Getting new treatments ready for release
Molecular radiotherapy involves the administration and selective delivery of radioisotope payloads to the tumour to cause localized cell death and tumour regression. Increasing focus has been given to the development of new alpha therapies, incorporating alpha-emitting radioisotope payloads. Before new radiotherapeutics are used in clinical settings, their efficacy and behaviour in the body must be investigated extensively, following various steps laid out in a preclinical workflow.
This is achieved largely through translational imaging and developing a mechanistic understanding of material trafficking; discovering how the radiopharmaceuticals interact with, and accumulate within, different parts of the body and its biological/biochemical processes.
During radiotherapy, a targeted carrier is used to ensure the radioisotope payload arrives at the tumour site. However, many radioisotopes decay through sequential daughter isotopes, which can be ejected from the carrier, and go elsewhere in the body. This is particularly true for alpha-emitting radioisotopes with high energy emissions. As a result, to understand the complete effect of novel alpha therapies on the body, these daughter isotopes need to be identified and quantified in the bodily tissues they’ve accumulated in.
Investigating these materials is time-dependent, as some daughter isotopes decay rapidly. Therefore, the technology used for such analysis must collect and analyse results quickly, and meet the demands of the preclinical workflows to complete effective and comprehensive preclinical studies.