Buccal tablets capable of resisting dentin hypersensitivity and preparation method of buccal tablets
A tooth sensitivity and buccal tablet technology, which is applied in the field of buccal tablets and its preparation, can solve the problems of slow effect, short retention time of toothpaste, anti-dentin sensitivity compounds can not fully exert the anti-dentin sensitivity effect, and achieve good taste , quick effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0041]The preparation method of the buccal tablet of the present invention comprises the following steps: (1) preparation of the first mixed powder; (2) preparation of the second mixed powder; (3) tabletting.
[0042] In step (1), the raw materials comprising potassium chloride, vitamin C, part of sugar alcohol, part of lactose and optional auxiliary materials are uniformly mixed and crushed to 30-70 mesh to obtain the first mixed powder; the part of sugar alcohol The quality of the part of lactose accounts for 30-60wt% of all sugar alcohols; the quality of said part of lactose accounts for 30-60wt% of the whole lactose;
[0043] The consumption of each component in the step (1) is as above, and will not be repeated here. Preferably, potassium chloride, vitamin C and auxiliary materials are firstly mixed uniformly to obtain a mixture; then the mixture is uniformly mixed with the part of sugar alcohol and part of lactose. Adopting the above-mentioned mixing method is conducive...
Embodiment 1
[0048] The formulation of the buccal tablet for anti-tooth hypersensitivity is as follows:
[0049] 8mg Potassium Chloride, 10mg Vitamin C, 400mg Xylitol, 75mg Lactose, 5mg Magnesium Stearate, 1mg Flavor.
[0050] The preparation method of above-mentioned buccal tablet is as follows:
[0051] (1) uniformly mix 8 mg of potassium chloride, 10 mg of vitamin C and 1 mg of essence to obtain a mixture; then uniformly mix the mixture with 200 mg of xylitol and 30 mg of lactose, and pulverize to 30-70 mesh to obtain the first mixed powder;
[0052] (2) Mix the first mixed powder, 200mg xylitol, 45mg lactose and 5mg magnesium stearate evenly to obtain the second mixed powder; the particle diameters of xylitol and lactose are both 20-50 mesh;
[0053] (3) Compress the second mixed powder into tablets with a pressure of 20kgf to obtain buccal tablets.
[0054] Refer to Table 3 for the oral test results of the buccal tablets.
Embodiment 2~5
[0056] Except that the formula quantity of potassium chloride is different, other conditions of embodiments 2-5 are respectively identical with embodiment 1. The formula quantity of the potassium chloride of embodiment 2~5 is referring to table 1. Refer to Table 3 for the oral test results of the buccal tablets of Examples 2-5.
[0057] The formula quantity of the potassium chloride of table 1 embodiment 2~5
[0058] serial number
PUM
Property | Measurement | Unit |
---|---|---|
Particle size | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com