Chin Frederick T, Namavari Mohammed, Levi Jelena, Subbarayan Murugesan, Ray Pritha, Chen Xiaoyuan, Gambhir Sanjiv S
Molecular Imaging Program at Stanford, Department of Radiology, Stanford University School of Medicine, Stanford, CA 94305-5484, USA.
Mol Imaging Biol. 2008 Mar-Apr;10(2):82-91. doi: 10.1007/s11307-007-0122-3. Epub 2007 Dec 22.
2'-deoxy-2'-[(18)F]fluoro-5-ethyl-1-beta-D-arabinofuranosyluracil ([(18)F]FEAU) is a promising radiolabeled nucleoside designed to monitor Herpes Simplex Virus Type 1 thymidine kinase (HSV1-tk) reporter gene expression with positron emission tomography (PET). However, the challenging radiosynthesis creates problems for being able to provide [(18)F]FEAU routinely. We have developed a routine method using a commercial GE TRACERlab FX-FN radiosynthesis module with customized equipment to provide [(18)F]FEAU. All radiochemical yields are decay corrected to end-of-bombardment and reported as means +/- SD. Radiofluorination (33 +/- 8%; n = 4), bromination (85 +/- 8%; n = 4), coupling reaction (83 +/- 6%; n = 4), base hydrolysis steps, and subsequent high-performance liquid chromatography purification afforded purified [(18)F]FEAU beta-anomer in 5 +/- 1% overall yield (n = 3 runs) after approximately 5.5 h and a beta/alpha-anomer ratio of 7.4. Radiochemical/chemical purities and specific activity exceeded 99% and 1.3 Ci/micromol (48 GBq/micromol), respectively. In cell culture, [(18)F]FEAU showed significantly (P < 0.05) higher accumulation in C6 cells expressing HSV1-tk/sr39tk as compared to wild-type C6 cells. Furthermore, [(18)F]FEAU showed slightly higher accumulation than 9-[4-[(18)F]fluoro-3-(hydroxymethyl)butylguanine ([(18)F]FHBG) in cells expressing HSV1-tk (P < 0.05), whereas [(18)F]FHBG showed significantly higher (P < 0.05) accumulation than [(18)F]FEAU in HSV1-sr39tk-expressing cells. micro-PET imaging of mice carrying tumor xenografts of C6 cells stably expressing HSV1-tk or HSV1-sr39tk are consistent with the cell uptake results. The [(18)F]FEAU mouse images also showed very low gastrointestinal signal with predominant renal clearance as compared to [(18)F]FHBG. The routine radiosynthesis of [(18)F]FEAU was successfully semiautomated using a commercial module along with customized equipment to provide the beta-anomer in modest yields. Although further studies are needed, early results also suggest [(18)F]FEAU is a promising PET radiotracer for monitoring HSV1-tk reporter gene expression.
2'-脱氧-2'-[(18)F]氟-5-乙基-1-β-D-阿拉伯呋喃糖基尿嘧啶([(18)F]FEAU)是一种很有前景的放射性标记核苷,旨在通过正电子发射断层扫描(PET)监测单纯疱疹病毒1型胸苷激酶(HSV1-tk)报告基因的表达。然而,具有挑战性的放射性合成给常规提供[(18)F]FEAU带来了问题。我们开发了一种常规方法,使用配备定制设备的商用GE TRACERlab FX-FN放射性合成模块来提供[(18)F]FEAU。所有放射化学产率均经衰变校正至轰击结束,并以平均值±标准差报告。放射性氟化(33±8%;n = 4)、溴化(85±8%;n = 4)、偶联反应(83±6%;n = 4)以及碱水解步骤,随后通过高效液相色谱纯化,在约5.5小时后以5±1%的总产率(n = 3次运行)得到纯化的[(18)F]FEAUβ-异构体,β/α-异构体比例为7.4。放射化学/化学纯度和比活分别超过99%和1.3 Ci/μmol(48 GBq/μmol)。在细胞培养中,与野生型C6细胞相比,[(18)F]FEAU在表达HSV1-tk/sr39tk的C6细胞中积累显著更高(P < 0.05)。此外,在表达HSV1-tk的细胞中,[(18)F]FEAU的积累略高于9-[4-[(18)F]氟-3-(羟甲基)丁基]鸟嘌呤([(18)F]FHBG)(P < 0.05),而在表达HSV1-sr39tk的细胞中,[(18)F]FHBG的积累显著高于[(18)F]FEAU(P < 0.05)。对携带稳定表达HSV1-tk或HSV1-sr39tk的C6细胞肿瘤异种移植的小鼠进行的微型PET成像与细胞摄取结果一致。与[(18)F]FHBG相比,[(18)F]FEAU小鼠图像还显示胃肠道信号非常低,主要通过肾脏清除。使用商用模块和定制设备成功地对[(18)F]FEAU的常规放射性合成进行了半自动操作,以适度的产率提供β-异构体。尽管还需要进一步研究,但早期结果也表明[(18)F]FEAU是一种用于监测HSV1-tk报告基因表达的有前景的PET放射性示踪剂。