The metal cation chelating capacity of astaxanthin. Does this have any influence on antiradical activity?

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Abstract

In this Density Functional Theory study, it became apparent that astaxanthin (ASTA) may form metal ion complexes with metal cations such as Ca +2, Cu +2, Pb +2, Zn +2, Cd +2 and Hg +2. The presence of metal cations induces changes in the maximum absorption bands which are red shifted in all cases. Therefore, in the case of compounds where metal ions are interacting with ASTA, they are redder in color. Moreover, the antiradical capacity of some ASTA-metal cationic complexes was studied by assessing their vertical ionization energy and vertical electron affinity, reaching the conclusion that metal complexes are slightly better electron donors and better electron acceptors than ASTA. © 2012 by the authors.

Figures

  • Figure 2. Optimized structures of [ASTA-Ca]+2, [ASTA-Ca2]+4, [ASTA-Cd2(H2O)2]+2, and [ASTA-Cd2(H2O)4]+4. Schematic representation of ASTA is also included.
  • Table 1. UV/vis maximum absorption wavelength, λmax in nm and oscillator strength (f), as well as the correspondent excitation energy (EE in eV) calculated in gas phase and in ethanol for ASTA and the ASTA-metal cationic complexes.
  • Figure 3. Optimized structures of [(ASTA-H)Pb(C2H 5OH)2]+1 and [(ASTA-2H)Pb2(C2H5OH)4]+2.
  • Table 2. UV/vis maximum absorption wavelength, λmax, in nm and oscillator strength (f), as well as the correspondent excitation energy (EE in eV) calculated including solvent (ethanol) effect via the PCM model. The optimized metal complexes considered the deprotonation of ASTA to form the metal compound.
  • Table 3. Energy differences in ethanol (reported in kcal/mol) for the formation of [(ASTA-nH)Mn C2H 5OH)2n]+n complexes.
  • Table 4. Vertical Ionization Energy (VIE) and Vertical Electron Affinity (VEA) in ethanol, calculated with the LC-wPBE functional.

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APA

Hernández-Marin, E., Barbosa, A., & Martínez, A. (2012). The metal cation chelating capacity of astaxanthin. Does this have any influence on antiradical activity? Molecules, 17(1), 1039–1054. https://doi.org/10.3390/molecules17011039

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