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Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry

Chloramphenicol (CAP), a bacteriostatic antibiotic, is used for the treatment of bacterial infections in human and animals. Continual exposure of CAP residues into animal tissues may lead to antibiotic resistance. For the protection of humans and animals from this problem, a fast and highly sensitiv...

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Autores principales: Akter Mou, Salma, Islam, Rafiza, Shoeb, Mohammad, Nahar, Nilufar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497835/
https://www.ncbi.nlm.nih.gov/pubmed/34646535
http://dx.doi.org/10.1002/fsn3.2530
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author Akter Mou, Salma
Islam, Rafiza
Shoeb, Mohammad
Nahar, Nilufar
author_facet Akter Mou, Salma
Islam, Rafiza
Shoeb, Mohammad
Nahar, Nilufar
author_sort Akter Mou, Salma
collection PubMed
description Chloramphenicol (CAP), a bacteriostatic antibiotic, is used for the treatment of bacterial infections in human and animals. Continual exposure of CAP residues into animal tissues may lead to antibiotic resistance. For the protection of humans and animals from this problem, a fast and highly sensitive analytical method based on ultra‐high‐performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS) was developed and validated in this study for the quantitative determination of CAP in poultry meat and beef samples. Quick, easy, cheap, effective, rugged, and safe (QuEChERS) method was used for the extraction of CAP residues. The developed method was validated in terms of linearity, accuracy, precision, and specificity. Poultry meat and beef samples were extracted with 20 ml water–acetonitrile (1:1, v/v) and cleaned up by MgSO(4), primary secondary amine, and C18 powder. The method was found to be linear in a wide concentration range, with correlation coefficient of higher than 0.999. The repeatability and reproducibility of this method were satisfactory. The achieved limit of detection and limit of quantification were 0.16 and 0.50 ng/g, respectively. Recoveries were estimated at 5 and 10 ng/g spiking levels in the range of 99%–111% with the coefficient of variation 0.48%–12.48% for spiked samples, and the matrix enhancement effects were mild in the range of 80%–85%. In this study, the levels of CAP residue in tested real samples were found below the detection limit. The method proved to be suitable for CAP determination in all kinds of samples tested and also efficient for the application of routine analysis.
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spelling pubmed-84978352021-10-12 Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry Akter Mou, Salma Islam, Rafiza Shoeb, Mohammad Nahar, Nilufar Food Sci Nutr Original Research Chloramphenicol (CAP), a bacteriostatic antibiotic, is used for the treatment of bacterial infections in human and animals. Continual exposure of CAP residues into animal tissues may lead to antibiotic resistance. For the protection of humans and animals from this problem, a fast and highly sensitive analytical method based on ultra‐high‐performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS) was developed and validated in this study for the quantitative determination of CAP in poultry meat and beef samples. Quick, easy, cheap, effective, rugged, and safe (QuEChERS) method was used for the extraction of CAP residues. The developed method was validated in terms of linearity, accuracy, precision, and specificity. Poultry meat and beef samples were extracted with 20 ml water–acetonitrile (1:1, v/v) and cleaned up by MgSO(4), primary secondary amine, and C18 powder. The method was found to be linear in a wide concentration range, with correlation coefficient of higher than 0.999. The repeatability and reproducibility of this method were satisfactory. The achieved limit of detection and limit of quantification were 0.16 and 0.50 ng/g, respectively. Recoveries were estimated at 5 and 10 ng/g spiking levels in the range of 99%–111% with the coefficient of variation 0.48%–12.48% for spiked samples, and the matrix enhancement effects were mild in the range of 80%–85%. In this study, the levels of CAP residue in tested real samples were found below the detection limit. The method proved to be suitable for CAP determination in all kinds of samples tested and also efficient for the application of routine analysis. John Wiley and Sons Inc. 2021-08-16 /pmc/articles/PMC8497835/ /pubmed/34646535 http://dx.doi.org/10.1002/fsn3.2530 Text en © 2021 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Akter Mou, Salma
Islam, Rafiza
Shoeb, Mohammad
Nahar, Nilufar
Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
title Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
title_full Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
title_fullStr Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
title_full_unstemmed Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
title_short Determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
title_sort determination of chloramphenicol in meat samples using liquid chromatography–tandem mass spectrometry
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497835/
https://www.ncbi.nlm.nih.gov/pubmed/34646535
http://dx.doi.org/10.1002/fsn3.2530
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