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Synthesis, Characterization, and Cytotoxicity Evaluation of Chlorambucil-Functionalized Mesoporous Silica Nanoparticles

dc.contributor.authorKarnopp, Juliana Camila Fischer
dc.contributor.authorJorge, Juliana
dc.contributor.authorda Silva, Jaqueline Rodrigues
dc.contributor.authorBoldo, Diego
dc.contributor.authorDel Pino Santos, Kristiane Fanti
dc.contributor.authorDuarte, Adriana Pereira
dc.contributor.authorde Castro, Gustavo Rocha [UNESP]
dc.contributor.authorde Azevedo, Ricardo Bentes
dc.contributor.authorPrada, Ariadna Lafourcade
dc.contributor.authorAmado, Jesús Rafael Rodríguez
dc.contributor.authorMartines, Marco Antonio Utrera
dc.contributor.institutionFederal University of Mato Grosso do Sul
dc.contributor.institutionUniversity of Brasilia
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionFederal University of Grande Dourados
dc.date.accessioned2025-04-29T20:13:49Z
dc.date.issued2024-08-01
dc.description.abstractThis study describes the synthesis and characterization of chlorambucil (CLB)-functionalized mesoporous silica nanoparticles (MSNs) for potential application in cancer therapy. The nanoparticles were designed with a diameter between 20 and 50 nm to optimize cellular uptake and avoid rapid clearance from the bloodstream. The synthesis method involved modifying a previously reported technique to reduce particle size. Successful functionalization with CLB was confirmed through various techniques, including Fourier transform infrared spectroscopy (FTIR) and elemental analysis. The cytotoxicity of the CLB-functionalized nanoparticles (MSN@NH2-CLB) was evaluated against human lung adenocarcinoma cells (A549) and colon carcinoma cells (CT26WT). The results suggest significantly higher cytotoxicity of MSN@NH2-CLB compared to unbound CLB, with improved selectivity towards cancer cells over normal cells. This suggests that MSN@NH2-CLB holds promise as a drug delivery system for targeted cancer therapy.en
dc.description.affiliationPostgraduate Program in Chemistry Chemistry Institute Federal University of Mato Grosso do Sul, Campo Grande, MS
dc.description.affiliationPostgraduate Program in Nanoscience and Nanotechnology Biological Science Institute University of Brasilia, DF
dc.description.affiliationPostgraduate Program in Environmental Biotechnology Bioscience Institute Sao Paulo State University, SP
dc.description.affiliationPostgraduate Program in Biotechnology Faculty of Pharmacy Food and Nutrition Federal University of Mato Grosso do Sul, Campo Grande, MS
dc.description.affiliationPostgraduate Program in Health Sciences Faculty of Health Sciences Federal University of Grande Dourados, MS
dc.description.affiliationUnespPostgraduate Program in Environmental Biotechnology Bioscience Institute Sao Paulo State University, SP
dc.description.sponsorshipUniversidade Federal de Mato Grosso do Sul
dc.identifierhttp://dx.doi.org/10.3390/pharmaceutics16081086
dc.identifier.citationPharmaceutics, v. 16, n. 8, 2024.
dc.identifier.doi10.3390/pharmaceutics16081086
dc.identifier.issn1999-4923
dc.identifier.scopus2-s2.0-85202587855
dc.identifier.urihttps://hdl.handle.net/11449/308862
dc.language.isoeng
dc.relation.ispartofPharmaceutics
dc.sourceScopus
dc.subjectcancer
dc.subjectchlorambucil
dc.subjectcytotoxicity
dc.subjectdrug delivery
dc.subjectmesoporous silica
dc.subjectnanocarriers
dc.subjecttargeted therapy
dc.titleSynthesis, Characterization, and Cytotoxicity Evaluation of Chlorambucil-Functionalized Mesoporous Silica Nanoparticlesen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0001-5755-9049[2]
unesp.author.orcid0000-0002-1218-2425[7]
unesp.author.orcid0000-0002-2137-9588[8]
unesp.author.orcid0000-0001-7574-6219[10]
unesp.author.orcid0000-0003-0405-6514[11]

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