Kondo Yuto, Kimura Hiroyuki, Sasaki Minon, Koike Sumina, Yagi Yusuke, Hattori Yasunao, Kawashima Hidekazu, Yasui Hiroyuki
Department of Analytical and Bioinorganic Chemistry, Division of Analytical and Physical Sciences, Kyoto Pharmaceutical University, 5 Nakauchi-cho, Misasagi, Yamashina-ku, Kyoto 607-8414, Japan.
Department of Radiological Technology, Faculty of Medicinal Science, Kyoto College of Medical Science, 1-3 Imakita, Oyama-higashi, Sonobe, Nantan, Kyoto 622-0022, Japan.
ACS Omega. 2023 Jun 27;8(27):24418-24425. doi: 10.1021/acsomega.3c01974. eCollection 2023 Jul 11.
Direct radioiodination of peptides using copper-mediated iododeboronation is a promising radiosynthetic method for solving issues of classical direct radiolabeling, such as toxicity of the organotin precursor (iododestannylation) or formation of radio byproducts (by electrophilic iodination of a tyrosine residue). However, the parameters for optimizing the reaction conditions for various peptides are not completely understood. In particular, considering peptide solubility, the effects of water-containing solvents on labeling efficiency should be thoroughly investigated. Herein, we describe the effect of water on copper-mediated radioiododeboronation and the key factors for ensuring the successful radiolabeling of small molecules and peptides in water-organic solvents. I-labeled substrates containing peptides ([I]/-IBTA) were obtained with high radiochemical conversions (RCCs: >95%) using an alcohol solvent, and a decrease in these RCCs was observed with increasing water content in the methanol solvent. Additionally, when using water-methanol solvents, a difference in RCC due to the substituent effect was also observed. However, the RCCs can be improved without the use of other additives by adjusting the copper catalyst and time of the labeling reaction or by utilizing substituent effects. This study contributes to the improvement of the design of boronic peptide precursors and radiolabeling protocols using copper-mediated iododeboronation.
使用铜介导的碘脱硼反应对肽进行直接放射性碘化是一种很有前景的放射性合成方法,可解决传统直接放射性标记的问题,如有机锡前体的毒性(碘脱锡反应)或放射性副产物的形成(通过酪氨酸残基的亲电碘化)。然而,各种肽的反应条件优化参数尚未完全明确。特别是,考虑到肽的溶解性,含水性溶剂对标记效率的影响应进行深入研究。在此,我们描述了水对铜介导的放射性碘脱硼反应的影响,以及在水 - 有机溶剂中确保小分子和肽成功进行放射性标记的关键因素。使用醇类溶剂可获得具有高放射化学转化率(RCCs:>95%)的含肽碘标记底物([I]/-IBTA),且在甲醇溶剂中随着水含量增加,这些RCCs会降低。此外,使用水 - 甲醇溶剂时,由于取代基效应也观察到RCCs存在差异。然而,通过调整铜催化剂和标记反应时间或利用取代基效应,无需使用其他添加剂即可提高RCCs。本研究有助于改进使用铜介导的碘脱硼反应的硼酸肽前体设计和放射性标记方案。