Please use this identifier to cite or link to this item: https://hdl.handle.net/1822/61975

TitleNanoemulsion-based delivery systems for curcumin: effect of carrier oil type on bioaccessibility and cell viability
Author(s)Vicente, A. A.
Gonçalves, Raquel Filipa Silva
Martins, Joana Teresa Rodrigues
Duarte, Catarina M.
Pinheiro, Ana Cristina
KeywordsNanoemulsions
Curcumin
In vitro digestion
Bioaccessibility
Cytotoxicity
Issue dateNov-2017
CitationVicente, António A.; Gonçalves, Raquel F. S.; Martins, Joana T.; Duarte, Catarina M.; Pinheiro, Ana Cristina, Nanoemulsion-based delivery systems for curcumin: effect of carrier oil type on bioaccessibility and cell viability. DoF 2017 - 7th International Symposium on Delivery of Functionality In Complex Food Systems. Auckland, New Zealand, Nov 5-8, 2017.
Abstract(s)Curcumin exerts a wide range of biological and pharmacological activities (e.g. anti-inflammatory and anticancer), however, its health benefits are limited by its poor solubility in aqueous media and low bioavailability. Nanoemulsions (NE) are particularly effective carriers for incorporating lipophilic bioactive compounds into many foods, improving their bioavailability and stability. The knowledge of NE and bioactive compounds behaviour during digestion/absorption is of utmost importance to assess their safety and to produce NE with optimized bioactivity. The purpose of this research was to evaluate the behaviour of curcumin NE formulated with two different carrier oils - long chain triglycerides (LCT) and medium chain triglycerides (MCT) - when submitted to an in vitro digestion. NE physicochemical properties (size, zeta-potential and morphology), free fatty acids release and curcumin bioaccessibility were evaluated. The impact of both formulations on Caco-2 cell viability was analyzed by MTT assay. In vitro digestion results indicated that both NE were only stable at mouth conditions, once they exhibited an increase in particle size from this stage on. Curcumin bioaccessibility increased 12 times when encapsulated in NE-MCT, compared with free curcumin. However, a low curcumin bioaccessibility was obtained for NE-LCT, and no significant differences were observed between NE-LCT and free curcumin. Overall, cell viability results demonstrated that curcumin encapsulated in NE-MCT and NE-LCT present no cytotoxic effects at curcumin concentrations lower than 20 and 25 g.mL-1, respectively. This work contributes to the development of NE with improved bioavailability and on their application in food sector by gathering fundamental data on digestion and safety of different NE.
TypeAbstract
URIhttps://hdl.handle.net/1822/61975
Publisher versionhttps://www.dof2017.org/
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Resumos em Livros de Atas / Abstracts in Proceedings

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