Gastric floating slow-release administrating system and its three-dimensional printing forming preparation method
A drug delivery system and gastric floating technology, applied in the field of medical drug preparation, can solve the problems of complex preparation process, many equipments, and difficulties in large-scale process, and achieve the effect of making up for prolongation, accelerating drug release, and compensating for the release route
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Embodiment 1
[0032] Embodiment 1: Layer powder and binder deployment
[0033] Pass hydroxypropyl methylcellulose HPMC 4M, paracetamol, polyvinylpyrrolidone K30, and cetyl alcohol through a 200-mesh sieve respectively, and mix the powder with a particle size of less than 74 μm evenly to obtain a layered powder. Its raw material composition and content (weight parts) are as follows:
[0034] Acetaminophen 100 parts
[0035] Hydroxypropyl methylcellulose HPMC 4M 12 parts
[0036] Polyvinylpyrrolidone K30 9 parts
[0037] Cetyl alcohol 10 parts
[0038] Weigh 2 grams of ethyl cellulose (EC) powder at 5 cps, and dissolve 5 grams of polyvinylpyrrolidone K30 powder in 100 mL of 90% ethanol aqueous solution to prepare spraying adhesive 1.
[0039] Weigh 5 grams of polyvinylpyrrolidone K30 powder and dissolve it in 100 mL of 90% ethanol aqueous solution to prepare spraying adhesive 2.
Embodiment 2
[0040] Example 2: Determining 3D printing forming parameters
[0041] Layer spraying method:
[0042] 1~10 layers Spraying the entire garden surface of Φ10mm
[0043] 11-20 layers Spray a circle with a circumference of 2mm
[0044] 21~30 layers Spraying the entire garden surface of Φ10mm
[0045] Spray forming parameters:
[0046] Layer interval time 2min
[0047] Powder layer thickness 100~200μm
[0048] Spraying rate [spraying drop volume (droplet quantity × droplet size) × spraying frequency] 4nL × 12kz
[0049] Spraying times 2 to 3 times
Embodiment 3
[0050] Example 3: Preparation of gastric floating sustained-release drug delivery system containing ethyl cellulose
[0051] The operation of the 3D printing system is directly controlled by the computer terminal output command: first spread a layer of mixed powder with a thickness of 200μm, spray the binder 1 for 2 times, and after 2 minutes, the piston rod drives the powder bed of the workbench to descend as a whole, and then spread another layer The mixed powder with a thickness of 200 μm is sprayed and bonded to form, so that the three-dimensional printing forming parameters determined in Example 2 are repeated continuously to obtain a gastric floating sustained and controlled release drug delivery system. Then the obtained drug delivery system is dried and depowdered to obtain the finished product.
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