Brassinolide water dispersible granule/tablet and preparation method thereof
A technology of brassinolide and dispersible granules, which is applied in botany equipment and methods, biocides, animal repellents, etc., and can solve problems such as environmentally unfriendly organic solvents, inconvenient transportation of emulsifiable concentrates, and inaccurate use and measurement , to achieve the effects of less drug damage, good storage stability, and fast disintegration speed
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Embodiment 1001
[0030] The preparation of embodiment 10.01% brassinolide water-dispersible granules
[0031] The selection and ratio of original drug and auxiliary agent are: 95% brassinolide original drug 0.011% (0.01%), the dispersant is sodium methylene dimethyl naphthalene sulfonate 2.0%, calcium lignosulfonate 4.0%, wetting agent sodium lauryl sulfate 2.0%, disintegrating agent is sodium carboxymethyl starch 9.0%, binder is dextrin 5.0%, filler is attapulgite to make up 100%
[0032] According to the above proportions, the dosage of each component is calculated, weighed, and mixed evenly; the formula is granulated by ultrafine / jet milling, dried, granulated, and selected. Product testing is carried out according to the quality control indicators of water-dispersible granules, including the content of active ingredients, wetting time, disintegration rate, suspension rate, foaming property, sieve analysis, shedding rate, pH range and thermal storage stability, etc. The specific method is ...
Embodiment 1
[0038] The brassinolide water-dispersible granule performance index prepared by embodiment 1 is: brassinolide content 0.0102%, wettability qualified (18 seconds), disintegration (46 seconds), foaming property qualified (22 milliliters ), moisture 1.5%, pH value 6.6, suspension rate 88%, shedding rate 0.8%, sieve analysis 99%, thermal storage stability qualified, active ingredient decomposition rate 0.3%.
Embodiment 2001
[0039] The preparation of embodiment 20.01% brassinolide water-dispersible tablet
[0040] The selection and ratio of the original drug and the auxiliary agent are: 0.011% (0.01%) of the original drug of 95% brassinolide, the dispersant is 3.0% of naphthalene sulfonate formaldehyde condensate, 3.0% of calcium lignosulfonate, The wetting agent is sodium lauryl sulfate 2.0%, the disintegrant is sodium carboxymethyl starch 13.0%, the binder is polyvinyl alcohol 5.0%, and the filler is talcum powder to make up 100%.
[0041] According to the above proportions, the dosage of each component is calculated, weighed, and mixed evenly; the formula is granulated by ultrafine / jet milling, dried, pressed into tablets, and selected. Product testing is carried out according to the quality control indicators of water-dispersible tablets, including the content of active ingredients, disintegration time limit, suspension rate, foaming property, sieve analysis, powder and fragment rate, pH range...
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