Article

Determination of flunixin and 5-hydroxy flunixin residues in livestock and fishery products using LC-MS/MS

Sunyoung Park1, Yong Seok Choi2, Ji Young Kim1,*, Jang-Deok Choi1, Guiim Moon1
Author Information & Copyright
1National Institute of Food & Drug Safety Evaluation, Pesticides & Veterinary Drug Residues Division, Cheongju-si 28159, Korea.
2College of Pharmacy, Dankook University, Cheonan 31116, Korea.
*Corresponding Author: Ji Young Kim. E-mail: jykim98@korea.kr.

© Copyright 2024 Korean Society for Food Science of Animal Resources. This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: Jan 29, 2024 ; Revised: Mar 12, 2024 ; Accepted: Mar 12, 2024

Published Online: Mar 21, 2024

Abstract

Flunixin is a veterinary nonsteroidal anti-inflammatory agent whose residues have been investigated in their original form within tissues such as muscle and liver. However, flunixin remains in milk as a metabolite, and 5-hydroxy flunixin has been used as the primary marker for its surveillance. This study aimed to develop a quantitative method for detecting flunixin and 5-hydroxy flunixin in milk and to strengthen the monitoring system by applying to other livestock and fishery products. Two different methods were compared, and the target compounds were extracted from milk using an organic solvent, purified with C18, concentrated, and reconstituted using a methanol-based solvent. Following filtering, the final sample was analyzed using liquid chromatography-tandem mass spectrometry. Method 1 is environmentally friendly due to the low use of reagents and is based on a multi-residue, multi-class analysis method approved by the Ministry of Food and Drug Safety. The accuracy and precision of both methods were 84.6−115% and 0.7−9.3%, respectively. Owing to the low matrix effect in milk and its convenience, Method 1 was evaluated for other matrices (beef, chicken, egg, flatfish, and shrimp) and its recovery and coefficient of variation are sufficient according to the Codex criteria (CAC/GL 71-2009). The limits of detection and quantification were 2−8 and 5−27 µg/kg for flunixin and 2−10 and 6−33 µg/kg for 5-hydroxy flunixin, respectively. This study can be used as a monitoring method for a positive list system that regulates veterinary drug residues for all livestock and fisheries products.

Keywords: Flunixin; Veterinary drug; Residues; Food safety; LC-MS/MS