ABSTRACT
Polymers of lactic and glycolic acid are often used for the production of injectible microparticles with controlled drug release. In the variety of processes used for the microparticle formulation, the Aerosol Solvent Extraction System (ASES) is rather special. Microparticle formation and drying take place in one step by precipitating a methylene chloride solution of the polymer in supercritical CO2. This process sets special requirements to the polymers in crystallinity, solubility, and thermal behavior that are best fulfilled by blocked copolymers. This study investigates a number of lactide-co-glycolide polymers with blocked distribution of the co-monomers by NMR spectroscopy and powder diffraction. The molar ratios are determined by 1H-NMR spectroscopy to verify the manufacturer's declarations of the purchased specimens. Additionally, the block length is determined by application of 13C-NMR. Therefore, a method reported in the literature was modified and evaluated in order to calculate the length of lactide and glycolide sequences in the polymer. Furthermore, this study looks at the impact of synthesis conditions on block length and crystallinity, and the impact of the blocking on both, crystallinity and solubility of the polymers.
Subject(s)
Biocompatible Materials/chemistry , Lactic Acid/chemistry , Polyglycolic Acid/chemistry , Polymers , Drug Carriers , Nuclear Magnetic Resonance, Biomolecular , Structure-Activity RelationshipABSTRACT
The Aerosol Solvent Extraction System (ASES) process uses supercritical carbon dioxide for the production of microparticles. Since the critical temperature for this gas is at 304 K, polymers that are used in this process must fulfil certain requirements in crystallinity, and thermal behavior. This can be achieved by the use of blocked copolymers and thus the presence of semicrystalline microdomains in the polymers. However, changing the sequences of the comonomers dilactide and lactide often leads to polymers of low solubility due to long glycolide blocks. In this study, the critical properties of two blocked co-polymers were investigated, such as the blocked structure itself by (1)H-NMR and (13)C-NMR, the thermal behavior by differential scanning calorimetry (DSC), and the crystallinity by powder diffraction. The impact of these properties on microparticles formed by those polymers was also object of these studies. Additionally, two different model drugs, albumin and estriolm were embedded to investigate the impact of different polymer properties on drug content and release.