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Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability
Resveratrol, because of its low solubility in water and its high membrane permeability, is collocated in the second class of the biopharmaceutical classification system, with limited bioavailability due to its dissolution rate. Solid dispersion of resveratrol supported on Magnesium DiHydroxide (Resv...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315708/ https://www.ncbi.nlm.nih.gov/pubmed/30563110 http://dx.doi.org/10.3390/nu10121925 |
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author | Spogli, Roberto Bastianini, Maria Ragonese, Francesco Iannitti, Rossana Giulietta Monarca, Lorenzo Bastioli, Federica Nakashidze, Irina Brecchia, Gabriele Menchetti, Laura Codini, Michela Arcuri, Cataldo Mancinelli, Loretta Fioretti, Bernard |
author_facet | Spogli, Roberto Bastianini, Maria Ragonese, Francesco Iannitti, Rossana Giulietta Monarca, Lorenzo Bastioli, Federica Nakashidze, Irina Brecchia, Gabriele Menchetti, Laura Codini, Michela Arcuri, Cataldo Mancinelli, Loretta Fioretti, Bernard |
author_sort | Spogli, Roberto |
collection | PubMed |
description | Resveratrol, because of its low solubility in water and its high membrane permeability, is collocated in the second class of the biopharmaceutical classification system, with limited bioavailability due to its dissolution rate. Solid dispersion of resveratrol supported on Magnesium DiHydroxide (Resv@MDH) was evaluated to improve solubility and increase bioavailability of resveratrol. Fluorimetric microscopy analysis displays three types of microparticles with similar size: Type 1 that emitted preferably fluorescence at 445 nm with bandwidth of 50 nm, type 2 that emitted preferably fluorescence at 605 nm with bandwidth of 70 nm and type 3 that is non-fluorescent. Micronized pure resveratrol displays only microparticles type 1 whereas type 3 are associated to pure magnesium dihydroxide. Dissolution test in simulated gastric environment resveratrol derived from Resv@MDH in comparison to resveratrol alone displayed better solubility. A 3-fold increase of resveratrol bioavailability was observed after oral administration of 50 mg/kg of resveratrol from Resv@MDH in rabbits. We hypothesize that type 2 microparticles represent magnesium dihydroxide microparticles with a resveratrol shell and that they are responsible for the improved resveratrol solubility and bioavailability of Resv@MDH. |
format | Online Article Text |
id | pubmed-6315708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63157082019-01-08 Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability Spogli, Roberto Bastianini, Maria Ragonese, Francesco Iannitti, Rossana Giulietta Monarca, Lorenzo Bastioli, Federica Nakashidze, Irina Brecchia, Gabriele Menchetti, Laura Codini, Michela Arcuri, Cataldo Mancinelli, Loretta Fioretti, Bernard Nutrients Article Resveratrol, because of its low solubility in water and its high membrane permeability, is collocated in the second class of the biopharmaceutical classification system, with limited bioavailability due to its dissolution rate. Solid dispersion of resveratrol supported on Magnesium DiHydroxide (Resv@MDH) was evaluated to improve solubility and increase bioavailability of resveratrol. Fluorimetric microscopy analysis displays three types of microparticles with similar size: Type 1 that emitted preferably fluorescence at 445 nm with bandwidth of 50 nm, type 2 that emitted preferably fluorescence at 605 nm with bandwidth of 70 nm and type 3 that is non-fluorescent. Micronized pure resveratrol displays only microparticles type 1 whereas type 3 are associated to pure magnesium dihydroxide. Dissolution test in simulated gastric environment resveratrol derived from Resv@MDH in comparison to resveratrol alone displayed better solubility. A 3-fold increase of resveratrol bioavailability was observed after oral administration of 50 mg/kg of resveratrol from Resv@MDH in rabbits. We hypothesize that type 2 microparticles represent magnesium dihydroxide microparticles with a resveratrol shell and that they are responsible for the improved resveratrol solubility and bioavailability of Resv@MDH. MDPI 2018-12-05 /pmc/articles/PMC6315708/ /pubmed/30563110 http://dx.doi.org/10.3390/nu10121925 Text en © 2018 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 Spogli, Roberto Bastianini, Maria Ragonese, Francesco Iannitti, Rossana Giulietta Monarca, Lorenzo Bastioli, Federica Nakashidze, Irina Brecchia, Gabriele Menchetti, Laura Codini, Michela Arcuri, Cataldo Mancinelli, Loretta Fioretti, Bernard Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability |
title | Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability |
title_full | Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability |
title_fullStr | Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability |
title_full_unstemmed | Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability |
title_short | Solid Dispersion of Resveratrol Supported on Magnesium DiHydroxide (Resv@MDH) Microparticles Improves Oral Bioavailability |
title_sort | solid dispersion of resveratrol supported on magnesium dihydroxide (resv@mdh) microparticles improves oral bioavailability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315708/ https://www.ncbi.nlm.nih.gov/pubmed/30563110 http://dx.doi.org/10.3390/nu10121925 |
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