Enhancing the Stability of 211At Radiopharmaceuticals: Insights from Ortho-Substituent Strategies
Year: 2025
Type: editorial
Abstract: High Resolution Image Download MS PowerPoint Slide Astatine-211 ( 211 At) is a promising alpha-emitting radionuclide for targeted alpha therapy (TAT), delivering high linear energy transfer (LET) and a short radiation range, making it ideal for cancer treatment while minimizing damage to surrounding healthy tissue. This viewpoint highlights recent advancements in the development of astatine-211 compounds for TAT, with a focus on the role of neighboring substituents in enhancing in vivo stability. By mitigating deastatination, these structural modifications improve radiopharmaceutical integrity, paving the way for more effective and clinically viable 211 At-based radiopharmaceuticals.
Source: ACS Medicinal Chemistry Letters
Authors: Taoqian Zhao, Steven H. Liang
Institution: Emory University
Language: English
Subfield: Radiology, Nuclear Medicine and Imaging
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4408665437
