Convenient tumor 3D spheroid arrays manufacturing via acoustic excited bubbles for in situ drug screening

被引:9
|
作者
Zheng, Jingjing [1 ,2 ]
Hu, Xuejia [3 ]
Gao, Xiaoqi [1 ,2 ]
Liu, Yantong [1 ,2 ]
Zhao, Shukun [1 ,2 ]
Chen, Longfei [1 ,2 ]
He, Guoqing [1 ,2 ]
Zhang, Jingwei [4 ]
Wei, Lei [5 ]
Yang, Yi [1 ,2 ]
机构
[1] Wuhan Univ, Renmin Hosp, Inst Med & Phys, Sch Phys & Technol,Key Lab Artificial Micro & Nano, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
[3] Xiamen Univ, Sch Elect Sci & Engn, Dept Elect Engn, Xiamen 361005, Peoples R China
[4] Wuhan Univ, Zhongnan Hosp, Dept Breast & Thyroid Surg, Wuhan 430071, Peoples R China
[5] Wuhan Univ, Zhongnan Hosp, Sch Basic Med Sci, Wuhan 430071, Peoples R China
关键词
DROPLET-BASED MICROFLUIDICS; MULTICELLULAR SPHEROIDS; MANIPULATION; GENERATION; CELLS;
D O I
10.1039/d2lc00973k
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The quick and convenient fabrication of in vitro tumor spheroids models has been pursued for clinical drug discovery and personalized therapy. Here, uniform three-dimensional (3D) tumor spheroids are quickly constructed by acoustically excited bubble arrays in a microfluidic chip and performed drug response testing in situ. In detail, bubble oscillation excited by acoustic waves induces second radiation force, resulting in the cells rotating and aggregating into tumor spheroids, which obtain controllable sizes ranging from 30 to 300 mu m. These spherical tumor models are located in microfluidic networks, where drug solutions with gradient concentrations are generated from 0 to 18 mg mL(-1), so that the cell spheroids response to drugs can be monitored conveniently and efficiently. This one-step tumor spheroids manufacturing method significantly reduces the model construction time to less than 15 s and increases efficiency by eliminating additional transfer processes. These significant advantages of convenience and high-throughput manufacturing make the tumor models promising for use in tumor treatment and point-of-care diagnosis.
引用
收藏
页码:1593 / 1602
页数:10
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