Key result
Flavonoids show negligible risk of displacing warfarin on albumin in molecular modeling studies.
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In vitro study shows minimal risk of warfarin-flavonoid interaction in binding to human serum albumin, suggesting safety in concurrent use.
Human serum albumin (HSA) binds a variety of xenobiotics, including flavonoids and warfarin. The binding of another ligand to the IIA binding site on HSA can cause warfarin displacement and potentially the elevation of its free concentration in blood. Studies dealing with flavonoid-induced warfarin displacement from HSA provided controversial results: estimated risk of displacement ranged from none to serious. To resolve these controversies, in vitro study of simultaneous binding of warfarin and eight different flavonoid aglycons and glycosides to HSA was carried out by fluorescence spectroscopy as well as molecular docking. Results show that warfarin and flavonoids do not share the same binding region in binding to HSA. Interactions were only observed at high warfarin concentrations not attainable under recommended dosing regimes. Docking experiments show that flavonoid aglycons and glycosides do not bind at warfarin high affinity sites, but rather to different regions within the IIA HSA subdomain. Thus, the risk of clinically significant warfarin-flavonoid interaction in binding to HSA should be regarded as negligible.
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Rimac et al. (2017) studied this question. Simultaneous binding of warfarin and flavonoid aglycons/glycosides was evaluated on Binding interaction and warfarin displacement from human serum albumin. In vitro and molecular docking studies revealed that warfarin and flavonoids do not share the same binding region on human serum albumin, making the risk of clinically significant interaction negligible.
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