Search results for "positron emitter"

showing 5 items of 5 documents

68Ga-BPAMD: PET-imaging of bone metastases with a generator based positron emitter

2012

Abstract Purpose Bone metastases are a serious aggravation for patients suffering from cancer. Therefore, early recognition of bone metastases is of great interest for further treatment of patients. Bisphosphonates are widely used for scintigraphy of bone lesions with 99m Tc. Using the 68 Ge/ 68 Ga generator together with a macroyclic bisphosphonate a comparable PET-tracer comes into focus. Procedures The bisphosphonate DOTA-conjugated ligand BPAMD was labelled with 68 Ga. [ 68 Ga]BPAMD was evaluated in vitro concerning binding to hydroxyapatite and stability. The tracer's in vivo accumulation was determined on healthy rats and bone metastases bearing animals by μ-PET. Results BPAMD was lab…

MaleCancer Researchmedicine.medical_treatmentBone NeoplasmsElectronsGallium RadioisotopesScintigraphyHeterocyclic Compounds 1-RingIn vivoCell Line TumormedicineAnimalsRadiology Nuclear Medicine and imagingRadiochemistryDiphosphonatesmedicine.diagnostic_testbusiness.industryChemistryPositron emittersCancerPet imagingBisphosphonateLigand (biochemistry)medicine.diseaseRatsDurapatiteBone lesionPositron-Emission TomographyMolecular MedicineNuclear medicinebusinessNuclear Medicine and Biology
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Impact of prompt gamma emission of 44Sc on quantification in preclinical and clinical PET systems

2021

Abstract 44Sc is an increasingly investigated positron emitter for use in positron emission tomography (PET) imaging. However, 44Sc is a non-pure positron emitter, since prompt photons are co-emitted during the decay process. This study investigates coincidence energy spectra of 44Sc and its impact on PET quantification on a preclinical and clinical PET system in comparison with 18F. The raw data of the coincidence events revealed characteristic differences comparing the photon energy distribution of 44Sc and 18F. Due to prompt gamma emission of 44Sc, activity recovery is underestimated on PET systems. However, clinical PET imaging of 44Sc with acceptable quantitative accuracy appears feasi…

RadiationMaterials sciencemedicine.diagnostic_testAstrophysics::High Energy Astrophysical PhenomenaPhysics::Medical PhysicsPositron emittersGamma rayPet imagingPhoton energy010403 inorganic & nuclear chemistry01 natural sciencesQuantitative accuracyCoincidence030218 nuclear medicine & medical imaging0104 chemical sciences03 medical and health sciences0302 clinical medicineNuclear magnetic resonancePositron emission tomographymedicinePhysics::Accelerator PhysicsPet quantificationApplied Radiation and Isotopes
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72/74As-labeling of HPMA based polymers for long-term in vivo PET imaging

2010

Abstract In the context of molecular imaging, various polymers based on the clinically approved N-(2-hydroxypropyl)-methacrylamide (HPMA) have been radio-labeled using longer-living positron emitters 72As t1/2 = 26 h or 74As t1/2 = 17.8 d. This approach may lead to non-invasive determination of the long-term in vivo fate of polymers by PET (positron emission tomography). Presumably, the radio label itself will not strongly influence the polymer structure due to the fact that the used nuclide binds to already existing thiol moieties within the polymer structure. Thus, the use of additional charges or bulky groups can be avoided.

Time FactorsClinical BiochemistryPharmaceutical ScienceContext (language use)BiochemistryArsenicIn vivoDrug DiscoveryPolymer chemistrymedicineMolecular BiologyRadioisotopeschemistry.chemical_classificationAcrylamidesmedicine.diagnostic_testOrganic ChemistryArsenic isotopePositron emittersPolymerPet imagingchemistryPositron emission tomographyPositron-Emission TomographyBiophysicsMolecular MedicineMolecular imagingBioorganic & Medicinal Chemistry Letters
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Post-Processing via Cation Exchange Cartridges: Versatile Options

2012

New 68Ge/68Ga radionuclide generators provide the positron emitter 68Ga (T½ = 67.7 min) as an easily available and relatively inexpensive source of a PET nuclide for labeling of interesting targeting vectors. However, currently available “ionic” 68Ge/68Ga radionuclide generators are not necessarily optimized for the routine synthesis of 68Ga-labeled radiopharmaceuticals in a clinical environment. Post-processing of 68Ge/68Ga generators using cation exchange resins provides chemically and radiochemically pure 68Ga with 97±2% within less than 4 min, with 68Ge almost completely removed, and ready for online labeling. This simple, fast, and efficient technology can be extended for new applicati…

chemistry.chemical_compoundCartridgechemistryRadiochemistrySynthonAcetonePositron emittersIonic bondingRadionuclide GeneratorIon-exchange resin
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Radiolabeling of Nanoparticles and Polymers for PET Imaging

2014

Nanomedicine has become an emerging field in imaging and therapy of malignancies. Nanodimensional drug delivery systems have already been used in the clinic, as carriers for sensitive chemotherapeutics or highly toxic substances. In addition, those nanodimensional structures are further able to carry and deliver radionuclides. In the development process, non-invasive imaging by means of positron emission tomography (PET) represents an ideal tool for investigations of pharmacological profiles and to find the optimal nanodimensional architecture of the aimed-at drug delivery system. Furthermore, in a personalized therapy approach, molecular imaging modalities are essential for patient screeni…

radiolabelingmedicine.medical_specialtyPharmaceutical ScienceNanoparticlelcsh:Medicinelcsh:RS1-441NanotechnologyReviewlcsh:Pharmacy and materia medicaDrug DiscoverymedicineMedical physicsPersonalized therapypolymersmedicine.diagnostic_testbusiness.industrylcsh:RPositron emittersimagingPet imagingnanomedicinepositron emitterPETPositron emission tomographyDrug deliverydrug deliveryMolecular MedicineNanomedicinenanoparticlesMolecular imagingbusinessPharmaceuticals
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