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Updated: May 2, 2026

Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis
Published on: March 7, 2018
Hierarchical Mesochannel-Confined Nanozyme Reactors Propelling Gold Amplification Immunoassays for Ultrasensitive
Huan Cai1, Zhujun Ai1,2, Xin Gao3
1Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, China.
Abstract:
Ultrasensitive, rapid, stable, and user-friendly point-of-care (POC) diagnostic technologies are imperative for disease screening and home healthcare. Herein, we propose a novel hierarchically mesoporous channel-confined nanozyme reactor (FeMPPt) as an enrichment-confinement nanoreactor to enhance gold plasmonic signal amplification, significantly boosting the sensitivity and stability of visual lateral flow immunoassays (vLFIAs) for ultrasensitive dual-mode (qualitative/quantitative) detection of multiplex disease biomarkers. The FeMPPt with high colorimetric signal brightness was synthesized through a spatially controlled assembly of polydopamine flexible scaffolds and platinum nanozymes within the hierarchical mesochannels of 3D magnetically core-shelled dendritic mesoporous silica. Through electrostatic adsorption, high-specific-surface-area interception, and mesoporous confinement catalysis, 125- and 5-fold enhancements were achieved compared to conventional gold nanoparticles (AuNPs) and nonporous nanozymes of almost equivalent size, respectively. The limit of detection for FeMPPt-labeled vLFIA for qualitative/quantitative detection of cardiac troponin I and alpha-fetoprotein was 125/230-fold and 1300/1300-fold lower than that for AuNP-labeled vLFIA, respectively. In addition, clinical practicality was validated using 234 serum samples from clinical laboratories and 34 samples from emergency departments, with quantitative performance comparable/superior to standard/miniaturized chemiluminescence immunoassay systems, demonstrating its considerable potential for real-time disease biomarker detection in both clinical and POC settings.
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