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...

Full description

Saved in:
Bibliographic Details
Main Authors: Siriporn Okonogi, Ornchuma Naksuriya, Suporn Charumanee, Jakkapan Sirithunyalug
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84995436892&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56272
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-56272
record_format dspace
spelling th-cmuir.6653943832-562722018-09-05T03:12:00Z Effect of aromatic substitution of curcumin nanoformulations on their stability Siriporn Okonogi Ornchuma Naksuriya Suporn Charumanee Jakkapan Sirithunyalug Pharmacology, Toxicology and Pharmaceutics © 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. 2018-09-05T03:12:00Z 2018-09-05T03:12:00Z 2016-12-01 Journal 22180532 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/6653943832/56272
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Pharmacology, Toxicology and Pharmaceutics
spellingShingle Pharmacology, Toxicology and Pharmaceutics
Siriporn Okonogi
Ornchuma Naksuriya
Suporn Charumanee
Jakkapan Sirithunyalug
Effect of aromatic substitution of curcumin nanoformulations on their stability
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 Siriporn Okonogi
Ornchuma Naksuriya
Suporn Charumanee
Jakkapan Sirithunyalug
author_facet Siriporn Okonogi
Ornchuma Naksuriya
Suporn Charumanee
Jakkapan Sirithunyalug
author_sort Siriporn Okonogi
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 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84995436892&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56272
_version_ 1681424661025390592