Patyra Ewelina, Kwiatek Krzysztof
Department of Hygiene of Animal Feedingstuffs, National Veterinary Research Institute, 24-100 Puławy, Poland.
J Vet Res. 2020 Jun 20;64(3):433-438. doi: 10.2478/jvetres-2020-0044. eCollection 2020 Sep.
A high-performance liquid chromatographic-diode array detector (HPLC-DAD) method for the determination of amoxicillin in medicated feedingstuffs was developed and validated. The method was used to investigate the quality requirements of animal feedingstuffs (declared content of active substance and feed homogeneity).
Two-gram samples were extracted by potassium phosphate buffer solution. Extracts were filtered and directly analysed by HPLC-DAD without further clean-up. Amoxicillin was separated by acetonitrile and 0.01M phosphate buffer (pH 5.0) on a Phenomenex Luna C18 column.
This method provided average recoveries of 76.1 to 81.6% with coefficients of variation (CV, %) for repeatability and reproducibility in the ranges of 3.7-7.2% and 5.3-7.6%, respectively. The limit of detection was 51.2 mg/kg and limit of quantification was 103.0 mg/kg.
The method was successfully validated and proved to be efficient, precise, and useful for quantification of amoxicillin in medicated feedingstuffs.
建立并验证了一种用于测定加药饲料中阿莫西林的高效液相色谱 - 二极管阵列检测器(HPLC - DAD)方法。该方法用于研究动物饲料的质量要求(活性物质的申报含量和饲料均匀性)。
取2克样品用磷酸钾缓冲溶液提取。提取物过滤后直接用HPLC - DAD分析,无需进一步净化。在Phenomenex Luna C18柱上,用乙腈和0.01M磷酸盐缓冲液(pH 5.0)分离阿莫西林。
该方法的平均回收率为76.1%至81.6%,重复性和再现性的变异系数(CV,%)分别在3.7 - 7.2%和5.3 - 7.6%范围内。检测限为51.2毫克/千克,定量限为103.0毫克/千克。
该方法成功验证,证明对加药饲料中阿莫西林的定量分析高效、精确且实用。