Sumatriptan pharmaceutical composition used in nasal cavity and preparation method thereof
A composition and drug technology, applied in the field of new formulations of sumatriptan, can solve problems such as inconvenient use of injections, easy to cause gastrointestinal adverse reactions, pain, etc.
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Embodiment 1
[0022] Raw materials g
[0023] Sumatriptan succinate 700 (equivalent to sumatriptan 500)
[0025] Methylparaben 5.0
[0026] Ethylparaben 5.0
[0027] Weigh the raw and auxiliary materials according to the prescription amount. First mix the excipients methylparaben and ethylparaben, then add about 8000ml of water, heat to 40°C, stir and dissolve, then add the weighed sumatriptan succinate and sodium chloride , stir and make it dissolve, cool to room temperature, add water to 10000ml, filter with a microporous membrane, pack in 10ml plastic bottles with quantitative valve caps, and prepare 1000 bottles of the medicine of the present invention.
Embodiment 2
[0036] Raw materials g
[0037] Sumatriptan 1000
[0039] Methylparaben 7.0
[0040] Ethylparaben 7.0
[0041] Weigh the raw and auxiliary materials according to the prescription amount; first mix the auxiliary materials methylparaben and ethylparaben, then add about 7500ml of water, heat to 45°C and stir to dissolve, then add the weighed succinic acid Sumatriptan and sodium chloride are stirred and dissolved, cooled to room temperature, added with water to 10000ml, filtered with a microporous membrane, and packed in 10ml plastic bottles with quantitative valve caps to prepare the medicine of the present invention 1000 bottles.
Embodiment 3
[0043] Raw materials g
[0044] Sumatriptan 500
[0045] Sodium chloride 18.0
[0046] Methylparaben 20.0
[0047] Ethylparaben 20.0
[0048] Weigh the raw and auxiliary materials according to the prescription amount; first mix the auxiliary materials methylparaben and ethylparaben, then add about 8500ml of water, heat to 50°C and stir to dissolve, then add the weighed succinic acid Sumatriptan and sodium chloride are stirred and dissolved, cooled to room temperature, added with water to 10000ml, filtered with a microporous membrane, and packed in 10ml plastic bottles with quantitative valve caps to prepare the medicine of the present invention 1000 bottles.
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