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Development of chrysin loaded oil-in-water nanoemulsion for improving bioaccessibility
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by นพพร ม่วงระย้า  
Metadata
Document Title
Development of chrysin loaded oil-in-water nanoemulsion for improving bioaccessibility
Author
Ting P., Srinuanchai W., Suttisansanee U., Tuntipopipat S., Charoenkiatkul S., Praengam K., Chantong B., Temviriyanukul P., Nuchuchua O.
Name from Authors Collection
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Affiliations
Faculty of Medicine Ramathibodi Hospital and Institute of Nutrition, Mahidol University, Bangkok, 10400, Thailand; Nano Agricultural Chemistry and Processing Research Team, National Nanotechnology Center (NANOTEC), National Science and Technology Development Agency (NSTDA), Klong Luang, Pathum Thani, 12120, Thailand; Institute of Nutrition, Mahidol University, Salaya, Phuttamonthon, Nakhon Pathom, 73170, Thailand; Department of Pre-Clinical and Applied Animal Science, Faculty of Veterinary Science, Mahidol University, Salaya, Phutthamonthon, Nakhon Pathom, 73170, Thailand
Type
Article
Source Title
Foods
ISSN
23048158
Year
2021
Volume
10
Issue
8
Open Access
Gold, Green
Publisher
MDPI AG
DOI
10.3390/foods10081912
Abstract
Chrysin (5,7-dihydroxyflavone) is a remarkable flavonoid exhibiting many health-promoting activities, such as antioxidant, anti-inflammatory, and anti-Alzheimer’s disease (AD). Nevertheless, chrysin has been addressed regarding its limited applications, due to low bioaccessibility. There-fore, to improve chrysin bioaccessibility, a colloidal delivery system involving nanoemulsion was developed as chrysin nanoemulsion (chrysin-NE) using an oil-in-water system. Our results show that chrysin can be loaded by approximately 174.21 µg/g nanoemulsion (100.29 ± 0.53% w/w) when medium chain triglyceride (MCT) oil was used as an oil phase. The nanocolloidal size, polydispersity index, and surface charge of chrysin-NE were approximately 161 nm, 0.21, and −32 mV, respectively. These properties were stable for at least five weeks at room temperature. Furthermore, in vitro chrysin bioactivities regarding antioxidant and anti-AD were maintained as pure chrysin, suggest-ing that multistep formulation could not affect chrysin properties. Interestingly, the developed chrysin-NE was more tolerant of gastrointestinal digestion and significantly absorbed by the human intestinal cells (Caco-2) than pure chrysin. These findings demonstrate that the encapsulation of chrysin using oil-in-water nanoemulsion could enhance the bioaccessibility of chrysin, which might be subsequently applied to food and nutraceutical industries. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Keyword
Funding Sponsor
National Science and Technology Development Agency; Thailand Graduate Institute of Science and Technology
License
CC BY
Rights
Author
Publication Source
Scopus