# Integrating Pt nanoparticles with 3D Cu2-  x Se/GO nanostructure to achieve nir-enhanced peroxidizing Nano-enzymes for dynamic monitoring the level of H2O2 during the inflammation

**Authors:** Man Shen, Xianling Dai, Dongni Ning, Hanqing Xu, Yang Zhou, Gangan Chen, Zhangyin Ren, Ming Chen, Mingxuan Gao, Jing Bao

PMC · DOI: 10.3389/fimmu.2024.1392259 · 2024-07-17

## TL;DR

This paper introduces a new sensor that uses nanostructures to detect hydrogen peroxide in wounds, improving treatment of inflammation.

## Contribution

A novel 3D Cu2- x Se/GO nanostructure decorated with Pt nanoparticles enables NIR-enhanced detection of H2O2 with high sensitivity.

## Key findings

- The Cu2- x Se/GO@Pt/SPCE sensor reduces H2O2 detection limit from 1.45 μM to 0.53 μM under NIR light.
- The sensor allows in-situ real-time monitoring of H2O2 released by cells.
- The nanostructure enhances catalytic efficiency through localized surface plasma effects.

## Abstract

The treatment of wound inflammation is intricately linked to the concentration of reactive oxygen species (ROS) in the wound microenvironment. Among these ROS, H2O2 serves as a critical signaling molecule and second messenger, necessitating the urgent need for its rapid real-time quantitative detection, as well as effective clearance, in the pursuit of effective wound inflammation treatment. Here, we exploited a sophisticated 3D Cu2-

x
Se/GO nanostructure-based nanonzymatic H2O2 electrochemical sensor, which is further decorated with evenly distributed Pt nanoparticles (Pt NPs) through electrodeposition. The obtained Cu2-

x
Se/GO@Pt/SPCE sensing electrode possesses a remarkable increase in specific surface derived from the three-dimensional surface constructed by GO nanosheets. Moreover, the localized surface plasma effect of the Cu2-

x
Se nanospheres enhances the separation of photogenerated electron-hole pairs between the interface of the Cu2-

x
Se NPs and the Pt NPs. This innovation enables near-infrared light-enhanced catalysis, significantly reducing the detection limit of the Cu2-

x
Se/GO@Pt/SPCE sensing electrode for H2O2 (from 1.45 μM to 0.53μM) under NIR light. Furthermore, this biosensor electrode enables in-situ real-time monitoring of H2O2 released by cells. The NIR-enhanced Cu2-

x
Se/GO@Pt/SPCE sensing electrode provide a simple-yet-effective method to achieve a detection of ROS (H2O2、-OH) with high sensitivity and efficiency. This innovation promises to revolutionize the field of wound inflammation treatment by providing clinicians with a powerful tool for accurate and rapid assessment of ROS levels, ultimately leading to improved patient outcomes.

## Linked entities

- **Chemicals:** H2O2 (PubChem CID 784), -OH (PubChem CID 961)

## Full-text entities

- **Diseases:** inflammation (MESH:D007249)
- **Chemicals:** Cu2- x Se (-), Pt (MESH:D010984), ROS (MESH:D017382), H2O2 (MESH:D006861)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11288797/full.md

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Source: https://tomesphere.com/paper/PMC11288797