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Published online on March 4, 2008, 10.1073/pnas.0711622105
PNAS | March 11, 2008 | vol. 105 | no. 10 | 3705-3710
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PHYSICAL SCIENCES / BIOLOGICAL SCIENCES / ENGINEERING / MEDICAL SCIENCES
Simultaneous in vivo positron emission tomography and magnetic resonance imaging

Ciprian Catana*,{dagger}, Daniel Procissi{ddagger}, Yibao Wu*, Martin S. Judenhofer§, Jinyi Qi*, Bernd J. Pichler§, Russell E. Jacobs{ddagger}, and Simon R. Cherry*

*Department of Biomedical Engineering, University of California, Genome and Biomedical Sciences Facility, 451 East Health Sciences Drive, Davis, CA 95616; {ddagger}Beckman Institute, California Institute of Technology, MC 139-74, 1200 East California Boulevard, Pasadena, CA 91125; and §Department of Radiology, Laboratory for Preclinical Imaging and Imaging Technology, University of Tübingen, Roentgenweg 11, 72076 Tübingen, Germany

Communicated by Michael E. Phelps, University of California School of Medicine, Los Angeles, CA, December 11, 2007 (received for review May 15, 2007)

Positron emission tomography (PET) and magnetic resonance imaging (MRI) are widely used in vivo imaging technologies with both clinical and biomedical research applications. The strengths of MRI include high-resolution, high-contrast morphologic imaging of soft tissues; the ability to image physiologic parameters such as diffusion and changes in oxygenation level resulting from neuronal stimulation; and the measurement of metabolites using chemical shift imaging. PET images the distribution of biologically targeted radiotracers with high sensitivity, but images generally lack anatomic context and are of lower spatial resolution. Integration of these technologies permits the acquisition of temporally correlated data showing the distribution of PET radiotracers and MRI contrast agents or MR-detectable metabolites, with registration to the underlying anatomy. An MRI-compatible PET scanner has been built for biomedical research applications that allows data from both modalities to be acquired simultaneously. Experiments demonstrate no effect of the MRI system on the spatial resolution of the PET system and <10% reduction in the fraction of radioactive decay events detected by the PET scanner inside the MRI. The signal-to-noise ratio and uniformity of the MR images, with the exception of one particular pulse sequence, were little affected by the presence of the PET scanner. In vivo simultaneous PET and MRI studies were performed in mice. Proof-of-principle in vivo MR spectroscopy and functional MRI experiments were also demonstrated with the combined scanner.

molecular imaging | small animal imaging | multimodality imaging


Freely available online through the PNAS open access option.

Author contributions: C.C., D.P., Y.W., M.S.J., B.J.P., R.E.J., and S.R.C. designed research; C.C., D.P., and Y.W. performed research; J.Q. contributed new reagents/analytic tools; C.C., D.P., Y.W., M.S.J., J.Q., B.J.P., R.E.J., and S.R.C. analyzed data; and C.C. wrote the paper.

The authors declare no conflict of interest.

This article contains supporting information online at www.pnas.org/cgi/content/full/0711622105/DC1.

{dagger}To whom correspondence should be addressed at: Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Building 149, Room 2301, 13th Street, Charlestown, MA 02129. E-mail: ccatana{at}nmr.mgh.harvard.edu

© 2008 by The National Academy of Sciences of the USA


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