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Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential
The flavonoid rutin (RU) is a known antioxidant substance of plant origin. Its potential application in pharmaceutical and cosmetic fields is, however, limited, due to its low water solubility. This limitation can be overcome by polymerization of the phenolic RU into polyrutin (PR). In this work, an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835416/ https://www.ncbi.nlm.nih.gov/pubmed/31561552 http://dx.doi.org/10.3390/polym11101566 |
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author | Pivec, Tanja Kargl, Rupert Maver, Uroš Bračič, Matej Elschner, Thomas Žagar, Ema Gradišnik, Lidija Stana Kleinschek, Karin |
author_facet | Pivec, Tanja Kargl, Rupert Maver, Uroš Bračič, Matej Elschner, Thomas Žagar, Ema Gradišnik, Lidija Stana Kleinschek, Karin |
author_sort | Pivec, Tanja |
collection | PubMed |
description | The flavonoid rutin (RU) is a known antioxidant substance of plant origin. Its potential application in pharmaceutical and cosmetic fields is, however, limited, due to its low water solubility. This limitation can be overcome by polymerization of the phenolic RU into polyrutin (PR). In this work, an enzymatic polymerization of RU was performed in water, without the addition of organic solvents. Further, the chemical structure of PR was investigated using (1)H NMR, and FTIR spectroscopy. Size-exclusion chromatography (SEC) was used to determine the molecular weight of PR, while its acid/base character was studied by potentiometric charge titrations. Additionally, this work investigated the antioxidant and free radical scavenging potential of PR with respect to its chemical structure, based on its ability to (i) scavenge non biological stable free radicals (ABTS), (ii) scavenge biologically important oxidants, such as O(2)•, NO•, and OH•, and (iii) chelate Fe(2+). The influence of PR on fibroblast and HaCaT cell viability was evaluated to confirm the applicability of water soluble PR for wound healing application. |
format | Online Article Text |
id | pubmed-6835416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68354162019-11-25 Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential Pivec, Tanja Kargl, Rupert Maver, Uroš Bračič, Matej Elschner, Thomas Žagar, Ema Gradišnik, Lidija Stana Kleinschek, Karin Polymers (Basel) Article The flavonoid rutin (RU) is a known antioxidant substance of plant origin. Its potential application in pharmaceutical and cosmetic fields is, however, limited, due to its low water solubility. This limitation can be overcome by polymerization of the phenolic RU into polyrutin (PR). In this work, an enzymatic polymerization of RU was performed in water, without the addition of organic solvents. Further, the chemical structure of PR was investigated using (1)H NMR, and FTIR spectroscopy. Size-exclusion chromatography (SEC) was used to determine the molecular weight of PR, while its acid/base character was studied by potentiometric charge titrations. Additionally, this work investigated the antioxidant and free radical scavenging potential of PR with respect to its chemical structure, based on its ability to (i) scavenge non biological stable free radicals (ABTS), (ii) scavenge biologically important oxidants, such as O(2)•, NO•, and OH•, and (iii) chelate Fe(2+). The influence of PR on fibroblast and HaCaT cell viability was evaluated to confirm the applicability of water soluble PR for wound healing application. MDPI 2019-09-26 /pmc/articles/PMC6835416/ /pubmed/31561552 http://dx.doi.org/10.3390/polym11101566 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pivec, Tanja Kargl, Rupert Maver, Uroš Bračič, Matej Elschner, Thomas Žagar, Ema Gradišnik, Lidija Stana Kleinschek, Karin Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential |
title | Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential |
title_full | Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential |
title_fullStr | Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential |
title_full_unstemmed | Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential |
title_short | Chemical Structure–Antioxidant Activity Relationship of Water–Based Enzymatic Polymerized Rutin and Its Wound Healing Potential |
title_sort | chemical structure–antioxidant activity relationship of water–based enzymatic polymerized rutin and its wound healing potential |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835416/ https://www.ncbi.nlm.nih.gov/pubmed/31561552 http://dx.doi.org/10.3390/polym11101566 |
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