Wang Xinyu, Cao Zhaoxin, Su Jingyi, Ma Yu, Zhang Siyu, Shao Zihan, Ge Xuemei, Cheng Xiaoliang, Zhou Zhiyong
Department of Food Science and Technology, College of Light Industry Science and Engineering, Nanjing Forestry University, Nanjing 210037, PR China.
Department of Food Science and Technology, College of Light Industry Science and Engineering, Nanjing Forestry University, Nanjing 210037, PR China; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, PR China.
Int J Biol Macromol. 2025 Mar;293:139392. doi: 10.1016/j.ijbiomac.2024.139392. Epub 2024 Dec 31.
Curcumin (CUR) is a polyphenolic compound extracted from plants with a wide range of pharmacological activities. However, the low stability and bioavailability limits its practical application. This work utilized the chitosan (CH) and sodium alginate (SA) to modify the surface of the liposome to improve the stability of curcumin. Studies on the adsorption of pepsin to the surface of liposomes and the formation of protein coronas (PCs) were also carried out to investigate the in vivo behavior of the sodium alginate and chitosan modified curcumin liposomes (SA-CH-LPs). The result shown that the average particle size of SA-CH-LPs was around 220.7 ± 1.68 nm. X-ray Diffractometer (XRD) and differential scanning calorimeter (DSC) confirmed the successful preparation of SA-CH-LPs and illustrated their crystalline characteristics. The cytotoxicity of SA-CH-LPs was determined by CCK-8 assay and the results showed that the cell viability was above 80 % at different concentrations. In vitro results showed that the bioaccessibility of SA-CH-LPs (87.9 %) was better than curcumin liposomes (LPs) (66.4 %), and could better resist to catabolic degradation in the gastrointestinal environment. This work could provide the feasibility for improving the stability and bioaccessibility of the curcumin liposome, as well as given the preliminary evidence for investigation of the interaction with enzyme during the in vivo digestion process for the further application in food.
姜黄素(CUR)是一种从植物中提取的具有广泛药理活性的多酚类化合物。然而,其低稳定性和生物利用度限制了它的实际应用。这项工作利用壳聚糖(CH)和海藻酸钠(SA)修饰脂质体表面以提高姜黄素的稳定性。还开展了胃蛋白酶在脂质体表面的吸附以及蛋白质冠(PCs)形成的研究,以探究海藻酸钠和壳聚糖修饰的姜黄素脂质体(SA-CH-LPs)的体内行为。结果表明,SA-CH-LPs的平均粒径约为220.7 ± 1.68 nm。X射线衍射仪(XRD)和差示扫描量热仪(DSC)证实了SA-CH-LPs的成功制备,并阐明了它们的晶体特性。通过CCK-8法测定SA-CH-LPs的细胞毒性,结果表明在不同浓度下细胞活力均高于80%。体外结果显示,SA-CH-LPs的生物可及性(87.9%)优于姜黄素脂质体(LPs)(66.4%),并且在胃肠道环境中能更好地抵抗分解代谢降解。这项工作可为提高姜黄素脂质体的稳定性和生物可及性提供可行性,同时为其在食品中的进一步应用研究体内消化过程中与酶的相互作用提供初步证据。