Radiolabelling and evaluation of novel haloethylsulfoxides as PET imaging agents for tumor hypoxia

详细信息    查看全文

• 作者：Evelyn Laurens ; Shinn Dee Yeoh ; Angela Rigopoulos ; Diana Cao ; Glenn A. Cartwright ; Graeme J. O'Keefe ; Henri J. Tochon-Danguy ; Jonathan M. White ; Andrew M. Scott ; Uwe Ackermann
• 关键词：Hypoxia ; Radiolabelling ; SK-RC-52 tumor model ; Radiotracer metabolism ; LCMS
• 刊名：Nuclear Medicine and Biology
• 出版年：2012
• 出版时间：August, 2012
• 年：2012
• 卷：39
• 期：6
• 页码：871-882
• 全文大小：478 K

文摘

The significance of imaging hypoxia with the PET ligand [¹⁸F]FMISO has been demonstrated in a variety of cancers. However, the slow kinetics of [¹⁸F]FMISO require a 2-h delay between tracer administration and patient scanning. Labelled chloroethyl sulfoxides have shown faster kinetics and higher contrast than [¹⁸F]FMISO in a rat model of ischemic stroke. However, these nitrogen mustard analogues are unsuitable for routine production and use in humans. Here we report on the synthesis and in vitro and in vivo evaluation of two novel sulfoxides which we synthesised from a single precursor molecule via either 2-[¹⁸F]fluoroethyl azide click chemistry or conventional nucleophilic displacement of a chloride leaving group. The yields of the click chemistry approach were 90¡À5 % of [¹⁸F] based on 2-[¹⁸F]fluoroethyl azide, and the yields for the S_N reaction were 15¡À5 % of [¹⁸F] based on K[¹⁸F]F. Both radiotracers underwent metabolism in an in vitro assay using S9 liver fractions with biological half-lives of 32.39 and 43.32 min, respectively. Imaging studies using an SK-RC-52 tumor model in BALB/c nude mice have revealed that only [¹⁸F] is retained in hypoxic tumors, whereas [¹⁸F] is cleared from those tumors at a rate similar to that of muscle tissue. [¹⁸F] has emerged as a promising new lead structure for further development of sulfoxide-based hypoxia imaging agents. In particular, the mechanism of uptake needs to be elucidated and changes to the chemical structure need to be made in order to reduce metabolism and improve radiotracer kinetics.