Rapid Communications in Mass Spectrometry 2012-06-15

Differentiation of enantiomeric drugs by iodo-substituted L-amino acid references under electrospray ionization mass spectrometric conditions.

R Karthikraj, S Prabhakar, M Vairamani

Index: Rapid Commun. Mass Spectrom. 26(11) , 1385-91, (2012)

Full Text: HTML

Abstract

In chiral differentiation by mass spectrometry, use of a single reference that differentiates various classes of compounds including drugs is ideal, but so far there are no such reports in the literature. We have successfully used iodo-substituted amino acids for the chiral differentiation of ten enantiomeric pairs of drugs.To achieve the chiral differentiation, the trimeric Cu complex ion consisting of two chiral reference molecules and an analyte molecule was generated under positive ion electrospray ionization (ESI) conditions and subsequently subjected for collision- induced dissociation (CID) experiments using an LCQ ion trap mass spectrometer. The spectra were recorded under identical experimental conditions for both the enantiomers, and were averages of 30 scans. Cooks' kinetic method and chiral recognition ratio method (CR method) were used to arrive at the R(chiral) /CR values, respectively.The R(chiral) or CR values of the studied drugs are higher for 3,5-diiodo-L-tyrosine as the reference, than for 4-iodo-L-phenylalanine, except for isoproterenol and atenolol. Both the references show the same selectivity (R- or S-selectivity) towards all the studied drugs. With 3,5-diiodo-L-tyrosine as the reference, an R(chiral) value of 12.75 is obtained for DOPA and this is the highest reported value in the literature till now. The suitability of the current method in measuring enantiomeric excess is also demonstrated for DOPA.The use of 4-iodo-L-phenylalanine or 3,5-diiodo-L-tyrosine as a chiral reference for the chiral differentiation of ten enantiomeric pairs of pharmaceutically important drugs has been demonstrated. The chiral differentiation of pregabalin, tenofovir and pramipexole is reported for the first time. This study shows that it is possible to develop a single chiral reference compound for the differentiation of a group of chiral drugs having some similarities.Copyright © 2012 John Wiley & Sons, Ltd.


Related Compounds

  • H-Phe(4-I)-OH

Related Articles:

A nonradioactive approach to investigate the metabolism of therapeutic peptides by tagging with 127i and using inductively-coupled plasma mass spectrometry analysis.

2015-01-01

[Drug Metab. Dispos. 43(1) , 17-26, (2014)]

An expanded eukaryotic genetic code.

2003-08-15

[Science 301(5635) , 964-7, (2003)]

p-[123I]iodo-L-phenylalanine for detection of pancreatic cancer: basic investigations of the uptake characteristics in primary human pancreatic tumour cells and evaluation in in vivo models of human pancreatic adenocarcinoma.

2004-04-01

[Eur. J. Nucl. Med. Mol. Imaging 31(4) , 532-41, (2004)]

Validation of brain tumour imaging with p-[123I]iodo-L-phenylalanine and SPECT.

2005-09-01

[Eur. J. Nucl. Med. Mol. Imaging 32(9) , 1041-9, (2005)]

One plasmid selection system for the rapid evolution of aminoacyl-tRNA synthetases.

2009-07-15

[Bioorg. Med. Chem. Lett. 19 , 3845-3847, (2009)]

More Articles...