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 inJournal of Nuclear Medicine Vol. 50; no. 6; pp. 999 - 1007
Main Authors Gore, John C, Yankeelov, Thomas E, Peterson, Todd. E, Avison, Malcolm J
Format Journal Article
LanguageEnglish
Published United States Soc Nuclear Med 01.06.2009
Society of Nuclear Medicine
Subjects
Online AccessGet full text
ISSN0161-5505
1535-5667
2159-662X
DOI10.2967/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.
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
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– 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
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  doi: 10.1016/j.rcl.2004.09.010
– ident: 2021051711590854000_50.6.999.33
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Snippet 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...
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StartPage 999
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?
URI http://jnm.snmjournals.org/cgi/content/abstract/50/6/999
https://www.ncbi.nlm.nih.gov/pubmed/19443583
https://www.proquest.com/docview/219230169
https://www.proquest.com/docview/67284535
https://pubmed.ncbi.nlm.nih.gov/PMC2719757
Volume 50
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