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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Towards anti-angiogenic activity of NiFe2O4 nanoparticles

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Autor(es):
Santos, J. G. [1] ; Lopes, H. [1] ; Moreno, H. [1] ; Ramirez, M. A. [1] ; Garcia, F. G. [2] ; Simoes, A. Z. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Sao Paulo State Univ UNESP, Sch Engn Guaratingueta, Sao Paulo, Guaratingueta - Brazil
[2] Fed Univ Itajuba UNIFEI, Inst Phys & Chem, Av BPS 1303, Itajuba, MG - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: CERAMICS INTERNATIONAL; v. 47, n. 11, p. 16152-16161, JUN 1 2021.
Citações Web of Science: 1
Resumo

In this study, NiFe2O4 nanoparticles (NPs) were prepared using the polymeric precursor method and calcined at 500?C for 4 h with (S? NiFe2O4) and without (NiFe2O4) CTAB as a surfactant, respectively. The magnetic and biological properties were evaluated based on the (micro)structure and electronic structure of the NPs. On sample S?NiFe2O4, the significant increase in magnetization saturation (Ms - 61.84 emu/g), magnetic remanence (Mr - 4.30 emu/g), and coercivity (Hc - 0.475 kOe) in comparison to sample NiFe2O4 (Ms - 24.81 emu/g, Mr - 1.00 emu/g, and Hc - 0.475 kOe) at room temperature (300 K) may be associated with the presence of oxygen vacancies the spinel lattice of NiFe2O4, generating magnetic moments. The concentration of 1 ?g/mL S?NiFe2O4 decreased in -50% angiogenesis in the chorioallantoic membrane (CAM). S?NiFe2O4 NPs showed high blood vessel affinity and anti-angiogenic activity; hence, effectively concentrating on tumoral vessels, which may enhance drug effectivity and enable simultaneous treatments, image diagnosis of solid tumors, etc. Thus, our results suggest that CTAB addition is an effective way to tune its magnetic response due to its excellent biocompatibility, high bulk saturation magnetization, and low magnetic anisotropy. (AU)

Processo FAPESP: 13/07296-2 - CDMF - Centro de Desenvolvimento de Materiais Funcionais
Beneficiário:Elson Longo da Silva
Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs