CN110169948A - A kind of canker sore of the material containing bioactive minerals repairs gel and preparation method thereof - Google Patents
A kind of canker sore of the material containing bioactive minerals repairs gel and preparation method thereof Download PDFInfo
- Publication number
- CN110169948A CN110169948A CN201910524322.9A CN201910524322A CN110169948A CN 110169948 A CN110169948 A CN 110169948A CN 201910524322 A CN201910524322 A CN 201910524322A CN 110169948 A CN110169948 A CN 110169948A
- Authority
- CN
- China
- Prior art keywords
- gel
- solution
- medium
- formula ratio
- agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 73
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims abstract description 57
- 239000011707 mineral Substances 0.000 title claims abstract description 57
- 230000000975 bioactive effect Effects 0.000 title claims abstract description 56
- 208000020670 canker sore Diseases 0.000 title claims abstract description 41
- 230000008439 repair process Effects 0.000 title claims abstract description 27
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 238000001879 gelation Methods 0.000 title abstract description 3
- 239000000227 bioadhesive Substances 0.000 claims abstract description 36
- 239000011159 matrix material Substances 0.000 claims abstract description 33
- 239000002994 raw material Substances 0.000 claims abstract description 31
- 239000002270 dispersing agent Substances 0.000 claims abstract description 26
- 239000003002 pH adjusting agent Substances 0.000 claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 158
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 63
- 235000010755 mineral Nutrition 0.000 claims description 54
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 36
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 34
- 229910052710 silicon Inorganic materials 0.000 claims description 34
- 239000010703 silicon Substances 0.000 claims description 32
- 239000000022 bacteriostatic agent Substances 0.000 claims description 30
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 28
- 230000000694 effects Effects 0.000 claims description 24
- 239000000843 powder Substances 0.000 claims description 23
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims description 22
- 229960000935 dehydrated alcohol Drugs 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 18
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 16
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 16
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 16
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 15
- 238000010438 heat treatment Methods 0.000 claims description 15
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 15
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 15
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 15
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 14
- 229920002125 Sokalan® Polymers 0.000 claims description 14
- 229960001631 carbomer Drugs 0.000 claims description 14
- 235000011187 glycerol Nutrition 0.000 claims description 14
- 239000011521 glass Substances 0.000 claims description 13
- 238000004090 dissolution Methods 0.000 claims description 12
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 11
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims description 11
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 claims description 11
- 229960002216 methylparaben Drugs 0.000 claims description 11
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 11
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 10
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 10
- 229940041616 menthol Drugs 0.000 claims description 10
- -1 phosphoric acid hydrogen Chemical class 0.000 claims description 10
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 9
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000005313 bioactive glass Substances 0.000 claims description 9
- 229940116229 borneol Drugs 0.000 claims description 9
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 claims description 9
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 claims description 9
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims description 7
- 235000010234 sodium benzoate Nutrition 0.000 claims description 7
- 239000004299 sodium benzoate Substances 0.000 claims description 7
- 206010028980 Neoplasm Diseases 0.000 claims description 6
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- 229920002678 cellulose Polymers 0.000 claims description 6
- 239000001913 cellulose Substances 0.000 claims description 6
- 235000010980 cellulose Nutrition 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000001103 potassium chloride Substances 0.000 claims description 6
- 235000011164 potassium chloride Nutrition 0.000 claims description 6
- 239000002210 silicon-based material Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 239000010642 eucalyptus oil Substances 0.000 claims description 4
- 229940044949 eucalyptus oil Drugs 0.000 claims description 4
- 238000005187 foaming Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 239000011574 phosphorus Substances 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 235000010241 potassium sorbate Nutrition 0.000 claims description 4
- 239000004302 potassium sorbate Substances 0.000 claims description 4
- 229940069338 potassium sorbate Drugs 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- FTLYMKDSHNWQKD-UHFFFAOYSA-N (2,4,5-trichlorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=C(Cl)C=C1Cl FTLYMKDSHNWQKD-UHFFFAOYSA-N 0.000 claims description 3
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims description 3
- 229920001661 Chitosan Polymers 0.000 claims description 3
- 229920000148 Polycarbophil calcium Polymers 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 3
- 239000003242 anti bacterial agent Substances 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 229910001424 calcium ion Inorganic materials 0.000 claims description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 3
- 229960001617 ethyl hydroxybenzoate Drugs 0.000 claims description 3
- 235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 claims description 3
- 239000004403 ethyl p-hydroxybenzoate Substances 0.000 claims description 3
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052588 hydroxylapatite Inorganic materials 0.000 claims description 3
- 239000004310 lactic acid Substances 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 claims description 3
- 229950005134 polycarbophil Drugs 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims description 3
- 229920000053 polysorbate 80 Polymers 0.000 claims description 3
- 229940085605 saccharin sodium Drugs 0.000 claims description 3
- 229960003885 sodium benzoate Drugs 0.000 claims description 3
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims description 3
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims description 3
- 239000001509 sodium citrate Substances 0.000 claims description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 3
- 239000001540 sodium lactate Substances 0.000 claims description 3
- 229940005581 sodium lactate Drugs 0.000 claims description 3
- 235000011088 sodium lactate Nutrition 0.000 claims description 3
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 2
- 241001474374 Blennius Species 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- 239000004408 titanium dioxide Substances 0.000 claims 1
- 208000025865 Ulcer Diseases 0.000 abstract description 41
- 231100000397 ulcer Toxicity 0.000 abstract description 40
- 208000027418 Wounds and injury Diseases 0.000 abstract description 14
- 239000003814 drug Substances 0.000 abstract description 9
- 229940079593 drug Drugs 0.000 abstract description 8
- 239000004615 ingredient Substances 0.000 abstract description 5
- 210000004400 mucous membrane Anatomy 0.000 abstract description 4
- 230000001681 protective effect Effects 0.000 abstract description 4
- 230000000638 stimulation Effects 0.000 abstract description 3
- 206010067484 Adverse reaction Diseases 0.000 abstract description 2
- 241000894006 Bacteria Species 0.000 abstract description 2
- 230000006838 adverse reaction Effects 0.000 abstract description 2
- 230000003115 biocidal effect Effects 0.000 abstract description 2
- 239000012567 medical material Substances 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 107
- 239000000499 gel Substances 0.000 description 97
- 235000019441 ethanol Nutrition 0.000 description 58
- 229960004756 ethanol Drugs 0.000 description 52
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 20
- 235000019796 monopotassium phosphate Nutrition 0.000 description 20
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 20
- 230000000052 comparative effect Effects 0.000 description 12
- 206010052428 Wound Diseases 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 8
- 230000036407 pain Effects 0.000 description 8
- 235000013406 prebiotics Nutrition 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 210000000214 mouth Anatomy 0.000 description 6
- 210000004027 cell Anatomy 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000004659 sterilization and disinfection Methods 0.000 description 5
- 239000003292 glue Substances 0.000 description 4
- 230000035876 healing Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000036961 partial effect Effects 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 235000005979 Citrus limon Nutrition 0.000 description 3
- 244000131522 Citrus pyriformis Species 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- TZBAVQKIEKDGFH-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-1-benzothiophene-2-carboxamide;hydrochloride Chemical compound [Cl-].C1=CC=C2SC(C(=O)NCC[NH+](CC)CC)=CC2=C1 TZBAVQKIEKDGFH-UHFFFAOYSA-N 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- 230000029663 wound healing Effects 0.000 description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 206010030113 Oedema Diseases 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 210000003296 saliva Anatomy 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000037314 wound repair Effects 0.000 description 2
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 240000001624 Espostoa lanata Species 0.000 description 1
- 235000009161 Espostoa lanata Nutrition 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 208000002399 aphthous stomatitis Diseases 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000035587 bioadhesion Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 230000004663 cell proliferation Effects 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 210000001650 focal adhesion Anatomy 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 230000003862 health status Effects 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- VAOCPAMSLUNLGC-UHFFFAOYSA-N metronidazole Chemical compound CC1=NC=C([N+]([O-])=O)N1CCO VAOCPAMSLUNLGC-UHFFFAOYSA-N 0.000 description 1
- 229960000282 metronidazole Drugs 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 210000002200 mouth mucosa Anatomy 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 229940037201 oris Drugs 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000001959 radiotherapy Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000009418 renovation Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 210000001584 soft palate Anatomy 0.000 description 1
- 210000004872 soft tissue Anatomy 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 230000001720 vestibular Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/42—Phosphorus; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/38—Cellulose; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/006—Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
Abstract
The invention belongs to medical material tech field, in particular to the canker sore of a kind of material containing bioactive minerals repairs gel and preparation method thereof.The raw material for repairing gel is by mass percentage, comprising: bioadhesive gel matrix 0.05%-5%, bioactive minerals material 0.05%-5%, dispersing agent 3%-20%, pH adjusting agent 0.01%-1%, medium surplus.Canker sore of the invention repairs gel; it can be according to the surface of a wound size when use; appropriate gel is taken to be applied to the canker sore surface of a wound; 30s or so can form one layer of adhesiveness protective film; perfection fitting ulcer wound surface; with excellent adhesiveness, closure, biocompatibility, be effectively prevented bacterium enters to invade stimulation of the foreign matter to ulcer surface and mucosal tissue.Present component safety, the ingredients such as hormone-free, antibiotic avoid drug-induced adverse reaction, and are not necessarily to special instrument, easy to operate, wide indications.
