Table 4.
The main nanotoxicological advantages and disadvantages of multi-cellular primary 3D liver MT in the assessment of the tissue as a potential in vivo surrogate
| Advantages | Disadvantages |
|---|---|
| Human tissue | Cost of plates can be potentially prohibitive to academia |
| Primary cells | Toxicological assessment beyond 2 weeks might not be ideal in a nano context |
| Incorporation of numerous liver cell populations - hepatocytes, Kupffer cells and endothelial cells | There is no physiological structure to the tissue - cells aggregate randomly |
| High metabolic activity | |
| In vitro model which allows for repeated long term exposure of xenobiotics | |
| Little variability between MT in wells and plates | |
| Scaffold-free with 100% endogenous extracellular matrix |