Veterinary antidysenteric powder suspension and preparation method thereof
A technology of Zhili powder and suspension, which is applied in the field of veterinary Zhili powder suspension and its preparation, can solve the problems that cannot meet the requirements of breeding modernization, intensification, scale, automation, intelligence, and development. It can maximize the pharmacological effect and inconvenient clinical application to achieve the effect of facilitating veterinary clinical application, regulating gastrointestinal function, and facilitating absorption
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Embodiment 1
[0033] The present invention is realized through the following technical scheme, a veterinary antidiarrheal powder suspension, specifically comprising the following components by weight: 30-50 parts of realgar, 0.2-0.5 parts of patchouli oil, 100-200 parts of talc, 5-5 parts of table salt 36 servings. It also includes an antifreeze agent, which is any one of glycerin or propylene glycol; the weight component of the antifreeze agent is 10-100 parts.
[0034] Other parts of this embodiment are the same as those of the foregoing embodiments, so details are not repeated here.
Embodiment 2
[0036] This example is further optimized on the basis of the above example, a veterinary Zhili powder suspension, which specifically includes the following components by weight: 40 parts of realgar, 0.33 parts of patchouli oil, 150 parts of talc, and 40 parts of glycerin.
[0037] It should be noted that, through the above improvements, 0.33 parts of patchouli oil is equivalent to 110 parts of patchouli.
[0038] Other parts of this embodiment are the same as those of the foregoing embodiments, so details are not repeated here.
Embodiment 3
[0040] This embodiment is further optimized on the basis of the above-mentioned embodiments, a preparation method of Zhili powder suspension for animals, which specifically includes the following steps:
[0041] Step S1: processing the raw medicinal material into powder;
[0042] Step S2: Weigh the raw medicinal materials in step S1 according to the weight components, and set aside;
[0043] Step S3: preparation of suspending agent; specifically, adding 5-36 g of salt to every 100 ml of pharmaceutical water and stirring evenly to obtain a salt solution with a salt concentration of 4.8%-26.5%; the salt concentration is 4.8%- 26.5% saline solution is used as a suspending agent and is used for standby;
[0044] Step S4: Mix the suspending agent prepared in step S3 with the original medicinal material in step S2 to prepare the first mixture; specifically, place the realgar powder, talc powder and patchouli oil weighed in step S2 in a container, Add the suspending agent prepared ...
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