| Literature DB >> 35745007 |
Shuang Liu1, Xingzhu Chen1, Mingyue Yu1, Jianing Li1, Jinyao Liu1, Zunxuan Xie1, Fengxiang Gao2, Yuyan Liu1.
Abstract
Breakthroughs in the field of nanotechnology, especially in nanochemistry and nanofabrication technologies, have been attracting much attention, and various nanomaterials have recently been developed for biomedical applications. Among these nanomaterials, nanoscale titanium dioxide (nano-TiO2) has been widely valued in stomatology due to the fact of its excellent biocompatibility, antibacterial activity, and photocatalytic activity as well as its potential use for applications such as dental implant surface modification, tissue engineering and regenerative medicine, drug delivery carrier, dental material additives, and oral tumor diagnosis and treatment. However, the biosafety of nano-TiO2 is controversial and has become a key constraint in the development of nano-TiO2 applications in stomatology. Therefore, in this review, we summarize recent research regarding the applications of nano-TiO2 in stomatology, with an emphasis on its performance characteristics in different fields, and evaluations of the biological security of nano-TiO2 applications. In addition, we discuss the challenges, prospects, and future research directions regarding applications of nano-TiO2 in stomatology that are significant and worthy of further exploration.Entities:
Keywords: antibacterial; dental implant surface modification; dental material additives; nanostructure; titanium dioxide
Mesh:
Substances:
Year: 2022 PMID: 35745007 PMCID: PMC9229536 DOI: 10.3390/molecules27123881
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.927
Figure 1Common forms of nano-TiO2 and its application in stomatology (the figure was drawn using Figdraw, and part of picture material is cited from https://smart.servier.com/ (accessed on 13 May 2022)).
Figure 2(A) The constructed coating. At a normal body temperature (37 °C), the hydrogel is in a sol state, which controls the continuous release of simvastatin and promotes long-term osteogenic differentiation. When the temperature rises to 40 °C, the hydrogel changes from sol to gel, releasing Gly to stimulate macrophages to polarize into a proinflammatory M1 phenotype to kill bacteria. (B) The results of the ALP activity of MC3T3-E1 after 14 days of culture. (C) E. coli colony count. Reprinted from Reference [63]; Copyright 2022, with permission from Elsevier. * p < 0.05; ** p < 0.01; *** p < 0.001.
Figure 3(A) Cell behavior in response to TNTs of different sizes in different microenvironments; (B) protective effect of large TNTs on ROS injury. Reprinted from Reference [81]; Copyright 2022, with permission from Elsevier. (a. The high expression of ITG α5β1 on TNT110 substrates promoted the early adhesion of osteo-blasts; b. The up-regulation of Bcl2 and down-regulation of Bax improved cell survival; c. High expression of p-FoxO3a and β-catenin proteins promoted the osteogenic differentiation).
Figure 4(A) Construction diagram of a nanofibrillated, chitosan-coated, highly ordered titania nanotube array/graphene nanocomposite; (B) release curves of vancomycin in different groups; (C) viability of MG63 cells in different groups; (D) colony count of Staphylococcus aureus in different groups. Reprinted from Reference [94]; Copyright 2022, with permission from Elsevier.
Figure 5Modification of the substrate to capture and release CTCs. Reprinted with permission from Reference [123]; Copyright 2022, American Chemical Society.