The in vitro effect of antimicrobial photodynamic therapy with indocyanine green on Enterococcus faecalis: Influence of a washing vs non-washing procedure

•The concentration of indocyanine green (ICG) as photosensitizer (PS) has an important role in eradication of Enterococcus faecalis..•It’s recommended to apply ICG accompanied by laser irradiation without being washed out before irradiation.•The concentration of PS should be considered as a crucial...

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Published inPhotodiagnosis and photodynamic therapy Vol. 16; pp. 119 - 123
Main Authors Chiniforush, Nasim, Pourhajibagher, Maryam, Parker, Steven, Shahabi, Sima, Bahador, Abbas
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.12.2016
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ISSN1572-1000
1873-1597
DOI10.1016/j.pdpdt.2016.09.007

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Abstract •The concentration of indocyanine green (ICG) as photosensitizer (PS) has an important role in eradication of Enterococcus faecalis..•It’s recommended to apply ICG accompanied by laser irradiation without being washed out before irradiation.•The concentration of PS should be considered as a crucial point in antimicrobial photodynamic therapy. The purpose of this study was to evaluate the in vitro effect of washing and non-washing of indocyanine green (ICG) as photosensitizer (PS) on bacterial count, biofilm formation, development and degradation of Enterococcus faecalis. The anti-bacterial, anti-biofilm formation, anti-biofilm development and biofilm degradation of anti-microbial photodynamic therapy (aPDT) against E. faecalis was determined at concentrations of 3 to 2000μg/mL of ICG, subject to 18J/cm2 dose of diode laser (808nm) in washing and non-washing producers. Bacterial viability measurements and biofilm assays were evaluated by broth microdilution method and crystal violet assays, respectively. ICG-mediated aPDT, using 25 to 2000μg/mL and 50 to 2000μg/mL showed significant reduction in E. faecalis growth when compared to the control in non-washing and washing producers, respectively (P<0.05). Also, ICG-mediated aPDT showed a significantly inhibitory effect on biofilm formation of E. faecalis in concentration of 6 to 2000μg/mL and 100 to 2000μg/mL in non-washing and washing groups (P<0.05). The biofilm development was inhibited by concentrations of 12 to 2000μg/mL and 100 to 2000μg/mL in non-washing and washing groups. The biofilm degradation increased from concentrations of 12 to 2000μg/mL and 250 to 2000μg/mL in non-washing and washing groups, respectively. This study shows that the application of ICG should be accompanied by laser irradiation without being washed out to achieve better result for bacterial count reduction and anti-biofilm effects.
AbstractList •The concentration of indocyanine green (ICG) as photosensitizer (PS) has an important role in eradication of Enterococcus faecalis..•It’s recommended to apply ICG accompanied by laser irradiation without being washed out before irradiation.•The concentration of PS should be considered as a crucial point in antimicrobial photodynamic therapy. The purpose of this study was to evaluate the in vitro effect of washing and non-washing of indocyanine green (ICG) as photosensitizer (PS) on bacterial count, biofilm formation, development and degradation of Enterococcus faecalis. The anti-bacterial, anti-biofilm formation, anti-biofilm development and biofilm degradation of anti-microbial photodynamic therapy (aPDT) against E. faecalis was determined at concentrations of 3 to 2000μg/mL of ICG, subject to 18J/cm2 dose of diode laser (808nm) in washing and non-washing producers. Bacterial viability measurements and biofilm assays were evaluated by broth microdilution method and crystal violet assays, respectively. ICG-mediated aPDT, using 25 to 2000μg/mL and 50 to 2000μg/mL showed significant reduction in E. faecalis growth when compared to the control in non-washing and washing producers, respectively (P<0.05). Also, ICG-mediated aPDT showed a significantly inhibitory effect on biofilm formation of E. faecalis in concentration of 6 to 2000μg/mL and 100 to 2000μg/mL in non-washing and washing groups (P<0.05). The biofilm development was inhibited by concentrations of 12 to 2000μg/mL and 100 to 2000μg/mL in non-washing and washing groups. The biofilm degradation increased from concentrations of 12 to 2000μg/mL and 250 to 2000μg/mL in non-washing and washing groups, respectively. This study shows that the application of ICG should be accompanied by laser irradiation without being washed out to achieve better result for bacterial count reduction and anti-biofilm effects.
