Implant Surface Decontamination Methods That Can Impact Implant Wettability
Abstract
:1. Introduction
2. Implant Surface Decontamination Methods
2.1. Physical Decontamination Methods
2.1.1. Surface Decontamination with Lasers
Impact of Lasers on Surface Wettability
2.1.2. Surface Decontamination with Air-Polishing
Air-Polishing and Surface Wettability
2.1.3. Surface Decontamination with UV Light
UV Light and Surface Wettability
2.1.4. Plasma Surface Decontamination
Plasma Decontamination and Surface Wettability
2.2. Chemical Treatment Decontamination Methods
2.2.1. Chlorhexidine (CHX) Decontamination
- 0.1% to 0.2% CHX—Lower concentrations, often used as mouth rinses or irrigation solutions, are less aggressive on tissues and can be effective for maintaining peri-implant health. For instance, 0.2% CHX has been used as an irrigation solution in cases of peri-implant mucositis to reduce the bacterial load [64].
- 1% CHX gel—This concentration is commonly applied directly to implant surfaces during non-surgical peri-implantitis treatments. It allows for localized application, reducing bacterial colonization while minimizing tissue irritation. Studies indicate that 1% CHX gel may be effective in reducing microbial contamination on implants [65].
- 2% CHX solution—Higher concentrations, such as 2%, are typically used in clinical settings for mechanical debridement or adjunctive surgical treatments of peri-implantitis. The 2% solution provides potent antimicrobial action, which is particularly useful when a more aggressive approach to decontamination is required [66].
Chlorhexidine (CHX) Decontamination and Surface Wettability
2.2.2. Hydrogen Peroxide (H2O2) Decontamination
Hydrogen Peroxide (H2O2) Decontamination and Surface Wettability
2.2.3. Citric Acid Decontamination
Citric Acid Decontamination and Surface Wettability
2.2.4. Ethylenediaminetetraacetic Acid (EDTA) Decontamination
Ethylenediaminetetraacetic Acid (EDTA) Decontamination and Surface Wettability
2.2.5. Sodium Hypochlorite (NaOCl) Decontamination
Sodium Hypochlorite and Surface Wettability
3. Summary and Conclusions
4. Challenges and Future Research
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Physical Decontamination Methods |
Lasers |
Air-polishing |
UV Light |
Plasma |
Chemical Treatment Decontamination Methods |
Chlorhexidine (CHX) |
Hydrogen Peroxide (H2O2) |
Citric Acid |
Ethylenediaminetetraacetic Acid (EDTA) |
Sodium Hypochlorite (NaOCl) |
Study: Lasers | Decontamination Method | Impact on Surface Roughness | Impact on Wettability | Biocompatibility/ Biological Effects | Key Findings |
---|---|---|---|---|---|
Kreisler et al. (2002) | Er:YAG laser | N/A | N/A | N/A | Decontamination of implant surfaces by means of the Er:YAG laser did not excessively heat the periimplant bone. |
Friedmann et al. (2006) | Er:YAG laser (23.5 s with a pulsed, water-cooled laser beam) | Er: YAG laser can create micro-textures that enhance the surface roughness. | Wettability is enhanced after laser treatment, promoting osteoblast attachment. | Osteoblasts show greater attachment on laser-treated surfaces. | Er:YAG laser removed P. gingivalis and cellular debris, providing a suitable surface for the attachment of new osteoblasts. |
Romanos et al. (2006) | CO2 laser (10,600 nm; 4–6 W; 20 Hz, dual cycle 6%) or Er,Cr:YSGG laser (2780 nm; 1.25 W; air 42; water 41) | N/A | N/A | Osteoblasts may be grown on all of the surfaces. | Laser irradiation of titanium surfaces with carbon dioxide or Er,Cr:YSGG lasers may promote osteoblast attachment and osteoblastic proliferation. |
Ayobian-Markazi et al. (2015) | Er:YAG laser (10 Hz; 230 μs pulse duration; 100 mJ/pulse; 12.8 J/cm2 energy density) with a cone-shaped fiber tip. SLA titanium surfaces. | Decreased surface roughness. | Increased wettability. | Biocompatibility is enhanced, showing better cell adhesion and growth. | Er:YAG laser irradiation (100 mJ/pulse, 10 Hz) enhances the biocompatibility and osteoblast response of SLA titanium surfaces, reducing the surface roughness and increasing the wettability. |
Amid et al. (2021) | Er:YAG, (MZ6 tip; 150 mJ/pulse; 1.5 W; 10 Hz frequency). Air-polishing with glycine. | N/A | Er:YAG and air-polishing both increased wettability. | N/A | Air-flow abrasion improved titanium surface characteristics without altering their topography or elements. |
