| Literature DB >> 16884807 |
Miechel L T Zweers1, Gerard H M Engbers, Dirk W Grijpma, Jan Feijen.
Abstract
Dexamethasone- or rapamycin-loaded nanoparticles based on poly(ethylene oxide) and poly(dl-lactic-co-glycolic acid) block copolymers (PEO-PLGA) were prepared without additional stabilizer using the salting-out method. A fast release of drug in PBS (pH 7.4) at 37 degrees C resulting in 100% release within 5 h was observed for both drugs. The rate of drug release was substantially reduced by treating the particles with gelatin or albumin after drug loading, resulting in a linear drug release in time. It was shown that the rate of drug release is related to the amount of protein associated with the nanoparticles. After gelatin treatment of drug-loaded nanoparticles, sustained release of dexamethasone for 17 days and of rapamycin for 50 days could be achieved.Entities:
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Year: 2006 PMID: 16884807 DOI: 10.1016/j.jconrel.2006.05.021
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776