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Multi-residue Determination of Veterinary Drugs in Fishery Products Using Liquid Chromatography-Tandem Mass Spectrometry

机译:使用液相色谱 - 串联质谱法测定渔业产品中兽药兽药

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The aim of the present study was to develop a multi-residue confirmation method for the analysis of veterinary drugs in fishery products using liquid chromatography-tandem mass spectrometry. The chosen veterinary drugs, which are legally authorized compounds in Korea, were categorized into chemical classes such as amphenicols, cephalosporins, fluoroquinolones, macrolides, penicillins, pleuromutilins, sulfonamides, and tetracyclines. Sample extraction and cleanup were evaluated based on a modified quick, easy, cheap, effective, rugged, and safe procedure using octadecylsilane and primary secondary amine sorbents for purification. Extractions were carried out using an ammonium acetate buffer and ethylenediaminetetraacetic acid disodium salt (pH 4.0) with the addition of ammonium formate in water/acetonitrile. Instrumental analysis was performed using positive/negative ionization in the multiple reaction monitoring mode. The chromatographic conditions were optimized to give run time of &20 min, and the developed method was validated according to the Codex Alimentarius Commission guidelines. Mean recoveries of the veterinary drugs ranged from 68.1 to 111%. At all target concentrations, the intraday precision was &15%, and the lowest limits of detection and quantification were &5 and &10 mu g kg(-1). To evaluate the imprecision arising from residual matrix components, the linearity of our method was determined as &0.98 using matrix-matched calibrations constructed at six different concentrations. The proposed method was applied to the analysis of 403 real samples obtained from domestic markets in Korea, and a number of samples tested positive (27.1%) for the targeted drugs. This analytical method is suitable for reliable detection of veterinary drug residues in fishery products.
机译:本研究的目的是利用液相色谱 - 串联质谱法开发用于分析渔业产品中兽药的多残余物证明方法。在韩国合法授权的化合物中所选择的兽医药物被分类为化学类别,例如杏仁溶胶,头孢菌素,氟喹啉,大环内酯,青霉素,葡萄牙,磺胺酰胺和四环素。使用八癸基硅烷和初级仲胺吸附剂的改进的快速,简单,廉价,有效,粗糙,安全程序评估样品萃取和清洁剂。用乙酸铵缓冲液和乙二胺四乙酸二钠(pH 4.0)在水/乙腈中加入甲酸铵进行萃取。使用多反应监测模式中的正/负电离进行仪器分析。优化色谱条件以提供& LT; 20分钟的运行时间,并根据Codex Alimentarius委员会准则进行验证发达的方法。兽药的平均恢复范围从68.1%到111%。在所有靶浓度下,盘中精度为& 15%,以及最低的检测和定量限制为& 5和& 10 mu g kg(-1)。为了评估残留基质组分引起的不精确,我们的方法的线性度被确定为& GT; 0.98使用以六种不同浓度构建的矩阵匹配的校准。将所提出的方法应用于韩国国内市场获得的403个真实样品的分析,并且许多样品测试了靶向药物的阳性(27.1%)。该分析方法适用于渔业产品中可靠地检测兽药残留物。

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