Sousa et al. (2022) | Ti brushes (TiB), TiB with photodynamic therapy (λ: 660–675 nm; 11 mW), TiB with 0.2% CHX/1% NaClO, and treatments with or without UV-C radiation. | TiB decreased Ra. | Increased wettability with TiB plus UV-C irradiation. | No treatment hindered titanium biocompatibility; however, chemical agents and micro-rough surfaces increased cytotoxicity in MG-63 cells, while smooth surfaces and TiO2 photofunctionalization improved cytocompatibility post-decontamination. | UV-C photofunctionalization improves Ti surface biocompatibility and MG-63 cell proliferation, with smooth surfaces and TiO2 photofunctiona-lization yielding optimal results. |
Rezeka et al. (2024) | Diode lasers (940 nm; 1 W, 2W, or 3W). All groups irradiated for 30 s in continuous mode. | Laser irradiation decreased the roughness by melting the surface. | Wettability increased after laser treatment. | Diode lasers (940 nm) at 2 W and 3 W enhanced titanium surface hydrophilicity, potentially improving implant osseointegration after decontamination. | Diode lasers (940 nm) at 2 W and 3 W power significantly altered the surface characteristics of the material. |
Al-Khafaji and Hamad (2020) | Laser structuring. | Ra for the dot-and-groove structuring design increased with an increasing number of laser scans. Laser structuring with the dot design for any laser scan caused and increase in Ra. | Wettability of commercial pure titanium disks for the dot-and-groove structuring design increased with an increasing number of laser scans. Laser structuring with the dot design for any laser scan caused increased wettability. | Laser structuring may enhance cell adhesion, including for osteoblasts, due to improved surface roughness and wettability. | Laser dot-and-groove structuring, especially with 25 laser scans, increased the surface roughness and wettability of CP Ti disks. |
Khosroshahi et al. (2009) | Nd-YAG laser (1.06 μm wavelength; 200 μs pulse duration and pulse energy of 50 J). | Increased Ra after Nd-YAG laser treatment from 0 J cm−2 to 100 J cm−2 and decreased Ra after laser radiation at 140 J cm−2. | Decreased wettability after laser radiation from 0 J cm−2 to 100 J cm−2 and increased wettability after laser radiation at 140 J cm−2. | Decrease in contact angle due to Nd-YAG laser treatment can cause more cell adhesion to the surface | SEM, contact angle, and preliminary in vitro/in vivo tests show that Nd laser treatment enhances cell adhesion and improves the physicochemical properties of the Ti6Al4V alloy. |
Lee et al. (2023) | Er,Cr:YSGG laser (2780 nm; 2 W; 300 mJ; 10 Hz; 10 sec), diode laser (940 nm; 2 W; 100 mJ; 10 Hz; 10 sec), and electrocautery. | Er,Cr:YSGG laser increased the roughness of SLA- and femtosecond-laser-treated disks compared with machined surfaces. | Er,Cr:YSGG laser on femtosecond-laser-treated surfaces showed statistically significant differences compared with other treatment methods. | Increased O2 levels after Er,Cr:YSGG laser (promotes formation of TiO2 layer) | Er,Cr:YSGG laser and electrocautery treatments signifi-cantly altered the surface roughness of titanium implant surfaces. |
Staehlike et al. (2022) | Laser structuring and cold atmospheric plasma. | Laser structuring increases Ra. | Laser-induced microstructures are hydrophobic, but they are hydrophilic after argon plasma activation. | Surface nano–microtopography combined with plasma chemistry enhances the strong attachment of human gingival HGF-1 fibroblasts to zirconia surfaces. | Both laser microstructuring and argon plasma activation of zirconia seems to be optimal for strong gingival cell attachment. |
Study | Decontamination Method | Impact on Surface Roughness | Impact on Wettability | Biocompatibility/Biological Effects | Key Findings |
---|---|---|---|---|---|
Bennani et al. (2015) | Air-polishing with glycine | Treated disks had a higher mean Ra | N/A | 88% reduction in the amount of biofilm on the air-polished disks | Air-polishing is effective in biofilm removal, maintaining surface integrity, and increasing the Ra. |
Petersilka et al. (2008) | Air-polishing with glycine or sodium bicarbonate | N/A | N/A | No adverse effects on gingival tissues; improved cleaning efficacy | Glycine powder results in less gingival erosion than hand instrumentation or sodium bicarbonate air-polishing. |
Cochis et al. (2013) | Air-polishing with glycine or sodium bicarbonate | Increased Ra with sodium bicarbonate; no change with glycine | Increased wettability | Glycine powder effectively inhibits bacterial recolonization on implants within 24 h | Air-polishing with glycine powder is an effective method for plaque removal from dental implants. |
