| Literature DB >> 27374627 |
Fang Du1, Stefan Hönzke2, Falko Neumann3, Juliane Keilitz1, Wei Chen1, Nan Ma3, Sarah Hedtrich2, Rainer Haag4.
Abstract
The topical application of drugs allows for a local application in skin disease and can reduce side effects. Here we present biodegradable core-multishell (CMS) nanocarriers which are composed of a hyperbranched polyglycerol core functionalized with diblock copolymers consisting of polycaprolactone (PCL) and poly(ethylene glycol) (mPEG) as the outer shell. The anti-inflammatory drug Dexamethasone (Dexa) was loaded into these CMS nanocarriers. DLS results suggested that Dexa loaded nanoparticles mostly act as a unimolecular carrier system. With longer PCL segments, a better transport capacity is observed. In vitro skin permeation studies showed that CMS nanocarriers could improve the Nile red penetration through the skin by up to 7 times, compared to a conventional cream formulation. Interestingly, covalently FITC-labeled CMS nanocarriers remain in the stratum corneum layer. This suggests the enhancement is due to the release of cargo after being transported into the stratum corneum by the CMS nanocarriers. In addition, the hPG-PCL-mPEG CMS nanocarriers exhibited good stability, low cytotoxicity, and their production can easily be scaled up, which makes them promising nanocarriers for topical drug delivery.Entities:
Keywords: Core-multishell (CMS) nanocarriers; Dexamethasone; Drug delivery systems; Topical application
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Year: 2016 PMID: 27374627 DOI: 10.1016/j.jconrel.2016.06.048
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776