In order to enable an iCal export link, your account needs to have an API key created. This key enables other applications to access data from within Indico even when you are neither using nor logged into the Indico system yourself with the link provided. Once created, you can manage your key at any time by going to 'My Profile' and looking under the tab entitled 'HTTP API'. Further information about HTTP API keys can be found in the Indico documentation.
Additionally to having an API key associated with your account, exporting private event information requires the usage of a persistent signature. This enables API URLs which do not expire after a few minutes so while the setting is active, anyone in possession of the link provided can access the information. Due to this, it is extremely important that you keep these links private and for your use only. If you think someone else may have acquired access to a link using this key in the future, you must immediately create a new key pair on the 'My Profile' page under the 'HTTP API' and update the iCalendar links afterwards.
Permanent link for public information only:
Permanent link for all public and protected information:
Nuclear imaging and therapy in the era of precision medicine
(Paul Scherrer Institut)
C. Villi meeting room (INFN-LNL)
C. Villi meeting room
Application of tumor-seeking molecules labeled with diagnostic radionuclides is currently one of the most sensitive methodologies for the non-invasive detection of cancer in vivo. At the same time, systemic delivery of molecules radiolabeled with particle emitting radionuclides such as α-, β-- and electron-emitters allow destruction of tumor cells with minimal side-effects for the patients. The key word behind the concept is “Theragnosis” with matched-pairs of diagnostic and therapeutic radionuclides with identical or similar chemical properties.
In the recent years “new” radiometals have found their way into preclinical and clinical development because of their favorable, physical decay properties (physical half-life, mode of radioactive decay, energy rage of emitted particles etc.) compared to the current isotopes. Among the most interesting radionuclides are 43/44/47Sc, 64/67Cu and 149/152/155/161Tb. The production and rapid purification and moreover their stable and efficient incorporation into tumor targeting molecules represent a challenge for inorganic and bioinorganic chemistry. New, metal selective, and functionalized chelating systems have been developed, which form in vivo stable complexes without negatively influencing the biological behavior of the targeting molecules.
This talk will highlight the latest, innovative strategies for the production and chemical separation of new radiometals as well as the latest developments of bifunctional metal chelating systems and their chemical and bio-orthogonal incorporation into targeting molecules.