TY - JOUR
T1 - Self-assembly properties of enzymatically treated oat oil
AU - Gladkauskas, Eimantas
AU - Gilbert, Jennifer
AU - Humphreys, Ben
AU - Montalvo Diaz, Scott
AU - Piña Cañaveras, Anna Maria
AU - Terry, Ann
AU - Lindberg Yilmaz, Jenny
AU - Nylander, Tommy
AU - Adlercreutz, Patrick
AU - Tullberg, Cecilia
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/11
Y1 - 2025/11
N2 - The enzymatic modification of natural oat oils enriched with polar lipids (PL), consisting mainly of equal mixture of phospholipids and galactolipids, offers a sustainable pathway to produce liquid crystalline phases (LCPs) with diverse structural arrangements, including micellar or bicontinuous cubic and hexagonal phases. These self-assembling lipid systems have potential applications in drug delivery, nutraceuticals, and food formulations due to their ability to encapsulate bioactive compounds, thereby enhancing their stability, and facilitate controlled release. This study introduces a novel, low-energy, and sustainable one-step enzymatic process that makes oat oil lipids self-assemble into desired types of LCPs without the need for additional surfactants or stabilisers. The polar lipid content was a critical factor in determining the curvature of the lipid-aqueous interface and hence the type of LCP formed. Small angle x-ray scattering (SAXS), cryogenic transmission electron microscopy (cryoTEM), and thin layer chromatography (TLC) was used to elucidate the phase behaviour, structure, and composition of the LCP. Functional additives, such as curcumin, vitamin D, and octyl glucoside (OG), were incorporated into the LCPs with concentrations up to 10 wt%, thereby highlighting the possibility to tailor the system for different applications. Dispersed LCP nanoparticles were successfully produced via sonication and have an internal hexagonal structure as verified by SAXS and cryoTEM. The obtained results show that enzymatic processing using lipolytic enzymes can be used to control the conversion of oat oil with the polar lipid content ranging from 15 to 60 wt% into LCPs with either lamellar, micellar cubic (Fd3m) or reversed hexagonal internal structure.
AB - The enzymatic modification of natural oat oils enriched with polar lipids (PL), consisting mainly of equal mixture of phospholipids and galactolipids, offers a sustainable pathway to produce liquid crystalline phases (LCPs) with diverse structural arrangements, including micellar or bicontinuous cubic and hexagonal phases. These self-assembling lipid systems have potential applications in drug delivery, nutraceuticals, and food formulations due to their ability to encapsulate bioactive compounds, thereby enhancing their stability, and facilitate controlled release. This study introduces a novel, low-energy, and sustainable one-step enzymatic process that makes oat oil lipids self-assemble into desired types of LCPs without the need for additional surfactants or stabilisers. The polar lipid content was a critical factor in determining the curvature of the lipid-aqueous interface and hence the type of LCP formed. Small angle x-ray scattering (SAXS), cryogenic transmission electron microscopy (cryoTEM), and thin layer chromatography (TLC) was used to elucidate the phase behaviour, structure, and composition of the LCP. Functional additives, such as curcumin, vitamin D, and octyl glucoside (OG), were incorporated into the LCPs with concentrations up to 10 wt%, thereby highlighting the possibility to tailor the system for different applications. Dispersed LCP nanoparticles were successfully produced via sonication and have an internal hexagonal structure as verified by SAXS and cryoTEM. The obtained results show that enzymatic processing using lipolytic enzymes can be used to control the conversion of oat oil with the polar lipid content ranging from 15 to 60 wt% into LCPs with either lamellar, micellar cubic (Fd3m) or reversed hexagonal internal structure.
KW - Enzymatic modification
KW - Lipolysis
KW - Liquid crystalline phases
KW - Micellar cubic phase
KW - Oat oil
KW - Polar lipids
KW - Triglyceride hydrolysis
U2 - 10.1016/j.foodhyd.2025.111378
DO - 10.1016/j.foodhyd.2025.111378
M3 - Article
AN - SCOPUS:105002123903
SN - 0268-005X
VL - 167
JO - Food Hydrocolloids
JF - Food Hydrocolloids
M1 - 111378
ER -