ Sci Pollut Res Int       Date:  2016-05-11       Impact factor: 4.223

2.  Nickel-iron layered double hydroxide nanostructures for micro solid phase extraction of nonsteroidal anti-inflammatory drugs, followed by quantitation by HPLC-UV.

Authors:  Shahram Seidi; Sasan Eshghi Sanàti
Journal:  Mikrochim Acta       Date:  2019-04-23       Impact factor: 5.833

3.  Simultaneous determination of mefenamic and tolfenamic acids in real samples by terbium-sensitized luminescence.

Authors:  J A Murillo Pulgarín; A Alañón Molina; F Martínez Ferreras
Journal:  J Fluoresc       Date:  2012-07-01       Impact factor: 2.217

4.  Validation of a UV Spectrometric Method for the Assay of Tolfenamic Acid in Organic Solvents.

Authors:  Sofia Ahmed; Nafeesa Mustaan; Muhammad Ali Sheraz; Syeda Ayesha Ahmed Un Nabi; Iqbal Ahmad
Journal:  J Pharm (Cairo)       Date:  2015-12-10

5.  The Surface Area to Volume Ratio Changes the Pharmacokinetic and Pharmacodynamic Parameters in the Subcutaneous Tissue Cage Model: As Illustrated by Carprofen in Sheep.

Authors:  Richard Munn; Ted Whittem; Andrew P Woodward
Journal:  Front Vet Sci       Date:  2022-07-01
  5 in total

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