Biomimetic nanosystems for pancreatic cancer therapy: A review

dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto de Materiais (iMATUS)
dc.contributor.authorPereira Silva, Miguel
dc.contributor.authorVeiga, Francisco José de Baptista
dc.contributor.authorSantos, Ana Cláudia Paiva
dc.contributor.authorConcheiro Nine, Ángel Joaquín
dc.contributor.authorÁlvarez Lorenzo, Carmen
dc.date.accessioned2025-11-27T10:00:33Z
dc.date.available2025-11-27T10:00:33Z
dc.date.issued2025-05-08
dc.description.abstractPancreatic cancer (PC) is a highly lethal and aggressive malignancy, currently one of the leading causes of cancer-related deaths worldwide, in both women and men. PC is highly resistant to standard chemotherapy (CT) because its immunosuppressive and hypoxic tumor microenvironment and a dense desmoplastic stroma compartment extensively limit drug accessibility and perfusion. Although CT is one of the main therapeutic strategies for PC management contributing to tumor eradication through a cytotoxic effect, CT is associated with a poor pharmacokinetic profile and provokes deleterious systemic toxicity. This low efficacy-poor safety scenario urgently calls for innovative and highly specific therapeutic strategies to counteract this urgent clinical challenge. Nanotechnology-based precision materials for cancer may help improve drug stability and minimize the systemic cytotoxic effects by increasing drug tumor accumulation and also enabling controlled release, but several drawbacks still persist, such as the poor targeting efficiency. In the last few years increased attention has been paid to bioinspired nanosystems that can mimic either partially or totally biological systems, including lipid layers as suitable stealth coatings resembling the composition of cell membranes, lipoprotein- and blood protein-based nanosystems, and cell membrane-derived systems, such as extracellular vesicles, cell membrane nanovesicles and cell membrane-coated nanosystems, which display intrinsic cancer-targeting abilities, enhanced biocompatibility, decreased immunogenicity, and prolonged blood circulation profile. This review covers the recent breakthroughs on advanced biomimetic PC-targeted nanosystems, focusing on their design, properties and applications as innovative, multifunctional and versatile tools paving the way to improved PC diagnosis and treatment.
dc.description.peerreviewedSI
dc.description.sponsorshipThis work was supported by the Fundaçao para a Ciencia e Tecnologia (FCT, Portugal) [FCT SFRH/BD/148771/2019] and the Ministerio de Ciencia e Innovacion MCIN/AEI/10.13039/501100011033 [PID2023-150422OB-I00] (Spain), Xunta de Galicia [ED431C 2024/ 09], and FEDER.
dc.identifier.citationPereira-Silva, M., Veiga, F., Paiva-Santos, A. C., Concheiro, A., & Alvarez-Lorenzo, C. (2025). Biomimetic nanosystems for pancreatic cancer therapy: A review. Journal of Controlled Release, 383, 113824. 10.1016/j.jconrel.2025.113824
dc.identifier.doi10.1016/j.jconrel.2025.113824
dc.identifier.issn0168-3659
dc.identifier.urihttps://hdl.handle.net/10347/44046
dc.journal.titleJournal of Controlled Release
dc.language.isoeng
dc.page.final51
dc.page.initial1
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2023-150422OB-I00/ES/SCAFFOLDS PIEZOELECTRICOS RECUBIERTOS CON MEMBRANAS CELULARES PARA MEDICINA REGENERATIVA PERSONALIZADA
dc.relation.publisherversionhttps://doi.org/10.1016/j.jconrel.2025.113824
dc.rights© 2025 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/).
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectPancreatic cancer
dc.subjectNanoparticle
dc.subjectChemotherapy
dc.subjectBiomimetic
dc.subjectExosome
dc.subjectCell membrane-coated
dc.titleBiomimetic nanosystems for pancreatic cancer therapy: A review
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number383
dspace.entity.typePublication
relation.isAuthorOfPublicationfbd9d3a4-b1f4-4aff-8472-de22b1c140c4
relation.isAuthorOfPublication44d6632e-65cd-485a-bb67-86df5567793a
relation.isAuthorOfPublication.latestForDiscoveryfbd9d3a4-b1f4-4aff-8472-de22b1c140c4

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