Simultaneous determination of sulfonamides, trimethoprim, amoxicillin and tylosin in medicated feed by high performance liquid chromatography with mass spectrometry

• Published in: Journal of veterinary research 2024-03, Vol.68 (1), p.129-136
• Main Authors: Patyra, Ewelina, Kwiatek, Krzysztof
• Format: Article
• Language: English
• Subjects: Acetonitrile; Amoxicillin; Chromatography; High-performance liquid chromatography; liquid chromatography–mass spectrometry (LC-MS); Mass spectrometry; Mass spectroscopy; medicated feed; Reproducibility; Scientific imaging; Sulfadiazine; Sulfamerazine; Sulfamethazine; Sulfamethoxazole; Sulfonamides; Trimethoprim; Tylosin
• ISSN: 2450-7393; 2450-8608; 2450-8608
• DOI: 10.2478/jvetres-2024-0011

The article presents a rapid and simple analytical procedure for determination of four sulfonamides (sulfadiazine, sulfamerazine, sulfamethazine and sulfamethoxazole), trimethoprim, tylosin and amoxicillin in animal medicated feed. Eighteen medicated feed samples were analysed for active substances. The analytical protocol used a mixture of acetonitrile and 0.05 M phosphoric buffer, pH 4.5 for the extraction of seven antibacterial substances. After extraction, the samples were diluted in Milli-Q water and analysed by liquid chromatography with mass spectrometry. The developed procedure was subjected to validation in terms of linearity, selectivity, limits of quantification and determination, repeatability, reproducibility and uncertainty. The validation of the method was carried out in accordance with the criteria set out in Commission Implementing Regulation (EU) 2021/808 and ICH guidelines. This method provided average recoveries of 90.8 to 104.5% with coefficients of variation for repeatability and reproducibility in the ranges of 3.2-6.9% and 5.2-8.3%, respectively for all analysed antibacterial substances. The limit of detection and limit of quantification for all seven analytes ranged from 5.4 mg/kg to 48.3 mg/kg and from 10.4 mg/kg to 119.3 mg/kg, respectively. The uncertainty of the method depending on the compound varied from 14.0% to 24.0%. The validated method was successfully applied to the 18 medicated feeds. The developed method can be successfully used to routinely control the content and homogeneity of seven antibacterial substances in medicated feed.