首页|磁性固相萃取净化-超高效液相色谱-串联质谱同时测定尿液中6种鹅膏肽类毒素

磁性固相萃取净化-超高效液相色谱-串联质谱同时测定尿液中6种鹅膏肽类毒素

扫码查看
目的 建立磁性纳米材料萃取净化结合超高效液相色谱-串联质谱(UPLC-MS/MS)同时测定尿液中α-鹅膏毒肽、β-鹅膏毒肽、γ-鹅膏毒肽、羧基二羟鬼笔毒肽、二羟鬼笔毒肽和羧基三羟鬼笔毒肽的检测方法.方法 尿液样本经C18功能化磁性纳米颗粒(Fe3O4@SiO2@C18)的萃取净化,采用超高效液相色谱-串联质谱电喷雾电离(ESI),多反应监测(MRM)模式测定6种鹅膏肽类毒素.结果 6种鹅膏肽类毒素的线性范围为0.50~50.00 ng/ml,均呈良好的线性关系;检出限为0.05~0.15 μg/kg,定量限为0.15~0.50 μg/kg,平均加标回收率为83.5%~102.3%之间,相对标准偏差(RSD)为2.55%-5.67%.结论 该方法简便快速,结果准确可靠,适用于尿液中6种鹅膏肽类毒素检测.
Simultaneous determination of six kinds of amanita peptide toxins in urine by ultra performance liquid chromatography-tandem mass spectrometry with magnetic solid-phase extraction
Objective To establish a method for the simultaneous determination of α-amanitin,β-amanitin,γ-amanitin,phallacidin,phalloidin and phallisacin in urine by ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS)with magnetic solid-phase extraction.Methods Urine samples were extracted and purified by C18 func-tionalized magnetic nanoparticles(Fe3O4@SiO2@C18).Six amanita peptide toxins were determined by a mass spectrometer coupled with electrospray ionization(ESI)and multiple reaction monitoring(MRM)mode.Results The linear range of six amanita peptide toxins was 0.50-50.00 ng/ml,and all showed good linear relationship.The limits of detection were 0.05-0.15 μg/kg and the limits of quantification were 0.15-0.50 μg/kg.The average recoveries of the method ranged from 83.5%to 102.3%,and the relative standard deviation(RSD)ranged from 2.55%to 5.67%.Conclusion The method is rapid,simple and accurate for the determination of six kinds of amanita peptide toxins in urine.

Amanita peptide toxinsMagnetic solid-phase extractionUrineUltra performance liquid chromatography-tandem mass spectrometry

崔勇、张冠英、刘智

展开 >

吉林省卫生监测检验中心理化检验所,吉林 长春 130062

长春中医药大学

鹅膏肽类毒素 磁性固相萃取 尿液 超高效液相色谱-串联质谱

2024

中国卫生工程学
中华预防医学会,吉林省预防医学会

中国卫生工程学

影响因子:0.416
ISSN:1671-4199
年,卷(期):2024.23(5)