| Literature DB >> 26198385 |
Maria Gregori1, Daniela Bertani2, Emanuela Cazzaniga3, Antonina Orlando3, Michele Mauri2, Alberto Bianchi2, Francesca Re3, Silvia Sesana3, Stefania Minniti3, Maura Francolini4, Alfredo Cagnotto5, Mario Salmona5, Luca Nardo3, Domenico Salerno3, Francesco Mantegazza3, Massimo Masserini3, Roberto Simonutti2.
Abstract
In the search of new drug delivery carriers for the brain, self-assembled nanoparticles (NP) were prepared from poly(N,N-dimethylacrylamide)-block-polystyrene polymer. NP displayed biocompatibility on cultured endothelial cells, macrophages and differentiated SH-SY5Y neuronal-like cells. The surface-functionalization of NP with a modified fragment of human Apolipoprotein E (mApoE) enhanced the uptake of NP by cultured human brain capillary endothelial cells, as assessed by confocal microscopy, and their permeability through a Transwell Blood Brain Barrier model made with the same cells, as assessed by fluorescence. Finally, mApoE-NP embedding doxorubicin displayed an enhanced release of drug at low pH, suggesting the potential use of these NP for the treatment of brain tumors.Entities:
Keywords: blood-brain barrier; controlled drug release; copolymers; drug delivery; nanoparticles
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Year: 2015 PMID: 26198385 DOI: 10.1002/mabi.201500172
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979