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Research Article | Open Access

Silk fibroin–gelatine haemostatic sponge loaded with thrombin for wound haemostasis and tissue regeneration

Yajun Zhang1,2,3,4,†, Ming Li2,3,4,†, Jing Chang2,3,4,† , Chang Li2,3,4, Yuwen Hui2,3,4, Yanhua Wang3,4,5( ), Weiguo Xu1( )
Clinical School/Colledge of Orthopedics, Tianjin Medical University, 406 South Jiefang Road, Hexi District, Tianjin 300270, China
Trauma Medicine Center, Peking University People’s Hospital, 39 Nanfeng West 1st Road, Tongzhou District, Beijing 100044, China
Key Laboratory of Trauma and Neural Regeneration, Ministry of Education, Peking University, 39 Nanfeng West 1st Road, Tongzhou District, Beijing 100044, China
National Center for Trauma Medicine, 39 Nanfeng West 1st Road, Tongzhou District, Beijing 100044, China
Department of Orthopedics and Trauma, Peking University People’s Hospital, 39 Nanfeng West 1st Road, Tongzhou District, Beijing 100044, China

†Yajun Zhang, Ming Li and Jing Chang are co-first authors.

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Highlights

• SFG composite haemostatic sponges were prepared using gelatine and silk fibroin, which can address the mechanical defects of gelatine and silk fibroin when used alone.

• Adding thrombin can further improved the haemostatic performance of the SFG@TB composite haemostatic sponge.

• The SFG@TB composite hemostatic sponge with outstanding mechanical properties, good hemostatic performance and high biosafety can promote wound hemostasis and tissue repair.

Abstract

Background

Wound haemostasis is an important part of clinical treatments, especially treatments for patients with avulsion injury, destructive injury and large-scale soft tissue injury. Therefore, developing fast and effective haemostatic materials is critical. This study aimed to design a novel and efficient silk fibroin–gelatine composite haemostatic sponge loaded with thrombin (SFG@TB) to assist in wound haemostasis.

Methods

The SFG@TB composite haemostatic sponge was formed with gelatine, silk fibroin and thrombin through a freeze-drying technique. First, the material characteristics of SFG@TB were measured, including the elastic modulus, swelling rate and porosity. Second, in vitro cell coculture experiments, in vivo embedding experiments and haemolytic analyses were performed to evaluate the biocompatibility of SFG@TB. Then, coagulation experiments and femoral artery and liver bleeding models were used to evaluate the haemostatic performance of SFG@TB. Finally, the ability of SFG@TB to promote tissue healing was evaluated through experiments with Sprague–Dawley rat models of injury.

Results

Compared with gelatine sponges, SFG@TB exhibited outstanding mechanical properties and water absorption properties. In addition, the excellent biosafety of the composite haemostatic sponge was confirmed by cell experiments, subcutaneous embedding experiments and haemolytic analysis. Based on the in vitro coagulation test results, SFG@TB exhibited greater adhesion of red blood cells and platelets and a shorter dynamic coagulation time. Compared to the use of silk fibroin–gelatine composite haemostatic sponges or gelatine sponges, the introduction of thrombin resulted in a shorter haemostasis time and a smaller bleeding volume, as revealed by in vivo coagulation tests. The experiments with Sprague–Dawley rat models of injury indicated that SFG@TB accelerated the wound healing process and reduced scar width, which was accompanied by thicker granulation tissue.

Conclusions

Overall, the SFG@TB composite haemostatic sponge, which exhibits outstanding mechanical properties, good haemostatic performance and high biosafety, promoted wound haemostasis and tissue repair. Therefore, the SFG@TB composite haemostatic sponge could be a promising material for wound haemostasis.

Graphical Abstract

References

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Burns & Trauma
Article number: tkae026

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Cite this article:
Zhang Y, Li M, Chang J, et al. Silk fibroin–gelatine haemostatic sponge loaded with thrombin for wound haemostasis and tissue regeneration. Burns & Trauma, 2024, 12: tkae026. https://doi.org/10.1093/burnst/tkae026

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Received: 18 November 2023
Revised: 27 April 2024
Published: 10 October 2026
© The Author(s) 2024. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com