Eriobotuya japonica extract, and composition containing same and use
A loquat flower and extract technology is applied in the field of extract prepared from loquat flower as a raw material medicine, and can solve the problems such as lack of effective quality control, complex and complicated efficacy of loquat flower, etc., and achieves that the quality control method is simple and easy to implement and has a wide range of use. , good reproducibility
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Embodiment 1
[0028] The preparation of embodiment 1 loquat flower extract of the present invention
[0029] Weigh 500g loquat flower sample, put it in a 5000ml round bottom flask, add ten times the amount of 75% ethanol, reflux at 70°C for 2h, and collect the reflux liquid. The residue was then condensed and refluxed with five times the volume of 75% ethanol for 2 h, and the two extracts were combined. The extract is packed into a flask, and on a rotary evaporator, the temperature of the water bath is 50° C., and the speed is 95 rpm, and it is spin-dried into a loquat flower extract extract.
Embodiment 2
[0030] Embodiment 2 The determination test of extraction solvent of the present invention
[0031] (1) Determination of solvent
[0032] Accurately weigh a certain amount of loquat flowers, add methanol, ethyl acetate, 95%, 75%, 50% ethanol and 100ml of water as solvents, reflux for 2.5h, rotary steam, constant volume in a 100ml volumetric flask, and determine the total flavonoids and the content of oleanolic acid and ursolic acid to obtain the best extraction solvent.
[0033] solvent
Total flavonoids (mg / g)
Ursolic acid (mg / g)
Oleanolic acid (mg / g)
6.33
34.9
6.6
4.07
35.6
5.9
95% ethanol
6.68
36.6
6.8
75% ethanol
19.76
35.8
6.1
[0034] 50% ethanol
28.89
10.7
2.1
water
20.45
none
none
[0035] To sum up, the content of total flavonoids in the water extract was the highest. Bas...
Embodiment 3
[0039] Embodiment 3 loquat flower extract HPLC fingerprint spectrum determination method of the present invention
[0040] The fingerprints of loquat flowers were determined by HPLC. Experiment with RP-C 18 The chromatographic column was used as the stationary phase, methanol-buffer was used as the mobile phase for linear gradient elution, and the pH of the buffer was adjusted to 3.4 with acetic acid. Gradient elution program: the ratio of methanol and buffer (pH=3.4) solution in 0-5min is 30:70 for 0-5min; 50:50 for 5-6min; 50:50 for 6-16min; 50:50 for 16-26min It was 94:6; 26~46min became 100:0; 46~70min was 100:0, the flow rate was 0.5mL / min, and the ultraviolet detection wavelength was 210nm.
[0041] The specific experimental method is:
[0042] 1. Instruments, reagents and materials
[0043] 1.1 Instrument
[0044] 1) U.S. DIONEX high performance liquid chromatography [SOR-100 Solvent Rack, P680 HPLC Pump, ASI-100 Automated Sample Injector, PDA-100 Photodiode Array ...
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