Extraction method and application of Hexagona apiaria fungal oil
A technology of cellulite bacteria and extraction method, which is applied in the extraction technology and application field of bacterial oil, can solve the problem of no hairy cellulite bacterial oil, etc., and achieve the effects of easy implementation, simple operation, and various types
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Embodiment 1
[0034] The preparation of embodiment 1 hair cellulum bacterium oil
[0035] Material: Hexagonia apiaria (Pers.) Fr. was collected from dry longan branches in Nandan Mountain Scenic Area, Sanshui District, Foshan City, Guangdong Province on October 27, 2018.
[0036] Diethyl ether: analytically pure;
[0037] n-Hexane: analytically pure;
[0038] Ethyl acetate: analytically pure.
[0039] Take the above-mentioned wild hair cellulite after natural air-drying, pulverize, and extract with diethyl ether at 50°C for 24 hours at a material-to-liquid ratio of 1:20. Oil;
[0040] The crude bacterial oil was purified by silica gel column chromatography, eluted with n-hexane-ethyl acetate with a volume ratio of 9:1, the eluate was collected, and the solvent was recovered by vacuum rotary distillation at 50°C to obtain the hair cellulite bacterial oil .
[0041] The oil yield of the above-mentioned extracted Trichocellus bacterium oil is 0.26%.
[0042] The inventor has also tried t...
Embodiment 2
[0043] The analysis of the chemical constituents of embodiment 2 hair cellulum bacterium oil
[0044] 2.1. Instruments and materials used
[0045] In embodiment 1, diethyl ether extracts the purified hair cellulite bacterium oil;
[0046] Agilent 7890A gas chromatograph coupled with Agilent 5975C mass spectrometer.
[0047] 2.2. Analytical conditions and methods
[0048] 1) Chromatographic conditions: HP-5MS quartz capillary column (30m×250μm×0.25μm) is used as the chromatographic column; the temperature is raised by program: the initial temperature is 40°C, the temperature is raised to 150°C at a speed of 5°C / min, and then the temperature is increased to 10°C / min The speed was raised to 280°C, and the temperature was kept constant for 10 minutes; the temperature of the injection port was 280°C, and the injection volume was 1 μL; the split ratio was 20:1; the carrier gas was helium.
[0049] 2) Mass spectrometry conditions: EI ion source, ion source temperature 280°C, elect...
Embodiment 3
[0057] Example 3 Evaluation of Antioxidant Activity of Hairy Cellular Bacteria Oil
[0058] 3.1 Materials
[0059] Reagents: 1,1-diphenyl-2-picrylhydrazyl (DPPH), ascorbic acid, absolute ethanol;
[0060] Sample: the hair cellulite bacterium oil prepared by the method described in embodiment 1;
[0061] 3.2 Experiment of scavenging DPPH free radicals with the oil of Trichomonas
[0062] A microplate reader was used to measure the in vitro scavenging ability of DPPH free radicals of different concentrations of sample solutions. Use a pipette gun to accurately pipette 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, and 50 μL of sample solution (initial concentration: 10 mg / mL) into the 96-well microtiter plate, and then add no Dilute with water and ethanol so that the total volume of each well is 50 μL, then use a pipette to accurately absorb 100 μL of the prepared DPPH solution (0.2 mmol / L) into the sample solution, and finally add absolute ethanol to make the total volume of each wel...
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