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dc.creatorMagalhães, Elisângela Jaqueline-
dc.creatorQueiroz, Maria Eliana Lopes Ribeiro de-
dc.creatorPenido, Marcus Luiz de Oliveira-
dc.creatorPaiva, Marco Antônio Ribeiro-
dc.creatorTeodoro, Janaína Aparecida Reis-
dc.creatorAugusti, Rodinei-
dc.creatorNascentes, Clésia Cristina-
dc.date.accessioned2018-02-16T11:36:17Z-
dc.date.available2018-02-16T11:36:17Z-
dc.date.issued2013-09-
dc.identifier.citationMAGALHÃES, E. J. et al. Determination of cocaine in postmortem human liver exposed to overdose. Application of an innovative and efficient extraction/clean up procedure and gas chromatography–mass spectrometry analysis. Journal of Chromatography A, Amsterdam, v. 1309, p. 15 – 21, Sept. 2013pt_BR
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0021967313012910pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/28575-
dc.description.abstractA simple and efficient method was developed for the determination of cocaine in post-mortem samples of human liver via solid–liquid extraction with low temperature partitioning (SLE–LTP) and analysis by gas chromatography coupled to mass spectrometry (GC–MS). The extraction procedure was optimized by evaluating the influence of the following variables: pH of the extract, volume and composition of the extractor solvent, addition of a sorbent material (PSA: primary–secondary amine) and NaCl to clean up and increase the ionic strength of the extract. A bovine liver sample that was free of cocaine was used as a blank for the optimization of the SLE–LTP extraction procedure. The highest recovery was obtained when crushed bovine liver (2 g) was treated with 2 mL of ultrapure water plus 8 mL of acetonitrile at physiological pH (7.4). The results also indicated no need for using PSA and NaCl. The complete analytical procedure was validated for the following figures of merit: selectivity, lower limit of quantification (LLOQ), calibration curve, recovery, precision and accuracy (for within-run and between-run experiments), matrix effect, dilution integrity and stability. The within-run and between-run precision (at four levels) varied from 2.1% to 9.4% and from 4.0% to 17.0%, respectively. A maximum deviation of 11.62% for the within-run and between-run accuracies in relation to the nominal concentrations was observed. Moreover, the LLOQ value for cocaine was 50.0 ng g−1 whereas no significant effects were noticed in the assays of dilution integrity and stability. To assess its overall performance, the optimized method was applied to the analysis of eight human liver samples collected from individuals who died due to the abusive consumption of cocaine. Due to the existence of a significant matrix effect, a blank human liver was used to construct a matrix-matched analytical curve. The concentrations of cocaine found in these samples ranged from 333.5 to 5969 ng g−1.pt_BR
dc.languageen_USpt_BR
dc.publisherElsevierpt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceJournal of Chromatography Apt_BR
dc.subjectCocainept_BR
dc.subjectLiverpt_BR
dc.subjectSample preparationpt_BR
dc.subjectExtraction procedurept_BR
dc.subjectGC-MS analysispt_BR
dc.subjectLow-temperature partitioningpt_BR
dc.titleDetermination of cocaine in postmortem human liver exposed to overdose. Application of an innovative and efficient extraction/clean up procedure and gas chromatography–mass spectrometry analysispt_BR
dc.typeArtigopt_BR
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