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Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers
Resveratrol, a naturally occurring polyphenol, has attracted significant attention due to its antioxidant, cardioprotective and anticancer potential. However, its low aqueous solubility limits resveratrol bioavailability and use. In this work, different mesoporous silica matrices were used to encaps...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780957/ https://www.ncbi.nlm.nih.gov/pubmed/35057098 http://dx.doi.org/10.3390/pharmaceutics14010203 |
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author | Ioniţă, Simona Lincu, Daniel Mitran, Raul-Augustin Ziko, Laila Sedky, Nada K. Deaconu, Mihaela Brezoiu, Ana-Maria Matei, Cristian Berger, Daniela |
author_facet | Ioniţă, Simona Lincu, Daniel Mitran, Raul-Augustin Ziko, Laila Sedky, Nada K. Deaconu, Mihaela Brezoiu, Ana-Maria Matei, Cristian Berger, Daniela |
author_sort | Ioniţă, Simona |
collection | PubMed |
description | Resveratrol, a naturally occurring polyphenol, has attracted significant attention due to its antioxidant, cardioprotective and anticancer potential. However, its low aqueous solubility limits resveratrol bioavailability and use. In this work, different mesoporous silica matrices were used to encapsulate the polyphenol and to increase its dissolution rate. Pristine MCM-41, MCM-48, SBA-15, SBA-16, FDU-12 and MCF silica were obtained. The influence of SBA-15 functionalized with aminopropyl, isocyanate, phenyl, mercaptopropyl, and propionic acid moieties on resveratrol loading and release profiles was also assessed. The cytotoxic effects were evaluated for mesoporous carriers and resveratrol-loaded samples against human lung cancer (A549), breast cancer (MDA-MB-231) and human skin fibroblast (HSF) cell lines. The effect on apoptosis and cell cycle were assayed for selected resveratrol-loaded carriers. The polyphenol molecules are encapsulated only inside the mesopores, mostly in amorphous state. All materials containing either pristine or functionalized silica carriers increased polyphenol dissolution rate. The influence of the physico-chemical properties of the mesoporous carriers and resveratrol–loaded supports on the kinetic parameters was identified. Resv@SBA-15-SH and Resv@SBA-15-NCO samples exhibited the highest anticancer effect against A549 cells (IC(50) values were 26.06 and 36.5 µg/mL, respectively) and against MDA-MB-231 (IC(50) values were 35.56 and 19.30 µg/mL, respectively), which highlights their potential use against cancer. |
format | Online Article Text |
id | pubmed-8780957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87809572022-01-22 Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers Ioniţă, Simona Lincu, Daniel Mitran, Raul-Augustin Ziko, Laila Sedky, Nada K. Deaconu, Mihaela Brezoiu, Ana-Maria Matei, Cristian Berger, Daniela Pharmaceutics Article Resveratrol, a naturally occurring polyphenol, has attracted significant attention due to its antioxidant, cardioprotective and anticancer potential. However, its low aqueous solubility limits resveratrol bioavailability and use. In this work, different mesoporous silica matrices were used to encapsulate the polyphenol and to increase its dissolution rate. Pristine MCM-41, MCM-48, SBA-15, SBA-16, FDU-12 and MCF silica were obtained. The influence of SBA-15 functionalized with aminopropyl, isocyanate, phenyl, mercaptopropyl, and propionic acid moieties on resveratrol loading and release profiles was also assessed. The cytotoxic effects were evaluated for mesoporous carriers and resveratrol-loaded samples against human lung cancer (A549), breast cancer (MDA-MB-231) and human skin fibroblast (HSF) cell lines. The effect on apoptosis and cell cycle were assayed for selected resveratrol-loaded carriers. The polyphenol molecules are encapsulated only inside the mesopores, mostly in amorphous state. All materials containing either pristine or functionalized silica carriers increased polyphenol dissolution rate. The influence of the physico-chemical properties of the mesoporous carriers and resveratrol–loaded supports on the kinetic parameters was identified. Resv@SBA-15-SH and Resv@SBA-15-NCO samples exhibited the highest anticancer effect against A549 cells (IC(50) values were 26.06 and 36.5 µg/mL, respectively) and against MDA-MB-231 (IC(50) values were 35.56 and 19.30 µg/mL, respectively), which highlights their potential use against cancer. MDPI 2022-01-16 /pmc/articles/PMC8780957/ /pubmed/35057098 http://dx.doi.org/10.3390/pharmaceutics14010203 Text en © 2022 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 Ioniţă, Simona Lincu, Daniel Mitran, Raul-Augustin Ziko, Laila Sedky, Nada K. Deaconu, Mihaela Brezoiu, Ana-Maria Matei, Cristian Berger, Daniela Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers |
title | Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers |
title_full | Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers |
title_fullStr | Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers |
title_full_unstemmed | Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers |
title_short | Resveratrol Encapsulation and Release from Pristine and Functionalized Mesoporous Silica Carriers |
title_sort | resveratrol encapsulation and release from pristine and functionalized mesoporous silica carriers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780957/ https://www.ncbi.nlm.nih.gov/pubmed/35057098 http://dx.doi.org/10.3390/pharmaceutics14010203 |
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