TY - JOUR
T1 - Liquid chromatography coupled to tandem mass spectrometry and high resolution mass spectrometry as analytical tools to characterize multi-class cytostatic compounds
AU - Gómez-Canela, Cristian
AU - Cortés-Francisco, Nuria
AU - Ventura, Francesc
AU - Caixach, Josep
AU - Lacorte, Silvia
N1 - Funding Information:
The Spanish Ministry of Science and Innovation is acknowledged for financial support (project CTQ2011-25875 ). Dr. Roser Chaler and Dori Fanjul are acknowledged for mass spectrometric assistance in LC–MS/MS and Dr. Cintia Flores and Oscar Palacios are acknowledged for mass spectrometric assistance in LC-Orbitrap-MS.
PY - 2013/2/8
Y1 - 2013/2/8
N2 - Cytostatic compounds used in the treatment of cancer have emerged as a new generation of water contaminants due to the continuous amounts administered to patients and to the fact that a variable proportion is excreted unchanged. In this study, we have evaluated the performance of liquid-chromatography-tandem mass spectrometry (LC-MS/MS) and high resolution mass spectrometry using an Orbitrap analyzer (LC-HRMS) for the multiresidue determination of multi-class cytostatic compounds. In a first step, ionization conditions were tested in positive electrospray mode and optimum fragmentation patterns were determined. For LC-MS/MS, two selected reaction monitoring (SRM) transitions were optimized and for LC-HRMS, the molecular ion with 5. ppm error and two product ions were defined. Following, the chromatographic conditions were optimized considering that compounds analyzed have a very different chemical structure and chromatographic behavior. The best performance was obtained with a Luna C18 column, which permitted the separation of the 26 compounds in 15. min. Finally, the performance of LC-MS/MS and LC-HRMS was compared in terms of linearity, sensitivity, intra and inter-day precision and overall robustness. While LC-MS/MS provided good identification capabilities due to selective SRM transitions, LC-Orbitrap proved to be 100 times more sensitive. This study provides a comprehensive overview on the MS conditions to determine the outmost used cytostatic compounds and provides a spectral library to be used for the identification of these compounds in water or biological matrices.
AB - Cytostatic compounds used in the treatment of cancer have emerged as a new generation of water contaminants due to the continuous amounts administered to patients and to the fact that a variable proportion is excreted unchanged. In this study, we have evaluated the performance of liquid-chromatography-tandem mass spectrometry (LC-MS/MS) and high resolution mass spectrometry using an Orbitrap analyzer (LC-HRMS) for the multiresidue determination of multi-class cytostatic compounds. In a first step, ionization conditions were tested in positive electrospray mode and optimum fragmentation patterns were determined. For LC-MS/MS, two selected reaction monitoring (SRM) transitions were optimized and for LC-HRMS, the molecular ion with 5. ppm error and two product ions were defined. Following, the chromatographic conditions were optimized considering that compounds analyzed have a very different chemical structure and chromatographic behavior. The best performance was obtained with a Luna C18 column, which permitted the separation of the 26 compounds in 15. min. Finally, the performance of LC-MS/MS and LC-HRMS was compared in terms of linearity, sensitivity, intra and inter-day precision and overall robustness. While LC-MS/MS provided good identification capabilities due to selective SRM transitions, LC-Orbitrap proved to be 100 times more sensitive. This study provides a comprehensive overview on the MS conditions to determine the outmost used cytostatic compounds and provides a spectral library to be used for the identification of these compounds in water or biological matrices.
KW - Cytostatic compounds
KW - LC-HRMS
KW - LC-MS/MS
KW - Orbitrap
KW - Quality parameters
UR - http://www.scopus.com/inward/record.url?scp=84872485476&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2012.12.031
DO - 10.1016/j.chroma.2012.12.031
M3 - Article
C2 - 23313302
AN - SCOPUS:84872485476
SN - 0021-9673
VL - 1276
SP - 78
EP - 94
JO - Journal of Chromatography A
JF - Journal of Chromatography A
ER -