Synthesis and Study of Antifungal Properties of New Cationic Beta-Glucan Derivatives

Bibliographic Details
Title: Synthesis and Study of Antifungal Properties of New Cationic Beta-Glucan Derivatives
Authors: Kamil Kaminski, Magdalena Skora, Paweł Krzyściak, Sylwia Stączek, Agnieszka Zdybicka-Barabas, Małgorzata Cytryńska
Source: Pharmaceuticals, Vol 14, Iss 9, p 838 (2021)
Publisher Information: MDPI AG, 2021.
Publication Year: 2021
Collection: LCC:Medicine
LCC:Pharmacy and materia medica
Subject Terms: antifungal, beta-glucan, polycations, Galleria mellonella model, Medicine, Pharmacy and materia medica, RS1-441
More Details: The interaction of positively charged polymers (polycations) with a biological membrane is considered to be the cause of the frequently observed toxicity of these macromolecules. If it is possible to obtain polymers with a predominantly negative effect on bacterial and fungal cells, such systems would have great potential in the treatment of infectious diseases, especially now when reports indicate the growing risk of fungal co-infections in COVID-19 patients. We describe in this article cationic derivatives of natural beta-glucan polymers obtained by reacting the polysaccharide isolated from Saccharomyces boulardii (SB) and Cetraria islandica (CI) with glycidyl trimethyl ammonium chloride (GTMAC). Two synthesis strategies were applied to optimize the product yield. Fungal diseases particularly affect low-income countries, hence the emphasis on the simplicity of the synthesis of such drugs so they can be produced without outside help. The three structures obtained showed selective anti-mycotic properties (against, i.e., Scopulariopsis brevicaulis, Aspergillus brasiliensis, and Fusarium solani), and their toxicity established using fibroblast 3T3-L1 cell line was negligible in a wide range of concentrations. For one of the polymers (SB derivative), using in vivo model of Aspergillus brasiliensis infection in Galleria mellonella insect model, we confirmed the promising results obtained in the preliminary study.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1424-8247
Relation: https://www.mdpi.com/1424-8247/14/9/838; https://doaj.org/toc/1424-8247
DOI: 10.3390/ph14090838
Access URL: https://doaj.org/article/e1d7413969c44a88a8d51c0d98ef7bf6
Accession Number: edsdoj.1d7413969c44a88a8d51c0d98ef7bf6
Database: Directory of Open Access Journals
More Details
ISSN:14248247
DOI:10.3390/ph14090838
Published in:Pharmaceuticals
Language:English