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Bioinspired Polyacrylic Acid-Based Dressing: Wet Adhesive, Self-Healing, and Multi-Biofunctional Coacervate Hydrogel Accelerates Wound Healing
被引:101
|作者:
Wang, Lingshuang
[1
]
Duan, Lian
[1
]
Liu, Ga
[1
]
Sun, Jianfeng
[2
]
Shahbazi, Mohammad-Ali
[3
]
Kundu, Subhas C. C.
[4
]
Reis, Rui L. L.
[4
]
Xiao, Bo
[1
]
Yang, Xiao
[1
]
机构:
[1] Southwest Univ, Coll Sericulture Text & Biomass Sci, State Key Lab Silkworm Genome Biol, Chongqing 400715, Peoples R China
[2] Univ Oxford, Botnar Res Ctr, Nuffield Dept Orthoped Rheumatol & Musculoskeletal, Oxford OX3 7LD, England
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Engn, Antonius Deusinglaan 1, NL-9713 AV Groningen, Netherlands
[4] Univ Minho, I3Bs Res Inst Biomat Biodegradables & Biomimet, Headquarters European Inst Excellence Tissue Engn, 3Bs Res Grp, AvePk, P-4805017 Barco, Guimaraes, Portugal
基金:
中国国家自然科学基金;
关键词:
antibacterial;
polyacrylic acid;
tannic acid;
wet adhesion;
wound healing;
TANNIC-ACID;
INSPIRED ADHESIVE;
TOUGH;
POLYMERS;
TISSUE;
PERFORMANCE;
EFFICIENT;
DESIGN;
D O I:
10.1002/advs.202207352
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Polyacrylic acid (PAA) and its derivatives are commonly used as essential matrices in wound dressings, but their weak wet adhesion restricts the clinical application. To address this issue, a PAA-based coacervate hydrogel with strong wet adhesion capability is fabricated through a facile mixture of PAA copolymers with isoprenyl oxy poly(ethylene glycol) ether and tannic acid (TA). The poly(ethylene glycol) segments on PAA prevent the electrostatic repulsion among the ionized carboxyl groups and absorbed TA to form coacervates. The absorbed TA provides solid adhesion to dry and wet substrates via multifarious interactions, which endows the coacervate with an adhesive strength to skin of 23.4 kPa and 70% adhesion underwater. This coacervate achieves desirable self-healing and extensible properties suitable for frequently moving joints. These investigations prove that the coacervate has strong antibacterial activity, facilitates fibroblast migration, and modulates M1/M2 polarization of macrophages. In vivo hemorrhage experiments further confirm that the coacervate dramatically shortens the hemostatic time from hundreds to tens of seconds. In addition, full-thickness skin defect experiments demonstrate that the coacervate achieves the best therapeutic effect by significantly promoting collagen deposition, angiogenesis, and epithelialization. These results demonstrate that a PAA-based coacervate hydrogel is a promising wound dressing for medical translation.
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页数:16
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