摘要
Phytosterols (PS) are natural steroidal compounds with multiple physiological functions, but their poor solubility, high crystallinity, and low bioavailability hinder effective utilization. In this study, PS-loaded nanostructured lipid carriers modified with cross-linked chitosan (CLCS-PS-NLCs) developed via emulsification-evaporation combined with high-pressure homogenization. The optimal formulation was achieved with 0.5 % (w/w) chitosan and a tripolyphosphate (TPP):chitosan (CS) mass ratio of 2:1 to enhance carrier stability and PS absorption. Structural characterization using dynamic light scattering (DLS) and transmission electron microscopy (TEM), along with fourier transform infrared (FTIR), X-ray diffraction (XRD), and differential scanning calorimetry (DSC), confirmed efficient PS encapsulation and successful chitosan modification. CLCS-PS-NLCs demonstrated excellent stability under varying pH, ionic strength, and storage conditions. In vitro and in vivo studies showed improved digestion and absorption of PS, achieving a bioaccessibility of 36.65 % compared to only 13.28 % for PS-NLCs, and enhancing its uptake in rats. This study provides a promising delivery system for PS with potential applications in functional foods and pharmaceuticals.
危险品化学品经营许可证(带存储)