Colloidal Dispersions
of Gramicidin D in Water: Preparation,
Characterization, and Differential Cytotoxicity
Posted on 2025-02-24 - 07:09
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.
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Márcio-e-Silva, Ricardo; Bazan, Bianca R.; Ribeiro, Rodrigo T.; Gimenes, Sarah N. C.; Távora, Bianca C. L. F.; Faquim-Mauro, Eliana L.; et al. (2025). Colloidal Dispersions
of Gramicidin D in Water: Preparation,
Characterization, and Differential Cytotoxicity. ACS Publications. Collection. https://doi.org/10.1021/acsomega.4c11133