The role of microfluidics and 3D-bioprinting in the future of exosome therapy

被引:23
作者
Amondarain, Mikele [1 ]
Gallego, Idoia [2 ,3 ,4 ]
Puras, Gustavo [2 ,3 ,4 ]
Saenz-del-Burgo, Laura [2 ,3 ,4 ]
Luzzani, Carlos [2 ]
Pedraz, Jose Luis [2 ,3 ,4 ]
机构
[1] Fdn Lucha Enfermedades Neurol Infancia FLENI, CONICET, Lab Invest Aplicada Neurociencias LIAN, Buenos Aires, Argentina
[2] Univ Basque Country UPV EHU, Fac Pharm, Lab Pharmaceut, NanoBioCel Grp, Vitoria, Spain
[3] Inst Hlth Carlos III, Biomed Res Networking Ctr Bioengn Biomat & Nanomed, Vitoria, Spain
[4] NanoBioCel Res Grp, Bioaraba, Vitoria, Spain
关键词
CELL-DERIVED EXOSOMES; EXTRACELLULAR VESICLES; DELIVERY; SCAFFOLD; BONE; NANOVESICLES; HYDROGEL; REPAIR; REGENERATION; STROKE;
D O I
10.1016/j.tibtech.2023.05.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Exosome-based strategies constitute a promising tool for therapeutics, avoiding potential immunogenic and tumorigenic side-effects of cell therapies. However, the collection of a suitable exosome pool, and the need for high doses with conventional administration approaches, hamper their clinical translation. To over -come these challenges, versatile exosome collection strategies together with advanced delivery platforms may represent major progress in this field. Microfluidics enables large-scale gathering of both natural and synthetic exosomes for their implementation into bioinks, while 3D-bioprinting holds great promise in regenerative medicine with the use of exosome-loaded scaffolds that mimic the target tissue with controlled pharmacokinetics and pharmacodynamics. Hence, the combination of both strategies might become the key for the translation of exosome therapies to clinical practice.
引用
收藏
页码:1343 / 1359
页数:17
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