FORMATION OF SOLID SHELL LIPID NANOPARTICLES WITH LIQUID FISH OIL CORE

Hanna Salminen 1 Thrandur Helgason 1 Bjarki Kristinsson 2 Kristberg Kristbergsson 2 Jochen Weiss 1
1Department of Food Physics and Meat Science, University of Hohenheim, Stuttgart, Baden-Württenberg
2Faculty of Food Science and Nutrition, University of Iceland, Reykjavik
Formation of physically and chemically stable delivery systems for bioactive compounds is a key challenge for food and pharmaceutical industries. Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) have emerged as potential structures to encapsulate unstable lipophilic bioactives. We hypothesized that by selecting appropriate surfactants (high- or low melting lecithin) we can control the crystallization behavior of the lipid nanoparticles, resulting in entrapment of ω-3 fatty acids inside the solid lipid matrix thereby preventing their oxidation. Therefore, we investigated the influence of surfactant type on physical and chemical stability of (i) NLC containing tristearin and ω-3 fish oil, (ii) tristearin SLN, and (iii) ω-3 fish oil-in-water emulsions. The physical and chemical stability of the nanoparticles was evaluated by light scattering, differential scanning calorimetry (DSC), gas chromatography, and cryo-transmission electron microscopy (TEM). Results showed that the presence of fish oil reduced the crystallization temperature, melting temperature, and melting enthalpy of tristearin. NLC stabilized with high melting lecithin inhibited the oxidation of ω-3 fatty acids ≥ 90% compared to those stabilized with low melting lecithin. This was attributed to the solidified surfactant layer of high melting lecithin inducing crystallization of the shell by interfacial heterogeneous nucleation. In contrast, low melting lecithin does not solidify before the tristearin and thus cannot control the crystallization behavior. This leads to disordered crystals structure and partial or full expulsion of the liquid ω-3 fatty acids. The results demonstrated that oxidation of unstable ω-3 fatty acids encapsulated in lipid nanoparticles was inhibited by the creation of an appropriate crystal structure - without the use of antioxidants. Our findings indicated that the saturated high melting lecithin was the key in controlling the crystallization behavior. This study shows that structure design can be used to control chemistry in a major way.

Principal investigator: Prof. Jochen Weiss j.weiss@uni-hohenheim.de








 




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