汤水粉,钱卓真,周佳敏,王丽娟,刘海新,罗方方,位绍红,陈燕婷.固相萃取-液相色谱-串联质谱法测定海参中62种兽药残留[J].食品安全质量检测学报,2024,15(12):230-239
固相萃取-液相色谱-串联质谱法测定海参中62种兽药残留
Determination of 62 kinds of veterinary drug residues in sea cucumber by solid phase extraction with liquid chromatography-tandem mass spectrometry
投稿时间:2024-04-02  修订日期:2024-06-26
DOI:
中文关键词:  固相萃取  高效液相色谱-串联质谱  海参  兽药残留
英文关键词:solid phase extraction  liquid chromatography tandem mass spectrometry  sea cucumber  veterinary drug residues
基金项目:福建省属公益类科研院所基本科研专项(2021R1013008)
作者单位
汤水粉 1. 福建省水产研究所, 福建省海洋生物增养殖与高值化利用重点实验室 
钱卓真 1. 福建省水产研究所, 福建省海洋生物增养殖与高值化利用重点实验室 
周佳敏 2. 厦门华厦学院 
王丽娟 1. 福建省水产研究所, 福建省海洋生物增养殖与高值化利用重点实验室 
刘海新 1. 福建省水产研究所, 福建省海洋生物增养殖与高值化利用重点实验室 
罗方方 1. 福建省水产研究所, 福建省海洋生物增养殖与高值化利用重点实验室 
位绍红 1. 福建省水产研究所, 福建省海洋生物增养殖与高值化利用重点实验室 
陈燕婷 3. 福建省水产技术推广总站 
AuthorInstitution
TANG Shui-Fen 1. Key Laboratory of Cultivation and High-value Utilization of Marine Organisms in Fujian Province, Fisheries Research Institute of Fujian 
QIAN Zhuo-Zhen 1. Key Laboratory of Cultivation and High-value Utilization of Marine Organisms in Fujian Province, Fisheries Research Institute of Fujian 
ZHOU Jia-Min 2. Xiamen Huaxia University 
WANG Li-Juan 1. Key Laboratory of Cultivation and High-value Utilization of Marine Organisms in Fujian Province, Fisheries Research Institute of Fujian 
LIU Hai-Xin 1. Key Laboratory of Cultivation and High-value Utilization of Marine Organisms in Fujian Province, Fisheries Research Institute of Fujian 
LUO Fang-Fang 1. Key Laboratory of Cultivation and High-value Utilization of Marine Organisms in Fujian Province, Fisheries Research Institute of Fujian 
WEI Shao-Hong 1. Key Laboratory of Cultivation and High-value Utilization of Marine Organisms in Fujian Province, Fisheries Research Institute of Fujian 
CHEN Yan-Ting 3. Fujian Fisheries Technology Extension Center 
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中文摘要:
      目的 建立固相萃取结合高效液相色谱-串联质谱同时测定海参中62种药物的检测方法。方法 样品加水分散后经1.0%甲酸乙腈溶液提取, PEP固相萃取柱净化后, 采用Waters X-Bridge-C18色谱柱分离、0.2%甲酸水溶液-甲醇为流动相进行梯度洗脱, 使用选择离子监测模式检测。结果 62种兽药在0.50~100.00 ng/mL范围内呈现出良好的线性关系, 线性相关系数r2在0.9953~1.0000范围内。方法检出限为0.25~2.50 μg/kg; 在3个不同浓度添加水平下, 62种兽药的平均回收率在70.3%~119.0%, 批内和批间的相对标准偏差(n=5)为0.13%~14.90%, 均小于15.00%。将该方法应用于30批次海参样品的检测, 其中4批次样品的喹诺酮检测结果阳性, 检出量为5.30~28.00 μg/kg, 与国家标准方法的检测结果相比, 该方法对于本次喹诺酮药物筛查的准确率为100%。结论 该方法灵敏度高, 准确度和精密度良好, 满足我国兽药残留检测要求, 可适用于海参中62种兽药多残留的定性定量分析检测。
英文摘要:
      Objective To establish a method for simultaneous determination of 62 kinds of veterinary drugs in sea cucumber by solid phase extraction combined with liquid chromatography tandem mass spectrometry. Methods The sample was extracted with 1.0% formic acid acetonitrile after dispersed with water. After purification by PEP solid-phase extraction column, 62 kinds of veterinary drugs were separated using Waters X-Bridge-C18 column with 0.2% formic acid aqueous solution and methanol as mobile phase. Detection was performed using selective ion monitoring mode. Results The results showed that 62 kinds of veterinary drugs exhibited good linearity in the range of 0.50–100.00 ng/mL, with a correlation coefficient r2 in the range of 0.9953~1.0000. The detection limit of the method is 0.25–2.50 μg/kg. Recovery test with 3 different addition contents showed the results in the range of 70.3%-119.0%, and all the relative standard deviation RSD (n=5) were 0.13%-14.90%, less than 15.00%. At last the method was applied to detection of 30 sea cucumber samples, among which 4 samples contained quinolone with the amount range from 5.30–28.00 μg/kg. Compared with the results of national standard method, the accuracy of this method for quinolone drug screening was 100% in this study. Conclusion This method has high sensitivity, good accuracy and precision, which meets the requirements of China’s veterinary drug residue detection, and can be applied to the qualitative and quantitative detection of 62 kinds of veterinary drug residues in sea cucumbers.
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