Collaborative Innovation Center for Green Chemical Manufacturing and Accurate Detection, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China.
Anal Chem. 2022 May 17;94(19):7132-7139. doi: 10.1021/acs.analchem.2c01162. Epub 2022 May 6.
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 CuCoO@CuO (HDS-CuCoO@CuO) 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 CuO nanoparticles (NPs) were formed in situ on the layered-hollow CuCoO nanospheres (NSs) to obtain HDS-CuCoO@CuO heterostructures. The formed heterojunctions supplied shorter charge transfer distance and better interfacial charge transfer efficiency as well as more effective separation performance. Consequently, HDS-CuCoO@CuO 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-CuCoO@CuO 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).
人们迫切期待在近红外(NIR)区域通过协同加速反应增强电化学发光(ECL)发射,从而实现对疾病生物标志物的超灵敏检测。在此,本文首次方便地制备了中空双壳 CuCoO@CuO(HDS-CuCoO@CuO)杂化结构,并将其用作有吸引力的协同加速反应剂,以改善金纳米团簇(AuNCs)的 NIR ECL 性能。得益于完美匹配的晶格间距,独特的 CuO 纳米颗粒(NPs)原位形成在层状中空 CuCoO 纳米球(NSs)上,得到 HDS-CuCoO@CuO 杂化结构。形成的异质结提供了更短的电荷转移距离和更好的界面电荷转移效率以及更有效的分离性能。因此,HDS-CuCoO@CuO 杂化结构作为一种理想的电活性基底,可以显著促进形成足够的反应中间自由基与 AuNCs 阳离子自由基反应,实现比单个 AuNCs 强约 3 倍的 NIR ECL 响应。此外,由 l-蛋氨酸(l-Met)模板化的 AuNCs 表现出约 830nm 的 NIR ECL 发射,这可以降低光化学损伤,甚至实现无损检测,具有更高的灵敏度和环境适应性。随后,引入一种基于 HWRGWVC 七肽的良好定位固定策略作为特异性抗体固定剂,进一步保持了抗体在 HDS-CuCoO@CuO 和 AuNCs 表面的生物活性,同时显著增强了孵育性能。基于这种渐进式传感机制,构建了一种用于超灵敏分析细胞角蛋白 19 片段 21-1(CYFRA21-1)的 NIR 免疫传感器,实现了从 2fg/mL 到 50ng/mL 的宽线性范围和 0.67fg/mL(S/N=3)的低检测限(LOD)。