Abstract
A new biodegradable polyanhydride copolymer, poly[bis(p-carboxyphenoxy)butane-sebacicacid] [poly(CPB:SA)], was synthesised using modified melt polycondensation. Microspheres
made using the new polyanhydride copolymers were prepared using a modified double emulsion, solvent evaporation technique using a model protein, bovine serum albumin (BSA) at a 10% w/w
theoretical load. The degradation studies of the polymers and microspheres were carried out in
PBS, with shaking, at 37°C and monitored using gel permeation chromatography (GPC), IR
spectroscopy and scanning electron microscopy (SEM). Water penetration and anhydride bond cleavage (polymer degradation) occurred rapidly (< 5 days) compared to the time scale of overall microsphere erosion (weeks to months) with different polymer compositions. Subsequent to bond cleavage, the ultimate erosion of the microsphere and release of entrapped BSA was due mainly
to the slow dissolution of the individual hydrophobic monomers (CPB and SA) from the
microsphere surface. This surface erosion mechanism leads to predictable drug release rates
which may be appropriate for the delivery of many protein therapeutics, especially vaccine
antigens. Protein release rates could be adjusted by changing monomer composition ratios. Due to the fast degradation of anhydride bonds relative to microsphere erosion, initial polymer molecular weight did not have a significant effect on macromolecule release rates. Instead, protein release rates from polymers of identical composition could be varied by changing the
amount of protein encapsulated.
Date of Award | Jun 2000 |
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Original language | English |
Awarding Institution |
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Keywords
- Biodegradable polyanhydride microspheres
- SynEncapsulation of proteins.