Creating tissue on chip constructs in microtitre plates for drug discovery.
Creating tissue on chip constructs in microtitre plates for drug discovery.
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DOI:
10.1039/c8ra00849c
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发表时间:
2018-03-05
期刊:
影响因子:
3.9
通讯作者:
Cooper, J. M.
中科院分区:
文献类型:
--
作者:
Macdonald, N. P.;Menachery, A.;Reboud, J.;Cooper, J. M.
We report upon a novel coplanar dielectrophoresis (DEP) based cell patterning system for generating transferrable hepatic cell constructs, resembling a liver-lobule, in culture. The use of paper reinforced gel substrates provided sufficient strength to enable these constructs to be transfered into 96-well plates for long term functional studies, including in the future, drug development studies. Experimental results showed that hepatic cells formed DEP field-induced structures corresponding to an array of lobule-mimetic patterns. Hepatic viability was observed over a period of 3 days by the use of a fluorescent cell staining technique, whilst the liver specific functionality of albumin secretion showed a significant enhancement due to the layer patterning of cell lines (HepG2/C3A), compared to 2D patterned cells and un-patterned control. This “build and transfer” concept could, in future, also be adapted for the layer-by-layer construction of organs-on-chip in microtitre formats. We report upon a novel coplanar dielectrophoresis (DEP) based cell patterning system for generating transferrable hepatic cell constructs, resembling a liver-lobule, in culture.
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影响因子:
--
作者:
Dvir-Ginzberg, M;Gamlieli-Bonshtein, I;Cohen, S
通讯作者:
Cohen, S
影响因子:
6.1
作者:
Albrecht, DR;Tsang, VL;Bhatia, SN
通讯作者:
Bhatia, SN
DOI:
10.1007/10_029
发表时间:
2007-01-01
期刊:
TISSUE ENGINEERING II: BASICS OF TISSUE ENGINEERING AND TISSUE APPLICATIONS
影响因子:
--
作者:
Nahmias, Yaakov;Berthiaume, Francois;Yarmush, Martin L.
通讯作者:
Yarmush, Martin L.
DOI:
10.1126/science.1188302
发表时间:
2010-06-25
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Huh D;Matthews BD;Mammoto A;Montoya-Zavala M;Hsin HY;Ingber DE
通讯作者:
Ingber DE
影响因子:
46.9
作者:
Bhatia, Sangeeta N.;Ingber, Donald E.
通讯作者:
Ingber, Donald E.