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A powder and preparation technology, which is applied in the fields of pharmaceutical formula, drug delivery, digestive system, etc., can solve the problems of slow onset of oral tablets, economic burden, inconvenient use, and high pain for patients
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Embodiment 1
[0014] Embodiment 1: Preparation of nasal powder containing granisetron hydrochloride:
[0015] Weigh 11.2 g of granisetron hydrochloride fine powder (calculated as granisetron 10.0 g) that has been pulverized through a 120 mesh sieve, and set aside. In addition, 388.8 g of lactose, which was accurately weighed and crushed through a 100-mesh sieve, was set aside. The above-mentioned granisetron hydrochloride and lactose were uniformly mixed in an equal-volume ascending method, and sieved again for 3 times to obtain a nasal powder containing granisetron hydrochloride.
Embodiment 2
[0016] Embodiment 2. After nasal powder of the present invention and tablet are administered, in blood drug concentration peak concentration time (T max ) and peak concentration (C max )Comparison
[0017] The nasal powder 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 powder 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.
[0018] Table 1
[0019] Comparison of blood concentration of granisetron nasal powder and tablet after administration
[0020] parameters
[0021] As can be seen from the data in Table 1, the granisetron nasal powder of the present invention is...
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