Document Type
Article
Publication Date
2013
Publication Title
IEEE Xplore
Abstract
We have developed a novel microfluidic device using poly-dimethylsiloxane (PDMS) microchannels for long term, layered co-culture of primary rat hepatocytes (PRH) and endothelial cells (EC) to mimic the liver sinusoid. Three microfluidic configurations were investigated as shown in Figure 1. In configuration 1, where PRH and rat adrenal medullary endothelial cells (RAMEC) were cocultured with matrigel in layers in a single PDMS microchannel, cells remained viable for 30 days. In configuration 3, where PRH and liver sinusoidal endothelial cells (LSEC) were cultured on the opposite sides of the microporous membrane between two microchannels under static and dynamic conditions, PRH retained their viability and normal morphology up to 35 days and 63 days, respectively. Thus, our novel liver models that closely mimic the liver sinusoid have been proven to facilitate long-term layered co-cultures of PRH and EC.
Keywords
Liver model, liver on a chip, liver co-culture, long term culture, primary hepatocytes, microfluidic platform
First Page
301
Last Page
304
DOI
10.1109/Transducers.2013.6626762
Recommended Citation
Kang, Young Bok (Abraham), "Liver on a Chip; Engineering the Liver Sinusoid" (2013). Faculty Publications - Biomedical, Mechanical, and Civil Engineering. 132.
https://digitalcommons.georgefox.edu/mece_fac/132
Comments
Originally published in Institute of Electrical and Electronics Engineers. 2013. Conference paper.Pages 301-304.
10.1109/Transducers.2013.6626762