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Controlled release of salicylic acid from poly(D,L-Lactide)
A G Andreopoulos1, E Hatzi, M Doxastakis
1Department of Chemical Engineering, National Technical University of Athens, 9 Iroon Polytechniou Str., 15780 Zografos, Greece. andreo@chemeng.ntua.gr
Journal of Materials Science. Materials in Medicine
|September 7, 2004
Summary
High molecular weight poly(D,L-Lactide) exhibited Fick
Area of Science:
- Polymer Chemistry
- Materials Science
- Biomedical Engineering
Background:
- Poly(D,L-Lactide) is a biodegradable polymer with potential applications in drug delivery.
- Understanding its degradation and drug release kinetics is crucial for optimizing its use.
Purpose of the Study:
- To prepare and characterize high molecular weight poly(D,L-Lactide).
- To investigate the swelling behavior and salicylic acid (SA) release from poly(D,L-Lactide) with varying molecular weights.
- To elucidate the release mechanism of SA from the polymer matrix.
Main Methods:
- Ring-opening bulk polymerization of D,L-Lactide to synthesize poly(D,L-Lactide).
- Characterization of polymer molecular weight (Mv), melting point, and swelling behavior.
- In vitro release studies of salicylic acid (SA) from polymer samples in a buffer solution.
Main Results:
- Poly(D,L-Lactide) swelling followed Fick's law, particularly for high molecular weight samples.
- Salicylic acid release demonstrated a time-linear relationship in the early stages.
- Higher SA content potentially accelerated the decomposition of high molecular weight poly(D,L-Lactide).
Conclusions:
- High molecular weight poly(D,L-Lactide) exhibits predictable swelling and drug release behavior.
- The release kinetics are influenced by polymer molecular weight and drug loading.
- Poly(D,L-Lactide) shows promise for controlled drug delivery applications, with release rates tunable by molecular weight and drug content.