Department of Pharmacy, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, China.
Shandong Xinhua Pharmaceutical Company Limited, Zibo, Shandong, China.
AAPS PharmSciTech. 2022 Mar 29;23(4):100. doi: 10.1208/s12249-022-02255-3.
Luteolin (Lu) is a kind of flavonoid that has been proved to treat non-alcoholic fatty liver disease by alleviating intestinal microbiota disorder. In this study, luteolin was coated with methoxy poly(ethylene glycol)-poly(dl-lactide-co-glycolic acid) (mPEG-PLGA) using an emulsion solvent evaporation method, and the optimum preparation process was determined by a single-factor experiment combined with response surface methodology (RSM). Methacrylic acid-methyl methacrylate (1:2) copolymer (Eudragit S100) was then used to coat the surface of Lu/mPEG-PLGA nanoparticles. The physical parameters of Eudragit S100-coated Lu/mPEG-PLGA nanoparticles (Lu-NPs), such as appearance, particle size, potential, particle size distribution and drug release, and stability in vitro, were evaluated. In addition, its cytotoxicity in vitro, pharmacokinetics, tissue distribution, and toxicity in vivo were also studied. The results showed that the prepared Lu-NPs had uniform particle size distribution, high encapsulation efficiency, and good stability. Normal colonic epithelial cells showed good tolerance to Lu-NPs. After oral administration, the blood concentration of luteolin peaked at 8 h, and the main tissue distribution was within the colon, confirming its colon-targeted profile. Safety assessments also indicated that no significant changes were observed in main organs after administration of Lu-NPs. The use of Eudragit S100-coated Lu/mPEG-PLGA nanoparticles is a new strategy for colon-targeted delivery of luteolin that encourages luteolin to fulfill its role in the colon.
木犀草素(Lu)是一种黄酮类化合物,已被证明通过缓解肠道微生物群失调来治疗非酒精性脂肪肝疾病。在本研究中,木犀草素采用乳液溶剂蒸发法用甲氧基聚(乙二醇)-聚(DL-乳酸-共-乙醇酸)(mPEG-PLGA)进行包衣,并通过单因素实验结合响应面法(RSM)确定最佳制备工艺。然后,用甲基丙烯酸甲酯-甲基丙烯酸(1:2)共聚物(Eudragit S100)对 Lu/mPEG-PLGA 纳米粒的表面进行包衣。对 Eudragit S100 包被的 Lu/mPEG-PLGA 纳米粒(Lu-NPs)的外观、粒径、电位、粒径分布和体外药物释放以及稳定性等物理参数进行了评价。此外,还研究了其体外细胞毒性、药代动力学、组织分布和体内毒性。结果表明,所制备的 Lu-NPs 具有均匀的粒径分布、高包封效率和良好的稳定性。正常结肠上皮细胞对 Lu-NPs 具有良好的耐受性。口服给药后,木犀草素的血药浓度在 8 h 时达到峰值,主要组织分布在结肠内,证实了其结肠靶向特征。安全性评估还表明,给药后主要器官没有观察到明显变化。使用 Eudragit S100 包被的 Lu/mPEG-PLGA 纳米粒是一种将木犀草素靶向递送至结肠的新策略,鼓励木犀草素在结肠中发挥作用。