Evidence map›Paper›PMID 39862190›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2025

Modification of Liposomal Properties by an Engineered Gemini Surfactant.

Ala'a F Eftaiha, Buti Suryabrahmam, Nicholas B Morris, Abdussalam K Qaroush, Khaleel I Assaf, Dina M Foudeh, Suhad B Hammad, Rana Ashkar

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Ala'a F EftaihaDepartment of Chemistry, Faculty of Science, The Hashemite University, Zarqa 13133, Jordan.ORCID 0000-0003-4285-2546
Buti SuryabrahmamDepartment of Physics, Virginia Tech, Blacksburg, Virginia 24061, United States.ORCID 0000-0002-8517-1604
Nicholas B MorrisDepartment of Physics, Virginia Tech, Blacksburg, Virginia 24061, United States.
Abdussalam K QaroushDepartment of Chemistry, Faculty of Science, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0001-6549-7693
Khaleel I AssafDepartment of Chemistry, Faculty of Science, Al-Balqa Applied University, Al-Salt 19117, Jordan.ORCID 0000-0003-4331-8492
Dina M FoudehDepartment of Chemistry, Faculty of Science, The University of Jordan, Amman 11942, Jordan.
Suhad B HammadDepartment of Chemistry, Faculty of Science, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0003-4449-5642
Rana AshkarDepartment of Physics, Virginia Tech, Blacksburg, Virginia 24061, United States.ORCID 0000-0003-4075-2330

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid membranes form the primary structure of cell membranes and serve as configurable interfaces across numerous applications including biosensing technologies, antifungal treatments, and therapeutic platforms. Therefore, the modification of lipid membranes by additives has important consequences in both biological processes and practical applications. In this study, we investigated a nicotinic-acid-based gemini surfactant (NAGS) as a chemically tunable molecular additive for modulating the structure and phase behavior of liposomal membranes. We specifically focused on NAGS with hydrocarbon chains that mirror those of lipid molecules. By introducing NAGS to phosphatidylcholine membranes with lipids of identical and varied chain lengths or degrees of unsaturation, we demonstrated the effects of headgroup interactions and chain mismatch between NAGS and membrane lipids. Using small-angle X-ray scattering, we showed that regardless of chain compatibility or mismatch, NAGS reduced the thickness and packing density of fluid lipid membranes. Further observations by fluorescence microscopy revealed the emergence of ordered-disordered domains upon cooling to room temperature. The observed phases were quite distinct from those of lipid membranes with analogous chain compositions, emphasizing the importance of NAGS headgroup chemistry in mediating domain formation and stabilization. These findings open new possibilities for exploiting NAGS in tuning the structure and organization of liposomal membranes with potential applications in drug delivery and biomedical imaging.

Indexed as

LiposomesSurface-Active AgentsPhosphatidylcholinesLiposomesPhosphatidylcholinesSurface-Active Agents

Identifiers

PMID39862190
PMCPMC11823631

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Registered trials

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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 OpenQuestion graph.