Description
Technical field
The invention belongs to medical material tech field, in particular to the canker sore of a kind of material containing bioactive minerals
Repair gel and preparation method thereof.
Background technique
Canker sore is a kind of superficial ulcer betided on oral mucosa, also known as " aphtha ", often hair in tongue, lip, cheek,
The positions such as vestibular ditch, soft palate, and have periodically, the disease incidence in general population is not less than 10%, in specific crowd, suffers from
Sick rate is up to 60%.Patient often feels in great pain, particularly evident when especially encountering the foods such as sour, salty, hot and cold, serious shadow
Ring the life and work for arriving patient.
Currently, the product clinically used is powder, paste, film, gargle etc., main purpose is relieved pain with anti-inflammatory and is
It is main, although the treatment to canker sore has certain curative effect, do not have the ability of the growth of induced tissue cell, for bursting
Reparation, the healing in ulcer face, lack enough facilitations;And the product of certain repair can be played, and mostly containing ground
The drug ingedients such as Sai meter Song, metronidazole;Along with existing product have focal adhesion it is poor, easily by saliva washout, using inadequate
The disadvantages of facilitating, the movement etc. of patient's masseter when speaking, feeding, the therapeutic effect of these products receive certain influence;
Such as powder canker sore product, after being applied to affected part, quickly as saliva is lost, when in use, foreign body sensation is stronger for film, and
The shape of film causes the two perfect cannot be bonded with the shape difference of ulcer surface.
Therefore, in the scientific research and practice of the department of stomatology, needing to develop a kind of can form physics screened film, promote cell raw
Novel canker sore that is long, accelerating wound healing, ingredient safety, good effect, patient's physiological pain few repairs gel.
Summary of the invention
The object of the present invention is to provide a kind of canker sore of material containing bioactive minerals to repair gel and its preparation
Method.The reparation gel can wound healing, and screened film, ingredient safety, good effect can be formed.
To achieve the goals above, the present invention adopts the following technical scheme:
A kind of canker sore reparation gel of the material containing bioactive minerals, the raw material for repairing gel press quality hundred
Score meter, comprising:
As preferred embodiment, the raw material for repairing gel is by mass percentage, further includes:
Corrigent 0.01%-0.5%
Bacteriostatic agent 0.01%-0.5%.
As preferred embodiment, the bioadhesive gel matrix is polyacrylic materials, cellulose family material
The combination of one or more of material, chitosan, polyvinyl alcohol, sodium alginate;Preferably, the polyacrylic materials are selected from card
The mixture of one or more of wave nurse, polycarbophil;It is fine that the cellulose material is selected from hydroxypropyl cellulose, ethoxy
Tie up the mixture of one or more of element, hydroxypropyl methyl cellulose, sodium carboxymethylcellulose.
As preferred embodiment, the dispersing agent is selected from propylene glycol, glycerine, polyethylene glycol, Tween-80, anhydrous
One or more of ethyl alcohol mixture.
As preferred embodiment, the pH adjusting agent is selected from citric acid, sodium citrate, triethanolamine, biphosphate
The mixture of one or more of salt, phosphoric acid hydrogen disalt, lactic acid;The dihydric phosphate particular certain cancers or sylvite, the phosphorus
Sour hydrogen disalt particular certain cancers or sylvite.
As preferred embodiment, the corrigent is any one in menthol, borneol, saccharin sodium, eucalyptus oil
Kind or several mixtures;The antibacterial agent is selected from methylparaben, ethylparaben, sodium benzoate, potassium sorbate, sodium lactate
One or more of mixture.
As preferred embodiment, the medium is dehydrated alcohol and water, in the medium, the volume of dehydrated alcohol
Percentage is 65%-95%.
As preferred embodiment, the bioactive minerals material be selected from bioactivity silicon, bioactivity glass,
The mixture of one or more of hydroxyapatite;Preferably, the bioactivity silicon has the inorganic of three-dimensional net structure
Silicon materials, the silica including 40-70wt%, the oxide of the phosphorus of 30-60wt%, calcium and sodium;Wherein silica is formed
Tridimensional network, calcium ion and phosphonium ion are orderly distributed among three-dimensional netted silicon atom.Preferably, the bioactivity glass
It is living that glass is selected from 45S5 bioactive glass powder, 58S bioactive glass powder, 70S bioactive glass powder, 77S biology
At least one of property glass powder.
When not containing corrigent and bacteriostatic agent in the raw material for repairing gel, preparation method, comprising the following steps:
Solution A preparation steps: the bioadhesive gel matrix is well-dispersed in 0.65-0.80 times of formula ratio
In the dispersing agent, the medium is then added and sufficiently dissolves, obtains solution A;When the bioadhesive gel matrix needs to add
When heat of solution, solution A is prepared as follows: the bioadhesive gel matrix is well-dispersed in formula ratio
In 0.65-0.80 times of the dispersing agent, the water being then added in the medium of formula ratio sufficiently dissolves, and obtains solution A, preferably
Ground, the temperature heated during the dissolution are 65-95 DEG C, preferably 70 DEG C;
Then plus the solution miscible step: dispersing the bioactive minerals material in remaining dispersing agent,
A;When the bioadhesive gel matrix needs to dissolve by heating, it is also necessary to add anhydrous in the medium of formula ratio
Ethyl alcohol;It is sufficiently stirred to obtain mixed liquor later;
It adjusts pH step: pH adjusting agent being added in Xiang Suoshu mixed liquor, adjusting pH is 3-8;
It stands de-foaming steps: after the mixed liquor after adjusting pH value is stood defoaming, obtaining the reparation gel.
When containing corrigent and bacteriostatic agent in the raw material for repairing gel, preparation method, comprising the following steps:
Solution A preparation steps: the bioadhesive gel matrix is well-dispersed in 0.65-0.80 times of formula ratio
In the dispersing agent, 0.7-0.9 times of the medium that formula ratio is then added sufficiently dissolves, and obtains solution A;When the biological slime
When attached property gel-type vehicle needs to dissolve by heating, solution A is prepared as follows: the bioadhesive gel matrix is abundant
It is scattered in the dispersing agent of 0.65-0.80 times of formula ratio, the water being then added in the medium of formula ratio is sufficiently molten
Solution, obtains solution A, it is preferable that the temperature heated during the dissolution is 65-95 DEG C, preferably 70 DEG C;
Solution B preparation steps: the corrigent or/and bacteriostatic agent are dissolved in the remaining medium, then with it is described
Solution A is uniformly mixed, and obtains solution B;When the bioadhesive gel matrix needs to dissolve by heating, the remaining medium
Refer to the dehydrated alcohol in the medium of formula ratio;
Miscible step: dispersing the bioactive minerals material in remaining dispersing agent, and then plus the B is molten
Liquid, and be sufficiently stirred, obtain mixed liquor;
It adjusts pH step: pH adjusting agent being added in Xiang Suoshu mixed liquor, adjusting pH is 3-8;
It stands de-foaming steps: after the mixed liquor after adjusting pH value is stood defoaming, obtaining the reparation gel.
