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Fast confirmation for marijuana metabolite: THC-COOH, ultra-fast LC—MS/MS run time, and application to routine samples

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A fast, reliable, inexpensive, and practical method with a low determination limit and high recovery has been developed for the determination of the marijuana metabolite in routine analysis. THC-COOH in urine was validated using liquid chromatography—tandem mass spectrometry (LC—MS/MS). Before an easy single-step extraction with Toxi-Tubes, basic hydrolysis was performed at 60 °C for 30 min. LC—MS/MS analysis takes 2.5 min for each sample, and the retention time of the analyte is 1.75 min. Specificity, linearity, limit of detection (LOD), limit of quantification (LOQ), accuracy, repeatability, and intermediate precision (inter-day) system suitability parameters were determined in the validation study. The recovery of the extraction method was 88.67 (±5.91). LOD and LOQ values were 1.41 and 5.00 ng mL−1, respectively. The method showed linear response between the values 5.00 and 500.00 ng mL−1. The repeatability was 9.64% (relative standard deviation, RSD%), and the intermediate precisions (RSDR%) were 10.73%, 13.74%, and 8.11% at 10.00, 100.00, and 200.00 ng mL−1 concentration levels, respectively. No statistically significant difference was found in ANOVA analysis, between three consecutive days in intermediate precision study, for 90% confidence level. HorRat values were between 0.34 and 0.61. The method was applied to CEDIA positive samples, obtained from the Trabzon Group Presidency of Turkish Council of Forensic Medicine, successfully.
Rocznik
Strony
253--265
Opis fizyczny
Bibliogr. 32 poz., rys.
Twórcy
autor
  • Trabzon Group Presidency of Turkish Council of Forensic Medicine, Trabzon, Turkey
  • Istanbul University Institute of Forensic Sciences, Cerrahpasa, Istanbul, Turkey
autor
  • Istanbul University Faculty of Medicine, Department of Microbiology, Institute of Forensic Sciences, Cerrahpasa, Istanbul, Turkey
autor
  • Istanbul University Institute of Forensic Sciences, Cerrahpasa, Istanbul, Turkey
Bibliografia
  • [1] A.C. Moffad, M.D. Osselton, and B. Widdop, Clarke’s Analysis of Drugs and Poisons, 3rd ed., Pharmaceutical Press, London, 1990, pp. 741
  • [2] M.A. Huestis, Drug Monographs: Marijuana. In: Current Approaches in Forensic - Toxicology, Forensic Toxicologist Certification Board, Inc., Florida, 1994, pp. 1–32
  • [3] A.C. Moffat, Sci. Justice, 42, 55 (2002)
  • [4] E. Lendoiro, A. Castro, H. Fernández-Vega, M.C. Cela-Pérez, J.M. López-Vilariño, M.V. González-Rodríguez, A. Cruz, and M. López-Rivadulla, Anal. Bioanal. Chem., 406, 3589 (2014)
  • [5] C. Montesano, M. Sergi, S. Odoardi, M.C. Simeoni, D. Compagnone, and R. Curini, J. Pharm. Biomed. Anal., 91, 169 (2014)
  • [6] R.C. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 6th edn., Biomedical Publication, Foster City, California, 2002.
  • [7] N.J. Giardino, J. Forensic Sci., 42, 323 (1997)
  • [8] D. Bourquin and R. Brenneisen, J. Chromatogr. A, 414, 187 (1987)
  • [9] B.J. Alan, H.N. ElSohly, S.A. ElSayed, and M.A. ElSohly, J. Anal. Chem., 8, 249 (1984)
  • [10] R.C. Meatherall and J.C. Garriot, J. Anal. Toxicol., 12, 136 (1988)
  • [11] B.M. Kapur, United Nations Office on Drugs and Crime Drug-Testing Methods and Clinical Interpretations of Test Results, United Nations Office on Drug and Crime (UNODC), 1993, pp. 115–154. Retrieved December 15, 2015, from http://www.unodc.org/unodc/en/data-and-analysis/bulletin/bulletin_1993-01-01_2_page005.html
  • [12] H.H. McCurdy, L.J. Lewellen, L.S. Callahan, and P.S. Childs, J. Anal. Toxicol., 10, 175 (1986)
  • [13] B.D. Paul, L.D. Mell, J.M. Mitchell, J.R.M. McKinley, and J. Irving, J. Anal. Toxicol., 11, 1 (1987)
  • [14] C.P. Ritchard, N. Lydia, E.S. Robert, D.W. George, and J.G. Daryl, J. Anal. Toxicol., 14, 46 (1990)
  • [15] M. Fellini, S. Martello, and M. Chiarotti, Forensic Sci. Int., 204, 67 (2011)
  • [16] W. Weinmann, S. Vogt, R. Goerke, C. Müller, and A. Bromberger, Forensic Sci. Int., 113, 381 (2000)
  • [17] M.A. ElSohly, E.S. Arafat, and A.B. Jones, J. Anal. Toxicol., 8, 7 (1984)
  • [18] H. Teixeira, A. Verstraete, P. Proença, F. Corte-Real, P. Monsanto, and D.N. Vieira, Forensic Sci. Int., 170, 148 (2007)
  • [19] S.S. Simões, I. Silva, A.C. Ajenjo, and M.J. Dias, Forensic Sci. Int., 243, 117 (2014)
  • [20] L. Vlase, D.S. Popa, D. Zaharia, and F. Loghin, RJML, 2, 133 (2010)
  • [21] S. Görög, Pharm. Biomed. Anal., 4, 267 (2000)
  • [22] M.C. Sonanis and A.P. Rajput, Int. J. Pharm. Pharm. Sci., 3, 145 (2011)
  • [23] B. Magnusson and U. Örnemark (Eds) Eurachem Guide: The Fitness for Purpose of Analytical Methods — A Laboratory Guide to Method Validation and Related Topics, 2nd edn., 2014.
  • [24] J. Mocak, A.M. Bond, S. Mitchell, and G.A. Scollary, J. Pure Appl., 69, 297 (1997)
  • [25] M.R. Ghante, H.K. Pannu, A. Loni, and T. Shivsharan, Int. J. Pharm. Pharm. Sci., 4, 241 (2012)
  • [26] M. Thompson, TrAC, 26, 1125 (2007)
  • [27] AOAC Official Methods of Analysis, Guidelines for Standard Method Performance Requirements, Appendix F, AOAC International, 16, 2012
  • [28] P.M. Kemp, I.K. Abukhalaf, J.E. Mano, B.R. Mano, D.D. Alford, M.E. McWilliams, F.E. Nixon, M.J. Fitzgerald, R.R. Reeves, and M.J. Wood, J. Anal. Toxicol., 19, 292 (1995)
  • [29] E. Jagerdeo, M.A. Montgomery, R.P. Karas, and M. Sibum, Anal. Bioanal. Chem., 398, 329 (2010)
  • [30] K. Sulic, S. Djordjevic, B. Rusic, K. Denic, V. Nesic, M. Antunovic, and M. Curcic, MD-Medical Data, 6, 051 (2014)
  • [31] W. Kwon, J.Y. Kim, S. Suh, and M. Kyo, Anal. Methods, 5, 3028 (2013)
  • [32] M.J. Rumpler, J. Chromatogr. B., 957, 77 (2014).
Uwagi
PL
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę (zadania 2017).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-c189a50e-85fe-47c2-854a-81448e5bbceb
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