Busca avançada
Ano de início
Entree
(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.)

Cyto-genotoxic evaluation of novel anti-tubercular copper (II) complexes containing isoniazid-based ligands

Texto completo
Autor(es):
Fregonezi, Nathalia Ferreira [1] ; de Souza, Fabiana Aparecida [1] ; Aleixo, Nadia Andrade [1] ; da Silva Gomes, Pietra Stefany [1] ; Silvestre, Rafaela Baldassari [1] ; De Grandis, Rone Aparecido [1, 2] ; da Silva, Patricia Bento [2] ; Pavan, Fernando Rogerio [2] ; Chorilli, Marlus [2] ; Resende, Flavia Aparecida [1]
Número total de Autores: 10
Afiliação do(s) autor(es):
[1] UNIARA Univ Araraquara, Dept Biol Sci & Hlth, Araraquara 14801340, SP - Brazil
[2] UNESP Sao Paulo State Univ, Fac Pharmaceut Sci Araraquara, Dept Biol Sci, Araraquara 14801902, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: REGULATORY TOXICOLOGY AND PHARMACOLOGY; v. 113, JUN 2020.
Citações Web of Science: 0
Resumo

Considering the promising previous results of Cu (II) complexes with isoniazid active ligand against Mycobacterium tuberculosis, the main causative agent of tuberculosis, novel biological assays evaluating its toxicogenic potential were performed to ensure the safe use. The genotoxicity/mutagenicity of the complexes CuCl2(INH)(2)center dot H2O (I1), Cu(NCS)(2)(INH)(2)center dot 5H(2)O (I2) and Cu(NCO)(2)(INH)(2)center dot 4H(2)O (I3) was evaluated by the Comet, Micronucleus-cytome and Salmonella microsome (Ames test) assays. The cell viability using resazurin assay indicated that I1, I2 e I3 had moderate to low capacity to reduce the viability of colorectal cells (Caco-2), liver cells (HepG2), lung cells (GM 07492-A and A549) and endothelial cells (HU-VE-C). On genotoxicity/mutagenicity, I1 complex did not induce sizable levels of DNA damage in HepG2 cells (Comet assay), and gene (Ames test) and chromosomal (Micronucleus-cytome assay) mutations. Already, I2 and I3 complexes were considered mutagenic in the highest concentrations used. In light of the above, these results contribute to valuable data on the safe use of Cu(II) complexes. Considering the absence of mutagenicity and cytotoxicity of I1, this complex is a potential candidate for the development of a new drug to the treatment tuberculosis, while I2 and I3 require caution in its use. (AU)

Processo FAPESP: 17/16278-9 - Estudo do potencial genotoxicológico e da permeabilidade em células Caco-2 de complexos metálicos com promissoras atividades biológicas
Beneficiário:Flávia Aparecida Resende Nogueira
Linha de fomento: Auxílio à Pesquisa - Regular