Molecular Imaging Without Radiopharmaceuticals?
The limitations on the sensitivity for detecting small changes in MRI, CT, and ultrasound pulse-echo images are used to estimate the practical requirements for molecular imaging and targeted contrast enhancement for these modalities. These types of imaging are highly unlikely to approach the sensiti...
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Published in | Journal of Nuclear Medicine Vol. 50; no. 6; pp. 999 - 1007 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Soc Nuclear Med
01.06.2009
Society of Nuclear Medicine |
Subjects | |
Online Access | Get full text |
ISSN | 0161-5505 1535-5667 2159-662X |
DOI | 10.2967/jnumed.108.059576 |
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Abstract | The limitations on the sensitivity for detecting small changes in MRI, CT, and ultrasound pulse-echo images are used to estimate the practical requirements for molecular imaging and targeted contrast enhancement for these modalities. These types of imaging are highly unlikely to approach the sensitivity for detecting molecular processes of radionuclear methods, and the prospects for achieving sufficient concentrations of appropriate agents in vivo are poor for several types of applications such as small-molecule targeting of specific receptors. However, using relatively large carrier systems such as particles and liposomes, sufficient concentrations of paramagnetic agents may be delivered to achieve MR-signal changes adequate for detection. The use of higher-resolution MR images will aid the prospects for molecular imaging in small animals. Theoretic considerations also predict that a similar approach, using rather large particles or carriers of materials with a high atomic number, may also be successful for CT, especially with additional developments such as the use of monochromatic x-rays. The prospects of molecular imaging by x-ray imaging may not be as bleak as has been predicted. For ultrasound detection, gas-filled bubbles can provide a sufficient backscattered sound intensity to be detectable at concentrations and sizes not much different from agents designed for these other modalities. |
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AbstractList | The limitations on the sensitivity for detecting small changes in MRI, CT, and ultrasound pulse-echo images are used to estimate the practical requirements for molecular imaging and targeted contrast enhancement for these modalities. These types of imaging are highly unlikely to approach the sensitivity for detecting molecular processes of radionuclear methods, and the prospects for achieving sufficient concentrations of appropriate agents in vivo are poor for several types of applications such as small-molecule targeting of specific receptors. However, using relatively large carrier systems such as particles and liposomes, sufficient concentrations of paramagnetic agents may be delivered to achieve MR-signal changes adequate for detection. The use of higher-resolution MR images will aid the prospects for molecular imaging in small animals. Theoretic considerations also predict that a similar approach, using rather large particles or carriers of materials with a high atomic number, may also be successful for CT, especially with additional developments such as the use of monochromatic x-rays. The prospects of molecular imaging by x-ray imaging may not be as bleak as has been predicted. For ultrasound detection, gas-filled bubbles can provide a sufficient backscattered sound intensity to be detectable at concentrations and sizes not much different from agents designed for these other modalities. The limitations on the sensitivity for detecting small changes in MRI, CT, and ultrasound pulse-echo images are used to estimate the practical requirements for molecular imaging and targeted contrast enhancement for these modalities. These types of imaging are highly unlikely to approach the sensitivity for detecting molecular processes of radionuclear methods, and the prospects for achieving sufficient concentrations of appropriate agents in vivo are poor for several types of applications such as small-molecule targeting of specific receptors. However, using relatively large carrier systems such as particles and liposomes, sufficient concentrations of paramagnetic agents may be delivered to achieve MR-signal changes adequate for detection. The use of higher-resolution MR images will aid the prospects for molecular imaging in small animals. Theoretic considerations also predict that a similar approach, using rather large particles or carriers of materials with a high atomic number, may also be successful for CT, especially with additional developments such as the use of monochromatic x-rays. The prospects of molecular imaging by x-ray imaging may not be as bleak as has been predicted. For ultrasound detection, gas-filled bubbles can provide a sufficient backscattered sound intensity to be detectable at concentrations and sizes not much different from agents designed for these other modalities.The limitations on the sensitivity for detecting small changes in MRI, CT, and ultrasound pulse-echo images are used to estimate the practical requirements for molecular imaging and targeted contrast enhancement