2015
DOI: 10.1016/j.jpba.2015.05.022
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Determination of XLR-11 and its metabolites in hair by liquid chromatography–tandem mass spectrometry

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Cited by 21 publications
(9 citation statements)
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“…Park et al . [ 38 ] described a quantitative analytical method for the determination of XLR-11 and its metabolites in hair using LC-MS/MS, since the latter drug has been widely abused in South Korea recently. The authors stated that the detection of the metabolites in hair samples could exclude external contamination and prove actual consumption.…”
Section: Analytical Methods For the Deter-mination Of Nps In Hairmentioning
confidence: 99%
“…Park et al . [ 38 ] described a quantitative analytical method for the determination of XLR-11 and its metabolites in hair using LC-MS/MS, since the latter drug has been widely abused in South Korea recently. The authors stated that the detection of the metabolites in hair samples could exclude external contamination and prove actual consumption.…”
Section: Analytical Methods For the Deter-mination Of Nps In Hairmentioning
confidence: 99%
“…Generally, the analytical methodology consisted of the following steps: hair decontamination from external contaminants, hair digestion or pulverization and analytes extraction from a hair amount ranging between 10−100 mg. The hair decontamination procedures used were washing with: (i) organic solvents, such as methanol [ 20 , 21 , 23 , 24 , 32 , 34 , 43 , 44 , 47 , 50 , 51 , 53 , 54 , 56 , 58 , 60 ], ethanol [ 35 ], acetone [ 19 , 22 , [25] , [26] , [27] , 37 , 38 , 41 , 46 , 49 , 57 , 61 , 63 ], hexane [ 27 ], petroleum ether [ 41 , 49 ], dichloromethane [ 20 , 21 , 23 , 24 , [28] , [29] , [30] , [31] , 33 , 34 , 36 , 39 , 40 , 42 , 45 , 48 , [52] , [53] , [54] , [55] , [56] , [58] , [59] , [60] , 62 ], isopropanol [ 23 , 28 ], isooctane [ 38 , 52 ]; (ii) sodium dodecyl sulfate solution [ 35 , …”
Section: Extraction and Detection Methods For The Determination Of Nps In Hairmentioning
confidence: 99%
“…Analytes’ extraction from hair, which followed hair digestion or pulverization, was achieved by either single step methanol extraction [ 20 , 25 , 27 , 43 , 44 , 47 , [49] , [50] , [51] , 53 , 56 , [58] , [59] , [60] , 62 ], or acidified methanol extraction [ 19 , 21 , 32 , 49 ], or ethanol extraction [ 41 ], or liquid-liquid extraction (LLE) with various mixtures of organic solvents [ 22 , 25 , 30 , 36 , 39 , 40 , 42 , 45 , 46 , 48 , 55 , 61 , 63 ], or extraction with aqueous buffers of organic solvents (methanol/ acetonitrile/ ammonium formate) [ 26 ], or (methanol/ acetonitrile/ trifluoroacetic acid (TFA)) [ 37 ] or (methanol/ TFA) [ 38 ] or (methanol/ acetonitrile/ ammonium acetate) [ 57 ], or solid phase extraction (SPE) on various cartridges [ 24 , 29 , 31 , 52 , 54 ] or mixed-mode solid phase extraction (MSPE) [ 33 , 34 ] or pressurized liquid extraction (PLE) [ 23 , 28 , 35 ], assisted in many cases by mild heat of the samples [ [19] , [20] , [21] , [22] , [23] , 25 , 26 , 29 , 34 , 36 , 39 , 40 , ...…”
Section: Extraction and Detection Methods For The Determination Of Nps In Hairmentioning
confidence: 99%
“…The methodology applied did not include parent compounds as the high hepatic metabolism showed by synthetic cannabinoids made quite improbable their detection in urine samples 67 . In the case of authentic hair samples, the parent compound XLR‐11 was the major compound found by LC–MS/MS (QqQ), while its major metabolites were determined at lower concentrations 68 …”
Section: Detection Of Nps Biomarkers In Toxicological Samples: From Quantitative Ms/ms Analysis To Hrms Screeningmentioning
confidence: 99%