Microenvironment self-adaptive multifunctional hydrogels elicit immunomodulation mediated wound healing

Herein, we report a microenvironment self-adaptive multifunctional hydrogel (GBOD-PF) dressing with intrinsic hemostasis, antimicrobial and anti-inflammatory properties that promotes collagen deposition, activates the immune response, and angiogenesis, accelerates large-scale chronic wound healing. To address these needs, aldehyde-functionalized dextran (ODT) was first synthesized through oxidation, and an injectable hydrogel was prepared by mixing Gel and ODT solutions in the presence of borax and paeoniflorin (PF) through the formation of dynamic Schiff base bonds (GBOD-PF). This multifunctional hydrogel exhibits remodeling and self-healing properties, enhanced adhesion strength and biocompatibility. Moreover, it possesses broad-spectrum antibacterial activity and superior hemostasis, providing early-stage protection for complex wounds. Notably, GBOD-PF targets the TLR4/NF-κB signaling pathway, a core mediator of inflammation, thereby dampening the inflammatory cascade. The results demonstrate the application of the GBOD-PF hydrogel in an infection wound and diabetic model wound healing model, which enhanced immune response, induced M1-to-M2 macrophage repolarization to establish anti-inflammatory microenvironment, regulated MMP-9, promoted angiogenesis, thereby inducing a pro-regenerative response. Therefore, this work provides an effective strategy for the treatment of chronic wound repair and tissue regeneration.

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Publication Details

Journal
Materials Today Bio
Published
2025-09-23
DOI
https://doi.org/10.1016/j.mtbio.2025.102340
Citations
1
Primary Topic
Wound Healing and Treatments
Type
article
Field-Weighted Citation Impact
1.03
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article

Microenvironment self-adaptive multifunctional hydrogels elicit immunomodulation mediated wound healing

Xijin Wu, Ping Ling, Shengyu Li, Xiaonian Zhu et al.
1 citations
Materials Today Bio
Wound Healing and Treatments
1.03
article

Microenvironment self-adaptive multifunctional hydrogels elicit immunomodulation mediated wound healing

Xijin Wu, Ping Ling, Shengyu Li, Xiaonian Zhu, Huiyin Fu, Qiyang Shou, Wenjun Xu, Dian Yu, YuJia Li, Yicheng Wang, Wei Zhang, Jin-Wei Wang, Weihan Zhu, Jintao Fang, Xia Qin, Junwen Hu, Jintao Shi
article en
1 citations

Abstract

Herein, we report a microenvironment self-adaptive multifunctional hydrogel (GBOD-PF) dressing with intrinsic hemostasis, antimicrobial and anti-inflammatory properties that promotes collagen deposition, activates the immune response, and angiogenesis, accelerates large-scale chronic wound healing. To address these needs, aldehyde-functionalized dextran (ODT) was first synthesized through oxidation, and an injectable hydrogel was prepared by mixing Gel and ODT solutions in the presence of borax and paeoniflorin (PF) through the formation of dynamic Schiff base bonds (GBOD-PF). This multifunctional hydrogel exhibits remodeling and self-healing properties, enhanced adhesion strength and biocompatibility. Moreover, it possesses broad-spectrum antibacterial activity and superior hemostasis, providing early-stage protection for complex wounds. Notably, GBOD-PF targets the TLR4/NF-κB signaling pathway, a core mediator of inflammation, thereby dampening the inflammatory cascade. The results demonstrate the application of the GBOD-PF hydrogel in an infection wound and diabetic model wound healing model, which enhanced immune response, induced M1-to-M2 macrophage repolarization to establish anti-inflammatory microenvironment, regulated MMP-9, promoted angiogenesis, thereby inducing a pro-regenerative response. Therefore, this work provides an effective strategy for the treatment of chronic wound repair and tissue regeneration.

Materials Today BioVol. 35
Zhejiang Chinese Medical University (CN), Zhejiang Lab (CN), Zhejiang Provincial People's Hospital (CN), Second Affiliated Hospital of Zhejiang University (CN), University of Chinese Academy of Sciences (CN), Zhejiang University (CN)
Openalex Percentile: Top 18%
Wound Healing and Treatments
1.03
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