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UPLC-MS/MS法检测中毒血液中α-茄碱和α-卡茄碱

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建立一种超高效液相色谱-三重四极杆串联质谱(UPLC-MS/MS)检验血液中α-茄碱和α-卡茄碱的方法.采用乙腈沉淀蛋白法提取目标物,电喷雾离子源正离子模式(ESI+)下,多反应监控(MRM)分析.结果表明,血液中α-茄碱和α-卡茄碱检出限分别为 0.10 ng/mL和 0.11 ng/mL;在0.5~50 ng/mL范围内线性关系良好,R2 均大于0.998;在低、中、高(0.5 ng/mL、5 ng/mL、50 ng/mL)3种添加浓度中基质效应在 92.64%~110.45%之间,提取回收率在89.23%~105.08%之间,日内、日间精密度RSD均不大于 5.94%.本方法专属性好、灵敏度高、准确性好,可用于快速检验中毒血液α-茄碱和α-卡茄碱.
Determination of α-solanine and α-chaconine in Poisoned Blood by UPLC-MS/MS
To establish a method for the determination of α-solanine and α-chaconine in blood by ultra performance liquid chromatography-triple quadrupole tandem mass spectrometry(UPLC-MS/MS).The target compounds were extracted by acetonitrile precipitation protein method,and analyzed by multiple reaction monitoring(MRM)under positive ion mode(ESI+)of the electrospray ion source.The results show that the detection limits of α-solanine and α-chaconine in blood were 0.10 ng/mL and 0.11 ng/mL,respectively.The linear relationship was good in the range of 0.5~50 ng/mL,and R2 was greater than 0.998.In the low,medium and high(0.5 ng/mL,5 ng/mL,50 ng/mL)concentrations,the matrix effect was between 92.64%and 110.45%,the extraction recovery was between 89.23%and 105.08%,and the intra-day and inter-day precision RSD was not above 5.94%.The method has good specificity,high sensitivity and good accuracy,and can be used for rapid detection of α-solanine and α-chaconine in blood.

α-solanineα-chaconinepoisoningbloodultra-performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS)

孙玉婷、李寅

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安徽全诚司法鉴定中心,安徽 合肥 230000

α-茄碱 α-卡茄碱 中毒 血液 超高效液相色谱-三重四极杆串联质谱

2024

山西化工
山西省煤化工发展促进中心 山西省化工学会

山西化工

影响因子:0.293
ISSN:1004-7050
年,卷(期):2024.44(6)