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Thermoacoustic molecular tomography with magnetic nanoparticle contrast agents for targeted tumor detection

Source: Med. Phys. 37, 4193 (2010); doi:10.1118/1.3466696

Published 21 July 2010

KEYWORDS and PACS
Keywords
PACS
  • 87.63.dh
    Ultrasonographic medical imaging
  • 87.85.Rs
    Nanotechnologies - applications in biomedical engineering
  • 87.64.M-
    Optical microscopy in biophysics and medical physics
  • YEAR: 2010
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PUBLICATION DATA
ISSN:
1553-9628 (online)
Publisher:
AIP is a member of CrossRef AAPM
Liming Nie, Zhongmin Ou, Sihua Yang, and Da Xing
MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, South China Normal University, Guangzhou 510631, China and College of Biophotonics, South China Normal University, Guangzhou 510631, China
Purpose: The primary feasibility steps of demonstrating the ability of microwave-induced thermoacoustic (TA) in phantoms have been previously reported. However, none were shown to target a diseased site in living subjects in thermoacoustic tomography (TAT) field so far. To determine the expressions of oncogenic surface molecules, it is quite necessary to image tumor lesions and acquire pathogenic status on them via TAT.Methods: Compared to biological tissues, iron oxide nanoparticles have a much higher microwave absorbance. Fe3O4/polyaniline (PANI) nanoparticles were prepared via polymerization of aniline in the Fe3O4 superparamagnetic fluids. Then Fe3O4/PANI was conjugated to folic acid (FA), which can bind specifically to the surface of the folate receptor used as a tumor marker. FA-Fe3O4/PANI targeted tumor was irradiated by pulsed microwave at 6 GHz for thermoacoustic detection and imaging.Results: The effect of the Fe3O4/PANI superparamagnetic nanoparticles for enhancing TAT images was successfully investigated in ex vivo human blood and in vivo mouse tail. Intravenous administration of the targeted nanoparticles to mice bearing tumors showed fivefold greater thermoacoustic signal and much longer elimination time than that of mice injected with nontargeted nanoparticles in the tumor. The specific targeting ability of FA-Fe3O4/PANI to tumor was also verified on fluorescence microscopy.Conclusions: Fabricated iron oxide nanoparticles conjugated with tumor ligands for targeted TAT tumor detection at the molecular level was reported for the first time. The results indicate that thermoacoustic molecular imaging with functionalized iron oxide nanoparticles may contribute to targeted and functional early cancer imaging. Also, the modified iron oxide nanoparticles combined with suitable tumor markers may also be used as novel nanomaterials for targeted and guided cancer thermal therapy. ©2010 American Association of Physicists in Medicine
History: Received 13 November 2009; revised 30 June 2010; accepted 30 June 2010; published 21 July 2010
Permalink: http://dx.doi.org/10.1118/1.3466696

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