Compared with prior art, technical benefits of the invention is as follows:
1, the canker sore of the material produced by the present invention containing bioactive minerals repairs gel, and when use can be according to the surface of a wound
Size, takes appropriate gel to be applied to the canker sore surface of a wound, and 30s or so can form one layer of adhesiveness protective film, perfection fitting
Ulcer wound surface has excellent adhesiveness, closure, biocompatibility, and be effectively prevented bacterium enters to invade foreign matter to ulcer
The stimulation in face and mucosal tissue.Meanwhile the bioactive minerals material in gel is after contacting the surface of a wound, can promote growth because
The proliferation of son secretion and cell, can promote wound repair ability, accelerate the healing rate of the surface of a wound, to more efficiently treat
Canker sore.
2, present component safety, the ingredients such as hormone-free, antibiotic avoid drug-induced adverse reaction, and nothing
Special instrument is needed, easy to operate, wide indications.
3, the selection proportion of each raw material of the invention is reasonable, acts synergistically, especially medium, bioadhesive gel base
Matter, bioactive minerals material are fitted to each other between this three, further improve the comprehensive performance of renovation agent jointly.
Detailed description of the invention
Fig. 1: the therapeutic effect diagram in the animal experiment of test case, after 5 days.
Specific embodiment
For further understanding of the invention, the present invention will be further described combined with specific embodiments below, is retouched
The embodiment stated is only a part of the embodiment of the present invention, instead of all the embodiments.Based on the embodiments of the present invention, originally
Field technical staff every other embodiment obtained without making creative work, belongs to protection of the present invention
Range.
In a first aspect, the canker sore that the present invention provides a kind of material containing bioactive minerals repairs gel, raw material
By mass percentage, comprising:
As preferred embodiment, the raw material of above-mentioned reparation gel is by mass percentage, further includes:
Corrigent 0.01%-0.5%
Bacteriostatic agent 0.01%-0.5%.
Illustratively, the mass percent of above-mentioned bioadhesive gel matrix can for 0.05%, 0.1%, 0.3%,
0.5%, the arbitrary value or any number in 0.75%, 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%
Range, the mass percent of above-mentioned bioactive minerals material can for 0.05%, 0.1%, 0.3%, 0.5%, 0.75%,
1%, the arbitrary value or any number range in 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, above-mentioned dispersion
The mass percent of agent can be the arbitrary value in 3%, 5%, 8%, 10%, 12%, 15%, 17%, 20% or any number
Range, the mass percent of above-mentioned pH adjusting agent can for 0.01%, 0.03%, 0.05%, 0.1%, 0.15%, 0.2%,
0.25%, 0.3%, 0.35%, 0.4%, 0.45%, 0.5%, 0.55%, 0.6%, 0.65%, 0.7%, 0.75%,
0.8%, the arbitrary value or any number range in 0.85%, 0.9%, 0.95%, 1%;The mass percent of above-mentioned corrigent
Can for 0.01%, 0.03%, 0.05%, 0.1%, 0.15%, 0.2%, 0.25%, 0.3%, 0.35%, 0.4%,
0.45%, the arbitrary value or any number range in 0.5%;The mass percent of above-mentioned bacteriostatic agent can for 0.01%,
0.03%, appointing in 0.05%, 0.1%, 0.15%, 0.2%, 0.25%, 0.3%, 0.35%, 0.4%, 0.45%, 0.5%
Meaning value or any number range.
Wherein, above-mentioned bioadhesive gel matrix (also known as gelling agent, bioadhesive material, gel-type vehicle) can be with
For the combination of one or more of polyacrylic materials, cellulose material, chitosan, polyvinyl alcohol, sodium alginate;It is above-mentioned
Polyacrylic materials are mixed selected from one or more of carbomer, polycarbophil;Above-mentioned cellulose material is selected from hydroxypropyl
The mixing of one or more of base cellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose, sodium carboxymethylcellulose.The life
Object adhesive gels matrix all has good bioadhesive and film forming as filmogen, can be formed in ulcer surface
One layer of isolation film mitigates ulcer pain to shield extraneous physics, chemical factor to the stimulation of ulcerative lesions mucous membrane tissue
Bitterly.Bioadhesive gel matrix is the essential ingredient of reparation gel of the invention, formula preparation according to the invention
Bioactive minerals material being uniformly distributed in ulcer surface can be guaranteed by repairing gel, thus with a small amount of functional material, that is, low at
This acquisition more preferably using effect.If being added without the gel-type vehicle, it is equivalent to " bioactive minerals material " is direct
It is added in dispersing agent and medium, bioactive minerals material can sink to bottom, in this way, bioactive minerals material will not
It can be effectively adhered to ulcer wound surface, so that cannot play the role of effective.
Above-mentioned bioactive minerals material is selected from one of bioactivity silicon, bioactivity glass, hydroxyapatite
Or it is a variety of;Bioactive minerals material plays the role of repair cell as functional material.When the bioactive minerals matter
Material is after especially bioactivity silicon is contacted with the surface of a wound, can promote the generation of growth factor and cell absorption, migration and increase
It grows, this material is can uniquely to be formed to be chemically bonded with bone tissue, and the material of bonding action can be equally formed with soft tissue.At this
In invention amount ranges, the additive amount of " bioactive minerals material " is more, can more promote cell Proliferation, wound repair,
But it is more than usage amount range of the present invention, will lead to facilitation reduction.
Above-mentioned dispersing agent be selected from propylene glycol, glycerine, polyethylene glycol (such as Macrogol 4000 or 6000), Tween-80,
One or more of dehydrated alcohol mixture.The effect of the dispersing agent is to play pre-dispersed effect, makes bioactive minerals
Material is evenly dispersed in ulcer gel, to keep product quality more uniform.
Above-mentioned pH adjusting agent be selected from citric acid, sodium citrate, triethanolamine, dihydric phosphate (particular certain cancers or sylvite),
The mixture of one or more of phosphoric acid hydrogen disalt (particular certain cancers or sylvite), lactic acid.The effect of the pH adjusting agent is to make to produce
Product keep specific pH value range.
Any one or a few mixture of the above-mentioned corrigent in menthol, borneol, saccharin sodium, eucalyptus oil.It should
The effect of corrigent is to mitigate patient pain, improves the mouthfeel of product, and patient is made to be easier to receive.
Above-mentioned bacteriostatic agent is selected from one of methylparaben, ethylparaben, sodium benzoate, potassium sorbate, sodium lactate
Or several mixture.The effect of the bacteriostatic agent is to inhibit microorganism growth in product, prevents from extending the shelf life.
Above-mentioned medium dehydrated alcohol and water, in the medium, the percent by volume of dehydrated alcohol are 65%-95%.It is excellent
Selection of land, when bioadhesive gel matrix is the matrix for not needing to dissolve by heating, the medium is that percentage by volume is 65%-
The ethanol water of 95% (such as: 65%, arbitrary value or any range between the two in 70%, 75%, 80%, 90%, 95%)
Solution.When bioadhesive gel matrix is the matrix for needing to dissolve by heating, the medium is the dehydrated alcohol independently used
With water.
Ethyl alcohol in the medium can not only play the role of disinfection, and evaporation rate is especially fast, and film formation time is short.Due to
The present invention repairs the ethanol solution containing debita spissitudo in gel, so in the case where being added without bacteriostatic agent, shelf-life also phase
To long.
Currently, there are no the mouths of addition bioactive minerals material especially bioactivity silicon materials in scientific research and practice
Chamber ulcer gel products, simple canker sore gel products are also less, and canker sore product occurs mostly in the form of film, patch;
Reparation gel of the invention has just filled up this blank.
Above-mentioned each raw material synergistic effect of the invention, jointly has further reparation gel of the invention and treats well
Effect, medium therein, bioadhesive gel matrix have good synergistic effect between bioactive minerals material.
