Enhanced Hemostatic and Procoagulant Efficacy of PEG/ZnO Hydrogels: A Novel Approach in Traumatic Hemorrhage Management.
Chuyue ZhangYifan WangYuan XueJunyao ChengPengfei ChiZhaohan WangBo LiTaoxu YanBing WuZheng WangPublished in: Gels (Basel, Switzerland) (2024)
Managing severe bleeding, particularly in soft tissues and visceral injuries, remains a significant challenge in trauma and surgical care. Traditional hemostatic methods often fall short in wet and dynamic environments. This study addresses the critical issue of severe bleeding in soft tissues, proposing an innovative solution using a polyethylene glycol (PEG)-based hydrogel combined with zinc oxide (ZnO). The developed hydrogel forms a dual-network structure through amide bonds and metal ion chelation, resulting in enhanced mechanical properties and adhesion strength. The hydrogel, exhibiting excellent biocompatibility, is designed to release zinc ions, promoting coagulation and accelerating hemostasis. Comprehensive characterization, including gelation time, rheological properties, microstructure analysis, and swelling behavior, demonstrates the superior performance of the PEG/ZnO hydrogel compared to traditional PEG hydrogels. Mechanical tests confirm increased compression strength and adhesive properties, which are crucial for withstanding tissue dynamics. In vitro assessments reveal excellent biocompatibility and enhanced procoagulant ability attributed to ZnO. Moreover, in vivo experiments using rat liver and tail bleeding models demonstrate the remarkable hemostatic performance of the PEG/ZnO hydrogel, showcasing its potential for acute bleeding treatment in both visceral and peripheral scenarios.
Keyphrases
- drug delivery
- quantum dots
- tissue engineering
- room temperature
- hyaluronic acid
- drug release
- atrial fibrillation
- reduced graphene oxide
- wound healing
- visible light
- gene expression
- spinal cord injury
- healthcare
- early onset
- palliative care
- insulin resistance
- metabolic syndrome
- type diabetes
- oxide nanoparticles
- liver failure
- oxidative stress
- white matter
- gold nanoparticles
- staphylococcus aureus
- single cell
- chronic pain
- trauma patients
- solid state
- chemotherapy induced