3,4-Dihydropyrimidin-2-(1H)-one-Based Cationic Surfactants: Synthesis, Self-Assembly, and Antimicrobial Activity

-average and surfactant hydrophobicity, which was further supported by transmission electron microscopy. The aggregation number was determined by fluorescence quenching. The antimicrobial efficacy of DHPM-based surfactants was evaluated against six pathogenic microbes, including both gram-positive and gram-negative bacteria and fungi, to assess differences in antimicrobial potency. Molecular docking revealed interactions between surfactant head groups and bacterial cell wall components.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-07-27
DOI
https://doi.org/10.1021/acsami.6c07588
Primary Topic
Surfactants and Colloidal Systems
Type
article
Field-Weighted Citation Impact
0.00
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article

3,4-Dihydropyrimidin-2-(1H)-one-Based Cationic Surfactants: Synthesis, Self-Assembly, and Antimicrobial Activity

Jamsheera Anjudikkal, Ajmal Koya Pulikkal, Salahudheen VP
ACS Applied Materials & Interfaces
Surfactants and Colloidal Systems
article

3,4-Dihydropyrimidin-2-(1H)-one-Based Cationic Surfactants: Synthesis, Self-Assembly, and Antimicrobial Activity

Jamsheera Anjudikkal, Ajmal Koya Pulikkal, Salahudheen VP
article en

Abstract

-average and surfactant hydrophobicity, which was further supported by transmission electron microscopy. The aggregation number was determined by fluorescence quenching. The antimicrobial efficacy of DHPM-based surfactants was evaluated against six pathogenic microbes, including both gram-positive and gram-negative bacteria and fungi, to assess differences in antimicrobial potency. Molecular docking revealed interactions between surfactant head groups and bacterial cell wall components.

ACS Applied Materials & Interfaces
Autonomous University of Aguascalientes (MX), Government of Mizoram (IN), Maulana Azad National Institute of Technology (IN)
Clean water and sanitation
Openalex Percentile: Top 16%
Surfactants and Colloidal Systems
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