Tinizadole dental plaster for treating buccal inflammation
An oral patch, tinidazole technology, applied in the directions of sheet delivery, medical preparations containing active ingredients, digestive system, etc., to achieve the effect of maintaining drug efficacy, reducing drug side effects, and reducing the degree of adverse reactions
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Embodiment 1
[0021] Grind the menthol into powder, sieve and set aside, and sieve the hydroxypropyl methylcellulose, protein sugar and lactose separately, set aside. Get 5g tinidazole, 13g hydroxypropyl methylcellulose, 0.5g carbomer, 2g protein sugar, 2g lactose, 0.03g menthol, 0.23g magnesium stearate and mix evenly, then press into tablets according to conventional methods, Each tablet contains 5mg of tinidazole.
Embodiment 2
[0023] Grind the menthol into powder and sieve it for later use; sieve the hydroxyethyl cellulose, protein sugar and lactose respectively for later use. Get 200g tinidazole, 440g hydroxyethyl cellulose, 213g carbomer 943, 123g protein sugar, 123g lactose, 1g menthol, 10g magnesium stearate and mix uniformly, then press into tablets according to the method of embodiment 1, wherein Each tablet contains 5 mg of tinidazole.
Embodiment 3
[0025] According to the State Food and Drug Administration New Drug Clinical Research Approval No. 2002HL0330, the concentration of tinidazole oral patch in the saliva of 10 healthy volunteers was determined by high performance liquid chromatography. Tests have shown that the tinidazole oral patch of Example 1 has a sticking time of 1.5-2.5 hours on the tooth surface, and the effective bacteriostatic concentration (greater than 0.12 μg / ml) in saliva can be maintained for 4 hours. The sticking time of the tinidazole oral patch of Example 2 on the tooth surface is 2-3 hours, and the effective bacteriostatic concentration (greater than 0.12 μg / ml) in saliva can be maintained for 5 hours. It shows that the adhesion and sustained release effect of the tinidazole oral patch of the present invention are obvious, and compared with the traditional regular release oral dosage form, it is very beneficial to exert the effect of inhibiting oral anaerobic bacteria.
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