Effects of an amino acid buffered hypochlorite solution as an adjunctive to air-powder abrasion in open-flap surface decontamination of implants failed for peri-implantitis: an ex vivo randomized clinical trial.

OBJECTIVES: To evaluate ex vivo the efficacy of an amino acid buffered hypochlorite solution supplemented to surface debridement with air-powder abrasion in removing bacterial biofilm following open-flap decontamination of implants failed due to peri-implantitis. MATERIALS AND METHODS: This study was an ex vivo, single-blind, randomized, intra-subject investigation. Study population consisted of 20 subjects with at least three implants failed for peri-implantitis (in function for > 12 months and progressive bone loss exceeding 50%) to be explanted. For each patient, implants were randomly assigned to surface decontamination with sodium bicarbonate air-powder abrasion (test-group 1) or sodium bicarbonate air-powder abrasion supplemented by amino acid buffered hypochlorite solution (test-group 2) or untreated control group. Following open-flap surgery, untreated implants (control group) were explanted. Afterwards, test implants were decontaminated according to allocation and explanted. Microbiological analysis was expressed in colony-forming units (CFU/ml). RESULTS: A statistically significant difference in the concentrations of CFU/ml was found between implants of test-group 1 (63,018.18 ± 228,599.36) (p = 0.007) and implants of test-group 2 (260.00 ± 375.80) (p < 0.001) compared to untreated implants (control group) (86,846.15 ± 266,689.44). The concentration of CFU/ml on implant surfaces was lower in test-group 2 than in test-group 1, with a statistically significant difference (p < 0.001). CONCLUSION: The additional application of amino acid buffered hypochlorite solution seemed to improve the effectiveness of implant surface decontamination with air-powder abrasion following open-flap surgery. CLINICAL RELEVANCE: Lacking evidence on the most effective method for biofilm removal from contaminated implant surfaces, the present experimental study provides further information for clinicians and researchers.

The stability of implants and microbiological effects following photobiomodulation therapy with one-stage placement: A randomized, controlled, single-blinded, and split-mouth clinical study.

BACKGROUND: Studies have reported a positive effect on bone healing and the elimination of microorganisms placed on the titanium implants, while others have not confirmed the positive photobiomodulation therapy (PBMT) effects on bone regeneration and bone structure around the implants. PURPOSE: The aim of the present study was to address the following questions: Does PBMT improve implant stability and affect microbiota around dental implants in the early stage of osseointegration? MATERIALS AND METHODS: This study was designed as randomized-controlled prospective, split mouth, single-blinded clinical trial. Implants were randomly divided into two groups and implants placed in the test group were treated with Gallium-aluminum-arsenide (GaAlAs) diode laser with PBMT immediately after surgery and for 15 days (n = 47). In the control group, implants were not irradiated(n = 46). The primary stability of the implants was measured by the Resonance frequency analysis (RFA) after insertion and the secondary stability values were recorded at 30th, 60th, and 90th days after surgery as implant stability quotient (ISQ). The hand-held RFA was held perpendicular to the jaw line as indicated by the manufacturer for buccal-lingual (BL), mesial-distal (MD), and lingual-buccal (LB) measurement and different measurements were analyzed as separately. RESULTS: Significantly higher magnetic RFA values were achieved on the 90th day in all measurement sides for both groups. ISQ levels in groups at baseline and the day-30, 60, and 90. ISQ readings were not statistically significant between test and control groups for each time point. A statistically significant increase in ISQ reading for BL, MD, and LB dimensions in both groups was noted from baseline to the day-90 (P < .05). CONCLUSION: It was concluded that PBMT did not have a clinically significant effect on implant stabilization, especially in terms of ISQ values at early alveolar bone healing term. Clinical trial number is NCT04495335.

Hydroxyl radicals generated by hydrogen peroxide photolysis recondition biofilm-contaminated titanium surfaces for subsequent osteoblastic cell proliferation.

