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Electrospinning Fibrous Polymer Scaffolds for Tissue Engineering and Cell Culture
Published on: October 21, 2009
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A simple route to functionalising electrospun polymer scaffolds with surface biomolecules
Karolina Dziemidowicz1, Steve Brocchini1, Gareth R Williams1
1UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
International Journal of Pharmaceutics
|January 23, 2021
Summary
This study shows that UV-initiated photografting of perfluorophenyl azide N-hydroxysuccinimide (PFPA-NHS) onto polycaprolactone (PCL) scaffolds effectively immobilizes therapeutic proteins like catalase, retaining their activity for potential regenerative medicine applications.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Regenerative Medicine
Background:
- Surface functionalization of electrospun scaffolds is crucial for regenerative medicine.
- Bioconjugation methods must preserve biomolecule activity.
- Perfluorophenyl azide N-hydroxysuccinimide (PFPA-NHS) enables UV-initiated covalent coupling to polymers.
Purpose of the Study:
- To explore the feasibility of PFPA-NHS functionalization of electrospun polycaprolactone (PCL) scaffolds.
- To assess the retention of biomolecule activity after conjugation.
- To investigate potential applications in oncological photodynamic therapy.
Main Methods:
- Photografting of PFPA-NHS onto electrospun PCL scaffolds.
- Protein conjugation using fluorescence staining and attachment studies.
- Cell viability assays (Caco-2) to optimize washing methods (sonication).
- Enzyme activity and stability assays for surface-attached catalase.
Main Results:
- PFPA-NHS photografting successfully functionalized PCL scaffolds, retaining amine coupling capability.
- Sonication washing is essential to prevent cell death caused by unreacted PFPA.
- Surface-attached catalase retained enzymatic activity and showed sustained binding (~60% after 6 days).
Conclusions:
- PFPA-NHS functionalization is a viable method for immobilizing active biomolecules onto PCL scaffolds.
- This technique offers potential for developing advanced protein-based therapies with prolonged presentation and sustained release.
- The method holds promise for applications in regenerative medicine and oncological photodynamic therapy.

