# Anodization and Its Role in Peri-Implant Tissue Adhesion: A Novel 3D Bioprinting Approach

## TL;DR

This study uses 3D bioprinting to compare how yellow anodized titanium abutments affect epithelial cell behavior compared to traditional ones, finding better cell organization on anodized surfaces.

## Contribution

A novel 3D bioprinted peri-implant mucosa model was developed to evaluate epithelial cell responses to yellow anodized titanium surfaces.

## Key findings

- Anodized titanium surfaces showed enhanced epithelial cytoskeletal organization compared to turned surfaces.
- TRITC-phalloidin signal intensity was significantly higher on anodized samples after 21 days.
- Both surfaces supported epithelial coverage in a 3D environment.

## Abstract

Background: Soft tissue stability around dental implant abutments is critical for maintaining a functional peri-implant seal. Yellow anodization is used to improve the aesthetic and surface characteristics of titanium abutments, yet its epithelial effects under more physiologically relevant 3D conditions remain insufficiently explored. Objective: To develop a 3D bioprinted in vitro peri-implant mucosa model and to compare epithelial cell responses on yellow anodized versus turned titanium abutment surfaces. Methods: Commercial Grade 5 (Ti6Al4V) titanium abutments were anodized and compared with turned controls. A collagen-based 3D bioprinted “collar-like” construct incorporating YD-38 epithelial cells was fabricated using a custom holder system to simulate peri-implant mucosal contact. Samples were cultured for 14 and 21 days. Cell distribution and morphology were assessed by optical microscopy and HE staining, while cytoskeletal organization was evaluated by TRITC-phalloidin/Hoechst staining and confocal microscopy. Quantitative fluorescence analysis was performed at 21 days. Results: Both surfaces supported epithelial coverage in the 3D environment. Anodized specimens showed more pronounced actin cytoskeletal organization and the presence of actin-rich, filamentous cellular extensions compared with turned controls. Quantitative image analysis demonstrated significantly higher TRITC-phalloidin signal intensity at 21 days on anodized samples (p < 0.001). Conclusions: Within the limitations of a 3D epithelial in vitro model using YD-38 cells, yellow anodization was associated with enhanced epithelial cytoskeletal organization compared with turned titanium. The presented 3D bioprinted platform may serve as a practical in vitro tool for screening abutment surface modifications relevant to peri-implant soft tissue integration.