EP2349199A2 - Pharmaceutical composition for the treatment of periodontal diseases - Google Patents
Pharmaceutical composition for the treatment of periodontal diseasesInfo
- Publication number
- EP2349199A2 EP2349199A2 EP09737192A EP09737192A EP2349199A2 EP 2349199 A2 EP2349199 A2 EP 2349199A2 EP 09737192 A EP09737192 A EP 09737192A EP 09737192 A EP09737192 A EP 09737192A EP 2349199 A2 EP2349199 A2 EP 2349199A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- mass
- pharmaceutical composition
- treatment
- human
- periodontal
- 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.)
- Withdrawn
Links
- 238000011282 treatment Methods 0.000 title claims abstract description 20
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 11
- 208000028169 periodontal disease Diseases 0.000 title description 11
- 230000000694 effects Effects 0.000 claims abstract description 17
- 201000001245 periodontitis Diseases 0.000 claims abstract description 15
- 239000000126 substance Substances 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims abstract description 9
- 102000002322 Egg Proteins Human genes 0.000 claims abstract description 8
- 108010000912 Egg Proteins Proteins 0.000 claims abstract description 8
- 108010010803 Gelatin Proteins 0.000 claims abstract description 8
- 241001465754 Metazoa Species 0.000 claims abstract description 8
- 239000008273 gelatin Substances 0.000 claims abstract description 8
- 229920000159 gelatin Polymers 0.000 claims abstract description 8
- 235000019322 gelatine Nutrition 0.000 claims abstract description 8
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229920000609 methyl cellulose Polymers 0.000 claims abstract description 7
- 239000001923 methylcellulose Substances 0.000 claims abstract description 7
- 235000010981 methylcellulose Nutrition 0.000 claims abstract description 7
- 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 abstract description 6
- 230000005764 inhibitory process Effects 0.000 claims abstract description 6
- 229920002307 Dextran Polymers 0.000 claims abstract description 4
- 239000000654 additive Substances 0.000 claims abstract description 4
- 239000009194 citrus pectin Substances 0.000 claims abstract description 4
- 229940040387 citrus pectin Drugs 0.000 claims abstract description 4
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims abstract description 4
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims abstract description 4
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims abstract description 4
- 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 abstract description 4
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 claims abstract description 3
- 210000004381 amniotic fluid Anatomy 0.000 claims abstract description 3
- 210000002700 urine Anatomy 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 31
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 30
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims description 18
- 235000018417 cysteine Nutrition 0.000 claims description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 10
- 229940122344 Peptidase inhibitor Drugs 0.000 claims description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 5
- -1 polyoxyethylene Polymers 0.000 claims description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 230000002335 preservative effect Effects 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims 1
- 239000008363 phosphate buffer Substances 0.000 claims 1
- 239000000499 gel Substances 0.000 abstract description 6
- 239000008055 phosphate buffer solution Substances 0.000 abstract description 5
- 101000749287 Clitocybe nebularis Clitocypin Proteins 0.000 abstract description 2
- 101000767029 Clitocybe nebularis Clitocypin-1 Proteins 0.000 abstract description 2
- 229940094664 Cysteine protease inhibitor Drugs 0.000 abstract description 2
- 150000001298 alcohols Chemical class 0.000 abstract description 2
- 239000004480 active ingredient Substances 0.000 abstract 1
- 230000003239 periodontal effect Effects 0.000 description 20
- 210000001519 tissue Anatomy 0.000 description 18
- 102000035195 Peptidases Human genes 0.000 description 14
- 108091005804 Peptidases Proteins 0.000 description 14
- 206010061218 Inflammation Diseases 0.000 description 12
- 239000012530 fluid Substances 0.000 description 12
- 230000004054 inflammatory process Effects 0.000 description 12
- 239000003112 inhibitor Substances 0.000 description 12
- 241000894006 Bacteria Species 0.000 description 11
- 235000019833 protease Nutrition 0.000 description 11
- 108050004038 cystatin Proteins 0.000 description 10
- 210000004261 periodontium Anatomy 0.000 description 10
- 208000007565 gingivitis Diseases 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 102000004190 Enzymes Human genes 0.000 description 8
- 108090000790 Enzymes Proteins 0.000 description 8
- 238000011161 development Methods 0.000 description 8
- 230000018109 developmental process Effects 0.000 description 8
- 229940088598 enzyme Drugs 0.000 description 8
- 102000015833 Cystatin Human genes 0.000 description 7
- 210000000988 bone and bone Anatomy 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 201000010099 disease Diseases 0.000 description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 210000003296 saliva Anatomy 0.000 description 5
