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Characterizing and optimizing poly-L-lactide-co-ε-caprolactone membranes for urothelial tissue engineering
Reetta Sartoneva1, Anne-Marie Haaparanta, Tuija Lahdes-Vasama
1Institute of Biomedical Technology, University of Tampere, Tampere, Finland. reetta.sartoneva@uta.fi
Journal of the Royal Society, Interface
|August 17, 2012
Summary
Smooth and textured poly-l-lactide-co-ε-caprolactone (PLCL) membranes effectively support human urothelial cell growth for tissue engineering. Texturing did not significantly improve cell attachment or proliferation over smooth surfaces.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Urology
Background:
- Synthetic biomaterials like polylactide (PLA) and polycaprolactone are explored for urothelial tissue engineering.
- Poly-l-lactide-co-ε-caprolactone (PLCL) shows promise, but surface optimization is needed for human urothelial cells (hUCs).
Purpose of the Study:
- To compare smooth (sPLCL), textured (tPLCL), and compression-moulded PLCL (cPLCL) membranes for hUC growth.
- To evaluate the impact of topographical texturing on cell response and mechanical properties.
Main Methods:
- Synthesized and characterized different PLCL-based membranes (sPLCL, tPLCL, cPLCL).
- Cultured hUCs on the membranes and assessed cell attachment, proliferation, viability, and phenotype.
- Evaluated mechanical properties, including elongation, under hydrolysis.
Main Results:
- Both sPLCL and tPLCL significantly outperformed cPLCL in supporting hUC growth.
- tPLCL offered no significant advantage over sPLCL for cell attachment or proliferation.
- Cells remained viable and maintained their phenotype on all tested membranes over 14 days.
- sPLCL and tPLCL demonstrated suitable mechanical properties for urothelial applications, with tPLCL showing higher elongation.
Conclusions:
- sPLCL and tPLCL are promising candidates for urothelial tissue engineering applications.
- Further investigation of sPLCL and tPLCL is warranted based on cell culture and mechanical data.
- Topographical texturing may not be essential for improved hUC growth on PLCL membranes.

