Preparation of a nanocomposite hydrogel with high adhesion, toughness, and inherent antibacterial properties by a one-pot method

被引:5
|
作者
Liu, Jianzhi [1 ,2 ]
Zhang, Zipeng [1 ]
Liu, Zhibang [1 ]
Yu, Yueqin [1 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, State Key Lab Ecochem Engn, Qingdao 266042, Shandong, Peoples R China
[2] Taishan Univ, Tai An 271021, Shandong, Peoples R China
[3] Jiangsu Qingkemucheng New Mat Res Inst, Xuzhou 221100, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanocomposite hydrogel; Antibacterial property; Adhesion; Mechanical properties; One-pot method; NA-MONTMORILLONITE;
D O I
10.1016/j.colsurfa.2022.130368
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the biomedical field, it is challenging to develop a multifunctional hydrogel with superior tissue adhesion, cell compatibility, inherent antibacterial properties, and excellent mechanical properties. Herein, we designed a material system with a synergistic effect and prepared a multifunctional nanocomposite hydrogel using a one-pot method, with N-maleyl dopamine (MDA), montmorillonite (MMT), chitosan-N-2-hydroxypropyl trimethy-lammonium chloride (HACC), and acrylamide as materials. As a nanofiller, montmorillonite enhanced the me-chanical properties of the hydrogel, achieving superior tensile strength (47 KPa), considerable tensile strain (660%), and desired compressive property. The cations exchange between HACC and MMT promoted the uni-form dispersion of MMT to synthesize hydrogels with a consistent structure. Antibacterial test results of hydrogels showed an excellent inhibitory effect against Escherichia coli (> 96%) and Staphylococcus aureus (> 98%). Moreover, these nanocomposite hydrogels exhibited excellent biocompatibility (> 88%) and superior adhesion (> 14 KPa), making them ideal as wound dressing materials. The full-thickness skin defect experiments in mice showed that nanocomposite hydrogel dressings significantly accelerated wound closure and promoted tissue regeneration and collagen deposition.
引用
收藏
页数:11
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