李献刚,李 芳,贾汶静,沈致淳,张学梅.三通道自动固相萃取-高效液相色谱四极杆串联质谱法检测水中8种痕量微囊藻毒素[J].食品安全质量检测学报,2021,12(2):540-545
三通道自动固相萃取-高效液相色谱四极杆串联质谱法检测水中8种痕量微囊藻毒素
Determination of 8 microcystins in the water by tri-channel automatic solid-phase extraction and high performance liquid chromatography- quadrupole tandem mass spectrometry
投稿时间:2020-09-18  修订日期:2021-01-05
DOI:
中文关键词:  三通道自动固相萃取  微囊藻毒素  高效液相色谱-四极杆串联质谱法
英文关键词:three-channel automatic solid phase extraction  microcystins  high performance liquid chromatography-quadrupole tandem mass spectrometry
基金项目:
作者单位
李献刚 东港海关综合技术服务中心, 国家级农兽药残留及海洋生物毒素检测重点实验室 
李 芳 东港海关综合技术服务中心, 国家级农兽药残留及海洋生物毒素检测重点实验室 
贾汶静 东港海关综合技术服务中心, 国家级农兽药残留及海洋生物毒素检测重点实验室 
沈致淳 东港海关综合技术服务中心, 国家级农兽药残留及海洋生物毒素检测重点实验室 
张学梅 东港海关综合技术服务中心, 国家级农兽药残留及海洋生物毒素检测重点实验室 
AuthorInstitution
LI Xian-Gang Integrated Technical Serivce Center of Donggang Cumstoms, National Level Key Laboratory of Veterinary Drug, Pesticid Residue & Marine Life’s Toxin Detection 
LI Fang Integrated Technical Serivce Center of Donggang Cumstoms, National Level Key Laboratory of Veterinary Drug, Pesticid Residue & Marine Life’s Toxin Detection 
JIA Wen-Jing Integrated Technical Serivce Center of Donggang Cumstoms, National Level Key Laboratory of Veterinary Drug, Pesticid Residue & Marine Life’s Toxin Detection 
SHEN Zhi-Chun Integrated Technical Serivce Center of Donggang Cumstoms, National Level Key Laboratory of Veterinary Drug, Pesticid Residue & Marine Life’s Toxin Detection 
ZHANG Xue-Mei Integrated Technical Serivce Center of Donggang Cumstoms, National Level Key Laboratory of Veterinary Drug, Pesticid Residue & Marine Life’s Toxin Detection 
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中文摘要:
      目的 建立三通道自动固相萃取-高效液相色谱-四极杆串联质谱法检测水中痕量的8种微囊藻毒素的分析方法。方法 采用高自动化的前处理设备, 采用C18固相萃取小柱富集浓缩, 应用液相色谱-四极杆串联质谱法定性定量地检测8种微囊藻毒素。结果 该方法检测水中的8种微囊藻毒素检出限为0.01~0.6 μg/L, 在0.25~62.5 μg/L的线性范围中, 线性相关系数大于0.99。结论 该方法自动化程度高、灵敏度高、定性定量准确、测定浓度范围广。
英文摘要:
      Objective To establish a method for determination of 8 microcystins in water by tri-channel automatic solid-phase extraction and high performance liquid chromatography-quadrupole tandem mass spectrometry. Methods The highly automated pre-processing equipment was adopted, the C18 solid phase extraction column was used for enrichment and concentration, and 8 microcystins were quantitatively and qualitatively determined by liquid chromatography-quadrupole tandem mass spectrometry. Results The limits of detection 8 microcystins in water by this method were 0.01?0.6 g/L. The linear correlation coefficient is greater than 0.99 in the linear range of 0.25?62.5 g/L. Conclusion This method has high automatization, high sensitivity, accurate qualitative and quantitative determination and wide concentration determination range.
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