Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/28290
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dc.contributor.authorTavares, Anabelapt_PT
dc.contributor.authorCarvalho, Carla M. B.pt_PT
dc.contributor.authorFaustino, Maria A.pt_PT
dc.contributor.authorNeves, Maria G. P. M. S.pt_PT
dc.contributor.authorTomé, João P. C.pt_PT
dc.contributor.authorTomé, Augusto C.pt_PT
dc.contributor.authorCavaleiro, José A. S.pt_PT
dc.contributor.authorCunha, Ângelapt_PT
dc.contributor.authorGomes, Newton C. M.pt_PT
dc.contributor.authorAlves, Elianapt_PT
dc.contributor.authorAlmeida, Adelaidept_PT
dc.date.accessioned2020-04-24T14:50:29Z-
dc.date.available2020-04-24T14:50:29Z-
dc.date.issued2010-01-20-
dc.identifier.issn1660-3397pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/28290-
dc.description.abstractAntimicrobial photodynamic therapy (aPDT) has emerged in the clinical field as a potential alternative to antibiotics to treat microbial infections. No cases of microbial viability recovery or any resistance mechanisms against it are yet known. 5,10,15-tris(1-Methylpyridinium-4-yl)-20-(pentafluorophenyl)-porphyrin triiodide (Tri-Py(+)-Me-PF) was used as photosensitizer. Vibrio fischeri and recombinant Escherichia coli were the studied bacteria. To determine the bacterial recovery after treatment, Tri-Py(+)-Me-PF (5.0 microM) was added to bacterial suspensions and the samples were irradiated with white light (40 W m(-2)) for 270 minutes. Then, the samples were protected from light, aliquots collected at different intervals and the bioluminescence measured. To assess the development of resistance after treatment, bacterial suspensions were exposed to white light (25 minutes), in presence of 5.0 microM of Tri-Py(+)-Me-PF (99.99% of inactivation) and plated. After the first irradiation period, surviving colonies were collected from the plate and resuspended in PBS. Then, an identical protocol was used and repeated ten times for each bacterium. The results suggest that aPDT using Tri-Py(+)-Me-PF represents a promising approach to efficiently destroy bacteria since after a single treatment these microorganisms do not recover their viability and after ten generations of partially photosensitized cells neither of the bacteria develop resistance to the photodynamic process.pt_PT
dc.language.isoengpt_PT
dc.publisherMDPIpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F41806%2F2007/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F38611%2F2007/PTpt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCationic porphyrinpt_PT
dc.subjectAntimicrobial photodynamic therapypt_PT
dc.subjectBacterial resistancept_PT
dc.subjectBacterial viabilitypt_PT
dc.subjectBioluminescencept_PT
dc.titleAntimicrobial photodynamic therapy: study of bacterial recovery viability and potential development of resistance after treatmentpt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage91pt_PT
degois.publication.issue1pt_PT
degois.publication.lastPage105pt_PT
degois.publication.titleMarine Drugspt_PT
degois.publication.volume8pt_PT
dc.identifier.doi10.3390/md8010091pt_PT
dc.identifier.essn1660-3397pt_PT
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