透明质酸
自愈水凝胶
胶粘剂
化学
高分子化学
化学工程
生物物理学
高分子科学
有机化学
解剖
医学
生物
工程类
图层(电子)
作者
Cameron Milne,Rijian Song,Melissa Johnson,Chunyu Zhao,Francesca Santoro Ferrer,A Sigen,Jing Lyu,Wenxin Wang
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-03-08
卷期号:25 (4): 2645-2655
被引量:35
标识
DOI:10.1021/acs.biomac.4c00194
摘要
High Resolution Image Download MS PowerPoint Slide Conventional techniques for the closure of wounds, such as sutures and staples, have significant drawbacks that can negatively impact wound healing. Tissue adhesives have emerged as promising alternatives, but poor adhesion, low mechanical properties, and toxicity have hindered their widespread clinical adoption. In this work, a dual modified, aldehyde and methacrylate hyaluronic acid (HA) biopolymer (HA-MA-CHO) has been synthesized through a simplified route for use as a double cross-linked network (DCN) hydrogel (HA-MA-CHO–DCN) adhesive for the effective closure and sealing of wounds. HA-MA-CHO–DCN cross-links in two stages: initial cross-linking of the aldehyde functionality (CHO) of HA-MA-CHO using a disulfide-containing cross-linker, 3,3′-dithiobis (propionic hydrazide) (DTPH), leading to the formation of a self-healing injectable gel, followed by further cross-linking via ultraviolet (UV) initiated polymerization of the methacrylate (MA) functionality. This hydrogel adhesive shows a stable swelling behavior and remarkable versatility as the storage modulus ( G ′) has shown to be highly tunable (10 3 –10 5 Pa) for application to many different wound environments. The new HA-MA-CHO–DCN hydrogel showed excellent adhesive properties by surpassing the burst pressure and lap-shear strength for the widely used bovine serum albumin-glutaraldehyde (BSAG) glue while maintaining excellent cell viability.
科研通智能强力驱动
Strongly Powered by AbleSci AI