Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56272
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dc.contributor.authorSiriporn Okonogien_US
dc.contributor.authorOrnchuma Naksuriyaen_US
dc.contributor.authorSuporn Charumaneeen_US
dc.contributor.authorJakkapan Sirithunyalugen_US
dc.date.accessioned2018-09-05T03:12:00Z-
dc.date.available2018-09-05T03:12:00Z-
dc.date.issued2016-12-01en_US
dc.identifier.issn22180532en_US
dc.identifier.issn00368709en_US
dc.identifier.other2-s2.0-84995436892en_US
dc.identifier.other10.3390/scipharm84040625en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84995436892&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56272-
dc.description.abstract© 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.en_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleEffect of aromatic substitution of curcumin nanoformulations on their stabilityen_US
dc.typeJournalen_US
article.title.sourcetitleScientia Pharmaceuticaen_US
article.volume84en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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