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Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives

This study investigated the antioxidant activity DPPH, ABTS, and Folin–Ciocalteu methods of betulin (compound 1) and its derivatives (compounds 2–11). Skin permeability and accumulation associated with compounds 1 and 8 were also examined. Identification of the obtained products (compound 2–11) and...

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Autores principales: Günther, Andrzej, Makuch, Edyta, Nowak, Anna, Duchnik, Wiktoria, Kucharski, Łukasz, Pełech, Robert, Klimowicz, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201114/
https://www.ncbi.nlm.nih.gov/pubmed/34198892
http://dx.doi.org/10.3390/molecules26113435
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author Günther, Andrzej
Makuch, Edyta
Nowak, Anna
Duchnik, Wiktoria
Kucharski, Łukasz
Pełech, Robert
Klimowicz, Adam
author_facet Günther, Andrzej
Makuch, Edyta
Nowak, Anna
Duchnik, Wiktoria
Kucharski, Łukasz
Pełech, Robert
Klimowicz, Adam
author_sort Günther, Andrzej
collection PubMed
description This study investigated the antioxidant activity DPPH, ABTS, and Folin–Ciocalteu methods of betulin (compound 1) and its derivatives (compounds 2–11). Skin permeability and accumulation associated with compounds 1 and 8 were also examined. Identification of the obtained products (compound 2–11) and betulin isolated from plant material was based on the analysis of (1)H- NMR and (13)C-NMR spectra. The partition coefficient was calculated to determine the lipophilicity of all compounds. In the next stage, the penetration through pig skin and its accumulation in the skin were evaluated of ethanol vehicles containing compound 8 (at a concentration of 0.226 mmol/dm(3)), which was characterized by the highest antioxidant activity. For comparison, penetration studies of betulin itself were also carried out. Poor solubility and the bioavailability of pure compounds are major constraints in combination therapy. However, we observed that the ethanol vehicle was an enhancer of skin permeation for both the initial betulin and compound 8. The betulin 8 derivative showed increased permeability through biological membranes compared to the parent betulin. The paper presents the transformation of polycyclic compounds to produce novel derivatives with marked antioxidant activities and as valuable intermediates for the pharmaceutical industry. Moreover, the compounds contained in the vehicles, due to their mechanism of action, can have a beneficial effect on the balance between oxidants and antioxidants in the body, minimizing the effects of oxidative stress. The results of this work may contribute to knowledge regarding vehicles with antioxidant potential. The use of vehicles for this type of research is therefore justified.
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spelling pubmed-82011142021-06-15 Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives Günther, Andrzej Makuch, Edyta Nowak, Anna Duchnik, Wiktoria Kucharski, Łukasz Pełech, Robert Klimowicz, Adam Molecules Article This study investigated the antioxidant activity DPPH, ABTS, and Folin–Ciocalteu methods of betulin (compound 1) and its derivatives (compounds 2–11). Skin permeability and accumulation associated with compounds 1 and 8 were also examined. Identification of the obtained products (compound 2–11) and betulin isolated from plant material was based on the analysis of (1)H- NMR and (13)C-NMR spectra. The partition coefficient was calculated to determine the lipophilicity of all compounds. In the next stage, the penetration through pig skin and its accumulation in the skin were evaluated of ethanol vehicles containing compound 8 (at a concentration of 0.226 mmol/dm(3)), which was characterized by the highest antioxidant activity. For comparison, penetration studies of betulin itself were also carried out. Poor solubility and the bioavailability of pure compounds are major constraints in combination therapy. However, we observed that the ethanol vehicle was an enhancer of skin permeation for both the initial betulin and compound 8. The betulin 8 derivative showed increased permeability through biological membranes compared to the parent betulin. The paper presents the transformation of polycyclic compounds to produce novel derivatives with marked antioxidant activities and as valuable intermediates for the pharmaceutical industry. Moreover, the compounds contained in the vehicles, due to their mechanism of action, can have a beneficial effect on the balance between oxidants and antioxidants in the body, minimizing the effects of oxidative stress. The results of this work may contribute to knowledge regarding vehicles with antioxidant potential. The use of vehicles for this type of research is therefore justified. MDPI 2021-06-05 /pmc/articles/PMC8201114/ /pubmed/34198892 http://dx.doi.org/10.3390/molecules26113435 Text en © 2021 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 Article
Günther, Andrzej
Makuch, Edyta
Nowak, Anna
Duchnik, Wiktoria
Kucharski, Łukasz
Pełech, Robert
Klimowicz, Adam
Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives
title Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives
title_full Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives
title_fullStr Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives
title_full_unstemmed Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives
title_short Enhancement of the Antioxidant and Skin Permeation Properties of Betulin and Its Derivatives
title_sort enhancement of the antioxidant and skin permeation properties of betulin and its derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201114/
https://www.ncbi.nlm.nih.gov/pubmed/34198892
http://dx.doi.org/10.3390/molecules26113435
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