Preparation and Performance Evaluation of a Zinc Oxide-Graphene Oxideloaded Chitosan-Based Thermosensitive Gel

被引:1
作者
Huang, Hao [1 ,2 ]
Han, Rui [1 ,2 ]
Huang, Ping-Ping [1 ,2 ]
Qiao, Chuan-Yue [1 ,2 ]
Bian, Shuang [1 ,2 ]
Xiao, Han [1 ,2 ]
Ma, Lei [1 ,2 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Prosthodont, Qingdao 266003, Peoples R China
[2] Qingdao Univ, Sch Stomatol, Qingdao 266023, Peoples R China
关键词
Thermosensitive hydrogel; graphene oxide; chitosan; nano zinc oxide; antibacterial; ZNO NANOPARTICLES; ANTIBACTERIAL ACTIVITY;
D O I
10.4014/jmb.2402.02055
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study aimed to develop and assess a chitosan biomedical antibacterial gel ZincOxideGrapheneOxide/Chitosan/13-Glycerophosphate (ZnO-GO/CS/13-GP) loaded with nano-zinc oxide (ZnO) and graphene oxide (GO), known for its potent antibacterial properties, biocompatibility, and sustained drug release. ZnO nanoparticles (ZnO-NPs) were modified and integrated with GO sheets to create 1% and 3% ZnO-GO/CS/13-GP thermo-sensitive hydrogels based on ZnO-GO to Chitosan (CS) mass ratio. Gelation time, pH, structural changes, and microscopic morphology were evaluated. The hydrogel's antibacterial efficacy against Porphyromonas gingivalis, biofilm biomass, and metabolic activity was examined alongside its impact (MC3T3-e1). The findings of this study revealed that both hydrogel formulations exhibited temperature sensitivity, maintaining a neutral pH. The ZnO-GO/CS/13-GP formulation effectively inhibited P. gingivalis bacterial activity and biofilm formation, with a 3% ZnO-GO/CS/13-GP antibacterial rate approaching 100%. MC3T3-e1 cells displayed good biocompatibility when cultured in the hydrogel extract.The ZnO-GO/CS/13-GP thermo-sensitive hydrogel demonstrates favorable physical and chemical properties, effectively preventing P. gingivalis biofilm formation. It exhibits promising biocompatibility, suggesting its potential as an adjuvant therapy for managing and preventing peri-implantitis, subject to further clinical investigations.
引用
收藏
页码:1229 / 1238
页数:10
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