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dc.contributor.authorFerreira, Maria do Perpétuo Socorro Borges Carriço-
dc.contributor.authorCardoso, M. F.C.-
dc.contributor.authorSilva, F. C. da-
dc.contributor.authorFerreira, V?tor Francisco-
dc.contributor.authorLima, Emerson Silva-
dc.contributor.authorSouza, João Vicente Braga de-
dc.date.accessioned2020-05-21T20:06:20Z-
dc.date.available2020-05-21T20:06:20Z-
dc.date.issued2014-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/15982-
dc.description.abstractThis study evaluated the antifungal activities of synthetic naphthoquinones against opportunistic and dermatophytic fungi and their preliminary mechanisms of action. The minimum inhibitory concentrations (MICs) of four synthetic naphthoquinones for 89 microorganisms, including opportunistic yeast agents, dermatophytes and opportunistic filamentous fungi, were determined. The compound that exhibited the best activity was assessed for its action against the cell wall (sorbitol test), for interference associated with ergosterol interaction, for osmotic balance (K+ efflux) and for membrane leakage of substances that absorb at the wavelength of 260 nm. All tested naphthoquinones exhibited antifungal activity, and compound IVS320 (3a,10b-dihydro-1H-cyclopenta [b] naphtho [2,3-d] furan-5,10-dione)-dione) demonstrated the lowest MICs across the tested species. The MIC of IVS320 was particularly low for dermatophytes (values ranging from 5-28 μg/mL) and Cryptococcus spp. (3-5 μg/mL). In preliminary mechanism-of-action tests, IVS320 did not alter the fungal cell wall but did cause problems in terms of cell membrane permeability (efflux of K+ and leakage of substances that absorb at 260 nm). This last effect was unrelated to ergosterol interactions with the membrane. © 2014 Ferreira et al.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 13, Número 1pt_BR
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Brazil*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subjectErgosterolen
dc.subjectNaphthoquinoneen
dc.subjectPerchloric Aciden
dc.subjectSorbitolen
dc.subject(naphtho[2,3 D]furan 5,10 Dione) Dioneen
dc.subject1,4 Naphthoquinone Derivativeen
dc.subject2,2 Dimethyl 2,3 Dihydronaphtho[1,2 B]furan 4,5 Dioneen
dc.subject2,2 Dimethyl 2,3 Dihydronaphtho[2,3 B]furan 4,9 Dioneen
dc.subject3a,10b Dihydro 1h Cyclopentaen
dc.subject7,9a Dihydro 6bh Cyclopentaen
dc.subjectAmphotericin Ben
dc.subjectAntifungal Agenten
dc.subjectNaphtho[2,1 D]furan 5,6 Dioneen
dc.subjectPerchloric Aciden
dc.subjectUnclassified Drugen
dc.subjectAnti-fungal Activityen
dc.subjectArthroderma Gypseumen
dc.subjectAspergillusen
dc.subjectAtomic Absorptionen
dc.subjectBroth Dilutionen
dc.subjectCandida Albicansen
dc.subjectCandida Parapsilosisen
dc.subjectCell Membrane Permeabilityen
dc.subjectControlled Studyen
dc.subjectCryptococcusen
dc.subjectCryptococcus Gattiien
dc.subjectCryptococcus Neoformansen
dc.subjectDermatophyteen
dc.subjectFilamentous Fungusen
dc.subjectFungal Cell Wallen
dc.subjectFungal Membraneen
dc.subjectFusariumen
dc.subjectMicrosporum Canisen
dc.subjectMinimum Inhibitory Concentrationen
dc.subjectNonhumanen
dc.subjectPotassium Transporten
dc.subjectCandida Albicansen
dc.subjectCytolysis Assayen
dc.subjectFungal Cellen
dc.subjectYeasten
dc.subjectAntifungal Agentsen
dc.subjectCell Membrane Permeabilityen
dc.subjectFungien
dc.subjectHumansen
dc.subjectMicrobial Sensitivity Testsen
dc.subjectMycosesen
dc.subjectNaphthoquinonesen
dc.titleAntifungal activity of synthetic naphthoquinones against dermatophytes and opportunistic fungi: Preliminary mechanism-of-action testsen
dc.typeArtigopt_BR
dc.identifier.doi10.1186/1476-0711-13-26-
dc.publisher.journalAnnals of Clinical Microbiology and Antimicrobialspt_BR
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