dc.creatorMartinez, Sol Romina
dc.creatorIbarra, Luis Exequiel
dc.creatorPonzio, Rodrigo Andrés
dc.creatorForcone, Maria Virginia
dc.creatorWendel, Ana Belén
dc.creatorChesta, Carlos Alberto
dc.creatorSpesia, Mariana Belen
dc.creatorPalacios, Rodrigo Emiliano
dc.date.accessioned2020-10-29T14:26:16Z
dc.date.accessioned2022-10-15T15:28:05Z
dc.date.available2020-10-29T14:26:16Z
dc.date.available2022-10-15T15:28:05Z
dc.date.created2020-10-29T14:26:16Z
dc.date.issued2020-06
dc.identifierMartinez, Sol Romina; Ibarra, Luis Exequiel; Ponzio, Rodrigo Andrés; Forcone, Maria Virginia; Wendel, Ana Belén; et al.; Photodynamic inactivation of ESKAPE group bacterial pathogens in planktonic and biofilm cultures using metallated porphyrin-doped conjugated polymer nanoparticles; American Chemical Society Inc; ACS Infectious Diseases; 6; 8; 6-2020; 2202-2213
dc.identifier2373-8227
dc.identifierhttp://hdl.handle.net/11336/117137
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4402829
dc.description.abstractPhotodynamic inactivation (PDI) protocols using photoactive metallated porphyrin-doped conjugated polymer nanoparticles (CPNs) and blue light were developed to eliminate multidrug-resistant pathogens. CPNs-PDI protocols using varying particle concentration and irradiation doses were tested against nine pathogenic bacterial strains including antibiotic-resistant bacteria of the ESKAPE pathogens group. Bactericidal effect was achieved in methicillin-resistant Sthaphylococus aureus strains using low light doses (9.6-14.4 J/cm2); while Gram-negative bacteria required a higher light dose (28.8 J/cm2). Bacteria-CPNs interaction was studied through flow cytometry taking advantage of the intrinsic CPNs fluorescence, demonstrating that CPNs efficiently bind to the bacterial envelope. Finally, the performance of CPNs-PDI was explored in biofilms; good antibiofilm ability and almost complete eradication were observed for S. aureus and Escherichia coli biofilms, respectively, using confocal microscopy. Overall, we demonstrated that CPNs-PDI is an efficient tool not only to kill superbugs as sessile cells but also to disrupt and eradicate biofilms of highly relevant pathogenic bacterial species.
dc.languageeng
dc.publisherAmerican Chemical Society Inc
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acsinfecdis.0c00268
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acsinfecdis.0c00268
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectBIOFILMS
dc.subjectESKAPE PATHOGENS
dc.subjectMETALLATED PORPHYRIN-DOPED CONJUGATED POLYMER NANOPARTICLES
dc.subjectPHOTODYNAMIC INACTIVATION PROTOCOLS
dc.titlePhotodynamic inactivation of ESKAPE group bacterial pathogens in planktonic and biofilm cultures using metallated porphyrin-doped conjugated polymer nanoparticles
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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