Bioavailability and structural study of 20-hydroxyecdysone complexes with cyclodextrins.

Abstract:

:20-Hydroxyecdysterone - (2β,3β,5β,22R)-2,3,14,20,22,25-hexahydroxycholest-7-en-6-one was isolated in satisfactory yield using ethanol extraction from the aerial part of Silene wolgensis (Hornem.) Otth; sometimes Silene wolgensis (Willd.) Bess. ex Spreng. The complexation of the phytoecdysteroid with β-cyclodextrin was studied by NMR spectroscopy. By studying the changes in chemical shifts of protons of substrates and receptors it was found that ecdysterone interacts with cyclodextrins to form supramolecular inclusion complexes of stoichiometric composition of 1:1 or 1:2. Ecdysterone-β-cyclodextrin complexes exhibit 100 times higher solubility in water than the parent compound.

journal_name

Steroids

journal_title

Steroids

authors

Temirgaziyev BS,Kučáková K,Baizhigit YA,Jurášek M,Džubák P,Hajdúch M,Dolenský B,Drašar PB,Tuleuov BI,Adekenov SM

doi

10.1016/j.steroids.2018.11.007

subject

Has Abstract

pub_date

2019-07-01 00:00:00

pages

37-41

eissn

0039-128X

issn

1878-5867

pii

S0039-128X(18)30211-3

journal_volume

147

pub_type

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