Nature of the main contaminant in the drug primaquine diphosphate: SFC and SFC-MS methods of analysis

被引:36
作者
Brondz, Ilia
Ekeberg, Dag
Bell, David S.
Annino, Amy R.
Hustad, Jan Arild
Svendsen, Robert
Vlachos, Vaso
Oakley, Paul
Langley, G. John
Mohini, Thite
Amaury, Cazenave-Gassiot
Mikhalitsyn, Felix
机构
[1] Univ Life Sci, Dept Chem Biotechnol & Food Sci, N-1432 As, Norway
[2] Sigma Aldrich Supelco, Bellefonte, PA USA
[3] Sigma Aldrich Norway AS, Oslo, Norway
[4] Mettler Toledo Berger SFC, Newark, DE USA
[5] Mettler Toledo AutoChem, Columbia, MD USA
[6] Univ Southampton, Dept Chem, Southampton SO9 5NH, Hants, England
[7] Martsinovsky Inst Med Parasitol & Trop Med, Moscow, Russia
关键词
primaquine; quinocide; positional isomers; chiral chromatography; SFC-MS; anti-malaria drug;
D O I
10.1016/j.jpba.2006.09.017
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The drug primaquine diphosphate is used for causative treatment of malaria. Using HPLC-MS and GC-MS,this research group was previously able to show that the main contaminant of primaquine is the positional isomer quinocide [I. Brondz, D. Mantzilas, U. Klein, D. Ekeberg, E. Hvattum, M.N. Lebedeva, F.S. Mikhailitsyn, G.D. Soulimanov, J. Roe, J. Chromatogr. B: Anal. Technol. Biomed. Life Sci. 800 (2004) 211-223; 1. Brondz, U. Klein, D. Ekeberg, D. Mantzilas, E. Hvattum, H. Schultz, F. S. Mikhailitsyn, Asian J. Chem. 17 (2005) 1678-1688]. Primaquine and quinocide are highly toxic substances which can have a number of side effects upon use in medical treatment. A standard for quinocide is not typically commercially available. In the present work, supercritical fluid chromatography-mass spectrometry (SFC-MS) with two different columns was used to achieve a shorter analysis time for the separation between the positional isomers quinocide and primaquine in primaquine diphosphate and to elucidate additional information about differences in their MS fragmentation. Unlike using HPLC-MS, it was possible to achieve the differential fragmentation of positional isomers at branching points using the SFC-MS technique. The desired short analysis time was achieved using SFC equipped with a Discovery HS F5 column and the differential fragmentation of positional isomers during SFC-MS provides information on the differences in the structure of these substances. Using a Chiralpak AD-H chiral column, it was possible to resolve the enantiomers in primaquine and separate quinocide from those enantiomers. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:937 / 944
页数:8
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