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FeMn single-atom nanozyme dual-readout HER2 test

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An etched FeMn–N–C nanozyme boosts peroxidase-like activity 2.03-fold and reports HER2 by electrochemistry and 808 nm photothermal readout.

Source

Bimetallic Single-Atom Nanozyme-Based Electrochemical-Photothermal Dual-Function Portable Immunoassay with Smartphone Imaging

Wang Y, Zeng R, Tian S, et al. · Analytical chemistry · 2024

doi.org/10.1021/acs.analchem.4c02606Read the full paper ↗115 citationscc by

What they did

Authors pyrolyzed ZnO@ZIF-8 to N-doped carbon, doped Fe/Mn, etched defects, assayed TMB/H2O2 POD activity, built a sandwich immunoassay, and compared five hospital sera to ELISA.

What they found

FeMn-NCetch/SAC is 2.03× more POD-active than Fe-NC/SAC. Dual electrochemical and 808 nm photothermal signals agree with a commercial HER2 ELISA (texp < 2.78).

The limits

What it doesn't show

This is a five-sample serum comparison, not a multicenter diagnostic trial; ‘biotherapeutic’ potential is speculative.

Key terms

Single-atom nanozyme
M–N–C sites that mimic peroxidase (POD) activity.
POD-like activity
Catalysis of TMB oxidation by H2O2, read at 652 nm.
HER2
Breast-cancer biomarker detected in the sandwich assay.
Photothermal readout
808 nm laser heating used as a second signal channel.
Dual-readout immunoassay
Independent electrochemical and thermal signals for the same capture event.

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POD-like activity rose by about:

Common questions

How much did bimetallic etching help POD activity?

2.03 times vs Fe-NC/SAC.

Second signal?

808 nm photothermal with a digital multimeter.

Clinical check?

Five sera vs commercial ELISA, t below 2.78.

TMB readout wavelength?

652 nm.

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