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超高效液相色谱-三重四极杆串联质谱法同时测定槟榔籽中四种生物碱含量
引用本文:郭晓杰,王盼,庞朝海,韩丙军,阳辛凤.超高效液相色谱-三重四极杆串联质谱法同时测定槟榔籽中四种生物碱含量[J].食品工业科技,2021,42(14):257-263.
作者姓名:郭晓杰  王盼  庞朝海  韩丙军  阳辛凤
作者单位:1.海南大学热带作物学院,海南海口 5702282.中国热带农业科学院分析测试中心,海南海口 5711013.中国热带农业科学院热带作物品种资源研究所,海南海口5700004.海南省热带果蔬产品质量安全重点实验室,海南海口 571101
基金项目:中国热带农业科学院2020年基本业务费专项资金项目(1630082020005);国家重点研发计划项目(2017YFF0207800)
摘    要:目的:采用超高效液相色谱-三重四极杆串联质谱(UPLC-MS/MS)建立槟榔籽中槟榔碱、槟榔次碱、去甲槟榔碱和去甲槟榔次碱含量的检测方法。方法:样品经45%乙醇水溶液提取,利用UPLC-MS/MS法进行检测。色谱条件:采用Waters Atlantis T3(2.1 mm×150 mm,5 μm)色谱柱分离,以0.1%甲酸水溶液-乙腈溶液为流动相进行梯度洗脱,流速0.5 mL·min?1,柱温40 ℃,进样量1 μL。质谱条件:采用电喷雾离子源(ESI+),检测方式多反应监测(MRM)模式扫描;外标法定量。结果:在50~500 ng/mL,槟榔碱、槟榔次碱、去甲槟榔碱和去甲槟榔次碱的质量浓度与峰面积都呈现良好的线性关系(R2>0.99);加样回收率均在规定范围70%~120%内,平均回收率在75.27%~96.70%,RSD<7.0%。结论:该方法的重复性、稳定性良好,仪器精密度较好。

关 键 词:槟榔    槟榔碱    槟榔次碱    去甲槟榔碱    去甲槟榔次碱    超高效液相色谱-串联质谱(UPLC-MS/MS)
收稿时间:2020-09-16

Simultaneous Determination of Four Alkaloids in Betel Nut Seeds by Ultra Performance Liquid Chromatography-Triple Quadrupole Tandem Mass Spectrometry
GUO Xiaojie,WANG Pan,PANG Zhaohai,HAN Bingjun,YANG Xinfeng.Simultaneous Determination of Four Alkaloids in Betel Nut Seeds by Ultra Performance Liquid Chromatography-Triple Quadrupole Tandem Mass Spectrometry[J].Science and Technology of Food Industry,2021,42(14):257-263.
Authors:GUO Xiaojie  WANG Pan  PANG Zhaohai  HAN Bingjun  YANG Xinfeng
Affiliation:1.College of Tropical Crops, Hainan University, Haikou 570228, China2.Analysis and Testing Center, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China3.Tropical Crops Genetic Resources Institute, Chinese Academy of Tropical Agricultural Sciences, Haikou 570000, China4.Hainan Provincial Key Laboratory of Quality and Safety for Tropical Fruits and Vegetables, Haikou 571101, China
Abstract:Objective: A method was developed for the determination of arecoline, arecaidine, guvacoline and guvacine hydrochloride in areca nut seeds by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). Methods: The sample were extracted with 45% ethanol aqueous solution, and detected by UPLC-MS/MS method. Chromatographic conditions: Separated by Waters Atlantis T3 (2.1 mm×150 mm, 5 μm) column, eluted by gradient with 0.1% formic acid aqueous solution-acetonitrile solution as mobile phase, with flow rate of 0.5 mL·min?1, column temperature of 40 ℃, injection volume of 1 μL. Mass spectrometry conditions: Using electrospray ion source (ESI+), detection method multiple reaction monitoring (MRM) mode scanning, the quantitative analysis by external standard method. Results: In the range of 50~500 ng/mL, the mass concentration and peak area of arecoline, arecaidine, guvacoline and guvacine hydrochloride showed a good linear relationship (R2>0.99), and the sample recovery rates were all within the specified range of 70%~120%, the average recovery rate was 75.27%~96.70%, and the RSD was less than 7%. Conclusion: The method was good repeatability, stability, and instrument precision.
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