药物输送
材料科学
外体
纳米医学
挤压
内体
阿霉素
生物医学工程
微泡
纳米技术
药品
药理学
纳米颗粒
化学
医学
生物化学
化疗
外科
小RNA
冶金
基因
细胞内
作者
Peng Guo,Sara Busatto,Jing Huang,Golnaz Morad,Marsha A. Moses
标识
DOI:10.1002/adfm.202008326
摘要
To date, the scaled-up manufacturing and efficient drug loading of exosomes are two existing challenges limiting the clinical translation of exosome-based drug delivery. Herein, we developed a facile magnetic extrusion method for preparing endosome-derived vesicles, also known as exosome mimetics (EMs), which share the same biological origin and similar morphology, composition, and biofunctions with native exosomes. The high yield and consistency of this magnetic extrusion method help to overcome the manufacturing bottleneck in exosome research. Moreover, the proposed standardized multi-step method readily facilitates the ammonium sulfate gradient approach to actively load chemodrugs such as doxorubicin into EMs. The engineered EMs developed and tested here exhibit comparable drug delivery properties as do native exosomes and potently inhibit tumor growth by delivering doxorubicin in an orthotopic breast tumor model. These findings demonstrate that EMs can be prepared in a facile and scaled-up manner as a promising biological nanomedicine for cancer drug delivery.
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