Magnetic targeting has been recently introduced to enhance cell retention in animals with acute myocardial infarction. However, it is unclear whether the magnetic accumulation of intravascular cells increases the risk of coronary embolism. Upon finite element analysis, we found that the permanent magnetic field was nonuniform, manifestated as attenuation along the vertical axis and polarisation along the horizontal axis. In the in vitro experiments, iron-labelled mesenchymal stem cells (MSCs) were accumulated in layers predominantly at the edge of the magnet. In an ischaemic rat model subjected to intracavitary MSCs injection, magnetic targeting induced unfavourable vascular embolisation and an inhomogeneous distribution of the donor cells, which prevented the enhanced cell retention from translating into additional functional benefit. These potential complications of magnetic targeting should be thoroughly investigated and overcome before clinical application.
Keywords: B; CE; Coronary artery; Embolisation; F(r); I/R; IC; MNCs; MR; MSCs; MagMSCs; Magnetic targeting; Nanoparticle; NdFeB; PLL; SPIO; SRY; Stem cell; capture efficiency; intracoronary injection; ischemia/reperfusion; magnetic field density; magnetic field gradient in r direction; magnetic force on cells in r direction; magnetic resonance; magnetically-loaded mesenchymal stem cells; mesenchymal stem cells; mononuclear cells; neodymium–iron–boron; poly-l-lysine; sex-determining region Y gene; superparamagnetic oxide nanoparticles; ∂B/∂r.
Copyright © 2013 Elsevier Ltd. All rights reserved.