Evidence map›Paper›PMID 41658063›Full record

ArticleACS omega2026

Direct Retrieval of Biomechanical and Hydrodynamic Parameters for Drug Carrier Liposomes Using Conventional Extrusion Processes.

Maria Victoria Heiderick Machado, Maria Luiza Barbosa Pertence, Caroline Mari Ramos Oda, Jaqueline Aparecida Duarte, Ubirajara Agero, Elaine Amaral Leite, Angelo Malachias

Abstract read
In one paragraph

Article in ACS omega, 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.

Maria Victoria Heiderick MachadoDepartamento de Física, ICEx, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.
Maria Luiza Barbosa PertenceDepartamento de Física, ICEx, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.
Caroline Mari Ramos OdaFaculdade de Farmácia, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.
Jaqueline Aparecida DuarteFaculdade de Farmácia, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.
Ubirajara AgeroDepartamento de Física, ICEx, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.
Elaine Amaral LeiteFaculdade de Farmácia, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.
Angelo MalachiasDepartamento de Física, ICEx, Universidade Federal de Minas Gerais - UFMG, Av. Antonio Carlos, 6627, Belo Horizonte - MG, CEP 30123-970, Brazil.ORCID https://orcid.org/0000-0002-8703-4283

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Physical parameters such as membrane elasticity and solution viscosity in a liquid medium play crucial roles in the effectiveness of drug delivery. Liposome formulations, used in both research and clinical contexts, are usually designed to achieve desired chemical stability, particle size, and drug encapsulation efficiency. However, meeting such requirements may not suffice in order to succeed in in vivo tests, which can be frustrated due to poor evaluation of biomechanical conditions. In this work, we introduce simple biomechanical evaluation protocols that make use of conventional pressure-based liposome extrusion as well as dynamic light scattering results to extract elastic (mechanical) and hydrodynamic (viscosity) properties of colloidal solutions of liposomes. We describe a sequence of analytical steps that need to be carried out in order to obtain macroscopic results that are directly comparable to those of other methods. Two distinct and complementary procedures are presented: the first uses a systematic variation of extrusion pressure, giving access to the viscosity of the solution, and the second being a statistical evaluation of the particle size distribution obtained by dynamic light scattering, providing elasticity constants for liposomal systems. Both methods carry the advantage of generating results for the liposome suspension that will be applied to real systems, thereby offering a more realistic and integrative characterization compared with microscopic techniques that usually present incomplete statistical coverage.

Identifiers

PMID41658063
PMCPMC12878738

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.