A Quantitative Method for Residues of Macrolide Antibiotics in Porcine Kidney by Liquid Chromatography/Tandem Mass Spectrometry

Abstract

Abstract An LC/MS/MS-based multiresidue quantitative method was developed for the macrolides erythromycin A, neospiramycin I, oleandomycin, spiramycin I, tilmicosin, and tylosin A in porcine kidney tissues. The Canadian Food Inspection Agency (CFIA) had as part of its analytical scope an LC/UV method for quantification of residues of two macrolide antibiotics, tilmicosin and tylosin A, in the kidney, liver, and muscle of cattle, swine, and poultry. The method could not reliably detect concentrations below 10 μg/kg. To increase the scope of the CFIA's analytical capabilities, a sensitive multiresidue quantitative method for macrolide residues in food animal tissues was required. Porcine kidney samples were extracted with acetonitrile and alkaline buffer and cleaned-up using silica-based C18 SPE cartridges. Sample extracts were analyzed using LC/MS/MS with positive electrospray ionization. Fitness for purpose was verified in a single- laboratory validation study using a second analyst. The working analytical range was 5 to 50 μg/kg. LOD and LOQ were 0.5 to 0.6 μg/kg and 1.5 to 3.0 μg/kg, respectively. Limits of identification were 0.5 to 2.0 μg/kg. Relative intermediate precisions were 8 to 17%. Average absolute recoveries were 68 to 76%.