(1) suitable medium is used to cooperate biogel matrix and bioactive minerals material.Above-mentioned reparation is solidifying
In glue, bioactive minerals material needs achieve the effect that steadily to be scattered in gel, it is therefore desirable to which gel has certain
Consistency;And the gel of the prior art takes water as a solvent more, in contrast, the solvent in the present invention is the aqueous solution of ethyl alcohol, wherein
Water is a small part, so needing bioadhesive gel matrix that can not only also be dissolved in water, while to be also dissolved in ethyl alcohol,
Said effect can be reached, not so gel consistency is inadequate, and is easy layering, and bioactive minerals material can not be made steady in gel
Determine, be evenly distributed.
(2) it uses suitable medium while playing the role of a variety of.Above-mentioned medium (i.e. solvent) be ethyl alcohol aqueous solution or
Dehydrated alcohol adds water, has effect: 1) dissolving gel-type vehicle as solvent;2) ethyl alcohol itself has the function of disinfection, can be right
Ulcer wound surface carries out sterilizing;3) because ethyl alcohol has the function of disinfection, it can make product that there is the longer shelf-life, even
Without adding antibacterial agent;4) evaporation rate of ethyl alcohol is especially fast, therefore after ulcer gel is applied to the surface of a wound, can be fast rapid-result
Film will lead to that film formation time is too long, and patient is difficult to receive if using other solvent instead.
(3) bioadhesive gel matrix has a variety of effects.1) after reparation gel is applied to ulcer surface, in bioadhesion
Layer protecting film can be formed under the action of property gel-type vehicle, ulcer surface is isolated with oral environment, avoids stimulating, slows down pain
Bitterly;2) after reparation gel is applied to the surface of a wound, then the ethyl alcohol elder generation disinfection and sterilization in medium is volatilized, gel-type vehicle film forming, therefore is protected
Cuticula and the isolated environment that ulcer surface forms be do not have it is germy, until protective film disappears;3) protective film is by bioactivity mine
Material is fixed on around ulcer surface, thus bioactive minerals material can be made to act only on ulcer surface, is concentrated
Dosage is repaired;It is all biology rather than as the preparation such as spray used otherwise, in whole oral cavity environment
Active mineral material, so bioactive minerals material of the invention is with least additive amount, it is maximum optimal to reach
Repairing effect.
(4) although bioactive minerals material itself has good acceleration repairing effect, and do not have adherency and make
With bioactive minerals material is just such as when bioactive minerals material being simply applied to ulcer surface, after gargling lower mouth
It is washed out, can not be retained for a long time on ulcer surface, do not have the good therapeutic effect to ulcer, it is therefore desirable to Yi Zhongjie
Bioactive minerals material is fixed on the surface of a wound by matter within a certain period of time;In this way, ulcer gel of the invention is after film forming,
Just play this fixed function.
It can be seen that reparation gel of the invention uses medium, bioadhesive gel matrix, bioactive minerals matter
Material is fitted to each other between this three, has synergistic effect, makes to repair gel curative effect and has achieved the effect that 1+1+1 > 3.
As preferred embodiment, above-mentioned bioactive minerals material selects bioactivity silicon, the bioactivity silicon
Refer to: the inorganic silicon materials with three-dimensional net structure comprising the silica of 40-70wt%, phosphorus, the calcium of 30-60wt%
With the oxide of sodium;Wherein silica forms tridimensional network, and calcium ion and phosphonium ion are orderly distributed in three-dimensional netted silicon
Among atom.In present invention bioactivity silicon used in the following embodiment for existing, commercially available, Beijing is happy prebiotic high-new
The Regesi of Technology Co., Ltd.'s production regenerates silicon materials (including I type and II type).Above-mentioned bioactivity silicon materials can add
Have reparation gel of the invention under conditions of dosage is little to have a better effect.Above-mentioned bioactive minerals material can also be with
Bioactivity glass is selected, which can be selected from commercially available 45S5 bioactive glass powder, 58S bioactivity glass
At least one of glass powder, 70S bioactive glass powder, 77S bioactive glass powder.
In the present invention, the used in amounts of above-mentioned raw materials will be limited in certain numberical range, otherwise will affect reparation gel
The quality of product.(1) for the mass percent of bioadhesive gel matrix if it is less than 0.05%, gel can be partially dilute, causes to hang
Buoyancy is bad, partially thick if it is greater than 5%, causes gel-type vehicle that cannot sufficiently dissolve.(2) if the mass percent of dispersing agent
Less than 3%, the dissolution time that will lead to gel-type vehicle is elongated, or even influences properties of product, leads to ethyl alcohol if it is greater than 20%
The amount of solution is reduced, i.e. gel retrogradation.(3) mass percent of bioactive minerals material cannot if it is less than 0.05%
Sufficiently play the role of promote repair, be greater than 5% be easy reunite, and the suspending power of gel be also not achieved can disperse suspension so
More bioactive minerals materials.(4) mass percent of pH adjusting agent is if it is less than 0.01% gel peracid, if greatly
Alkali is crossed in 1% gel.
As preferred embodiment, above-mentioned its raw material of reparation gel is by mass percentage, comprising:
Further preferably further include:
Corrigent 0.03%-0.4%
Bacteriostatic agent 0.03%-0.4%.
Embodiment more preferably, above-mentioned its raw material of reparation gel is by mass percentage, comprising:
Further preferably further include:
Corrigent 0.05%-0.3%
Bacteriostatic agent 0.05%-0.3%.
Second aspect, the canker sore reparation that the present invention provides the material containing bioactive minerals described in first aspect are solidifying
The preparation method of glue.
When not containing corrigent and bacteriostatic agent in the raw material for repairing gel, preparation method includes:
Step 1: solution A is prepared: above-mentioned bioadhesive gel matrix is well-dispersed in the 0.65-0.80 of formula ratio
In the above-mentioned dispersing agent of times (such as: arbitrary value or any range between the two in 0.65 times, 0.7 times, 0.75 times, 0.8 times),
Then it sufficiently dissolves plus giving an account of matter, obtains solution A.
If selecting the bioadhesive gel of the needs such as polyvinyl alcohol heating, medium water is only added in this step, no
Medium dehydrated alcohol is added.
Step 2: miscible: it disperses above-mentioned bioactive minerals material in remaining dispersing agent, it is then molten plus stating
Liquid A, and be sufficiently stirred, obtain mixed liquor.
If selecting the bioadhesive gel of the needs such as polyvinyl alcohol heating, need to add in medium in this step
Dehydrated alcohol.
Be added pH adjusting agent Step 3: adjusting in pH: Xiang Shangshu mixed liquor, adjustings pH for 3-8 (such as: 3,4,5,6,7,8
Middle arbitrary value or any range between the two).
Step 4: standing defoaming: after the mixed liquor after adjusting pH value is stood defoaming, obtaining above-mentioned reparation gel.
In above step one, two, dispersing agent is divided into two parts addition;In step 1 be added 0.65-0.8 (such as: 0.65
Times, 0.7 times, 0.75 times, arbitrary value or any range between the two in 0.8 times) times formula ratio is used to pre-dispersed gel-type vehicle,
Dosage excessively then causes the part of the pre-dispersed bioactive minerals material of dosage in step 2 to tail off, and makes bioactive minerals matter
Material cannot be sufficiently pre-dispersed, reunites in gel, and dosage is excessively few then to cause gel-type vehicle sufficiently pre-dispersed, adds medium
After cannot quickly dissolve, or even cannot sufficiently dissolve.When containing corrigent or/and bacteriostatic agent in the raw material for repairing gel, system
Preparation Method includes:
It weighs step: weighing each raw material according to said ratio, it is spare.
Step 1: solution A is prepared: above-mentioned bioadhesive gel matrix is well-dispersed in 0.7-0.9 times of formula ratio
In (such as: arbitrary value or any range between the two in 0.7 times, 0.75 times, 0.8 times, 0.85 times, 0.9 times) dispersing agent, so
0.7-0.9 times (such as: arbitrary value or any range between the two in 0.75 times, 0.8 times, 0.85 times) of formula ratio is added afterwards
Medium (herein medium be dehydrated alcohol and water mixed liquor) sufficiently dissolution, obtain solution A.
