3D Printing of a Biocompatible Scaffold and a Real-Time Imaging Window for Monitoring Rat Spinal Cord Regeneration
Mihir A. Madhaparia
University of Minnesota – Twin Cities | Advisors: Dr. Michael C. McAlpine & Dr. Ann M. Parr
PCL scaffold selection
PCL with 400 µm pores delivered the strongest balance of toughness and neural stem cell viability at 50 days post-differentiation.
In vivo imaging window
A chronic dorsal spinal imaging window was fabricated and validated in a rat model without foreign body rejection.
Structural analysis
ANSYS FEA validated the frame against physiological muscle loads to support long-term structural performance.
Bioprinting comparison
Comparative evaluation of EBB, SLA, MEW, inkjet, and DIW bioprinting modalities for neural tissue engineering.
Read abstract
The development of effective regenerative therapies for spinal cord injury is hindered by two major barriers: the lack of structurally optimized bridging scaffolds and the inability to monitor biological integration in real time. This thesis addresses both challenges through a dual-objective framework.
Three scaffold materials — polycaprolactone, poly(lactic-co-glycolic acid), and silicone — were evaluated through extrusion-based direct ink writing at channel widths of 200 µm, 400 µm, and 600 µm. PCL with a 400 µm pore size emerged as the strongest candidate because it combined surgical toughness with strong in vitro support for neural progenitor cell viability. PLGA was found to create cytotoxic acidic microenvironments through hydrolytic degradation.
Complementing the scaffold work, a chronic dorsal spinal imaging window was designed and surgically validated in a rat model. Inspired by surgical retractors, the device used 3D-printed teeth to hold tissue open and a flush-mounted PET optical film to provide stable, long-term in vivo visualization.