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Adhesive Hemostatic Conducting Injectable Composite Hydrogels with Sustained Drug Release and Photothermal Antibacterial Activity to Promote Full‐Thickness Skin Regeneration During Wound Healing

Yongping LiangFrontier Institute of Science and Technology, and State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 ChinaXin ZhaoFrontier Institute of Science and Technology, and State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 ChinaTianli HuFrontier Institute of Science and Technology, and State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 ChinaBaojun ChenDepartment of Orthopaedics The First Affiliated Hospital College of Medicine Xi'an Jiaotong University Xi'an 710061 ChinaZhanhai YinDepartment of Orthopaedics The First Affiliated Hospital College of Medicine Xi'an Jiaotong University Xi'an 710061 ChinaX. PeterDepartment of Materials Science and Engineering University of Michigan Ann Arbor MI 48109 USABaolin GuoFrontier Institute of Science and Technology, and State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 China
2019en
ABI

Аннотация

Abstract Developing injectable nanocomposite conductive hydrogel dressings with multifunctions including adhesiveness, antibacterial, and radical scavenging ability and good mechanical property to enhance full‐thickness skin wound regeneration is highly desirable in clinical application. Herein, a series of adhesive hemostatic antioxidant conductive photothermal antibacterial hydrogels based on hyaluronic acid‐graft‐dopamine and reduced graphene oxide (rGO) using a H 2 O 2 /HPR (horseradish peroxidase) system are prepared for wound dressing. These hydrogels exhibit high swelling, degradability, tunable rheological property, and similar or superior mechanical properties to human skin. The polydopamine endowed antioxidant activity, tissue adhesiveness and hemostatic ability, self‐healing ability, conductivity, and NIR irradiation enhanced in vivo antibacterial behavior of the hydrogels are investigated. Moreover, drug release and zone of inhibition tests confirm sustained drug release capacity of the hydrogels. Furthermore, the hydrogel dressings significantly enhance vascularization by upregulating growth factor expression of CD31 and improve the granulation tissue thickness and collagen deposition, all of which promote wound closure and contribute to a better therapeutic effect than the commercial Tegaderm films group in a mouse full‐thickness wounds model. In summary, these adhesive hemostatic antioxidative conductive hydrogels with sustained drug release property to promote complete skin regeneration are an excellent wound dressing for full‐thickness skin repair.

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