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Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities

Glycolipids are biocompatible and biodegradable amphiphilic compounds characterized by a great scientific interest for their potential applications in various technological areas, including pharmaceuticals, cosmetics, agriculture, and food production. This report summarizes the available synthetic m...

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Autores principales: Verboni, Michele, Perinelli, Diego Romano, Buono, Alessandro, Campana, Raffaella, Sisti, Maurizio, Duranti, Andrea, Lucarini, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604170/
https://www.ncbi.nlm.nih.gov/pubmed/37887201
http://dx.doi.org/10.3390/antibiotics12101500
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author Verboni, Michele
Perinelli, Diego Romano
Buono, Alessandro
Campana, Raffaella
Sisti, Maurizio
Duranti, Andrea
Lucarini, Simone
author_facet Verboni, Michele
Perinelli, Diego Romano
Buono, Alessandro
Campana, Raffaella
Sisti, Maurizio
Duranti, Andrea
Lucarini, Simone
author_sort Verboni, Michele
collection PubMed
description Glycolipids are biocompatible and biodegradable amphiphilic compounds characterized by a great scientific interest for their potential applications in various technological areas, including pharmaceuticals, cosmetics, agriculture, and food production. This report summarizes the available synthetic methodologies, physicochemical properties, and biological activity of sugar fatty acid ester surfactants, with a particular focus on 6-O-glucose, 6-O-mannose, 6-O-sucrose, and 6′-O-lactose ones. In detail, the synthetic approaches to this class of compounds, such as enzymatic lipase-catalyzed and traditional chemical (e.g., acyl chloride, Steglich, Mitsunobu) esterifications, are reported. Moreover, aspects related to the surface activity of these amphiphiles, such as their ability to decrease surface tension, critical micelle concentration, and emulsifying and foaming ability, are described. Biological applications with a focus on the permeability-enhancing effect across the skin or mucosa, antimicrobial and antifungal activities, as well as antibiofilm properties, are also presented. The information reported here on sugar-based ester surfactants is helpful to broaden the interest and the possible innovative applications of this class of amphiphiles in different technological fields in the future.
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spelling pubmed-106041702023-10-28 Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities Verboni, Michele Perinelli, Diego Romano Buono, Alessandro Campana, Raffaella Sisti, Maurizio Duranti, Andrea Lucarini, Simone Antibiotics (Basel) Review Glycolipids are biocompatible and biodegradable amphiphilic compounds characterized by a great scientific interest for their potential applications in various technological areas, including pharmaceuticals, cosmetics, agriculture, and food production. This report summarizes the available synthetic methodologies, physicochemical properties, and biological activity of sugar fatty acid ester surfactants, with a particular focus on 6-O-glucose, 6-O-mannose, 6-O-sucrose, and 6′-O-lactose ones. In detail, the synthetic approaches to this class of compounds, such as enzymatic lipase-catalyzed and traditional chemical (e.g., acyl chloride, Steglich, Mitsunobu) esterifications, are reported. Moreover, aspects related to the surface activity of these amphiphiles, such as their ability to decrease surface tension, critical micelle concentration, and emulsifying and foaming ability, are described. Biological applications with a focus on the permeability-enhancing effect across the skin or mucosa, antimicrobial and antifungal activities, as well as antibiofilm properties, are also presented. The information reported here on sugar-based ester surfactants is helpful to broaden the interest and the possible innovative applications of this class of amphiphiles in different technological fields in the future. MDPI 2023-09-30 /pmc/articles/PMC10604170/ /pubmed/37887201 http://dx.doi.org/10.3390/antibiotics12101500 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Verboni, Michele
Perinelli, Diego Romano
Buono, Alessandro
Campana, Raffaella
Sisti, Maurizio
Duranti, Andrea
Lucarini, Simone
Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities
title Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities
title_full Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities
title_fullStr Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities
title_full_unstemmed Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities
title_short Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities
title_sort sugar-based monoester surfactants: synthetic methodologies, properties, and biological activities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604170/
https://www.ncbi.nlm.nih.gov/pubmed/37887201
http://dx.doi.org/10.3390/antibiotics12101500
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