Evidence map›Paper›PMID 40060847›Full record

ArticleACS omega2025

Colloidal Dispersions of Gramicidin D in Water: Preparation, Characterization, and Differential Cytotoxicity.

Ricardo Márcio-E-Silva, Bianca R Bazan, Rodrigo T Ribeiro, Sarah N C Gimenes, Bianca C L F Távora, Eliana L Faquim-Mauro, Ana M Carmona-Ribeiro

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Ricardo Márcio-E-SilvaBiocolloids Laboratory, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP 05508-000, Brazil.ORCID https://orcid.org/0009-0004-4916-4118
Bianca R BazanBiocolloids Laboratory, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP 05508-000, Brazil.
Rodrigo T RibeiroBiocolloids Laboratory, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP 05508-000, Brazil.ORCID https://orcid.org/0000-0002-5099-4256
Sarah N C GimenesImmunopathology Laboratory, Butantan Institute, Av. Vital Brasil, 1500, São Paulo 05503-900, Brazil.
Bianca C L F TávoraImmunopathology Laboratory, Butantan Institute, Av. Vital Brasil, 1500, São Paulo 05503-900, Brazil.
Eliana L Faquim-MauroImmunopathology Laboratory, Butantan Institute, Av. Vital Brasil, 1500, São Paulo 05503-900, Brazil.
Ana M Carmona-RibeiroBiocolloids Laboratory, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP 05508-000, Brazil.ORCID https://orcid.org/0000-0001-8500-2707

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gramicidin D (Gr) is a natural mixture of channel peptides A-C with minor differences in chemical structure, which are able to span cell membranes as dimers. These Gr channels allow single-file diffusion of cations, thereby disrupting the usual ionic balance in biological cells and inducing cell lysis. The microbicidal activity of Gr using different carriers such as bilayer vesicles or bilayer disks, supported bilayers on silica, or polystyrene nanoparticles has been described. Gr antimicrobial activity was found to depend strongly on its formulation. Preliminary description of self-assembled Gr nanoparticles (Gr NPs) by our group showed a superior antimicrobial performance for these Gr self-assembled nanospheres. In this work, we further characterize Gr colloidal dispersions in aqueous solution over a range of micromolar concentrations from turbidimetry, obedience to the Rayleigh law for light scattered by NPs smaller than the wavelength of the incident light, dynamic light scattering to ascertain the reproducibility of physical characteristics of Gr NPs, and effects of Gr NPs on the cell viability of five different mammalian cell lines in culture over a micromolar range of Gr concentrations (0.5-5.0 μM). Thereby, the differential cytotoxicity of Gr NPs is inferred from the comparison between effects on microbial cell viability and mammalian cell viability. The results suggest that the simple and efficacious formulation of Gr NPs obtained directly from Gr self-assembly in aqueous solution deserves to be further exploited, aiming at systemic biomedical uses of Gr in vivo against infectious diseases and cancers.

Identifiers

PMID40060847
PMCPMC11886900

What Socratic holds

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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 Socratic graph.