Tramadol chronic abuse: An evidence from hair analysis by LC tandem MS

•An analytical method for tramadol and its three metabolites was validated.•The validated method was applied in four authentic hair samples.•N,O-didesmethyltramadol has been determined for the first time in hair matrix.•Metabolite to parent drug ratios reveal to be a helpful tool for abuse monitorin...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2015-01, Vol.102, p.450-458
Hauptverfasser: Verri, Patrizia, Rustichelli, Cecilia, Palazzoli, Federica, Vandelli, Daniele, Marchesi, Filippo, Ferrari, Anna, Licata, Manuela
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container_title Journal of pharmaceutical and biomedical analysis
container_volume 102
creator Verri, Patrizia
Rustichelli, Cecilia
Palazzoli, Federica
Vandelli, Daniele
Marchesi, Filippo
Ferrari, Anna
Licata, Manuela
description •An analytical method for tramadol and its three metabolites was validated.•The validated method was applied in four authentic hair samples.•N,O-didesmethyltramadol has been determined for the first time in hair matrix.•Metabolite to parent drug ratios reveal to be a helpful tool for abuse monitoring. Hair analysis, as complementary matrix, has expanded across the spectrum of toxicological investigations for misuse drug monitoring. Hair has become an important matrix for drug analysis, owing to the possibility to detect target analytes for long time periods, depending on hair length. A liquid chromatography–tandem mass spectrometry (LC–MS/MS) method has been developed for the quantitation of tramadol, a widely used centrally acting analgesic, and its main metabolites in hair (ODMT, NDMT, NOT). Hair samples were decontaminated and incubated overnight in diluted hydrochloric acid; the extracts were purified by mixed-mode solid phase cartridges and analyzed by LC–MS/MS in positive ionization mode monitoring two transitions per analyte. The procedure was fully validated in terms of linearity, limit of detection and lower limit of quantitation (LLOQ), accuracy, precision, recovery, matrix effect and selectivity. The linear regression analysis was calibrated by deuterated internal standards; for all analytes, responses were linear over the range 0.04–40.00ng/mg hair, with R2 values of at least 0.995. The method offered satisfactory precision (RSD90%) values. The found LLOQ values for tramadol and metabolites were in the range 0.010–0.030ng/mg hair. The proposed procedure was successfully applied to quantify tramadol and metabolites in real hair samples submitted to our laboratory: three cases of tramadol assumption within the therapeutic dosage (3×2 segments) and one case of tramadol abuse in a binge pattern (8 segments). The ranges found for TRAM, ODMT, NDMT and NOT were markedly higher in the abuse case (63.42–107.30, 3.76–6.26, 24.88–45.66, 0.22–1.18ng/mg hair, respectively) compared to the other case reports (3.29–20.12, 0.28–1.87, 0.45–4.32, 0.07–0.80ng/mg, respectively); also the values of NMDT/ODMT ratio differed significantly. According to the obtained data, we hypothesized that the binge pattern may influence the metabolites’ to parent drug concentration ratios; therefore this parameter could represent a target assessment tool to monitor abuse cases.
doi_str_mv 10.1016/j.jpba.2014.10.002
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Hair analysis, as complementary matrix, has expanded across the spectrum of toxicological investigations for misuse drug monitoring. Hair has become an important matrix for drug analysis, owing to the possibility to detect target analytes for long time periods, depending on hair length. A liquid chromatography–tandem mass spectrometry (LC–MS/MS) method has been developed for the quantitation of tramadol, a widely used centrally acting analgesic, and its main metabolites in hair (ODMT, NDMT, NOT). Hair samples were decontaminated and incubated overnight in diluted hydrochloric acid; the extracts were purified by mixed-mode solid phase cartridges and analyzed by LC–MS/MS in positive ionization mode monitoring two transitions per analyte. The procedure was fully validated in terms of linearity, limit of detection and lower limit of quantitation (LLOQ), accuracy, precision, recovery, matrix effect and selectivity. 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Hair analysis, as complementary matrix, has expanded across the spectrum of toxicological investigations for misuse drug monitoring. Hair has become an important matrix for drug analysis, owing to the possibility to detect target analytes for long time periods, depending on hair length. A liquid chromatography–tandem mass spectrometry (LC–MS/MS) method has been developed for the quantitation of tramadol, a widely used centrally acting analgesic, and its main metabolites in hair (ODMT, NDMT, NOT). Hair samples were decontaminated and incubated overnight in diluted hydrochloric acid; the extracts were purified by mixed-mode solid phase cartridges and analyzed by LC–MS/MS in positive ionization mode monitoring two transitions per analyte. The procedure was fully validated in terms of linearity, limit of detection and lower limit of quantitation (LLOQ), accuracy, precision, recovery, matrix effect and selectivity. 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According to the obtained data, we hypothesized that the binge pattern may influence the metabolites’ to parent drug concentration ratios; therefore this parameter could represent a target assessment tool to monitor abuse cases.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>25459945</pmid><doi>10.1016/j.jpba.2014.10.002</doi><tpages>9</tpages></addata></record>
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subjects Adult
Analgesics, Opioid - analysis
Analgesics, Opioid - metabolism
Binge pattern
Chromatography, Liquid - methods
Female
Hair - chemistry
Hair samples
Humans
LC–MS/MS
Male
Metabolites
Substance Abuse Detection - methods
Substance-Related Disorders - metabolism
Tandem Mass Spectrometry - methods
Tramadol
Tramadol - analysis
Tramadol - metabolism
Young Adult
title Tramadol chronic abuse: An evidence from hair analysis by LC tandem MS
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