Evidence map›Paper›PMID 41125729›Full record

ArticleScientific reports2025

The surface and micellar properties of ethanolamine based surface active ionic liquids in the presence of drug aspirin.

Elaheh Janbezar, Hemayat Shekaari, Shima Ghasemzadeh, Mohammad Bagheri Hokm Abad

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Elaheh JanbezarDepartment of Physical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, 5166616471, Iran.
Hemayat ShekaariDepartment of Physical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, 5166616471, Iran. hemayatt@yahoo.com.
Shima GhasemzadehDepartment of Physical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, 5166616471, Iran.
Mohammad Bagheri Hokm AbadDepartment of Physical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, 5166616471, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bio-based surface-active ionic liquids (SAILs) offer promising advantages for pharmaceutical applications, particularly in enhancing drug solubility and bioavailability. Aspirin, classified under the Biopharmaceutics Classification System (BCS) as poorly soluble in the gastrointestinal tract, require effective solubilization strategies for improved therapeutic efficacy. This study investigates the micellization behavior and thermophysical properties of three natural based SAILs (2-hydroxyethyl)ammonium oleate ([2-HEA][Ole]), bis(2-hydroxyethyl)ammonium oleate ([BHEA][Ole]), and tris(2-hydroxyethyl)ammonium oleate ([THEA][Ole]) in aqueous solutions of aspirin at 298 K. Micellization characteristics, including critical micelle concentration (CMC), were determined using electrical conductivity and surface tension measurements for SAILs in the presence of the aspirin aqueous solutions systems at 298 K. Key interfacial parameters such as interface surface pressure (Π), minimum surface area occupied per molecule ([Formula: see text]), Gibbs maximum excess surface concentration ([Formula: see text]) were also calculated. Additionally, the Conductor-like Screening Model (COSMO) was employed to elucidate molecular interactions between SAILs and the studied drug. The results indicate that CMC values decrease in the presence of aspirin. Among the studied systems, [THEA][Ole] exhibited the lowest CMC, as determined by electrical conductivity and surface tension measurements, particularly in the presence of higher concentrations of aspirin in aqueous media. Furthermore, COSMO analysis revealed that [THEA][Ole], possessing the highest surface cavity volume (V), demonstrated the most favorable interactions with aspirin, highlighting its potential as an effective solubilizing agent. Finally, interactions between SAILs and aspirin were investigated through limiting molar conductivity [Formula: see text] , and association constant [Formula: see text] , determination.

Indexed as

AspirinIonic LiquidsMicellesSurface-Active AgentsElectric ConductivitySolubilitySurface PropertiesSurface TensionAspirinIonic LiquidsMicellesSurface-Active AgentsAspirinBiobased surface-active ionic liquidsCOSMO analysisElectrical conductivitySurface tension

Identifiers

PMID41125729
PMCPMC12546906

What Socratic holds

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.