Covalently reactive microparticles imbibe blood to form fortified clots for rapid hemostasis and prevention of rebleeding

T Ting Chen C Chaonan Xiao X Xianjun Chen (Optogenetics & Synthetic Biology Interdisciplinary Research Center, Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China) Z Ziyi Yang J Jingwei Zhao B Bingkun Bao (School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China) Q Qingmei Zeng L Li Jiang (Department of Radiation Oncology The First Affiliated Hospital of Guangxi Medical University Nanning China) X Xinyi Huang (School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China) Y Yi Yang Q Qiuning Lin (School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China) W Wei Gong L Linyong Zhu (School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China)

Abstract

Abstract Owing to the inherently gradual nature of coagulation, the body fails in covalently crosslinking to stabilize clots rapidly, even with the aid of topical hemostats, thus inducing hemostatic failure and potential rebleeding. Although recently developed adhesives confer sealing bleeding sites independently of coagulation, interfacial blood hampers their adhesion and practical applications. Here, we report a covalently reactive hemostat based on blood-imbibing and -crosslinking microparticles. Once contacting blood, the microparticles automatically mix with blood via imbibition and covalently crosslink with blood proteins and the tissue matrix before natural coagulation operates, rapidly forming a fortified clot with enhanced mechanical strength and tissue adhesion. In contrast to commercial hemostats, the microparticles achieve rapid hemostasis (within 30 seconds) and less blood loss (approximately 35 mg and 1 g in the rat and coagulopathic pig models, respectively), while effectively preventing blood-pressure-elevation-induced rebleeding in a rabbit model. This work advances the development and clinical translation of hemostats for rapid hemostasis and rebleeding prevention.

Article Details

Volume / Issue Vol. 16, Issue 1
Published April 18, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (13)

T

Ting Chen

C

Chaonan Xiao

X

Xianjun Chen

Optogenetics & Synthetic Biology Interdisciplinary Research Center, Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China

Z

Ziyi Yang

J

Jingwei Zhao

B

Bingkun Bao

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China

Q

Qingmei Zeng

L

Li Jiang

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

X

Xinyi Huang

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China

Y

Yi Yang

Q

Qiuning Lin

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China

W

Wei Gong

L

Linyong Zhu

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dong Chuan Road, Shanghai 200240, China