Alkaline earth metal ion coordination increases the radical scavenging efficiency of kaempferol
Open Access
- 14 August 2020
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 10 (50) , 30035-30047
Abstract
Flavonoids are used as natural additives and antioxidants in foods, and after coordination to metal ions, as drug candidates, depending on the flavonoid structure. The rate of radical scavenging of the ubiquitous plant flavonoid kaempferol (3,5,7,4′-tetrahydroxyflavone, Kaem) was found to be significantly enhanced by coordination of Mg(II), Ca(II), Sr(II), and Ba(II) ions, whereas the radical scavenging rate of apigenin (5,7,4′-trihydroxyflavone, Api) was almost unaffected by alkaline earth metal (AEM) ions, as studied for short-lived β-carotene radical cations (β-Car˙+) formed by laser flash photolysis in chloroform/ethanol (7 : 3) and for the semi-stable 2,2-diphenyl-1-picrylhydrazyl radical, DPPH˙, in ethanol at 25 °C. A 1 : 1 Mg(II)–Kaem complex was found to be in equilibrium with a 1 : 2 Mg(II)–Kaem2 complex, while for Ca(II), Sr(II) and Ba(II), only 1 : 2 AEM(II)–Kaem complexes were detected, where all complexes showed 3-hydroxyl and 4-carbonyl coordination and stability constants of higher than 109 L2 mol−2. The 1 : 2 Ca(II)–Kaem2 complex had the highest second order rate constant for both β-Car˙+ (5 × 108 L mol−1 s−1) and DPPH˙ radical (3 × 105 L mol−1 s−1) scavenging, which can be attributed to the optimal combination of the stronger electron withdrawing capability of the (n − 1)d orbital in the heavier AEM ions and their spatially asymmetrical structures in 1 : 2 AEM–Kaem complexes with metal ion coordination of the least steric hindrance of two perpendicular flavone backbones as ligands in the Ca(II) complex, as shown by density functional theory calculations.Keywords
Funding Information
- National Natural Science Foundation of China (21573284, 21673288)
This publication has 41 references indexed in Scilit:
- Flavonoid–Metal Ion Complexes: A Novel Class of Therapeutic AgentsMedicinal Research Reviews, 2013
- β-Carotene Radical Cation Addition to Green Tea Polyphenols. Mechanism of Antioxidant Antagonism in Peroxidizing LiposomesJournal of Agricultural and Food Chemistry, 2011
- Synthesis and evaluation of antioxidant and antibacterial properties of morin complexesJournal of Coordination Chemistry, 2011
- Polyphenol-modified glassy carbon electrodes for copper detectionSensors and Actuators B: Chemical, 2011
- Fast Regeneration of Carotenoids from Radical Cations by Isoflavonoid Dianions: Importance of the Carotenoid Keto Group for Electron TransferThe Journal of Physical Chemistry A, 2009
- Radical-Scavenging Activity and Mechanism of Resveratrol-Oriented Analogues: Influence of the Solvent, Radical, and SubstitutionThe Journal of Organic Chemistry, 2009
- Kinetic Study of Flavonoid Reactions with Stable RadicalsJournal of Agricultural and Food Chemistry, 2004
- Calcium signalling: dynamics, homeostasis and remodellingNature Reviews Molecular Cell Biology, 2003
- Anti- and pro-oxidative effects of flavonoids on metal-induced lipid hydroperoxide-dependent lipid peroxidation in cultured hepatocytes loaded with α-linolenic acidFree Radical Biology and Medicine, 1999
- Thermodynamics of the Electron and the ProtonThe Journal of Physical Chemistry, 1994