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一种用于表皮生长因子受体成像的新型氟-18糖基化“点击”氰基喹啉的合成。

Synthesis of a new fluorine-18 glycosylated 'click' cyanoquinoline for the imaging of epidermal growth factor receptor.

作者信息

Pisaneschi Federica, Slade Rozanna L, Iddon Lisa, George Guillaume P C, Nguyen Quang-Dé, Spivey Alan C, Aboagye Eric O

机构信息

Faculty of Medicine, Comprehensive Cancer Imaging Centre, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK; Department of Chemistry, Imperial College London, South Kensington Campus, London, SW7 2AZ, UK.

出版信息

J Labelled Comp Radiopharm. 2014 Feb;57(2):92-6. doi: 10.1002/jlcr.3170. Epub 2013 Dec 5.

Abstract

This study reports the radiosynthesis of a new fluorine-18 glycosylated 'click' cyanoquinoline [(18) F]5 for positron emission tomography imaging of epidermal growth factor receptor (EGFR). The tracer was obtained in 47.7 ± 7.5% (n = 3) decay-corrected radiochemical yield from 2-[(18) F]fluoro-2-deoxy-β-d-glucopyranosyl azide, and the overall nondecay-corrected radiochemical yield from aqueous fluoride was 8.6 ± 2.3% (n = 3). An in vitro preliminary cellular uptake study showed selectivity of the tracer for EGFR-positive A431 cell lines versus EGFR-negative MCF-7 cell lines. [(18) F]5 tracer uptake in A431 cells was significantly reduced by addition of the cold isotope analogue compound 5.

摘要

本研究报告了一种用于表皮生长因子受体(EGFR)正电子发射断层显像的新型氟-18糖基化“点击”氰基喹啉[(18)F]5的放射性合成。该示踪剂由2-[(18)F]氟-2-脱氧-β-D-吡喃葡萄糖基叠氮化物经衰变校正后的放射化学产率为47.7±7.5%(n = 3),以氟化物水溶液计,未衰变校正的总放射化学产率为8.6±2.3%(n = 3)。一项体外初步细胞摄取研究表明,该示踪剂对EGFR阳性A431细胞系相对于EGFR阴性MCF-7细胞系具有选择性。添加冷同位素类似物化合物5后,A431细胞中[(18)F]5示踪剂的摄取显著降低。

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