| Literature DB >> 24706613 |
Lena Figge1, Franziska Appler, Howard H Chen, David E Sosnovik, Jörg Schnorr, Oliver Seitz, Matthias Taupitz, Bernd Hamm, Eyk Schellenberger.
Abstract
Annexin A5 (Anx) has been extensively used for imaging apoptosis by single-photon emission computed tomography, positron emission tomography, optical imaging and MRI. Recently we introduced ultrasmall Anx-VSOP (very small iron oxide particles)--the smallest high-relaxivity probe for MRI of apoptosis. Here we present a simplified method for the direct coupling of Anx to VSOP, which resulted in nanoparticles that are nearly completely covered with human Anx. These superparamagnetic nanoparticles are only 14.4 ± 2.3 nm in diameter and have higher T2* relaxivity. Compared with existing probes, the small size and the Anx shielding provide prerequisites for good biocompatibility and bioavailability in target tissues. In vitro characterization showed specific binding of Anx-VSOP to apoptotic cells, which led to a signal loss in T2*-weighted MR measurements, while control probe M1324-VSOP produced no such change. Exploratory MRI was done in vivo in a cardiac model of ischemia-reperfusion damage illustrating the potential of the probe for future studies.Entities:
Keywords: Annexin A5; VSOP; apoptosis; magnetic resonance imaging; very small iron oxide particles
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Year: 2014 PMID: 24706613 DOI: 10.1002/cmmi.1575
Source DB: PubMed Journal: Contrast Media Mol Imaging ISSN: 1555-4309 Impact factor: 3.161