Microtissues®

Summary

Published in Applied In Vitro Toxicology (2016), this peer-reviewed study used 3D Petri Dish® micro-molds to form scaffold-free 3D microtissues. Full citation: Jakubek, Lorin M., et al. Hepatic Spheroids for Long-Term Toxicity Studies

🫁 Hepatic & Liver

Hepatic Spheroids for Long-Term Toxicity Studies

Applied In Vitro Toxicology 2016 Jakubek, Lorin M., et al
Cite as: Jakubek, Lorin M., et al. Hepatic Spheroids for Long-Term Toxicity Studies. Applied In Vitro Toxicology (2016). doi:10.1089/aivt.2016.0016 doi.org/10.1089/aivt.2016.0016

Research Overview

Drug-induced liver injury is a leading cause of drug failure and market withdrawal, yet in vitro screening still relies on primary hepatocyte monolayers that lose their phenotype and metabolic function within days — a narrow experimental window that limits what assays can detect.

Hepatocyte spheroids avoid that decay: they develop structural polarity, functional bile canaliculi, and long-term viability. Because common spheroid formation methods lose cells, stress them, or demand special equipment, this study developed a rat primary hepatocyte spheroid system suited to pharmaceutical screening, capable of maintaining hepatic function over the long term.

Key Discoveries

  • Primary hepatocyte spheroids retain polarity, bile canaliculi, and long-term viability lost by monolayers
  • System designed to avoid the cell loss, stress, and equipment demands of other spheroid methods
  • Extends the experimental window for long-term hepatotoxicity screening