Medicament for inhibiting oral bacterial plaque and preparation method thereof
A technology for medicines and plaques, applied in the field of medicines for inhibiting oral plaques and their preparation, can solve the problems of short action time of mouthwash, occurrence of staining, inconvenience in carrying, etc. The effect of dissolution and absorption
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Embodiment 1
[0036] The preferred raw material components of the medicine of the present invention are as follows, and the following parts are parts by weight:
[0037]
[0038] The above raw material components are prepared according to the following scheme.
[0039] The preparation of the adhesive solution, the adhesive is povidone K-30 (PVP-K30), the wetting agent is 95% ethanol, the adhesive is dissolved in the wetting agent, and the concentration is 3%, that is, ;
[0040] Sucrose granulation, making sucrose with a binder (95% ethanol solution of 3% povidone K-30) into a soft material, granulating with a 24 mesh sieve, drying in an oven at 60°C for 5 hours, and sizing with a 20 mesh sieve;
[0041] Mix well, sieve galla tannic acid, citric acid, blueberry essence, magnesium stearate and mix well; mix mannitol and sucrose granules; then mix the above two parts;
[0042] For tableting, a 10mm die is sufficient for tableting. During the tableting process, the temperature in the oper...
Embodiment 2
[0044] The ratio of parts by weight of the raw material components of the medicine of the present invention is as follows:
[0045]
[0046] The above raw material components are prepared according to the following scheme.
[0047] The preparation of the adhesive solution, the adhesive is povidone K-30 (PVP-K30), the wetting agent is 95% ethanol, the adhesive is dissolved in the wetting agent, and the concentration is 3%, that is, ;
[0048] Sucrose granulation, the sucrose is made into a soft material with a binder solution (95% ethanol solution of 3% povidone K-30), granulated through a 24-mesh sieve, dried in an oven at 60°C for 5 hours, and granulated through a 20-mesh sieve;
[0049] Mix well, sieve galla tannic acid, citric acid, blueberry essence, magnesium stearate and mix well; mix mannitol and sucrose granules; then mix the above two parts;
[0050] For tableting, a 10mm die is enough for tableting. During the tableting process, the temperature in the operation ...
Embodiment 3
[0052] The ratio of parts by weight of the raw material components of the medicine of the present invention is as follows:
[0053]
[0054]
[0055] The above raw material components are prepared according to the following scheme.
[0056] The preparation of the adhesive solution, the adhesive is povidone K-30 (PVP-K30), the wetting agent is 95% ethanol, the adhesive is dissolved in the wetting agent, and the concentration is 3%, that is, ;
[0057] Sucrose granulation, the sucrose is made into a soft material with a binder (95% ethanol solution of 3% povidone K-30), granulated through a 24-mesh sieve, dried in an oven at 60°C for 5 hours, and granulated through a 20-mesh sieve;
[0058] Mix well, will. Gallnut tannic acid, citric acid, blueberry essence, and magnesium stearate are sieved and mixed; mannitol and sucrose granules are mixed; the above two parts are mixed;
[0059] For tableting, a 10mm die is sufficient for tableting. During the tableting process, the te...
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