Determination of phosphatidylethanol 16:0/18:1 in whole blood by 96-well supported liquid extraction and UHPLC-MS/MS.
96-well supported liquid extraction
Alcohol
LC-MS/MS
PEth 16:0/18:1
phosphatidylethanol
Journal
Journal of clinical laboratory analysis
ISSN: 1098-2825
Titre abrégé: J Clin Lab Anal
Pays: United States
ID NLM: 8801384
Informations de publication
Date de publication:
Jan 2019
Jan 2019
Historique:
revised:
20
06
2018
received:
25
04
2018
accepted:
05
07
2018
pubmed:
27
7
2018
medline:
16
2
2019
entrez:
27
7
2018
Statut:
ppublish
Résumé
Phosphatidylethanols (PEths) are specific, direct alcohol biomarkers that can be determined in human blood to distinguish between heavy and social drinking. PEth 16:0/18:1 is among the most predominant PEth homologues in human blood. The aim of the study was to develop a high throughput and sensitive UHPLC-MS/MS method for the determination of PEth 16:0/18:1 in whole blood. Whole blood samples were prepared by 96-well supported liquid extraction (SLE). Extracted samples were analyzed for PEth 16:0/18:1 by reversed phase UHPLC-MS/MS. The developed UHPLC-MS/MS method was fully validated in whole blood with PEth 16:0/18:1-D For the first time, 96-well SLE was used for preparation of a PEth homologue in biological samples. A mixture of tert-butyl methyl ether and 2-propanol (5:1, v:v) was chosen as organic eluent based on an evaluation of extraction recovery, purity of extracts, and evaporation time. The developed UHPLC-MS/MS method can be used for high throughput analyses and sensitive determinations of PEth 16:0/18:1 in whole blood.
Sections du résumé
BACKGROUND
BACKGROUND
Phosphatidylethanols (PEths) are specific, direct alcohol biomarkers that can be determined in human blood to distinguish between heavy and social drinking. PEth 16:0/18:1 is among the most predominant PEth homologues in human blood. The aim of the study was to develop a high throughput and sensitive UHPLC-MS/MS method for the determination of PEth 16:0/18:1 in whole blood.
METHODS
METHODS
Whole blood samples were prepared by 96-well supported liquid extraction (SLE). Extracted samples were analyzed for PEth 16:0/18:1 by reversed phase UHPLC-MS/MS.
RESULTS
RESULTS
The developed UHPLC-MS/MS method was fully validated in whole blood with PEth 16:0/18:1-D
CONCLUSION
CONCLUSIONS
For the first time, 96-well SLE was used for preparation of a PEth homologue in biological samples. A mixture of tert-butyl methyl ether and 2-propanol (5:1, v:v) was chosen as organic eluent based on an evaluation of extraction recovery, purity of extracts, and evaporation time. The developed UHPLC-MS/MS method can be used for high throughput analyses and sensitive determinations of PEth 16:0/18:1 in whole blood.
Identifiants
pubmed: 30047172
doi: 10.1002/jcla.22631
pmc: PMC6430335
doi:
Substances chimiques
Glycerophospholipids
0
phosphatidylethanol
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e22631Informations de copyright
© 2018 Wiley Periodicals, Inc.
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