Anti-parasitic ivermectin transdermal solution used for livestock and preparation method thereof
An ivermectin and anti-parasitic technology, applied to the field of ivermectin transdermal solution for anti-parasitic disease in livestock and its preparation field, can solve the problems of reduced feed utilization rate, decreased feed utilization rate, slow growth of livestock and the like , to reduce the decomposition rate, reduce inter-individual differences, and increase the effect of percutaneous absorption
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Embodiment 1
[0025] A kind of anti-parasitic ivermectin transdermal solution for livestock, its constituents and parts by weight thereof are respectively (by every 100ml proportioning of raw and auxiliary materials, the following examples are the same):
[0026] Ivermectin 0.5g
[0027] Ethyl acetate 10ml
[0028] Dimethyl sulfoxide 25ml
[0029] Azone 4ml
[0030] Isopropanol 2ml
[0031] Propylene Glycol 59ml.
[0032] The crude drug of the ivermectin transdermal solution involved in the present invention is ivermectin, and its alias is: 22,23-dihydroabamectin.
[0033] A method for preparing an anti-parasitic ivermectin transdermal solution for livestock, comprising the steps of:
[0034] (1) get the ivermectin of prescription quantity and dissolve to dissolve with ethyl acetate, obtain ivermectin solution;
[0035] (2) add dimethyl sulfoxide, isopropanol, azone while stirring in the above-mentioned ivermectin according to the prescription amount, and mix well;
[0036] (3) After...
Embodiment 2
[0040] An animal anti-parasitic ivermectin transdermal solution, its constituents and parts by weight are respectively:
[0041] Ivermectin 0.5g
[0042] Ethyl acetate 10ml
[0043] Dimethyl sulfoxide 25ml
[0044] Azone 4ml
[0045] Isopropanol 2ml
[0046] Propylene glycol 59ml
[0047] The steps of the preparation method of this embodiment are the same as those in Example 1.
Embodiment 3
[0049] An animal anti-parasitic ivermectin transdermal solution, its constituents and parts by weight are respectively:
[0050] Ivermectin 0.5g
[0051] Ethyl acetate 10ml
[0052] Dimethyl sulfoxide 30ml
[0053] Azone 5ml
[0054] Isopropanol 2ml
[0055] Propylene glycol 53ml
[0056] The steps of the preparation method of this embodiment are the same as those in Example 1.
[0057] Test data: after 8 hours of administration of azone and dimethyl sulfoxide in the drug formula, the penetration rate reaches 90.5%, exceeding the standard penetration rate.
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