The purpose of this study was to evaluate the in vitro effect of washing and non-washing of indocyanine green (ICG) as photosensitizer (PS) on bacterial count, biofilm formation, development and degradation of Enterococcus faecalis. The anti-bacterial, anti-biofilm formation, anti-biofilm development and biofilm degradation of anti-microbial photodynamic therapy (aPDT) against E. faecalis was determined at concentrations of 3 to 2000μg/mL of ICG, subject to 18J/cm dose of diode laser (808nm) in washing and non-washing producers. Bacterial viability measurements and biofilm assays were evaluated by broth microdilution method and crystal violet assays, respectively. ICG-mediated aPDT, using 25 to 2000μg/mL and 50 to 2000μg/mL showed significant reduction in E. faecalis growth when compared to the control in non-washing and washing producers, respectively (P<0.05). Also, ICG-mediated aPDT showed a significantly inhibitory effect on biofilm formation of E. faecalis in concentration of 6 to 2000μg/mL and 100 to 2000μg/mL in non-washing and washing groups (P<0.05). The biofilm development was inhibited by concentrations of 12 to 2000μg/mL and 100 to 2000μg/mL in non-washing and washing groups. The biofilm degradation increased from concentrations of 12 to 2000μg/mL and 250 to 2000μg/mL in non-washing and washing groups, respectively. This study shows that the application of ICG should be accompanied by laser irradiation without being washed out to achieve better result for bacterial count reduction and anti-biofilm effects.
Highlights • The concentration of indocyanine green (ICG) as photosensitizer (PS) has an important role in eradication of Enterococcus faecalis.. • It’s recommended to apply ICG accompanied by laser irradiation without being washed out before irradiation. • The concentration of PS should be considered as a crucial point in antimicrobial photodynamic therapy.
Author Shahabi, Sima
Pourhajibagher, Maryam
Chiniforush, Nasim
Bahador, Abbas
Parker, Steven
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Keywords Enterococcus faecalis
Biofilm degradation
Indocyanine green
Biofilm formation
Endodontic infection
Biofilm development
Language English
License Copyright © 2016 Elsevier B.V. All rights reserved.
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Snippet •The concentration of indocyanine green (ICG) as photosensitizer (PS) has an important role in eradication of Enterococcus faecalis..•It’s recommended to apply...
Highlights • The concentration of indocyanine green (ICG) as photosensitizer (PS) has an important role in eradication of Enterococcus faecalis.. • It’s...
The purpose of this study was to evaluate the in vitro effect of washing and non-washing of indocyanine green (ICG) as photosensitizer (PS) on bacterial count,...
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SourceType Index Database
Enrichment Source
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StartPage 119
SubjectTerms Bacterial Load - drug effects
Biofilm degradation
Biofilm development
Biofilm formation
Biofilms - drug effects
Biofilms - growth & development
Biofilms - radiation effects
Cell Survival - drug effects
Cell Survival - radiation effects
Disinfection - methods
Dose-Response Relationship, Drug
Dose-Response Relationship, Radiation
Endodontic infection
Enterococcus faecalis
Enterococcus faecalis - drug effects
Enterococcus faecalis - radiation effects
Hematology, Oncology and Palliative Medicine
Humans
Indocyanine green
Indocyanine Green - administration & dosage
Internal Medicine
Photochemotherapy - methods
Photosensitizing Agents - administration & dosage
Treatment Outcome
Title The in vitro effect of antimicrobial photodynamic therapy with indocyanine green on Enterococcus faecalis: Influence of a washing vs non-washing procedure
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https://www.clinicalkey.es/playcontent/1-s2.0-S1572100016301582
https://dx.doi.org/10.1016/j.pdpdt.2016.09.007
https://www.ncbi.nlm.nih.gov/pubmed/27640733
Volume 16
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