If selecting the bioadhesive gel of the needs such as polyvinyl alcohol heating, formula ratio described in this step
0.7-0.9 times of medium is replaced by the water in the medium of formula ratio, is added without dehydrated alcohol.
When bioadhesive gel matrix selects the needs such as polyvinyl alcohol to heat the substance that could be dissolved, need above-mentioned
Heated in course of dissolution, temperature be 65-95 DEG C (such as: arbitrary value or any in 65 DEG C, 70 DEG C, 75 DEG C, 80 DEG C, 85 DEG C, 90 DEG C
Range between the two), preferably 70 DEG C.
Step 2: solution B is prepared: above-mentioned corrigent, bacteriostatic agent being dissolved in remaining medium and (refer to remaining dehydrated alcohol
With the mixed liquor of water) in, it is then uniformly mixed with above-mentioned solution A, obtains solution B.If selecting the heating of the needs such as polyvinyl alcohol
Bioadhesive gel, then remaining medium refers to the dehydrated alcohol in the medium of formula ratio in this step.
Step 3: miscible: dispersing above-mentioned bioactive minerals material in remaining dispersing agent, then add and state B
Solution, and be sufficiently stirred, obtain mixed liquor.In this step, bioactive minerals material is first scattered in dispersing agent, then with it is molten
Liquid B mixing, can make bioactive minerals material be well-dispersed in solution B, without reuniting.
Be added pH adjusting agent Step 4: adjusting in pH: Xiang Shangshu mixed liquor, adjustings pH for 3-8 (such as: 3,4,5,6,7,8
Middle arbitrary value or any range between the two).
Step 5: standing defoaming: the mixed liquor after above-mentioned adjusting pH value being stood and is coagulated after defoaming to get canker sore reparation
Glue.
In the step of above two preparation method one, gel-type vehicle is first scattered in dispersing agent, and medium dissolution, energy is then added
Enough accelerate solution rate, dissolves also more abundant;In the step of above two preparation method three/step 4, pH is finally just adjusted,
Because pH is too high or too low, influence whether that the course of dissolution of gel-type vehicle impacts, so this operation is placed on last.
If above two preparation method in the order described above, is not likely to result in (1) bioactive minerals material dough
Poly-, (2) gel-type vehicle cannot sufficiently dissolve, to influence the product quality and curative effect of reparation gel.
Embodiment 1:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 2.5%, propylene glycol 8%, bioactivity silicon
1% (Regesi of the commercially available prebiotic new and high technology Co., Ltd production of Beijing happiness regenerates silicon), menthol 0.1%, nipalgin
Methyl esters 0.2%, citric acid 0.06%, surplus are that volume fraction is 75% ethanol solution.
Hydroxypropyl cellulose is well-dispersed in first in 0.7 times of formula ratio of propylene glycol, 0.8 times of formula ratio of second is added
Alcoholic solution is sufficiently dissolved and is sufficiently swollen, and obtains solution A.Then corrigent menthol, bacteriostatic agent methylparaben are dissolved in residue
Ethanol solution in sufficiently dissolve, then be uniformly mixed with above-mentioned solution A, obtain solution B.Bioactivity silicon is well-dispersed in residue
Propylene glycol in, the solution B then added is sufficiently stirred.It is eventually adding lemon acid for adjusting pH, and is stirred evenly, it is quiet under room temperature
It sets and repairs gel after defoaming to get canker sore.
Embodiment 2:
Raw material is weighed according to following mass percent formula: carbomer 0.2%, propylene glycol 5%, bioactivity silicon 0.5%
(Regesi of the commercially available prebiotic new and high technology Co., Ltd production of Beijing happiness regenerates silicon), borneol 0.1%, methylparaben
0.2%, triethanolamine 0.2%, potassium dihydrogen phosphate 0.4%, surplus is 70% ethyl alcohol (volume fraction).
Carbomer is well-dispersed in 0.75 times of propylene glycol of formula ratio first, 0.8 times of formula ratio of ethyl alcohol is added
Solution is sufficiently dissolved and is sufficiently swollen, and obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and sufficiently dissolved, then
It is uniformly mixed with above-mentioned solution A, obtains solution B.Bioactivity silicon is well-dispersed in propylene glycol, after then adding sufficiently swelling
B solution, be sufficiently stirred.It is eventually adding triethanolamine, potassium dihydrogen phosphate adjusts pH, and stirs evenly, standing defoaming under room temperature
Gel is repaired afterwards to get canker sore.
Embodiment 3:
Weigh raw material according to following mass percent formula: hydroxypropyl methyl cellulose 3%, propylene glycol 10%, biology are living
Property silicon 0.1% (Regesi of the prebiotic new and high technology Co., Ltd production of commercially available Beijing happiness regenerates silicon), menthol 0.2%,
Sodium benzoate 0.2%, potassium dihydrogen phosphate 0.3%, surplus are 80% ethyl alcohol (volume fraction).
Hydroxypropyl methyl cellulose is well-dispersed in first in 0.8 times of formula ratio of propylene glycol, is added 0.8 times of formula ratio
Ethanol solution sufficiently dissolve and be sufficiently swollen, obtain solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution sufficiently
Dissolution, then be uniformly mixed with above-mentioned solution A, obtain solution B.Bioactivity silicon is well-dispersed in remaining propylene glycol, then
In addition B solution, is sufficiently stirred.Be eventually adding potassium dihydrogen phosphate and adjust pH, and stir evenly, stood under room temperature after defoaming to get
Canker sore repairs gel.
Embodiment 4:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 2%, hydroxypropyl methyl cellulose 0.5%,
Glycerine 15%, (the Regesi regeneration of the commercially available prebiotic new and high technology Co., Ltd production of Beijing happiness of bioactivity silicon 2%
Silicon), borneol 0.2%, methylparaben 0.2%, citric acid 0.06%, potassium dihydrogen phosphate 0.4%, surplus is 80% ethyl alcohol (body
Fraction).
Hydroxypropyl cellulose, hydroxypropyl methyl cellulose are well-dispersed in 0.65 times of glycerine of formula ratio first
In, 0.8 times of formula ratio of ethanol solution is added and sufficiently dissolves and is sufficiently swollen, obtains solution A.Corrigent, bacteriostatic agent are dissolved in surplus
It sufficiently dissolves in remaining ethanol solution, then is uniformly mixed with above-mentioned solution A, obtain solution B.Bioactivity silicon is well-dispersed in surplus
In remaining glycerine, B solution is then added, is sufficiently stirred.It is eventually adding potassium dihydrogen phosphate and adjusts pH, and stir evenly, room temperature
Gel is repaired after lower standing defoaming to get canker sore.
Embodiment 5:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 1.5%, carbomer 0.1%, glycerine
15%, bioactivity silicon 3% (Regesi of the commercially available prebiotic new and high technology Co., Ltd production of Beijing happiness regenerates silicon), peppermint
Brain 0.1%, sodium benzoate 0.2%, triethanolamine 0.1%, citric acid 0.06%, potassium dihydrogen phosphate 0.4%, surplus are 70% second
Alcohol (volume fraction).
Hydroxypropyl cellulose, carbomer are well-dispersed in 0.65 times of glycerine of formula ratio first, formula is added
0.8 times of ethanol solution of amount sufficiently dissolves, and obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining remaining ethanol solution and filled
Divide and dissolve and be sufficiently swollen, then be uniformly mixed with above-mentioned solution A, obtains solution B.Bioactivity silicon is well-dispersed in remaining third
In triol, B solution is then added, is sufficiently stirred.It is eventually adding triethanolamine, potassium dihydrogen phosphate adjusting pH, and is stirred evenly, often
Gel is repaired after the lower standing defoaming of temperature to get canker sore.
Embodiment 6:
Raw material is weighed according to following mass percent formula: hydroxypropyl methyl cellulose 1.5%, carbomer 0.1%, the third three
Alcohol 10%, bioactivity silicon 0.5% (Regesi of the commercially available prebiotic new and high technology Co., Ltd production of Beijing happiness regenerates silicon),
Borneol 0.1%, methylparaben 0.2%, triethanolamine 0.1%, potassium dihydrogen phosphate 0.4%, surplus are 80% ethyl alcohol (volume point
Number).
