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Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies

PURPOSE: To investigate the effectiveness of antimicrobial blue light (aBL) as an alternative or adjunctive therapeutic for infectious keratitis. METHODS: We developed an ex vivo rabbit model and an in vivo mouse model of infectious keratitis. A bioluminescent strain of Pseudomonas aeruginosa was us...

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Autores principales: Zhu, Hong, Kochevar, Irene E., Behlau, Irmgard, Zhao, Jie, Wang, Fenghua, Wang, Yucheng, Sun, Xiaodong, Hamblin, Michael R., Dai, Tianhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283079/
https://www.ncbi.nlm.nih.gov/pubmed/28129422
http://dx.doi.org/10.1167/iovs.16-20272
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author Zhu, Hong
Kochevar, Irene E.
Behlau, Irmgard
Zhao, Jie
Wang, Fenghua
Wang, Yucheng
Sun, Xiaodong
Hamblin, Michael R.
Dai, Tianhong
author_facet Zhu, Hong
Kochevar, Irene E.
Behlau, Irmgard
Zhao, Jie
Wang, Fenghua
Wang, Yucheng
Sun, Xiaodong
Hamblin, Michael R.
Dai, Tianhong
author_sort Zhu, Hong
collection PubMed
description PURPOSE: To investigate the effectiveness of antimicrobial blue light (aBL) as an alternative or adjunctive therapeutic for infectious keratitis. METHODS: We developed an ex vivo rabbit model and an in vivo mouse model of infectious keratitis. A bioluminescent strain of Pseudomonas aeruginosa was used as the causative pathogen, allowing noninvasive monitoring of the extent of infection in real time via bioluminescence imaging. Quantitation of bacterial luminescence was correlated to colony-forming units (CFU). Using the ex vivo and in vivo models, the effectiveness of aBL (415 nm) for the treatment of keratitis was evaluated as a function of radiant exposure when aBL was delivered at 6 or 24 hours after bacterial inoculation. The aBL exposures calculated to reach the retina were compared to the American National Standards Institute standards to estimate aBL retinal safety. RESULTS: Pseudomonas aeruginosa keratitis fully developed in both the ex vivo and in vivo models at 24 hours post inoculation. Bacterial luminescence in the infected corneas correlated linearly to CFU (R(2) = 0.921). Bacterial burden in the infected corneas was rapidly and significantly reduced (>2-log(10)) both ex vivo and in vivo after a single exposure of aBL. Recurrence of infection was observed in the aBL-treated mice at 24 hours after aBL exposure. The aBL toxicity to the retina is largely dependent on the aBL transmission of the cornea. CONCLUSIONS: Antimicrobial blue light is a potential alternative or adjunctive therapeutic for infectious keratitis. Further studies of corneal and retinal safety using large animal models, in which the ocular anatomies are similar to that of humans, are warranted.
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spelling pubmed-52830792017-02-01 Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies Zhu, Hong Kochevar, Irene E. Behlau, Irmgard Zhao, Jie Wang, Fenghua Wang, Yucheng Sun, Xiaodong Hamblin, Michael R. Dai, Tianhong Invest Ophthalmol Vis Sci Cornea PURPOSE: To investigate the effectiveness of antimicrobial blue light (aBL) as an alternative or adjunctive therapeutic for infectious keratitis. METHODS: We developed an ex vivo rabbit model and an in vivo mouse model of infectious keratitis. A bioluminescent strain of Pseudomonas aeruginosa was used as the causative pathogen, allowing noninvasive monitoring of the extent of infection in real time via bioluminescence imaging. Quantitation of bacterial luminescence was correlated to colony-forming units (CFU). Using the ex vivo and in vivo models, the effectiveness of aBL (415 nm) for the treatment of keratitis was evaluated as a function of radiant exposure when aBL was delivered at 6 or 24 hours after bacterial inoculation. The aBL exposures calculated to reach the retina were compared to the American National Standards Institute standards to estimate aBL retinal safety. RESULTS: Pseudomonas aeruginosa keratitis fully developed in both the ex vivo and in vivo models at 24 hours post inoculation. Bacterial luminescence in the infected corneas correlated linearly to CFU (R(2) = 0.921). Bacterial burden in the infected corneas was rapidly and significantly reduced (>2-log(10)) both ex vivo and in vivo after a single exposure of aBL. Recurrence of infection was observed in the aBL-treated mice at 24 hours after aBL exposure. The aBL toxicity to the retina is largely dependent on the aBL transmission of the cornea. CONCLUSIONS: Antimicrobial blue light is a potential alternative or adjunctive therapeutic for infectious keratitis. Further studies of corneal and retinal safety using large animal models, in which the ocular anatomies are similar to that of humans, are warranted. The Association for Research in Vision and Ophthalmology 2017-01 /pmc/articles/PMC5283079/ /pubmed/28129422 http://dx.doi.org/10.1167/iovs.16-20272 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Cornea
Zhu, Hong
Kochevar, Irene E.
Behlau, Irmgard
Zhao, Jie
Wang, Fenghua
Wang, Yucheng
Sun, Xiaodong
Hamblin, Michael R.
Dai, Tianhong
Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies
title Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies
title_full Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies
title_fullStr Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies
title_full_unstemmed Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies
title_short Antimicrobial Blue Light Therapy for Infectious Keratitis: Ex Vivo and In Vivo Studies
title_sort antimicrobial blue light therapy for infectious keratitis: ex vivo and in vivo studies
topic Cornea
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283079/
https://www.ncbi.nlm.nih.gov/pubmed/28129422
http://dx.doi.org/10.1167/iovs.16-20272
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