Nasal spray agent
A technology for nasal sprays and sprays, applied in the field of sprays, which can solve the problems of economic burden and inconvenient use, slow onset of oral tablets, and low bioavailability
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Embodiment 1
[0013] Weigh 1.12 g of granisetron hydrochloride fine powder (calculated as granisetron 1.0 g) that has been pulverized through an 80-mesh sieve, and set aside. Dissolve 0.06g of ethyl p-hydroxybenzoate and 1.8g of sodium chloride in 200ml of distilled water and set aside. Put the above-mentioned granisetron hydrochloride in a 100ml volumetric flask, add 90ml of the above-mentioned mixed solution, shake to dissolve, add the solution to the full amount of 100ml, and filter under reduced pressure with a G3 or G4 vertical fusing glass funnel to obtain granisetron hydrochloride Liquid medicine for nasal spray. Embodiment 2. After the spray of the present invention and tablet are administered, in blood drug concentration peak concentration time (T max ) and peak concentration (C max )Comparison
Embodiment 2
[0014] The nasal spray containing 2mg granisetron (hereinafter referred to as preparation A) was prepared according to the method of Example 1; in addition, a tablet containing 2mg granisetron was used. Divide 8 Beagles into two groups, with 4 Beagles in each group. The above-mentioned granisetron nasal spray and granisetron tablet were given to the above-mentioned two groups of animals respectively, and the time (T max ) and the corresponding maximum blood concentration C max , and the results are shown in Table 1 below.
[0015] Table 1
[0016] parameters
[0017] As can be seen from the data in Table 1, the granisetron nasal spray of the present invention is significantly better than the granisetron tablet in the absorption and onset of the drug.
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