Advancing Microphysiological System Development to Bridge 2D & 3D Model Translation Gaps

  • Comparing 2D versus 3D microphysiological systems to identify optimal validation approaches for preclinical development
  • Evaluating neuronal and intestinal model systems to establish disease-specific benchmarking criteria and translational readiness
  • Implementing barrier function and inflammation assessments to demonstrate physiological relevance in complex tissue models