Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/45002
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dc.contributor.authorFerreira, Natalia Noronha-
dc.contributor.authorLeite, Celisnolia Morais-
dc.contributor.authorMoreno, Natalia Sanchez-
dc.contributor.authorMiranda, Renata Rank-
dc.contributor.authorPINCELA LINS, Paula-
dc.contributor.authorRodero, Camila Fernanda-
dc.contributor.authorde Oliveira Junior, Edilson-
dc.contributor.authorLima, Eliana Martins-
dc.contributor.authorReis, Rui M.-
dc.contributor.authorZucolotto, Valtencir-
dc.date.accessioned2025-01-08T12:58:36Z-
dc.date.available2025-01-08T12:58:36Z-
dc.date.issued2024-
dc.date.submitted2025-01-08T10:12:37Z-
dc.identifier.citationACS Applied Materials & Interfaces, 17 (1) , p. 484 -499-
dc.identifier.urihttp://hdl.handle.net/1942/45002-
dc.description.abstractGlioblastoma (GBM) is an extremely aggressive form of brain cancer that remains challenging to treat, especially owing to the lack of effective targeting and drug delivery concerns. Due to its anatomical advantages, the nose-to-brain strategy is an interesting route for drug delivery. Nanoengineering has provided technological tools and innovative strategies to overcome biotechnological limitations, which is promising for improving the effectiveness of conventional therapies. Herein, we designed a biomimetic multifunctional nanostructure produced by polymeric poly(d,l-lactic-co-glycolic) acid (PLGA) core loaded with Temozolomide (TMZ) coated with cell membrane isolated from glioma cancer cells. The developed nanostructures (NP-MB) were fully characterized, and their biological performance was investigated extensively. The results indicate that NP-MB could control TMZ release and promote TMZ permeation in the ex vivo nasal porcine mucosa. The higher cytotoxicity of NP-MB in different glioma cell lines, particularly against U251 cells, reinforces their potential for homotypic targeting. The chicken chorioallantoic membrane assay revealed a tumor size reduction and antiangiogenic activity. In vivo biodistribution studies showed that NP-MB effectively reaches the brain following nasal administration. These findings suggest that NP-MB holds promise as a biomimetic nanoplatform for effective targeting and homotypic recognition in GBM therapy with high potential for clinical translation.-
dc.description.sponsorshipThe Article Processing Charge for the publication of this research was funded by the Coordination for the Improvement of Higher Education Personnel - CAPES (ROR identifier:00x0ma614).-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.rights2024 The Authors. Published by American Chemical Society. This article is licensed under CC-BY 4.0-
dc.subject.otherbiomimetic delivery systems-
dc.subject.otherTemozolomide-
dc.subject.othernanotechnology-
dc.subject.otherPLGA-based nanoparticles-
dc.subject.otherglioblastomatreatment-
dc.subject.otherhomotypic recognition-
dc.subject.othernose-to-braindelivery-
dc.titleNose-to-Brain Delivery of Biomimetic Nanoparticles for Glioblastoma Targeted Therapy-
dc.typeJournal Contribution-
dc.identifier.epage499-
dc.identifier.issue1-
dc.identifier.spage484-
dc.identifier.volume17-
local.format.pages16-
local.bibliographicCitation.jcatA1-
dc.description.notesFerreira, NN; Zucolotto, V (corresponding author), Univ Sao Paulo, Phys Inst Sao Carlos, Nanomed & Nanotoxicol Grp, BR-13560970 Sao Carlos, SP, Brazil.-
dc.description.notesnoronhanat@hotmail.com; zuco@ifsc.usp.br-
local.publisher.place1155 16TH ST, NW, WASHINGTON, DC 20036 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.statusEarly view-
dc.identifier.doi10.1021/acsami.4c16837-
dc.identifier.pmid39692595-
dc.identifier.isi001379953300001-
local.provider.typewosris-
local.description.affiliation[Ferreira, Natalia Noronha; Leite, Celisnolia Morais; Moreno, Natalia Sanchez; Miranda, Renata Rank; Rodero, Camila Fernanda; Zucolotto, Valtencir] Univ Sao Paulo, Phys Inst Sao Carlos, Nanomed & Nanotoxicol Grp, BR-13560970 Sao Carlos, SP, Brazil.-
local.description.affiliation[Lins, Paula Maria Pincela] Hasselt Univ, Biomed Res Inst BIOMED, Fac Med & Life Sci, B-3590 Diepenbeek, Belgium.-
local.description.affiliation[de Oliveira Junior, Edilson; Lima, Eliana Martins] Univ Fed Goias UFG, Fac Farm, Lab Nanotecnol Farmaceut & Sistemas Liberacao Far, FarmaTec, 5a Ave C Rua 240 S-N,Praca Univ, BR-74605170 Goiania, Go, Brazil.-
local.description.affiliation[Reis, Rui M.] Barretos Canc Hosp, Mol Oncol Res Ctr, BR-14784400 Barretos, SP, Brazil.-
local.description.affiliation[Reis, Rui M.] Univ Minho, Life & Hlth Sci Res Inst ICVS, Sch Med, Campus Gualtar, P-4710057 Braga, Portugal.-
local.uhasselt.internationalyes-
item.contributorFerreira, Natalia Noronha-
item.contributorLeite, Celisnolia Morais-
item.contributorMoreno, Natalia Sanchez-
item.contributorMiranda, Renata Rank-
item.contributorPINCELA LINS, Paula-
item.contributorRodero, Camila Fernanda-
item.contributorde Oliveira Junior, Edilson-
item.contributorLima, Eliana Martins-
item.contributorReis, Rui M.-
item.contributorZucolotto, Valtencir-
item.fullcitationFerreira, Natalia Noronha; Leite, Celisnolia Morais; Moreno, Natalia Sanchez; Miranda, Renata Rank; PINCELA LINS, Paula; Rodero, Camila Fernanda; de Oliveira Junior, Edilson; Lima, Eliana Martins; Reis, Rui M. & Zucolotto, Valtencir (2024) Nose-to-Brain Delivery of Biomimetic Nanoparticles for Glioblastoma Targeted Therapy. In: ACS Applied Materials & Interfaces, 17 (1) , p. 484 -499.-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
crisitem.journal.issn1944-8244-
crisitem.journal.eissn1944-8252-
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