Study on pharmacological properties and cell absorption metabolism of novel daidzein napsylates. Issue 1 (13th January 2021)

• Record Type: Journal Article
• Authors: Jiao, Yanxiao; Peng, Jing; Ye, Xinglin; Hu, Huanan; Gan, Lijun; Yang, Jianyuan; Peng, You
• Is Part Of: Royal Society open science. Volume 8:Issue 1(2021)
• Publication Date: 2021-01-13
• Subjects: daidzein napsylates -- lipophilicity -- HAVSMCs -- cell absorption and metabolism -- structure–property relationship -- metabolic pathway in vitro; Science -- Periodicals; 500
• DOI: 10.1098/rsos.201475
• Languages: English
• ISSNs: 2054-5703

Abstract

Abstract : Novel daidzein napsylates (DD4 and DD5) were synthesized by microwave irradiation, according to structural modification of daidzein (DAI) using the principle of pharmacokinetic transformation. The pharmacological properties of DD4 and DD5 were evaluated via high performance liquid chromatography (HPLC) and calculated based on the drug design software Chem Axon 16.1.18. The cell uptake changes of DD4 and DD5 were investigated to analyse the structure–property relationship. The metabolisms of DD4 and DD5 were analysed by HPLC-mass spectrometry in human aortic vascular smooth muscle cells (HAVSMCs) and their possible metabolic pathways were inferred in vivo . The results showed that the solubility of DD4 and DD5 was increased by 2.79 × 10 5 and 2.16 × 10 5 times compared to that of DAI, separately, in ethyl acetate. The maximum absorption rates of DD4 and DD5 were enhanced by 4.3–4.5 times relative to DAI. Preliminary studies on metabolites of DD4 and DD5 in HAVSMCs showed that DD4 and DD5 were hydrolysed into DAI under the action of intracellular hydrolase in two ways, ester hydrolysis or ether hydrolysis. Then, DAI was combined with glucuronic acid to form daidzein monoglucuronate under the action of uridine diphosphate (UDP)-glucuronidase. Meanwhile, it was also found that metabolite M5 of DD5 could undergo glucuronidation under the action of UDP-glucuronosyltransferase and competitive sulphation under the action of sulphotransferase to produce its sulfate conjugate M7. Analysis of structure–property relationships indicated that the absorption and utilization of drugs is closely relative to the physical properties and could be improved by adjusting the liposolubility. The pharmaceutical properties were optimized comprehensively after DAI was modified by naphthalene sulphonate esterification. This indicates that this kind of derivatives may have relatively good absorption and transport characteristics and biological activities in vivo . The research on biological activities of the new derivatives (DD4 and DD5) is ongoing in our laboratory.