Microvalve-Assisted Patterning Platform for Measuring Cellular Dynamics Based on 3D Cell Culture
被引:18
作者:
Kim, Minseok S.
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Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South KoreaKorea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
Kim, Minseok S.
[1
]
Lee, Wonhye
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Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South KoreaKorea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
Lee, Wonhye
[1
]
Kim, Yu Chang
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Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
Korea Inst Machinery & Mat, Taejon, South KoreaKorea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
Kim, Yu Chang
[1
,2
]
Park, Je-Kyun
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Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon, South KoreaKorea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
Park, Je-Kyun
[1
,3
]
机构:
[1] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
[2] Korea Inst Machinery & Mat, Taejon, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon, South Korea
A microfluidic platform to satisfy both 3D cell culture and cell-based assay is required for credible assay results and improved assay concept in drug discovery. In this article, we demonstrate a microvalve-assisted patterning (MAP) platform to provide a new method for investigating cellular dynamics by generating a linear concentration gradient of a drug as well as to realize 3D cell culture in a microenvironment. The MAP platform was fabricated by multilayer soft lithography and several microvalves made it possible to pattern a cell-matrix (scaffold) and to exchange media solutions without breaking cell-matrix structure in a microchannel. This approach provides not only exact fluids control, bubble removal, and stable solution exchange in a microchannel, but also reliable scaffold fabrication and 3D cell culture. In this study, hepatotoxicity tests with human hepatocellular liver carcinoma cells (HepG2) were also performed in real-time monitoring where cell morphologies exposed to different drug concentrations were observed at a time. Compared to 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay, the MAP platform could be used to reduce drug amount and assay time for cell-based assays as much as 10 and 3 times, respectively.
机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Bissell, MJ
;
Rizki, A
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Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Rizki, A
;
Mian, IS
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Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Bissell, MJ
;
Rizki, A
论文数: 0引用数: 0
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机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Rizki, A
;
Mian, IS
论文数: 0引用数: 0
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机构:
Lawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USALawrence Berkeley Lab, Div Life Sci, Dept Cell & Mol Biol, Berkeley, CA 94720 USA