何宗剑, 朱定姬, 朱杰, 黄克建. 气相色谱-质谱法快速检测全血和尿液中百草枯、敌草快[J]. 职业卫生与应急救援, 2020, 38(4): 419-423. DOI: 10.16369/j.oher.issn.1007-1326.2020.04.025
引用本文: 何宗剑, 朱定姬, 朱杰, 黄克建. 气相色谱-质谱法快速检测全血和尿液中百草枯、敌草快[J]. 职业卫生与应急救援, 2020, 38(4): 419-423. DOI: 10.16369/j.oher.issn.1007-1326.2020.04.025
HE Zongjian, ZHU Dingji, ZHU Jie, HUANG Kejian. Rapid detection of paraquat and diquat in whole blood and urine by gas chromatography-mass spectrometry[J]. Occupational Health and Emergency Rescue, 2020, 38(4): 419-423. DOI: 10.16369/j.oher.issn.1007-1326.2020.04.025
Citation: HE Zongjian, ZHU Dingji, ZHU Jie, HUANG Kejian. Rapid detection of paraquat and diquat in whole blood and urine by gas chromatography-mass spectrometry[J]. Occupational Health and Emergency Rescue, 2020, 38(4): 419-423. DOI: 10.16369/j.oher.issn.1007-1326.2020.04.025

气相色谱-质谱法快速检测全血和尿液中百草枯、敌草快

Rapid detection of paraquat and diquat in whole blood and urine by gas chromatography-mass spectrometry

  • 摘要:
    目的 建立测定全血、尿液中百草枯和敌草快的气相色谱-质谱(GC-MS)方法。
    方法 以乙基百草枯为内标,含体积分数10%高氯酸的乙醇溶液沉淀蛋白,加入硼氢化钠-氯化镍还原体系,在60℃下还原反应40 min,经1.0 mL乙酸乙酯萃取,在GC-MS选择离子监测模式(SIM)下测定。
    结果 百草枯、敌草快在质量浓度范围0.05~2.0 μg/mL(全血)、0.02~2.0 μg/mL(尿液)内的线性关系良好,相关系数分别为0.999 5~0.999 9,方法检出限分别为0.004~0.008 μg/mL,加标回收率为94.1%~115.0%,相对标准偏差(RSD)为1.1%~6.6%。全血、尿液中百草枯和敌草快在4℃冰箱中至少可以保存7 d。
    结论 该方法简单准确、灵敏度高,能够满足全血和尿液样品中百草枯、敌草快的快速检测。

     

    Abstract:
    Objective To establish a method for determination of paraquat and diquat in whole blood and urine by gas chromatography-mass spectrometry(GC-MS).
    Methods Ethyl paraquat was used as internal standard, 10% perchloric acid-ethanol solution (V/V) was added to precipitate protein, and sodium borohydride-nickel chloride(NaBH4-NiCl2) were used in the reduction system. The reaction time was 40 minutes at 60℃, then the analytes were extracted with 1.0 mL ethyl acetate, and finally detected in GC-MS selective ion monitoring mode(SIM).
    Results The linearities were good within investigated mass concentration ranges of 0.05 to 2.0 μg/mL in the whole blood and 0.02 to 2.0 μg/mL in urine of the paraquat and diquat. The correlation coefficients were 0.999 5 to 0.999 9, the detection limits of the method were 0.004 to 0.008 μg/mL, and the recoveries at three spiked levels were within 94.1%-115.0%, with 1.1%-6.6% of the relative standard deviation (RSD). Paraquat and diquat in blood and urine could be stored for at least 7 days at 4℃.
    Conclusion The established method is simple, accurate, and sensitive for rapid detection of paraquat and diquat in whole blood and urine samples.

     

/

返回文章
返回