A Shape‐Recovery Polycationic Fibroin for Hemostasis‐Regeneration Transition by Recapitulating Natural Coagulation Networks

Y Yuxiang Wang (Key Laboratory of Photochemical Conversion and Optoelectronic Materials & CAS-HKU Joint Laboratory on New Materials) X Xing Li (Interdisciplinary Science Center, State Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology) Z Zhulian Li X Xiaowen Han G Gong Li C Chen Zhou (Department of Chemistry) P Peiyang Gu (Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering) Y Yaping Zou (National Engineering Research Center for Biomaterials Sichuan University 29# Wangjiang Road Chengdu Sichuan 610064 China) X Xiaolin Xiao Y Yong Jiang L Li Jiang (Department of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning China) L Lang Bai H Hong Yan (State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry) J Jie Liang (School of Energy and Power Engineering) X Xingdong Zhang Y Yujiang Fan Y Yong Sun (Department of Pharmaceutics, School of Pharmacy)

Abstract

Abstract Large‐scale and deep trauma restricts the effective hemostasis and tissue regeneration management, even causing death. The formation of the fibrin network is the initial stage of wound control. Inspired by Fn's characteristics during coagulation, an artificial polycationic fibroin (pCSF/β) is designed to achieve hemostasis‐regeneration transition. pCSF/β replicates the aggregation state and maturation process of Fn through intermolecular interaction and subsequent strain hardening originating from ethanol‐inducing β‐sheet to recapitulate natural coagulation networks, achieving mechanical reinforcement and shape recovery. Proteomics and transcriptomics analyses reveal that pCSF/β connects hemostasis and regeneration through platelet contents’ release and the PI3K/Akt signaling pathway. The results of incompressible hemostasis, large‐area skin repair, and penetrating liver regeneration in animal models such as minipigs confirm pCSF/β is superior to clinical products in rapid hemostasis and synchronous tissue regeneration. The molecular design of pCSF/β provides new insights for developing biomaterials in rapid hemostasis and simultaneous regeneration.

Article Details

Volume / Issue Vol. 37, Issue 45
Published November 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (17)

Y

Yuxiang Wang

Key Laboratory of Photochemical Conversion and Optoelectronic Materials & CAS-HKU Joint Laboratory on New Materials

X

Xing Li

Interdisciplinary Science Center, State Key Laboratory of Animal Biodiversity Conservation and Integrated Pest Management, Institute of Zoology

Z

Zhulian Li

X

Xiaowen Han

G

Gong Li

C

Chen Zhou

Department of Chemistry

P

Peiyang Gu

Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering

Y

Yaping Zou

National Engineering Research Center for Biomaterials Sichuan University 29# Wangjiang Road Chengdu Sichuan 610064 China

X

Xiaolin Xiao

Y

Yong Jiang

L

Li Jiang

Department of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning China

L

Lang Bai

H

Hong Yan

State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry

J

Jie Liang

School of Energy and Power Engineering

X

Xingdong Zhang

Y

Yujiang Fan

Y

Yong Sun

Department of Pharmaceutics, School of Pharmacy