Mistretta et al. (2024) | Air-polishing with glycine or erythritol | Increased Ra | Increased wettability after erythritol air-polishing | Erythritol air-polishing could improve the predictability of regenerative grafting techniques. | Erythritol increased the surface wettability of zirconia disks significantly better than glycine air-polishing. |
Francis et al. (2023) | Air-polishing with sodium bicarbonate, glycine, erythritol, or calcium carbonate | No change | N/A | All treated surfaces showed minimal bacterial residues compared with untreated ones | Treatment with different air–powders for 20 s did not alter the surface topography of both M and MRS surfaces. |
Drago et al. (2014) | Air-polishing with glycine or erythritol–chlorhexidine powders | N/A | N/A | Erythritol–chlorhexidine air-polishing seemed to display stronger activity than glycine against all the microbial strains tested. | Air-polishing with erythritol-chlorhexidine seems to be a valuable alternative to the traditional glycine treatment. |
Kim et al. (2023) | Air-polishing with glycine, 0.12% chlorhexidine and Er:YAG laser | N/A | N/A | Enhanced osseointegra-tion and cell attachment in vivo | Air–powder decontamination improved titanium surface properties and promoted osseointegration in a rabbit tibia model. |
Toma et al. (2019) | Plastic curettes, air-polishing with glycine and a titanium brush (Ti-Brush®) | N/A | N/A | Different treatments influenced soft-tissue healing and implant stability | Air-polishing and Ti-Brush® protocols were more effective than plastic curettes. |
Hentenaar et al. (2022) | Air-polishing with erythritol | N/A | N/A | No significant differences between both groups for mean peri-implant log-transformed bacterial counts. | Erythritol air-polishing was not more effective than saline for implant surface cleansing during peri-implantitis surgery. |
Huang et al. (2019) | Air-polishing with glycine, titanium curette treatment, carbon-fiber-reinforced plastic curette treatment, ultrasonic scaling with carbon-fiber-tip treatment | No change Curettes on Ti disks increased Ra | Air-polishing treatment groups showed significan-tly reduced hydrophili- city | For titanium disks, curettes were shown to create deep scratches and increased surface roughness, thereby facilitating the adhesion of bacteria. | Zirconia showed superior resistance to damage from all of the cleaning procedures. |
Toma et al. (2016) | Plastic curette, air-polishing with glycine, Ti-Brush and implantoplasty | N/A | Increased wettability after implantoplasty. Decrease in the surface wettability of the plastic curette disks. Hydrophobic character of control-, plastic curette-, Perio-Flow- and Ti-Brush-treated surfaces. | All treatments improved cell adhesion and proliferation and promoted a mature osteoblastic phenotype. | Laser and chemical methods were more effective in improving osteoblast attachment and cell viability compared with mechanical decontamination. |
Matthes et al. (2017) | Air-polishing with erythritol, cold atmospheric pressure argon plasma, or both | N/A | Increased wettability for all methods | Air-polishing restores cell compatibility with microbially contaminated implant surfaces. | Plaque removal with air-polishing rendered specimen conducive to cell growth. |
Kister et al. (2017) | Diamond burs, polishers, plastic and metal hand instruments, air scalers, and air-polishing with sodium bicarbonate | Air-flow device and plastic curette both showed a minor increase in Ra | Increased wettability after use of an air scaler, air-polishing device, and ProCup treatments | Different cleaning instruments affected the nanocoating integrity and biocompatibi-lity. | Air–powder abrasives and plastic instruments did not damage titanium implant surfaces. |
Study | Decontamination Method | Impact on Surface Roughness | Impact on Wettability | Biocompatibility/ Biological Effects | Key Findings |
---|---|---|---|---|---|
Rupp et al. (2010) | UV irradiation | N/A | - Anatase surfaces became superhydrophilic (contact angle < 5°) after 75 s of UV treatment with a dosage of 1.9 J/cm2. - Ti surfaces showed minimal reduction in contact angle (from 65° to ~58°). | - Enhanced superhydrophilicity on anatase surfaces. - Increased hydroxyl group formation and reduced hydrocarbons, improving surface cleanliness. - Effectively decomposed protein layers on anatase under UV. | UV irradiation removed ~76% of the adsorbed human serum albumin (HSA) on anatase but had no effect on Ti. |
