Bratteby Klas, Denholt Charlotte Lund, Lehel Szabolcs, Petersen Ida Nymann, Madsen Jacob, Erlandsson Maria, Ohlsson Tomas, Herth Matthias Manfred, Gillings Nic
Department of Drug Design and Pharmacology, University of Copenhagen, Jagtvej 160, 2100 Copenhagen, Denmark.
Department of Clinical Physiology Nuclear Medicine PET, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.
Pharmaceuticals (Basel). 2021 Jun 22;14(7):601. doi: 10.3390/ph14070601.
In the struggle to understand and accurately diagnose Parkinson's disease, radiopharmaceuticals and medical imaging techniques have played a major role. By being able to image and quantify the dopamine transporter density, noninvasive diagnostic imaging has become the gold standard. In the shift from the first generation of SPECT tracers, the fluorine-18-labeled tracer [F]FE-PE2I has emerged as the agent of choice for many physicians. However, implementing suitable synthesis for the production of [F]FE-PE2I has proved more challenging than expected. Through a thorough analysis of the relevant factors affecting the final radiochemical yield, we were able to implement high-yielding fully automated GMP-compliant synthesis of [F]FE-PE2I on a Synthera+ platform. By reaching RCYs up to 62%, it allowed us to isolate 25 GBq of the formulated product, and an optimized formulation resulted in the shelf life of 6 h, satisfying the increased demand for this radiopharmaceutical.
在理解和准确诊断帕金森病的努力中,放射性药物和医学成像技术发挥了重要作用。通过能够对多巴胺转运体密度进行成像和量化,非侵入性诊断成像已成为金标准。在从第一代单光子发射计算机断层扫描(SPECT)示踪剂的转变过程中,氟-18标记的示踪剂[F]FE-PE2I已成为许多医生的首选药物。然而,事实证明,实施适合生产[F]FE-PE2I的合成方法比预期更具挑战性。通过对影响最终放射化学产率的相关因素进行全面分析,我们能够在Synthera+平台上实现符合药品生产质量管理规范(GMP)的[F]FE-PE2I高产率全自动合成。通过达到高达62%的放射化学产率,我们能够分离出25吉贝可(GBq)的制剂产品,并且优化的制剂使保质期达到6小时,满足了对这种放射性药物不断增长的需求。