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Interaction of Graphene Oxide Particles and Dendrimers with Human Breast Cancer Cells by Real-Time Microscopy

dc.contributor.authorRibeiro, Beatriz Fumelli Monti
dc.contributor.authorChaves, Julyane Batista
dc.contributor.authorDe Souza, Marcelo Medina
dc.contributor.authorKeppler, Artur Franz
dc.contributor.authorDo Carmo, Devaney Ribeiro [UNESP]
dc.contributor.authorMachado-Santelli, Gláucia M.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionButantan Institute
dc.contributor.institutionFederal University of ABC
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:12:24Z
dc.date.issued2023-12-01
dc.description.abstractGraphene oxide (GOX) has become attractive due to its unique physicochemical properties. This nanomaterial can associate with other dendrimers, making them more soluble and allowing better interaction with biomacromolecules. The present study aimed to investigate, by real-time microscopy, the behavior of human breast cancer cells exposed to particles of materials based on graphene oxide. The MCF-7 cell line was exposed to GOX, GOX associated with Polypropylenimine hexadecaamine Dendrimer, Generation 3.0—DAB-AM-16 (GOXD) and GOX associated with polypropyleneimine—PAMAM (GOXP) in the presence or absence of fetal bovine serum (FBS). GOX, GOXD and GOXP were taken up by the cells in clusters and then the clusters were fragmented into smaller ones inside the cells. Real-time microscopy showed that the presence of FBS in the culture medium could allow a more efficient internalization of graphene materials. After internalizing the materials, cells can redistribute the clumps to their daughter cells. In conclusion, the present study showed that the particles can adhere to the cell surface, favoring their internalization. The presence of FBS contributed to the formation of smaller aggregates of particles, avoiding the formation of large ones, and thus transmitted a more efficient internalization of the materials through the interaction of the particles with the cell membrane.en
dc.description.affiliationDepartment of Cell and Developmental Biology Institute of Biomedical Sciences University of São Paulo
dc.description.affiliationCentre of Excellence in New Target Discovery (CENTD) Butantan Institute
dc.description.affiliationCentre of Natural and Human Sciences (CCNH) Federal University of ABC
dc.description.affiliationDepartment of Physics and Chemistry Paulista State University
dc.description.affiliationUnespDepartment of Physics and Chemistry Paulista State University
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdFAPESP: 2015/20397-8
dc.description.sponsorshipIdFAPESP: 2017/16893-5
dc.description.sponsorshipIdFAPESP: 2018/22882-9
dc.description.sponsorshipIdFAPESP: 2019/21841-0
dc.description.sponsorshipIdCNPq: 316504/2021-1
dc.description.sponsorshipIdCAPES: 33002010024P6
dc.identifierhttp://dx.doi.org/10.3390/pharmaceutics15122655
dc.identifier.citationPharmaceutics, v. 15, n. 12, 2023.
dc.identifier.doi10.3390/pharmaceutics15122655
dc.identifier.issn1999-4923
dc.identifier.scopus2-s2.0-85180640883
dc.identifier.urihttps://hdl.handle.net/11449/308415
dc.language.isoeng
dc.relation.ispartofPharmaceutics
dc.sourceScopus
dc.subjectbreast cancer cell culture
dc.subjectgraphene
dc.subjectnanoparticles internalization
dc.subjectreal-time microscopy
dc.titleInteraction of Graphene Oxide Particles and Dendrimers with Human Breast Cancer Cells by Real-Time Microscopyen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-5637-1463[2]
unesp.author.orcid0000-0003-2046-9693[6]

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