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dc.contributor.authorGonzález-Domínguez, José Miguel
dc.contributor.authorGrasa, Laura
dc.contributor.authorFrontiñán, Javier
dc.contributor.authorAbás, Elisa
dc.contributor.authorDomínguez-Alfaro, Antonio
dc.contributor.authorMesonero, J. E.
dc.contributor.authorCriado, Alejandro
dc.contributor.authorAnsón-Casaos, Alejandro
dc.date.accessioned2022-09-08T08:58:45Z
dc.date.available2022-09-08T08:58:45Z
dc.date.issued2022-01-25
dc.identifier.citationJ.M. González-Domínguez, L. Grasa, J. Frontiñán-Rubio, E. Abás, A. Domínguez-Alfaro, J.E. Mesonero, A. Criado, A. Ansón-Casaos, Intrinsic and selective activity of functionalized carbon nanotube/nanocellulose platforms against colon cancer cells, Colloids and Surfaces B: Biointerfaces. 212 (2022). https://doi.org/10.1016/j.colsurfb.2022.112363es_ES
dc.identifier.issn0927-7765
dc.identifier.urihttp://hdl.handle.net/2183/31531
dc.description.abstract[Abstract] Given their large surface area and versatile chemical reactivity, single-walled carbon nanotubes (SWCNTs) are regarded as the basis of new pharmacological complexes. In this study, SWCNTs are chemically functionalized with fluorescein, folic acid, and capecitabine, a drug that is commonly used against colorectal cancer. These functionalized SWCNTs are dispersed in water by taking advantage of their synergistic interaction with type-II nanocrystalline cellulose (II-NCC), and the resulting colloidal system is tested in vitro on both normal (differentiated) and cancerous (proliferative) human colon cells (Caco-2). The functionalized SWCNT/II-NCC hybrids show a higher activity than the reference (capecitabine) against the Caco-2 cancer cell line. However, this effect appears to be intrinsically associated with the SWCNT/II-NCC complex, particularly boosted by fluorescein, as the presence of capecitabine is not required. In addition, confocal microscopy fluorescence imaging using cell cultures highlights the enormous potential of this nanohybrid platform for colon cancer theranostics.es_ES
dc.description.sponsorshipThis research was funded by the regional government of Aragón, DGA (Grupos Reconocidos DGA-T03_17R, DGA-T03_20R and DGA-A20_20R), together with associated EU Regional Development Funds, and also the Spanish MINEICO through a “Juan de la Cierva Incorporación” contract, and their associated research funds (ref. IJCI-2016–27789). A.C. thanks the Xunta de Galicia for an “Atracción de Talento” research grant (no. ED431H 2020/17)es_ES
dc.description.sponsorshipGobierno de Aragón; DGA-T03_17Res_ES
dc.description.sponsorshipGobierno de Aragón; DGA-T03_20Res_ES
dc.description.sponsorshipGobierno de Aragón; DGA-A20_20Res_ES
dc.description.sponsorshipXunta de Galicia; ED431H 2020/17es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/IJCI-2016–27789/ES/
dc.relation.urihttps://doi.org/10.1016/j.colsurfb.2022.112363es_ES
dc.rightsAtribución-NoComercial-SinDerivadas 4.0 Internacionales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCarbon nanotubeses_ES
dc.subjectNanocellulosees_ES
dc.subjectFluoresceines_ES
dc.subjectCaco-2 cellses_ES
dc.subjectChemotherapyes_ES
dc.subjectTheranosticses_ES
dc.titleIntrinsic and Selective Activity of Functionalized Carbon Nanotube/Nanocellulose Platforms Against Colon Cancer Cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleColloids and Surfaces B: Biointerfaceses_ES
UDC.volume212es_ES
UDC.startPage112363es_ES
dc.identifier.doi10.1016/j.colsurfb.2022.112363


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