Robust and Facile Automated Radiosynthesis of [18F]FSPG on the GE FASTlab

Purpose (S)-4-(3- 18 F-Fluoropropyl)-ʟ-Glutamic Acid ([ 18 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 C - , whose expression is upregulated in many cancer types. To increase the clinical a...

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Veröffentlicht in:Molecular imaging and biology 2021-12, Vol.23 (6), p.854-864
Hauptverfasser: Edwards, Richard, Greenwood, Hannah E., McRobbie, Graeme, Khan, Imtiaz, Witney, Timothy H.
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Sprache:eng
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Zusammenfassung:Purpose (S)-4-(3- 18 F-Fluoropropyl)-ʟ-Glutamic Acid ([ 18 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 C - , whose expression is upregulated in many cancer types. To increase the clinical adoption of this radiotracer, reliable and facile automated procedures for [ 18 F]FSPG production are required. Here, we report a cassette-based method to produce [ 18 F]FSPG at high radioactivity concentrations from low amounts of starting activity. Procedures An automated synthesis and purification of [ 18 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 [ 18 F]FSPG and by assessing radiochemical purity using radio-HPLC. Purification of [ 18 F]FSPG was conducted by trapping and washing of the radiotracer on Oasis MCX SPE cartridges, followed by a reverse elution of [ 18 F]FSPG in phosphate-buffered saline. Subsequently, the [ 18 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 [ 18 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 100 MBq/ml. The improved radiotracer concentration allowed for the imaging of up to 20 mice, starting with just 1.5 GBq of [ 18 F]Fluoride. Conclusions We have developed a robust and facile method for [ 18 F]FSPG radiosynthesis in high radiotracer concentration, radiochemical yield, and radiochemical purity. This cassette-based method enabled the production of [ 18 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.
ISSN:1536-1632
1860-2002
DOI:10.1007/s11307-021-01609-w