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dc.contributor.authorZapata Zapata, Carolina-
dc.contributor.authorLoaiza Oliva, Manuela-
dc.contributor.authorMartínez Pabón, María Cecilia-
dc.contributor.authorStashenko, Elena-
dc.contributor.authorMesa Arango, Ana Cecilia-
dc.date.accessioned2024-11-18T18:43:07Z-
dc.date.available2024-11-18T18:43:07Z-
dc.date.issued2022-
dc.identifier.citationZapata-Zapata C, Loaiza-Oliva M, Martínez-Pabón MC, Stashenko EE, Mesa-Arango AC. In Vitro Activity of Essential Oils Distilled from Colombian Plants against Candidaauris and Other Candida Species with Different Antifungal Susceptibility Profiles. Molecules. 2022 Oct 12;27(20):6837. doi: 10.3390/molecules27206837.spa
dc.identifier.urihttps://hdl.handle.net/10495/43568-
dc.description.abstractABSTRACT: Multi-drug resistant species such as Candida auris are a global health threat. This scenario has highlighted the need to search for antifungal alternatives. Essential oils (EOs), or some of their major compounds, could be a source of new antifungal molecules. The aim of this study was to evaluate the in vitro activity of EOs and some terpenes against C. auris and other Candida spp. The eleven EOs evaluated were obtained by hydro-distillation from different Colombian plants and the terpenes were purchased. EO chemical compositions were obtained by gas chromatography/mass spectrometry (GC/MS). Antifungal activity was evaluated following the CLSI standard M27, 4th Edition. Cytotoxicity was tested on the HaCaT cell line and fungal growth kinetics were tested by time-kill assays. Candida spp. showed different susceptibility to antifungals and the activity of EOs and terpenes was strain-dependent. The Lippia origanoides (thymol + p-cymene) chemotype EO, thymol, carvacrol, and limonene were the most active, mainly against drug-resistant strains. The most active EOs and terpenes were also slightly cytotoxic on the HaCaT cells. The findings of this study suggest that some EOs and commercial terpenes can be a source for the development of new anti-Candida products and aid the identification of new antifungal targets or action mechanisms.spa
dc.format.extent13 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherMDPIspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleIn Vitro Activity of Essential Oils Distilled from Colombian Plants against Candidaauris and Other Candida Species with Different Antifungal Susceptibility Profilesspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGRID - Grupo de Investigación Dermatológicaspa
dc.publisher.groupGrupo de Investigación en Patología Oral Periodoncia y Cirugía Alvéolo-Dentaria (POPCAD)spa
dc.identifier.doi10.3390/molecules27206837-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1420-3049-
oaire.citationtitleMoleculesspa
oaire.citationstartpage1spa
oaire.citationendpage13spa
oaire.citationvolume27spa
oaire.citationissue20spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
oaire.fundernameColombia. Ministerio de Ciencia, Tecnología e Innovación - MinCienciasspa
oaire.fundernameColombia. Ministerio de Educación Nacional - MinEducaciónspa
oaire.fundernameColombia. Ministerio de Comercio, Industria y Turismo - MinCITspa
oaire.fundernameICETEX (Instituto Colombiano de Crédito Educativo y Estudios Técnicos en el Exterior)spa
dc.publisher.placeBasilea, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsAntifúngicos-
dc.subject.decsAntifungal Agents-
dc.subject.decsCandida-
dc.subject.decsLimoneno-
dc.subject.decsLimonene-
dc.subject.decsPruebas de Sensibilidad Microbiana-
dc.subject.decsMicrobial Sensitivity Tests-
dc.subject.decsAceites Volátiles-
dc.subject.decsOils, Volatile-
dc.subject.decsTerpenos-
dc.subject.decsTerpenes-
dc.subject.decsTimol-
dc.subject.decsThymol-
oaire.funderidentifier.isni0000000106611468-
oaire.funderidentifier.isni0000000403726245-
oaire.funderidentifier.localQ3146540-
dc.description.researchgroupidCOL0050839spa
dc.description.researchgroupidCOL0010074spa
oaire.awardnumberRC-FP44842- 212-2018spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000935-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D002175-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000077222-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D008826-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D009822-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D013729-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D013943-
dc.relation.ispartofjournalabbrevMoleculesspa
oaire.funderidentifier.rorRoR:03fd5ne08-
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