Park et al. (2011) | UV irradiation | No significant change in surface roughness (Sa: 0.833 ± 0.032 μm for the control samples; 0.854 ± 0.026 μm for the test samples). | Significant increase in hydrophilicity (contact angle: 22.69° ± 4.35° for test samples; 77.43° ± 3.80° for control samples). | Enhanced initial cellular attachment (p = 0.004), increased cell proliferation (p = 0.009), and higher ALP synthesis (p = 0.016 at day 3; p = 0.009 at days 7 and 14). | UV irradiation after 24 h improved wettability, leading to enhanced cellular attachment, proliferation, and differentiation without significant changes in the surface roughness or the oxide layer phase. Carbon content decreased after UV treatment. |
Wantanabe et al. (2012) | UV irradiation | No significant change in surface roughness. | Increased wettability. Contact angle = 0° (superhydrophi-lic). | Enhanced cell attachment. | UV treatment (2 h at 19 mW/cm2 with UV-C and UV-A radiation) promoted superhydrophilicity and improved osteoblast attachment. |
Tuna et al. (2015) | UV irradiation | No topographic changes; roughened surfaces remained rough (Zr1-r, Zr2-r), smooth surfaces remained smooth (Zr1-m, Zr2-m). | Significant shift from hydrophobic to hydrophilic. Contact angles decreased to 2.5–14.1° from 56.4–68.8° before treatment. | UV treatment led to a substantial decrease in surface carbon content (43–81%) and increased oxygen (19–45%) and zirconia (9–41%). The UV treatment increased the monoclinic phase in the Zr1 material by 19–25%. | 15 min of UV applied on zirconia surfaces changed the surface properties and significantly improved the wettability. |
Rutkunas et al. (2022) | UV irradiation | No significant difference in surface roughness (Ra = 0.094 ± 0.027 µm for ZrO-HT; Ra = 0.11 ± 0.036 µm for ZrO-UTML). | Slight increase in contact angle, but no significant difference (F(16) = 3.50; p = 0.292). | No significant difference in cytotoxicity; significant material-dependent changes in fibroblast proliferation (F(8) = 9.58; p = 0.005). | UV treatment altered cell viability and promoted cell proliferation in a material-dependent manner. - UV photofunctionalization enhanced HGF cell proliferation, particularly in ultra-translucent zirconia at 72 h. |
Hui et al. (2020) | Cold atmospheric plasma | No significant alterations to titanium surface features; preserved implant topography. | No reported changes in wettability. | No adverse biological effects; treatments did not compromise implant biocompatibility. | - CAP alone removed 52.10% of the biofilm, while combining CAP with air abrasion (AA) removed 95.32%. - AA and CAP combined yielded the best decontamination results. - CAP alone showed minimal biofilm removal; this requires further investigation for its potential as a standalone treatment. |
Flörke et al. (2022) | Cold atmospheric plasma | No significant change in surface roughness; titanium implant topography preserved. | No significant effect on wettability. | No adverse effects on biocompatibility; significant reduction in bacterial load. | - CAP treatment resulted in the lowest bacterial count (1.24 × 105 CFU/mL), which was significantly lower than that of PDT (8.28 × 106 CFU/mL) and PAG (3.14 × 106 CFU/mL). - CAP also showed the highest reduction in live bacteria and superior antimicrobial effectiveness. - Despite a significant reduction in bacterial load, complete decontamination was not achieved. |
Martins et al. (2024) | Cold atmospheric plasma | No significant change in surface roughness. | Significant reduction in contact angle from 59 ± 1.8° (untreated) to 14 ± 2.2° (CAP-treated), indicating improved wettability. | - Improved hemocompatibility with faster clot formation (shorter PT and APTT times). - Increased platelet activation, density, and thrombus formation. - Reduced bacterial colony formation by Pseudomonas aeruginosa. | CAP treatment enhanced the surface wettability, improved the interaction with blood components, and reduced bacterial colonization, making it a promising method for decontaminating titanium implants while enhancing biocompatibility. |
Study | Decontamination Method | Impact on Surface Roughness | Impact on Wettability | Biocompatibility/Biological Effects | Key Findings |
---|---|---|---|---|---|
Stuani et al. (2021) | CHX | Decreased roughness. | No significant differences in wettability. | Residual CHX remained on the surface of the titanium implant, even after rinsing. | CHX displayed substantivity on titanium surfaces. |
