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Chitosan-coated MIL-100(Fe) nanoparticles for enhanced piperine release in breast cancer treatment

dc.contributor.authorQuijia, Christian Rafael [UNESP]
dc.contributor.authorOcaña, Alberto
dc.contributor.authorAlonso‑Moreno, Carlos
dc.contributor.authorGalvão Frem, Regina Célia [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionYachay Tech University
dc.contributor.institutionSTART
dc.contributor.institutionUniversidad de Castilla-La Mancha
dc.date.accessioned2025-04-29T18:37:58Z
dc.date.issued2024-06-05
dc.description.abstractBreast cancer is one of the leading causes of death among women with cancer worldwide. Piperine (PIP) is a promising compound with potential chemotherapeutic activity for the treatment of breast cancer due to its antitumor activity, but its toxicity has limited its introduction in preclinical studies. An attractive platform for the treatment of breast cancer is represented by PIP@MIL-100(Fe), a metal-organic framework (MOF) network encapsulated with PIP and used as a release system. An engineering strategy in nanotechnology is the surface modification of nanosystems, such as chitosan (CHI), which is used to increase resistance to degradation and enable controlled drug release. Based on these scientific and technological advances, the aim of this study is to evaluate the therapeutic potential of PIP encapsulated in metal-organic frameworks coated with CHI in the treatment of breast cancer. The CHI@PIP@MIL-100(Fe) was successfully synthesized, which consists of MIL-100(Fe) containing PIP and coated with CHI, using the impregnation method. The infrared spectroscopy analysis showed major absorption bands such as the saccharide structure (1042, 1092, and 1164cm−1), confirming the presence of CHI in the MOFs. The cytotoxicity tests conducted on breast cancer cells, including SKBR3, MCF-7, MDA-MB-231, and BT549, using CHI@PIP@MIL-100(Fe), exhibited lower cytotoxicity indices in comparison to free PIP, which showed an index that was three to four times higher. Therefore, these nanostructures show potential as PIP-based therapies for breast cancer.en
dc.description.affiliationDepartment of Drugs and Medicines School of Pharmaceutical Sciences of São Paulo State University (UNESP), Rodovia Araraquara Jau, Km 01 – s/n – Campos Ville, Sao Paulo
dc.description.affiliationSchool of Biological Sciences and Engineering Yachay Tech University, Hda. San José s/n y Proyecto Yachay
dc.description.affiliationExperimental Therapeutics Unit Hospital Clínico San Carlos IdISSC Fundación Jiménez Díaz START
dc.description.affiliationUnidad NanoDrug Facultad de Farmacia Universidad de Castilla-La Mancha
dc.description.affiliationInstitute of Chemistry São Paulo State University (UNESP), Prof. Francisco Degni 55, Sao Paulo
dc.description.affiliationUnespDepartment of Drugs and Medicines School of Pharmaceutical Sciences of São Paulo State University (UNESP), Rodovia Araraquara Jau, Km 01 – s/n – Campos Ville, Sao Paulo
dc.description.affiliationUnespInstitute of Chemistry São Paulo State University (UNESP), Prof. Francisco Degni 55, Sao Paulo
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: CPP2021-008597
dc.identifierhttp://dx.doi.org/10.1016/j.molstruc.2024.137801
dc.identifier.citationJournal of Molecular Structure, v. 1305.
dc.identifier.doi10.1016/j.molstruc.2024.137801
dc.identifier.issn0022-2860
dc.identifier.scopus2-s2.0-85185404461
dc.identifier.urihttps://hdl.handle.net/11449/298731
dc.language.isoeng
dc.relation.ispartofJournal of Molecular Structure
dc.sourceScopus
dc.subjectCytotoxicity
dc.subjectMetal-organic framework
dc.subjectNanostructures
dc.subjectVesicle
dc.titleChitosan-coated MIL-100(Fe) nanoparticles for enhanced piperine release in breast cancer treatmenten
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0002-4370-8960 0000-0002-4370-8960[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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