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在 GE FASTlab 上稳健且简便的自动化 [F]FSPG 放射性合成

Robust and Facile Automated Radiosynthesis of [F]FSPG on the GE FASTlab.

机构信息

School of Biomedical Engineering & Imaging Sciences, King's College London, St. Thomas' Hospital, London, SE1 7EH, UK.

Pharmaceutical Diagnostics, Life Sciences, GE Healthcare, Pollards Wood, Nightingales Lane, Chalfont St. Giles, Buckinghamshire, HP8 4SP, UK.

出版信息

Mol Imaging Biol. 2021 Dec;23(6):854-864. doi: 10.1007/s11307-021-01609-w. Epub 2021 May 20.

Abstract

PURPOSE

(S)-4-(3-F-Fluoropropyl)-ʟ-Glutamic Acid ([F]FSPG) is a radiolabeled non-natural amino acid that is used for positron emission tomography (PET) imaging of the glutamate/cystine antiporter, system x, whose expression is upregulated in many cancer types. To increase the clinical adoption of this radiotracer, reliable and facile automated procedures for [F]FSPG production are required. Here, we report a cassette-based method to produce [F]FSPG at high radioactivity concentrations from low amounts of starting activity.

PROCEDURES

An automated synthesis and purification of [F]FSPG was developed using the GE FASTlab. Optimization of the reaction conditions and automated manipulations were performed by measuring the isolated radiochemical yield of [F]FSPG and by assessing radiochemical purity using radio-HPLC. Purification of [F]FSPG was conducted by trapping and washing of the radiotracer on Oasis MCX SPE cartridges, followed by a reverse elution of [F]FSPG in phosphate-buffered saline. Subsequently, the [F]FSPG obtained from the optimized process was used to image an animal model of non-small cell lung cancer.

RESULTS

The optimized protocol produced [F]FSPG in 38.4 ± 2.6 % radiochemical yield and >96 % radiochemical purity with a molar activity of 11.1 ± 7.7 GBq/μmol. Small alterations, including the implementation of a reverse elution and an altered Hypercarb cartridge, led to significant improvements in radiotracer concentration from <10 MBq/ml to >100 MBq/ml. The improved radiotracer concentration allowed for the imaging of up to 20 mice, starting with just 1.5 GBq of [F]Fluoride.

CONCLUSIONS

We have developed a robust and facile method for [F]FSPG radiosynthesis in high radiotracer concentration, radiochemical yield, and radiochemical purity. This cassette-based method enabled the production of [F]FSPG at radioactive concentrations sufficient to facilitate large-scale preclinical experiments with a single prep of starting activity. The use of a cassette-based radiosynthesis on an automated synthesis module routinely used for clinical production makes the method amenable to rapid and widespread clinical translation.

摘要

目的

(S)-4-(3-氟丙基)-L-谷氨酸([F]FSPG)是一种放射性标记的非天然氨基酸,用于正电子发射断层扫描(PET)成像谷氨酸/胱氨酸转运体,系统 x,其表达在许多癌症类型中上调。为了增加这种示踪剂的临床应用,需要可靠且简便的自动化程序来生产[F]FSPG。在这里,我们报告了一种基于盒式的方法,可从低起始活度的量中以高放射性浓度生产[F]FSPG。

过程

使用 GE FASTlab 开发了[F]FSPG 的自动化合成和纯化。通过测量[F]FSPG 的分离放射性化学产率并使用放射性 HPLC 评估放射性化学纯度,对反应条件和自动化操作进行了优化。[F]FSPG 的纯化是通过在 Oasis MCX SPE 小柱上捕获和洗涤示踪剂来进行的,然后在磷酸盐缓冲盐水(PBS)中反洗脱[F]FSPG。随后,使用从优化过程中获得的[F]FSPG 来对非小细胞肺癌动物模型进行成像。

结果

优化的方案以 38.4±2.6%的放射性化学产率和>96%的放射性化学纯度生产[F]FSPG,摩尔活性为 11.1±7.7GBq/μmol。小的改动,包括实施反洗脱和改变 Hypercarb 小柱,导致放射性示踪剂浓度从<10MBq/ml 显著提高到>100MBq/ml。改进的放射性示踪剂浓度允许在仅 1.5GBq [F]氟化物的起始活性下,对多达 20 只小鼠进行成像。

结论

我们已经开发了一种用于[F]FSPG 高放射性示踪剂浓度、放射性化学产率和放射性化学纯度的稳健而简便的方法。这种基于盒式的方法能够以足以促进具有单个起始活性预实验的大规模临床前实验的放射性浓度生产[F]FSPG。基于自动化合成模块的盒式放射合成的使用,该模块通常用于临床生产,使得该方法易于快速和广泛的临床转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0a3/8578107/586ecfcb6731/11307_2021_1609_Fig1_HTML.jpg

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