Sanguisorba officinalis sapogenin oral emulsion as well as preparation method and applications thereof
A technology of Ulmus saponin oral emulsion and Sangui saponin, which is applied in the field of Sangui saponin oral emulsion and its preparation, to achieve the effects of treatment and/or prevention, and improvement of drug solubility and dissolution
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Embodiment 1
[0030] The preparation of embodiment 1 oral emulsion of the present invention
[0031] Weigh the raw materials according to the following ratio:
[0032] Sanguigenin 1mg, soybean oil 100mg, egg yolk lecithin 20mg, glycerin 2mg.
[0033] The preparation method is as follows:
[0034] Take Sanguigenin, soybean oil, and egg yolk lecithin, mix them, dissolve them in ethanol, remove the ethanol by rotary evaporation under reduced pressure, add glycerin and appropriate amount of water under high-speed stirring, so that the concentration of Sanguigenin in the emulsion is 0.3mg / mL, 10000rpm Under high-speed shearing for 5 minutes, high-pressure homogenization under 800 bar pressure for 4 times, and high-pressure sterilization to obtain the oral emulsion of the present invention.
Embodiment 2
[0035] Embodiment 2 Preparation of oral emulsion of the present invention
[0036] Weigh the raw materials according to the following ratio:
[0037] Burnet genin 1mg, medium chain triglyceride 300mg, egg yolk lecithin 20mg, glycerin 3mg.
[0038] The preparation method is as follows:
[0039] Take Sanguigenin, medium-chain triglycerides, and egg yolk lecithin, mix them, dissolve them in ethanol, remove the ethanol by rotary evaporation under reduced pressure, add glycerin and appropriate amount of water under high-speed stirring, so that the concentration of Sanguigenin in the emulsion is 0.3mg / mL, high-speed shearing at 10000rpm for 5min, high-pressure homogenization at 800bar pressure for 4 times, and autoclaving to obtain the oral emulsion of the present invention.
Embodiment 3
[0040] Embodiment 3 Preparation of oral emulsion of the present invention
[0041] Weigh the raw materials according to the following ratio:
[0042] Sanguigenin 2mg, fish oil 300mg, egg yolk lecithin 20mg, glycerin 5mg.
[0043] The preparation method is as follows:
[0044] Take Sanguigenin, fish oil, and egg yolk lecithin, mix them, dissolve them in ethanol, remove the ethanol by rotary evaporation under reduced pressure, add glycerin and appropriate amount of water under high-speed stirring, so that the concentration of Sanguigenin in the emulsion is 0.3mg / mL, at 10000rpm High-speed shearing for 5 minutes, high-pressure homogenization under 800 bar pressure for 4 times, and high-pressure sterilization to obtain the oral emulsion of the present invention.
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