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Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol
Resveratrol (tran-3,5,4′-trihydroxystibene, RSV) is a kind of polyphenol which has anti-inflammatory, antioxidant, anti-allergy, and anti-cancer properties, as well as being a scavenger of free radicals and preventing cardiovascular diseases. However, it is quite unstable in light, heat, and other c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384602/ https://www.ncbi.nlm.nih.gov/pubmed/30743989 http://dx.doi.org/10.3390/molecules24030600 |
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author | Wu, Pey-Shiuan Li, Yu-Syuan Kuo, Yi-Ching Tsai, Suh-Jen Jane Lin, Chih-Chien |
author_facet | Wu, Pey-Shiuan Li, Yu-Syuan Kuo, Yi-Ching Tsai, Suh-Jen Jane Lin, Chih-Chien |
author_sort | Wu, Pey-Shiuan |
collection | PubMed |
description | Resveratrol (tran-3,5,4′-trihydroxystibene, RSV) is a kind of polyphenol which has anti-inflammatory, antioxidant, anti-allergy, and anti-cancer properties, as well as being a scavenger of free radicals and preventing cardiovascular diseases. However, it is quite unstable in light, heat, and other conditions, and decays easily due to environmental factors. For these reasons, this study used a new type of carrier, transfersome, to encapsulate RSV. Transfersome consists of phosphatidyl choline (PC) from a liposomal system and non-ionic edge activators (EA). EA are an important ingredient in the formulation of transfersome; they can enhance the flexibility of the lipid bimolecular membrane of transfersome. Due to its ultradeformability, it also allows drugs to penetrate the skin, even through the stratum corneum. We hope that this new encapsulation technique will improve the stability and enhance the permeability of RSV. Concluding all the tested parameters, the best production condition was 5% PC/EA (3:1) and 5% ethanol in distilled water, with an ultrasonic bath and stirring at 500 rpm, followed by high pressure homogenization. The optimal particle size was 40.13 ± 0.51 nm and the entrapment efficiency (EE) was 59.93 ± 0.99%. The results of antioxidant activity analysis showed that transfersomes were comparable to the RSV group (unencapsulated). During in vitro transdermal delivery analysis, after 6 h, D1-20(W) increased 27.59% by accumulation. Cell viability assay showed that the cytotoxicity of D3-80(W) was reduced by 34.45% compared with the same concentration of RSV. Therefore, we successfully prepared RSV transfersomes and also improved the stability, solubility, and safety of RSV. |
format | Online Article Text |
id | pubmed-6384602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63846022019-02-23 Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol Wu, Pey-Shiuan Li, Yu-Syuan Kuo, Yi-Ching Tsai, Suh-Jen Jane Lin, Chih-Chien Molecules Article Resveratrol (tran-3,5,4′-trihydroxystibene, RSV) is a kind of polyphenol which has anti-inflammatory, antioxidant, anti-allergy, and anti-cancer properties, as well as being a scavenger of free radicals and preventing cardiovascular diseases. However, it is quite unstable in light, heat, and other conditions, and decays easily due to environmental factors. For these reasons, this study used a new type of carrier, transfersome, to encapsulate RSV. Transfersome consists of phosphatidyl choline (PC) from a liposomal system and non-ionic edge activators (EA). EA are an important ingredient in the formulation of transfersome; they can enhance the flexibility of the lipid bimolecular membrane of transfersome. Due to its ultradeformability, it also allows drugs to penetrate the skin, even through the stratum corneum. We hope that this new encapsulation technique will improve the stability and enhance the permeability of RSV. Concluding all the tested parameters, the best production condition was 5% PC/EA (3:1) and 5% ethanol in distilled water, with an ultrasonic bath and stirring at 500 rpm, followed by high pressure homogenization. The optimal particle size was 40.13 ± 0.51 nm and the entrapment efficiency (EE) was 59.93 ± 0.99%. The results of antioxidant activity analysis showed that transfersomes were comparable to the RSV group (unencapsulated). During in vitro transdermal delivery analysis, after 6 h, D1-20(W) increased 27.59% by accumulation. Cell viability assay showed that the cytotoxicity of D3-80(W) was reduced by 34.45% compared with the same concentration of RSV. Therefore, we successfully prepared RSV transfersomes and also improved the stability, solubility, and safety of RSV. MDPI 2019-02-08 /pmc/articles/PMC6384602/ /pubmed/30743989 http://dx.doi.org/10.3390/molecules24030600 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 Wu, Pey-Shiuan Li, Yu-Syuan Kuo, Yi-Ching Tsai, Suh-Jen Jane Lin, Chih-Chien Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol |
title | Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol |
title_full | Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol |
title_fullStr | Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol |
title_full_unstemmed | Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol |
title_short | Preparation and Evaluation of Novel Transfersomes Combined with the Natural Antioxidant Resveratrol |
title_sort | preparation and evaluation of novel transfersomes combined with the natural antioxidant resveratrol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384602/ https://www.ncbi.nlm.nih.gov/pubmed/30743989 http://dx.doi.org/10.3390/molecules24030600 |
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