2018
DOI: 10.1016/j.forc.2017.12.007
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LC–MS/MS screening strategy for cannabinoids, opiates, amphetamines, cocaine, benzodiazepines and methadone in human serum, urine and post-mortem blood as an effective alternative to immunoassay based methods applied in forensic toxicology for preliminary examination

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Cited by 29 publications
(30 citation statements)
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“…The calibration curves for each analytical in blood were determined taking into account, where possible, the therapeutic and toxic concentrations of each substance. The concentration ranges in blood determined in this study are in agreement with those reported by Dziadosz et al that stipulated values between 2 and 50 ng mL −1 . Arora et al used working concentrations between 7.8 and 250 ng mL −1 .…”
Section: Resultssupporting
confidence: 92%
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“…The calibration curves for each analytical in blood were determined taking into account, where possible, the therapeutic and toxic concentrations of each substance. The concentration ranges in blood determined in this study are in agreement with those reported by Dziadosz et al that stipulated values between 2 and 50 ng mL −1 . Arora et al used working concentrations between 7.8 and 250 ng mL −1 .…”
Section: Resultssupporting
confidence: 92%
“…These results were considered more significant than the values reported by Steuer et al 29 and Sempio et al 37 In our study, we determined that LLOQs for whole blood ranged from 0.5 to 10 ng mL −1 for benzodiazepines and antidepressants, while Mut et al 38 reported in recent publications using the techniques of GC-MS and LC-MS. 25,29,30 The calibration curves for each analytical in blood were determined taking into account, where possible, the therapeutic and toxic concentrations of each substance. The concentration ranges in blood determined in this study are in agreement with those reported by Dziadosz et al 39 that stipulated values between 2 and 50 ng mL −1 .…”
Section: Methods Validationsupporting
confidence: 92%
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“…After shaking (15 minutes) and centrifugation (5 minutes), the organic layer was mixed with 10 μL 2‐propanol solution with 0.1 mol/L HCl and was evaporated to dryness under a stream of nitrogen at 35°C. “The residue was reconstituted in 100 μL of mobile phase at starting conditions.”…”
Section: Methodsmentioning
confidence: 99%
“…"The residue was reconstituted in 100 μL of mobile phase at starting conditions." 21 A comparison plasma solution was prepared in an appropriate manner to estimate the proven analytes quantitatively in the femoral blood samples by screening.…”
Section: Preparation Of Femoral Blood and Heart Blood Samples For Smentioning
confidence: 99%