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Rapid differentiation of nucleotide phosphoramidate diastereomers by electrospray ionization tandem mass spectrometry
RATIONALE Nucleotide phosphoramidates are prodrugs which effectively deliver the active nucleotide to target tissues. It was shown that the individual phosphoramidate diastereomers have different antiviral activity, although the active nucleotide is the same. Therefore, a fast and simple analytical...
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Published in: | Rapid communications in mass spectrometry 2012-08, Vol.26 (16), p.1887-1892 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | RATIONALE
Nucleotide phosphoramidates are prodrugs which effectively deliver the active nucleotide to target tissues. It was shown that the individual phosphoramidate diastereomers have different antiviral activity, although the active nucleotide is the same. Therefore, a fast and simple analytical method is needed to characterize the individual diastereomeric phosphoramidate prodrugs.
METHODS
Stock solutions of diastereomeric nucleotide phosphoramidate prodrugs, i.e., 5′‐phosphate derivatives of the β‐D‐2′‐deoxy‐2′‐α‐fluoro‐2′‐β‐C‐methyluridine nucleotide, were made in 25% acetonitrile to achieve a final concentration of 10 µg/mL. The samples were studied using high‐performance liquid chromatography (HPLC) coupled with electrospray ionization tandem mass spectrometry (ESI‐MS/MS).
RESULTS
The MS/MS spectra of diastereomeric pairs showed substantial differences in the relative abundances of a characteristic ion in negative mode, which is proposed to be a cyclic phosphoramidate ion. Results were confirmed by the MS/MS spectrum of an analog without the NH proton and deuterium exchange experiment. Furthermore, the diastereomer‐specific fragmentation behavior in negative ESI‐MS was used to characterize a series of nucleotide phosphoramidates with different amino acid and aromatic substituents.
CONCLUSIONS
An HPLC/MS/MS method was developed for the differentiation of the diastereomers of phosphoramidate prodrugs. In negative mode MS/MS spectra, the cyclic phosphoramidate ions yielded unambiguous distinction. This method presented a rapid and simple way for the characterization of nucleotide phosphoramidates. Copyright © 2012 John Wiley & Sons, Ltd. |
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ISSN: | 0951-4198 1097-0231 |
DOI: | 10.1002/rcm.6307 |