4.8 Article

Rapid Production of Cell-Laden Microspheres Using a Flexible Microfluidic Encapsulation Platform

期刊

SMALL
卷 15, 期 47, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201902058

关键词

biomanufacturing; hydrogel microspheres; microfluidic encapsulation; photocrosslink; regenerative medicine

资金

  1. American Heart Association [AM HEART-14SDG18610002]
  2. National Science Foundation Chemical, Bioengineering, Environmental, and Transport Systems program [NSF-CBET-1150854]
  3. Auburn University Research Initiative in Cancer (AURIC)
  4. AL EPSCOR

向作者/读者索取更多资源

This study establishes a novel microfluidic platform for rapid encapsulation of cells at high densities in photocrosslinkable microspherical hydrogels including poly(ethylene glycol)-diacrylate, poly(ethylene glycol)-fibrinogen, and gelatin methacrylate. Cell-laden hydrogel microspheres are advantageous for many applications from drug screening to regenerative medicine. Employing microfluidic systems is considered the most efficient method for scale-up production of uniform microspheres. However, existing platforms have been constrained by traditional microfabrication techniques for device fabrication, restricting microsphere diameter to below 200 mu m and making iterative design changes time-consuming and costly. Using a new molding technique, the microfluidic device employs a modified T-junction design with readily adjustable channel sizes, enabling production of highly uniform microspheres with cell densities (10-60 million cells mL(-1)) and a wide range of diameters (300-1100 mu m), which are critical for realizing downstream applications, through rapid photocrosslinking (approximate to 1 s per microsphere). Multiple cell types are encapsulated at rates of up to 1 million cells per min, are evenly distributed throughout the microspheres, and maintain high viability and appropriate cellular activities in long-term culture. This microfluidic encapsulation platform is a valuable and readily adoptable tool for numerous applications, including supporting injectable cell therapy, bioreactor-based cell expansion and differentiation, and high throughput tissue sphere-based drug testing assays.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据