Advances in antimicrobial photodynamic inactivation at the nanoscale

The alarming worldwide increase in antibiotic resistance amongst microbial pathogens necessitates a search for new antimicrobial techniques, which will not be affected by, or indeed cause resistance themselves. Light-mediated photoinactivation is one such technique that takes advantage of the whole...

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Main Authors: Kashef Nasim, Huang Ying-Ying, Hamblin Michael R.
Format: Article
Language:English
Published: De Gruyter 2017-08-01
Series:Nanophotonics
Subjects:
Online Access:https://doi.org/10.1515/nanoph-2016-0189
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spelling doaj-66a8e5f348484edf93cef11deaa194a82021-09-06T19:20:30ZengDe GruyterNanophotonics2192-86142017-08-016585387910.1515/nanoph-2016-0189nanoph-2016-0189Advances in antimicrobial photodynamic inactivation at the nanoscaleKashef Nasim0Huang Ying-Ying1Hamblin Michael R.2Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA 02114, USAWellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA 02114, USAWellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA 02114, USAThe alarming worldwide increase in antibiotic resistance amongst microbial pathogens necessitates a search for new antimicrobial techniques, which will not be affected by, or indeed cause resistance themselves. Light-mediated photoinactivation is one such technique that takes advantage of the whole spectrum of light to destroy a broad spectrum of pathogens. Many of these photoinactivation techniques rely on the participation of a diverse range of nanoparticles and nanostructures that have dimensions very similar to the wavelength of light. Photodynamic inactivation relies on the photochemical production of singlet oxygen from photosensitizing dyes (type II pathway) that can benefit remarkably from formulation in nanoparticle-based drug delivery vehicles. Fullerenes are a closed-cage carbon allotrope nanoparticle with a high absorption coefficient and triplet yield. Their photochemistry is highly dependent on microenvironment, and can be type II in organic solvents and type I (hydroxyl radicals) in a biological milieu. Titanium dioxide nanoparticles act as a large band-gap semiconductor that can carry out photo-induced electron transfer under ultraviolet A light and can also produce reactive oxygen species that kill microbial cells. We discuss some recent studies in which quite remarkable potentiation of microbial killing (up to six logs) can be obtained by the addition of simple inorganic salts such as the non-toxic sodium/potassium iodide, bromide, nitrite, and even the toxic sodium azide. Interesting mechanistic insights were obtained to explain this increased killing.https://doi.org/10.1515/nanoph-2016-0189antimicrobial photodynamic inactivationphotochemical mechanismsdrug delivery nanovehiclesfullerenestitanium dioxide photocatalysispotentiationdrug-resistant microbial cellsnanotechnology-based drug deliverytitania photocatalysisefflux-pump inhibition
collection DOAJ
language English
format Article
sources DOAJ
author Kashef Nasim
Huang Ying-Ying
Hamblin Michael R.
spellingShingle Kashef Nasim
Huang Ying-Ying
Hamblin Michael R.
Advances in antimicrobial photodynamic inactivation at the nanoscale
Nanophotonics
antimicrobial photodynamic inactivation
photochemical mechanisms
drug delivery nanovehicles
fullerenes
titanium dioxide photocatalysis
potentiation
drug-resistant microbial cells
nanotechnology-based drug delivery
titania photocatalysis
efflux-pump inhibition
author_facet Kashef Nasim
Huang Ying-Ying
Hamblin Michael R.
author_sort Kashef Nasim
title Advances in antimicrobial photodynamic inactivation at the nanoscale
title_short Advances in antimicrobial photodynamic inactivation at the nanoscale
title_full Advances in antimicrobial photodynamic inactivation at the nanoscale
title_fullStr Advances in antimicrobial photodynamic inactivation at the nanoscale
title_full_unstemmed Advances in antimicrobial photodynamic inactivation at the nanoscale
title_sort advances in antimicrobial photodynamic inactivation at the nanoscale
publisher De Gruyter
series Nanophotonics
issn 2192-8614
publishDate 2017-08-01
description The alarming worldwide increase in antibiotic resistance amongst microbial pathogens necessitates a search for new antimicrobial techniques, which will not be affected by, or indeed cause resistance themselves. Light-mediated photoinactivation is one such technique that takes advantage of the whole spectrum of light to destroy a broad spectrum of pathogens. Many of these photoinactivation techniques rely on the participation of a diverse range of nanoparticles and nanostructures that have dimensions very similar to the wavelength of light. Photodynamic inactivation relies on the photochemical production of singlet oxygen from photosensitizing dyes (type II pathway) that can benefit remarkably from formulation in nanoparticle-based drug delivery vehicles. Fullerenes are a closed-cage carbon allotrope nanoparticle with a high absorption coefficient and triplet yield. Their photochemistry is highly dependent on microenvironment, and can be type II in organic solvents and type I (hydroxyl radicals) in a biological milieu. Titanium dioxide nanoparticles act as a large band-gap semiconductor that can carry out photo-induced electron transfer under ultraviolet A light and can also produce reactive oxygen species that kill microbial cells. We discuss some recent studies in which quite remarkable potentiation of microbial killing (up to six logs) can be obtained by the addition of simple inorganic salts such as the non-toxic sodium/potassium iodide, bromide, nitrite, and even the toxic sodium azide. Interesting mechanistic insights were obtained to explain this increased killing.
topic antimicrobial photodynamic inactivation
photochemical mechanisms
drug delivery nanovehicles
fullerenes
titanium dioxide photocatalysis
potentiation
drug-resistant microbial cells
nanotechnology-based drug delivery
titania photocatalysis
efflux-pump inhibition
url https://doi.org/10.1515/nanoph-2016-0189
work_keys_str_mv AT kashefnasim advancesinantimicrobialphotodynamicinactivationatthenanoscale
AT huangyingying advancesinantimicrobialphotodynamicinactivationatthenanoscale
AT hamblinmichaelr advancesinantimicrobialphotodynamicinactivationatthenanoscale
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