Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry

Introduction: The main problem in determination of chloramphenicol in food of animal origin is a large number of matrices. The main target of this study was to create a method for determination and confirmation of chloramphenicol in products and food of animal origin. Material and Methods: Each 5 g...

Full description

Bibliographic Details
Main Authors: Śniegocki Tomasz, Gbylik-Sikorska Małgorzata, Posyniak Andrzej
Format: Article
Language:English
Published: Sciendo 2017-09-01
Series:Journal of Veterinary Research
Subjects:
Online Access:https://doi.org/10.1515/jvetres-2017-0032
id doaj-87622149c0444e74bb32b03b4fb0d27b
record_format Article
spelling doaj-87622149c0444e74bb32b03b4fb0d27b2021-09-06T19:40:55ZengSciendoJournal of Veterinary Research2450-86082017-09-0161332132710.1515/jvetres-2017-0032jvetres-2017-0032Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometryŚniegocki Tomasz0Gbylik-Sikorska Małgorzata1Posyniak Andrzej2Department of Pharmacology and Toxicology National Veterinary Research Institute, 24-100 Pulawy, PolandDepartment of Pharmacology and Toxicology National Veterinary Research Institute, 24-100 Pulawy, PolandDepartment of Pharmacology and Toxicology National Veterinary Research Institute, 24-100 Pulawy, PolandIntroduction: The main problem in determination of chloramphenicol in food of animal origin is a large number of matrices. The main target of this study was to create a method for determination and confirmation of chloramphenicol in products and food of animal origin. Material and Methods: Each 5 g matrix sample was mixed with 5 mL of water and 10 mL of acetonitrile/ethyl acetate, homogenised, and centrifuged. The organic layer was evaporated and redissolved in 6 mL of 4% NaCl. The extract was cleaned up by SPE technique. Chloramphenicol was analysed by LC-MS/MS in electrospray mode. Results: The procedure was validated according to the Commission Decision No. 2002/657/EC. The apparent recoveries were in the range of 92.1% to 107.1% with a repeatability less than 11.0% (4.4%-11.0%) and within-laboratory reproducibility below 13.6% (4.7%-13.6%). Conclusion: The method was successfully validated and proved to be efficient, precise, and useful for quantification of chloramphenicol in more than 20 different matrices.https://doi.org/10.1515/jvetres-2017-0032food of animal originchloramphenicolresiduesanalytical method
collection DOAJ
language English
format Article
sources DOAJ
author Śniegocki Tomasz
Gbylik-Sikorska Małgorzata
Posyniak Andrzej
spellingShingle Śniegocki Tomasz
Gbylik-Sikorska Małgorzata
Posyniak Andrzej
Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
Journal of Veterinary Research
food of animal origin
chloramphenicol
residues
analytical method
author_facet Śniegocki Tomasz
Gbylik-Sikorska Małgorzata
Posyniak Andrzej
author_sort Śniegocki Tomasz
title Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
title_short Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
title_full Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
title_fullStr Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
title_full_unstemmed Analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
title_sort analytical strategy for determination of chloramphenicol in different biological matrices by liquid chromatography - mass spectrometry
publisher Sciendo
series Journal of Veterinary Research
issn 2450-8608
publishDate 2017-09-01
description Introduction: The main problem in determination of chloramphenicol in food of animal origin is a large number of matrices. The main target of this study was to create a method for determination and confirmation of chloramphenicol in products and food of animal origin. Material and Methods: Each 5 g matrix sample was mixed with 5 mL of water and 10 mL of acetonitrile/ethyl acetate, homogenised, and centrifuged. The organic layer was evaporated and redissolved in 6 mL of 4% NaCl. The extract was cleaned up by SPE technique. Chloramphenicol was analysed by LC-MS/MS in electrospray mode. Results: The procedure was validated according to the Commission Decision No. 2002/657/EC. The apparent recoveries were in the range of 92.1% to 107.1% with a repeatability less than 11.0% (4.4%-11.0%) and within-laboratory reproducibility below 13.6% (4.7%-13.6%). Conclusion: The method was successfully validated and proved to be efficient, precise, and useful for quantification of chloramphenicol in more than 20 different matrices.
topic food of animal origin
chloramphenicol
residues
analytical method
url https://doi.org/10.1515/jvetres-2017-0032
work_keys_str_mv AT sniegockitomasz analyticalstrategyfordeterminationofchloramphenicolindifferentbiologicalmatricesbyliquidchromatographymassspectrometry
AT gbyliksikorskamałgorzata analyticalstrategyfordeterminationofchloramphenicolindifferentbiologicalmatricesbyliquidchromatographymassspectrometry
AT posyniakandrzej analyticalstrategyfordeterminationofchloramphenicolindifferentbiologicalmatricesbyliquidchromatographymassspectrometry
_version_ 1717767480208785408