Folic acid-conjugated curcumin-loaded bioMOF-101 for breast cancer therapy
| dc.contributor.author | Alves, Renata Carolina [UNESP] | |
| dc.contributor.author | Quijia, Christian Rafael [UNESP] | |
| dc.contributor.author | Bento da Silva, Patrícia | |
| dc.contributor.author | Faria, Raquel Santos | |
| dc.contributor.author | Cabral Morais, Amanda Alencar | |
| dc.contributor.author | Vasconcelos Morais, José Athayde | |
| dc.contributor.author | de Araújo, Henrique Loback Lopes | |
| dc.contributor.author | Frem, Regina Célia Galvão [UNESP] | |
| dc.contributor.author | de Azevedo, Ricardo Bentes | |
| dc.contributor.author | Chorilli, Marlus [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
| dc.contributor.institution | University of Brasilia (UnB) | |
| dc.date.accessioned | 2025-04-29T18:40:47Z | |
| dc.date.issued | 2023-09-01 | |
| dc.description.abstract | Breast cancer ranks as the primary cause of cancer-related mortality among women and stands as the fifth leading cause of cancer death overall. Biocompatible metal-organic frameworks (bioMOFs) emerge as highly attractive and promising platforms for efficient drug absorption and delivery. Thus, our objective was to develop drug delivery systems using bioMOF-101 materials, incorporating curcumin (CCM). The materials were enhanced by coating with folate molecules, facilitating targeted delivery to the tumor region. BioMOF-101 was meticulously synthesized, characterized using various techniques, and subsequently subjected to drug encapsulation tests. Remarkably, CCM@bioMOF-101-1D achieved an impressive encapsulation efficiency of 99.42%. To evaluate the impact of the MOF on cell viability, both breast tumor and normal cell lines were examined, revealing that the materials exhibited no toxicity. In vivo studies, bio-MOFs did not induce a reduction in the tumor region; however, the CCM@bioMOF-101-1D/FA caused a reduction in alveolar volume, which is indicative of its effectiveness in the model employed. In conclusion, the matrices studied herein can be considered promising alternatives for the treatment of breast cancer. | en |
| dc.description.affiliation | Department of Drugs and Medicines School of Pharmaceutical Sciences of São Paulo State University (UNESP), Rodovia Araraquara Jau, Km 01 – S/n – Campos Ville, Araraquara | |
| dc.description.affiliation | Department of Genetics and Morphology Institute of Biological Sciences University of Brasilia (UnB) Campus Universitario Darcy Ribeiro, Asa Norte, Federal District | |
| dc.description.affiliation | Institute of Chemistry São Paulo State University (UNESP), Prof. Francisco Degni 55, Araraquara | |
| dc.description.affiliationUnesp | Department of Drugs and Medicines School of Pharmaceutical Sciences of São Paulo State University (UNESP), Rodovia Araraquara Jau, Km 01 – S/n – Campos Ville, Araraquara | |
| dc.description.affiliationUnesp | Institute of Chemistry São Paulo State University (UNESP), Prof. Francisco Degni 55, Araraquara | |
| dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description.sponsorshipId | FAPESP: 2017/26065–2 | |
| dc.identifier | http://dx.doi.org/10.1016/j.jddst.2023.104702 | |
| dc.identifier.citation | Journal of Drug Delivery Science and Technology, v. 86. | |
| dc.identifier.doi | 10.1016/j.jddst.2023.104702 | |
| dc.identifier.issn | 1773-2247 | |
| dc.identifier.scopus | 2-s2.0-85165237597 | |
| dc.identifier.uri | https://hdl.handle.net/11449/298900 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Journal of Drug Delivery Science and Technology | |
| dc.source | Scopus | |
| dc.subject | Delivery system | |
| dc.subject | Functionalization | |
| dc.subject | Metal-organic frameworks | |
| dc.title | Folic acid-conjugated curcumin-loaded bioMOF-101 for breast cancer therapy | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isOrgUnitOfPublication | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
| relation.isOrgUnitOfPublication | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
| relation.isOrgUnitOfPublication.latestForDiscovery | 95697b0b-8977-4af6-88d5-c29c80b5ee92 | |
| unesp.author.orcid | 0000-0002-4370-8960[2] | |
| unesp.author.orcid | 0000-0002-6698-0545[10] | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara | pt |
| unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Química, Araraquara | pt |

