Synthesis, Antioxidant and Antimicrobial Activity of a New Phloridzin Derivative for Dermo-Cosmetic Applications

被引:43
作者
Baldisserotto, Anna [1 ]
Malisardi, Gemma [1 ]
Scalambra, Emanuela [1 ]
Andreotti, Elisa [2 ]
Romagnoli, Carlo [2 ]
Vicentini, Chiara Beatrice [1 ,3 ]
Manfredini, Stefano [1 ,3 ]
Vertuani, Silvia [1 ,3 ]
机构
[1] Univ Ferrara, Dept Life Sci & Biotechnol, I-44121 Ferrara, Italy
[2] Univ Modena & Reggio Emilia, Dept Life Sci, I-41121 Modena, Italy
[3] Ambrosialab, I-44121 Ferrara, Italy
关键词
phloridzin; F2; antioxidant activity; PCL; HPLC analysis; stability in dermocosmetic formulations; antifungal activity; POTENT ANTIOXIDANT; APPLE; PHLORETIN; FLAVONOIDS; METABOLISM; CANCER; CHOLESTEROL; POLYPHENOL; ABSORPTION; EXPRESSION;
D O I
10.3390/molecules171113275
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:13275 / 13289
页数:15
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