Chiral separation of atropine by high-performance liquid chromatography

被引:28
作者
Breton, D
Buret, D
Clair, P
Lafosse, A
机构
[1] Pharm Cent Armees, F-45998 Orleans, France
[2] Inst Chim Organ & Analyt, UFR Sci, F-45067 Orleans, France
关键词
enantiomers; atropine; liquid chromatography; mass spectrometry;
D O I
10.1016/j.chroma.2005.02.073
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The separation and quantitation of the enantiomers and also the determination of the enantiomeric purity are now current and indispensable tasks for the pharmaceutical analysis. Among the various techniques, liquid chromatography remains the best modality owing to several advantages. High speed, sensitivity, and reproducible results make LC the method of choice in almost all laboratories. Phases that contain a I acid glycoprotein as chiral selector are suitable for separation of charged and uncharged enantiomers with widely different structure. Atropine is widely used as parasympatolytic, anticholinergic and antiemetic drugs. It is one of the preferred antidote for immediate management of toxicity associated with nerve agents. Stereoselective separation was achieved with a prepacked alpha(1)-acid glycoprotein column without any derivatization procedure. The liquid chromatography system is coupled to mass spectrometry with an atmospheric pressure chemical ionization interface in the positive-ion mode. The chromatographed analytes are detected in selective ion monitoring after optimisation using factorial experimental design. Small amount of enantiomeric composition can be evaluated either by MS or by UV spectrometry (less than 5%). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 109
页数:6
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