Alzheimer's disease (AD) is a neurodegenerative disorder with increasing global prevalence and accounts for over half of all dementia cases. Early diagnosis is paramount for not only the management of the disease, but also for the development of new AD treatments. The current golden standard for diagnosis is performed by positron emission tomography (PET) scans with the tracer [C]Pittsburg Compound B ([C]PiB), which targets amyloid beta protein (A) that builds up as plaques in the brain of AD patients. The increasing demand for AD diagnostics is in turn expected to drive an increase in [C]PiB-PET scans and the setup of new [C]PiB production lines at PET centers globally. Here, we present the [C]PiB production setups, experiences, and use from four Danish PET facilities and discuss the challenges and potential pitfalls of [C]PiB production. We report on the [C]PiB production performed with the 6-OH-BTA-0 precursor dissolved in either dry acetone or 2-butanone and by using either [C]CO or [C]CH as C- precursors on three different commercial synthesis modules: TracerLab FX C Pro, ScanSys, or TracerMaker. It was found that the [C]CO method gives the highest radioactive yield (1.5 to 3.2 GBq vs. 0.8 ± 0.3 GBq), while the highest molar activity (98.0 ± 61.4 GBq/μmol vs. 21.2 to 95.6 GBq/μmol) was achieved using [C]CH. [C]PiB production with [C]CO on a TracerLab FX C Pro offered the most desirable results, with the highest yield of 3.17 ± 1.20 GBq and good molar activity of 95.6 ± 44.2 GBq/μmol. Moreover, all reported methods produced [C]PiB in quantities suitable for clinical applications, thus providing a foundation for other PET facilities seeking to establish their own [C]PiB production.
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http://dx.doi.org/10.3390/ph17020217 | DOI Listing |
A successful positron emission tomography imaging program involving carbon-11 radiotracers demands fast, efficient, and reliable synthesis methods, requiring an on-site cyclotron and radiochemistry group, as well as clinical staff trained to operate under the unique constraints of the carbon-11 radionuclide. This study examines the merits and advantages of a captive solvent 'loop method' of radiolabeling four tracers with the carbon-11 radionuclide, producing the radioligands [C]ER-176, [C]MRB, [C]mHED, and [C]PiB. The 'loop method' is compared against the traditional reactor-based method of carbon-11 methylation in the course of synthesizing the same radiotracers on the identical automated platform.
View Article and Find Full Text PDFAm J Nucl Med Mol Imaging
February 2024
Translational Imaging Program, Wake Forest School of Medicine Winston-Salem, NC 27157, USA.
Because carbon-11 (C) 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, C-labeled Pittsburgh compound B ([C]PiB) has been the gold standard PET radiotracer for imaging of amyloid β (Aβ) 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.
View Article and Find Full Text PDFCurr Radiopharm
July 2024
Department of Nuclear Medicine, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.
Aim: Efficient synthesis of precursor from commercially available starting materials and automated radiosynthesis of [C]PiB using commercially available dedicated [C]- Chemistry module from the synthesized precursor.
Background: [C]PiB is a promising radiotracer for PET imaging of β-Amyloid, advancing Alzheimer's disease research. The availability of precursors and protocols for efficient radiolabelling foster the applications of any radiotracer.
Pharmaceuticals (Basel)
February 2024
Department of Nuclear Medicine, Copenhagen University Hospital, Herlev and Gentofte, Borgmester Ib Juuls Vej 1, 2730 Herlev, Denmark.
Alzheimer's disease (AD) is a neurodegenerative disorder with increasing global prevalence and accounts for over half of all dementia cases. Early diagnosis is paramount for not only the management of the disease, but also for the development of new AD treatments. The current golden standard for diagnosis is performed by positron emission tomography (PET) scans with the tracer [C]Pittsburg Compound B ([C]PiB), which targets amyloid beta protein (A) that builds up as plaques in the brain of AD patients.
View Article and Find Full Text PDFActa Neuropathol Commun
February 2024
Department of Public Health and Caring Sciences, Geriatrics, Uppsala University, Uppsala, Sweden.
Deposition of amyloid beta (Aβ) into plaques is a major hallmark of Alzheimer's disease (AD). Different amyloid precursor protein (APP) mutations cause early-onset AD by altering the production or aggregation properties of Aβ. We recently identified the Uppsala APP mutation (APPUpp), which causes Aβ pathology by a triple mechanism: increased β-secretase and altered α-secretase APP cleavage, leading to increased formation of a unique Aβ conformer that rapidly aggregates and deposits in the brain.
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