Hood Joshua L
University of Louisville, Department of Pharmacology & Toxicology & the James Graham Brown Cancer Center, Clinical and Translational Research Building, 505 South Hancock Street, Louisville, KY 40202, USA.
Nanomedicine (Lond). 2016 Jul;11(13):1745-56. doi: 10.2217/nnm-2016-0102. Epub 2016 Jun 27.
Exosomes are extracellular nanovesicles. They innately possess ideal structural and biocompatible nanocarrier properties. Exosome components can be engineered at the cellular level. Alternatively, when exosome source cells are unavailable for customized exosome production, exosomes derived from a variety of biological origins can be modified post isolation which is the focus of this article. Modification of exosome surface structures allows for exosome imaging and tracking in vivo. Exosome membranes can be loaded with hydrophobic therapeutics to increase drug stability and efficacy. Hydrophilic therapeutics such as RNA can be encapsulated in exosomes to improve cellular delivery. Despite advances in post isolation exosome modification strategies, many challenges to effectively harnessing their therapeutic potential remain. Future topics of exploration include: matching exosome subtypes with nanomedicine applications, optimizing exosomal nanocarrier formulation and investigating how modified exosomes interface with the immune system. Research into these areas will greatly facilitate personalized exosome-based nanomedicine endeavors.
外泌体是细胞外纳米囊泡。它们天生具有理想的结构和生物相容性纳米载体特性。外泌体成分可在细胞水平上进行工程改造。另外,当无法获得外泌体来源细胞用于定制外泌体生产时,可以在分离后对源自多种生物学来源的外泌体进行修饰,这也是本文的重点。外泌体表面结构的修饰可实现外泌体在体内的成像和追踪。外泌体膜可负载疏水性治疗药物以提高药物稳定性和疗效。亲水性治疗药物(如RNA)可封装在外泌体中以改善细胞递送。尽管分离后外泌体修饰策略取得了进展,但有效发挥其治疗潜力仍面临许多挑战。未来的探索主题包括:使外泌体亚型与纳米医学应用相匹配、优化外泌体纳米载体制剂以及研究修饰后的外泌体如何与免疫系统相互作用。对这些领域的研究将极大地促进基于外泌体的个性化纳米医学研究。