Oil or fat composition
A kind of oil composition and composition technology, applied in the direction of pharmaceutical combination, inorganic/element cleaning composition, edible oil/fat, etc., can solve the problems of processability, flavor, and insufficient technology
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Embodiment 1
[0039] Embodiment 1 Manufacture of oil composition
[0040] The following oil and fat compositions were produced. The composition of the obtained oil composition is shown in Table 1. Glyceride composition was determined by HPLC method, wherein the column used "TSKgelG2500H" manufactured by Tosoh Co., Ltd., THF was used as the elution solvent, the solvent flow rate was set to 0.4mL / min, and the detector was RI. The composition of fatty acids was determined by GLC method after methyl esterification (Japan Oil Chemistry Association "Standard Oil Analysis Test Method" 2.4.1.2-1996, 2.4.2.2-1996).
[0041] Fat composition 1 (product of the present invention)
[0042] Add 422.9g of 2,2-dimethyl-1,3-dioxolane-4-methanol and 0.64g of sodium hydroxide into a four-neck flask, dehydrate and alcoholize under reduced pressure at 80°C, and then cool to 50°C . Further, 355.3 g of high DHA content oil "DHA-22" (manufactured by MARUHA Co., Ltd.) was added thereto, and after reacting for 1....
Embodiment 2
[0051] Example 2 PPARγ activation test
[0052] The small intestinal epithelial cell line IEC-6 was spread on a 12-well plate and cultured in DMEM (5% FCS) for one day. Here, using a transfection reagent (Superfect transfection reagent; QIAGEN), at the amount of 0.5 μg / well each, the chimeric molecules expressing the GAL4-DNA-binding fragment (DBD) and the PPARγ coordination-binding fragment (LBD) were simultaneously The plastid (pGAL4-PPARγ-LBD) and the marker plastid (pREP) containing the GAL4 binding sequence upstream of the firefly luciferase gene were introduced. In order to improve the transfection efficiency, at the same time, the luciferase gene of the sea shiitake was programmed into pGAL4-PPARγ-LBD. Then, the culture solution was replaced with the DMEM (+250 μM BSA) medium containing the test substance (500 μM), and the culture was continued for 24 hours. After washing with PBS, the cells were lysed using the Dual Luciferase Assay System (Promega). Add the matrix ...
Embodiment 3
[0055] Example 3 Gelation evaluation
[0056] Each oil and fat: water=70:30 (weight / weight), gelation property was observed visually, and it evaluated by the following evaluation criteria. The results are shown in Table 1.
[0057] A: No fluidity, gelation.
[0058] B: Almost no fluidity, slightly gelled.
[0059] C: Fluid and partially gelled.
[0060] D: Fluidity, no gelation at all.
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