Quantification of acetaminophen (paracetamol) in human plasma and urine by stable isotope-dilution GC–MS and GC–MS/MS as pentafluorobenzyl ether derivative

We report on the quantitative determination of acetaminophen (paracetamol; NAPAP-d 0) in human plasma and urine by GC–MS and GC–MS/MS in the electron-capture negative-ion chemical ionization (ECNICI) mode after derivatization with pentafluorobenzyl (PFB) bromide (PFB-Br). Commercially available tetr...

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Veröffentlicht in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2011-08, Vol.879 (23), p.2274-2280
Hauptverfasser: Trettin, Arne, Zoerner, Alexander A., Böhmer, Anke, Gutzki, Frank-Mathias, Stichtenoth, Dirk O., Jordan, Jens, Tsikas, Dimitrios
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Sprache:eng
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Zusammenfassung:We report on the quantitative determination of acetaminophen (paracetamol; NAPAP-d 0) in human plasma and urine by GC–MS and GC–MS/MS in the electron-capture negative-ion chemical ionization (ECNICI) mode after derivatization with pentafluorobenzyl (PFB) bromide (PFB-Br). Commercially available tetradeuterated acetaminophen (NAPAP-d 4) was used as the internal standard. NAPAP-d 0 and NAPAP-d 4 were extracted from 100-μL aliquots of plasma and urine with 300 μL ethyl acetate (EA) by vortexing (60 s). After centrifugation the EA phase was collected, the solvent was removed under a stream of nitrogen gas, and the residue was reconstituted in acetonitrile (MeCN, 100 μL). PFB-Br (10 μL, 30 vol% in MeCN) and N, N-diisopropylethylamine (10 μL) were added and the mixture was incubated for 60 min at 30 °C. Then, solvents and reagents were removed under nitrogen and the residue was taken up with 1000 μL of toluene, from which 1-μL aliquots were injected in the splitless mode. GC–MS quantification was performed by selected-ion monitoring ions due to [M−PFB] − and [M−PFB−H] −, m/ z 150 and m/ z 149 for NAPAP-d 0 and m/ z 154 and m/ z 153 for NAPAP-d 4, respectively. GC–MS/MS quantification was performed by selected-reaction monitoring the transition m/ z 150 → m/ z 107 and m/ z 149 → m/ z 134 for NAPAP-d 0 and m/ z 154 → m/ z 111 and m/ z 153 → m/ z 138 for NAPAP-d 4. The method was validated for human plasma (range, 0–130 μM NAPAP-d 0) and urine (range, 0–1300 μM NAPAP-d 0). Accuracy (recovery, %) ranged between 89 and 119%, and imprecision (RSD, %) was below 19% in these matrices and ranges. A close correlation ( r > 0.999) was found between the concentrations measured by GC–MS and GC–MS/MS. By this method, acetaminophen can be reliably quantified in small plasma and urine sample volumes (e.g., 10 μL). The analytical performance of the method makes it especially useful in pediatrics.
ISSN:1570-0232
1873-376X
DOI:10.1016/j.jchromb.2011.06.012