Bayrak et al. (2022) | CHX | No significant change in surface roughness. | Significant increase in wettability. | CHX residue adsorbed onto the titanium SLA surface. | The use of 0.2% CHX solution for 60 s improved surface wettability. |
Mouhyi et al. (2000) | H2O2 + CO2 laser | N/A | Significant increase in wettability. | Restoration of the oxide layer onto the titanium implant surface. | A combination of H2O2 + CO2 laser seems effective in the re-establishment of the atomic composition and oxide structure of contaminated titanium surfaces. |
Yoneyama et al. (2013) | H2O2 hydrothermal oxidation | SEM analysis showed increased surface roughness after treatment. | Significant increase in wettability. | Loading with fibroblast growth factor-2 (FGF-2) promoted the initial cell adhesion, proliferation, and osteodifferentiation, and enhanced bone bioactivity. | This treatment increased the initial adhesion, proliferative, and osteodifferentiation capacities of cells on the surface of titanium disks and promoted bone formation around a mini-implant. |
Lee et al. (2021) | Brushing implant surfaces with 3% H2O2 | N/A | N/A | This treatment restrained biofilm growth. | Compared with mechanical debridement, brushing implant surfaces with 3% H2O2 superiorly restrained biofilm regrowth. |
Noro et al. (2013) | Immersion in 150 mM H2O2 solution at 60 °C for 1 day | N/A | No significant differences in wettability on zirconia surfaces. | Introduction of hydroxyl groups onto zirconia surfaces can decrease the carbon content and therefore improve wettability. | No significant differences in wettability on zirconia surfaces. |
Tuna et al. (2023) | Immersion in 20% H2O2 for two hours | No significant change in surface roughness. | Significant increase in wettability. | Treatment with H2O2 appears to have no effect on the mineralization capacity of osteoblasts. However, the risk of thermal degradation of zirconia polycrystals does increase. | H2O2 treatment increases wettability and has no influence on osteoblast behavior. However, this treatment can be detrimental to material stability. |
Wheelis et al. (2016) | 40% citric acid | Significant increase in surface roughness | N/A | 40% citric acid is corrosive and disrupts the oxide layer on the titanium implant. The authors assume this has a negative effect on wettability. | While no investigation of wettability was performed, the authors assume that disruption of the oxide layer will hinder re-osseointegration. |
Souza et al. (2019) | Citric acid | Increased surface roughness. | N/A | Treatment significantly hindered the re-colonization of bacterial biofilms. | No effect on the oxide layer was observed. The treatment statistically enhanced the electrochemical stability of the titanium disk. |
Kotsakis et al. (2016) | 24% EDTA/1.5% NaOCl solution | N/A; the analysis only mentioned that the treatment left elemental surface contaminants. | Significant increase in surface wettability. | A significant increase in osteoblast proliferation was observed compared with surfaces decontaminated with CHX. | Osteoblast proliferation and differentiation did not significantly differ between decontaminated surfaces and controls. |
Kono et al. (2015) | 5% NaOCl for 24 h | No significant changes in surface roughness. | Significant increase in surface wettability. | Biomechanical push-in test indicated that the bone–titanium integration strength was significantly stronger in decontaminated surfaces. | NaOCl pretreatment enhanced the osseointegration capability of titanium and converted the surfaces from hydrophobic to superhydrophilic. |
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Romanos, G.E.; Mistretta, L.; Newman, A.; Ohana, D.; Delgado-Ruiz, R.A. Implant Surface Decontamination Methods That Can Impact Implant Wettability. Materials 2024, 17, 6249. https://doi.org/10.3390/ma17246249
Romanos GE, Mistretta L, Newman A, Ohana D, Delgado-Ruiz RA. Implant Surface Decontamination Methods That Can Impact Implant Wettability. Materials. 2024; 17(24):6249. https://doi.org/10.3390/ma17246249
Chicago/Turabian StyleRomanos, Georgios E., Lauren Mistretta, Allyson Newman, Danielle Ohana, and Rafael A. Delgado-Ruiz. 2024. "Implant Surface Decontamination Methods That Can Impact Implant Wettability" Materials 17, no. 24: 6249. https://doi.org/10.3390/ma17246249
APA StyleRomanos, G. E., Mistretta, L., Newman, A., Ohana, D., & Delgado-Ruiz, R. A. (2024). Implant Surface Decontamination Methods That Can Impact Implant Wettability. Materials, 17(24), 6249. https://doi.org/10.3390/ma17246249