Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Science, Nanjing Normal University, Nanjing 210046, China.
Jiangsu Key Laboratory for Molecular and Medical Biotechnology, College of Life Science, Nanjing Normal University, Nanjing 210046, China.
Carbohydr Polym. 2017 Oct 15;174:182-189. doi: 10.1016/j.carbpol.2017.06.061. Epub 2017 Jun 17.
To overcome barriers for oral delivery of insulin, the chitosan(CS)-based nanocarriers with a novel cell penetrating peptide (SAR6EW) have been prepared and evaluated in this study. Characterization measurements showed that SAR6EW/CS/insulin-NPs displayed global particles with smooth surfaces and an average diameter about 150nm. The entrapment efficiency and loading rates of insulin were 75.36% and 7.58%, respectively. Insulin could be released constantly from SAR6EW/CS/insulin-NPs in vitro. Furthermore, SAR6EW/CS/insulin-NPs could facilitate the uptake of insulin and induce a significantly higher internalization of insulin via adding clathrin and caveolae mediated endocytosis. In addition, in vivo hypoglycemic studies showed that orally administrated SAR6EW/CS/insulin-NPs produced a better hypoglycemic effect as compared with CS/insulin-NPs in diabetic rats. Meanwhile, no significant cytotoxicity of the nanoparticles was observed. In conclusion, SAR6EW-mediated chitosan nanocarriers showed sufficient effectiveness for oral delivery of insulin. This delivery system is also promising for the delivery of other protein drugs by oral administration.
为了克服胰岛素口服传递的障碍,本研究制备了基于壳聚糖(CS)的新型细胞穿透肽(SAR6EW)纳米载体,并对其进行了评价。特征测量表明,SAR6EW/CS/胰岛素-NPs 显示出具有光滑表面的整体颗粒,平均直径约为 150nm。胰岛素的包封效率和载药量分别为 75.36%和 7.58%。胰岛素可以在体外从 SAR6EW/CS/胰岛素-NPs 中持续释放。此外,SAR6EW/CS/胰岛素-NPs 可以通过增加网格蛋白和小窝介导的内吞作用促进胰岛素的摄取,并诱导胰岛素的内化显著增加。此外,体内降血糖研究表明,与 CS/胰岛素-NPs 相比,口服给予 SAR6EW/CS/胰岛素-NPs 在糖尿病大鼠中产生了更好的降血糖效果。同时,没有观察到纳米颗粒的显著细胞毒性。总之,SAR6EW 介导的壳聚糖纳米载体显示出足够的有效性,可用于胰岛素的口服传递。该递药系统也有望通过口服给予其他蛋白质药物。