Dental ulcer spray and preparation method thereof
An oral ulcer and spray technology, which is applied in the field of oral ulcer spray and its preparation, can solve the problems such as inability to achieve wound surface isolation, no pain relief function, prolonged treatment period, etc., so as to facilitate ulcer healing, prevent ulcer infection, avoid ulcer The effect of cross infection
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Embodiment 1
[0023] Oral ulcer spray, in parts by mass, consists of 1-3 parts of regenerative agent, 0.3-0.5 part of anti-inflammatory agent, 1-4 parts of film-forming agent, 0.5-2.5 parts of porogen, and 0.1-0.2 part of suspending agent 0.1-0.2 parts of antioxidant, 0.1-0.2 parts of astringent and 92-98 parts of solvent.
[0024] In the present embodiment, described regenerative agent is alanyl glutamine; Anti-inflammatory agent is the mixture of nano-silver, nano-zinc and chitosan, and wherein, the weight ratio of nano-silver, nano-zinc and chitosan is 1: 2:0.5; the film-forming agent is polyvinyl butyral; the porogen is a mixture of polyvinylpyrrolidone and glycerin, wherein the mass ratio of polyvinylpyrrolidone and glycerin is 1:1.26; the suspending agent is sodium alginate; the antioxidant is water-soluble coenzyme Q10; the astringent is calamine; the solvent is ethanol.
[0025] In this embodiment, the model of the polyvinyl butyral has a viscosity of 250CPS-280CPS or 10s-15s; the ...
Embodiment 2
[0033] Oral ulcer spray, in parts by mass, consists of 1-3 parts of regenerative agent, 0.3-0.5 part of anti-inflammatory agent, 1-4 parts of film-forming agent, 0.5-2.5 parts of porogen, and 0.1-0.2 part of suspending agent 0.1-0.2 parts of antioxidant, 0.1-0.2 parts of astringent and 92-98 parts of solvent.
[0034]In the present embodiment, described regenerative agent is alanyl glutamine; Anti-inflammatory agent is the mixture of nano-silver, nano-zinc and chitosan, and wherein, the weight ratio of nano-silver, nano-zinc and chitosan is 1: 2:0.5; the film-forming agent is polyvinyl butyral; the porogen is a mixture of polyvinylpyrrolidone and glycerin, wherein the mass ratio of polyvinylpyrrolidone and glycerin is 1:1.26; the suspending agent is sodium alginate; the antioxidant is water-soluble coenzyme Q10; the astringent is calamine; the solvent is ethanol.
[0035] In this embodiment, the model of the polyvinyl butyral has a viscosity of 250CPS-280CPS or 10s-15s; the s...
Embodiment 3
[0043] Oral ulcer spray, in parts by mass, consists of 1-3 parts of regenerative agent, 0.3-0.5 part of anti-inflammatory agent, 1-4 parts of film-forming agent, 0.5-2.5 parts of porogen, and 0.1-0.2 part of suspending agent 0.1-0.2 parts of antioxidant, 0.1-0.2 parts of astringent and 92-98 parts of solvent.
[0044] In the present embodiment, described regenerative agent is alanyl glutamine; Anti-inflammatory agent is the mixture of nano-silver, nano-zinc and chitosan, and wherein, the weight ratio of nano-silver, nano-zinc and chitosan is 1: 2:0.5; the film-forming agent is polyvinyl butyral; the porogen is a mixture of polyvinylpyrrolidone and glycerin, wherein the mass ratio of polyvinylpyrrolidone and glycerin is 1:1.26; the suspending agent is sodium alginate; the antioxidant is water-soluble coenzyme Q10; the astringent is calamine; the solvent is ethanol.
[0045] In this embodiment, the model of the polyvinyl butyral has a viscosity of 250CPS-280CPS or 10s-15s; the ...
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