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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...

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Autores principales: Okonogi, Siriporn, Naksuriya, Ornchuma, Charumanee, Suporn, Sirithunyalug, Jakkapan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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.
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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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