Titanium dental implants have been successfully used for decades; however, some implants are affected by peri-implantitis due to bacterial infection, resulting in loss of supporting bone. This study aimed to evaluate the effect of an antimicrobial chemotherapy employing H2O2 photolysis-developed to treat peri-implantitis-on biofilm-contaminated titanium surfaces in association with osteoblastic cell proliferation on the treated surface. Titanium discs were sandblasted and acid-etched, followed by contamination with a three-species biofilm composed of Porphyromonas gingivalis, Fusobacterium nucleatum, and Streptococcus mitis. This biofilm model was used as a simplified model of clinical peri-implantitis biofilm. The discs were subjected to ultrasound scaling, followed by H2O2 photolysis, wherein 365-nm LED irradiation of the disc immersed in 3% H2O2 was performed for 5 min. We analysed proliferation of mouse osteoblastic cells (MC3T3-E1) cultured on the treated discs. Compared with intact discs, biofilm contamination lowered cell proliferation on the specimen surface, whereas H2O2 photolysis recovered cell proliferation. Thus, H2O2 photolysis can recover the degraded biocompatibility of biofilm-contaminated titanium surfaces and can potentially be utilised for peri-implantitis treatment. However, to verify the findings of this study in relation to clinical settings, assessment using a more clinically relevant multi-species biofilm model is necessary.

Efficiency of Nanotube Surface-Treated Dental Implants Loaded with Doxycycline on Growth Reduction of Porphyromonas gingivalis.

PURPOSE: The prevalence of peri-implant infection in patients with dental implants has been shown to range from 28% to 56%. A nanotube-modified implant surface can deliver antibiotics locally and suppress periodontal pathogenic bacterial growth. The aim of this study was to evaluate the deliverability of antibiotics via a nanotube-modified implant. MATERIALS AND METHODS: Dental implants with a nanotube surface were fabricated and loaded with doxycycline. Afterward, each dental implant with a nanotube surface was placed into 2-mL tubes, removed from solution, and placed in a fresh solution daily for 28 days. Experimental samples from 1, 2, 4, 16, 24, and 28 days were used for this evaluation. The concentration of doxycycline was measured using spectrophotometric analysis at 273-nm absorbance. The antibacterial effect of doxycycline was evaluated by supplementing Porphyromonas gingivalis (P gingivalis) growth media with the solution collected from the dental implants at the aforementioned time intervals for a period of 48 hours under anaerobic conditions. A bacterial viability assay was used to evaluate P gingivalis growth at 550-nm absorbance. RESULTS: Doxycycline concentration varied from 0.33 to 1.22 µg/mL from day 1 to day 28, respectively. A bacterial viability assay showed the highest P gingivalis growth at day 1 (2 nm) and the lowest at day 4 (0.17 nm), with a gradual reduction from day 1 to day 4 of approximately 87.5%. The subsequent growth pattern was maintained and slightly increased from baseline in approximately 48.3% from day 1 to day 24. The final P gingivalis growth measured at day 28 was 29.4% less than the baseline growth. CONCLUSION: P gingivalis growth was suppressed in media supplemented with solution collected from dental implants with a nanotube surface loaded with doxycycline during a 28-day time interval.

Antimicrobial mouthrinse use as an adjunct method in peri-implant biofilm control.

Great possibilities for oral rehabilitation emerged as a result of scientific consolidation, as well as a large number of dental implant applications. Along with implants appeared diseases such as mucositis and peri-implantitis, requiring management through several strategies applied at different stages. Biofilm accumulation is associated with clinical signs manifest by both tooth and implant inflammation. With this in mind, regular and complete biofilm elimination becomes essential for disease prevention and host protection. Chemical control of biofilms, as an adjuvant to mechanical oral hygiene, is fully justified by its simplicity and efficacy proven by studies based on clinical evidence. The purpose of this review was to present a consensus regarding the importance of antimicrobial mouthrinse use as an auxiliary method in chemical peri-implant biofilm control. The active ingredients of the several available mouthrinses include bis-biguanide, essential oils, phenols, quaternary ammonium compounds, oxygenating compounds, chlorine derivatives, plant extracts, fluorides, antibiotics and antimicrobial agent combinations. It was concluded that there is strong clinical evidence that at least two mouthrinses have scientifically proven efficacy against different oral biofilms, i.e., chlorhexidine digluconate and essential oils; however, 0.12% chlorhexidine digluconate presents a number of unwanted side effects and should be prescribed with caution. Chemical agents seem beneficial in controlling peri-implant inflammation, although they require further investigation. We recommend a scientifically proven antiseptic, with significant short and long term efficacy and with no unwanted side effects, for the prevention and/or treatment of peri-implant disease.

