Application of probe electrospray ionization-tandem mass spectrometry to ultra-rapid determination of glufosinate and glyphosate in human serum.


Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
10 Sep 2019
Historique:
received: 31 01 2019
revised: 16 05 2019
accepted: 20 05 2019
pubmed: 7 6 2019
medline: 6 2 2020
entrez: 7 6 2019
Statut: ppublish

Résumé

Glufosinate and glyphosate, which are non-selective herbicides that include an amino acid moiety in their structures, are frequently used worldwide to control unwanted vegetation. Unfortunately, these readily available herbicides are also used by people to commit suicide, and thus represent important chemicals of interest in the fields of clinical medicine and forensics. Because of the high water solubility of these herbicides, most analytical methods for their detection require a derivatization step, which results in longer analysis times. Therefore, derivatization-based methods do not currently contribute to judgements on treatment decisions in emergency medicine. In this study, we addressed this limiting factor by developing an ultra-rapid and simple analytical technique using a combination of probe electrospray ionization (PESI) and tandem mass spectrometry (MS/MS), which gives quantitative results within 0.3 min. Herbicide standards were added to human serum that was then subjected to analysis (N = 5 per concentration). The analysis was repeated daily over eight consecutive days. The limit of detection (LOD) was 0.59 μg/mL for glufosinate and 0.20 μg/mL for glyphosate. The limit of quantitation (LOQ), i.e., the lowest point on the calibration curves, was 1.56 μg/mL for both the herbicides. The matrix effects were observed at three different concentrations (between 95.7%-104% for glufosinate, and between 90.7%-95.7% for glyphosate). When applied to samples taken from actual poisoning cases (six samples for each herbicide), the present method gave almost the same quantitative values as those obtained by conventional high-performance liquid chromatography with fluorescence detection. Thus, we believe that PESI-MS/MS could emerge as a rapid diagnosis method in the clinical emergency field.

Identifiants

pubmed: 31170631
pii: S0731-7085(19)30278-X
doi: 10.1016/j.jpba.2019.05.040
pii:
doi:

Substances chimiques

Aminobutyrates 0
Herbicides 0
phosphinothricin 51276-47-2
Glycine TE7660XO1C

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

175-181

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Kiyotaka Usui (K)

Division of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan. Electronic address: usui@forensic.med.tohoku.ac.jp.

Eriko Minami (E)

Division of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

Yuji Fujita (Y)

Division of Emergency Medicine, Iwate Medical University, Morioka 020-8505, Japan.

Eito Kubota (E)

Division of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

Haruka Kobayashi (H)

Division of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

Tomoki Hanazawa (T)

Emergency Medical Center and Poison Center, Saitama Medical University Hospital, Saitama 350-0495, Japan.

Tomohiro Yoshizawa (T)

Emergency Medical Center and Poison Center, Saitama Medical University Hospital, Saitama 350-0495, Japan.

Yoshito Kamijo (Y)

Emergency Medical Center and Poison Center, Saitama Medical University Hospital, Saitama 350-0495, Japan.

Masato Funayama (M)

Division of Forensic Medicine, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

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Classifications MeSH