Colloidal bismuth pectin capsule preparation and preparation method
A technology of colloidal bismuth pectin and capsules, which is applied in the field of medicine and can solve problems such as easy agglomeration, high viscosity, and poor effect
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Embodiment 1
[0033] Example 1 Preparation of Capsule Shells Containing Hydroxypropyl Starch
[0034] prescription:
[0035] Raw materials
Dosage
Hydroxypropyl starch
80g
7g
5g
sodium citrate
3.5g
2.7g
2g
[0036] Preparation:
[0037] (1) Chemical glue: put purified water into the chemical glue tank, heat to 80-100°C, then add hydroxypropyl starch, keep warm and stir for 90-180 minutes; then add the remaining ingredients, stir for 10-15 minutes, add activated carbon and stir for decolorization 15min, filter to temporary storage in the insulation barrel;
[0038] (2) The obtained glue solution is processed into a hydroxypropyl starch hollow capsule shell by a full-automatic hollow capsule manufacturing machine.
Embodiment 2a
[0060] Example 2a Preparation of the contents of colloidal bismuth pectin capsules
[0061] Specification 50mg batch 1000 capsules
[0062] prescription
[0063] components
weight
Colloidal bismuth pectin
50g
50g
Povidone K30
2g
18g
1g
[0064] making process:
[0065] (1) adhesive preparation: the povidone K30 of recipe quantity is dissolved in purified water as adhesive, for subsequent use;
[0066] (2) Mixing: take by weighing colloidal bismuth pectin and microcrystalline cellulose of prescription quantity and cross 60 mesh sieves, mix until uniform;
[0067] (3) Granulation: Add binder to the above-mentioned mixed powder to make soft material, pass through 24 mesh sieve and granulate;
[0068] (4) Drying: place the above-mentioned wet granules at 60° C. and blow dry for 1 hour;
Embodiment 2b
[0070] Example 2b Preparation of the contents of colloidal bismuth pectin capsules
[0071] Specification 50mg
[0072] Batch 1000 capsules
[0073] prescription
[0074]
[0075]
[0076] making process:
[0077] (1) adding colloidal bismuth pectin and diatomaceous earth to pulverize in a ball mill to obtain a drug-containing adsorbate, and controlling the average particle diameter of the drug-containing adsorbate to be less than 30 microns;
[0078] (2) The drug-containing adsorbate obtained in the step (1) is uniformly mixed with crospovidone and sodium stearate fumarate to obtain the required capsule contents.
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