| Literature DB >> 32475681 |
Abstract
Rapid imaging acquisition, high spatial resolution and sensitivity, powered by advancements in solid-state detector technology, are significantly changing the perspective of single photon emission tomography (SPECT). In particular, this evolutionary step is fueling a rediscovery of technetium-99m, a still unique radionuclide within the nuclear medicine scenario because of its ideal nuclear properties and easy preparation of its radiopharmaceuticals that does not require a costly infrastructure and complex procedures. Scope of this review is to show that the arsenal of technetium-99m radiopharmaceuticals is already equipped with imaging agents that may complement and integrate the role played by analogous tracers developed for positron emission tomography (PET). These include, in particular, somatostatin (SST) and prostate-specific membrane antigen (PSMA) receptor targeting agents, and a number of peptide-derived radiopharmaceuticals. Additionally, these recent technological developments, combined with new myocardial perfusion tracers having more favorable biodistribution and pharmacokinetic properties as compared to current commercial agents, may also reinvigorate the prevailing position still hold by technetium-99m radiopharmaceuticals in nuclear cardiology.Entities:
Keywords: Peptide radiopharmaceuticals; Prostate specific membrane antigen; Radiopharmaceuticals; SPECT myocardial perfusion imaging agents; Solid-state detectors; Somatostatin receptors; Technetium; Technetium-99m PSMA radiopharmaceuticals; Technetium-99m radiopharmaceuticals; Ultrafast SPECT cameras
Year: 2020 PMID: 32475681 DOI: 10.1016/j.nucmedbio.2020.05.005
Source DB: PubMed Journal: Nucl Med Biol ISSN: 0969-8051 Impact factor: 2.408