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作 者:侯冰 HOU Bing(Dandong Market Supervision Service Center(Dandong Inspection,Examination&Certification Centre),Dandong 118000,China)
机构地区:[1]丹东市市场监管事务服务中心(丹东市检验检测认证中心),辽宁丹东118000
出 处:《现代食品》2024年第15期173-175,共3页Modern Food
基 金:2022年度辽宁省市场监督管理局科技计划项目(2022ZC008)。
摘 要:采用超高效液相色谱串联质谱法建立了牛、羊脂肪中三氯苯达唑及其代谢物三氯苯达唑酮残留量的测定方法。样品用乙腈提取,正己烷净化,采用BEH C_(18)色谱柱、乙腈-0.1%甲酸溶液梯度洗脱分离,电喷雾负离子模式测定。结果显示,三氯苯达唑和三氯苯达唑酮在5~500 ng·mL^(-1)浓度范围内线性关系良好(R^(2)>0.99);方法检出限和定量限均为0.5μg·kg^(-1)和1μg·kg^(-1);在1μg·kg^(-1)、10μg·kg^(-1)、50μg·kg^(-1)添加水平下平均回收率在81.6%~102.3%,批内(n=6)及批间(n=3)相对标准偏差≤14.0%。方法准确度高,精密度好,适用于牛、羊脂肪中三氯苯达唑及其代谢物残留量的测定。A method for the determination of residues of triclabendazole and its metabolite ketotriclabendazole in cattle and sheep fat was established using ultra performance liquid chromatography-tandem mass spectrometry.The sample was extracted with acetonitrile,purified with hexane,separated by BEH C18 chromatographic column,gradient elution with acetonitrile and 0.1%formic acid solution,and determined by electrospray negative ion mode.The results showed that there was a good linear relationship(R^(2)>0.99)between triclabendazole and ketotriclabendazole in the range of 5~500 ng·mL^(-1);the detection limit and quantification limit of the method were both 0.5μg·kg^(-1)and 1μg·kg^(-1);the average recoveries were between 81.6%and 102.3%at the addition levels of 1μg·kg^(-1),10μg·kg^(-1),and 50μg·kg^(-1),and the relative standard deviations within the batch(n=6)and between batches(n=3)were≤14.0%.This method has high accuracy and good precision,which is suitable for determination of residues of triclabendazole and its metabolite in cattle and sheep fat.
关 键 词:牛羊脂肪 三氯苯达唑 三氯苯达唑酮 超高效液相色谱串联质谱
分 类 号:TS207.3[轻工技术与工程—食品科学]
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