| Literature DB >> 29133360 |
Ryan M Williams1, Janki Shah1, Helen S Tian1, Xi Chen1, Frederic Geissmann1, Edgar A Jaimes1, Daniel A Heller2.
Abstract
Direct targeting to the kidneys is a promising strategy to improve drug therapeutic index for the treatment of kidney diseases. We sought to investigate the renal selectivity and safety of kidney-targeted mesoscale nanoparticle technology. We found that direct intravenous administration of these particles resulted in 26-fold renal selectivity and localized negligibly in the liver or other organs. The nanoparticles targeted the renal proximal tubular epithelial cells, as evidenced by intravital microscopy and ex vivo imaging. Mice treated with the nanoparticles exhibited no negative systemic consequences, immune reaction, liver impairment, or renal impairment. The localization of material selectively to the renal tubules is uncommon, and this work portends the development of renal-targeted drugs for the treatment of kidney diseases.Entities:
Keywords: biomaterials; drug carriers; kidney; nanoparticles; pharmacokinetics
Mesh:
Year: 2017 PMID: 29133360 PMCID: PMC5730475 DOI: 10.1161/HYPERTENSIONAHA.117.09843
Source DB: PubMed Journal: Hypertension ISSN: 0194-911X Impact factor: 10.190