The use of laser therapy for dental implant surface decontamination: a narrative review of in vitro studies.

The aim of this narrative review was to critically evaluate in vitro studies assessing the efficacy of lasers in the bacterial decontamination of titanium implant surfaces. The MEDLINE, Web of Knowledge and Embase electronic databases were used to search for articles relating to the use of lasers in the bacterial decontamination of titanium specimen surfaces using predetermined search statements. Clinical studies, case reports, case series, review articles and animal models were excluded. Study selection was carried out independently and then cross-checked by two authors through abstract viewing. Eighteen articles were selected for full-text analysis. Erbium-doped yttrium-aluminium-garnet lasers had a wide range of powers capable of inducing bacterial decontamination. While carbon dioxide and gallium-aluminium-arsenide diode lasers demonstrated the ability to produce bacterial decontamination, the bacterial sensitivity to each varied depending on the species involved. There is no concensus on the laser type or settings that are optimal for bacterial decontamination of titanium implant surfaces as studies employ various test specimens, contamination methodologies, irradiation settings and protocols, and outcome measures resulting in limited study comparability. More investigations are required to provide guidelines for the use of laser therapy in the decontamination of implant surfaces.

Essential oils and zirconia dental implant materials.

PURPOSE: This study was conducted to evaluate the effectiveness of natural antimicrobial agents in reducing biofilm development on different titanium and zirconia dental implant materials in vitro using a constant depth film fermentor (CDFF). MATERIALS AND METHODS: Contact angles and surface free energy were determined for all surfaces. Biofilms were grown on disks of polished partially stabilized zirconia, titanium blasted with zirconia, titanium blasted with zirconia and acid-etched, and polished titanium using a CDFF to simulate oral cavity conditions. Antimicrobials (cinnamon oil, clove oil, chlorhexidine gluconate, or 0.5% Tween 80) were pulsed twice daily to the biofilm to mimic application in the oral cavity. Samples were taken after 6, 24, and 48 hours. Serial dilutions were made and plated onto agar. Bacterial colonies were counted to determine colony-forming units/mL. RESULTS: Treatment of different implant material surfaces with the various antimicrobial agents led to significant increases in wettability and free energy on all surfaces. All surfaces showed a remarkable decrease in bacterial adhesion in the first 2 days in a relatively similar manner, with significant reduction in most of them, particularly after 48 hours. CONCLUSIONS: Functionalization of different dental implant material surfaces with essential oils resulted in immediate and ongoing antibacterial and antiplaque activities, and this antibacterial effect was enhanced with increased plaque age. Differences in the type of material seemed to have little effect on bacterial adhesion after treatment with antimicrobial agents. Expansion of this work with in vivo studies and clinical trials would be valuable.

Laser therapy as an effective method for implant surface decontamination: a histomorphometric study in rats.

