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Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability
Curcumin, a poorly water-soluble bioactive compound, was successfully loaded into three different aromatic contents of hydroxypropylmethacrylamide (HPMA)-based polymeric micelles in order to develop water-soluble curcumin nanoformulations (Cur-Nano). The stability study of Cur-Nano was done by keepi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198022/ https://www.ncbi.nlm.nih.gov/pubmed/28656941 http://dx.doi.org/10.3390/scipharm84040625 |
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author | Okonogi, Siriporn Naksuriya, Ornchuma Charumanee, Suporn Sirithunyalug, Jakkapan |
author_facet | Okonogi, Siriporn Naksuriya, Ornchuma Charumanee, Suporn Sirithunyalug, Jakkapan |
author_sort | Okonogi, Siriporn |
collection | PubMed |
description | Curcumin, a poorly water-soluble bioactive compound, was successfully loaded into three different aromatic contents of hydroxypropylmethacrylamide (HPMA)-based polymeric micelles in order to develop water-soluble curcumin nanoformulations (Cur-Nano). The stability study of Cur-Nano was done by keeping the formulations at 4, 30, and 40 °C for 90 days. The physical appearance, curcumin remaining, and particle size of Cur-Nano were examined by visual inspection, high-performance liquid chromatography, and dynamic light scattering, respectively. After the storage period, the Cur-Nano composed of 100% aromatic-substituted polymer exhibited the highest stability of curcumin (80% of curcumin remaining) with a similar particle size as measured on the first day (50–60 nm) in all storage conditions. Curcumin in Cur-Nano composed of 25% and 0% aromatic-substituted polymer was significantly less stable accordingly. The results suggested that aromatic substitution to HPMA-based polymeric micelles can significantly enhance the stability of the loaded curcumin, considerably due to the π-π stacking interactions between the aromatic groups of curcumin and the polymer. It is concluded that curcumin-loaded polymeric micelles with high substituted aromatic content can be promising candidates with good storage stability for further clinical evaluations. |
format | Online Article Text |
id | pubmed-5198022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-51980222017-01-13 Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability Okonogi, Siriporn Naksuriya, Ornchuma Charumanee, Suporn Sirithunyalug, Jakkapan Sci Pharm Article Curcumin, a poorly water-soluble bioactive compound, was successfully loaded into three different aromatic contents of hydroxypropylmethacrylamide (HPMA)-based polymeric micelles in order to develop water-soluble curcumin nanoformulations (Cur-Nano). The stability study of Cur-Nano was done by keeping the formulations at 4, 30, and 40 °C for 90 days. The physical appearance, curcumin remaining, and particle size of Cur-Nano were examined by visual inspection, high-performance liquid chromatography, and dynamic light scattering, respectively. After the storage period, the Cur-Nano composed of 100% aromatic-substituted polymer exhibited the highest stability of curcumin (80% of curcumin remaining) with a similar particle size as measured on the first day (50–60 nm) in all storage conditions. Curcumin in Cur-Nano composed of 25% and 0% aromatic-substituted polymer was significantly less stable accordingly. The results suggested that aromatic substitution to HPMA-based polymeric micelles can significantly enhance the stability of the loaded curcumin, considerably due to the π-π stacking interactions between the aromatic groups of curcumin and the polymer. It is concluded that curcumin-loaded polymeric micelles with high substituted aromatic content can be promising candidates with good storage stability for further clinical evaluations. MDPI 2016-04-19 2016 /pmc/articles/PMC5198022/ /pubmed/28656941 http://dx.doi.org/10.3390/scipharm84040625 Text en © 2016 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 Okonogi, Siriporn Naksuriya, Ornchuma Charumanee, Suporn Sirithunyalug, Jakkapan Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability |
title | Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability |
title_full | Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability |
title_fullStr | Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability |
title_full_unstemmed | Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability |
title_short | Effect of Aromatic Substitution of Curcumin Nanoformulations on Their Stability |
title_sort | effect of aromatic substitution of curcumin nanoformulations on their stability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198022/ https://www.ncbi.nlm.nih.gov/pubmed/28656941 http://dx.doi.org/10.3390/scipharm84040625 |
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