Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/78453

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dc.contributor.authorOliveira, Anapor
dc.contributor.authorAraújo, Anapor
dc.contributor.authorRodrigues, Luísa C.por
dc.contributor.authorSilva, Catarina S.por
dc.contributor.authorReis, R. L.por
dc.contributor.authorNeves, N. M.por
dc.contributor.authorLeão, Pedropor
dc.contributor.authorMartins, Albinopor
dc.date.accessioned2022-06-21T15:10:40Z-
dc.date.issued2022-05-
dc.date.submitted2022-06-
dc.identifier.citationOliveira A., Araujo A., Rodrigues L.C., Silva C. S., Reis R. L., Neves N. M., Leão P., Martins A. Metronidazole Delivery Nanosystem Able To Reduce the Pathogenicity of Bacteria in Colorectal Infection, Biomacromolecules, Vol. 23, Issue 6, pp. 2415-2427, doi:10.1021/acs.biomac.2c00186, 2022por
dc.identifier.issn2415-2427por
dc.identifier.urihttps://hdl.handle.net/1822/78453-
dc.description.abstractMetronidazole (MTZ) is a drug potentially used for the treatment of intestinal infections, namely, the ones caused by colorectal surgery. The traditional routes of administration decrease its local effectiveness and present off-site effects. To circumvent such limitations, herein a drug delivery system (DDS) based on MTZ-loaded nanoparticles (NPs) immobilized at the surface of electrospun fibrous meshes is proposed. MTZ at different concentrations (1, 2, 5, and 10 mg mLâ 1) was loaded into chitosanâ sodium tripolyphosphate NPs. The MTZ loaded into NPs at the highest concentration showed a quick release in the first 12 h, followed by a gradual release. This DDS was not toxic to human colonic cells. When tested against different bacterial strains, a significant reduction of Escherichia coli and Staphylococcus aureus was observed, but no effect was found against Enterococcus faecalis. Therefore, this DDS offers high potential to locally prevent the occurrence of infections after colorectal anastomosis.por
dc.description.sponsorshipThe authors thank the Portuguese Foundation for Science and Technology (FCT) and CUF, S.A. for the Ph.D. scholarship of A.O. (PD/BDE/142979/2018). Also, the authors thank the FCT for the financial support of L.C.R. (SFRH/BPD/93697/ 2013). This work was also financially supported by the project Bluebiolab − Transboundary Marine Biotechnology Laboratory (0474_BLUEBIOLAB_1_E) financed by the Interreg programme Spain-Portugal through the European Regional Development Fund (ERDF), and by the FCT projects PTDC/CTM-CTM/29813/2017-(POCI-01-0145-FEDER-029813), UIDB/50026/2020, and UIDP/50026/2020por
dc.language.isoengpor
dc.publisherACS Publicationspor
dc.relationinfo:eu-repo/grantAgreement/FCT/OE/PD%2FBDE%2F142979%2F2018/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/FARH/SFRH%2FBPD%2F93697%2F2013/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FCTM-CTM%2F29813%2F2017/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50026%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50026%2F2020/PTpor
dc.rightsrestrictedAccesspor
dc.subjectAntibacterialpor
dc.subjectColorectalpor
dc.subjectElectrospun fibrous meshespor
dc.subjectMetronidazolepor
dc.subjectNanoparticlespor
dc.titleMetronidazole delivery nanosystem able to reduce the pathogenicity of bacteria in colorectal infectionpor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://doi.org/10.1021/acs.biomac.2c00186por
dc.commentshttp://3bs.uminho.pt/node/20782por
oaire.citationStartPage2415por
oaire.citationEndPage2427por
oaire.citationIssue6por
oaire.citationVolume23por
dc.date.updated2022-06-20T16:25:25Z-
dc.identifier.doi10.1021/acs.biomac.2c00186por
dc.date.embargo10000-01-01-
dc.identifier.pmid35623028por
dc.subject.wosScience & Technologypor
sdum.journalBiomacromoleculespor
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals
ICVS - Artigos em revistas internacionais / Papers in international journals

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