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Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications
The phenolic compound phloridzin (phloretin 2′-O-glucoside, variously named phlorizin, phlorrhizin, phlorhizin or phlorizoside) is a prominent member of the chemical class of dihydrochalcones, which are phenylpropanoids. Phloridzin is specifically found in apple and apple juice and known for its bio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268407/ https://www.ncbi.nlm.nih.gov/pubmed/23135632 http://dx.doi.org/10.3390/molecules171113275 |
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author | Baldisserotto, Anna Malisardi, Gemma Scalambra, Emanuela Andreotti, Elisa Romagnoli, Carlo Vicentini, Chiara Beatrice Manfredini, Stefano Vertuani, Silvia |
author_facet | Baldisserotto, Anna Malisardi, Gemma Scalambra, Emanuela Andreotti, Elisa Romagnoli, Carlo Vicentini, Chiara Beatrice Manfredini, Stefano Vertuani, Silvia |
author_sort | Baldisserotto, Anna |
collection | PubMed |
description | The phenolic compound phloridzin (phloretin 2′-O-glucoside, variously named phlorizin, phlorrhizin, phlorhizin or phlorizoside) is a prominent member of the chemical class of dihydrochalcones, which are phenylpropanoids. Phloridzin is specifically found in apple and apple juice and known for its biological properties. In particular we were attracted by potential dermo-cosmetic applications. Here we report the synthesis, stability studies and antimicrobial activity of compound F2, a new semi-synthetic derivative of phloridzin. The new derivative was also included in finished formulations to evaluate its stability with a view to a potential topical use. Stability studies were performed by HPLC; PCL assay and ORAC tests were used to determine the antioxidant activity. F2 presented an antioxidant activity very close to that of the parent phloridzin, but, unlike the latter, was more stable in formulations. To further explore potential health claims, antifungal activity of phloridzin and its derivative F2 were determined; the results, however, were rather low; the highest value was 31,6% of inhibition reached by F2 on Microsporum canis at the highest dose. |
format | Online Article Text |
id | pubmed-6268407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62684072018-12-13 Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications Baldisserotto, Anna Malisardi, Gemma Scalambra, Emanuela Andreotti, Elisa Romagnoli, Carlo Vicentini, Chiara Beatrice Manfredini, Stefano Vertuani, Silvia Molecules Article The phenolic compound phloridzin (phloretin 2′-O-glucoside, variously named phlorizin, phlorrhizin, phlorhizin or phlorizoside) is a prominent member of the chemical class of dihydrochalcones, which are phenylpropanoids. Phloridzin is specifically found in apple and apple juice and known for its biological properties. In particular we were attracted by potential dermo-cosmetic applications. Here we report the synthesis, stability studies and antimicrobial activity of compound F2, a new semi-synthetic derivative of phloridzin. The new derivative was also included in finished formulations to evaluate its stability with a view to a potential topical use. Stability studies were performed by HPLC; PCL assay and ORAC tests were used to determine the antioxidant activity. F2 presented an antioxidant activity very close to that of the parent phloridzin, but, unlike the latter, was more stable in formulations. To further explore potential health claims, antifungal activity of phloridzin and its derivative F2 were determined; the results, however, were rather low; the highest value was 31,6% of inhibition reached by F2 on Microsporum canis at the highest dose. MDPI 2012-11-07 /pmc/articles/PMC6268407/ /pubmed/23135632 http://dx.doi.org/10.3390/molecules171113275 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Baldisserotto, Anna Malisardi, Gemma Scalambra, Emanuela Andreotti, Elisa Romagnoli, Carlo Vicentini, Chiara Beatrice Manfredini, Stefano Vertuani, Silvia Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications |
title | Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications |
title_full | Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications |
title_fullStr | Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications |
title_full_unstemmed | Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications |
title_short | Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications |
title_sort | synthesis, antioxidant and antimicrobial activity of a new phloridzin derivative for dermo-cosmetic applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268407/ https://www.ncbi.nlm.nih.gov/pubmed/23135632 http://dx.doi.org/10.3390/molecules171113275 |
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