| Literature DB >> 27697619 |
Hannah Pischon1, Moritz Radbruch1, Anja Ostrowski1, Pierre Volz2, Christian Gerecke3, Michael Unbehauen4, Stefan Hönzke5, Sarah Hedtrich5, Joachim W Fluhr6, Rainer Haag4, Burkhard Kleuser3, Ulrike Alexiev2, Achim D Gruber1, Lars Mundhenk7.
Abstract
Inflammatory disorders of the skin pose particular therapeutic challenges due to complex structural and functional alterations of the skin barrier. Penetration of several anti-inflammatory drugs is particularly problematic in psoriasis, a common dermatitis condition with epidermal hyperplasia and hyperkeratosis. Here, we tested in vivo dermal penetration and biological effects of dendritic core-multishell-nanocarriers (CMS) in a murine skin model of psoriasis and compared it to healthy skin. In both groups, CMS exclusively localized to the stratum corneum of the epidermis with only very sporadic uptake by Langerhans cells. Furthermore, penetration into the viable epidermis of nile red as a model for lipophilic compounds was enhanced by CMS. CMS proved fully biocompatible in several in vitro assays and on normal and psoriatic mouse skin. The observations support the concept of CMS as promising candidates for drug delivery in inflammatory hyperkeratotic skin disorders in vivo.Entities:
Keywords: CMS; FLIM; Fluorescence microscopy; Mouse model; Nile red
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Year: 2016 PMID: 27697619 DOI: 10.1016/j.nano.2016.09.004
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307