Development of 11C-labeled CRANAD-102 for positron emission tomography imaging of soluble Aβ-species
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Development of 11C-labeled CRANAD-102 for positron emission tomography imaging of soluble Aβ-species. / Staudt, Markus; Shalgunov, Vladimir; Nedergaard, Maiken; Herth, Matthias M.
In: Journal of Labelled Compounds and Radiopharmaceuticals, Vol. 66, No. 12, 2023, p. 393-399.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Development of 11C-labeled CRANAD-102 for positron emission tomography imaging of soluble Aβ-species
AU - Staudt, Markus
AU - Shalgunov, Vladimir
AU - Nedergaard, Maiken
AU - Herth, Matthias M.
N1 - Funding information: Danmarks Frie Forskningsfond,Grant/Award Number: 2035-00077B
PY - 2023
Y1 - 2023
N2 - CRANAD-102, a selective near-infrared fluorescent tracer targeting soluble amyloid-β (Aβ) species, has recently attracted attention due to its potential to be used as a diagnostic tool for early stages of Alzheimer's disease (AD). Development of a positron emission tomography (PET) tracer based on CRANAD-102 could as such allow to noninvasively study soluble and protofibrillar species of Aβ in humans. These soluble and protofibrillar species are thought to be responsible to cause AD. Within this work, we successfully 11C-labeled CRANAD-102 via a Suzuki–Miyaura reaction in a RCС of 48 ± 9%, with a RCP of >96% and a molar activity (Am) of 25 ± 7 GBq/μmol. Future studies have to be conducted to evaluate if [11C]CRANAD-102 can be used to detect soluble protofibrils in vivo and if [11C]CRANAD-102 can be used to detect AD earlier as possible with current diagnostics.
AB - CRANAD-102, a selective near-infrared fluorescent tracer targeting soluble amyloid-β (Aβ) species, has recently attracted attention due to its potential to be used as a diagnostic tool for early stages of Alzheimer's disease (AD). Development of a positron emission tomography (PET) tracer based on CRANAD-102 could as such allow to noninvasively study soluble and protofibrillar species of Aβ in humans. These soluble and protofibrillar species are thought to be responsible to cause AD. Within this work, we successfully 11C-labeled CRANAD-102 via a Suzuki–Miyaura reaction in a RCС of 48 ± 9%, with a RCP of >96% and a molar activity (Am) of 25 ± 7 GBq/μmol. Future studies have to be conducted to evaluate if [11C]CRANAD-102 can be used to detect soluble protofibrils in vivo and if [11C]CRANAD-102 can be used to detect AD earlier as possible with current diagnostics.
KW - Alzheimer's disease
KW - amyloid beta
KW - carbon-11
KW - radiolabeling
KW - radiosynthesis
U2 - 10.1002/jlcr.4060
DO - 10.1002/jlcr.4060
M3 - Journal article
C2 - 37653688
AN - SCOPUS:85169168693
VL - 66
SP - 393
EP - 399
JO - Journal of Labelled Compounds and Radiopharmaceuticals
JF - Journal of Labelled Compounds and Radiopharmaceuticals
SN - 0362-4803
IS - 12
ER -
ID: 366507564