Digitální knihovnaUPCE
 

Optimization of Gradient Reversed Phase High Performance Liquid Chromatography Analysis of Acetaminophen Oxidation Metabolites using Linear and Non-linear Retention Model

ČlánekOmezený přístuppeer-reviewedpublished
Náhled

Datum publikování

2022

Autoři

Váňová, Jana
Dávid, Maliňák
Rudolf, Andrýs
Kubát, Miroslav
Mikysek, Tomáš
Roušarová, Erika
Kamil, Musílek
Roušar, Tomáš
Česla, Petr

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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

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Zdrojový dokument

Journal of Chromatography A, volume 1669, issue: April

Vydavatelská verze

https://www.sciencedirect.com/science/article/pii/S0021967322001546

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pouze v rámci univerzity

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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

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