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氟-18 标记叶酸衍生物的快速合成及其用于叶酸受体阳性肿瘤的 PET 成像的体外与体内评价。

Rapid synthesis and in vitro and in vivo evaluation of folic acid derivatives labeled with fluorine-18 for PET imaging of folate receptor-positive tumors.

机构信息

Cyclotron and Radiopharmaceuticals Department, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Kingdom of Saudi Arabia.

出版信息

Nucl Med Biol. 2011 Oct;38(7):1019-28. doi: 10.1016/j.nucmedbio.2011.03.004. Epub 2011 Jun 22.

Abstract

In an attempt to visualize folate receptors that overexpress on many cancers, [(18)F]-fluorobenzene and pyridinecarbohydrazide-folate/methotrexate conjugates ([(18)F]-1, [(18)F]-2-folates and [(18)F]-8, [(18)F]-9-MTXs) were synthesized by the nucleophilic displacement reactions using ethyl-trimethylammonium-benzoate and pyridinecarboxylate precursors. The intermediates ethyl [(18)F]-fluorinated benzene and pyridine esters were reacted with hydrazine to produce the [(18)F]-fluorobenzene and pyridinecarbohydrazides, followed by coupling with N-hydroxysuccinimide-folate/MTX. Radiochemical yields were greater than 80% (decay corrected), with total synthesis time of less than 45 min. Radiochemical purities were always greater than 97% without high-performance liquid chromatography purification. These synthetic approaches hold considerable promise as rapid and simple method for the radiofluorination of folate derivatives with high radiochemical yield in short synthesis time. In vitro tests on KB cell line showed that significant amount of the radioconjugates were associated with cell fractions, and in vivo characterization in normal Balb/c mice revealed rapid blood clearance of these radioconjugates with excretion predominantly by the urinary and partially by the hepatobiliary systems. Biodistribution studies in nude mice bearing human KB cell line xenografts demonstrated significant tumor uptake and favorable biodistribution profile for [(18)F]-2-folate over the other conjugates. The uptake in the tumors was blocked by excess coinjection of folic acid, suggesting a receptor-mediated process. Micro-positron emission tomography images of nude mice bearing human KB cell line xenografts confirmed these observations. These results demonstrate that [(18)F]-2-folate may be useful as molecular probe for detecting and staging of folate receptor-positive cancers, such as ovarian cancer and their metastasis as well as monitoring tumor response to treatment.

摘要

为了可视化许多癌症过度表达的叶酸受体,通过亲核取代反应使用乙基-三甲基铵苯甲酸酯和吡啶羧酸酯前体合成了 [(18)F]-氟苯和吡啶甲酰肼-叶酸/氨甲喋呤缀合物 [(18)F]-1、[(18)F]-2-叶酸和 [(18)F]-8、[(18)F]-9-MTXs)。中间体乙基 [(18)F]-氟化苯和吡啶酯与肼反应生成 [(18)F]-氟苯和吡啶甲酰肼,然后与 N-羟基琥珀酰亚胺-叶酸/氨甲喋呤偶联。放射性化学产率大于 80%(衰变校正),总合成时间不到 45 分钟。放射性化学纯度始终大于 97%,无需高效液相色谱纯化。这些合成方法具有很大的潜力,可作为快速简便的方法,在短时间内以高放射性化学产率对叶酸衍生物进行放射性氟化。在 KB 细胞系上的体外测试表明,大量放射性缀合物与细胞部分相关,在正常 Balb/c 小鼠中的体内表征表明,这些放射性缀合物在血液中迅速清除,主要通过泌尿系统和部分肝胆系统排泄。在携带人 KB 细胞系异种移植物的裸鼠中进行的生物分布研究表明,[(18)F]-2-叶酸的肿瘤摄取量显著,且具有良好的生物分布特征,优于其他缀合物。肿瘤摄取被过量注射的叶酸阻断,表明这是一种受体介导的过程。携带人 KB 细胞系异种移植物的裸鼠的微正电子发射断层扫描图像证实了这些观察结果。这些结果表明,[(18)F]-2-叶酸可作为检测和分期叶酸受体阳性癌症(如卵巢癌及其转移)以及监测肿瘤对治疗反应的分子探针。

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