Journal
FORENSIC TOXICOLOGY
Volume 37, Issue 1, Pages 215-223Publisher
SPRINGER
DOI: 10.1007/s11419-018-0458-1
Keywords
Novel synthetic opioids; U-47700; W-18; W-15; Method validation; LC - MS; MS
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PurposeThe objective of this study was to develop, optimize, and validate a method for the simultaneous quantification of U-47700, AH-7921, U-49900, U-50488, MT-45, W-18, and W-15 in whole blood using liquid chromatography-tandem mass spectrometry (LC-MS/MS).MethodsBlood samples (500 mu L) were fortified with mixed calibrator or quality control (25 mu L) and internal standard (10 mu L) solutions. Analytes were isolated via a solid-phase extraction procedure. Analysis was performed using an Agilent 1290 Infinity II liquid chromatograph coupled to an Agilent 6470 triple quadrupole mass spectrometer. The method was validated in accordance with Scientific Working Group for Forensic Toxicology (SWGTOX) standard practices for method validation in forensic toxicology and applied to the analysis of postmortem blood specimens.ResultsLower limits of quantification were 0.25-1ng/mL and the upper limits of quantification were 100ng/mL. The coefficients of determination (R-2) for the calibration curves were>0.99. Analytical bias, within-run imprecision, and between-run imprecision were within15%,16%, and17%, respectively. All analytes were found to be stable at room temperature for 24h, refrigerated (4 degrees C) for 72h, and in the autosampler (4 degrees C) for 72h. Authentic blood samples (n=30) were analyzed using the validated method. Mean (range) U-47700 concentrations were 214 (3.2-1448) ng/mL in 15 cases.Conclusions A quantification method for seven synthetic opioids (U-47700, AH-7921, U-49900, U-50488, MT-45, W-18, and W-15) in whole blood was developed, optimized, and validated in accordance with SWGTOX standard practices for method validation in forensic toxicology. This sensitive method was successfully applied to postmortem casework.
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