The flavanoid hesperidin (Hsd) is one of the major polyphenols in citrus fruits. Hsd and its aglycone hesperetin (Hst) have a broad array of bioactivities; however, their low aqueous solubility and low intestinal permeability lead to their limited oral bioavailability. In the present study, we generated two water-soluble derivatives of Hst, namely, Hst 7--phosphate and Hst3'--phosphate, by a unique bioconversion process of var. BCRC80517. The phosphorylated products showed superior aqueous solubility and distinct physicochemical properties compared with the original Hst. The Hst phosphate derivatives (HstPs) remained stable in simulated gastric and intestinal fluids for 240 min and could revert to the original Hst form by alkaline phosphatase treatment in Caco-2 cells, showing enhanced intestinal permeability . After oral administration in rats, HstPs greatly elevated plasma exposure to Hst and showed better bioavailability than did Hsd. HstPs may be a potential and efficient alternative to Hst.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.jafc.1c04298DOI Listing

Publication Analysis

Top Keywords

oral bioavailability
8
hst
8
aqueous solubility
8
intestinal permeability
8
hst hst
8
original hst
8
microbial phosphorylation
4
phosphorylation product
4
product hesperetin
4
hesperetin bcrc
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!