Optimization of Gradient Reversed Phase High Performance Liquid Chromatography Analysis of Acetaminophen Oxidation Metabolites using Linear and Non-linear Retention Model
ČlánekOmezený přístuppeer-reviewedpublishedDatum publikování
2022
Autoři
Váňová, Jana
Dávid, Maliňák
Rudolf, Andrýs
Kubát, Miroslav
Mikysek, Tomáš
Roušarová, Erika
Kamil, Musílek
Roušar, Tomáš
Česla, Petr
Vedoucí práce
Oponent
Název časopisu
Název svazku
Vydavatel
Abstrakt
Acetaminophen (paracetamol, APAP) is one of the most widely used drugs worldwide. Unfortunately, its overdose, which is caused by predominant oxidation of APAP, can lead to acute liver injury. In liver, oxidized APAP is conjugated with glutathione, leading to APAP-glutathione conjugate, which is metabolized to APAP-cysteine and APAP-N-acetylcysteine conjugates. Thus, all of those compounds could be used to monitor APAP metabolism in the overdosed patients. To date, only a limited number of rapid and accurate methods have been reported for the assessment of APAP oxidation metabolites using simple instrumentation, and thus this work was aimed at developing a fast and convenient gradient HPLC-UV/MS method. For this purpose, APAP conjugates with glutathione, cysteine, and N-acetylcysteine were synthesized, purified by preparative liquid chromatography, and characterized by NMR and high-resolution mass spectrometry. The gradient elution conditions were optimized using the window diagram approach and the effects of mobile phase composition and additives on separation and detection sensitivity were evaluated using two, i.e., linear and non-linear isocratic retention models. Quantitative parameters of the developed method were evaluated and the effectiveness, sensitivity, and specificity of the method were demonstrated on the analysis of human kidney HK-2 cell lysates, confirming the suitability of the method for routine use in studies on APAP toxicity.
Rozsah stran
article 462956
ISSN
0021-9673
Trvalý odkaz na tento záznam
Projekt
Zdrojový dokument
Journal of Chromatography A, volume 1669, issue: April
Vydavatelská verze
https://www.sciencedirect.com/science/article/pii/S0021967322001546
Přístup k e-verzi
pouze v rámci univerzity
Název akce
ISBN
Studijní obor
Studijní program
Signatura tištěné verze
Umístění tištěné verze
Přístup k tištěné verzi
Klíčová slova
acetaminophen, acetaminophen-S-conjugates, metabolites, gradient elution, optimization, isocratic retention models, window diagram, acetaminofen, S-konjugáty acetaminofenu, metabolity, gradientová eluce, optimalizace, isokratický retenční model, okénkový diagram