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当前位置: 首页 > 文章 > 分散固相萃取-超高效液相色谱-串联质谱法测定不同茶类中2,4-表芸苔素内酯残留 茶叶科学 2018 (6) 589-594
Position: Home > Articles > Determination of 2,4-Epibrassinolide in Different Teas by Ultra Performance Liquid Chromatography Coupled to Tandem Mass Spectrometry with Dispersive Solid Phase Extraction Journal of Tea Science 2018 (6) 589-594

分散固相萃取-超高效液相色谱-串联质谱法测定不同茶类中2,4-表芸苔素内酯残留

作  者：
诸力;陈红平;柴云峰;马桂岑;郝振霞;王晨;刘新;鲁成银
单  位：
农业农村部茶叶质量监督检验测试中心中国农业科学院茶叶研究所农业农村部茶叶产品质量安全风险评估实验室(杭州)农业部茶叶质量安全控制重点实验室
关键词：
茶叶;2,4-表芸苔素内酯;天丰素;油菜素甾醇;超高效液相色谱串联质谱;分散固相萃取
摘  要：
建立了一种分散固相萃取-超高效液相色谱-串联质谱快速测定不同茶类中2,4-表芸苔素内酯的方法。样品经乙腈均质提取,通过C18、强阴离子交换剂(SAX)和石墨化碳黑(GCB)混合吸附剂分散萃取前处理,以HSS T3色谱柱分离,采用ESI正离子扫描和可编程多反应监测模式(SMRM)检测,基质匹配溶液外标法定量。2,4-表芸苔素内酯在0.8～800μg·L~(-1)范围内线性良好(R2>0.999)。在不同茶类(绿茶、红茶、白茶、黑茶、乌龙茶)中标准样含量20、40和200μg·kg~(-1)添加水平下,目标化合物回收率均介于75.5%～93.6%之间,相对标准偏差RSD值在0.4%～7.0%之间(n=6),方法定量限(LOQ,S/N=10)在0.55～1.46μg·kg~(-1)之间。该方法稳定、准确、灵敏,能够满足各茶类检测需求。
译  名：
Determination of 2,4-Epibrassinolide in Different Teas by Ultra Performance Liquid Chromatography Coupled to Tandem Mass Spectrometry with Dispersive Solid Phase Extraction
作  者：
ZHU Li;CHEN Hongping;CHAI Yunfeng;MA Guicen;HAO Zhenxia;WANG Chen;LIU Xin;LU Chengyin;Tea Quality and Supervision Testing Center, Ministry of Agriculture and Rural Affairs, Tea Research Institute, Chinese Academy of Agricultural Sciences, Laboratory of Quality and Safety Risk Assessment for Tea, Ministry of Agriculture and Rural Affairs (Hangzhou),Key Laboratory of Tea Quality and Safety Control, Ministry of Agriculture and Rural Affairs;
单  位：
Hangzhou
关键词：
tea;;2,4-Epibrassinolide;;brassinolide;;brassinosteroids;;ultra performance liquid chromatographytandem mass spectrometry;;dispersive solid phase extraction
摘  要：
An efficient method for analyzing 2,4-Epibrassinolide in different teas was developed based on ultra-performance liquid chromatography coupled to tandem mass spectrometry(UPLC-MS/MS). Homogenized samples were extracted with acetonitrile solution, cleaned up with three sorbents including C18, strong anion exchanger(SAX) and graphitized carbon black(GCB). The compound was separated on a HSS T3 column using electrospray Ionization(ESI) mode, detected by scheduled multiple reaction monitoring(SMRM) and quantified bymatrix-matched external standard curves. The compound showed good linearity between the concentration of 0.8-800 μg·L~(-1), with high significant correlation(R2>0.999). The limit of quantitation(LOQ, S/N=10) ranged from 0.55 to 1.46 μg·kg~(-1). In addition, the spiked(20, 40, 200 μg·kg~(-1)) recoveries of tea samples were 75.5%-93.6%, and RSDs were 0.4%-7.0%. The method was accurately and sensitively applied to commercial tea samples, which fulfilled all requirement for the determination of 2,4-Epibrassinolide in tea samples.

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