In-situ gel preparation of potassium dehydroandrographolide succinate and preparation method thereof
A technology of in-situ gel and tranexine, which is applied in the directions of anti-inflammatory agents, pharmaceutical formulations, antiviral agents, etc., to achieve the effect of significant medicinal effect, stable properties and good antipyretic effect.
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Embodiment 1
[0027] Prescription: Chuanhuning 30.0g, poloxamer 40719.0g, poloxamer 1886.0g, sodium benzoate 0.5g, appropriate amount of triethanolamine, distilled water to make up to 100g.
[0028] Preparation method: Dissolve the prescribed amount of sodium benzoate in an appropriate amount of distilled water, add the prescribed amount of Chuanhuning, adjust the pH to about 5.8, and obtain Chuanhuning water; take the prescribed amount of poloxamer 188, put it in the Chuanhuning aqueous solution, and stir to dissolve at room temperature , then add the prescribed amount of poloxamer 407, stir to disperse evenly, refrigerate in a refrigerator at 4°C for more than 48 hours to obtain a yellow and clear solution, adjust the pH to 5.8-6.2, add water to make it 100g, and fill it.
Embodiment 2
[0030] Prescription is the same as embodiment 1
[0031] Preparation method: Take the prescribed amount of sodium benzoate, poloxamer 188, and poloxamer 407, put them in an appropriate amount of distilled water, stir to disperse evenly, and refrigerate in a refrigerator at 4°C for 24 hours to obtain a transparent glue, add the prescribed amount of Chuanhuning, Adjust the pH to 5.8-6.2, add water to make 100g, fill it, and get ready.
Embodiment 3
[0033] Prescription: Chuanhuning 10g, poloxamer 40720.0g, poloxamer 1881.0g, hydroxypropyl β-cyclodextrin 6.0g, sodium benzoate 0.5g, triethanolamine amount, distilled water to make up to 100g.
[0034] Preparation method: Dissolve 6.0 g of sodium benzoate and 6.0 g of hydroxypropyl β-cyclodextrin in the prescribed amount of distilled water, and the remaining operating steps and methods are the same as in Example 2.
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