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      Antimicrobial Photodynamic Therapy against Endodontic Enterococcus faecalis and Candida albicans Mono and Mixed Biofilms in the Presence of Photosensitizers: A Comparative Study with Classical Endodontic Irrigants

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          Abstract

          Endodontic biofilms eradication from the infected root canal system remains as the primary focus in endodontic field. In this study, it was assessed the efficacy of antimicrobial Photodynamic Therapy (aPDT) with the Zn(II)chlorin e6 methyl ester (Zn(II)e 6Me) activated by red light against monospecies and mixed biofilms of Enterococcus faecalis and Candida albicans. The results were compared with the ones obtained with Rose Bengal (RB), Toluidine Blue-O (TBO), the synthetic tetracationic porphyrin (TMPyP) as well as classical endodontic irrigants (3% NaOCl, 17% EDTA and 2% CHX). The antimicrobial efficacy of aPDT toward monospecies and mixed biofilms was quantified resorting to safranin red method. The changes of biofilm organization and of cellular ultrastructure were evaluated through several microscopy techniques (light, laser confocal and transmission electron microscopy). Zn(II)e 6Me once activated with light for 60 or 90 s was able to remove around 60% of the biofilm’s biomass. It was more efficient than TBO and RB and showed similar efficiency to TMPyP and classical irrigants, CHX and EDTA. As desirable in a PS, Zn(II)e 6Me in the dark showed smaller activity than TMPyP. Only NaOCl revealed higher efficiency, with 70–90% of the biofilm’s biomass removal. The organization of biofilms and the normal microbial cell ultrastructure were extensively damaged by the presence of Zn(II)e 6Me. aPDT with Zn(II)e 6Me showed to be an efficient antimicrobial strategy deserving further studies leading to a future clinical usage in endodontic disinfection.

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          Photosensitizers of the porphyrin and phthalocyanine series for photodynamic therapy

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            Influence of infection at the time of root filling on the outcome of endodontic treatment of teeth with apical periodontitis.

            This study investigated the role of infection on the prognosis of endodontic therapy by following-up teeth that had had their canals cleaned and obturated during a single appointment. The root canals of 55 single-rooted teeth with apical periodontitis were thoroughly instrumented and irrigated with sodium hypochlorite solution. Using advanced anaerobic bacteriological techniques, post-instrumentation samples were taken and the teeth were then root-filled during the same appointment. All teeth were initially infected; after instrumentation low numbers of bacteria were detected in 22 of 55 root canals. Periapical healing was followed-up for 5 years. Complete periapical healing occurred in 94% of cases that yielded a negative culture. Where the samples were positive prior to root filling, the success rate of treatment was just 68%--a statistically significant difference. Further investigation of three failures revealed the presence of Actinomyces species in each case; no other specific bacteria were implicated in failure cases. These findings emphasize the importance of completely eliminating bacteria from the root canal system before obturation. This objective cannot be reliably achieved in a one-visit treatment because it is not possible to eradicate all infection from the root canal without the support of an inter-appointment antimicrobial dressing.
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              Photodynamic therapy for localized infections--state of the art.

              Photodynamic therapy (PDT) was discovered over 100 years ago by observing the killing of microorganisms when harmless dyes and visible light were combined in vitro. Since then it has primarily been developed as a treatment for cancer, ophthalmologic disorders and in dermatology. However, in recent years interest in the antimicrobial effects of PDT has revived and it has been proposed as a therapy for a large variety of localized infections. This revival of interest has largely been driven by the inexorable increase in drug resistance among many classes of pathogen. Advantages of PDT include equal killing effectiveness regardless of antibiotic resistance, and a lack of induction of PDT resistance. Disadvantages include the cessation of the antimicrobial effect when the light is turned off, and less than perfect selectivity for microbial cells over host tissue. This review will cover the use of PDT to kill or inactivate pathogens in ex vivo tissues and in biological materials such as blood. PDT has been successfully used to kill pathogens and even to save life in several animal models of localized infections such as surface wounds, burns, oral sites, abscesses and the middle ear. A large number of clinical studies of PDT for viral papillomatosis lesions and for acne refer to its antimicrobial effect, but it is unclear how important this microbial killing is to the overall therapeutic outcome. PDT for periodontitis is a rapidly growing clinical application and other dental applications are under investigation. PDT is being clinically studied for other dermatological infections such as leishmaniasis and mycobacteria. Antimicrobial PDT will become more important in the future as antibiotic resistance is only expected to continue to increase.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                30 March 2017
                2017
                : 8
                : 498
                Affiliations
                [1] 1Faculty of Medicine, University of Coimbra Coimbra, Portugal
                [2] 2Department of Dentistry, Faculty of Medicine, University of Coimbra Coimbra, Portugal
                [3] 3Centre for Neuroscience and Cell Biology, University of Coimbra Coimbra, Portugal
                [4] 4Laboratory for Biostatistics and Medical Informatics, Faculty of Medicine, University of Coimbra Coimbra, Portugal
                [5] 5Department of Microbiology, Faculty of Medicine, University of Porto Porto, Portugal
                [6] 6Departamento de Química and Unidade de Investigação de Química Orgânica, Produtos Naturais e Agroalimentares, University of Aveiro Aveiro, Portugal
                [7] 7Department of Chemistry, Federal University of São Carlos São Carlos, Brazil
                Author notes

                Edited by: Octavio Luiz Franco, Universidade Católica de Brasília, Brazil

                Reviewed by: Efstathios D. Giaouris, University of the Aegean, Greece; Fabian Cieplik, University of Regensburg, Germany; Masoomeh Shams-Ghahfarokhi, Tarbiat Modares University, Iran

                *Correspondence: Teresa Gonçalves, tmfog@ 123456ci.uc.pt

                This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2017.00498
                5371592
                28424663
                13c060f7-4e93-4021-ab12-8ddcfe447d5f
                Copyright © 2017 Diogo, Fernandes, Caramelo, Mota, Miranda, Faustino, Neves, Uliana, de Oliveira, Santos and Gonçalves.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 December 2016
                : 10 March 2017
                Page count
                Figures: 6, Tables: 2, Equations: 0, References: 61, Pages: 11, Words: 0
                Funding
                Funded by: Fundação para a Ciência e a Tecnologia 10.13039/501100001871
                Award ID: UID / NEU / 04539 / 2013
                Award ID: UID/QUI/00062/2013
                Award ID: SFRH/BPD/63733/2009
                Award ID: SFRH/BPD/113285/2015
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                antimicrobial photodynamic therapy,endodontic biofilms,chlorin e6,enterococcus faecalis,candida albicans

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