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 |
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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. |
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ISSN: | 1570-0232 1873-376X |
DOI: | 10.1016/j.jchromb.2011.06.012 |