Effect of aromatic substitution of curcumin nanoformulations on their stability

© 2016 by the authors; licensee MDPI, Basel, Switzerland. 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 (Cu...

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Main Authors: Okonogi S., Naksuriya O., Charumanee S., Sirithunyalug J.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84995436892&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/41224
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-412242017-09-28T04:20:00Z Effect of aromatic substitution of curcumin nanoformulations on their stability Okonogi S. Naksuriya O. Charumanee S. Sirithunyalug J. © 2016 by the authors; licensee MDPI, Basel, Switzerland. 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. 2017-09-28T04:20:00Z 2017-09-28T04:20:00Z 2016-12-01 Journal 00368709 2-s2.0-84995436892 10.3390/scipharm84040625 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84995436892&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41224
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description © 2016 by the authors; licensee MDPI, Basel, Switzerland. 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 Journal
author Okonogi S.
Naksuriya O.
Charumanee S.
Sirithunyalug J.
spellingShingle Okonogi S.
Naksuriya O.
Charumanee S.
Sirithunyalug J.
Effect of aromatic substitution of curcumin nanoformulations on their stability
author_facet Okonogi S.
Naksuriya O.
Charumanee S.
Sirithunyalug J.
author_sort Okonogi S.
title Effect of aromatic substitution of curcumin nanoformulations on their stability
title_short 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_sort effect of aromatic substitution of curcumin nanoformulations on their stability
publishDate 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84995436892&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/41224
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