Optimization of Lactoferrin-Derived Amyloid Coating for Enhancing Soft Tissue Seal and Antibacterial Activity of Titanium Implants

Wan rong Wang, Jing Li, Jun ting Gu, Bo wen Hu, Wen Qin, Yi na Zhu, Zhen xing Guo, Yu Xuan Ma, Franklin Tay, Kai Jiao, Lina Niu

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

A poor seal of the titanium implant–soft tissue interface provokes bacterial invasion, aggravates inflammation, and ultimately results in implant failure. To ensure the long-term success of titanium implants, lactoferrin-derived amyloid is coated on the titanium surface to increase the expression of cell integrins and hemidesmosomes, with the goal of promoting soft tissue seal and imparting antibacterial activity to the implants. The lactoferrin-derived amyloid coated titanium structures contain a large number of amino and carboxyl groups on their surfaces, and promote proliferation and adhesion of epithelial cells and fibroblasts via the PI3K/AKT pathway. The amyloid coating also has a strong positive charge and possesses potent antibacterial activities against Staphylococcus aureus and Porphyromonas gingivalis. In a rat immediate implantation model, the amyloid-coated titanium implants form gingival junctional epithelium at the transmucosal region that resembles the junctional epithelium in natural teeth. This provides a strong soft tissue seal to wall off infection. Taken together, lactoferrin-derived amyloid is a dual-function transparent coating that promotes soft tissue seal and possesses antibacterial activity. These unique properties enable the synthesized amyloid to be used as potential biological implant coatings.

Original languageEnglish (US)
Article number2203086
JournalAdvanced Healthcare Materials
Volume12
Issue number11
DOIs
StatePublished - Apr 26 2023

Keywords

  • antibacterial implants
  • lactoferrin amyloid
  • soft tissue seals
  • titanium implants

ASJC Scopus subject areas

  • Biomaterials
  • Biomedical Engineering
  • Pharmaceutical Science

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