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May 3, 20260 citations

Hierarchical Mesochannel-Confined Nanozyme Reactors Propelling Gold Amplification Immunoassays for Ultrasensitive Point-of-Care Diagnostics.

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HCHuan CaiZAZhujun AiXGXin Gao

Key Points

  • This research aims to develop a novel nanozyme reactor to improve the sensitivity and stability of diagnostics for disease biomarkers.
  • Developed a hierarchically mesoporous channel-confined nanozyme reactor (FeMPPt) for signal amplification.
  • Conducted tests on clinical samples from 234 serum samples and 34 emergency department samples.
  • Compared performance with standard and miniaturized chemiluminescence immunoassay systems.
  • Achieved 125- and 5-fold signal enhancement over conventional gold nanoparticles and nonporous nanozymes, respectively.
  • Demonstrated limits of detection for cardiac troponin I and alpha-fetoprotein 125/230-fold and 1300/1300-fold lower than AuNP-labeled assays.
  • Showed quantitative performance comparable or superior to existing systems in clinical applications.

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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Cite This Study

Cai et al. (2026) studied this question.

synapsesocial.com/papers/69f6e5308071d4f1bdfc5f2dhttps://doi.org/10.1021/acs.analchem.6c00438
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