| Literature DB >> 28881095 |
Dmitry Gil1, Anastasia Frank-Kamenetskii1, John Barry1, Vladimir Reukov1,2, Yun Xiang1, Arabinda Das3, Abhay K Varma3,4, Mark S Kindy5, Naren L Banik3,4, Alexey Vertegel1.
Abstract
Polymeric nanoparticles have been extensively studied as drug delivery vehicles both in vitro and in vivo for the last two decades. In vitro methods to assess drug release profiles usually utilize degradation of nanoparticles in aqueous medium, followed by the measurement of the concentration of the released drug. This method, however, is difficult to use for drugs that are poorly water soluble. In this study, a protocol for measuring drug release kinetic using albumin solution as the medium is described. Albumin is a major blood transport protein, which mediates transport of many lipid soluble compounds including fatty acids, hormones, and bilirubin. The use of a dialysis-based system utilizing albumin dialysate solution allows hydrophobic drug release from a diverse set of drug delivery modalities is demonstrated. The method using liposomes and PLGA nanoparticles as drug carriers, and two model hydrophobic drugs, 17β-estradiol, and dexamethasone is validated.Entities:
Keywords: albumin; drug release; liposomes; membrane dialysis; nanoparticles
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Year: 2017 PMID: 28881095 DOI: 10.1002/biot.201700337
Source DB: PubMed Journal: Biotechnol J ISSN: 1860-6768 Impact factor: 4.677