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Development of a LC–MS/MS method for determination of propofol-glucuronide in hair and preliminary study on relationships between dose and hair concentration

•The abuse of propofol have been reported steadily around the world.•Simple, fast, and sensitive method was established using LC–MS/MS.•The developed method for determination propofol glucuronide in hair was validated.•Segmental hair samples are able to identify chronic use of propofol.•The relation...

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Published in:Forensic science international 2020-01, Vol.306, p.110070-110070, Article 110070
Main Authors: Kwon, Nam ji, Kim, Hyo Jeong, Cho, Sungnam, Lee, Min Ah, Han, Eunyoung
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description •The abuse of propofol have been reported steadily around the world.•Simple, fast, and sensitive method was established using LC–MS/MS.•The developed method for determination propofol glucuronide in hair was validated.•Segmental hair samples are able to identify chronic use of propofol.•The relationship between propofol use and analytical results was investigated. Propofol abuse has been reported worldwide, suggesting the need to establish analytical methods for human biological samples to investigate the abuse of propofol. This study aimed to investigate the relationship between dose and hair concentration using a simple and rapid analytical method developed and validated in this study. In the sample preparation, hair samples were washed with distilled water and methanol and extracted in methanol during 16h at room temperature. After centrifugation and evaporation, the residue was reconstituted and filtered through a 0.22μm membrane filter before LC–MS/MS analysis. The precursor-to-product ion transitions were 353 → 175, 113 for propofol glucuronide and m/z 370 → 175, 113 for internal standard(propofol glucuronide-d17). The calibration curves were satisfactory (R2=0.9997) and the limits of detection and quantification were 2 and 5pg/mg, respectively. In addition, this study collected the history of propofol use from subjects using a questionnaire and analyzed subjects' hair samples using a validated analytical method. As a result, the concentrations of propofol glucuronide ranged from 7 to 122pg/mg (mean : 51pg/mg). There were cases of positive relationships, but generally there was no correlation between dose and hair concentration.
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Propofol abuse has been reported worldwide, suggesting the need to establish analytical methods for human biological samples to investigate the abuse of propofol. This study aimed to investigate the relationship between dose and hair concentration using a simple and rapid analytical method developed and validated in this study. In the sample preparation, hair samples were washed with distilled water and methanol and extracted in methanol during 16h at room temperature. After centrifugation and evaporation, the residue was reconstituted and filtered through a 0.22μm membrane filter before LC–MS/MS analysis. The precursor-to-product ion transitions were 353 → 175, 113 for propofol glucuronide and m/z 370 → 175, 113 for internal standard(propofol glucuronide-d17). The calibration curves were satisfactory (R2=0.9997) and the limits of detection and quantification were 2 and 5pg/mg, respectively. In addition, this study collected the history of propofol use from subjects using a questionnaire and analyzed subjects' hair samples using a validated analytical method. As a result, the concentrations of propofol glucuronide ranged from 7 to 122pg/mg (mean : 51pg/mg). 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Propofol abuse has been reported worldwide, suggesting the need to establish analytical methods for human biological samples to investigate the abuse of propofol. This study aimed to investigate the relationship between dose and hair concentration using a simple and rapid analytical method developed and validated in this study. In the sample preparation, hair samples were washed with distilled water and methanol and extracted in methanol during 16h at room temperature. After centrifugation and evaporation, the residue was reconstituted and filtered through a 0.22μm membrane filter before LC–MS/MS analysis. The precursor-to-product ion transitions were 353 → 175, 113 for propofol glucuronide and m/z 370 → 175, 113 for internal standard(propofol glucuronide-d17). The calibration curves were satisfactory (R2=0.9997) and the limits of detection and quantification were 2 and 5pg/mg, respectively. 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identifier ISSN: 0379-0738
ispartof Forensic science international, 2020-01, Vol.306, p.110070-110070, Article 110070
issn 0379-0738
1872-6283
language eng
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source Elsevier
subjects Abuse
Adult
Analytical methods
Biological properties
Biological samples
Calibration
Centrifugation
Chromatography
Chromatography, Liquid
Distilled water
Drug dosages
Efficiency
Evaporation
Female
Forensic sciences
Forensic Toxicology
Gas flow
Glucuronides - administration & dosage
Glucuronides - analysis
Hair
Hair - chemistry
Hair analysis
Humans
Hypnotics and Sedatives - administration & dosage
Hypnotics and Sedatives - analysis
LC–MS/MS
Male
Mass spectrometry
Mathematical analysis
Metabolism
Metabolites
Methanol
Middle Aged
Propofol
Propofol - administration & dosage
Propofol - analysis
Propofol glucuronide
Questionnaires
Retention
Room temperature
Sample preparation
Sampling methods
Scientific imaging
Segmental hair analysis
Substance Abuse Detection - methods
Substance-Related Disorders - diagnosis
Tandem Mass Spectrometry
Urine
Young Adult
title Development of a LC–MS/MS method for determination of propofol-glucuronide in hair and preliminary study on relationships between dose and hair concentration
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