Oridonin solid dispersion preparation
A technology of oridonin and solid dispersion, applied in the field of biomedicine, can solve the problems of less gastrointestinal absorption, incomplete dissolution, slow dissolution, etc., and achieve high bioavailability, good dissolution in vitro, and high dissolution rate Effect
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Embodiment 1
[0027] Embodiment 1, Rubescensin A Solid Dispersion No. 1
[0028] Take 5g Rubescensin A and crush it through a 100-mesh sieve, mix it with 50g polyethylene glycol 4000, heat together, stir, and Rubescensin A is basically dissolved, and quickly pour it on a cold stainless steel plate to cool, and it becomes a white waxy solid. It is the polyethylene glycol solid dispersion of oridonin. The solid dispersion is rapidly soluble in water.
Embodiment 2
[0029] Embodiment 2, Rubescensin A solid dispersion No. 2
[0030] Take 5g Rubescensin A and dissolve it in hot 100ml ethanol, mix it with 300ml ethanol solution containing 10% polyvinylpyrrolidone K30, and then evaporate the ethanol under reduced pressure in a rotary evaporator to obtain a white powdery solid, which is winter A polyvinylpyrrolidone solid dispersion of lobeidin. The solid dispersion is rapidly soluble in water.
Embodiment 3
[0031] Embodiment 3, Rubescensin A solid dispersion No. 3
[0032]Get 5g Rubescensin A and dissolve it in 50ml ethyl acetate, add 25g poloxamer P188 to dissolve, and then evaporate the acetone under reduced pressure in a rotary evaporator to obtain a white waxy solid, which is the product of Rubescensin A. Poloxamer solid dispersion. The solid dispersion is rapidly soluble in water.
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Abstract
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