Surface-activated chemical ionization-electrospray ionization mass spectrometry combined with two-dimensional serial chromatography is a powerful tool for drug stability studies

被引:3
作者
Conti, Matteo [1 ]
Motta, Roberto [1 ]
Puggioli, Cristina [2 ]
Brambilla, Paolo [3 ,4 ]
机构
[1] St Orsola Malpighi Hosp, Cent Lab, Dept Haematol Oncol & Lab Med, Bologna, Italy
[2] St Orsola Malpighi Hosp, Dept Clin Pharm, Bologna, Italy
[3] Hosp Desio, Desio, Italy
[4] Bicocca Univ, Milan, Italy
关键词
Chemical stability - Computerized tomography - Degradation - Drug products - Liquid chromatography - Mass spectrometry - System stability;
D O I
10.1002/rcm.6567
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RATIONALE Drug stability is an important quality-control issue for pharmaceutical and clinical practices. Among the analytical techniques that address this issue, liquid chromatography/mass spectrometry (LC/MS) can be very useful, especially when assessing the quality of liquid formulations, because it is intrinsically sensitive, selective, and a rapid analytical technique. However, LC/MS suffers from technical drawbacks, e.g., matrix effects, and the production of in-source degradation products, which can limit its usefulness. METHODS To overcome the aforementioned drawbacks associated with LC/MS, we introduce an innovative approach (2D-LC/SACI-ESI-MS/MS) that incorporates two-dimensional liquid chromatography (2D-LC) in conjunction with an MS system consisting of a surface-activated chemical ionization-electrospray ionization chamber (SACI-ESI), an ion trap MS analyzer, and tandem mass spectrometry. RESULTS To validate our 2D-LC/SACI-ESI-MS/MS system stability studies were performed on the computerized tomography contrast agents, iohexol, iodixanol, iopamidol, iomeprol, iopromide, and iobitridol, either alone or in binary combination. The matrix effects, in-source analyte degradation, and analytical performance were compared with those obtained using a one-dimensional LC/MS configuration. The accuracy coefficient of variance (CV)=14%, and degradation (loss of water and other chemical moieties) was greatly reduced, attesting to the usefulness of this system for drug stability measurements. CONCLUSIONS Our new approach improves the performance (sensitivity, accuracy, and signal stability) of LC/MS instrumentation for drug stability measurements by reducing signal suppression effects and in-source chemical reactions. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1231 / 1236
页数:6
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