BACKGROUND: To the best of the authors' knowledge, a standard protocol for treating peri-implantitis is not yet established. METHODS: A total of 150 titanium disks with smooth or rough surfaces contaminated with microbial biofilm were implanted subcutaneously in rats after undergoing one of three treatments: 1) low-intensity laser (LIL); 2) antimicrobial photodynamic therapy (aPDT); or 3) toluidine blue O (TBO). Sterile and contaminated disks served as negative (NC) and positive (C) control groups, respectively. After days 7, 28, and 84, tissue inflammation was evaluated microscopically by measuring the density of collagen fibers (degree of fibrosis) and concentration of polymorphonuclear neutrophils. RESULTS: Surface texture did not affect the degree of inflammation, but the area of reactive tissue was significantly greater for rough implants (2.6 ± 3.7 × 10(6) µm(2)) than for smooth ones (1.9 ± 2.6 × 10(6) µm(2); P = 0.0377). Group C presented the lowest and group NC presented the highest degree of fibrosis with significance only after day 7; these groups had the highest and lowest scores, respectively, for degree of inflammation. Group C showed the largest area of reactive tissue (9.11 ± 2.10 × 10(6) µm(2)), but it was not significantly larger than group LIL (P = 0.3031) and group TBO (P = 0.1333). Group aPDT showed the smallest area (4.34 ± 1.49 × 10(6) µm(2)) of reactive tissue among the treatment groups. After day 28, groups LIL, aPDT, TBO, and C resembled group NC in all the studied parameters. CONCLUSION: Group aPDT showed more favorable results in parameter area of reactive tissue than the other methods after day 7, but over longer time periods all methods produced outcomes equivalent to sterile implants.

Comparative analysis of microorganism species succession on three implant surfaces with different roughness: an in vivo study.

PURPOSE: Because almost all implant systems reveal marginal bone loss and some implants can be affected by periimplantitis, to realize an effective maintenance treatment it is important to understand the biofilm development over different implant surfaces. The objective of this human study is to comparatively analyze the kinetics of microorganism species succession on 3 surfaces. MATERIALS AND METHODS: Three commercially pure titanium sheets with different roughness were randomly fixed bilaterally on the lingual regions of Hawley-type plates of 6 volunteers. The participants used the apparatuses in the following experimental periods: 1, 3, 7, 14, and 21 days, and were instructed to remove the acrylic plates only during oral hygiene procedures. Samples of biofilm were harvested from the central areas of each sheet, and the presence of 24 bacterial species was identified using Checkerboard DNA-DNA Hybridization method. RESULTS: The results showed no statistically significant differences with regard to the kinetics of bacterial species succession on the different surfaces, in all periods of time. Rough surfaces were not more prone to colonization by pathogenic bacteria than the smooth surfaces. CONCLUSION: The surface roughness does not affect the bacterial species succession in the biofilm. The succession of species was similar during all periods of the study.

Efeitos do laser em baixa intensidade, da terapia fotodinâmica e do azul de toluidina O na descontaminação de superfícies de implantes metálicos: estudo microscópico em subcutâneo de ratos / Effect of low intensity laser, photodynamic therapy and toluidine blue O the on decontamination of metallic implants surfaces: microscopic study in rats' subcutaneous tissue

A peri-implantite acomete um número crescente de indivíduos e os protocolos de tratamento objetivam descontaminar as superfícies dos implantes e torná-las novamente osseointegráveis. Porém, ainda não foi estabelecido um padrão ouro de tratamento para peri-implantite. Este estudo testa o poder de descontaminação do laser em baixa intensidade (LBI), da terapia fotodinâmica (PDT) e do azul de toluidina O (TBO). Sobre discos de titânio de 1,5 mm de espessura e 4,0 mm de diâmetro de superfícies lisas ou rugosas foi permitida a deposição natural de biofilme microbiano por 7 dias após os quais os discos foram divididos em grupos experimentais (15 discos por grupo), de acordo com o método de descontaminação: grupo LBI (laser de InGaAlP de 660 nm, 30 mW, 45 J/cm2 no modo continuo por 30 s); grupo PDT; grupo TBO (aplicação de TBO por 60 s); grupo controle positivo (C) sem tratamento e grupo controle negativo (NC) estéril. Os discos foram implantados em tecido conjuntivo subcutâneo de ratos e, após 7, 28 e 84 dias, foram obtidas 5 biópsias de cada grupo para análise em microscopia óptica. Implantes lisos e rugosos não diferiram com relação ao grau de fibrosamento e severidade do infiltrado inflamatório, mas a área do tecido reacional perimaterial foi maior nos rugosos (2,6 ± 3,7 x 106 µm2) do que nos lisos (1,9 ± 2,6 x 106 µm2). O grupo C foi o que apresentou menor grau de fibrosamento do tecido reacional (1), mas somente houve diferença estatisticamente significante (p = 0,0230) entre os grupos C e NC. A severidade do infiltrado inflamatório somente diferiu significantemente entre os grupos aos 7 dias, quando o grupo NC apresentou o menor escore (2) em comparação aos demais grupos (3). Com relação à área do tecido reacional perimaterial, só houve diferenças entre os grupos aos 7 dias, quando o grupo C apresentou maior área que os demais grupos (9,11 ± 2,10 x 106 µm2), porém, sem diferença estatisticamente significante em comparação aos grupos LBI e TBO...

