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Food, fibre and pharmaceuticals from animals
RESEARCH ARTICLE

Multi-residue analysis of eight veterinary drugs in buffalo milk using liquid chromatography-tandem mass spectrometry

Xingchen Huang https://orcid.org/0000-0002-5892-8173 A # , Pingchuan Zhu B # , Qinqiang Sun C , Runfeng Liu C , Pengfei Zhang D , Yuqi Liu A , Wei Hu B , Huiyan Xu C , Yangqing Lu https://orcid.org/0000-0003-1641-6142 C * and Qiang Fu https://orcid.org/0000-0003-4192-6427 B *
+ Author Affiliations
- Author Affiliations

A College of Life Science and Technology, Guangxi University, Nanning, China.

B State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi University, Nanning, China.

C College of Animal Science and Technology, Guangxi University, Nanning, China.

D Guangxi Academy of Sciences, Nanning, China.

* Correspondence to: luyangqing@gxu.edu.cn, gxfuq@163.com
# These authors contributed equally to this paper

Handling Editor: Sathya Velmurugan

Animal Production Science 63(14) 1435-1444 https://doi.org/10.1071/AN22437
Submitted: 25 November 2022  Accepted: 13 June 2023   Published: 4 July 2023

© 2023 The Author(s) (or their employer(s)). Published by CSIRO Publishing

Abstract

Context: There are still comparatively few methods for the detection of drug residues in buffalo milk.

Aims: This study aims to develop a method for the detection of drug residues in buffalo milk.

Methods: In this study, we developed an analytical method for veterinary drug residues in buffalo milk using liquid chromatography–tandem mass spectrometry. The multi-residue method was established for the simultaneous identification and quantitation of eight common veterinary drugs, including metronidazole, salbutamol, atropine, trimethoprim, hydrocortisone, kitasamycin, roxithromycin and tylosin.

Key results: The sample processing method for buffalo milk was compared and optimised. The precision, recovery and matrix effects of the method were validated. The precision and accuracy of all analytes ranged from 1.81% to 12.35% and 1.25% to 14.57%, respectively. The average recovery percentages varied between 93.59% and 114.57%, and the average matrix effect ranged from 87.12% to 103.76%. All eight analytes in buffalo milk exhibited stability under different treatment conditions.

Conclusions: The developed method was successfully applied to laboratory analysis and routine sample analysis. The method was demonstrated to be rapid, sensitive and reliable for the rapid monitoring of veterinary drug residues in buffalo milk.

Implications: The findings of this study contribute to the risk assessment of veterinary drug residues for preventing the human consumption of contaminated buffalo milk and its derivatives.

Keywords: analytical method development, average matrix effect, buffalo milk, kitasamycin, LC-MS/MS, multi-residue analysis, validation, veterinary drugs.


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