A Novel Biodegradable System Based on Gelatin Nanoparticles and Poly(lactic-co-glycolic acid) Microspheres for Protein and Peptide Drug Delivery
- 1 August 1997
- journal article
- Published by American Geophysical Union (AGU) in Journal of Pharmaceutical Sciences
- Vol. 86 (8), 891-895
- https://doi.org/10.1021/js970084i
Abstract
Gelatin nanoparticle-poly(lactic-co-glycolic acid) (PLGA) microsphere composites were prepared by encapsulating protein-loaded gelatin nanoparticles in PLGA microspheres. This encapsulation was conducted by using a phase separation method and a solvent extraction method. The average diameter of the gelatin nanoparticle-PLGA microsphere composites is between 160 and 175 microm. Protein loading efficiency is 93.2% for the nanoparticle-microsphere composite prepared by the phase separation method, while it is 31.31% for the composite prepared by the solvent extraction method. Protein release experiments indicate that this new composite system possesses sustained release characteristics. This system also demonstrates the capability of preventing the denaturation of protein drugs.Keywords
This publication has 12 references indexed in Scilit:
- Kinetics of insulin aggregation in aqueous solutions upon agitation in the presence of hydrophobic surfaces.Proceedings of the National Academy of Sciences, 1991
- In vivo peptide release from poly(dl-lactic acid-co-glycolic acid) copolymerJournal of Controlled Release, 1991
- Factors influencing the profiles of TRH release from copoly(d,l-lactic/glycolic acid) microspheresInternational Journal of Pharmaceutics, 1991
- Controlled Delivery Systems for Proteins Based on Poly(Lactic/Glycolic Acid) MicrospheresPharmaceutical Research, 1991
- Release of Human Serum Albumin from Poly(lactide-co-glycolide) MicrospheresPharmaceutical Research, 1990
- Synthesis of Gelatin Microspheres Containing InterferonPharmaceutical Research, 1989
- In vivo release profiles of leuprolide acetate from microcapsules prepared with polylactic acids or copoly(lactic/glycolic) acids and in vivo degradation of these polymers.CHEMICAL & PHARMACEUTICAL BULLETIN, 1988
- An explanation for the controlled release of macromolecules from polymersJournal of Controlled Release, 1985
- Controlled Release of Polypeptides and Other MacromoleculesPharmaceutical Research, 1984
- Morphological changes of ethylene/vinyl acetate-based controlled delivery systems during release of water-soluble solutesJournal of Membrane Science, 1983