Compound triamcinolone acetonide salicylic acid liniment
A technology of triamcinolone acetonide acetate and salicylic acid is applied in the pharmaceutical field to achieve the effects of improving the transdermal absorption rate, inhibiting the generation of impurities and improving the curative effect of use
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Embodiment 1
[0030] Example 1 of the present invention compound triamcinolone acetonide salicylic acid liniment F1
[0031] 0.05g triamcinol acetonide acetate, 2g chloramphenicol and 2g salicylic acid dissolved in an appropriate amount of 95% ethanol aqueous solution to give a pharmaceutical solution; 2ml of azotone, 3ml dimethyl sulfoxide and 10ml of propylene glycol dispersed in an appropriate amount of 95% ethanol aqueous solution to give an excipient solution; after the above-described pharmaceutical solution and excipient solution were mixed, continue to add 95% ethanol aqueous solution, volume to 100ml, fully mixed, i.e., to obtain a compound triamcinol acetonide salicylic acid liniment F1.
Embodiment 2
[0032] Example 2 of the present invention compound triamcinolone acetonide salicylic acid liniment F2
[0033] Adjust the skin impermeable agent ratio, the skin impermeable agent consisting of 2ml of azosterone and 3ml dimethyl sulfoxide in Example 1 is replaced with 1ml of nitridone and 4ml dimethyl sulfoxide, the remaining prescription and preparation process is the same as Example 1, i.e., to obtain the present invention compound triamcinolone salicylic acid liniment F2.
Embodiment 3
[0034] Example 3 of the present invention compound triamcinolone acetonide salicylate liniment F3
[0035] Adjust the skin permeator ratio, the skin impermeable agent consisting of 2ml of nitrotonone and 3ml of dimethyl sulfoxide in Example 1 is replaced with 4ml of nitrogen ketone and 1ml of dimethyl sulfoxide, the remaining prescription and preparation process is the same as Example 1, i.e., the present invention compound triamcinolone salicylic acid liniment F3.
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