A kind of microporous release osmotic pump controlled release tablet and preparation method thereof
An osmotic pump controlled-release and microporous technology, which is applied in pharmaceutical formulations and drug delivery, can solve the problems of restricting the promotion of osmotic pump products, difficult production, and long production cycle, so as to improve reliability, stability, and labor intensity. Reduction, the effect of equipment cost reduction
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Embodiment 1
[0035] Chip composition:
[0036]
[0037] Coating film composition:
[0038] Cellulose acetate 21g
[0039] Hydroxypropylcellulose (KlucelLF) 9g
[0040] Dibutyl sebacate 2g
[0041] Make 1000 tablets by the following preparation method:
[0042] (1) Tablet core preparation Take sodium chloride and pulverize, pass through a 100-mesh sieve, mix evenly with medicine and microcrystalline cellulose, use ethanol as a wetting agent, make a soft material, pass through a 30-mesh sieve to granulate, and dry at 50°C for 2 hour, granulate, add magnesium stearate, mix, tabletting, adopt conventional tabletting technology to compress 1000 tablets.
[0043] (2) Tablet core coating: take cellulose acetate, add acetone 600ml, stir to dissolve; take another hydroxypropyl cellulose (KlucelLF) and put it in a 50ml measuring bottle, add water to dissolve it, and add it to the above 1500ml cellulose acetate In the plain acetone solution, stir while adding to dissolve all the hydroxypropyl c...
Embodiment 2
[0046] Chip composition:
[0047]
[0048] Coating film composition:
[0049] Ethylcellulose 6.25g
[0050] Poloxamer 2376.75g
[0051] Triethyl citrate 2g
[0052] Make 1000 tablets by the following preparation method:
[0053] (1) Tablet core preparation Take mannitol and crush it, pass through a 100-mesh sieve, mix evenly with desvenlafaxine succinate, HPMC-K4M, HPMC-K100LV, use ethanol as a wetting agent, make a soft material, pass through a 30-mesh Sieve and granulate, dry at 45°C for 2 hours, granulate, add magnesium stearate, mix well, compress into tablets, and compress 1000 tablets by conventional tablet technology.
[0054] (2) Tablet core coating: Take poloxamer 237, ethyl cellulose and hydroxypropyl cellulose, add 1500 ml of ethanol, stir to dissolve. Add triethyl citrate and shake well to obtain a coating solution. Put the tablet cores prepared above in a coating machine, pass hot air, keep the temperature between 30-40°C, and spray into the coating solut...
Embodiment 3
[0057] Chip composition:
[0058]
[0059]
[0060] Coating film composition:
[0061] Cellulose diacetate 26.5g
[0062] Hydroxypropyl Cellulose KlucelGF1.5g
[0063] Dibutyl sebacate 2g
[0064] The composition of the film coating layer containing the main drug:
[0065] Desvenlafaxine Succinate 15g
[0066] Hypromellose 20g
[0067] Polyethylene glycol (1000) 2g
[0068] Make 1000 tablets by the following preparation method:
[0069] (1) Tablet core preparation: crush sodium chloride, add the main ingredient and 1 / 2 microcrystalline cellulose, pass through a 60-mesh sieve, and mix well. Add appropriate amount of 10% polyvinylpyrrolidone k-30 ethanol solution to make a soft material, pass through a 30-mesh sieve to granulate, and place in an oven to heat and dry at 50°C. The prepared granules are mixed with the remaining microcrystalline cellulose and magnesium stearate, and then added into a tablet machine for tablet compression.
[0070] (2) Tablet core coat...
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