Hydroxypropyl methyl cellulose, carbomer are well-dispersed in 0.75 times of glycerine of formula ratio first, are added
The ethanol solution that 0.8 times of formula ratio is sufficiently dissolved and is sufficiently swollen, and obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethyl alcohol
It sufficiently dissolves in solution, then is uniformly mixed with above-mentioned solution A, obtain solution B.Bioactivity silicon is well-dispersed in remaining the third three
In alcohol, above-mentioned solution B is then added, is sufficiently stirred.It is eventually adding potassium dihydrogen phosphate, triethanolamine adjusting pH, and is stirred evenly,
It is stood under room temperature and repairs gel after defoaming to get canker sore.
Comparative example 1:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 2.5%, propylene glycol 8%, menthol
0.1%, methylparaben 0.2%, citric acid 0.001%, surplus is that volume fraction is 75% ethanol solution.
Hydroxypropyl cellulose is well-dispersed in propylene glycol first, it is sufficiently molten that 0.8 times of formula ratio of ethanol solution is added
It solves and is sufficiently swollen, obtain solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and sufficiently dissolved, then with above-mentioned solution
A is uniformly mixed, and obtains solution B.It is eventually adding lemon acid for adjusting pH, and is stirred evenly, is burst after defoaming is stood under room temperature to get oral cavity
Ulcer repairs gel.
Comparative example 2:
Raw material is weighed according to following mass percent formula: carbomer 0.2%, propylene glycol 5%, borneol 0.1%, nipalgin
Methyl esters 0.2%, triethanolamine 0.2%, potassium dihydrogen phosphate 0.2%, surplus are 70% ethyl alcohol (volume fraction).
Carbomer is well-dispersed in propylene glycol first, 0.8 times of formula ratio of ethanol solution is added and sufficiently dissolves and fills
Divide swelling, obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining remaining ethanol solution and sufficiently dissolved, then with above-mentioned solution A
It is uniformly mixed, obtains solution B.It is eventually adding triethanolamine, potassium dihydrogen phosphate adjusts pH, and stirs evenly, standing defoaming under room temperature
Gel is repaired afterwards to get canker sore.
Comparative example 3:
Raw material is weighed according to following mass percent formula: hydroxypropyl methyl cellulose 3%, propylene glycol 10%, menthol
0.2%, sodium benzoate 0.2%, potassium dihydrogen phosphate 0.2%, surplus is 80% ethyl alcohol (volume fraction).
Hydroxypropyl methyl cellulose is well-dispersed in propylene glycol first, 0.8 times of formula ratio of ethanol solution is added and fills
Divide and dissolve and be sufficiently swollen, obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and sufficiently dissolved, then with it is above-mentioned
Solution A is uniformly mixed, and obtains solution B.It is eventually adding potassium dihydrogen phosphate and adjusts pH, and stir evenly, after standing defoaming under room temperature, i.e.,
It obtains canker sore and repairs gel.
Comparative example 4:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 2%, hydroxypropyl methyl cellulose 0.5%,
Glycerine 15%, borneol 0.2%, methylparaben 0.2%, citric acid 0.001%, potassium dihydrogen phosphate 0.2%, surplus 80%
Ethyl alcohol (volume fraction).
Hydroxypropyl cellulose and hydroxypropyl methyl cellulose are well-dispersed in glycerine first, formula ratio 0.8 is added
Ethanol solution again is sufficiently dissolved and is sufficiently swollen, and obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and filled
Divide dissolution, then be uniformly mixed with above-mentioned solution A, obtains solution B.It is eventually adding citric acid, potassium dihydrogen phosphate adjusting pH, and is stirred equal
It is even, it is stood under room temperature and repairs gel after defoaming to get canker sore.
Comparative example 5:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 1.5%, carbomer 0.1%, glycerine
15%, menthol 0.1%, sodium benzoate 0.2%, triethanolamine 0.1%, citric acid 0.001%, potassium dihydrogen phosphate 0.2% is remaining
Amount is 70% ethyl alcohol (volume fraction).
Hydroxypropyl cellulose, carbomer are well-dispersed in glycerine first, 0.8 times of formula ratio of ethanol solution is added
Sufficiently dissolution, obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and sufficiently dissolved, then is mixed with above-mentioned solution A
It closes uniformly, obtains solution B.It is eventually adding triethanolamine, citric acid, potassium dihydrogen phosphate to adjust pH, and stir evenly, be stood under room temperature
Gel is repaired after defoaming to get canker sore.
Comparative example 6:
Raw material is weighed according to following mass percent formula: hydroxypropyl methyl cellulose 1.5%, carbomer 0.1%, the third three
Alcohol 10%, borneol 0.1%, methylparaben 0.2%, triethanolamine 0.1%, potassium dihydrogen phosphate 0.2%, surplus are 80% ethyl alcohol
(volume fraction).
Hydroxypropyl methyl cellulose, carbomer are well-dispersed in glycerine first, 0.8 times of formula ratio of ethyl alcohol is added
Solution is sufficiently dissolved and is sufficiently swollen, and obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and sufficiently dissolved, then
It is uniformly mixed with above-mentioned solution A, obtains solution B.It is eventually adding potassium dihydrogen phosphate, triethanolamine adjusts pH, and stirs evenly, room temperature
Gel is repaired after lower standing defoaming to get canker sore.
Embodiment 7:
Raw material is weighed according to following mass percent formula: hydroxypropyl cellulose 2.5%, propylene glycol 8%, bioactivity glass
Glass (also known as bioactive minerals powder) 1%, menthol 0.1%, methylparaben 0.2%, citric acid 0.1%, surplus are
Volume fraction is 75% ethanol solution.
The bioactive minerals powder is by following weight percent at being grouped as: SiO240%, CaO 24%, Na2O
20%, P2O56%, SrO 10%;Wherein, each partial size accounts for the weight percent of bioactive minerals powder are as follows: and partial size 0.01~
15 μm of powder content is 25%, and the powder content that 15~60 μm of partial size is 65%, and the powder content that 60~150 μm of partial size is
10%.
Hydroxypropyl cellulose is well-dispersed in first in 0.7 times of formula ratio of propylene glycol, 0.8 times of formula ratio of second is added
Alcoholic solution sufficiently dissolves, and obtains solution A.Corrigent, bacteriostatic agent are dissolved in remaining ethanol solution and sufficiently dissolved, then with it is above-mentioned molten
Liquid A is uniformly mixed, and obtains solution B.Bioactive minerals powder is well-dispersed in remaining propylene glycol, B solution is then added,
It is sufficiently stirred.It is eventually adding lemon acid for adjusting pH, and is stirred evenly, is coagulated after defoaming is stood under room temperature to get canker sore reparation
Glue.
Embodiment 8
Weigh raw material according to following mass percent formula: (average degree of polymerization 1700, alcoholysis degree are polyvinyl alcohol 1788
88) 4%, Macrogol 4000 5%, (the prebiotic new and high technology Co., Ltd of commercially available Beijing happiness is raw for bioactivity silicon 0.1%
The Regesi of production regenerates silicon), disodium hydrogen phosphate 0.3%, eucalyptus oil 0.1%, potassium sorbate 0.2%, surplus is dehydrated alcohol, water
(volume ratio of dehydrated alcohol and water is 65/35).
Polyvinyl alcohol is well-dispersed in 0.75 times of Macrogol 4000 of formula ratio first, adds formula ratio
Water, heating makes it sufficiently dissolve swelling under the conditions of 70 DEG C, obtains solution A.Corrigent, bacteriostatic agent are dissolved in the anhydrous second of formula ratio
It sufficiently dissolves in alcohol, then is uniformly mixed with above-mentioned solution A, obtain solution B.Bioactivity silicon is well-dispersed in remaining poly- second two
In alcohol 4000, the B solution then added is sufficiently stirred.It is eventually adding disodium hydrogen phosphate and adjusts pH, and stir evenly, under room temperature
It stands and repairs gel after defoaming to get canker sore.
