Effects of nanomodified titanium surfaces considering bacterial colonization and viability of osteoblasts and fibroblasts

Abstract This study investigates nanostructured titanium surfaces (Ti2 spikes) that promote the viability of osteoblasts and fibroblasts and prevent bacterial colonisation. Helium ion irradiation was adopted to produce nanometric‐sized cones on titanium. Human osteoblasts (hFOB) and human gingiva fibroblasts (hGF) were used for analysis. A viability and a cytotoxicity assay were conducted to evaluate the lactate dehydrogenase (LDH) activity and assess cell damage in Ti2 spikes compared to titanium discs with a sandblasted and acid‐etched (Ti2 SLA) surface. The antibacterial activity was investigated against Escherichia coli , Streptococcus mutans , Fusobacterium nucleatum , and Porphyromonas gingivalis . In the course of the cultivation, both hGF and hFOB demonstrated significantly reduced viability on the Ti2 spikes surface. hGF cells exhibited a slight but significant increase in LDH release. In contrast, hFOB showed reduced cytotoxicity on this surface. On the Ti2 spikes surface, hGF cells exhibited a significant reduction in gene expression of VCL, Src‐1, and ITGα5. However, the integrin subunits ITGα1 and ITGα3 showed upregulation on the Ti2 spikes surface. The Ti2 spikes surface significantly increased the expression of almost all osteogenic markers. The results of conventional culturing demonstrated a statistically significant decrease in the number of viable cells for S . mutans , F . nucleaum , and greater quantities of P . gingivalis on Ti2 spikes surface compared to control. However, no such reduction was detected for E . coli . The long‐term success of implants relies on establishing and maintaining hard and soft peri‐implant tissues. Ti2 spikes represent a novel and promising approach to enhance osseointegration and optimize biocompatibility.