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Antimicrobial activity of new green-functionalized oxazoline-based oligomers against clinical isolates

dc.contributor.authorMartins, Celso
dc.contributor.authorCorreia, Vanessa G.
dc.contributor.authorAguiar-Ricardo, Ana
dc.contributor.authorCunha, Ângela
dc.contributor.authorMoutinho, Maria Guilhermina M.
dc.date.accessioned2016-04-29T08:42:41Z
dc.date.available2016-04-29T08:42:41Z
dc.date.issued2015-07-28
dc.descriptionThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.pt_PT
dc.description.abstract"Background: The search for new antimicrobial compounds able to overcome the global issue of microbial resistance to antibiotics is a priority worldwide. Moreover, several commensal microorganisms have been increasingly associated to opportunistic microbial infections. Having previously disclosed the green synthesis and preliminary characterization of the oligomers [linear oligo(ethylenimine) hydrochloride and oligo(2-methyl-2-oxazoline) quaternized with N,Ndimethyldodecylamine] we herein report on the screening of these oligomers against a battery of 69 clinical isolates of Aerococcus spp., Candida spp., Staphylococcus spp. and Streptococcus spp. Findings: The isolates’ susceptibility to both oligomers was evaluated by determining their minimal inhibitory concentration (MIC) and the biocidal effectiveness of each compound was further confirmed through spectrophotometric measurements and fluorescence microscopy. The MIC values of the 69 isolates were highly variable, yet favourably comparable with those of other antimicrobial polymers. The viability assays resulted in 100% of microbial killing rate after only 5 min, highlighting the promising antimicrobial action of these oligomers. Conclusions: Though further studies are required, evidence suggests that a strong effort should be done in order to confirm these compounds as valid alternatives for several clinical applications. This is reinforced by their well described biocompatibility with human tissues and by their proposed mechanism of action which difficult the development of microbial resistance to these compounds."pt_PT
dc.description.sponsorshipThis work was partially supported by Fundação para a Ciência e Tecnologia (FCT), Project PTDC/QUI/73939/2006, and by Instituto Superior de Ciências da Saúde Egas Moniz (ISCSEM).pt_PT
dc.identifier.citationMartins et al. SpringerPlus (2015) 4:382pt_PT
dc.identifier.doi10.1186/s40064-015-1166-5pt_PT
dc.identifier.issn2193-1801
dc.identifier.urihttp://hdl.handle.net/10400.26/13372
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringerpt_PT
dc.relationActivPOL - Development of oxazoline and aziridine-based antimicrobial polymers using supercritical carbon dioxide technology
dc.relation.publisherversionhttp://springerplus.springeropen.com/articles/10.1186/s40064-015-1166-5pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectAntimicrobial oxazolinespt_PT
dc.subjectOpportunistic pathogenspt_PT
dc.subjectMICpt_PT
dc.subjectViability assaypt_PT
dc.subjectClinical isolatespt_PT
dc.titleAntimicrobial activity of new green-functionalized oxazoline-based oligomers against clinical isolatespt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleActivPOL - Development of oxazoline and aziridine-based antimicrobial polymers using supercritical carbon dioxide technology
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FQUI%2F73939%2F2006/PT
oaire.citation.startPage382pt_PT
oaire.citation.titleSpringerPluspt_PT
oaire.citation.volume4pt_PT
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication56fb922b-b9fb-499f-80e3-103f86a78468
relation.isProjectOfPublication.latestForDiscovery56fb922b-b9fb-499f-80e3-103f86a78468

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