Journal of Lipid Research (May 2012)

OxLDL-targeted iron oxide nanoparticles for in vivo MRI detection of perivascular carotid collar induced atherosclerotic lesions in ApoE-deficient mice

  • Song Wen (文颂),
  • Dong-Fang Liu (柳东芳),
  • Zhen Liu (刘振),
  • Steven Harris,
  • Yu-Yu Yao (姚玉宇),
  • Qi Ding (丁琪),
  • Fang Nie (聂芳),
  • Tong Lu (卢瞳),
  • Hua-Jun Chen (陈华俊),
  • Yan-Li An (安艳丽),
  • Feng-Chao Zang (臧凤超),
  • Gao-Jun Teng (滕皋军)

Journal volume & issue
Vol. 53, no. 5
pp. 829 – 838

Abstract

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Atherosclerotic disease is a leading cause of morbidity and mortality in developed countries, and oxidized LDL (OxLDL) plays a key role in the formation, rupture, and subsequent thrombus formation in atherosclerotic plaques. In the current study, anti-mouse OxLDL polyclonal antibody and nonspecific IgG antibody were conjugated to polyethylene glycol-coated ultrasmall superparamagnetic iron oxide (USPIO) nanoparticles, and a carotid perivascular collar model in apolipoprotein E-deficient mice was imaged at 7.0 Tesla MRI before contrast administration and at 8 h and 24 h after injection of 30 mg Fe/kg. The results showed MRI signal loss in the carotid atherosclerotic lesions after administration of targeted anti-OxLDL-USPIO at 8 h and 24 h, which is consistent with the presence of the nanoparticles in the lesions. Immunohistochemistry confirmed the colocalization of the OxLDL/macrophages and iron oxide nanoparticles. The nonspecific IgG-USPIO, unconjugated USPIO nanoparticles, and competitive inhibition groups had limited signal changes (p < 0.05). This report shows that anti-OxLDL-USPIO nanoparticles can be used to directly detect OxLDL and image atherosclerotic lesions within 24 h of nanoparticle administration and suggests a strategy for the therapeutic evaluation of atherosclerotic plaques in vivo.

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