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Fluorine-18: Radiochemistry and Target-Specific PET Molecular Probes Design [PDF]

open access: yesFrontiers in Chemistry, 2022
The positron emission tomography (PET) molecular imaging technology has gained universal value as a critical tool for assessing biological and biochemical processes in living subjects.
Yunze Wang   +11 more
doaj   +3 more sources

Preparation of Fluorine-18 [PDF]

open access: bronzeJournal of Nuclear Science and Technology, 1964
Fluorine-18 was prepared by neutron irradiation of lithium carbonate in the reactor JRR-1. Five grams of lithium carbonate was irradiated for 2hr with a thermal neutron flux of 6×1011 n/cm2/sec. An alumina column was used to separate 18F from the irradiated material.
Eiji Shikata
openalex   +3 more sources

Isotopic Radiolabeling of Crizotinib with Fluorine-18 for In Vivo Pet Imaging [PDF]

open access: yesPharmaceuticals, 2022
Crizotinib is a tyrosine kinase inhibitor approved for the treatment of non-small-cell lung cancer, but it is inefficient on brain metastases. Crizotinib is a substrate of the P-glycoprotein, and non-invasive nuclear imaging can be used to assess the ...
Malvika Sardana   +14 more
doaj   +2 more sources

Synthesis and Evaluation of Fluorine-18-Labeled L-Rhamnose Derivatives [PDF]

open access: yesMolecules, 2023
The use of radiolabeled glucose for PET imaging resulted in the most commonly used tracer in the clinic, 2-deoxy-2-[18F]fluoroglucose (FDG). More recently, other radiolabeled sugars have been reported for various applications, including imaging tumors ...
Xiang Zhang   +9 more
doaj   +2 more sources

Fluorine-18 Labelled Radioligands for PET Imaging of Cyclooxygenase-2 [PDF]

open access: yesMolecules, 2022
Molecular imaging probes enable the early and accurate detection of disease-specific biomarkers and facilitate personalized treatment of many chronic diseases, including cancer.
Jatinder Kaur   +2 more
doaj   +2 more sources

Fluorine-18 Radiochemistry, Labeling Strategies and Synthetic Routes [PDF]

open access: yesBioconjugate Chemistry, 2014
Fluorine-18 is the most frequently used radioisotope in positron emission tomography (PET) radiopharmaceuticals in both clinical and preclinical research.
Orit Jacobson   +2 more
semanticscholar   +4 more sources

Sulfonium Salts as Leaving Groups for Aromatic Labelling of Drug-like Small Molecules with Fluorine-18 [PDF]

open access: goldScientific Reports, 2015
Positron emission tomography (PET) is unique in that it allows quantification of biochemical processes in vivo, but difficulties with preparing suitably labelled radiotracers limit its scientific and diagnostic applications. Aromatic [18F]fluorination of
Kerstin Sander   +6 more
openalex   +2 more sources

Recent Trends in Bioorthogonal Click-Radiolabeling Reactions Using Fluorine-18

open access: yesMolecules, 2013
The increasing application of positron emission tomography (PET) in nuclear medicine has stimulated the extensive development of a multitude of novel and versatile bioorthogonal conjugation techniques especially for the radiolabeling of biologically ...
Doreen Pietzsch   +2 more
doaj   +2 more sources

Performance of Positron Emission Tomography and Positron Emission Tomography/Computed Tomography Using Fluorine-18-Fluorodeoxyglucose for the Diagnosis, Staging, and Recurrence Assessment of Bone Sarcoma

open access: goldMedicine, 2015
To investigate the performance of fluorine-18-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) and PET/computed tomography (CT) in the diagnosis, staging, restaging, and recurrence surveillance of bone sarcoma by systematically reviewing ...
Fanxiao Liu   +8 more
openalex   +2 more sources

Fluorine-18 isotope scans of the sacroiliac joints. [PDF]

open access: bronzeAnnals of the Rheumatic Diseases, 1972
J. Webb   +3 more
openalex   +4 more sources

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