Amorphous zinc phosphate nanoclusters loaded polycarbonate thermosensitive hydrogel: An innovative strategy for promoting wound healing

被引:0
|
作者
Chen, Siwen [1 ,2 ]
Li, Yutong [3 ]
Ren, Sihang [4 ]
Yang, Yuanyuan [2 ]
Hou, Zhipeng [2 ]
Han, Siyu [1 ]
Zhang, Wanhong [1 ]
Guo, Jing [5 ]
Hu, Jianshe [1 ]
Zhang, Xing [3 ]
Yang, Liqun [2 ]
机构
[1] Center for Molecular Science and Engineering, College of Science, Northeastern University, Shenyang,110819, China
[2] Research Center for Biomedical Materials, Engineering Research Center of Ministry of Education for Minimally Invasive Gastrointestinal Endoscopic Techniques, Shengjing Hospital of China Medical University, Shenyang,110004, China
[3] Institute of Metal Research, Chinese Academy of Sciences, Shenyang,110016, China
[4] Department of Plastic Surgery, The Second Hospital of Dalian Medical University, Dalian,116027, China
[5] Liaoning Research Institute for Eugenic Birth & Fertility, China Medical University, Shenyang,110031, China
来源
Materials Today Bio | 2024年 / 29卷
关键词
Endothelial cells - Medicinal chemistry - Nanoclay - Nanoclusters - Platelets - Tissue regeneration;
D O I
10.1016/j.mtbio.2024.101266
中图分类号
学科分类号
摘要
Skin trauma is a matter of great concern for public health, emphasizing the importance of reconstructing the microenvironment at the trauma site to facilitate tissue regeneration. Therefore, the investigation of innovative wound dressings has significant research and clinical implications. In this study, we prepared a thermosensitive hydrogel based on a hydrophilic-hydrophobic-hydrophilic triblock polycarbonate polymer (PTP), and created a composite hydrogel, PTPH-AZP, by incorporating amorphous zinc phosphate (AZP) nanoclusters. We evaluated the effects of PTPH-AZP on human umbilical vein endothelial cells (HUVECs) and the ability to promote skin wound healing. According to the results, PTPH-AZP was found to promote the proliferation, migration, and tube formation of HUVECs through the sustained release of Zn2+ at appropriate concentrations. In vivo experiments demonstrated that in the early-mid stages of wound healing, PTPH-AZP promotes increases in Platelet Endothelial Cell Adhesion Molecule-1 (CD31) and α-Smooth Muscle Actin (α-SMA) content within the wound area, facilitating accelerated re-epithelialization and enhanced collagen deposition. In later healing stages, epidermal thickness in the PTPH-AZP treated group was significantly improved, aligning with surrounding intact skin with no instances of attenuated or hypertrophic scarring observed. The findings from the in vivo study suggested that PTPH-AZP may have a positive impact on vascularization and wound healing. In conclusion, this study presents a promising strategy for skin wound healing, highlighting the potential of PTPH-AZP as an effective therapeutic approach. © 2024 The Author(s)
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