Adsorptive Surface Modification of Cellulose Nanocrystals to Stabilize Nutraceuticals Loaded Lipid Carriers for Food Application
General Material Designation
[Thesis]
First Statement of Responsibility
Patel, Avinash Singh
Subsequent Statement of Responsibility
Camire, Mary E.
.PUBLICATION, DISTRIBUTION, ETC
Name of Publisher, Distributor, etc.
The University of Maine
Date of Publication, Distribution, etc.
2020
GENERAL NOTES
Text of Note
203 p.
DISSERTATION (THESIS) NOTE
Dissertation or thesis details and type of degree
Ph.D.
Body granting the degree
The University of Maine
Text preceding or following the note
2020
SUMMARY OR ABSTRACT
Text of Note
Lipid carriers such as emulsions and liposomes have been widely studied as carriers for different nutraceuticals. However, lipid carriers' physicochemical instability results in the leakage of loaded nutraceuticals and the low solubility into the digestion medium, thus reducing the bioaccessibility. Cellulose nanocrystals (CNC) are nano-sized cellulose derivatives obtained after hydrolysis of cellulosic matrices that possess potential applications in functional foods and nutraceuticals. However, hydrophilicity, anionic surface potential, and poor re-dispersibility limit CNC's applications. The primary objectives of this research were 1) to modify CNC via adsorbing polyethylene glycol (PEG) to stabilize liposomes and to study its physiochemical stability at different in vitro gastrointestinal tract (GIT) conditions, pH levels (1-11), temperatures (4-100°C) and illumination periods (4-72 hours); 2) to modify CNC via adsorbing lauric acid to stabilize O/W emulsion and to study its physicochemical stability at different pH (1-11), dilution factors (1-10 times), storage period (up to 30 days) and GIT conditions. Phycobiliprotein and beta-carotene were chosen as model nutraceuticals. In study 1, particle size and microscopic analysis revealed a better physical/kinetic stability for the liposomes stabilized with PEG-adsorbed CNC than the liposomes stabilized with unmodified CNC, resulting in significantly (p≤0.05) smaller average particle size during the initial and mouth phases of the in vitro GIT study, nonetheless a significant (p≤0.05) increase in the particle size from ~300 nm to ~5500 nm at gastric phase due to lower pH. Moreover, stabilized liposomes retained the attributes of phycobiliprotein against pH, illumination, and a temperature of 60 °C. In study 2, lauric acid-adsorbed CNC affirmed the kinetic/physical stability of emulsions throughout the GIT phases. Results exhibited a maximum of 65% beta-carotene bioaccessibility for the emulsion stabilized with modified CNC, and 71% for the emulsion stabilized with unmodified CNC. Moreover, a higher amount of lipid oxidation was recorded for the emulsion with stabilized modified CNC than the emulsion stabilized with gum Arabic. Although modified CNC retains the kinetic/physical stability of lipid carriers; however, it increases lipid carriers' chemical instability and decreases the loaded nutraceuticals' bioaccessibility. A strategic modification of CNC is needed to ensure the stability of lipid carriers and increased nutraceuticals bioaccessibility.