Simultaneous determination of residues of chloramphenicol, thiamphenicol, florfenicol, and florfenicol amine in farmed aquatic species by liquid chromatography/mass spectrometry

• Published in: Journal of AOAC International 2003-05, Vol.86 (3), p.510-514
• Main Authors: VAN DE RIET, Jeffery M, POTTER, Ross A, CHRISTIE-FOUGERE, Melissa, BURNS, B. Garth
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Chloramphenicol - analysis; Chromatography, Liquid; Drug Residues - analysis; Fish and seafood industries; Fishes; Food industries; Fundamental and applied biological sciences. Psychology; General aspects; Mass Spectrometry; Methods of analysis, processing and quality control, regulation, standards; Salmonidae; Thiamphenicol - analogs & derivatives; Thiamphenicol - analysis
• ISSN: 1060-3271; 1944-7922
• DOI: 10.1093/jaoac/86.3.510

A liquid chromatographic (LC)/mass spectrometric (MS) method was developed for determining the residues of chloramphenicol, thiamphenicol, florfenicol, and florfenicol amine in a number of aquatic species. The phenicols are extracted with acetone, the extracts are partitioned with dichloromethane, the aqueous layer is removed, and the organic layer is evaporated to dryness. The residue is dissolved in dilute acid and defatted with hexane, and the aqueous layer is prepared for analysis by LC. The phenicols are determined by reversed-phase LC by using a Hypersil C18-BD column with a water-acetonitrile gradient and MS detection using selected-ion recording. Calibration curves were linear for all analytes between 0.015 and 0.425 ng injected. The relative standard deviations for measurements by the proposed method were < 10% for all of the analytes studied, with recoveries ranging from 71% for florfenicol amine to 107% for florfenicol in salmon tissue spiked at the 2 ng/g level. Detection limits of 0.1 ng/g for florfenicol and chloramphenicol, 0.3 ng/g for thiamphenicol, and 1.0 ng/g for florfenicol amine are easily obtainable. The operational errors, interferences, and recoveries for spiked samples compare favorably with those obtained by established LC methodology. The proposed method is simple, rapid, and specific for monitoring residues of chloramphenicol, thiamphenicol, florfenicol, and florfenicol amine in a number of aquatic species.