Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.biomaterials.2009.07.022
Title: Laminar-flow immediate-overlay hepatocyte sandwich perfusion system for drug hepatotoxicity testing
Authors: Xia, L. 
Ng, S.
Han, R.
Tuo, X. 
Xiao, G.
Leo, H.L. 
Cheng, T. 
Yu, H. 
Keywords: Mass transfer
Perfusion bioreactor
Polarity
Sandwich culture
Shear stress
Stable functions
Issue Date: 2009
Source: Xia, L., Ng, S., Han, R., Tuo, X., Xiao, G., Leo, H.L., Cheng, T., Yu, H. (2009). Laminar-flow immediate-overlay hepatocyte sandwich perfusion system for drug hepatotoxicity testing. Biomaterials 30 (30) : 5927-5936. ScholarBank@NUS Repository. https://doi.org/10.1016/j.biomaterials.2009.07.022
Abstract: Drug hepatotoxicity testing requires in vitro hepatocyte culture to maintain the long-term and stable liver specific functions. We developed a drug testing platform based on laminar-flow immediate-overlay hepatocyte sandwich perfusion culture. The immediate-overlay sandwich (collagen-coated porous polymeric membrane as top overlay) protects the cells and integrity of the top collagen matrix from the impact of flow. A bioreactor was designed that allowed proper control of shear stress and mass transfer. The culture parameters such as the optimal perfusion initiation time and flow rate were systematically and mechanistically determined. The optimized system could re-establish hepatocyte polarity to support biliary excretion and to maintain other liver specific functions, such as the biotransformation enzyme activities, for two weeks that extended the usable in vitro hepatocyte-based drug testing window. When the perfusion cultured hepatocytes from days 7 or 14 were used for drug testing, the APAP-induced hepatotoxicity measurements were more sensitive and consistent over time than the static culture control, enabling further exploitations in large-scale drug testing applications. © 2009 Elsevier Ltd. All rights reserved.
Source Title: Biomaterials
URI: http://scholarbank.nus.edu.sg/handle/10635/25166
ISSN: 01429612
DOI: 10.1016/j.biomaterials.2009.07.022
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