ArticleACS omega2025
Colloidal Dispersions of Gramicidin D in Water: Preparation, Characterization, and Differential Cytotoxicity.
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.
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.
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.
Who cites it
1 citing paper in PubMed.
- Gramicidin D as a Multi-Target Antimicrobial Against Staphylococcus aureus: Biofilm Disruption, Virulence Attenuation, Antibiotic Potentiation, and Protein-Peptide Docking Insight.Probiotics and antimicrobial proteins · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
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
What Socratic holds
Registered trials
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.