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dc.contributor.authorSoria, F.
dc.contributor.authorMartínez-Pla, L.
dc.contributor.authorAznar-Cervantes, S.D.
dc.contributor.authorde la Cruz, J.E.
dc.contributor.authorFernández, T.
dc.contributor.authorPérez Fentes, Daniel Adolfo
dc.contributor.authorLlanes, L.
dc.contributor.authorSánchez-Margallo, F.M.
dc.date.accessioned2025-08-26T11:02:42Z
dc.date.available2025-08-26T11:02:42Z
dc.date.issued2022
dc.identifier.citationSoria F, Martínez-Pla L, Aznar-Cervantes SD, de la Cruz JE, Fernández T, Pérez-Fentes D, et al. Cytotoxicity Assessment of a New Design for a Biodegradable Ureteral Mitomycin Drug-Eluting Stent in Urothelial Carcinoma Cell Culture. Polymers. 2022;14(19).
dc.identifier.issn2073-4360
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/6416a50b5db420433b7b6310*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20833
dc.description.abstractUrothelial tumour of the upper urinary tract is a rare neoplasm, but unfortunately, it has a high recurrence rate. The reduction of these tumour recurrences could be achieved by the intracavitary instillation of adjuvant chemotherapy after nephron-sparing treatment in selected patients, but current instillation methods are ineffective. Therefore, the aim of this in vitro study is to evaluate the cytotoxic capacity of a new instillation technology through a biodegradable ureteral stent/scaffold coated with a silk fibroin matrix for the controlled release of mitomycin C as an anti-cancer drug. Through a comparative study, we assessed, in urothelial carcinoma cells in a human cancer T24 cell culture for 3 and 6 h, the cytotoxic capacity of mitomycin C by viability assay using the CCK-8 test (Cell counting Kit-8). Cell viability studies in the urothelial carcinoma cell line confirm that mitomycin C embedded in the polymeric matrix does not alter its cytotoxic properties and causes a significant decrease in cell viability at 6 h versus in the control groups. These findings have a clear biomedical application and could be of great use to decrease the recurrence rate in patients with upper tract urothelial carcinomas by increasing the dwell time of anti-cancer drugs.en
dc.description.sponsorshipThis research was funded by Instituto de Salud Carlos III (ISCIII, Spain) through the projects PI16/01707 and PI20/01188. Additionally, project IB18107 was funded by Consejeria de Economia, Ciencia y Agenda Digital-Junta de Extremadura (Spain) and co-funded by the European Union. This study has been partially supported (80%) by the European Commission ERDF/FEDER Operational Programme `Murcia' CCI No 2007ES161PO001 (Project No. 14-20/20).en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleCytotoxicity Assessment of a New Design for a Biodegradable Ureteral Mitomycin Drug-Eluting Stent in Urothelial Carcinoma Cell Culture*
dc.typeArticleen
dc.authorsophosSoria, F. M. F.
dc.authorsophosMartínez-Pla, L.
dc.authorsophosAznar-Cervantes, S. D.
dc.authorsophosde la Cruz, J. E.
dc.authorsophosFernández, T.
dc.authorsophosPérez-Fentes, D.
dc.authorsophosLlanes, L.
dc.authorsophosSánchez, Margallo
dc.identifier.doi10.3390/polym14194081
dc.identifier.sophos6416a50b5db420433b7b6310
dc.issue.number19
dc.journal.titlePolymers*
dc.relation.projectIDInstituto de Salud Carlos III (ISCIII, Spain) [PI16/01707, PI20/01188]; Consejeria de Economia, Ciencia y Agenda Digital-Junta de Extremadura (Spain) [IB18107]; European Union; European Commission ERDF/FEDER Operational Programme 'Murcia' CCI [2007ES161PO001, 14-20/20]
dc.relation.publisherversionhttps://ddfv.ufv.es/bitstream/10641/3611/1/polymers-14-04081.pdf;https://mdpi-res.com/d_attachment/polymers/polymers-14-04081/article_deploy/polymers-14-04081.pdf?version=1664432504es
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number14


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Atribución 4.0 Internacional
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