| Full text | |
| Author(s): |
João Honorato
[1]
;
Katia M. Oliveira
[2]
;
Celisnolia M. Leite
[3]
;
Legna Colina-Vegas
;
Joaquim A. Nóbrega
[5]
;
Eduardo E. Castellano
[6]
;
Javier Ellena
[7]
;
Rodrigo S. Correa
[8]
;
Alzir A. Batista
Total Authors: 9
|
| Affiliation: | [1] Universidade Federal de São Carlos (UFSCar). Departamento de Química - Brasil
[2] Universidade Federal de Ouro Preto (UFOP). Instituto de Ciências Exatas e Biológicas (ICEB). Departamento de Química - Brasil
[3] Universidade Federal de São Carlos (UFSCar). Departamento de Química - Brasil
[5] Universidade Federal de São Carlos (UFSCar). Departamento de Química - Brasil
[6] Universidade de São Paulo (USP). Instituto de Física de São Carlos - Brasil
[7] Universidade de São Paulo (USP). Instituto de Física de São Carlos - Brasil
[8] Universidade Federal de Ouro Preto (UFOP). Instituto de Ciências Exatas e Biológicas (ICEB). Departamento de Química - Brasil
Total Affiliations: 9
|
| Document type: | Journal article |
| Source: | Journal of the Brazilian Chemical Society; v. 31, n. 11, p. 2237-2249, 2020-10-30. |
| Abstract | |
Mononuclear and binuclear RuII/arene/triphenylphosphine complexes with p-substituted benzoic acid derivatives were prepared and characterized. These monocationic complexes of type [Ru(η6-p-cymene)(PPh3)L] (L = benzoic acid (1), p-hydroxybenzoic acid (2), p-nitrobenzoic acid (3) and terephthalic acid (4)) were characterized using various techniques, such as nuclear magnetic resonance (NMR) and matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry, and the crystal structure of 1, 3 and 4 were determined by X-ray diffraction analysis. The cytotoxicity of the complexes was evaluated, in vitro, against tumorigenic [MDA-MB-231, MCF-7 (breast), A549 (lung) and DU-145 (prostate)] and non-tumorigenic [MCF-10A (breast), MRC-5 (lung) and PNT-2 (prostate)] cells. The binuclear complex (4) was inactive due to its low solubility. Complexes 1, 2 and 3 showed similar cytotoxicity, however, complex 1 presented better selectivity index against MDA-MB-231 than compounds 2 and 3. Cellular ruthenium absorption was explored by inductively coupled plasma mass spectrometry (ICP-MS) analyzing the whole cells and the culture medium. Complementary studies showed that complex 1 inhibited colony formation, induced morphology changes in cells and promoted cell cycle arrest in the Sub-G1 phase for the MDA-MB-231 cells. (AU) | |
| FAPESP's process: | 16/23130-5 - Determination of cellular biodistribution of Cu, Ru and Pt in human tumor and non tumor breast cells by Inductively Coupled Plasma Mass Spectrometry |
| Grantee: | Legna Andreina Colina Vegas |
| Support Opportunities: | Scholarships in Brazil - Post-Doctoral |