Autor(es): Pereira, AR ; Bravo, C ; Ramos, RM ; Carina Costa ; Rodrigues, A ; de Freitas, V ; Mateus, N ; Dias, R ; Soares, S ; Joana Oliveira
Data: 2024
Identificador Persistente: https://hdl.handle.net/10216/164988
Origem: Repositório Aberto da Universidade do Porto
Anthocyanins have limited application as natural colorants and antioxidants due to their color loss and instability under certain conditions. This research explores the formation of a complex between lignosulfonates (LS) and cyanidin-3-O-glucoside (C3G) using a multitechnique approach as well as the effect on C3G ' s red color, oxidative stability, and antioxidant activity in acidic mediums. All data revealed pH-dependent LS-C3G interactions. The thermodynamic parameters showed weak noncovalent interactions, mainly electrostatic interactions, hydrogen bonds, and hydrophobic effect, with a higher association constant determined at pH 3. Fourier-transform infrared spectroscopy and Zeta-potential experiments further corroborate evidence of these LS-C3G interactions. Fluorescence quenching and lifetime experiments revealed static and dynamic quenching at pH 1 and 3, respectively. UV-visible spectroscopy demonstrated a bathochromic shift upon complex formation and a hyperchromic effect at pH 3 and 4, as a consequence of the improved red color of C3G. Electrochemical results suggested that at pH 3 the LS enhances C3G stability by protecting its oxidizable moieties over time, as well as improving the antioxidant activity of the anthocyanin in the complex.
