Towards understanding the low bioavailability of quercetin: a study of its interaction with intestinal lipids

Rich G. T., Buchweitz M., Winterbone M., Kroon P. A., Wilde P. J.. (2017)

Nutrients, 9, 111

We have studied the uptake of quercetin aglycone into CaCo-2/TC7 cells in the presence and absence of mixed micelles that are present in the human small intestine. The micelles inhibited the transport of quercetin into the cells. To gain understanding of why this is the case we examined solubilisation of quercetin in micelles of differing composition and into pure lipid phases. We did this by using the environmental sensitivity of quercetin’s UV-visible absorption spectra and measurement of free quercetin by filtration of the micellar solutions. The nature of the micelles was also studied by pyrene fluorescence. We found that partition of quercetin into simple bile salt micelles was low and for mixed micelles was inhibited by increasing bile salt concentration. The affinity of quercetin decreased in the order egg phosphatidylcholine (PC) = lysoPC > mixed micelles > bile salts. These results together with the innate properties of quercetin contribute to understanding the low bioavailability of quercetin.

Nutrients, 9, 111

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