Comparison of electrochemical and chemical approaches to forced oxidative degradation studies: Abacavir case study

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F24%3A10482522" target="_blank" >RIV/00216208:11310/24:10482522 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=WXh_9G.Wfe" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=WXh_9G.Wfe</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.rechem.2024.101336" target="_blank" >10.1016/j.rechem.2024.101336</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Comparison of electrochemical and chemical approaches to forced oxidative degradation studies: Abacavir case study

Popis výsledku v původním jazyce

This article demonstrates the potential of electrochemical oxidation as an alternative approach to studying the effect of oxidation on active pharmaceutical ingredients. The performance and the outcomes of the electrochemical approach are compared to those of the more common approaches such as peroxide mediated, radical, or metal ion oxidation. The effect of oxidation on abacavir and the effect of the solvent were studied. Electrochemical oxidation was performed using an electrochemical flow cell in static mode, with a glassy carbon electrode (working potential 1.3 V) and a boron-doped diamond electrode (working potential 2.5 V) used as the working electrodes. The glassy carbon electrode was used to monitor the oxidative degradation by electron transfer mechanism and boron-doped diamond electrode was used to monitor the degradation by electron transfer and radical mechanism. The largest amounts of degradation products formed by electrochemical oxidation were observed in a cosolvent consisting of 0.5 M aqueous ammonium acetate pH 7.0 with MeOH (1:9; v/v) in 5 h, 10.6 % and 7.1 % of degradation products were formed on glassy carbon electrode and boron-doped diamond electrode, respectively. Peroxide mediated oxidation in 0.3 % hydrogen peroxide for 72 h at ambient temperature yielded the most degradation products, i.e., 8.7 %, in cosolvent consisting of 0.5 M ammonium acetate, pH 7.0, with MeOH (1:1; v/v). The third approach was radical oxidation using AIBN as a radical initiator at a concentration of 20 mol % at 50 C for 7 days. The most degradation products, i.e., 34.2 %, formed by radical oxidation were observed in pure MeOH. The last approach tested was oxidation using metal ions. A 1.0 mmol/l FeCl3 solution was used and the oxidation took place for 7 days at 50 C. During the metal ion oxidation, the most degradation products, i.e., 25.7 % were formed in pure MeOH.

Název v anglickém jazyce

Comparison of electrochemical and chemical approaches to forced oxidative degradation studies: Abacavir case study

Popis výsledku anglicky

This article demonstrates the potential of electrochemical oxidation as an alternative approach to studying the effect of oxidation on active pharmaceutical ingredients. The performance and the outcomes of the electrochemical approach are compared to those of the more common approaches such as peroxide mediated, radical, or metal ion oxidation. The effect of oxidation on abacavir and the effect of the solvent were studied. Electrochemical oxidation was performed using an electrochemical flow cell in static mode, with a glassy carbon electrode (working potential 1.3 V) and a boron-doped diamond electrode (working potential 2.5 V) used as the working electrodes. The glassy carbon electrode was used to monitor the oxidative degradation by electron transfer mechanism and boron-doped diamond electrode was used to monitor the degradation by electron transfer and radical mechanism. The largest amounts of degradation products formed by electrochemical oxidation were observed in a cosolvent consisting of 0.5 M aqueous ammonium acetate pH 7.0 with MeOH (1:9; v/v) in 5 h, 10.6 % and 7.1 % of degradation products were formed on glassy carbon electrode and boron-doped diamond electrode, respectively. Peroxide mediated oxidation in 0.3 % hydrogen peroxide for 72 h at ambient temperature yielded the most degradation products, i.e., 8.7 %, in cosolvent consisting of 0.5 M ammonium acetate, pH 7.0, with MeOH (1:1; v/v). The third approach was radical oxidation using AIBN as a radical initiator at a concentration of 20 mol % at 50 C for 7 days. The most degradation products, i.e., 34.2 %, formed by radical oxidation were observed in pure MeOH. The last approach tested was oxidation using metal ions. A 1.0 mmol/l FeCl3 solution was used and the oxidation took place for 7 days at 50 C. During the metal ion oxidation, the most degradation products, i.e., 25.7 % were formed in pure MeOH.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10406 - Analytical chemistry

Projekt

—

Návaznosti

S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2024

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Results in Chemistry

ISSN

2211-7156

e-ISSN

2211-7156

Svazek periodika

7

Číslo periodika v rámci svazku

January

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

8

Strana od-do

101336

Kód UT WoS článku

001179022200001

EID výsledku v databázi Scopus

2-s2.0-85183923753