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dc.creatorCepeda-Franco, C. (Carmen)-
dc.creatorMitxelena-Iribarren, O. (Oihane)-
dc.creatorCalero-Castro, F.J.(Francisco José)-
dc.creatorAstigarraga, M.(Malen)-
dc.creatorLaga, I. (Iman)-
dc.creatorPereira, S. (Sheila)-
dc.creatorArana-Alonso, S. (Sergio)-
dc.creatorMujika-Garmendia, M. (Maite)-
dc.creatorPadillo-Ruiz, J. (Javier)-
dc.date.accessioned2023-05-17T09:12:21Z-
dc.date.available2023-05-17T09:12:21Z-
dc.date.issued2023-02-
dc.identifier.citationCepeda-Franco, C. (Carmen); Mitxelena-Iribarren, O. (Oihane); Calero-Castro, F.J.(Francisco José); et al. "TARTESSUS: A customized electrospun drug delivery system loaded with Irinotecan for Local and sustained chemotherapy release in pancreatic cancer". Bioengineering. 10 (2), 2023-02,es
dc.identifier.issn2306-5354-
dc.identifier.urihttps://hdl.handle.net/10171/66278-
dc.description.abstractPost-surgical chemotherapy in pancreatic cancer has notorious side effects due to the high dose required. Multiple devices have been designed to tackle this aspect and achieve a delayed drug release. This study aimed to explore the controlled and sustained local delivery of a reduced drug dose from an irinotecan-loaded electrospun nanofiber membrane (named TARTESSUS) that can be placed on the patients' tissue after tumor resection surgery. The drug delivery system formulation was made of polycaprolactone (PCL). The mechanical properties and the release kinetics of the drug were adjusted by the electrospinning parameters and by the polymer ratio between 10 w.t.% and 14 w.t.% of PCL in formic acid:acetic acid:chloroform (47.5:47.5:5). The irinotecan release analysis was performed and three different release periods were obtained, depending on the concentration of the polymer in the dissolution. The TARTESSUS device was tested in 2D and 3D cell cultures and it demonstrated a decrease in cell viability in 2D culture between 72 h and day 7 from the start of treatment. In 3D culture, a decrease in viability was seen between 72 h, day 7 (p < 0.001), day 10 (p < 0.001), 14 (p < 0.001), and day 17 (p = 0.003) as well as a decrease in proliferation between 72 h and day 10 (p = 0.030) and a reduction in spheroid size during days 10 (p = 0.001), 14 (p < 0.001), and 17 (p < 0.001). In conclusion, TARTESSUS showed a successful encapsulation of a chemotherapeutic drug and a sustained and delayed release with an adjustable releasing period to optimize the therapeutic effect in pancreatic cancer treatment.es_ES
dc.format.extent183es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectElectrospinninges_ES
dc.subjectNanofiber membranees_ES
dc.subjectPancreatic canceres_ES
dc.subjectDrug delivery systemes_ES
dc.subjectIrinotecanes_ES
dc.titleTARTESSUS: A customized electrospun drug delivery system loaded with Irinotecan for Local and sustained chemotherapy release in pancreatic canceres_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.publisher.placeSWITZERLANDes_ES
dc.editorial.noteThis article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY)es_ES
dc.identifier.doi10.3390/bioengineering10020183-
dadun.citation.number2es_ES
dadun.citation.publicationNameBioengineeringes_ES
dadun.citation.volume10es_ES
dc.identifier.pmid36829677-

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