高效液相色谱-串联质谱法测定野生蘑菇中毒样品中5种鹅膏肽类毒素
Determination of five peptide toxins in wild mushroom poisoning samples by high performance liquid chromatography-tandem mass spectrometry
投稿时间:2024-12-12  修订日期:2025-04-03
DOI:
中文关键词:  高效液相色谱-串联质谱法  食物中毒;鹅膏肽类毒素;鹅膏毒肽  鬼笔毒肽
英文关键词:high performance liquid chromatography-tandem mass spectrometry  food poisoning  peptide toxins  amatoxins  phallotoxins
基金项目:深圳市龙岗区科技创新专项资金(LGWJ2023-002)
作者单位
韦慧慰 龙岗区疾病预防控制中心 
刘金明 龙岗区疾病预防控制中心 
孙金影 龙岗区疾病预防控制中心 
唐亮 龙岗区疾病预防控制中心 
郑权东 龙岗区疾病预防控制中心 
AuthorInstitution
WEI Hui-wei Longgang Center for Disease Control and Prevention 
LIU Jin-ming Longgang Center for Disease Control and Prevention 
SUN Jin-ying Longgang Center for Disease Control and Prevention 
TANG Liang Longgang Center for Disease Control and Prevention 
ZHENG Quan-dong Longgang Center for Disease Control and Prevention 
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中文摘要:
      建立高效液相色谱-串联质谱法快速测定野生蘑菇中毒样品中5种鹅膏肽类毒素的分析方法。方法 剩余蘑菇和患者尿液经甲醇提取,250 mgN-丙基乙二胺(N-propyl ethylenediamine, PSA)吸附剂净化,采用Waters CORTECS C18+液相色谱柱分离待测物,以甲醇-2 mmol/L乙酸铵(含0.1%甲酸)为流动相,进行梯度洗脱。采用高效液相色谱-串联质谱检测。结果 5种鹅膏肽类毒素在10.0~500 μg/L质量浓度范围内线性关系良好(r>0.997),蘑菇样品中5种毒素检出限为2.0~3.0 μg/kg,定量限为5.0~10 μg/kg,尿液样品中5种毒素检出限为0.8~1.2 μg/L,定量限为2.0~4.0 μg/L。方法回收率范围为60.1%~94.9%,相对标准偏差为2.0%~17.7% (n=6)。结论 该方法准确、快速,适用于食用野生蘑菇中毒事件剩余蘑菇样品和患者尿液样品中鹅膏肽类毒素的检测。
英文摘要:
      Objective To establish an analytical method for the rapid determination of five peptide toxins in samples from wild mushroom poisoning incidents by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Methods The remaining mushrooms and patient urine samples were extracted by methanol, purified by 250 mg N-propyl ethylenediamine (PSA), and separated by Waters CORTECS C18+ liquid chromatography column. The mobile phase consisted of methanol and 2 mmol/L ammonium acetate (containing 0.1% formic acid) under gradient elution. Determined by HPLC-MS/MS. Results The five peptide toxins had a good linear relationship (r > 0.997) at the concentration10.0-500 μg/L. The limits of detection (LODs) of the five peptide toxins in the mushroom samples were 2.0-3.0 μg/kg, the limits of quantification (LOQs) were 5.0-10 μg/kg. In the urine samples, the LODs of the five peptide toxins were 0.8-1.2 μg/L, the LOQs were 2.0-4.0 μg/L. The recoveries were 60.1%-94.9%, and the relative standard deviations were 2.0%-17.7% (n = 6). Conclusion This method accurate and rapid, suitable for determination of peptide toxins in residual mushroom and patient urine samples from wild mushroom poisoning incidents.
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