Patyra Ewelina, Kwiatek Krzysztof
Department of Hygiene and Animal Feedingstuffs, National Veterinary Research Institute, 24-100 Puławy, Poland.
J Vet Res. 2024 Mar 23;68(1):129-136. doi: 10.2478/jvetres-2024-0011. eCollection 2024 Mar.
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.
本文介绍了一种快速简便的分析方法,用于测定动物药饵中的四种磺胺类药物(磺胺嘧啶、磺胺甲基嘧啶、磺胺二甲嘧啶和磺胺甲恶唑)、甲氧苄啶、泰乐菌素和阿莫西林。
对18个药饵样品进行活性物质分析。分析方案使用乙腈和pH值为4.5的0.05 M磷酸缓冲液的混合物来提取七种抗菌物质。提取后,样品用超纯水稀释,并用液相色谱-质谱联用仪进行分析。所开发的方法在线性、选择性、定量限和测定限、重复性、再现性和不确定度方面进行了验证。
该方法的验证是按照欧盟委员会实施条例(EU)2021/808和国际人用药品注册技术协调会(ICH)指南规定的标准进行的。对于所有分析的抗菌物质,该方法的平均回收率为90.8%至104.5%,重复性和再现性的变异系数分别在3.2 - 6.9%和5.2 - 8.3%范围内。所有七种分析物的检测限和定量限分别为5.4 mg/kg至48.3 mg/kg和10.4 mg/kg至119.3 mg/kg。该方法的不确定度因化合物而异,范围为14.0%至24.0%。经过验证的方法成功应用于18个药饵样品。
所开发的方法可成功用于常规控制药饵中七种抗菌物质的含量和均匀性。