Implantable Graphene Fiber Sensor Functionalized with Enzyme-Mimicking Fe-Porphyrin for In Vivo Simultaneous Monitoring of NO and H2O2 in Cancer

Nitric oxide (NO) and hydrogen peroxide (H2O2) are critical in redox homeostasis, cell signaling, and tumor progression, yet the simultaneous detection of both remains challenging due to their low concentrations and high reactivity. Herein, we developed an implantable, fully flexible electrochemical biosensor based on a Fe-porphyrin metal-organic framework (i.e., PCN-224(Fe)) for real-time monitoring of NO and H2O2 in complex biological environments. This platform employs PCN-224(Fe) with enzyme-mimicking activity as the catalytic material, combined with nitrogen and boron codoped graphene fiber as the freestanding and flexible microelectrode substrate. The resultant electrochemical sensor demonstrated outstanding performance, with detection limits of 3.0 nM for NO and 0.5 μM for H2O2, and sensitivities of 2.99 mA cm-2 mM-1 and 1.04 mA cm-2 mM-1, respectively. This performance surpasses most previously reported electrochemical sensors. The sensor also shows excellent selectivity and reproducibility, facilitating continuous monitoring of NO and H2O2 signals in the tumor microenvironment. The proposed fiber-based sensor enables in situ, real-time, continuous monitoring of NO and H2O2 in cancer cells, tissues, and living organisms, thereby effectively discriminating between cancerous and normal samples based on significantly elevated biomarker levels in malignant tissues. When implanted directly into living tissues, the sensing device captures dynamic biomarker fluctuations in vivo with high fidelity, offering a distinct advantage over traditional in vitro assays, which often introduce signal loss and concentration artifacts during sample processing. As a result, this approach provides a more accurate reflection of actual in vivo conditions and holds great promise for assessing tumor progression as well as monitoring therapeutic responses.

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Publication Details

Journal
ACS Sensors
Published
2026-09-11
DOI
https://doi.org/10.1021/acssensors.6c02929
Primary Topic
Electrochemical sensors and biosensors
Type
article
Field-Weighted Citation Impact
0.00

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article

Implantable Graphene Fiber Sensor Functionalized with Enzyme-Mimicking Fe-Porphyrin for In Vivo Simultaneous Monitoring of NO and H2O2 in Cancer

Kaiyuan Yao, Min Hu, Anshun Zhao, Fei Xiao et al.
ACS Sensors
Electrochemical sensors and biosensors
article

Implantable Graphene Fiber Sensor Functionalized with Enzyme-Mimicking Fe-Porphyrin for In Vivo Simultaneous Monitoring of NO and H2O2 in Cancer

Kaiyuan Yao, Min Hu, Anshun Zhao, Fei Xiao, Hengrui Zhang, Shanting Li, Tengyun Chang, Wei Huang, Dan Wang
article en

Abstract

Nitric oxide (NO) and hydrogen peroxide (H2O2) are critical in redox homeostasis, cell signaling, and tumor progression, yet the simultaneous detection of both remains challenging due to their low concentrations and high reactivity. Herein, we developed an implantable, fully flexible electrochemical biosensor based on a Fe-porphyrin metal-organic framework (i.e., PCN-224(Fe)) for real-time monitoring of NO and H2O2 in complex biological environments. This platform employs PCN-224(Fe) with enzyme-mimicking activity as the catalytic material, combined with nitrogen and boron codoped graphene fiber as the freestanding and flexible microelectrode substrate. The resultant electrochemical sensor demonstrated outstanding performance, with detection limits of 3.0 nM for NO and 0.5 μM for H2O2, and sensitivities of 2.99 mA cm-2 mM-1 and 1.04 mA cm-2 mM-1, respectively. This performance surpasses most previously reported electrochemical sensors. The sensor also shows excellent selectivity and reproducibility, facilitating continuous monitoring of NO and H2O2 signals in the tumor microenvironment. The proposed fiber-based sensor enables in situ, real-time, continuous monitoring of NO and H2O2 in cancer cells, tissues, and living organisms, thereby effectively discriminating between cancerous and normal samples based on significantly elevated biomarker levels in malignant tissues. When implanted directly into living tissues, the sensing device captures dynamic biomarker fluctuations in vivo with high fidelity, offering a distinct advantage over traditional in vitro assays, which often introduce signal loss and concentration artifacts during sample processing. As a result, this approach provides a more accurate reflection of actual in vivo conditions and holds great promise for assessing tumor progression as well as monitoring therapeutic responses.

ACS Sensors
First Affiliated Hospital of Henan University of Science and Technology (CN), Huazhong University of Science and Technology Hospital (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China
Reduced inequalities
Openalex Percentile: Top 20%
Electrochemical sensors and biosensors
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