Differential internalization of brick shaped iron oxide nanoparticles by endothelial cells. Issue 35 (19th August 2016)

• Record Type: Journal Article
• Authors: Sun, Zhizhi; Worden, Matthew; Wroczynskyj, Yaroslav; Manna, Palash K.; Thliveris, James A.; van Lierop, Johan; Hegmann, Torsten; Miller, Donald W.
• Is Part Of: Journal of materials chemistry. Volume 4:Issue 35(2016)
• Page Start: 5913
• Page End: 5920
• Publication Date: 2016-08-19
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c6tb01480a
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : Nonspherical iron oxide core "nanobricks" have enhanced uptake in endothelial cells through caveolae-mediated endocytosis mechanism. Abstract : Nanoparticles targeting endothelial cells to treat diseases such as cancer, oxidative stress, and inflammation have traditionally relied on ligand–receptor based delivery. The present studies examined the influence of nanoparticle shape in regulating preferential uptake of nanoparticles in endothelial cells. Spherical and brick shaped iron oxide nanoparticles (IONPs) were synthesized with identical negatively charged surface coating. The nanobricks showed a significantly greater uptake profile in endothelial cells compared to nanospheres. Application of an external magnetic field significantly enhanced the uptake of nanobricks but not nanospheres. Transmission electron microscopy revealed differential internalization of nanobricks in endothelial cells compared to epithelial cells. Given the reduced uptake of nanobricks in endothelial cells treated with caveolin inhibitors, the increased expression of caveolin-1 in endothelial cells compared to epithelial cells, and the ability of IONP nanobricks to interfere with caveolae-mediated endocytosis process, a caveolae-mediated pathway is proposed as the mechanism for differential internalization of nanobricks in endothelial cells.