首页|基于复合纳米材料比色/荧光双信号的黄曲霉毒素B1检测

基于复合纳米材料比色/荧光双信号的黄曲霉毒素B1检测

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以黄曲霉毒素B1(aflatoxin B1,AFB1)为检测目标物,使用二氧化硅纳米颗粒为载体富集谷胱甘肽和黄曲霉毒素适配体制备识别探针,二氧化锰纳米颗粒与石墨烯量子点偶联的复合纳米材料为底物,通过谷胱甘肽与底物的反应构建了一种比色和荧光双模信号输出的高灵敏便携式检测平台.在优化条件下,对本方法的检测性能及特异性进行研究,得到比色信号的回归方程为△A=-0.275-0.0211gC,检出限为2.732× 10-12g/mL;荧光信号的回归方程为△F=928.733+71.7791gC,检出限为1.667×10-12g/mL,两种方法都具备良好检测特异性.将该方法用于牛奶、大米、麦片、酱油和白醋5种实际样品中AFB1的检测,并与传统方法进行对比,本方法结果具有较高的准确度.
Colorimetric and Fluorescent Dual-Mode Detection of Aflatoxin B1 Using Composite Nanomaterial
In this study,a highly sensitive portable platform with colorimetric and fluorescent dual-mode signal output for the detection of aflatoxin B,(AFB1)was developed based on the reaction between glutathione and a composite nanomaterial consisting of manganese dioxide(MnO2)nanoparticles and graphene quantum dots(GQDs)as a substrate.The recognition probe was prepared by using silica nanoparticles as a carrier to enrich glutathione and AFB1 aptamers.Under optimal conditions,analytical figures of merit such as specificity of this method were studied.The regression equation for colorimetric signal was △A=-0.275-0.02 1lgC and the detection limit was 2.732 × 10-12 g/mL;the regression equation for fluorescence signal was △F=928.733+71.7791gC and the detection limit was 1.667 × 10-12 g/mL.Both methods had good detection specificity.The proposed method was applied in the detection of food samples,such as milk,rice,oatmeal,soy sauce and white vinegar with higher accuracy,compared with the traditional method.

aflatoxin B1manganese dioxide nanoparticlesgraphene quantum dotsaptamerdual-mode signal

李阳、鲁迨、周州、陈丽叶、谢新辉、吴家浩、赵倩、石星波

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湖南农业大学食品科学技术学院,食品科学与生物技术湖南省重点实验室,湖南长沙 410128

湖南省产商品质量监督检验研究院,湖南长沙 410007

黄曲霉毒素B1 二氧化锰纳米颗粒 石墨烯量子点 核酸适配体 双模信号

国家自然科学基金青年科学基金

32001778

2023

食品科学
北京食品科学研究院

食品科学

CSTPCDCSCD北大核心
影响因子:1.327
ISSN:1002-6630
年,卷(期):2023.44(24)
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