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Targeted Polymeric Nanoparticles as a Strategy for the Treatment of Glioblastoma: A Review

dc.contributor.authorde Paula, Geanne Aparecida [UNESP]
dc.contributor.authorde Paula, Mariana Carlomagno [UNESP]
dc.contributor.authorDutra, Jessyca Aparecida Paes [UNESP]
dc.contributor.authorCarvalho, Suzana Gonçalves [UNESP]
dc.contributor.authorDi Filippo, Leonardo Delello [UNESP]
dc.contributor.authorVillanova, Janaína Cecília Oliveira
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)pt
dc.date.accessioned2026-07-24T13:31:08Z
dc.date.issued2025-01-01
dc.description.abstractGlioblastoma multiforme is the most common and aggressive malignant tumor that affects the central nervous system, with high mortality and low survival. Glioblastoma multiforme treatment includes resection tumor surgery, followed by radiotherapy and chemotherapy adjuvants. However, the drugs used in chemotherapy present some limitations, such as the difficulty of crossing the bloodbrain barrier and resisting the cellular mechanisms of drug efflux. The use of polymeric nanoparticles has proven to be an effective alternative to circumvent such limitations, as it allows the exploration of a range of polymeric structures that can be modified in order to control the biodistribution and cytotoxic effect of the drug delivery systems. Nanoparticles are nanometric in size and allow the incorporation of targeting ligands on their surface, favoring the transposition of the blood-brain barrier and the delivery of the drug to specific sites, increasing the selectivity and safety of chemotherapy. The present review has described the characteristics of chitosan, poly(vinyl alcohol), poly(lactic-coglycolic acid), poly(ethylene glycol), poly(β-amino ester), and poly(ε-caprolactone), which are some of the most commonly used polymers in the manufacture of nanoparticles for the treatment of glioblastoma multiforme. In addition, some of the main targeting ligands used in these nanosystems are presented, such as transferrin, chlorotoxin, albumin, epidermal growth factor, and epidermal growth factor receptor blockers, explored for the active targeting of antiglioblastoma agents.
dc.description.affiliationSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, Brazil.
dc.description.affiliationCenter for Exact, Natural and Health Sciences - CCENS, Federal University of Espírito Santo (UFES), Alegre, Espírito Santo, Brazil.
dc.description.affiliationUnespSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, Brazil.
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1166403793
dc.identifier.dimensionspub.1166403793
dc.identifier.doi10.2174/0115672018257713231107060630
dc.identifier.issn1567-2018
dc.identifier.issn1875-5704
dc.identifier.orcid0000-0002-8637-6783
dc.identifier.orcid0000-0001-8802-0054
dc.identifier.orcid0000-0002-0139-457X
dc.identifier.orcid0000-0001-6365-8756
dc.identifier.orcid0000-0001-6166-1724
dc.identifier.orcid0000-0002-6698-0545
dc.identifier.pmid38013438
dc.identifier.urihttps://hdl.handle.net/11449/328588
dc.publisherBentham Science Publishers
dc.relation.ispartofCurrent Drug Delivery; n. 4; v. 22; p. 413-430
dc.rights.accessRightsAcesso restritopt
dc.rights.sourceRightsclosed
dc.sourceDimensions
dc.titleTargeted Polymeric Nanoparticles as a Strategy for the Treatment of Glioblastoma: A Review
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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