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当前位置: 首页 > 文章 > β-环糊精及其衍生物对黄曲霉毒素B_1荧光增强机理研究 食品科学 2012,33 (15) 28-33
Position: Home > Articles > Mechanisms Underlying Fluorescence Enhancement of Aflatoxin B_1 by β-Cyclodextrin and Its Derivatives FOOD SCIENCE 2012,33 (15) 28-33

β-环糊精及其衍生物对黄曲霉毒素B_1荧光增强机理研究

作  者：
张敏;郭婷;刘馨;肖洁;张宇昊;马良
单  位：
西南大学食品科学学院;四川省资阳产品质量监督检验所;重庆市特色食品工程技术研究中心
关键词：
β-环糊精;AFB1;荧光增强;超分子包络物
摘  要：
利用光谱法、Benesi-Hildebrand法、热力学方法研究β-环糊精(β-CD)及其衍生物对黄曲霉毒素B1(AFB1)荧光增强机理,探讨溶剂中甲醇体积比、M-β-CD浓度、时间、干扰离子等因素对荧光增强作用的影响。根据Benesi-Hildebrand法确定7种β-环糊精及其衍生物在低浓度时与AFB1包络比为1:1,高浓度时包络比为2:1。采用热力学方法计算了包合常数最大的M-β-CD与AFB1包合过程的熵变(ΔS)、焓变(ΔH)及自由能变化(ΔG)均为负值,说明包合反应是放热反应且能自发进行,焓变是形成超分子包络物的主要驱动力。紫外吸收光谱及KI淬灭实验表明AFB1进入M-β-CD空腔从而使荧光得到保护。得出结论:7种β-环糊精及其衍生物与AFB1通过形成超分子包络物可大幅增强AFB1荧光发射强度,提高AFB1荧光分析法的检测灵敏度。
译  名：
Mechanisms Underlying Fluorescence Enhancement of Aflatoxin B_1 by β-Cyclodextrin and Its Derivatives
作  者：
ZHANG Min 1,2,GUO Ting 1,LIU Xin 1,XIAO Jie 1,ZHANG Yu-hao 1,3,MA Liang 1,3,(1.College of Food Science,Southwest University,Chongqing 400716,China;2.Product Quality Supervision and Assay Office of Ziyany,Ziyang 641300,China;3.Chongqing Special Food Programme and Technology Research Center,Chongqing 400716,China)
关键词：
β-cyclodextrin;aflatoxin B1;fluorescence enhancement;supramolecular inclusion
摘  要：
The mechanisms underlying fluorescence enhancement of aflatoxin B1(AFB1) by β-cyclodextrin(β-CD) and its derivatives were explored using spectroscopy,Benesi-Hidebrand analysis and thermodynamics.Moreover the effects of methanol volume percentage,M-β-CD concentration,reaction time and interfering ions on fluorescence enhancement were analyzed.β-CD and its six derivatives showed an inclusion ratio to AFB1 of 1:1 at low concentrations and 2:1 at high concentrations.The thermodynamic parameters entropy change(ΔS),enthalpy change(ΔH) and free energy change(ΔG) for maximum inclusion constant between M-β-CD and AFB1 were negative,suggesting that the inclusion reaction is exothermic and can occur spontaneously.Enthalpy change was the dominant force during the formation of inclusion complexes.UV absorption spectra and KI quenching experiments showed that AFB1 could enter M-β-CD cavity to protect fluorescence.Therefore,β cyclodextrin and its derivatives can allow considerable enhancement in the fluorescence emission intensity of AFB1 by the formation of supramolecular inclusion complexes,resulting in increased sensitivity of AFB1fluorescence analysis.

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