Development of WPI/Inulin Maillard Conjugate Based Nanoemulsion Delivery System to Enhance the Bioaccessibility of LycopeneDevelopment of WPI/Inulin Maillard Conjugate Based Nanoemulsion Delivery System to Enhance the Bioaccessibility of Lycopene
- Other Titles
- Development of WPI/Inulin Maillard Conjugate Based Nanoemulsion Delivery System to Enhance the Bioaccessibility of Lycopene
- Authors
- 이세희; 김연우; 이원재
- Issue Date
- Apr-2024
- Publisher
- 농업생명과학연구원
- Keywords
- Bioaccessibility; Lycopene; Maillard conjugate; Nanoemulsion; Whey protein isolate
- Citation
- 농업생명과학연구, v.58, no.2, pp 125 - 135
- Pages
- 11
- Indexed
- KCI
- Journal Title
- 농업생명과학연구
- Volume
- 58
- Number
- 2
- Start Page
- 125
- End Page
- 135
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/70527
- DOI
- 10.14397/jals.2024.58.2.125
- ISSN
- 1598-5504
2383-8272
- Abstract
- This study investigated the effect of manufacturing variables (including heating temperature) on the physicochemical properties ofnanoemulsion delivery system (NDS) prepared with WPI/Inulin Maillard conjugate and to study how the physicochemical propertiesof NDS affected the bioaccessibility of lycopene. The functional properties of the WPI/Inulin Maillard conjugate were determined usingthe OPA method, interfacial tension, and EAI. The physicochemical and morphological properties of NDS were measured using Zetasizerand TEM, respectively. The bioaccessibility of lycopene in the WPI/Inulin Maillard conjugate based NDS was measured using aspectrophotometer. As the pH and heating temperature increased, the Maillard conjugation efficiency increased significantly (p<0.0001).
The emulsifying properties of the WPI/Inulin Maillard conjugate were greater than those of WPI. A WPI/Inulin Maillard conjugate basedNDS with a size of ~180 nm was observed in TEM images while the droplet size of the WPI/Inulin Maillard conjugate based NDSwas smaller than that of the WPI based NDS. During in vitro digestion, no significant changes in the droplet size and PDI of NDSwere observed in the mouth and stomach phases, whereas in the intestinal phase, the droplet size and PDI increased significantly (p<0.0001).
Moreover, the bioaccessibility of lycopene in the WPI/Inulin Maillard conjugate based NDS significantly increased (p<0.0001), comparedwith that of the WPI based NDS. There was a significant (p<0.05) increase in the bioaccessibility of lycopene with a decrease in theinterfacial tension and droplet size of NDS. In conclusion, WPI/Inulin Maillard conjugate based NDS can be used to enhance thebioaccessibility of lycopene.
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