Boosting the Clinical Translation of Organ-on-a-Chip Technology

被引:5
|
作者
Caballero, David [1 ,2 ]
Reis, Rui L. [1 ,2 ]
Kundu, Subhas C. [1 ,2 ]
机构
[1] Univ Minho, Headquarters European Inst Excellence Tissue Engn, I3Bs Res Inst Biomat Biodegradables & Biomimet, 3Bs Res Grp, AvePk,Parque Ciencia & Tecnol, P-4805017 Barco, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, P-4704553 Braga, Portugal
来源
BIOENGINEERING-BASEL | 2022年 / 9卷 / 10期
关键词
organ-on-a-chip; microfluidics; drug screening; drug discovery; disease modelling; clinical translation; personalized medicine;
D O I
10.3390/bioengineering9100549
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
Organ-on-a-chip devices have become a viable option for investigating critical physiological events and responses; this technology has matured substantially, and many systems have been reported for disease modeling or drug screening over the last decade. Despite the wide acceptance in the academic community, their adoption by clinical end-users is still a non-accomplished promise. The reasons behind this difficulty can be very diverse but most likely are related to the lack of predictive power, physiological relevance, and reliability necessary for being utilized in the clinical area. In this Perspective, we briefly discuss the main attributes of organ-on-a-chip platforms in academia and how these characteristics impede their easy translation to the clinic. We also discuss how academia, in conjunction with the industry, can contribute to boosting their adoption by proposing novel design concepts, fabrication methods, processes, and manufacturing materials, improving their standardization and versatility, and simplifying their manipulation and reusability.
引用
收藏
页数:12
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