Iron oxide nanoparticle-containing microbubble composites as contrast agents for MR and ultrasound dual-modality imaging

被引:149
作者
Liu, Zhe [1 ]
Lammers, Twan [1 ]
Ehling, Josef [1 ,2 ]
Fokong, Stanley [1 ]
Bornemann, Joerg [3 ]
Kiessling, Fabian [1 ]
Gaetjens, Jessica [1 ]
机构
[1] Rhein Westfal TH Aachen, Fac Med, Helmholtz Inst Biomed Engn, Dept Expt Mol Imaging ExMI, D-52074 Aachen, Germany
[2] Univ Hosp Aachen UKA, Inst Pathol, D-52074 Aachen, Germany
[3] Univ Hosp Aachen UKA, Elect Microscop Facil, D-52074 Aachen, Germany
关键词
Nanoparticle; MRI (magnetic resonance imaging); Contrast agent; Polymerization; Molecular imaging; CYANOACRYLATE NANOPARTICLES; MAGNETIC NANOPARTICLES; IN-VITRO; DELIVERY; GENE;
D O I
10.1016/j.biomaterials.2011.05.019
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Magnetic resonance (MR) and ultrasound (US) imaging are widely used diagnostic modalities for various experimental and clinical applications. In this study, iron oxide nanoparticle-embedded polymeric microbubbles were designed as multi-modal contrast agents for hybrid MR US imaging. These magnetic nano-in-micro imaging probes were prepared via a one-pot emulsion polymerization to form poly(butyl cyanoacrylate) microbubbles, along with the oil-in-water (O/W) encapsulation of iron oxide nanoparticles in the bubble shell. The nano-in-micro embedding strategy was validated using NMR and electron microscopy. These hybrid imaging agents exhibited strong contrast in US and an increased transversal relaxation rate in MR. Moreover, a significant increase in longitudinal and transversal relaxivities was observed after US-induced bubble destruction, which demonstrated triggerable MR imaging properties. Proof-of-principle in vivo experiments confirmed that these nanoparticle-embedded microbubble composites are suitable contrast agents for both MR and US imaging. In summary, these magnetic nano-in-micro hybrid materials are highly interesting systems for bimodal MR US imaging, and their enhanced relaxivities upon US-induced destruction recommend them as potential vehicles for MR-guided US-mediated drug and gene delivery. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6155 / 6163
页数:9
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