中国中药杂志2025,Vol.50Issue(23):6505-6514,10.DOI:10.19540/j.cnki.cjcmm.20250916.302
淫羊藿多糖组分介导的自组装纳米粒对淫羊藿苷增溶促渗研究
Solubilization and permeation enhancement of icariin by Epimedium polysaccharide-mediated self-assembled nanoparticles
摘要
Abstract
In recent years,self-assembled nanostructures of TCM polysaccharides have attracted widespread attention in drug delivery systems.This study investigated the effects of two Epimedium polysaccharides,a neutral polysaccharide(EPSN)and an acidic polysaccharide(EPSA),on the loading of the active component icariin(ICA)and their influence on biopharmaceutical properties.Structural characterization revealed EPSN as a glucan and EPSA as an acidic heteropolysaccharide,both exhibiting triple-helix conformations.Dynamic light scattering(DLS),critical aggregation concentration(CAC),and electron microscopy demonstrated that the polysaccharides self-assembled into nanoparticles in aqueous solutions.Fourier transform infrared spectroscopy(FT-IR)and differential scanning calorimetry(DSC)revealed that hydrogen bonding and π-π stacking interactions occurred between the polysaccharides and ICA.Solubility testing using the saturation shake-flask method,gastrointestinal stability assays,parallel artificial membrane permeability assay(PAMPA),and single-pass intestinal perfusion(SPIP)in rats were used to evaluate and compare the effects of the two polysaccharides on ICA solubility,stability,and permeability.The results showed that both polysaccharides enhanced ICA solubility,stability,and permeability,with EPSA showing superior solubility and stability enhancement,while EPSN exhibited better permeability-promoting effects.关键词
淫羊藿多糖/淫羊藿苷/自组装纳米粒/功能组分Key words
Epimedium polysaccharide/icariin/self-assembled nanoparticles/functional components引用本文复制引用
HUANG Bin,YANG Yan-jun,YANG Bing,ZHU Mao-mao,FENG Liang,JIA Xiao-bin..淫羊藿多糖组分介导的自组装纳米粒对淫羊藿苷增溶促渗研究[J].中国中药杂志,2025,50(23):6505-6514,10.基金项目
国家自然科学基金重点项目(82230117) (82230117)
国家自然科学基金面上项目(82474093) (82474093)
江苏省卓越博士后科研基金计划项目(2022ZB317) (2022ZB317)
中国药科大学双一流建设创新团队项目(CPU2018GF07) (CPU2018GF07)