This work involved the validation of a multiresidue method according to the Normative Instruction 24/2009-MAPA for determining 25 analytes, among fluoroquinolones, sulfonamides and trimethoprim in samples of poultry and porcine kidney. The extraction procedure was based on a QuEChERS approach. A liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed using the selected reaction monitoring mode (SRM) and ESI+ ionization. All of the validated figures of merit were evaluated as satisfactory. Accuracy was assessed by recovery studies, varying from 82.7 to 115.5% for porcine kidney and from 91.5 to 110.4% for poultry kidney. Relative standard deviations were lower than 25.5% for porcine kidney, and 29.8% for poultry kidney. Decision limits (CCα) comprised values from 10.37 to 3298.43 μg kg-1 for porcine kidney and 10.08 to 3176.59 μg kg-1 for poultry kidney. Detection capabilities (CCβ) varied from 10.73 to 3396.86 μg kg-1 for porcine kidney and 10.67 to 3253.19 μg kg-1 for poultry kidney. The developed method has been successfully employed in the routine analysis of incurred samples.
CITATION STYLE
Rocha, D. G., Santos, F. A., Gomes, A. A., & Faria, A. F. (2017). Validation of a LC-MS/MS multiresidue methodology based on a QuEChERS approach for the determination of fluoroquinolones, sulfonamides and trimethoprim in poultry and porcine kidney according to the normative instruction 24/2009-MAPA. Journal of the Brazilian Chemical Society, 28(1), 76–86. https://doi.org/10.5935/0103-5053.20160147
Mendeley helps you to discover research relevant for your work.