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dc.contributor.authorGonzález Garcinuño, Álvaro 
dc.contributor.authorTabernero de Paz, Antonio 
dc.contributor.authorNieto Jiménez, Celia 
dc.contributor.authorMartín del Valle, Eva María 
dc.contributor.authorKenjeres, Sasa
dc.date.accessioned2026-01-16T10:14:50Z
dc.date.available2026-01-16T10:14:50Z
dc.date.issued2025
dc.identifier.citationÁlvaro González-Garcinuño, Antonio Tabernero, Celia Nieto, Eva Martín del Valle, Sasa Kenjeres, Multiphysics simulation of liposome release from hydrogels for cavity filling following patient-specific breast tumor surgery, European Journal of Pharmaceutical Sciences, Volume 204, 2025, 106966, ISSN 0928-0987, https://doi.org/10.1016/j.ejps.2024.106966. (https://www.sciencedirect.com/science/article/pii/S0928098724002793)es_ES
dc.identifier.issn0928-0987
dc.identifier.urihttp://hdl.handle.net/10366/168905
dc.description.abstract[EN]Several studies have recommended the use of hydrogels for localized targeted delivery of chemotherapeutic drugs following tumor removal surgery. This approach aims to both fill the cavity and prevent cancer recurrence. The use of Multiphysics-based simulation emerges as a valuable strategy for minimizing experimental work, providing detailed insights into how drug release occurs in the tissue, and enabling the optimization of the design. In this study, we introduced a mathematical model, utilizing experimental data, to investigate the transport of liposomes carrying MZ1 from a thermosensitive hydrogel and their impact on the viability of breast cancer cells. The proposed comprehensive model considers not just the transport within the interstitial tissue, represented as a porous medium, but also the uptake by cells and its influence on cell viability, along with the potential lymphatic drainage. The six real patient-specific tumor shapes extracted from MRI scans were used to investigate how the size and form of the tumor can modify the transport pattern. The computational results revealed that the concentration of liposomes in the tissue is significantly influenced by their release from the hydrogel, which proved to be the limiting step. Liposome concentrations of approximately 0.1 % weight were found to be sufficient in ensuring minimal cell survival in the vicinity of the tumor.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.subjectMultiphysics simulationes_ES
dc.subjectBreast canceres_ES
dc.subjectLiposomeses_ES
dc.subjectThermosensitive hydrogelses_ES
dc.subjectMass transferes_ES
dc.titleMultiphysics simulation of liposome release from hydrogels for cavity filling following patient-specific breast tumor surgeryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1016/j.ejps.2024.106966es_ES
dc.identifier.doi10.1016/j.ejps.2024.106966
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titleEuropean Journal of Pharmaceutical Scienceses_ES
dc.volume.number204es_ES
dc.page.initial106966es_ES
dc.type.hasVersioninfo:eu-repo/semantics/draftes_ES


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