Electrospun nanocomposite dressing integrating cerium dioxide and collagen accelerates pressure injury healing

<h2>Summary</h2> Pressure injuries (PIs) involve a pathological cycle of oxidative stress, inflammation, and impaired angiogenesis. To address this, we engineered an electrospun nanocomposite dressing—CePC—incorporating cerium dioxide nanoparticles into a polycaprolactone collagen matrix. This dressing could modulate the wound microenvironment. <i>In vitro</i>, it could scavenge reactive oxygen species, protect endothelial cells, enhance vascular endothelial growth factor (VEGF) expression, and reduce pro-inflammatory cytokines. In a murine PI model, the treatment accelerated wound closure, promoted granulation tissue formation and dermal regeneration, and improved functional angiogenesis. Mechanistically, the dressing shifted the macrophage phenotype from a pro-inflammatory to a pro-healing state. These findings demonstrate a strategy that combines nanomaterials and biomaterials to regulate inflammation and vascularization, providing a potential therapeutic approach for PI repair.

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Publication Details

Journal
iScience
Published
2026-05-23
DOI
https://doi.org/10.1016/j.isci.2026.116096
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
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article

Electrospun nanocomposite dressing integrating cerium dioxide and collagen accelerates pressure injury healing

Jiani Wu, 钱彩艳, Zhikang Mo, Yue Tang et al.
iScience
Advanced Nanomaterials in Catalysis
article

Electrospun nanocomposite dressing integrating cerium dioxide and collagen accelerates pressure injury healing

Jiani Wu, 钱彩艳, Zhikang Mo, Yue Tang, Huiyu Tan, Lu Zhang, Haibin Chen, Yumei Zhong
article en

Abstract

<h2>Summary</h2> Pressure injuries (PIs) involve a pathological cycle of oxidative stress, inflammation, and impaired angiogenesis. To address this, we engineered an electrospun nanocomposite dressing—CePC—incorporating cerium dioxide nanoparticles into a polycaprolactone collagen matrix. This dressing could modulate the wound microenvironment. <i>In vitro</i>, it could scavenge reactive oxygen species, protect endothelial cells, enhance vascular endothelial growth factor (VEGF) expression, and reduce pro-inflammatory cytokines. In a murine PI model, the treatment accelerated wound closure, promoted granulation tissue formation and dermal regeneration, and improved functional angiogenesis. Mechanistically, the dressing shifted the macrophage phenotype from a pro-inflammatory to a pro-healing state. These findings demonstrate a strategy that combines nanomaterials and biomaterials to regulate inflammation and vascularization, providing a potential therapeutic approach for PI repair.

iScienceVol. 29(6)
Sun Yat-sen University (CN), The Seventh Affiliated Hospital of Sun Yat-sen University (CN)
Openalex Percentile: Top 11%
Advanced Nanomaterials in Catalysis
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