Persulfated Ascorbic Acid Glycoside as a Safe and Stable Derivative of Ascorbic Acid for Skin Care Application
Authors:
- Ana JesusAJAna Jesus
- Marta Correia-Da-SilvaMarta Correia-Da-Silva
- Catarina ConfrariaCCCatarina Confraria
- Sílvia SilvaSílvia Silva
- Gonçalo BritesGonçalo Brites
- Ana I. SebastiãoASAna I. Sebastião
- Mylène CarrascalMylène Carrascal
- Madalena PintoMadalena Pinto
- Honorina CidadeHonorina Cidade
- Paulo CostaPCPaulo Costa
- Maria T. CruzMaria T. Cruz
- Emília SousaEmília Sousa
Open Access
- 27 September 2024
- Vol. 29 (19) , 4604
Abstract
The pursuit of cosmetic ingredients with proven efficacy and safety that meet consumer needs drives the advancement of new products. Ascorbic acid (AA) is utilized in cosmetic products, predominantly for its potent antioxidant properties. Nonetheless, its instability compromises its efficacy. In this work, ascorbyl 2-O-glucoside persulfate (AAGS) was synthesized, characterized, and evaluated regarding its safety profile and potential bioactivities and the results were compared to AA and its glycoside AAG. Pre-formulation studies were performed to assess the stability of the compounds and their compatibility with typical excipients commonly used in topical formulations. AAGS did not affect the metabolic activity of keratinocyte, macrophage, and monocyte cell lines, up to 500 µM. AAGS also exhibited a non-prooxidant and non-sensitizing profile and anti-allergic activity by impeding the allergen-induced maturation of THP-1 cells. When compared to AA and AAG, AAGS was shown to be more stable at pH values between 5 and 7, as well as superior thermostability and photostability. AAGS demonstrated higher stability in metal solutions of Fe(II) and Mg(II) than AA. AAGS demonstrated similar DPPH radical scavenging activity compared to AA. These results provide useful information for the development of new AA derivatives, highlighting AAGS as a novel cosmetic ingredient.Keywords
Funding Information
- FCT-Fundação para a Ciência e a Tecnologia (UIDP/04378/2020, LA/P/0140/2020, UIDP/04539/2020, UIDP/04423/2020, LA/P/0058/2020, CENTRO-01-0145-FEDER-000012, UI/BD/151319/2021, PD/BDE/142926/2018)
- Associate Laboratory Institute for Health and Bioeconomy-i4HB (UIDP/04378/2020, LA/P/0140/2020, UIDP/04539/2020, UIDP/04423/2020, LA/P/0058/2020, CENTRO-01-0145-FEDER-000012, UI/BD/151319/2021, PD/BDE/142926/2018)
- Group of Marine Natural Products and Medicinal Chemistry-CIIMAR (UIDP/04378/2020, LA/P/0140/2020, UIDP/04539/2020, UIDP/04423/2020, LA/P/0058/2020, CENTRO-01-0145-FEDER-000012, UI/BD/151319/2021, PD/BDE/142926/2018)
- European Regional Development Fund (ERDF) (UIDP/04378/2020, LA/P/0140/2020, UIDP/04539/2020, UIDP/04423/2020, LA/P/0058/2020, CENTRO-01-0145-FEDER-000012, UI/BD/151319/2021, PD/BDE/142926/2018)
- Ph.D. Grants (UIDP/04378/2020, LA/P/0140/2020, UIDP/04539/2020, UIDP/04423/2020, LA/P/0058/2020, CENTRO-01-0145-FEDER-000012, UI/BD/151319/2021, PD/BDE/142926/2018)
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