High-content toltrazuril soluble powder, as well as preparation method and application thereof
A technology of soluble powder and toltrazuril, which is applied in powder delivery, drug combination, anti-infective drugs, etc., can solve the problems of poor water solubility of toltrazuril preparations, limited therapeutic effect and application, prone to precipitation and discoloration, etc. To achieve the effect of improving bioavailability, increasing drug content, and fast dissolution speed
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specific Embodiment approach 1
[0028] Specific embodiment one: present embodiment is a kind of high-content toltrazuril soluble powder, and it is made up of 1 part to 60 parts of toltrazuril, 5 parts to 40 parts of alkaline pH regulator, It is prepared by 4-40 parts of co-solvent and 1-89 parts of soluble filler.
[0029] This embodiment has the following advantages: 1. A kind of high-content toltrazuril soluble powder of this embodiment has added solubilizing adjuvant in toltrazuril, has greatly improved the toltrazuril preparation. The high drug content improves the bioavailability; two, a high-content toltrazuril soluble powder of the present embodiment has a fast dissolution rate and stable preparation, and there is no agglomeration and discoloration phenomenon at room temperature for three years; three, The high-content toltrazuril soluble powder of this embodiment can be directly added to the drinking water of animals for administration, and can also be used as a raw material and mixed with auxiliary ...
specific Embodiment approach 2
[0030] Specific embodiment two: the difference between this embodiment and specific embodiment one is that: the alkaline pH regulator is an alkaline inorganic salt; wherein, the alkaline inorganic salt is sodium hydroxide, potassium hydroxide, One or a mixture of sodium hydrogen phosphate, sodium dihydrogen phosphate, sodium bicarbonate, sodium carbonate and potassium carbonate. Others are the same as in the first embodiment.
[0031] Each component in the mixture described in this embodiment is in any ratio.
specific Embodiment approach 3
[0032] Embodiment 3: The difference between this embodiment and Embodiment 1 or 2 is that the co-solvent is polyethylene glycol polymer compound, polyvinylpyrrolidone polymer compound, polyvinyl alcohol polymer compound , sodium benzoate, sodium salicylate, p-aminobenzoic acid, urea and acetamide, or a mixture of several of them. Others are the same as in the first or second embodiment.
[0033] Each component in the mixture described in this embodiment is in any ratio.
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