Effects of the application of low-temperature atmospheric plasma on titanium implants on wound healing in peri-implant connective tissue in rats

• Published in: International journal of implant dentistry 2024-03, Vol.10 (1), p.15, Article 15
• Main Authors: Harada, Atsuro, Sasaki, Hodaka, Asami, Yosuke, Hanazawa, Kiyotoshi, Miyazaki, Sota, Sekine, Hideshi, Yajima, Yasutomo
• Format: Article
• Language: English
• Subjects: Acceleration; Animals; Atmospheric pressure; Cell adhesion; Collagen; Connective tissue; Connective Tissue - pathology; Connective tissues; Contact angle; Contact pressure; Dental Implants; Dentistry; Gene expression; In vivo methods and tests; Low temperature; Maturation; Medicine; Plasma; Polymerase chain reaction; Rats; Sealing; Soft tissues; Surface Properties; Surgical implants; Temperature; Titanium; Transplants & implants; Wound Healing
• ISSN: 2198-4034; 2198-4034
• DOI: 10.1186/s40729-024-00524-3

Purpose This study aimed to clarify the effects of surface modification of titanium (Ti) implants by low-temperature atmospheric pressure plasma treatment on wound healing and cell attachment for biological sealing in peri-implant soft tissue. Methods Hydrophilization to a Ti disk using a handheld low-temperature atmospheric pressure plasma device was evaluated by a contact angle test and compared with an untreated group. In in vivo experiments, plasma-treated pure Ti implants using a handheld plasma device (experimental group: PL) and untreated implants (control group: Cont) were placed into the rat upper molar socket, and samples were harvested at 3, 7 and 14 days after surgery. Histological evaluation was performed to assess biological sealing, collagen- and cell adhesion-related gene expression by reverse transcription quantitative polymerase chain reaction, collagen fiber detection by Picrosirius Red staining, and immunohistochemistry for integrins. Results In in vivo experiments, increased width of the peri-implant connective tissue (PICT) and suppression of epithelial down growth was observed in PL compared with Cont. In addition, high gene expression of types I and XII collagen at 7 days and acceleration of collagen maturation was recognized in PL. Strong immunoreaction of integrin α2, α5, and β1 was observed at the implant contact area of PICT in PL. Conclusions The handheld low-temperature atmospheric pressure plasma device provided hydrophilicity on the Ti surface and maintained the width of the contact area of PICT to the implant surface as a result of accelerated collagen maturation and fibroblast adhesion, compared to no plasma application.