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An Ultrasensitive Electrochemiluminescent Immunoassay for Aflatoxin M1 in Milk Based on Extraction by Magnetic Graphene and Detection by Antibody-Labeled CdTe Quantumn Dots-Carbon Nanotubes Nanocomposite

机译:牛奶中黄曲霉毒素M1的超灵敏化学发光免疫分析基于磁性石墨烯的提取和抗体标记的CdTe量子点碳纳米管纳米复合材料的检测

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摘要

An ultrasensitive electrochemiluminescent immunoassay (ECLIA) for aflatoxins M1 (ATM1) in milk using magnetic Fe3O4-graphene oxides (Fe-GO) as the absorbent and antibody-labeled cadmium telluride quantum dots (CdTe QDs) as the signal tag is presented. Firstly, Fe3O4 nanoparticles were immobilized on GO to fabricate the magnetic nanocomposites, which were used as absorbent to ATM1. Secondly, aflatoxin M1 antibody (primary antibody, ATM1 Ab1), was attached to the surface of the CdTe QDs-carbon nanotubes nanocomposite to form the signal tag (ATM1 Ab1/CdTe-CNT). The above materials were characterized. The optimal experimental conditions were obtained. Thirdly, Fe-GO was employed for extraction of ATM1 in milk. Results indicated that it can adsorb ATM1 efficiently and selectively within a large extent of pH from 3.0 to 8.0. Adsorption processes reached 95% of the equilibrium within 10 min. Lastly, the ATM1 with a serial of concentrations absorbed on Fe-GO was conjugated with ATM1 Ab1/CdTe-CNT signal tag based on sandwich immunoassay. The immunocomplex can emit a strong ECL signal whose intensity depended linearly on the logarithm of ATM1 concentration from 1.0 to 1.0 × 105 pg/mL, with the detection limit (LOD) of 0.3 pg/mL (S/N = 3). The method was more sensitive for ATM1 detection compared to the ELISA method. Finally, ten samples of milk were tested based on the immunoassay. The method is fast and requires very little sample preparation, which was suitable for high-throughput screening of mycotoxins in food.
机译:介绍了使用磁性Fe3O4-氧化石墨烯(Fe-GO)作为吸收剂和抗体标记的碲化镉量子点(CdTe QDs)作为信号标签的牛奶中黄曲霉毒素M1(ATM1)的超灵敏电化学发光免疫分析(ECLIA)。首先,将Fe3O4纳米颗粒固定在GO上以制备磁性纳米复合材料,将其用作ATM1的吸收剂。其次,将黄曲霉毒素M1抗体(一抗,ATM1 Ab1)连接到CdTe QDs-碳纳米管纳米复合材料的表面,形成信号标签(ATM1 Ab1 / CdTe-CNT)。表征了以上材料。获得了最佳实验条件。第三,用Fe-GO提取牛奶中的ATM1。结果表明,它可以在3.0至8.0的较大pH范围内有效且选择性地吸附ATM1。吸附过程在10分钟内达到平衡的95%。最后,基于三明治免疫分析,将一系列在Fe-GO上吸收的浓度的ATM1与ATM1 Ab1 / CdTe-CNT信号标签缀合。免疫复合物可以发出强的ECL信号,其强度与ATM1浓度的对数从1.0到1.0×10 5 pg / mL线性相关,检测极限(LOD)为0.3 pg / mL(S / N = 3)。与ELISA方法相比,该方法对ATM1检测更敏感。最后,基于免疫测定法测试了十份牛奶样品。该方法快速且几乎不需要样品制备,适用于食品中真菌毒素的高通量筛选。

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