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Nanomedicine (Lond) ; 12(20): 2503-2517, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28882086

ABSTRACT

AIM: To improve the in vivo delivery of gold nanorods (GNRs) to the central nervous system of rats, these gold nanoparticles were conjugated to Angiopep-2, a shuttle peptide that can cross the blood-brain barrier. MATERIALS & METHODS: GNRs were synthesized and modified using polyethylene glycol and Angiopep-2 (GNR-PEG-Angiopep-2). The physicochemical properties, in vitro cytotoxicity and ex vivo biodistribution of the conjugate were examined. RESULTS: GNR-PEG-Angiopep-2 was stable over the following days, and the different concentrations that were tested did not affect the viability of microvascular endothelial cells. The conjugation of Angiopep-2 to GNRs enhanced the endocytosis of these particles (in vitro) and the accumulation in brains (in vivo), when compared with GNRs modified only with PEG. CONCLUSION: This study provides evidence that Angiopep-2 improves the delivery of GNRs to the brain parenchyma. This property is highly relevant for future applications of GNRs as platforms for photothermal and theranostic purposes.


Subject(s)
Central Nervous System/drug effects , Gold/chemistry , Nanotubes/chemistry , Peptides/chemistry , Peptides/pharmacology , Animals , Biological Transport , Blood-Brain Barrier/metabolism , Brain/metabolism , Cell Survival , Drug Carriers/chemistry , Drug Liberation , Endothelial Cells , Fluorescent Dyes/chemistry , Humans , Male , Microscopy, Electron, Transmission/methods , Optical Imaging/methods , Particle Size , Peptides/toxicity , Permeability , Polyethylene Glycols/chemistry , Rats , Rats, Sprague-Dawley , Surface Properties , Tissue Distribution
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