TY - JOUR
T1 - Simultaneous determination of 11 aconitum alkaloids in human serum and urine using liquid chromatography-tandem mass spectrometry
AU - Usui, Kiyotaka
AU - Hayashizaki, Yoshie
AU - Hashiyada, Masaki
AU - Nakano, Anri
AU - Funayama, Masato
PY - 2012/5
Y1 - 2012/5
N2 - A liquid chromatography-tandem mass spectrometry method was developed and validated for simultaneous determination of four aconitines (aconitine, mesaconitine, hypaconitine, jesaconitine) and seven of their hydrolysis products (benzoylmesaconine, benzoylhypaconine, 14-O-anisoylaconine, benzoylaconine, aconine, mesaconine, hypaconine) in human serum and urine samples. Extraction was undertaken using a mixed-mode cation-exchange cartridge (OASIS MCX), and D 5-aconitine was used as an internal standard. Separation of aconitum alkaloids was carried out using an L-column ODS with the mobile phase consisting of 10mM ammonium formate and methanol. The intra- and inter-day precisions were 0.3% to 9.9% and 3.2% to 12.8%, respectively. Intra- and inter-day accuracies were -14.1% to 7.3%, and -10.6% to 8.3%, respectively. The limit of detection and limit of quantification of analytes were 0.04-0.38ng/mL and 0.12-1.15ng/mL respectively. This method was applied in an autopsy case and successfully detected aconitines and their metabolites as well as some anti-psychiatric drugs.
AB - A liquid chromatography-tandem mass spectrometry method was developed and validated for simultaneous determination of four aconitines (aconitine, mesaconitine, hypaconitine, jesaconitine) and seven of their hydrolysis products (benzoylmesaconine, benzoylhypaconine, 14-O-anisoylaconine, benzoylaconine, aconine, mesaconine, hypaconine) in human serum and urine samples. Extraction was undertaken using a mixed-mode cation-exchange cartridge (OASIS MCX), and D 5-aconitine was used as an internal standard. Separation of aconitum alkaloids was carried out using an L-column ODS with the mobile phase consisting of 10mM ammonium formate and methanol. The intra- and inter-day precisions were 0.3% to 9.9% and 3.2% to 12.8%, respectively. Intra- and inter-day accuracies were -14.1% to 7.3%, and -10.6% to 8.3%, respectively. The limit of detection and limit of quantification of analytes were 0.04-0.38ng/mL and 0.12-1.15ng/mL respectively. This method was applied in an autopsy case and successfully detected aconitines and their metabolites as well as some anti-psychiatric drugs.
KW - Aconitine
KW - Aconitum alkaloids
KW - Liquid chromatography-tandem mass spectrometry
UR - http://www.scopus.com/inward/record.url?scp=84858333284&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84858333284&partnerID=8YFLogxK
U2 - 10.1016/j.legalmed.2012.01.006
DO - 10.1016/j.legalmed.2012.01.006
M3 - Article
C2 - 22342149
AN - SCOPUS:84858333284
SN - 1344-6223
VL - 14
SP - 126
EP - 133
JO - Legal Medicine
JF - Legal Medicine
IS - 3
ER -