Ultra-high performance hydrophilic interaction liquid chromatography - Triple quadrupole tandem mass spectrometry method for determination of cysteine, homocysteine, cysteinyl-glycine and glutathione in rat plasma.
Animals
Chemical Fractionation
/ instrumentation
Chromatography, High Pressure Liquid
/ instrumentation
Cysteine
/ blood
Dipeptides
/ blood
Disease Models, Animal
Glutathione
/ blood
Homocysteine
/ blood
Humans
Hydrophobic and Hydrophilic Interactions
Maleimides
/ chemistry
Rats
Rats, Inbred SHR
Rats, Transgenic
Sensitivity and Specificity
Tandem Mass Spectrometry
/ instrumentation
Tauopathies
/ blood
tau Proteins
/ genetics
Derivatization
LC–MS/MS
N-phenylmaleimide
Tauopathy
Thiols
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:
05 Feb 2019
05 Feb 2019
Historique:
received:
21
09
2018
revised:
08
10
2018
accepted:
29
10
2018
pubmed:
18
11
2018
medline:
20
3
2019
entrez:
18
11
2018
Statut:
ppublish
Résumé
An ultra-high performance hydrophilic interaction liquid chromatography - triple quadrupole tandem mass spectrometry method was developed for the determination of biologically important thiols, namely cysteine, homocysteine, cysteinyl-glycine, glutathione, in rat plasma. The sample preparation procedure as well as the analytical method were comprehensively optimized and subsequently validated. An optimum sample preparation protocol was based on the simple and fast derivatization of the thiols with new derivatization reagent, N-phenylmaleimide, enabling highly selective and sensitive quantification in plasma matrices. The method, characterized by favourable performance parameters and meeting the FDA criteria for biomedical analysis, was successfully applied for monitoring the concentration levels of the selected thiols in the samples from transgenic rat model for tauopathy. The study revealed significant changes in homocysteine and glutathione levels related to tauopathy while other thiols did not indicate such relationship. Indeed, these findings could play an important role in further understanding of tauopathy process in the brain. Moreover, the proposed highly effective, reliable and robust analytical protocol can be easily adapted for other thiol compounds, spreading its application range in this biomedical field.
Identifiants
pubmed: 30447532
pii: S0731-7085(18)32157-5
doi: 10.1016/j.jpba.2018.10.053
pii:
doi:
Substances chimiques
Dipeptides
0
MAPT protein, human
0
Maleimides
0
tau Proteins
0
Homocysteine
0LVT1QZ0BA
cysteinylglycine
384644SZ9T
N-phenylmaleimide
9U9KT462VW
Glutathione
GAN16C9B8O
Cysteine
K848JZ4886
Types de publication
Journal Article
Validation Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
442-451Informations de copyright
Copyright © 2018 Elsevier B.V. All rights reserved.