Evidence map›Paper›PMID 33315962›Full record

ArticlePloS one2020

Synthesis and analysis of 4-(3-fluoropropyl)-glutamic acid stereoisomers to determine the stereochemical purity of (4S)-4-(3-[18F]fluoropropyl)-L-glutamic acid ([18F]FSPG) for clinical use.

Kai-Ting Shih, Ya-Yao Huang, Chia-Ying Yang, Mei-Fang Cheng, Yu-Wen Tien, Chyng-Yann Shiue, Rouh-Fang Yen, Ling-Wei Hsin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Simplified and highly-reliable automated production of [EJNMMI radiopharmacy and chemistry · 2023
    Article
  2. Article
  3. Radiosynthesis and Analysis of (S)-4-(3-[Molecular imaging and biology · 2023
    Article
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Kai-Ting ShihSchool of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.
Ya-Yao HuangDepartment of Nuclear Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Chia-Ying YangSchool of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.
Mei-Fang ChengDepartment of Nuclear Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Yu-Wen TienDepartment of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Chyng-Yann ShiueDepartment of Nuclear Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Rouh-Fang YenDepartment of Nuclear Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Ling-Wei HsinSchool of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.ORCID 0000-0001-5018-4491
National Taiwan University · TWNational Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(4S)-4-(3-[18F]Fluoropropyl)-L-glutamic acid ([18F]FSPG) is a positron emission tomography (PET) imaging agent for measuring the system xC- transporter activity. It has been used for the detection of various cancers and metastasis in clinical trials. [18F]FSPG is also a promising diagnostic tool for evaluation of multiple sclerosis, drug resistance in chemotherapy, inflammatory brain diseases, and infectious lesions. Due to the very short half-life (110 min) of 18F nuclide, [18F]FSPG needs to be produced on a daily basis; therefore, fast and efficient synthesis and analytical methods for quality control must be established to assure the quality and safety of [18F]FSPG for clinical use. To manufacture cGMP-compliant [18F]FSPG, all four nonradioactive stereoisomers of FSPG were prepared as reference standards for analysis. (2S,4S)-1 and (2R,4R)-1 were synthesized starting from protected L- and D-glutamate derivatives in three steps, whereas (2S,4R)-1 and (2R,4S)-1 were prepared in three steps from protected (S)- and (R)-pyroglutamates. A chiral HPLC method for simultaneous determination of four FSPG stereoisomers was developed by using a 3-cm Chirex 3126 column and a MeCN/CuSO4(aq) mobile phase. In this method, (2R,4S)-1, (2S,4S)-1, (2R,4R)-1, and (2S,4R)-1 were eluted in sequence with sufficient resolution in less than 25 min without derivatization. Scale-up synthesis of intermediates for the production of [18F]FSPG in high optical purity was achieved via stereo-selective synthesis or resolution by recrystallization. The enantiomeric excess of intermediates was determined by HPLC using a Chiralcel OD column and monitored at 220 nm. The nonradioactive precursor with >98% ee can be readily distributed to other facilities for the production of [18F]FSPG. Based on the above accomplishments, cGMP-compliant [18F]FSPG met the acceptance criteria in specifications and was successfully manufactured for human use. It has been routinely prepared and used in several pancreatic ductal adenocarcinoma metastasis-related clinical trials.

Indexed as

Chromatography, High Pressure LiquidCrystallizationGlutamatesHumansInjectionsStereoisomerism4-(3-fluoropropyl)glutamic acidGlutamates

Identifiers

PMID33315962
PMCPMC7735610
OpenAlexW3111585833

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.