Effect of 1‐Hexyl‐3Methylimidazolium Bromide on the Antioxidant Property of Polyphenols: An Ecofriendly Alternative

ABSTRACT Polyphenols are naturally high‐valued secondary plant metabolites that demonstrate strong antimicrobial potential besides their well‐established health‐promoting benefits. The conventional polyphenolic extraction process mostly includes organic solvents, which cause environmental harm. In this context, ionic liquids (ILs) have emerged as an environmentally friendly substitute for traditional solvents to extract various active substances from plants such as coumarins, terpenoids, phenylpropanoids, and flavonoids. This study investigates the synthesis of 1‐hexyl‐3‐methylimidazolium bromide [HMIm][Br], an IL, and studies its impact on the antioxidant and antimicrobial properties of two polyphenolic compounds, gallic acid (GA) and tannic acid (TA), so that it can be effectively used in the extraction process. [HMIm][Br] was synthesized via alkylation and characterized through UV‐Vis, FTIR, and NMR techniques. The mixture of [HMIm][Br] with GA and TA demonstrated enhanced antioxidant activity in DPPH assays; 77% and 82%, respectively, in comparison to pure GA (64%) and TA (73%), suggesting improved free radical scavenging due to synergistic effects. Antibacterial and antibiofilm assays against Escherichia coli and Staphylococcus aureus revealed that when [HMIm][Br] was combined with GA or TA, antimicrobial efficacy was enhanced specifically for S. aureus when compared to the individual components. The zone of inhibition reported in case of S. aureus (GA: 9 mm; [HMIm][Br] + GA: 18 mm; TA: 9 mm; [HMIm][Br] + TA: 14 mm) and E. coli (GA: 8 mm; [HMIm][Br] + GA: 15 mm; TA: 10 mm; [HMIm][Br] + GA: 10 mm). Molecular docking studies supported these findings, indicating binding affinity of ([HMIm][Br]) to bacterial proteins, S. aureus (−5.0 kcal/mol) and E. coli (−4.0 kcal/mol). These results highlight the potential of [HMIm][Br] in improving the solubility, stability, and bioactivity of polyphenols, making the combination a promising candidate for applications in pharmaceuticals, food preservation, and cosmetics. The study contributes to the development of sustainable and effective polyphenol‐based formulations.

Authors

Institutions

Publication Details

Journal
Environmental Quality Management
Published
2025-12-01
DOI
https://doi.org/10.1002/tqem.70246
Primary Topic
Ionic liquids properties and applications
Type
article
Field-Weighted Citation Impact
0.00

Funders

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

Effect of 1‐Hexyl‐3Methylimidazolium Bromide on the Antioxidant Property of Polyphenols: An Ecofriendly Alternative

Tanushree Sahoo, Sangram Keshari Samal, Swaraj Kumar Beriha, Sanghamitra Pradhan et al.
Environmental Quality Management
Ionic liquids properties and applications
article

Effect of 1‐Hexyl‐3Methylimidazolium Bromide on the Antioxidant Property of Polyphenols: An Ecofriendly Alternative

Tanushree Sahoo, Sangram Keshari Samal, Swaraj Kumar Beriha, Sanghamitra Pradhan, Sangeeta Raut, Ananya Pattnaik, Itishree Panda, Vibek Srichandan
article en

Abstract

ABSTRACT Polyphenols are naturally high‐valued secondary plant metabolites that demonstrate strong antimicrobial potential besides their well‐established health‐promoting benefits. The conventional polyphenolic extraction process mostly includes organic solvents, which cause environmental harm. In this context, ionic liquids (ILs) have emerged as an environmentally friendly substitute for traditional solvents to extract various active substances from plants such as coumarins, terpenoids, phenylpropanoids, and flavonoids. This study investigates the synthesis of 1‐hexyl‐3‐methylimidazolium bromide [HMIm][Br], an IL, and studies its impact on the antioxidant and antimicrobial properties of two polyphenolic compounds, gallic acid (GA) and tannic acid (TA), so that it can be effectively used in the extraction process. [HMIm][Br] was synthesized via alkylation and characterized through UV‐Vis, FTIR, and NMR techniques. The mixture of [HMIm][Br] with GA and TA demonstrated enhanced antioxidant activity in DPPH assays; 77% and 82%, respectively, in comparison to pure GA (64%) and TA (73%), suggesting improved free radical scavenging due to synergistic effects. Antibacterial and antibiofilm assays against Escherichia coli and Staphylococcus aureus revealed that when [HMIm][Br] was combined with GA or TA, antimicrobial efficacy was enhanced specifically for S. aureus when compared to the individual components. The zone of inhibition reported in case of S. aureus (GA: 9 mm; [HMIm][Br] + GA: 18 mm; TA: 9 mm; [HMIm][Br] + TA: 14 mm) and E. coli (GA: 8 mm; [HMIm][Br] + GA: 15 mm; TA: 10 mm; [HMIm][Br] + GA: 10 mm). Molecular docking studies supported these findings, indicating binding affinity of ([HMIm][Br]) to bacterial proteins, S. aureus (−5.0 kcal/mol) and E. coli (−4.0 kcal/mol). These results highlight the potential of [HMIm][Br] in improving the solubility, stability, and bioactivity of polyphenols, making the combination a promising candidate for applications in pharmaceuticals, food preservation, and cosmetics. The study contributes to the development of sustainable and effective polyphenol‐based formulations.

Environmental Quality ManagementVol. 35(2)
Siksha O Anusandhan University (IN), Regional Medical Research Center (IN), Regional Medical Research Centre (IN)
Indian Council of Medical Research
Openalex Percentile: Top 72%
Ionic liquids properties and applications
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.