State Key Laboratory of Natural Medicines, Department of Pharmaceutical Science, China Pharmaceutical University, Nanjing 210009, China.
NMPA Key Laboratory for Research and Evaluation of Pharmaceutical Preparations and Excipients, China Pharmaceutical University, Nanjing 210009, China.
Nanoscale. 2023 Mar 9;15(10):5063-5073. doi: 10.1039/d2nr05744a.
Accuratly controlling drug release from a smart "self-regulated" drug delivery system is still an ongoing challenge. Herein, we developed a surface decoration strategy to achieve an efficient drug encapsulation with precise ratiometric control. Thanks to the surface decoration with cationic carrier materials by electrostatic attraction, the surface properties of different protein and peptide nanoparticles were uniformed to those adsorbed carrier materials. These carrier materials endowed protein and peptide nanoparticles with good dispersity in the oil phase and significantly inhibited the drug transfer from oil to water. With uniform surface properties, we realized the co-encapsulation of multiple types of proteins and peptides with precise ratiometric control. The encapsulation efficiency was higher than 87.8% for insulin. After solidification, the adsorbed materials on the surface of nanoparticles formed a solid protection layer, which prolonged the mean residence time of insulin from 3.3 ± 0.1 h (for insulin solution) to 47.5 ± 1.3 h. In type 1 diabetes, the spermine-modified acetalated dextran microparticle co-loaded with insulin, glucose oxidase and catalase maintained the blood glucose level within the normal range for 7 days.
准确控制智能“自我调节”药物输送系统的药物释放仍然是一个持续的挑战。在此,我们开发了一种表面修饰策略,通过精确的比例控制实现高效的药物包封。由于通过静电吸引用阳离子载体材料进行表面修饰,不同蛋白质和肽纳米颗粒的表面性质均均匀化为吸附的载体材料。这些载体材料使蛋白质和肽纳米颗粒在油相中有良好的分散性,并显著抑制药物从油相转移到水相。通过均匀的表面性质,我们实现了多种类型蛋白质和肽的共包封,并具有精确的比例控制。胰岛素的包封效率高于 87.8%。固化后,纳米颗粒表面吸附的材料形成了固体保护层,将胰岛素的平均停留时间从 3.3±0.1 h(胰岛素溶液)延长至 47.5±1.3 h。在 1 型糖尿病中,同时负载胰岛素、葡萄糖氧化酶和过氧化氢酶的 spermine 修饰的缩醛化葡聚糖微球使血糖水平在 7 天内保持在正常范围内。