Literature DB >> 15905064

Application of GC-EI-MS for the identification and investigation of positional isomer in primaquine, an antimalarial drug.

Vaijanath G Dongre1, Pravin P Karmuse, M M Nimbalkar, Dharmendra Singh, Ashok Kumar.   

Abstract

A major impurity associated with primaquine drug samples obtained from European Pharmacopoeia (EP) and other commercial sources was detected and identified using HPLC, photo diode array (PDA), LC-MS/MS and gas chromatograph-electron impact-mass spectrometer (GC-EI-MS). PDA and LC-ESI-MS/MS data provided an evidence for it being isomeric in nature. However, spectral data obtained from the newly developed GC-EI-MS method has been utilised for structural elucidation and found to be conclusive to characterize this impurity as positional isomer, i.e. 8-(4-amino-4-methylbutyl amino)-6 methoxyquinoline. The structure of this impurity has been confirmed by its synthesis. Precursor of primaquine was also investigated using GC-EI-MS. The data obtained confirmed the origin of isomeric impurity in precursor.

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Year:  2005        PMID: 15905064     DOI: 10.1016/j.jpba.2005.03.019

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  1 in total

1.  Electrospray ionization-ion trap mass spectrometry study of PQAAPro and PQProAA mimetic derivatives of the antimalarial primaquine.

Authors:  Nuno Vale; Joana Matos; Rui Moreira; Paula Gomes
Journal:  J Am Soc Mass Spectrom       Date:  2008-07-01       Impact factor: 3.109

  1 in total

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