scholarly journals Targeted Nanoparticles for Cardiovascular Molecular Imaging

2013 ◽  
Vol 1 (3) ◽  
pp. 191-204 ◽  
Author(s):  
Gustav J. Strijkers
Circulation ◽  
2008 ◽  
Vol 118 (suppl_18) ◽  
Author(s):  
Hoon Sim ◽  
Anne Neubauer ◽  
Shelton Caruthers ◽  
Gregory Lanza ◽  
Samuel Wickline ◽  
...  

Cardiovascular molecular imaging with targeted nanoparticles has emerged as a promising method for early detection of atherosclerosis and vulnerable plaque. However, traditional pharmacokinetic models for diffusible drugs are inadequate to describe the efficacy of nanoparticle carriers of diagnostic and therapeutic cargos. To quantify blood and MRI tissue signals from gadolinium-loaded nanoparticles (Gd-NP) targeted to avb3 integrins expressed on angiogenic capillaries in the aortas of cholesterol-fed rabbit, a novel 4 compartment open PK model was developed that utilized a unique simultaneous fitting scheme. In 10 rabbits fed 0.25% cholesterol for 3 months, the concentration of nanoparticles was measured serially from blood samples after injection of 1 ml/kg of targeted or nontargeted Gd-NP. The MRI proton signatures emanating from nanoparticles bound to the expanded vasa vasorum of the descending thoracic aorta was computed for all aortic cross sections in 1.5T T1w fa-suppressed spin-echo images. Based on the PK analysis, the concentration of targeted nanoparticles in the aortic wall is double that of non-targeted nanoparticles. Notably, this signal enhancement is achieved with 20x less gadolinium (4.6x10 −3 mmol Gd/kg BW) as compared with the dose of conventional gadolinium agents (0.1 mmol/kg). Further, the PK analysis shows that the targeted nanoparticles are more than three times more effective at reaching the aortic wall. These results should facilitate development and use of nanotechnologies intended for early detection of atherosclerosis and provide enhanced understanding of the kinetics and mechanisms of active targeting of plaque angiogenesis.


2012 ◽  
Vol 53 (5) ◽  
pp. 673-676 ◽  
Author(s):  
M. D. Majmudar ◽  
M. Nahrendorf

2009 ◽  
Vol 2 (1) ◽  
pp. 56-70 ◽  
Author(s):  
Matthias Nahrendorf ◽  
David E. Sosnovik ◽  
Brent A. French ◽  
Filip K. Swirski ◽  
Frank Bengel ◽  
...  

Author(s):  
Alan R. Morrison ◽  
Joseph C. Wu ◽  
Mehran M. Sadeghi

Cardiovascular molecular imaging is a relatively young but rapidly expanding discipline that consists of a biologically-targeted approach to the assessment of physiologic and pathologic processes in vivo. This novel approach to imaging involves the integration of multiple disciplines such as cell and molecular biology, chemistry, and imaging sciences. The ultimate goal is quantitative assessment of cardiovascular processes at the cellular and molecular level, moving beyond traditional diagnostic information, in order to guide individually tailored therapy. In fact, it is likely that specific approaches to molecular imaging will be developed in tandem with the development of novel therapeutic strategies. Recent advances in probe development and imaging systems have contributed to evolution of molecular imaging toward clinical translational. These include technological progress in traditional imaging platforms; along with the emergence of newer imaging modalities such as photoacoustic imaging. In addition, hybrid imaging (e.g. nuclear imaging with CT or MRI) has the potential for improved spatial localization, and more accurate quantification by coupling anatomic and biological information. In addition to potential clinical applications that address existing diagnostic gaps in cardiovascular medicine, molecular imaging allows for unique approaches to studying pathophysiology. This chapter is intended to provide an overview of the state of the art in cardiovascular molecular imaging, highlighting how it may improve the management of major cardiovascular diseases.


2009 ◽  
Vol 7 (1) ◽  
pp. 38-47 ◽  
Author(s):  
Lawrence W. Dobrucki ◽  
Albert J. Sinusas

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