A Quantitative Method for Simultaneous Determination of 5-Methoxy-N,N-Diisopropyltryptamine and its Metabolites in Urine Using Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry
- Authors
- Jin, Ming J.; Jin, Changbae; Kim, Jin Y.; In, Moon K.; Kwon, Oh S.; Yoo, Hye H.
- Issue Date
- Jul-2011
- Publisher
- American Society for Testing and Materials
- Keywords
- forensic science; 5-MeO-DIPT; 5-OH-DIPT; 5-MeO-IPT; urine; LC/MS/MS
- Citation
- Journal of Forensic Sciences, v.56, no.4, pp 1044 - 1048
- Pages
- 5
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Journal of Forensic Sciences
- Volume
- 56
- Number
- 4
- Start Page
- 1044
- End Page
- 1048
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/37324
- DOI
- 10.1111/j.1556-4029.2011.01753.x
- ISSN
- 0022-1198
1556-4029
- Abstract
- 5-Methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT) is a designer hallucinogen derived from tryptamine and is reportedly abused and involved in criminal activities. For the detection of 5-MeO-DIPT use, a liquid chromatography-tandem mass spectrometric method for 5-MeO-DIPT and its metabolites, 5-hydroxy-N,N-diisopropyltryptamine (5-OH-DIPT) and 5-methoxy-N,N-isopropyltryptamine (5-MeO-IPT) was developed and validated in rat urine. The urine samples were pretreated by protein precipitation with acetonitrile and introduced into a BDS HYPERSIL C-18 column (50 x 2.0 mm, 5 mu m) for chromatographic separation. Mobile phases consisted of methanol, water, and 1% formic acid, and gradient elution was used at a flow rate of 0.2 mL/min. For the MS detection, multiple-reaction monitoring analysis was adopted. The linear range was 0.01-10 mu g/mL, and the lower limit of quantification was 10 ng/mL for all analytes. The intra- and interday accuracies and precisions met the criteria (< 15%). The developed method was successfully applied to the drug-treated rat urine.
- Files in This Item
-
Go to Link
- Appears in
Collections - COLLEGE OF PHARMACY > DEPARTMENT OF PHARMACY > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.