Evidence map›Paper›PMID 42579469›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2026

Erythrocyte Membrane Incorporation Modulates the Stability and Fusion-Associated Behavior of Biomimetic Liposomes.

Lucas R Sousa, Luciano V Sá, Tacio G Hayasaki, Leticia S O Freitas, Karin A Riske, Sebastião A Mendanha, Eliana M Lima

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2026. 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

7 authors.

Lucas R SousaFarmaTec - Laboratory for RD&I in Pharmaceutical Nanotechnology and Drug Delivery Systems , Samambaia Technology Park, 74690-631Goiânia, Goiás, Brazil.
Luciano V SáFarmaTec - Laboratory for RD&I in Pharmaceutical Nanotechnology and Drug Delivery Systems , Samambaia Technology Park, 74690-631Goiânia, Goiás, Brazil.
Tacio G HayasakiFarmaTec - Laboratory for RD&I in Pharmaceutical Nanotechnology and Drug Delivery Systems , Samambaia Technology Park, 74690-631Goiânia, Goiás, Brazil.
Leticia S O FreitasFarmaTec - Laboratory for RD&I in Pharmaceutical Nanotechnology and Drug Delivery Systems , Samambaia Technology Park, 74690-631Goiânia, Goiás, Brazil.ORCID 0009-0009-6531-0695
Karin A RiskeDepartment of Biophysics, Federal University of São Paulo, 04039-032São Paulo, São Paulo, Brazil.ORCID 0000-0003-4080-1358
Sebastião A MendanhaFarmaTec - Laboratory for RD&I in Pharmaceutical Nanotechnology and Drug Delivery Systems , Samambaia Technology Park, 74690-631Goiânia, Goiás, Brazil.ORCID 0000-0002-9545-5248
Eliana M LimaFarmaTec - Laboratory for RD&I in Pharmaceutical Nanotechnology and Drug Delivery Systems , Samambaia Technology Park, 74690-631Goiânia, Goiás, Brazil.ORCID 0000-0003-1231-5803

Funding

Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico 304122/2019-0Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico 315885/2021-1
6 · The paper itself

Abstract

This study investigates how membrane composition governs the stability and fusogenic behavior of biomimetic hybrid liposomes composed of phosphatidylcholine (PC) and red blood cell (RBC) membrane fragments. While prior work on RBC-derived hybrid systems has largely focused on biological performance metrics such as circulation time, cellular uptake, and immune evasion, the biophysical and thermodynamic consequences of membrane hybridization at the molecular level remain poorly explored. Here, we address this gap through a systematic, multitechnique physicochemical characterization of a series of RBC-hybrid liposome formulations spanning a range of lipid:protein ratios. A comprehensive physicochemical characterization was performed using electron spin resonance (ESR) to probe membrane dynamics, microdifferential scanning calorimetry (microDSC) to assess thermotropic behavior, and isothermal titration calorimetry (ITC) to examine membrane energetics, solubilization, and intervesicular interactions. Incorporation of RBC membrane fragments increased membrane rigidity, as indicated by ESR and microDSC, and was associated with enhanced resistance to Triton X-100-induced solubilization, a finding attributed to compositional heterogeneity and protein-lipid organization introduced by membrane hybridization. ITC-based interaction assays further showed that cationic hybrid liposomes exhibited stronger fusion-associated signatures than their conventional counterparts, indicating that RBC membrane incorporation significantly alters interfacial membrane behavior in ways that cannot be explained by lipid composition alone. Together, these results show that RBC membrane content modulates both the structural stability and interaction profile of liposomes, establishing a biophysical framework for understanding how biomembrane-derived components reshape vesicle behavior and providing insights and useful design parameters for the development of robust biomimetic lipid-based delivery systems.

Indexed as

Biomimetic MaterialsErythrocyte MembraneLiposomesBiomimeticsHumansMembrane FusionPhosphatidylcholinesThermodynamicsLiposomesPhosphatidylcholines

Identifiers

PMID42579469
PMCPMC13472161

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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.