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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.)

Structural effects on the hesperidin properties obtained by chelation to magnesium complexes

Texto completo
Autor(es):
Oliveira, Regina M. M. [1] ; de Souza Daniel, Juliana F. [2] ; de Aguiar, Inara [1] ; das Gracas Fernandes da Silva, Maria Fatima [1] ; Fernandes, Joao Batista [1] ; Carlos, Rose M. [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Univ Fed Sao Carlos, Dept Quim, BR-13565905 Sao Carlos, SP - Brazil
[2] Univ Tecnol Fed Parana, BR-86036370 Londrina, PR - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: Journal of Inorganic Biochemistry; v. 129, p. 35-42, DEC 2013.
Citações Web of Science: 12
Resumo

The magnesium complex {[}Mg( hesp)(2)(phen)] (1), where hesp = hesperidin and phen = 1,10'-phenanthroline, was synthesized and characterized by Elemental Analysis (C,H,N), atomic absorption and spectroscopic (FTIR, UV-visible, H-1 NMR) techniques. The congested structure facilitates the tilting and contact of the two hesperidin ligands by hydrogen bonding interactions having a stabilizer effect on the hesperidin. The hydrogen bonds are strongly affected by the solvent used which can lead to changes in the physical-chemical, luminescence and biologic properties of complex 1. Complex 1 is more hydrosoluble (S = 472 +/- 3.05 mu g mL(-1)) and liposoluble (log P = -0.15 +/- 0.01) than free hesperidin (S = 5.92 +/- 0.49 mu g mL(-1), log P = 0.30). Oxidation of the complex in an aqueous solution and room temperature investigated by cyclic voltammetry resulted in a very stable two-electron cyclic process to form the phenoxonium neutral, cation and dication radicals. The stability of the voltammetric process indicates that the species produced are never exhausted and does not lead to changes in the coordination sphere composition. The complex was found to be a better radical scavenger for superoxide radical (IC50 = 68.3 mu M at pH 7.8) than free hesperidin (IC50 = 116.68 mu mol L-1) and vitamin C (IC50 = 852 mu mol L-1). The strong blue fluorescence of complex 1 switches through loss of luminescence in pure water/protic organic solvents or when protected from water (in octanol for example as a model of phospholipid membranes). These features provide an opportunity to map the reactivity of hesperidin in the physiologic medium. In this context, a high uptake of complex into HeLa cells was detected by fluorescence microscopy. The blue fluorescence was uniformly distributed mainly in per nucleic region. (C) 2013 Elsevier Inc All rights reserved. (AU)

Processo FAPESP: 09/08218-0 - Novos complexos do tipo Mn(I)-fotosensibilizador: modelos minéticos para o lado doador do PSII em fotossíntese artificial
Beneficiário:Rose Maria Carlos
Linha de fomento: Auxílio à Pesquisa - Regular
Processo FAPESP: 08/57859-5 - Controle biorracional de insetos pragas
Beneficiário:Maria Fátima das Graças Fernandes da Silva
Linha de fomento: Auxílio à Pesquisa - Temático