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Effect of plasticization on heparin release from biodegradable matrices
L P Tan1, S S Venkatraman, P F Sung
1School of Materials Engineering, Nanyang Technological University, N4.1-1-30 Nanyang Avenue, Singapore 639798, Singapore.
International Journal of Pharmaceutics
|September 15, 2004
Summary
Plasticizers affect heparin release from polymer films differently based on polymer type. Poly-L-lactide (PLLA) films showed reduced burst release, while poly-L-lactide-co-glycolide (PLLGA) films were largely unaffected by plasticizers.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Heparin is a crucial anticoagulant drug.
- Polymer films are investigated for controlled drug release applications.
- Understanding polymer-drug interactions is key for effective delivery systems.
Purpose of the Study:
- To investigate the effect of polyethylene glycol (PEG) plasticizer on heparin release from poly-L-lactide (PLLA), poly-L-lactide-co-glycolide (PLLGA), and poly-DL-lactide-co-glycolide (PLGA) films.
- To analyze the influence of polymer composition and plasticizer on drug release kinetics and degradation.
- To correlate release profiles with polymer properties like hydrophilicity and crystallinity.
Main Methods:
- Fabrication of heparin-loaded polymer films using PLLA, PLLGA, and PLGA.
- Incorporation of polyethylene glycol (PEG) as a plasticizer.
- In vitro release studies to determine heparin release profiles.
- Analysis of degradation kinetics and polymer properties.
Main Results:
- Heparin release generally followed a burst, diffusion, and degradation-controlled pattern.
- PEG accelerated degradation in all tested polymers.
- PEG significantly altered release profiles: reduced burst and accelerated diffusion in PLLA, but had minimal effect on PLLGA 80/20.
- Observed differences were attributed to polymer hydrophilicity and crystallinity.
Conclusions:
- Plasticizer effectiveness in modulating heparin release is polymer-dependent.
- PLLA and PLLGA 80/20 exhibit distinct responses to PEG, highlighting the importance of polymer selection for drug delivery.
- Hydrophilicity and crystallinity are critical factors influencing drug release from biodegradable polymer matrices.