for these modalities. These types of imaging are highly unlikely to approach the sensitivity for detecting molecular processes of radionuclear methods, and the prospects for achieving sufficient concentrations of appropriate agents in vivo are poor for several types of applications such as small-molecule targeting of specific receptors. However, using relatively large carrier systems such as particles and liposomes, sufficient concentrations of paramagnetic agents may be delivered to achieve MR-signal changes adequate for detection. The use of higher-resolution MR images will aid the prospects for molecular imaging in small animals. Theoretic considerations also predict that a similar approach, using rather large particles or carriers of materials with a high atomic number, may also be successful for CT, especially with additional developments such as the use of monochromatic x-rays. The prospects of molecular imaging by x-ray imaging may not be as bleak as has been predicted. For ultrasound detection, gas-filled bubbles can provide a sufficient backscattered sound intensity to be detectable at concentrations and sizes not much different from agents designed for these other modalities. The limitations on the sensitivity for detecting small changes in MRI, CT, and ultrasound pulse-echo images are used to estimate the practical requirements for molecular imaging and targeted contrast enhancement for these modalities. These types of imaging are highly unlikely to approach the sensitivity for detecting molecular processes of radionuclear methods, and the prospects for achieving sufficient concentrations of appropriate agents in vivo are poor for several types of applications such as small-molecule targeting of specific receptors. However, using relatively large carrier systems such as particles and liposomes, sufficient concentrations of paramagnetic agents may be delivered to achieve MR-signal changes adequate for detection. The use of higher-resolution MR images will aid the prospects for molecular imaging in small animals. Theoretic considerations also predict that a similar approach, using rather large particles or carriers of materials with a high atomic number, may also be successful for CT, especially with additional developments such as the use of monochromatic x-rays. The prospects of molecular imaging by x-ray imaging may not be as bleak as has been predicted. For ultrasound detection, gas-filled bubbles can provide a sufficient backscattered sound intensity to be detectable at concentrations and sizes not much different from agents designed for these other modalities. [PUBLICATION ABSTRACT] |
Author | Yankeelov, Thomas E Avison, Malcolm J Peterson, Todd. E Gore, John C |
AuthorAffiliation | 1 Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee 8 Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 6 Department of Cancer Biology, Vanderbilt University, Nashville, Tennessee 3 Department of Physics and Astronomy, Vanderbilt University, Nashville, Tennessee 2 Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, Tennessee 4 Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 5 Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee 7 Department of Neurology, Vanderbilt University, Nashville, Tennessee |
AuthorAffiliation_xml | – name: 6 Department of Cancer Biology, Vanderbilt University, Nashville, Tennessee – name: 1 Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee – name: 2 Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, Tennessee – name: 3 Department of Physics and Astronomy, Vanderbilt University, Nashville, Tennessee – name: 5 Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee – name: 4 Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee – name: 8 Department of Pharmacology, Vanderbilt University, Nashville, Tennessee – name: 7 Department of Neurology, Vanderbilt University, Nashville, Tennessee |
Author_xml | – sequence: 1 fullname: Gore, John C – sequence: 2 fullname: Yankeelov, Thomas E – sequence: 3 fullname: Peterson, Todd. E – sequence: 4 fullname: Avison, Malcolm J |
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Cites_doi | 10.1002/mrm.1910090205 10.1002/jcb.10632 10.1016/S0079-6565(97)00014-9 10.1016/j.jmr.2007.01.017 10.1517/17425247.4.2.149 10.2174/187152007780618135 10.1088/0031-9155/51/17/012 10.1158/0008-5472.CAN-08-0749 10.1021/ar020228m 10.1148/radiol.2463070471 10.2741/2796 10.1002/jmri.20970 10.1088/0031-9155/23/6/014 10.1007/s00330-003-1912-x 10.1101/gad.1047403 10.1039/b509907m 10.1002/mrm.21256 10.1038/sj.bmt.1701439 10.1148/radiology.199.3.8638019 10.1021/ja8001293 10.1073/pnas.1733836100 10.1038/ncpcardio0659 10.1088/0031-9155/22/2/011 10.1146/annurev.bioeng.9.060906.151929 10.1002/mrm.21145 10.1038/370199a0 10.1002/jcb.10660 10.1016/j.mri.2007.11.002 10.1016/j.rcl.2004.09.010 |
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SubjectTerms | Diagnostic Imaging - methods Human subjects Humans Magnetic Resonance Imaging - methods Medical imaging Methods Molecular biology Molecules Nanoparticles Nuclear medicine Protons Radiopharmaceuticals Studies Success Tomography, X-Ray Computed - methods Ultrasonography - methods |
Title | Molecular Imaging Without Radiopharmaceuticals? |
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