Preparation method of cassia bark extract, cassia bark extract and composition and application thereof
A technology of cinnamon extract and composition, which is applied in the field of preparation of drugs or health care products with dual effects and liver function, and the preparation of cinnamon extract, which can solve problems such as unclear mechanism of action, and achieve improvement of liver function, Effects of lowering blood sugar and increasing sensitivity
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Embodiment 1
[0112] Embodiment 1. Preparation of Cinnamon Water Extract
[0113] Process flow of cinnamon water extract
[0114] Mix the cinnamon raw material and double-distilled water in a certain ratio (10g+100ml), extract with a rotary evaporator under vacuum, control the water temperature at 45°C, filter with qualitative filter paper after extraction for 6 hours, and filter out the residue , to obtain 50ml of cinnamon aqueous extract, and the resulting concentration is 0.2g / ml.
[0115] Physicochemical properties of cinnamon water extract
[0116] Cinnamon water extract is a mixture containing cinnamyl alcohol, cinnamic acid, cinnamaldehyde, eugenol and other organic compounds. The appearance is a yellow clear liquid with a pH of 4.6, slightly acidic, with a special fragrance and a light and slightly sweet taste.
[0117] HPLC spectrum
[0118] The HPLC collection of illustrative plates of cinnamon aqueous extract of the present invention is as figure 1 shown.
[0119] The ...
Embodiment 2
[0127] The preparation of embodiment 2 cinnamon-ethanol / water (10:90, v / v) extract
[0128] The ethanol extract of cinnamon was prepared according to the process of Example 1, except that the double distilled water was replaced by a mixed solvent system of ethanol / water (10:90, v / v), and the extraction temperature was 40°C. The dried extract is a yellowish powder, which can be dissolved in water to obtain a clear yellow liquid with a pH of 4.3.
[0129] The cinnamon water extract (indicated by CE) prepared in Example 1 was used in the following examples. In the experiment, 1 μl, 3 μl, and 6 μl of the extract of Example 1 were added to a 24-well cell culture plate, the cell culture medium was 1 ml, and the obtained concentrations were 0.2 mg / ml, 0.6 mg / ml, and 1.2 mg / ml, respectively.
Embodiment 3
[0130] Example 3. The induction of cinnamon water extract to the differentiation of 3T3-L1 cells into adipocytes
[0131] 3T3-L1 cells were seeded in 24-well plates, cultured for 2 days, and induced to differentiate with DM (10 μg / ml insulin, 1 μM dexamethasone, 0.5 mM cadenosine inhibitor), while adding different concentrations of CE (0.2 mg / ml , 0.6mg / ml). After 5 days, they were stained with Oil Red and observed under a microscope. Observation results such as figure 2 shown.
[0132] The results showed that CE could significantly promote the differentiation of 3T3-L1 cells into adipocytes. Since PPARγ is a sufficient and necessary condition for adipocyte differentiation, it is speculated that CE may stimulate the expression of PPARγ.
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