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Validation of a high-throughput MPS for 3D culturing of primary hepatocytes
Filed under: ADME, DILI, Drug metabolism, General OOC, and Safety toxicology
A high-throughput 3D MPS model supported the long-term culture of primary human hepatocytes under perfused conditions. Across two donors, the Liver-48 format maintained hepatocyte viability and consistent liver-specific function over 14 days, including robust albumin production. Minimal differences in lactate dehydrogenase release and uniform microtissue formation were observed compared with the established Liver-12 format
Engineering and biological validation demonstrated consistent flow across the Liver-48 plate and showed that scaling experimental capacity four-fold did not compromise liver-specific function or physiological relevance. Together, these findings support the use of high-throughput 3D MPS models to generate robust, reproducible, and human-relevant data at greater scale for drug discovery and development.