Polyvinyl alcohol is first dissolved in water above and then is mixed again with ethyl alcohol, without being directly added to ethanol solution
In, be because heating can make ethyl alcohol rapid evaporation, it is difficult to operate, thus just by medium ethyl alcohol and water dissolve respectively it is different
Raw material is to avoid the operation heated to ethyl alcohol.
Detect example:
One, animal experiment:
The foundation and grouping of model: 40 SD mouse, after anesthesia, under the cotton balls calcination mouse tongue for speckling with phenol solution
Side 60s is randomly divided into experimental group 1, experimental group 2, experimental group 3, model group to prepare diameter as the ulcer surface of 5mm, and every group each
10 cavys.
Medication: experimental group 1 smears canker sore and repairs gel (embodiment 1), each thickness 2mm, 3 times a day, even
It is 5 days continuous.Experimental group 2 smears canker sore and repairs gel (embodiment 7), each thickness 2mm, 3 times a day, continuous 5 days.Experimental group
3, which smear canker sore, repairs gel (comparative example 1), each thickness 2mm, 3 times a day, continuous 5 days.Model group is not dealt with.
Effect assessment: 0 degree: mucous membrane is without ulcer;I degree: ulcer exists, without obvious pseudomembrane at ulcer;II degree: surface at ulcer
The pseudomembrane for having one layer of yellow-white thin;III degree: skin surface has thicker pseudomembrane, there is inflammatory edema situation around ulcer;IV degree:
Skin surface pseudomembrane is thick, and periulcerous inflammation oedema is serious.
Experimental result after being repaired gel for treating 5 days using canker sore is as shown in table 1, Fig. 1:
Table 1: the treatment effectiveness evaluation statistics after test 5 days
By above-described embodiment 2 and comparative example 2, embodiment 3 and comparative example 3, embodiment 4 and comparative example 4, embodiment 5 with it is right
Ratio 5, embodiment 6 and comparative example 6 carry out above-mentioned animal experiment, and the curative effect of each embodiment is better than corresponding comparative example
Curative effect.
Two, clinical test:
Patient data: canker sore patient totally 200, male, female each 100, the age 20-65 years old.When this ulcer occurs
Between within 48h, and not yet by treatment, patient health status is good.
Exclusion criteria: participating in drug study in 3 months, with immune systems such as other diseases of cari oris mucosa and rheumatoids
Disease, there is the disease of diabetic history, diabetes or other influences wound healing, used radiotherapy, chemotherapy in the recent period and was immunized and controls
It treats, to this medicine composition allergy, doctor is deemed unsuitable for selected subject etc. according to clinical experience.
Group technology: agreeing to through patient, patient is divided into 2 groups, each 100, control group gives oral cavity ulcer powder treatment (north
Capital limited liability company, Tongrentang), treatment group, which is given, prepares canker sore reparation gel for treating in this patent embodiment 1.Through uniting
Meter analysis, the patient in experimental group and control group, the age, gender, the course of disease, ulcer area and in terms of without aobvious
Sex differernce is write, is comparable.
Treatment method:
Experimental group: patient will be dried first with sanitary cotton swab at ulcer, is then taken in appropriate embodiment 1 and is prepared canker sore
Gel is repaired, affected part is applied to, continues the 30s or so that dehisces, gel can form one layer of barrier protection film.3 times a day, continuous 7
It.
Control group: patient will be dried first with sanitary cotton swab at ulcer, then take appropriate oral cavity ulcer powder, be applied to trouble
Place, 3 times a day, continuous 7 days.
Judging index:
It is effective: 1-3 days ulcer healings of medication and pain disappearance;
It is effective: 4-5 days ulcer healings of medication and pain disappearance;
Invalid: ulcer does not heal within medication 6 days or more.
Clinical test results:
Remarks: total effective rate is calculated with the sum of effective and effective.
Claims (10)
1. a kind of canker sore of material containing bioactive minerals repairs gel, it is characterised in that: the original for repairing gel
Material is by mass percentage, comprising:
2. repairing gel according to claim 1, it is characterised in that: it is described repair gel raw material by mass percentage,
Further include:
Corrigent 0.01%-0.5%
Bacteriostatic agent 0.01%-0.5%.
3. repairing gel according to claim 1, it is characterised in that:
The bioadhesive gel matrix is polyacrylic materials, cellulose material, chitosan, polyvinyl alcohol, seaweed
The combination of one or more of sour sodium;
Preferably, the polyacrylic materials are selected from the mixture of one or more of carbomer, polycarbophil;The fibre
Tie up one of plain class material in hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose, sodium carboxymethylcellulose
Kind or several mixtures.
4. repairing gel according to claim 1, it is characterised in that:
The dispersing agent is mixed selected from one or more of propylene glycol, glycerine, polyethylene glycol, Tween-80, dehydrated alcohol
Object.
5. repairing gel according to claim 1, it is characterised in that:
The pH adjusting agent in citric acid, sodium citrate, triethanolamine, dihydric phosphate, phosphoric acid hydrogen disalt, lactic acid one
Kind or several mixtures;
The dihydric phosphate particular certain cancers or sylvite, the phosphoric acid hydrogen disalt particular certain cancers or sylvite.
6. repairing gel according to claim 2, it is characterised in that:
Any one or a few mixture of the corrigent in menthol, borneol, saccharin sodium, eucalyptus oil;
The antibacterial agent is selected from one of methylparaben, ethylparaben, sodium benzoate, potassium sorbate, sodium lactate or several
The mixture of kind.
7. repairing gel according to claim 1, it is characterised in that:
The medium is dehydrated alcohol and water, and in the medium, the percent by volume of dehydrated alcohol is 65%-95%.
8. repairing gel according to claim 1, it is characterised in that: the bioactive minerals material is selected from bioactivity
The mixture of one or more of silicon, bioactivity glass, hydroxyapatite;
Preferably, the bioactivity silicon has the inorganic silicon materials of three-dimensional net structure, the titanium dioxide including 40-70wt%
Silicon, the oxide of the phosphorus of 30-60wt%, calcium and sodium;Wherein silica forms tridimensional network, and calcium ion and phosphonium ion have
Sequence is distributed among three-dimensional netted silicon atom.
Preferably, it is raw to be selected from 45S5 bioactive glass powder, 58S bioactive glass powder, 70S for the bioactivity glass
At least one of object activity glass powder, 77S bioactive glass powder.
9. described in any one of claim 1,3-5,7-8 repair gel preparation method, it is characterised in that: this method include with
Lower step:
Solution A preparation steps: the bioadhesive gel matrix is well-dispersed in described in 0.65-0.80 times of formula ratio
In dispersing agent, the medium is then added and sufficiently dissolves, obtains solution A;
When the bioadhesive gel matrix needs to dissolve by heating, solution A is prepared as follows: by the biological slime
Attached property gel-type vehicle is well-dispersed in 0.65-0.80 times of the dispersing agent of formula ratio, and the described of formula ratio is then added
Water in medium sufficiently dissolves, and obtains solution A, it is preferable that the temperature heated during the dissolution is 65-95 DEG C, preferably
It is 70 DEG C;
Then plus the solution A miscible step: dispersing the bioactive minerals material in remaining dispersing agent,;When
When the bioadhesive gel matrix needs to dissolve by heating, it is also necessary to add the anhydrous second in the medium of formula ratio
Alcohol;It is sufficiently stirred to obtain mixed liquor later;
It adjusts pH step: pH adjusting agent being added in Xiang Suoshu mixed liquor, adjusting pH is 3-8;
It stands de-foaming steps: after the mixed liquor after adjusting pH value is stood defoaming, obtaining the reparation gel.
