4.8 Article

Hollow Double-Shell CuCo2O4@Cu2O Heterostructures as a Highly Efficient Coreaction Accelerator for Amplifying NIR Electrochemiluminescence of Gold Nanoclusters in Immunoassay

Journal

ANALYTICAL CHEMISTRY
Volume 94, Issue 19, Pages 7132-7139

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c01162

Keywords

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Funding

  1. National Natural Science Foundation of China [21627809, 21827812]
  2. Special Foundation for Taishan Scholar Professorship of Shandong Province [TS201712052]
  3. Innovation Team Project of Colleges and Universities in Jinan [2019GXRC027]

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The utilization of HDS-CuCo2O4@Cu2O heterostructures as coreaction accelerators greatly enhances the NIR ECL performance of AuNCs. The use of L-methionine templated AuNCs allows for nondestructive detection with improved susceptibility and circumambient adaptability. The introduction of a well site-oriented fixation strategy preserves the bioactivity of antibodies and enhances the incubation performance. The NIR immunosensor achieved ultrasensitive analysis of CYFRA21-1 with a wide linear range and low limit of detection.
The evolution of electrochemiluminescence (ECL) emission amplified by coreaction accelerator in near-infrared (NIR) area has been overwhelmingly anticipated for ultrasensitive detection of disease biomarkers. Herein, the hollow double-shell CuCo2O4@Cu2O (HDS-CuCo2O4@Cu2O) heterostructures were conveniently prepared and utilized as an attractive coreaction accelerator to improve the NIR ECL performance of gold nanoclusters (AuNCs) for the first time. Benefiting from perfect-matched lattice spacing, unique Cu2O nanoparticles (NPs) were formed in situ on the layered-hollow CuCo2O4 nanospheres (NSs) to obtain HDS-CuCo2O4@Cu2O heterostructures. The formed heterojunctions supplied shorter charge transfer distance and better interfacial charge transfer efficiency as well as more effective separation performance. Consequently, HDS-CuCo2O4@Cu2O heterostructures as an admirable electroactive substrate could significantly promote the formation of sufficient coreactant intermediate radicals to react with AuNCs cationic radicals, realizing about 3-folds stronger NIR ECL response than that of individual AuNCs. In addition, the AuNCs templated by L-methionine (L-Met) exhibited NIR ECL emission around 830 nm, which could decrease the photochemical damage to even realize a nondestructive detection with improved susceptibility and circumambient adaptability. Subsequently, a well site-oriented fixation strategy utilizing HWRGWVC heptapeptide as the specific antibody immobilizer was introduced to further preserve the bioactivity of antibody on the HDS-CuCo2O4@Cu2O and AuNCs surface along with enhancing the incubation performance markedly. In view of the progressive sensing mechanism, a NIR immunosensor was obtained for the ultrasensitive analysis of CYFRA21-1, which achieved a broad linear ranging from 2 fg/mL to 50 ng/mL and a low limit of detection (LOD) of 0.67 fg/mL (S/N = 3).

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