| Literature DB >> 12615416 |
Giuseppe De Rosa1, Amélie Bochot, Fabiana Quaglia, Madeleine Besnard, Elias Fattal.
Abstract
Microspheres for the controlled release of an antisense oligonucleotide against the Transforming growth factor beta(1) were designed. Free oligonucleotide or its solid complexes with polyethylenimine (PEI) at different nitrogen/phosphate (N/P) ratios, were encapsulated within poly(lactide-co-glycolide) (PLGA) microspheres prepared by the multiple emulsion-solvent evaporation technique. The encapsulation of the oligonucleotide in form of solid complexes, the N/P ratio, as well as the PLGA type affected microspheres characteristics in term of loading, morphology, oligonucleotide distribution inside matrix and in vitro release profile. The designed microspheres allow the encapsulation and slow release of oligonucleotide/PEI solid complexes that should be effectively internalized inside cells. Copyright 2002 Elsevier Science B.V.Entities:
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Year: 2003 PMID: 12615416 DOI: 10.1016/s0378-5173(02)00689-0
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875