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

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

ACS Omega

Biocolloids Laboratory, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Avenida Professor Lineu Prestes, 748, Butantan, São Paulo, SP 05508-000, Brazil.

Published: March 2025

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11886900PMC
http://dx.doi.org/10.1021/acsomega.4c11133DOI Listing

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