Antioxidant Activity of Prochlorperazine Dimaleate

Reactive oxygen species participate in many physiological processes of the body, but their excess disturbs the metabolic balance and leads to an unfavorable phenomenon called oxidative stress. Several mechanisms account for ROS elimination. One of the antioxidants may be phenothiazine derivatives because of the basic chemical structure – the phenothiazine ring. The study aimed to assess the antioxidant activity of prochlorperazine dimaleate, a phenothiazine derivative, and compare it with reference antioxidants (Trolox and ascorbic acid). Thus, we investigated ABTS, DPPH, CUPRAC, FRAP, and scavenging superoxide anion radical (O2•) assays. It was shown that prochlorperazine dimaleate does not reduce ABTS radicals; meanwhile, Trolox significantly decreased these radicals dose-dependently. Moreover, prochlorperazine dimaleate scavenges DPPH radicals, but it is much less efficient than ascorbic acid. Noteworthy, we noticed that the analyzed drug significantly reduces Fe3+ and Cu2+ ions, as well as scavenges O2• radicals. Based on the obtained IC50 values, the antioxidant activity of prochlorperazine dimaleate could be as follows: CUPRAC > FRAP > O2• > DPPH > ABTS. Of course, to present a full view of the potential antioxidant activity of phenothiazine derivatives, further experiments must be performed using other derivatives.

Authors

Publication Details

Journal
Acta Poloniae Pharmaceutica - Drug Research
Published
2025-04-09
DOI
https://doi.org/10.32383/appdr/200888
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Antioxidant Activity of Prochlorperazine Dimaleate

Jerzy Stojko, Agata Kabała‐Dzik, Michał Otręba, Anna Rzepecka‐Stojko et al.
Acta Poloniae Pharmaceutica - Drug Research
Synthesis and biological activity
article

Antioxidant Activity of Prochlorperazine Dimaleate

Jerzy Stojko, Agata Kabała‐Dzik, Michał Otręba, Anna Rzepecka‐Stojko, Tiago Rodrigues, Anna Kleczka
article en

Abstract

Reactive oxygen species participate in many physiological processes of the body, but their excess disturbs the metabolic balance and leads to an unfavorable phenomenon called oxidative stress. Several mechanisms account for ROS elimination. One of the antioxidants may be phenothiazine derivatives because of the basic chemical structure – the phenothiazine ring. The study aimed to assess the antioxidant activity of prochlorperazine dimaleate, a phenothiazine derivative, and compare it with reference antioxidants (Trolox and ascorbic acid). Thus, we investigated ABTS, DPPH, CUPRAC, FRAP, and scavenging superoxide anion radical (O2•) assays. It was shown that prochlorperazine dimaleate does not reduce ABTS radicals; meanwhile, Trolox significantly decreased these radicals dose-dependently. Moreover, prochlorperazine dimaleate scavenges DPPH radicals, but it is much less efficient than ascorbic acid. Noteworthy, we noticed that the analyzed drug significantly reduces Fe3+ and Cu2+ ions, as well as scavenges O2• radicals. Based on the obtained IC50 values, the antioxidant activity of prochlorperazine dimaleate could be as follows: CUPRAC > FRAP > O2• > DPPH > ABTS. Of course, to present a full view of the potential antioxidant activity of phenothiazine derivatives, further experiments must be performed using other derivatives.

Acta Poloniae Pharmaceutica - Drug ResearchVol. 81(6)
Śląski Uniwersytet Medyczny w Katowicach, Uniwersytet Śląski w Katowicach
Openalex Percentile: Top 95%
Synthesis and biological activity
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.