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Abstract
Developing superporous hemostatic sponges with simultaneously enhanced permeability and mechanical properties remains challenging but highly desirable to achieve rapid hemostasis for non-compressible hemorrhage. Typical approaches to improve the permeability of hemostatic sponges by increasing porosity sacrifice mechanical properties and yield limited pore interconnectivity, thereby undermining the hemostatic efficacy and subsequent tissue regeneration. Herein, we propose a temperature-assisted secondary network compaction strategy following the phase separation-induced primary compaction to fabricate the superporous chitosan sponge with highly-interconnected porous structure, enhanced blood absorption rate and capacity, and fatigue resistance. The superporous chitosan sponge exhibits rapid shape recovery after absorbing blood and maintains sufficient pressure on wounds to build a robust physical barrier to greatly improve hemostatic efficiency. Furthermore, the superporous chitosan sponge outperforms commercial gauze, gelatin sponges, and chitosan powder by enhancing hemostatic efficiency, cell infiltration, vascular regeneration, and in-situ tissue regeneration in non-compressible organ injury models, respectively. We believe the proposed secondary network compaction strategy provides a simple yet effective method to fabricate superporous hemostatic sponges for diverse clinical applications.
Developing porous hemostatic sponges remains challenging. Here, authors proposed a temperature-assisted secondary network compaction strategy following the phase separation induced primary compaction to fabricate the superporous chitosan sponges.
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1 South China University of Technology, School of Biomedical Sciences and Engineering, Guangzhou International Campus, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838); South China University of Technology, National Engineering Research Center for Tissue Restoration and Reconstruction, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838)
2 The Seventh Affiliated Hospital of Sun Yat-sen University, Department of Orthopedic Surgery, Shenzhen, China (GRID:grid.511083.e) (ISNI:0000 0004 7671 2506)
3 Huazhong University of Science and Technology, Department of Orthopedics, Union Hospital, Tongji Medical College, Wuhan, China (GRID:grid.33199.31) (ISNI:0000 0004 0368 7223)
4 First Affiliated Hospital of Sun Yat-sen University, Department of Joint Surgery, Guangzhou, China (GRID:grid.412615.5) (ISNI:0000 0004 1803 6239)
5 South China University of Technology, School of Biomedical Sciences and Engineering, Guangzhou International Campus, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838); South China University of Technology, National Engineering Research Center for Tissue Restoration and Reconstruction, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838); South China University of Technology, Guangdong Provincial Key Laboratory of Biomedical Engineering, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838); South China University of Technology, Key Laboratory of Biomedical Materials and Engineering of the Ministry of Education, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838)
6 The Seventh Affiliated Hospital of Sun Yat-sen University, Department of Orthopedic Surgery, Shenzhen, China (GRID:grid.511083.e) (ISNI:0000 0004 7671 2506); Shenzhen Key Laboratory of Bone Tissue Repair and Translational Research, Shenzhen, China (GRID:grid.511083.e)