Cargando…

Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study

The long-term success of dental implant rehabilitation depends significantly on proper peri-implant soft tissue integration. Therefore, decontamination of abutments prior to their connection to the implant is beneficial to enhance soft tissue attachment and to aid in maintaining marginal bone around...

Descripción completa

Detalles Bibliográficos
Autores principales: Sharon, Esi, Pietrokovski, Yoav, Engel, Ilana, Assali, Rula, Houri-Haddad, Yael, Beyth, Nurit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254387/
https://www.ncbi.nlm.nih.gov/pubmed/37297212
http://dx.doi.org/10.3390/ma16114080
_version_ 1785056630656729088
author Sharon, Esi
Pietrokovski, Yoav
Engel, Ilana
Assali, Rula
Houri-Haddad, Yael
Beyth, Nurit
author_facet Sharon, Esi
Pietrokovski, Yoav
Engel, Ilana
Assali, Rula
Houri-Haddad, Yael
Beyth, Nurit
author_sort Sharon, Esi
collection PubMed
description The long-term success of dental implant rehabilitation depends significantly on proper peri-implant soft tissue integration. Therefore, decontamination of abutments prior to their connection to the implant is beneficial to enhance soft tissue attachment and to aid in maintaining marginal bone around the implant. Consequently, different implant abutment decontamination protocols were evaluated regarding biocompatibility, surface morphology, and bacterial load. The protocols evaluated were autoclave sterilization, ultrasonic washing, steam cleaning, chlorhexidine chemical decontamination, and sodium hypochlorite chemical decontamination. The control groups included: (1) implant abutments prepared and polished in a dental lab without decontamination and (2) unprepared implant abutments obtained directly from the company. Surface analysis was performed using scanning electron microscopy (SEM). Biocompatibility was evaluated using XTT cell viability and proliferation assays. Biofilm biomass and viable counts (CFU/mL) (n = 5 for each test) were used for surface bacterial load evaluation. Surface analysis revealed areas of debris and accumulation of materials, such as iron, cobalt, chromium, and other metals, in all abutments prepared by the lab and with all decontamination protocols. Steam cleaning was the most efficient method for reducing contamination. Chlorhexidine and sodium hypochlorite left residual materials on the abutments. XTT results showed that the chlorhexidine group (M = 0.7005, SD = 0.2995) had the lowest values (p < 0.001) (autoclave: M = 3.6354, SD = 0.1510; ultrasonic: M = 3.4077, SD = 0.3730; steam: M = 3.2903, SD = 0.2172; NaOCl: M = 3.5377, SD = 0.0927; prep non-decont.: M = 3.4815, SD = 0.2326; factory: M = 3.6173, SD = 0.0392). Bacterial growth (CFU/mL) was high in the abutments treated with steam cleaning and ultrasonic bath: 2.93 × 10(9), SD = 1.68 × 10(12) and 1.83 × 10(9), SD = 3.95 × 10(10), respectively. Abutments treated with chlorhexidine showed higher toxicity to cells, while all other samples showed similar effects to the control. In conclusion, steam cleaning seemed to be the most efficient method for reducing debris and metallic contamination. Bacterial load can be reduced using autoclaving, chlorhexidine, and NaOCl.
format Online
Article
Text
id pubmed-10254387
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-102543872023-06-10 Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study Sharon, Esi Pietrokovski, Yoav Engel, Ilana Assali, Rula Houri-Haddad, Yael Beyth, Nurit Materials (Basel) Article The long-term success of dental implant rehabilitation depends significantly on proper peri-implant soft tissue integration. Therefore, decontamination of abutments prior to their connection to the implant is beneficial to enhance soft tissue attachment and to aid in maintaining marginal bone around the implant. Consequently, different implant abutment decontamination protocols were evaluated regarding biocompatibility, surface morphology, and bacterial load. The protocols evaluated were autoclave sterilization, ultrasonic washing, steam cleaning, chlorhexidine chemical decontamination, and sodium hypochlorite chemical decontamination. The control groups included: (1) implant abutments prepared and polished in a dental lab without decontamination and (2) unprepared implant abutments obtained directly from the company. Surface analysis was performed using scanning electron microscopy (SEM). Biocompatibility was evaluated using XTT cell viability and proliferation assays. Biofilm biomass and viable counts (CFU/mL) (n = 5 for each test) were used for surface bacterial load evaluation. Surface analysis revealed areas of debris and accumulation of materials, such as iron, cobalt, chromium, and other metals, in all abutments prepared by the lab and with all decontamination protocols. Steam cleaning was the most efficient method for reducing contamination. Chlorhexidine and sodium hypochlorite left residual materials on the abutments. XTT results showed that the chlorhexidine group (M = 0.7005, SD = 0.2995) had the lowest values (p < 0.001) (autoclave: M = 3.6354, SD = 0.1510; ultrasonic: M = 3.4077, SD = 0.3730; steam: M = 3.2903, SD = 0.2172; NaOCl: M = 3.5377, SD = 0.0927; prep non-decont.: M = 3.4815, SD = 0.2326; factory: M = 3.6173, SD = 0.0392). Bacterial growth (CFU/mL) was high in the abutments treated with steam cleaning and ultrasonic bath: 2.93 × 10(9), SD = 1.68 × 10(12) and 1.83 × 10(9), SD = 3.95 × 10(10), respectively. Abutments treated with chlorhexidine showed higher toxicity to cells, while all other samples showed similar effects to the control. In conclusion, steam cleaning seemed to be the most efficient method for reducing debris and metallic contamination. Bacterial load can be reduced using autoclaving, chlorhexidine, and NaOCl. MDPI 2023-05-30 /pmc/articles/PMC10254387/ /pubmed/37297212 http://dx.doi.org/10.3390/ma16114080 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sharon, Esi
Pietrokovski, Yoav
Engel, Ilana
Assali, Rula
Houri-Haddad, Yael
Beyth, Nurit
Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study
title Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study
title_full Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study
title_fullStr Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study
title_full_unstemmed Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study
title_short Biocompatibility, Surface Morphology, and Bacterial Load of Dental Implant Abutments following Decontamination Protocols: An In-Vitro Study
title_sort biocompatibility, surface morphology, and bacterial load of dental implant abutments following decontamination protocols: an in-vitro study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254387/
https://www.ncbi.nlm.nih.gov/pubmed/37297212
http://dx.doi.org/10.3390/ma16114080
work_keys_str_mv AT sharonesi biocompatibilitysurfacemorphologyandbacterialloadofdentalimplantabutmentsfollowingdecontaminationprotocolsaninvitrostudy
AT pietrokovskiyoav biocompatibilitysurfacemorphologyandbacterialloadofdentalimplantabutmentsfollowingdecontaminationprotocolsaninvitrostudy
AT engelilana biocompatibilitysurfacemorphologyandbacterialloadofdentalimplantabutmentsfollowingdecontaminationprotocolsaninvitrostudy
AT assalirula biocompatibilitysurfacemorphologyandbacterialloadofdentalimplantabutmentsfollowingdecontaminationprotocolsaninvitrostudy
AT hourihaddadyael biocompatibilitysurfacemorphologyandbacterialloadofdentalimplantabutmentsfollowingdecontaminationprotocolsaninvitrostudy
AT beythnurit biocompatibilitysurfacemorphologyandbacterialloadofdentalimplantabutmentsfollowingdecontaminationprotocolsaninvitrostudy