Two decades of [11C]PiB synthesis, 2003-2023: a review

被引:2
|
作者
Myburgh, Paul Josef [1 ]
Sai, Kiran Kumar Solingapuram [1 ,2 ]
机构
[1] Wake Forest Sch Med, Translat Imaging Program, Winston Salem, NC 27157 USA
[2] Wake Forest Sch Med, Dept Radiol, Winston Salem, NC 27157 USA
关键词
Alzheimer's disease (AD); positron emission tomography (PET); 11; C-tracer; 11C]PiB; clinical radiochemistry; ALZHEIMERS-DISEASE; A-BETA; AMYLOID DEPOSITION; COMPOUND-B; NEUROPATHOLOGIC ASSESSMENT; QUALITY-CONTROL; WHITE-MATTER; PET; RADIOSYNTHESIS; C-11-PIB;
D O I
10.62347/ADSK6584
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Because carbon-11 (11C) radiotracers cannot be shipped over long distances, their use in routine positron emission tomography (PET) studies is dependent on the production capabilities of individual radiochemistry laboratories. Since 2003, 11 C-labeled Pittsburgh compound B ([11C]PiB) has been the gold standard PET radiotracer for in vivo imaging of amyloid [3 (A[3) plaques. For more than two decades, researchers have been working to develop faster, higher-yielding, more robust, and optimized production methods with higher radiochemical yields for various imaging applications. This review evaluates progress in [11C]PiB radiochemistry. An introductory overview assesses how it has been applied in clinical neurologic imaging research. We examine the varying approaches reported for radiolabeling, purification, extraction, and formulation. Further considerations for QC methods, regulatory considerations, and optimizations were also discussed.
引用
收藏
页码:48 / 62
页数:15
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