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Highlights in targeted nanoparticles as a delivery strategy for glioma treatment

dc.contributor.authorLuiz, Marcela Tavares
dc.contributor.authorDelello Di Filippo, Leonardo [UNESP]
dc.contributor.authorTofani, Larissa Bueno [UNESP]
dc.contributor.authorde Araújo, Jennifer Thayanne Cavalcante [UNESP]
dc.contributor.authorDutra, Jessyca Aparecida Paes [UNESP]
dc.contributor.authorMarchetti, Juliana Maldonado
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T11:18:25Z
dc.date.available2021-06-25T11:18:25Z
dc.date.issued2021-07-15
dc.description.abstractGlioma is the most common type of Central Nervous System (CNS) neoplasia and it arises from glial cells. As glial cells are formed by different types of cells, glioma can be classified according to the cells that originate it or the malignancy grade. Glioblastoma multiforme is the most common and aggressive glioma. The high lethality of this tumor is related to the difficulty in performing surgical removal, chemotherapy, and radiotherapy in the CNS. To improve glioma treatment, a wide range of chemotherapeutics have been encapsulated in nanosystems to increase their ability to overcome the blood–brain barrier (BBB) and specifically reach the tumoral cells, reducing side effects and improving drug concentration in the tumor microenvironment. Several studies have investigated nanosystems covered with targeting ligands (e.g., proteins, peptides, aptamers, folate, and glucose) to increase the ability of drugs to cross the BBB and enhance their specificity to glioma through specific recognition by receptors on BBB and glioma cells. This review addresses the main targeting ligands used in nanosystems to overcome the BBB and promote the active targeting of drugs for glioma. Furthermore, the advantages of using these molecules in glioma treatment are discussed.en
dc.description.affiliationSchool of Pharmaceutical Science of Ribeirao Preto University of Sao Paulo (USP)
dc.description.affiliationSchool of Pharmaceutical Science of Sao Paulo State University (UNESP)
dc.description.affiliationUnespSchool of Pharmaceutical Science of Sao Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.1016/j.ijpharm.2021.120758
dc.identifier.citationInternational Journal of Pharmaceutics, v. 604.
dc.identifier.doi10.1016/j.ijpharm.2021.120758
dc.identifier.issn1873-3476
dc.identifier.issn0378-5173
dc.identifier.scopus2-s2.0-85107556811
dc.identifier.urihttp://hdl.handle.net/11449/208753
dc.language.isoeng
dc.relation.ispartofInternational Journal of Pharmaceutics
dc.sourceScopus
dc.subjectActive targeting
dc.subjectDrug delivery systems
dc.subjectGlioblastoma multiforme
dc.subjectNanoparticles
dc.titleHighlights in targeted nanoparticles as a delivery strategy for glioma treatmenten
dc.typeResenhapt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.departmentFármacos e Medicamentos - FCFpt

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