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
  • [1] Performance evaluation of the whole-body PET scanner ECAT EXACT HR+ following the IEC standard
    Adam, LE
    Zaers, J
    Ostertag, H
    Trojan, H
    Bellemann, ME
    Brix, G
    [J]. IEEE TRANSACTIONS ON NUCLEAR SCIENCE, 1997, 44 (03) : 1172 - 1179
  • [2] Beanlands R, 1996, CAN J CARDIOL, V12, P875
  • [3] Cardiac positron emission tomography
    Bergmann, SR
    [J]. SEMINARS IN NUCLEAR MEDICINE, 1998, 28 (04) : 320 - 340
  • [4] Cerebral hyperglycolysis following severe traumatic brain injury in humans: A positron emission tomography study
    Bergsneider, M
    Hovda, DA
    Shalmon, E
    Kelly, DF
    Vespa, PM
    Martin, NA
    Phelps, ME
    McArthur, DL
    Caron, MJ
    Kraus, JF
    Becker, DP
    [J]. JOURNAL OF NEUROSURGERY, 1997, 86 (02) : 241 - 251
  • [5] Beyer T, 2000, J NUCL MED, V41, P1369
  • [6] THE DESIGN AND PHYSICAL CHARACTERISTICS OF A SMALL ANIMAL POSITRON EMISSION TOMOGRAPH
    BLOOMFIELD, PM
    RAJESWARAN, S
    SPINKS, TJ
    HUME, SP
    MYERS, R
    ASHWORTH, S
    CLIFFORD, KM
    JONES, WF
    BYARS, LG
    YOUNG, J
    ANDREACO, M
    WILLIAMS, CW
    LAMMERTSMA, AA
    JONES, T
    [J]. PHYSICS IN MEDICINE AND BIOLOGY, 1995, 40 (06) : 1105 - 1126
  • [7] Brooks DJ, 1997, BAILLIERE CLIN NEUR, V6, P69
  • [8] PET instrumentation: What are the limits?
    Budinger, TF
    [J]. SEMINARS IN NUCLEAR MEDICINE, 1998, 28 (03) : 247 - 267
  • [9] Positron emission tomography neuroreceptor imaging as a tool in drug discovery, research and development
    Burns, HD
    Hamill, TG
    Eng, W
    Francis, B
    Fioravanti, C
    Gibson, RE
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (04) : 388 - 394
  • [10] Chatziioannou AF, 1999, J NUCL MED, V40, P1164