首页|超高效液相色谱-三重四极杆串联质谱法检测凉茶中的碱性嫩黄O

超高效液相色谱-三重四极杆串联质谱法检测凉茶中的碱性嫩黄O

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建立了超高效液相色谱-三重四极杆串联质谱法(Ultra Performance Liquid Chromatography-Triple Quadrupole Mass Spectrometry,UPLC-MS/MS)测定凉茶中碱性嫩黄O的快速分析方法.以乙腈作为提取剂,样品经过涡旋混合、超声提取 12 min和高速离心后,所得上清液用微孔滤膜过滤,采用UPLC-MS/MS进行测定,以外标法定量.在质量浓度为0.10~20.00 ng·mL-1 时,碱性嫩黄O具有良好的线性关系,相关系数为 0.999 8,方法检出限为 0.5 μg·kg-1,定量限为 1.0 μg·kg-1.添加水平为 2.0~25.0 μg·kg-1 时,样品加标回收率为 86.7%~95.5%,相对标准偏差为 3.5%~3.9%.该方法精密度好,准确度高,方便快捷,适用于凉茶中碱性嫩黄O含量的测定.
Determination of Auramine O in Herbal Tea by Ultra Performance Liquid Chromatography-Triple Quadrupole Mass Spectrometry
A rapid analytical method for the determination of auramine O in herbal tea was developed using ultra-performance liquid chromatography-triple quadrupole mass spectrometry(UPLC-MS/MS).Acetonitrile was used as the extraction solvent,and the samples were vortex-mixed,subjected to ultrasonic extraction for 12 minutes,and then centrifuged at high speed.The supernatant was filtered through a membrane and analyzed using UPLC-MS/MS with external standard quantification.Auramine O exhibited a good linear relationship in the concentration was 0.10 to 20.00 ng·mL-1,with a correlation coefficient was 0.999 8.The method's limit of detection was 0.5 μg·kg-1,and the limit of quantification was 1.0 μg·kg-1.The recovery rate at spiking levels ranging from 2.0 μg·kg-1 to 25.0 μg·kg-1 was between 86.7%and 95.5%,with the relative standard deviation was 3.5%to 3.9%.This method demonstrates high precision,accuracy,and efficiency,making it suitable for the quantification of auramine O in herbal tea.

auramine Oultra performance liquid chromatography-tandem mass spectrometryherbal tea

黄志宁、郭新东、寻知庆、钟俊威、刘庆

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广州质量监督检测研究院(广州市NQI-质量安全科技协同创新中心),广东广州 511447

碱性嫩黄O 超高效液相色谱-串联质谱法 凉茶

广州市科技计划项目广东省重点领域研发计划项目

2023B04J04072019B020211001

2024

食品安全导刊
商业科技质量中心 北京肉类食品协会

食品安全导刊

影响因子:0.065
ISSN:1674-0270
年,卷(期):2024.(23)