Fundamentals of positron emission tomography and applications in preclinical drug development

被引:113
作者
Cherry, SR
机构
[1] Univ Calif Los Angeles, Sch Med, Crump Inst Mol Imaging, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
关键词
D O I
10.1177/00912700122010357
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Positron emission tomography (PET) is a nuclear imaging technique that can dynamically image trace amounts of positron-labeled radiopharmaceuticals in vivo. Tracer concentrations can be determined quantitatively, and by application of appropriate tracer kinetic models, the rates of a wide range of different biological processes can be measured noninvasively in humans. PET has been used as a research tool for more than 25 years and has also found clinical applications, particularly in oncology, neurological disorders, and cardiovascular disease. Recently, there has been tremendous interest in applying PET technology to in vivo small-animal imaging. Significant improvements in the imaging technology now permit a wide range of PET studies in mice and rats, using compact, relatively low-cost, dedicated small-animal PET scanners. This article reviews the fundamental basis of PET imaging and discusses the development of small-animal PET scanners and their possible application in preclinical drug development. (C) 2001 the American College of Clinical Pharmacology.
引用
收藏
页码:482 / 491
页数:10
相关论文
共 56 条
  • [31] Initial results from the Sherbrooke avalanche photodiode positron tomograph
    Lecomte, R
    Cadorette, J
    Rodrigue, S
    Lapointe, D
    Rouleau, D
    Bentourkia, M
    Yao, R
    Msaki, P
    [J]. IEEE TRANSACTIONS ON NUCLEAR SCIENCE, 1996, 43 (03) : 1952 - 1957
  • [32] Investigation of the performance of the general electric ADVANCE positron emission tomograph in 3D mode.
    Lewellen, TK
    Kohlmyer, SG
    Miyaoka, RS
    Kaplan, MS
    [J]. IEEE TRANSACTIONS ON NUCLEAR SCIENCE, 1996, 43 (04) : 2199 - 2206
  • [33] Repetitive, non-invasive imaging of the dopamine D2 receptor as a reporter gene in living animals
    MacLaren, DC
    Gambhir, SS
    Satyamurthy, N
    Barrio, JR
    Sharfstein, S
    Toyokuni, T
    Wu, L
    Berk, AJ
    Cherry, SR
    Phelps, ME
    Herschman, HR
    [J]. GENE THERAPY, 1999, 6 (05) : 785 - 791
  • [34] MARRIOTT CJ, 1994, J NUCL MED, V35, P1390
  • [35] The state of positron emitting radionuclide production in 1997
    McCarthy, TJ
    Wetch, MJ
    [J]. SEMINARS IN NUCLEAR MEDICINE, 1998, 28 (03) : 235 - 246
  • [36] Mielke R, 1998, J NEURAL TRANSM-SUPP, P237
  • [37] Quantitative assessment of longitudinal metabolic changes in vivo after traumatic brain injury in the adult rat using FDG-MicroPET
    Moore, AH
    Osteen, CL
    Chatziioannou, AF
    Hovda, DA
    Cherry, SR
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (10) : 1492 - 1501
  • [38] The role of positron emission tomography in the drug development of M100907, a putative antipsychotic with a novel mechanism of action
    Offord, SJ
    Wong, DF
    Nyberg, S
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 39 : 17S - 24S
  • [39] OLLINGER J, 1997, IEEE SIGNAL PROC MAG, P43
  • [40] PHELPS ME, 1986, POSITRON EMISSION TO