@article {Aithal:2007:1550-7033:254,
title = "Viability, Proliferation and Functionality of Hepatocytes Cultured on Self-Assembled Monolayers (SAMs)-Modified Indium Tin Oxide (ITO)",
journal = "Journal of Biomedical Nanotechnology",
parent_itemid = "infobike://asp/jbn",
publishercode ="asp",
year = "2007",
volume = "3",
number = "3",
publication date ="2007-09-01T00:00:00",
pages = "254-263",
itemtype = "ARTICLE",
issn = "1550-7033",
url = "https://www.ingentaconnect.com/content/asp/jbn/2007/00000003/00000003/art00006",
doi = "doi:10.1166/jbn.2007.030",
keyword = "HEPATOCYTE, PROLIFERATION AND FUNCTIONALITY, SELF-ASSEMBLED MONOLAYER, AMINO GROUP, L-GLUTAMINE",
author = "Aithal, Rajendra K. and Kumaraswamy, Deepak P. and Mills, David K. and Kuila, Debasish",
abstract = "Hepatocyte-based cell culture platforms find their use in diverse applications ranging from drug toxicity platforms to bioartificial livers. Maintenance of hepatocyte specific functions even for a short duration of time, in vitro, is a major challenge. In this report, we have
cultured primary rat hepatocytes on indium tin oxide (ITO) substrates modified with organic self-assembled monolayers (SAMs) containing methyl (CH3), amino (NH2), thiol (SH) terminating groups with different degrees of wettability and surface charge.
SAM modified surfaces were characterized using water contact angle measurements and infrared spectroscopy, and the cells were assessed for their viability and functionality using standard assays. Morphological responses of hepatocyte cell culture indicate characteristic cell clustering and
the presence of binucleate cells predominantly on ITO, ITO-NH2 and ITO-CH3, but not on ITO-SH surface. The initial attachment of the cells may be attributed to the charge and the hydrophobic nature of the SAM end groups under physiological conditions. Cells proliferate
in the presence of L-glutamine and produce Type I collagen and other proteins with low release of lactate dehydrogenase (LDH). These results suggest that SAM-based cell culture platform may be used to have a better understanding of cell-substrate interactions and make a suitable choice of
substrate for use in clinical research.",
}