The peri-implantitis is a disease that is increasing in a number of individuals and the protocols of treatment has intended to decontaminate the implant surfaces and makes this biocompatible again. However, until this moment, a gold standard for peri-implantitis treatment was not established. The present study tests the power of decontamination of low intensity laser (LBI), photodynamic therapy (PDT) and toluidine blue O (TBO). The natural deposition of microbian biofilm was allowed on titanium discs with 1,5 mm of thickness and 4,0 mm of diameter and smooth and grooved surfaces during 7 days when the discs were separated in experimental groups (15 discs each group), in accordance with the decontamination method: LBI group (decontamination with InGaAlP laser, 660 nm, 30 mW, 45 J/cm2 in continuous way during 30 s); PDT group; TBO group (application of TBO during 60 s); controlled positive group (C) without any kind of treatment and controlled negative group (NC), sterile. The discs had been implanted in rats subcutaneous connective tissue and, after 7, 28 and 84 days, had been gotten 5 biopsies from each group for histology processing. Smooth and grooved implants did not differ on fibrosis grade and severity of the inflammatory infiltrate, however the perimaterial reaction tissue area was bigger on grooved implants (2,6 ± 3,7 x 106 µm2) that on smooth implants (1,9 ± 2,6 x 106 µm2). The C group was the one that showed the smallest reaction tissue fibrosis grade (1), but only was significant statistical difference (p = 0,0230) between C and NC groups. The severity of inflammatory infiltrate only significant differed between the groups on 7 days, when the NC group showed the smallest score (2) in comparison to the others groups (3). In relation to the perimaterial reaction tissue area, only were differences between the groups on 7 days, when C group showed bigger area than the others (9,11 ± 2,10 x 106 µm2), nevertheless, without significant statistical...

Biofilms inducing ultra-low friction on titanium.

Biofilm formation is widely reported in the literature as a problem in the healthcare, environmental, and industrial sectors. However, the role of biofilms in sliding contacts remains unclear. Friction during sliding was analyzed for titanium covered with mixed biofilms consisting of Streptococcus mutans and Candida albicans. The morphology of biofilms on titanium surfaces was evaluated before, during, and after sliding tests. Very low friction was recorded on titanium immersed in artificial saliva and sliding against alumina in the presence of biofilms. The complex structure of biofilms, which consist of microbial cells and their hydrated exopolymeric matrix, acts like a lubricant. A low friction in sliding contacts may have major significance in the medical field. The composition and structure of biofilms are shown to be key factors for an understanding of friction behavior of dental implant connections and prosthetic joints. For instance, a loss of mechanical integrity of dental implant internal connections may occur as a consequence of the decrease in friction caused by biofilm formation. Consequently, the study of the exopolymeric matrix can be important for the development of high-performance novel joint-based systems for medical and other engineering applications.

Implant surface analysis and microbiologic evaluation of failed implants retrieved from smokers.

The aim of this study was to evaluate the microbiota and surface of failed titanium dental implants from 4 manufacturers. Twelve mobile dental implants were retrieved from 10 smokers after 3 to 10 years of functional loading. Before implant removal, microbial samples were taken and evaluated using polymerase chain reaction. After implant removal, analyses of the failed implant surfaces were performed using scanning electron microscopy and energy-dispersive spectrometer x-ray. Periodontal pathogens such as Aggregactibacter actinomycetemcomitans, Campylobacter rectus, Eikenella corrodens, Fusobacterium nucleatum, Porphyromonas gingivalis, Prevotella intermedia, Tannerella forsythia, and Treponema denticola were detected in all implants in different proportions. Surface analysis showed varying degrees of surface roughness between the samples and the presence of proteinaceous material, appearing mainly as dark stains. Foreign carbon, oxygen, sodium, calcium, aluminum, and silicon elements were also found. Although no material-related causes of implant failure were detected, several periodontal pathogens were identified independently of the surface topography or manufacturer.

