首页|液相色谱串联质谱法检测草铵膦、草甘膦及其代谢物在水和土壤中的残留

液相色谱串联质谱法检测草铵膦、草甘膦及其代谢物在水和土壤中的残留

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利用超高效液相色谱-串联质谱仪(UHPLC-MS/MS),结合固相萃取净化建立了在水和土壤中同时快速测定草甘膦、草铵膦及其6种代谢物的多残留分析方法.前处理采用Oasis MCX和Oasis MAX固相萃取柱提取,2%甲酸甲醇-水(体积比为1∶1)洗脱,旋干后0.1%氨水定容,UHPLC-MS/MS检测.方法的线性范围为0.02~0.5 mg/L;在水中添加水平为0.000 1 mg/L和0.001 mg/L时,草甘膦、草铵膦及其代谢物的回收率为72.8%~94.2%,RSD为2.3%~16.1%;土壤中添加水平为0.001 mg/kg和0.01 mg/kg时,草甘膦、草铵膦及其代谢物的回收率为70.6%~88.5%,RSD为3.6%~12.8%.本方法准确、灵敏、全面,适用于草甘膦、草铵膦及其代谢物在水土环境中的残留检测及监测.
Determination of glufosinate-ammonium,glyphosate and their metabolites in soil and water by HPLC-MS/MS
An ultra-high performance liquid chromatography-tandem mass spectrometry(UHPLC-MS/MS)combined with solid-phase extraction purification was used to establish a multi-residue analysis method for the simultaneous determination of glyphosate,glufosinate-ammonium and their six metabolites in water or soil.Oasis MCX and Oasis MAX solid phase extraction columns were used in pre-treatment,and then 2%formic acid methanol water(volume ratio of 1∶1)was used for elution.The eluent collected was evaporated to dryness by a rotary evaporator and diluted with 0.1%ammonia.The linear range of the method was 0.02-0.5 mg/L.Under the spiked level of 0.000 1 and 0.001 mg/L in the purified water,the recoveries were 72.8%-94.2%and the relative standard deviations were 2.3%-16.1%,respectively.Under the spiked level of 0.001 mg/kg and 0.01 mg/kg in the soil,the recoveries were 70.6%-88.5%and the relative standard deviations were 3.6%-12.8%,respectively.The method is accurate,sensitive and comprehensive,which could be used to analyze the content of glyphosate,glufosinate-ammonium and their metabolites in low concentration samples in environmental test.

water and soilglufosinate-ammoniumglyphosatemetaboliteUHPLC-MS/MSresidue analysis

姬乐园、王平平、朱丽珍、毛连纲、张兰、蒋红云、刘新刚

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中国农业科学院植物保护研究所,植物病虫害综合治理全国重点实验室,北京 100193

水和土壤 草铵膦 草甘膦 代谢物 UHPLC-MS/MS 残留检测

国家自然科学基金国际(地区)合作与交流项目

32261133527

2024

植物保护
中国植物保护学会 中国农业科学院植物保护研究所

植物保护

CSTPCD北大核心
影响因子:1.004
ISSN:0529-1542
年,卷(期):2024.50(2)
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