TY - JOUR
T1 - The rapid identification and quantification of iso-alpha-acids and reduced iso-alpha-acids in blood using UHPLC-MS/MS: validation of a novel marker for beer consumption
AU - Rodda, Luke
AU - Gerostamoulos, Dimitri
AU - Drummer, Olaf Heino
PY - 2013
Y1 - 2013
N2 - A method for the detection of iso-a-acid (IAA) type ingredient congeners that are derived from the hop plant
(Humulus lupulus L.) was developed to detect recent consumption
of beer in blood. Three structurally similar but
chemically altered IAA, also used as beer-specific ingredients,
are known as ?reduced IAA?, consisting of the rho-,
tetrahydro-, and hexahydro-IAA were also targeted. The use
of a simple protein precipitation extraction and ultrahighperformance
liquid chromatography system coupled with a
tandem mass spectrometer system enabled detection of these
analytes in both antemortem and postmortem blood. Extracts
were injected onto a C18 solid-core column under gradient
elution to achieve separation of isobaric analogs and isomers
within a 10-min run time. Electrospray ionization in negative
multiple reaction monitoring mode was used to monitor three
transitions for each of the analytes that were ultimately
grouped together to form a calibration curve for quantification
of each of the four IAA groups. The method was fully validated
according to international guidelines that included extraction
efficiency, matrix effects, process efficiency, ion
suppression/enhancement of co-eluting analytes, selectivity,
crosstalk, accuracy and precision, stabilities, and lower limits
of quantification. Finally, applicability of the method described
was demonstrated by the detection of IAA ingredient
congeners in the blood of a volunteer following the consumption
of a relatively small amount of beer in a pilot study.
AB - A method for the detection of iso-a-acid (IAA) type ingredient congeners that are derived from the hop plant
(Humulus lupulus L.) was developed to detect recent consumption
of beer in blood. Three structurally similar but
chemically altered IAA, also used as beer-specific ingredients,
are known as ?reduced IAA?, consisting of the rho-,
tetrahydro-, and hexahydro-IAA were also targeted. The use
of a simple protein precipitation extraction and ultrahighperformance
liquid chromatography system coupled with a
tandem mass spectrometer system enabled detection of these
analytes in both antemortem and postmortem blood. Extracts
were injected onto a C18 solid-core column under gradient
elution to achieve separation of isobaric analogs and isomers
within a 10-min run time. Electrospray ionization in negative
multiple reaction monitoring mode was used to monitor three
transitions for each of the analytes that were ultimately
grouped together to form a calibration curve for quantification
of each of the four IAA groups. The method was fully validated
according to international guidelines that included extraction
efficiency, matrix effects, process efficiency, ion
suppression/enhancement of co-eluting analytes, selectivity,
crosstalk, accuracy and precision, stabilities, and lower limits
of quantification. Finally, applicability of the method described
was demonstrated by the detection of IAA ingredient
congeners in the blood of a volunteer following the consumption
of a relatively small amount of beer in a pilot study.
UR - http://download.springer.com/static/pdf/678/art%253A10.1007%252Fs00216-013-7413-0.pdf?auth66=1392517614_b8bfcd197ec42bb58947b4740a598b82&ext=.pdf
U2 - 10.1007/s00216-013-7413-0
DO - 10.1007/s00216-013-7413-0
M3 - Article
SN - 1618-2642
VL - 405
SP - 9755
EP - 9767
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
IS - 30
ER -