Literature DB >> 24021831

A fluoro versus a nitro derivative-a high-performance liquid chromatography study of two basic analytes with different reversed phases and silica phases as basis for the separation of a positron emission tomography radiotracer.

Barbara Wenzel1, Robert Günther, Peter Brust, Jörg Steinbach.   

Abstract

To develop a basis for the separation of a (18)F-labeled PET radiotracer from its nitro precursor, we performed an analytical HPLC study using the unlabeled reference compound and the corresponding nitro precursor. Aim of the study was to find a separation in which the fluoro derivative elutes in front of the nitro precursor with appropriate separation parameters. Several RP phases as well as a bare silica column were investigated with ACN and MeOH as organic modifiers and aqueous NH4OAc because of the basic character of the analytes. Four types of separation were observed based on different interaction mechanisms. When ACN/20mM NH4OAc aq. was used mainly cationic-exchange and hydrophobic interactions contributed to the retention. A reversal of elution order could be observed starting from 95% ACN and subsequent increasing of the water content. This phenomenon was observed for all RP phases and seems to be independent of the different spacers bound to the silica. By contrast, using MeOH/20mM NH4OAc aq. the elution order depends on the phase material. Two columns with the potential to perform π-π interactions showed different separation behavior compared to the other RP phases.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ACN; Basic analytes; Cationic-exchange; MeOH; PET; PFP; RP phases; Silanol sites; VAChT; acetonitrile; methanol; pentafluorophenyl; positron emission tomography; vesicular acetylcholine transporter

Mesh:

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Year:  2013        PMID: 24021831     DOI: 10.1016/j.chroma.2013.08.068

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  3 in total

1.  Synthesis and evaluation of an (18)F-labeled pyrimidine-pyridine amine for targeting CXCR4 receptors in gliomas.

Authors:  Dustin Wayne Demoin; Masahiro Shindo; Hanwen Zhang; Kimberly J Edwards; Inna Serganova; Naga Vara Kishore Pillarsetty; Jason S Lewis; Ronald G Blasberg
Journal:  Nucl Med Biol       Date:  2016-05-14       Impact factor: 2.408

2.  Radiosynthesis and Biological Investigation of a Novel Fluorine-18 Labeled Benzoimidazotriazine- Based Radioligand for the Imaging of Phosphodiesterase 2A with Positron Emission Tomography.

Authors:  Rien Ritawidya; Barbara Wenzel; Rodrigo Teodoro; Magali Toussaint; Mathias Kranz; Winnie Deuther-Conrad; Sladjana Dukic-Stefanovic; Friedrich-Alexander Ludwig; Matthias Scheunemann; Peter Brust
Journal:  Molecules       Date:  2019-11-15       Impact factor: 4.411

3.  Synthesis and Biological Evaluation of a Novel 18F-Labeled Radiotracer for PET Imaging of the Adenosine A2A Receptor.

Authors:  Thu Hang Lai; Magali Toussaint; Rodrigo Teodoro; Sladjana Dukić-Stefanović; Mathias Kranz; Winnie Deuther-Conrad; Rareş-Petru Moldovan; Peter Brust
Journal:  Int J Mol Sci       Date:  2021-01-25       Impact factor: 5.923

  3 in total

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