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Three-Dimensional Bioprinted MR-Trackable Regenerative Scaffold for Postimplantation Monitoring on T1-Weighted MRI
Sadi Loai1,2, Daniel A Szulc1,2, Hai-Ling Margaret Cheng1,2,3
1Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada.
This study developed an MRI-detectable bioprinted scaffold using a manganese-based contrast agent. While cell viability was maintained, the scaffolds migrated, highlighting challenges in in vivo tracking for tissue regeneration.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Medical Imaging
Background:
- Three-dimensional (3D) bioprinted tissue scaffolds offer precise control for tissue regeneration.
- In vivo confirmation of scaffold placement and retention is critical postimplantation.
- Detecting unwanted implant migration is essential for therapeutic success.
Purpose of the Study:
- To integrate a safe, effective Magnetic Resonance (MR) contrast agent into a bioprinting workflow.
- To enable bright-contrast scaffold monitoring in vivo after implantation.
- To assess the feasibility of MR-guided scaffold tracking.
Main Methods:
- Bioprinted gelatin/alginate scaffolds were labeled with MnPNH2.
- In vitro and in vivo MRI (7.0 T) assessed scaffold T1 relaxation times.
- Cell viability and proliferation were evaluated over two weeks.
- Scaffold implantation in Sprague Dawley rats followed by longitudinal imaging.
Main Results:
- Cell viability remained high (>90%) after labeling and bioprinting.
- Labeled scaffolds showed significantly reduced T1 values in vitro and in vivo.
- In vivo imaging at 24 hours postimplantation and gross pathology confirmed scaffold migration beyond the imaging field.
- No significant differences in T1 values were observed between in vivo and in vitro labeled scaffolds.
Conclusions:
- An MR-detectable, cell-compatible bioprinted scaffold was successfully created.
- The T1-weighting contrast agent enabled high-resolution postimplantation scaffold tracking.
- Scaffold migration was observed, indicating a need for improved retention strategies.
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