10. repairing the preparation method of gel described in claim 1-8, it is characterised in that: method includes the following steps:
Solution A preparation steps: the bioadhesive gel matrix is well-dispersed in described in 0.65-0.80 times of formula ratio
In dispersing agent, 0.7-0.9 times of the medium that formula ratio is then added sufficiently dissolves, and obtains solution A;
When the bioadhesive gel matrix needs to dissolve by heating, solution A is prepared as follows: by the biological slime
Attached property gel-type vehicle is well-dispersed in 0.65-0.80 times of the dispersing agent of formula ratio, and the described of formula ratio is then added
Water in medium sufficiently dissolves, and obtains solution A, it is preferable that the temperature heated during the dissolution is 65-95 DEG C, preferably
It is 70 DEG C;
Solution B preparation steps: the corrigent or/and bacteriostatic agent are dissolved in the remaining medium, then with the solution A
It is uniformly mixed, obtains solution B;When the bioadhesive gel matrix needs to dissolve by heating, the remaining medium refers to
Dehydrated alcohol in the medium of formula ratio;
Miscible step: dispersing the bioactive minerals material in remaining dispersing agent, then plus the B solution, and
It is sufficiently stirred, obtains mixed liquor;
It adjusts pH step: pH adjusting agent being added in Xiang Suoshu mixed liquor, adjusting pH is 3-8;
It stands de-foaming steps: after the mixed liquor after adjusting pH value is stood defoaming, obtaining the reparation gel.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910524322.9A CN110169948A (en) | 2019-06-17 | 2019-06-17 | A kind of canker sore of the material containing bioactive minerals repairs gel and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910524322.9A CN110169948A (en) | 2019-06-17 | 2019-06-17 | A kind of canker sore of the material containing bioactive minerals repairs gel and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN110169948A true CN110169948A (en) | 2019-08-27 |
Family
ID=67697433
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910524322.9A Pending CN110169948A (en) | 2019-06-17 | 2019-06-17 | A kind of canker sore of the material containing bioactive minerals repairs gel and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110169948A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111840295A (en) * | 2020-08-18 | 2020-10-30 | 隆琰 | Insomnia treatment medicine, preparation method and application thereof in treating insomnia |
CN113842493A (en) * | 2021-09-13 | 2021-12-28 | 深圳先进技术研究院 | Preparation method of temperature-sensitive hydrogel and temperature-sensitive hydrogel |
CN114209604A (en) * | 2022-01-12 | 2022-03-22 | 北京幸福益生再生医学科技有限公司 | Oral care anhydrous composition and preparation method and application thereof |
CN115444992A (en) * | 2022-05-20 | 2022-12-09 | 北京幸福益生再生医学科技有限公司 | Absorbable anti-adhesion material and preparation method thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101347388A (en) * | 2008-02-27 | 2009-01-21 | 徐阳波 | Oral cavity nursing agent and preparation technique thereof |
CN104248775A (en) * | 2014-09-22 | 2014-12-31 | 片仔癀(上海)生物科技研发有限公司 | Hydroxyapatite-chitosan compound gel and preparation process and application thereof |
CN105709271A (en) * | 2016-03-24 | 2016-06-29 | 广东泰宝医疗科技股份有限公司 | Glass wound repair gel with biological activity and preparation method thereof |
CN106362214A (en) * | 2016-08-24 | 2017-02-01 | 北京幸福益生高新技术有限公司 | Regenerated silicon material as well as preparation method and application thereof |
CN106890355A (en) * | 2017-01-18 | 2017-06-27 | 烟台正海生物科技股份有限公司 | A kind of bioactivity glass/carboxymethyl chitosan wound repair gel and preparation method thereof |
CN107412200A (en) * | 2017-04-27 | 2017-12-01 | 哈尔滨乾佰纳生物药业有限公司 | A kind of spacetabs type stomatocace film with bioadhesive and preparation method thereof |
-
2019
- 2019-06-17 CN CN201910524322.9A patent/CN110169948A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101347388A (en) * | 2008-02-27 | 2009-01-21 | 徐阳波 | Oral cavity nursing agent and preparation technique thereof |
CN104248775A (en) * | 2014-09-22 | 2014-12-31 | 片仔癀(上海)生物科技研发有限公司 | Hydroxyapatite-chitosan compound gel and preparation process and application thereof |
CN105709271A (en) * | 2016-03-24 | 2016-06-29 | 广东泰宝医疗科技股份有限公司 | Glass wound repair gel with biological activity and preparation method thereof |
CN106362214A (en) * | 2016-08-24 | 2017-02-01 | 北京幸福益生高新技术有限公司 | Regenerated silicon material as well as preparation method and application thereof |
CN106890355A (en) * | 2017-01-18 | 2017-06-27 | 烟台正海生物科技股份有限公司 | A kind of bioactivity glass/carboxymethyl chitosan wound repair gel and preparation method thereof |
CN107412200A (en) * | 2017-04-27 | 2017-12-01 | 哈尔滨乾佰纳生物药业有限公司 | A kind of spacetabs type stomatocace film with bioadhesive and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
HAMADA ELASYED等: "Bioactive Glass-Ceramic Foam Scaffolds from "Inorganic Gel Casting" and Sinter-Crystallization", 《MATERIALS (BASEL)》 * |
谢梦生等: "口腔组织再生领域应用中的纳米生物活性玻璃材料", 《中国组织工程研究》 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111840295A (en) * | 2020-08-18 | 2020-10-30 | 隆琰 | Insomnia treatment medicine, preparation method and application thereof in treating insomnia |
CN113842493A (en) * | 2021-09-13 | 2021-12-28 | 深圳先进技术研究院 | Preparation method of temperature-sensitive hydrogel and temperature-sensitive hydrogel |
CN113842493B (en) * | 2021-09-13 | 2022-12-02 | 深圳先进技术研究院 | Preparation method of temperature-sensitive hydrogel and temperature-sensitive hydrogel |
CN114209604A (en) * | 2022-01-12 | 2022-03-22 | 北京幸福益生再生医学科技有限公司 | Oral care anhydrous composition and preparation method and application thereof |
CN114209604B (en) * | 2022-01-12 | 2024-01-12 | 北京幸福益生高新技术有限公司 | Anhydrous composition for oral care and preparation method and application thereof |
CN115444992A (en) * | 2022-05-20 | 2022-12-09 | 北京幸福益生再生医学科技有限公司 | Absorbable anti-adhesion material and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110169948A (en) | A kind of canker sore of the material containing bioactive minerals repairs gel and preparation method thereof | |
CN102600494B (en) | Polysaccharide combination and preparation method and application thereof | |
Hasnain et al. | Use of alginates for drug delivery in dentistry | |
CN103961371B (en) | A kind of dental treatment thing with multi-efficiency and compositions thereof | |
CN105169458A (en) | Biological activity mineral substance material and application of biological activity mineral substance material to soft tissue anabrosis and long-time erosion wound cell regeneration and melanoma restraining | |
CN100457084C (en) | Nanometer silver type external use antibiotic gel for female external use and its prepn. method | |
CN105213298A (en) | A kind of oral care gels and preparation method thereof | |
CN101444555A (en) | Purely Chinese traditional medical film for curing oral ulcer and method for preparing same | |
CN108159024A (en) | A kind of sustained release pad pasting for treating canker sore and preparation method thereof | |
CN105168238A (en) | Hyaluronic temperature-sensitive gel and preparation method and application thereof | |
CN102579286A (en) | Traditional Chinese medicine and Western medicine combined strong-efficacy desensitization toothpaste | |
CN106063798B (en) | Oral ulcer treatment patch film and preparation method thereof | |
CN107596435A (en) | A kind of gel of wound repair containing bioactivity glass | |
CN110917120A (en) | Sticky antibacterial repairing material and preparation method and application thereof | |
CN112023123B (en) | Antibacterial gel material for oral restoration and preparation method thereof | |
CN108079013B (en) | Preparation method and application of pain-relieving bioactive glass powder | |
CN108339122B (en) | Preparation method and application of anti-allergy bioactive glass powder | |
CN1739580A (en) | Recipe and prepn process of Chinese medicine gel prepn | |
CN106581741A (en) | Reconstructed human source collagen paste and preparation method thereof | |
CN112773816B (en) | Wound repair spray and preparation method and application thereof | |
CN101156849B (en) | An alepsin slow-releasing gel for promoting paradontal part reborn as well as preparation method and application | |
CN105343927A (en) | Composition for treating dry socket and preparation method of composition | |
CN108264235A (en) | A kind of preparation method and application of the bioactivity glass powder of wound healing | |
CN103381196A (en) | Composition used for treating cervical erosion and application thereof | |
CN113440434A (en) | Pregnant woman toothpaste containing bioactive glass and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20190827 |