Electrochemiluminescent determination of prostate-specific antigen using Au@(MoS2/GO/o-MWNTs) nanohybrids as co-reaction accelerator and hyperbranched hybridization chain reaction for signal amplification

电化学发光 检出限 连锁反应 化学 发光体 胶体金 线性范围 凝聚体 纳米化学 化学发光 材料科学 纳米颗粒 色谱法 纳米技术 光化学 发光 有机化学 光电子学 生物化学 基因 基因组
作者
Yingying Sun,Qin Yan,Jun Zhang,Qunxiang Ren
出处
期刊:Mikrochimica Acta [Springer Nature]
卷期号:188 (9) 被引量:7
标识
DOI:10.1007/s00604-021-04957-0
摘要

Three-dimensional flowerlike Au@(MoS2/GO/o-MWNTs) nanohybrids (abbreviated as AMGMs) were synthesized and then introduced into an electrochemiluminescence (ECL) system as a new co-reaction accelerator for the ultrasensitive prostate-specific antigen (PSA). The AMGMs not only served as a substrate with good conductivity and a large specific surface area for loading abundant primary antibodies but also acted as an effective co-reaction accelerator; the co-reaction accelerator could interact with a co-reactant rather than the luminophore to boost the generation of free radical intermediates, thereby producing abundant excited states of luminophores to amplify the ECL signal response. Additionally, an anticipated signal amplification strategy based on the hybridization chain reaction (HCR) was developed by gathering a large amount of a DNA initiator on gold nanoparticles. These gathered DNA initiators could generate multiple DNA concatemers and attach more signal molecules, which resulted in outstanding exponential signal amplification. Consequently, the ECL immunosensor demonstrated high sensitivity, with a linear range from 0.1 pg mL−1 to 50 ng mL−1 and a detection limit of 0.028 pg mL−1. In addition, the immunosensor displayed excellent stability and selectivity. It was evaluated by analyzing human serum sample. The recovery obtained was 98.80–112.00% and the RSD was 1.73–3.12%, indicating the immunosensor could be applied to the simultaneous detection of PSA in human serum samples.

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