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.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117 Anal+Chem
2014 ; 86
(20
): 10397-405
Nephropedia Template TP
gab.com Text
Twit Text FOAVip
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English Wikipedia
Simultaneous measurement of tabun, sarin, soman, cyclosarin, VR, VX, and VM
adducts to tyrosine in blood products by isotope dilution UHPLC-MS/MS
#MMPMID25286390
Crow BS
; Pantazides BG
; Quiñones-González J
; Garton JW
; Carter MD
; Perez JW
; Watson CM
; Tomcik DJ
; Crenshaw MD
; Brewer BN
; Riches JR
; Stubbs SJ
; Read RW
; Evans RA
; Thomas JD
; Blake TA
; Johnson RC
Anal Chem
2014[Oct]; 86
(20
): 10397-405
PMID25286390
show ga
This work describes a new specific, sensitive, and rapid stable isotope dilution
method for the simultaneous detection of the organophosphorus nerve agents
(OPNAs) tabun (GA), sarin (GB), soman (GD), cyclosarin (GF), VR, VX, and VM
adducts to tyrosine (Tyr). Serum, plasma, and lysed whole blood samples (50 ?L)
were prepared by protein precipitation followed by digestion with Pronase.
Specific Tyr adducts were isolated from the digest by a single solid phase
extraction (SPE) step, and the analytes were separated by reversed-phase ultra
high performance liquid chromatography (UHPLC) gradient elution in less than 2
min. Detection was performed on a triple quadrupole tandem mass spectrometer
using time-triggered selected reaction monitoring (SRM) in positive electrospray
ionization (ESI) mode. The calibration range was characterized from 0.100-50.0
ng/mL for GB- and VR-Tyr and 0.250-50.0 ng/mL for GA-, GD-, GF-, and VX/VM-Tyr
(R(2) ? 0.995). Inter- and intra-assay precision had coefficients of variation of
?17 and ?10%, respectively, and the measured concentration accuracies of spiked
samples were within 15% of the targeted value for multiple spiking levels. The
limit of detection was calculated to be 0.097, 0.027, 0.018, 0.074, 0.023, and
0.083 ng/mL for GA-, GB-, GD-, GF-, VR-, and VX/VM-Tyr, respectively. A
convenience set of 96 serum samples with no known nerve agent exposure was
screened and revealed no baseline values or potential interferences. This method
provides a simple and highly specific diagnostic tool that may extend the time
postevent that a confirmation of nerve agent exposure can be made with
confidence.