Neodymium:yttrium aluminum garnet laser irradiation with low pulse energy: a potential tool for the treatment of peri-implant disease.

Bacterial contamination may seriously compromise successful implant osteointegration in the clinical practice of dental implantology. Several methods for eliminating bacteria from the infected implants have been proposed, but none of them have been shown to be an effective tool in the treatment of peri-implantitis. In the present study, we investigated the efficacy of pulsed neodymium:yttrium aluminum garnet laser irradiation (Nd:YAG) in achieving bacterial ablation while preserving the surface properties of titanium implants. For this purpose, suspensions of Escherichia coli or Actinobacillus (Haemophilus) actinomycetemcomitans were irradiated with different laser parameters, both streaked on titanium implants, and in broth medium. It was found, by light and atomic force microscopy, that Nd:YAG laser, when used with proper working parameters, was able to bring about a consistent microbial ablation of both aerobic and anaerobic species, without damaging the titanium surface.

Self-reinforced ciprofloxacin-releasing polylactide-co-glycolide 80/20 inhibits attachment and biofilm formation by Staphylococcus epidermidis: an in vitro study.

We have observed the efficiency of antibiotic-releasing polylactide-co-glycolide (PLGA) 80/20 in preventing Staphylococcus epidermidis attachment and biofilm formation in vitro. The aim of the present study was to evaluate the effect of self-reinforced (SR) implants with enhanced antibiotic release on bacterial attachment and biofilm formation rates, and also on growth inhibition of Staphylococcus epidermidis. Cylindrical SR-PLGA+AB specimens (length 30 mm, diameter 3 mm) were examined by scanning electron microscopy (SEM) for attachment of S. epidermidis ATCC 35989 on biomaterial surface and formation of biofilm, after incubating with bacterial suspension of ca. 10 cfu/mL for 1, 3, 7, 14 and 21 days. SR-PLGA and SR-PLGA+AB implants were tested on agar plates by measuring the inhibition distance around implants. On the surface of SR-PLGA+AB, at days 1, 3, 7, 14 and 21, the percentage of areas with not a single bacteria attached, was 88.6%, 71.1%, 73.7%, 73.7%, and 68.4%, respectively. On the areas where bacteria were detected, the number of bacterial cells remained low during whole study period, and no significant increase by time was seen. There was no biofilm observed on 97-99% of the examined areas during the whole study period on SR-PLGA+AB. In agar plates, the SR-PLGA+AB showed inhibition of bacterial growth, with (mean) 53.2 mm diameter of inhibition area with peeled implants and 50.5 mm with non-peeled implants. There was no inhibition seen around implants without ciprofloxacin. Bioabsorbable ciprofloxacin-releasing self-reinforced PLGA (SR-PLGA+AB) was superior to plain SR-PLGA in preventing bacterial attachment, biofilm formation, and also the growth of Staphylococcus epidermidis.

Treatment of the contaminated implant surface using the Er,Cr:YSGG laser.

Treatment of the contaminated implant surface by mechanical and chemotherapeutic means has met with mixed success. Incomplete surface debridement or alteration of the implant surface could compromise attempts at grafting and reintegration of the implant body. Development of a laser system operating at 2780 nm and using an ablative hydrokinetic process offers the possibility for more efficient decontamination and debridement. The Er,Cr: YSGG laser is evaluated and compared with the most commonly used chemotherapeutic modality for treatment of the implant surface. A scanning electron microscope study is presented comparing YSGG ablation to citric acid treatment of the titanium plasma sprayed and HA-coated implant surface. We can conclude that laser ablation using the YSGG laser is highly efficient at removing potential contaminants on the roughened implant surface while demonstrating no effects on the titanium substrate.