Effects of TiO 2 Nanotubes and Reduced Graphene Oxide on Streptococcus mutans and Preosteoblastic Cells at an Early Stage.
Min-Kyung JiHyeonji KimGeonwoo JeongWon-Jae KimJe-Hwang RyuHoonsung ChoHyun-Pil LimPublished in: International journal of molecular sciences (2024)
The effects of TiO 2 nanotube (TNT) and reduced graphene oxide (rGO) deposition onto titanium, which is widely used in dental implants, on Streptococcus mutans ( S. mutans ) and preosteoblastic cells were evaluated. TNTs were formed through anodic oxidation on pure titanium, and rGO was deposited using an atmospheric plasma generator. The specimens used were divided into a control group of titanium specimens and three experimental groups: Group N (specimens with TNT formation), Group G (rGO-deposited specimens), and Group NG (specimens under rGO deposition after TNT formation). Adhesion of S. mutans to the surface was assessed after 24 h of culture using a crystal violet assay, while adhesion and proliferation of MC3T3-E1 cells, a mouse preosteoblastic cell line, were evaluated after 24 and 72 h through a water-soluble tetrazolium salt assay. TNT formation and rGO deposition on titanium decreased S. mutans adhesion ( p < 0.05) and increased MC3T3-E1 cell adhesion and proliferation ( p < 0.0083). In Group NG, S. mutans adhesion was the lowest ( p < 0.05), while MC3T3-E1 cell proliferation was the highest ( p < 0.0083). In this study, TNT formation and rGO deposition on a pure titanium surface inhibited the adhesion of S. mutans at an early stage and increased the initial adhesion and proliferation of preosteoblastic cells.
Keyphrases
- biofilm formation
- reduced graphene oxide
- candida albicans
- pseudomonas aeruginosa
- induced apoptosis
- staphylococcus aureus
- gold nanoparticles
- early stage
- escherichia coli
- cell cycle arrest
- cell adhesion
- signaling pathway
- cell proliferation
- water soluble
- cell death
- visible light
- squamous cell carcinoma
- cystic fibrosis
- nitric oxide
- air pollution
- hydrogen peroxide
- quantum dots
- rectal cancer
- cell cycle
- sentinel lymph node
- cell migration
- single cell