铜绿假单胞菌
药物输送
细胞外小泡
膜
微生物学
化学
免疫
药品
胞外囊泡
细菌
微泡
细胞生物学
生物
纳米技术
免疫系统
免疫学
药理学
材料科学
生物化学
小RNA
基因
遗传学
作者
Jin Gao,Mindy Lee,Xinyue Dong,Zhenjia Wang
标识
DOI:10.1007/978-1-0716-1811-0_30
摘要
Extracellular vesicles (EVs) derived from cell membranes act as therapeutics and targeted drug carriers. However, the production scalability and reproducibility of EVs limit their biomedical applications. In the past few years, our lab has developed a nitrogen cavitation approach to efficiently produce EVs from any types of eukaryotic cells and bacteria. We have demonstrated that EVs derived from differentiated HL-60 cells can improve the treatment of inflammatory diseases. In addition, we have showed an increased survival of animals from bacterial infections by Pseudomonas aeruginosa after the mice were immunized with the nanovesicles derived from Pseudomonas aeruginosa membrane.
科研通智能强力驱动
Strongly Powered by AbleSci AI