Background:The main goal of the study was to find the magnetic resonance imaging (MRI) parameters that optimize contrast between tissue and thermal lesions produced by focused ultrasound (FUS) using T1-weighted (T1-W) and T2-weighted (T2-W) fast spin echo (FSE) sequences.Methods:FUS sonications were performed in ex vivo porcine tissue using a single-element FUS transducer of 2.6 MHz in 1.5 and 3 T MRI scanners. The difference in relaxation times as well as the impact of critical MRI parameters on the resultant contrast-to-noise ratio (CNR) between coagulated and normal tissues were assessed. Discrete and overlapping lesions were inflicted in tissue with simultaneous acquisition of T2-W FSE images.Results:FUS lesions are characterized by lower relaxation times than intact porcine tissue. CNR values above 80 were sufficient for proper lesion visualization. For T1-W imaging, repetition time values close to 1500 ms were considered optimum for obtaining sufficiently high CNR at the minimum time cost. Echo time values close to 50 ms offered the maximum lesion contrast in T2-W FSE imaging. Monitoring of acute FUS lesions during grid sonications was performed successfully. Lesions appeared as hypointense spots with excellent contrast from surrounding tissue.Conclusion:MRI monitoring of signal intensity changes during FUS sonication in grid patterns using optimized sequence parameters can provide useful information about lesion progression and the success of ablation. This preliminary study demonstrated the feasibility of the proposed monitoring method in ex vivo porcine tissue and should be supported by in vivo studies to assess its clinical potential.
机构:
Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Calif Nano Syst Inst CNSI, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Deng, Tian
Zhang, Le
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiol Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Zhang, Le
Li, Xinzhou
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiol Sci, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Li, Xinzhou
Zink, Jeffrey, I
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Univ Calif Los Angeles, Calif Nano Syst Inst CNSI, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiol Sci, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Zink, Jeffrey, I
Wu, Holden H.
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Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Calif Nano Syst Inst CNSI, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
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Toronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, CanadaToronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, Canada
Nguyen, Michael
Zhao, Na
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Toronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, CanadaToronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, Canada
Zhao, Na
Xu, Yuan
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Toronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, CanadaToronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, Canada
Xu, Yuan
Tavakkoli, Jahangir
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Toronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, Canada
St Michaels Hosp, Inst Biomed Engn Sci & Technol iBEST, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada
KHE 332C,350 Victoria St, Toronto, ON M5B 2K3, CanadaToronto Metropolitan Univ, Dept Phys, 350 Victoria St, Toronto, ON, Canada