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Signal Amplification Strategy for Highly Sensitive Detecting Brombuterol with Electrochemiluminescent Immunoassay by Using CdSe QDs as Label and Gold Nanoparticle as Substrate

机译:以CdSe QDs为标记物和金纳米颗粒为底物的电化学发光免疫分析灵敏检测溴索丁醇的信号放大策略

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摘要

A signal amplification strategy for electrochemiluminescence (ECL) immunosensor was designed based on gold nanoparticles (AuNPs) and L-cysteine capped CdSe QDs for highly sensitive detection of brombuterol (Brom) in the presence of K2S2O8 as the co-reactant. Therein, AuNPs as the substrate can simplify the experiment process, accelerate the electron transfer rate, and enhance the ECL signal. In the presence of Brom standard solution, coating antigen immobilized on the electrode surface via AuNPs would compete with Brom for the limited binding sites of the CdSe QDs labeled Brom antibody. There was a linear relationship between the logarithm of the Brom concentration and ECL signal. Under the optimal conditions, immunosensor had a good linear range in 0.01-1000ngmL(-1) and a lower detection limit at 0.003ngmL(-1). The specificity and stability of the immuneosensor was also studied, it has been used for the determination of Brom in real samples with satisfactory results. The proposed immunosensor will extend the application of QDs in ECL immunoassays and open a new road for the detection of other small molecules in the future.
机译:基于金纳米颗粒(AuNPs)和L-半胱氨酸封端的CdSe QD设计了电化学发光(ECL)免疫传感器的信号放大策略,用于在K2S2O8作为共反应物的情况下高灵敏度地检测溴酚(Brom)。其中,以AuNPs为底物可以简化实验过程,加快电子传递速率,增强ECL信号。在存在Brom标准溶液的情况下,通过AuNPs固定在电极表面的包被抗原将与Brom竞争CdSe QD标记的Brom抗体的有限结合位点。 Brom浓度的对数与ECL信号之间存在线性关系。在最佳条件下,免疫传感器的线性范围在0.01-1000ngmL(-1)内,检出限在0.003ngmL(-1)下。还对免疫传感器的特异性和稳定性进行了研究,已用于实际样品中溴的测定,结果令人满意。拟议中的免疫传感器将扩展QD在ECL免疫分析中的应用,并为将来检测其他小分子开辟一条新路。

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