Abstract

The fields of molecular biology, immunology and genetics have generated many important developments that advance the understanding of the induction and progression of oncological, cardiological and neurological diseases as well as the identification of disease-associated molecules and drugs that specifically target diseased cells during therapy. These insights have triggered the development of targeted radiopharmaceuticals which open up a new dimension of radiopharmaceutical sciences in nuclear medicine. Radiopharmaceuticals, also called radiotracers, are radiolabelled molecules, bearing a “radioactive lantern”, and used as molecular probes to address clinically relevant biological targets such as receptors, enzymes, transport systems and others. Positron emission tomography (PET) and single photon emission computed tomography (SPECT) realised in the en-vogue hybrid technologies PET/CT, SPECT/CT and PET/MRI represent the state-of-the-art diagnostic imaging technologies in nuclear medicine which are used to follow the trace of the administered radiopharmaceutical noninvasively thereby in vivo visualising and assessing biological processes at the subcellular and molecular level in a highly sensitive manner. In this connexion novel radiopharmaceuticals for the noninvasive molecular imaging of early disease states and monitoring of treatment responses in vivo by means of PET/CT, SPECT/CT and PET/MRI are indispensable prerequisites to further advance and strengthen the unique competence of radiopharmaceutical sciences. In the era of personalised medicine the diagnostic potential of radiopharmaceuticals is directly linked to a subsequent individual therapeutic approach called endoradiotherapy. Depending on the “radioactive lantern” (gamma or particle emitter) used for radiolabelling of the respective tracer molecule, the field of Radiopharmaceutical Chemistry can contribute to the set-up of an “in vivo theranostic” approach especially in tumour patients by offering tailor-made (radio)chemical entities labelled either with a diagnostic or a therapeutic radionuclide. [...]

Highlights

  • Klaus KopkaDivision of Radiopharmaceutical Chemistry, Research Program Imaging and Radiooncology, German

  • The fields of molecular biology, immunology and genetics have generated many important developments that advance the understanding of the induction and progression of oncological, cardiological and neurological diseases as well as the identification of disease-associated molecules and drugs that target diseased cells during therapy

  • These insights have triggered the development of targeted radiopharmaceuticals which open up a new dimension of radiopharmaceutical sciences in nuclear medicine

Read more

Summary

Klaus Kopka

Division of Radiopharmaceutical Chemistry, Research Program Imaging and Radiooncology, German. One contribution shows an example of a 177Lu-labelled NTS1 radioligand for endoradiotherapy of a preclinical colon tumour model and subsequent imaging of successful therapy by μPET using [68Ga]Ga-DOTA-RGD as a specific radiotracer for imaging angiogenesis (Figure 4) [8] Another attractive receptor which is important for the progression of cancer represents the epidermal growth factor receptor (EGFR). One additional representative PSMA inhibitor, CHX-A''-DTPA-DUPAPep, potentially applicable both as diagnostic and therapeutic radiopharmaceutical was radiolabelled with the PET radionuclide gallium-68 (68Ga) as well as with the beta-minus particle emitters yttrium (90Y) and lutetium-177 (177Lu) which are clinically relevant for systemic radionuclide therapy (i.e., endoradiotherapy) (Scheme 3) [12]

Cell surface bound
Kry in Buffer
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call