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Published on: August 19, 2015
Tailored protein release from biodegradable poly(ε-caprolactone-PEG)-b-poly(ε-caprolactone) multiblock-copolymer
Milica Stanković1, Jasmine Tomar1, Christine Hiemstra2
1Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, Groningen, The Netherlands.
This study explored protein release from biodegradable poly(ε-caprolactone-PEG)-block-poly(ε-caprolactone) copolymers. Higher PEG content and lower protein molecular weight enhanced release rates, enabling tailored protein delivery.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Biodegradable polymers are crucial for controlled drug release.
- Poly(ε-caprolactone)-based copolymers offer tunable properties for biomedical applications.
- Phase-separated multiblock copolymers present unique characteristics for protein encapsulation.
Purpose of the Study:
- To investigate in vitro protein release from novel [PCL-PEG]-b-[PCL] multiblock copolymers.
- To evaluate the impact of polymer block ratio and polyethylene glycol (PEG) content on protein release kinetics.
- To determine the influence of protein molecular weight on release profiles from these biodegradable implants.
Main Methods:
- Synthesis of poly(ε-caprolactone-PEG)-block-poly(ε-caprolactone) ([PCL-PEG]-b-[PCL]) multiblock copolymers with varying PEG content (22.5-52.5 wt%).
- Spray-drying of proteins (goserelin, insulin, lysozyme, carbonic anhydrase, albumin) with inulin stabilizer.
- Incorporation of spray-dried proteins into polymeric implants via hot melt extrusion.
- In vitro release studies of proteins with molecular weights ranging from 1.2 to 66 kDa.
Main Results:
- All incorporated proteins maintained structural integrity post-extraction.
- Protein release rate increased with decreasing protein molecular weight.
- Higher PEG content in the [PCL-PEG]-b-[PCL] copolymer led to increased protein release rates.
- Increased PEG content also enhanced copolymer swelling and degradation rates.
Conclusions:
- The release rate of proteins from [PCL-PEG]-b-[PCL] copolymers is significantly influenced by protein molecular weight and polymer PEG content.
- Tailoring the PEG content in these biodegradable multiblock copolymers allows for controlled release of proteins with varying molecular weights.
- These findings support the potential of [PCL-PEG]-b-[PCL] copolymers as versatile platforms for advanced protein delivery systems.
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