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A microfluidic device for study of the effect of tumor vascular structures on the flow field and HepG2 cellular flow behaviors.
Ke, Ming; Cai, Shaoxi; Zou, Misha; Zhao, Yi; Li, Bo; Chen, Sijia; Chen, Longcong.
Affiliation
  • Ke M; College of Bioengineering, Chongqing University, Chongqing, 400044, China.
  • Cai S; College of Bioengineering, Chongqing University, Chongqing, 400044, China. Electronic address: sxcai@cqu.edu.cn.
  • Zou M; College of Bioengineering, Chongqing University, Chongqing, 400044, China.
  • Zhao Y; College of Bioengineering, Chongqing University, Chongqing, 400044, China.
  • Li B; College of Bioengineering, Chongqing University, Chongqing, 400044, China; School of Education, Chongqing Normal University, Chongqing, China.
  • Chen S; College of Bioengineering, Chongqing University, Chongqing, 400044, China.
  • Chen L; College of Bioengineering, Chongqing University, Chongqing, 400044, China; School of Basic Medical Sciences, Chongqing Medical University, Chongqing, China.
Biochem Biophys Res Commun ; 496(1): 238-243, 2018 01 29.
Article in En | MEDLINE | ID: mdl-29309789
To build a microfluidic device with various morphological features of the tumor vasculature for study of the effects of tumor vascular structures on the flow field and tumor cellular flow behaviors. The designed microfluidic device was able to approximatively simulate the in vivo structures of tumor vessels and the flow within it. In this models, the influences of the angle of bifurcation, the number of branches, and the narrow channels on the flow field and the influence of vorticity on the retention of HepG2 cells were significant. Additionally, shear stress below physiological conditions of blood circulation has considerable effect on the formation of the lumen-like structures (LLSs) of HepG2 cells. These results can provide some data and reference in the understanding of the interaction between hemorheological properties and tumor vascular structures in solid tumors.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Separation / Cell Culture Techniques / Bioreactors / Hep G2 Cells / Lab-On-A-Chip Devices / Neovascularization, Pathologic Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2018 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Separation / Cell Culture Techniques / Bioreactors / Hep G2 Cells / Lab-On-A-Chip Devices / Neovascularization, Pathologic Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2018 Type: Article Affiliation country: China