Seminars in Nuclear Medicine
Volume 38, Issue 1 , Pages 20-31, January 2008

Radiopharmaceuticals for Renal Positron Emission Tomography Imaging

  • Zsolt Szabo, MD, PhD

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Zsolt Szabo, MD, PhD, Russell H. Morgan Department of Radiology and Radiological Sciences, Division of Nuclear Medicine, The Johns Hopkins Medical Institutions, 601 N Caroline St, Room # JHOC 3233, Baltimore, MD 21287.
  • ,
  • Jinsong Xia, MD, PhD
  • ,
  • William B. Mathews, PhD

Russell H. Morgan Department of Radiology and Radiological Sciences, Division of Nuclear Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Radiopharmaceuticals for functional renal imaging, including renal blood flow, renal blood volume, glomerular excretion, and metabolism have been available for some time. This review outlines radiopharmaceuticals for functional renal imaging as well as those that target pertinent molecular constituents of renal injury and repair. The angiotensin and endothelin receptors are particularly appealing molecular targets for renal imaging because of their association with renal physiology and pathology. Other targets such as the vascular endothelial growth factor (VEGF) receptor, integrin, or phosphatidylserine have been investigated at length for cancer imaging, but they are just as important constituents of the renal injury/repair process. Various diseases can involve identical mechanisms, such as angiogenesis and apoptosis, and radiopharmaceuticals developed for these processes in other organs can also be used for renal imaging. The sensitivity and spatial resolution of positron emission tomography makes it an ideal tool for molecular and functional kidney imaging. Radiopharmaceutical development for the kidneys must focus on achieving high target selectivity and binding affinity, stability and slow metabolism in vivo, and minimal nonspecific accumulation and urinary excretion.

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 The research related to this publication has been supported by NIH grants DK-50,183 and CA-115532 and by a grant from the Center for Biological Modulators/KRICT Korea.

PII: S0001-2998(07)00114-6

doi:10.1053/j.semnuclmed.2007.09.008

Seminars in Nuclear Medicine
Volume 38, Issue 1 , Pages 20-31, January 2008