Three-species biofilm model onto plasma-treated titanium implant surface

• Published in: Colloids and surfaces, B, Biointerfaces Vol. 152; pp. 354 - 366
• Main Authors: Matos, Adaias O., Ricomini-Filho, Antônio P., Beline, Thamara, Ogawa, Erika S., Costa-Oliveira, Bárbara E., de Almeida, Amanda B., Nociti Junior, Francisco H., Rangel, Elidiane C., da Cruz, Nilson C., Sukotjo, Cortino, Mathew, Mathew T., Barão, Valentim A.R.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-04-2017
• Subjects: Actinomyces - growth & development; Animals; Bacterial Adhesion; Biocompatible Materials; Biofilms; Biofilms - growth & development; Cell Line; Dental Implants - microbiology; Fusobacterium nucleatum - growth & development; Glow discharge plasma; Mice; Micro-arc oxidation; Microscopy, Atomic Force; Microscopy, Confocal; Microscopy, Electron, Scanning; Oxidation-Reduction; Streptococcus sanguis - growth & development; Surface Properties; Titanium; Titanium - chemistry; Titanium; Glow discharge plasma; Biofilms; Micro-arc oxidation
• ISSN: 0927-7765; 1873-4367
• DOI: 10.1016/j.colsurfb.2017.01.035

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•MAO treatment promoted greater wettability and roughness.•GDP treatment was able to increase the wettability and surface free energy of cpTi.•Plasma technology maintained the bacterial proliferation under control.•Plasma treatments did not reduce cell viability.
In this study, titanium (Ti) was modified with biofunctional and novel surface by micro-arc oxidation (MAO) and glow discharge plasma (GDP) and we tested the development of a three-species periodontopatogenic biofilm onto the treated commercially-pure titanium (cpTi) surfaces. Machined and sandblasted surfaces were used as control group. Several techniques for surface characterizations and monoculture on bone tissue cells were performed. A multispecies biofilm composed of Streptococcus sanguinis, Actinomyces naeslundii and Fusobacterium nucleatum was developed onto cpTi discs for 16.5h (early biofilm) and 64.5h (mature biofilm). The number of viable microorganisms and the composition of the extracellular matrix (proteins and carbohydrates) were determined. The biofilm organization was analyzed by scanning electron microscopy (SEM) and Confocal laser scanning microscopy (CLSM). In addition, MC3T3-E1 cells were cultured on the Ti surfaces and cell proliferation (MTT) and morphology (SEM) were assessed. MAO treatment produced oxide films rich in calcium and phosphorus with a volcano appearance while GDP treatment produced silicon-based smooth thin-film. Plasma treatments were able to increase the wettability of cpTi (p<0.05). An increase of surface roughness (p<0.05) and formation of anatase and rutile structures was noted after MAO treatment. GDP had the greatest surface free energy (p<0.05) while maintaining the surface roughness compared to the machined control (p>0.05). Plasma treatment did not affect the viable microorganisms counts, but the counts of F. nucleatum was lower for MAO treatment at early biofilm phase. Biofilm extracellular matrix was similar among the groups, excepted for GDP that presented the lowest protein content. Moreover, cell proliferation was not significantly affected by the experimental, except for MAO at 6days that resulted in an increased cell proliferative. Together, these findings indicate that plasma treatments are a viable and promising technology to treat bone-integrated dental implants as the new surfaces displayed improved mechanical and biological properties with no increase in biofilm proliferation.