- 108010005843 Cysteine Proteases Proteins 0.000 description 4
- 102000005927 Cysteine Proteases Human genes 0.000 description 4
- 241000605862 Porphyromonas gingivalis Species 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 210000001847 jaw Anatomy 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 235000018102 proteins Nutrition 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 210000003079 salivary gland Anatomy 0.000 description 4
- 238000001356 surgical procedure Methods 0.000 description 4
- 241001432959 Chernes Species 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 230000008929 regeneration Effects 0.000 description 3
- 238000011069 regeneration method Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 108010061642 Cystatin C Proteins 0.000 description 2
- 102100026897 Cystatin-C Human genes 0.000 description 2
- 102100028036 Cystatin-S Human genes 0.000 description 2
- 108090000395 Cysteine Endopeptidases Proteins 0.000 description 2
- 102000003950 Cysteine Endopeptidases Human genes 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 108010026774 Salivary Cystatins Proteins 0.000 description 2
- 208000008312 Tooth Loss Diseases 0.000 description 2
- 206010052428 Wound Diseases 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- BNGRKDJZQIGWQF-UHFFFAOYSA-N [4-benzamido-5-(naphthalen-2-ylamino)-5-oxopentyl]-(diaminomethylidene)azanium;chloride Chemical compound Cl.C=1C=C2C=CC=CC2=CC=1NC(=O)C(CCCNC(=N)N)NC(=O)C1=CC=CC=C1 BNGRKDJZQIGWQF-UHFFFAOYSA-N 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 description 2
- 210000004195 gingiva Anatomy 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 230000008076 immune mechanism Effects 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 244000000010 microbial pathogen Species 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 239000000419 plant extract Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- 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 1
- OTLLEIBWKHEHGU-UHFFFAOYSA-N 2-[5-[[5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy]-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-4-phosphonooxyhexanedioic acid Chemical compound C1=NC=2C(N)=NC=NC=2N1C(C(C1O)O)OC1COC1C(CO)OC(OC(C(O)C(OP(O)(O)=O)C(O)C(O)=O)C(O)=O)C(O)C1O OTLLEIBWKHEHGU-UHFFFAOYSA-N 0.000 description 1
- 241000186361 Actinobacteria <class> Species 0.000 description 1
- 208000010266 Aggressive Periodontitis Diseases 0.000 description 1
- 108010007570 Amelogenin Proteins 0.000 description 1
- 102000007325 Amelogenin Human genes 0.000 description 1
- 208000004099 Angle Class III Malocclusion Diseases 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 241001092371 Bergenia Species 0.000 description 1
- 208000006386 Bone Resorption Diseases 0.000 description 1
- 206010065687 Bone loss Diseases 0.000 description 1
- 101000806820 Capnocytophaga gingivalis Aminopeptidase Proteins 0.000 description 1
- 102000003908 Cathepsin D Human genes 0.000 description 1
- 108090000258 Cathepsin D Proteins 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 102100028007 Cystatin-SA Human genes 0.000 description 1
- 101710144510 Cysteine proteinase inhibitor Proteins 0.000 description 1
- 208000002064 Dental Plaque Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000186394 Eubacterium Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 108091020100 Gingipain Cysteine Endopeptidases Proteins 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 101000572796 Hepatitis E virus genotype 1 (isolate Human/China/HeBei/1987) RNA-directed RNA polymerase Proteins 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 108010077861 Kininogens Proteins 0.000 description 1
- 102000010631 Kininogens Human genes 0.000 description 1
- 206010061274 Malocclusion Diseases 0.000 description 1
- 206010027439 Metal poisoning Diseases 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- DEFAKPKFXYITPZ-FQEVSTJZSA-N N-benzoyl-L-arginine 2-naphthylamide Chemical compound N([C@@H](CCCN=C(N)N)C(=O)NC=1C=C2C=CC=CC2=CC=1)C(=O)C1=CC=CC=C1 DEFAKPKFXYITPZ-FQEVSTJZSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 208000006650 Overbite Diseases 0.000 description 1
- 102000016387 Pancreatic elastase Human genes 0.000 description 1
- 108010067372 Pancreatic elastase Proteins 0.000 description 1
- 206010072574 Periodontal inflammation Diseases 0.000 description 1
- 102000001938 Plasminogen Activators Human genes 0.000 description 1
- 108010001014 Plasminogen Activators Proteins 0.000 description 1
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 208000033608 aggressive 1 periodontitis Diseases 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229940058679 baza Drugs 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000005312 bioglass Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 230000024279 bone resorption Effects 0.000 description 1
- 235000010410 calcium alginate Nutrition 0.000 description 1
- 239000000648 calcium alginate Substances 0.000 description 1
- 229960002681 calcium alginate Drugs 0.000 description 1
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002852 cysteine proteinase inhibitor Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 108010074702 enamel matrix proteins Proteins 0.000 description 1
- 239000002095 exotoxin Substances 0.000 description 1
- 231100000776 exotoxin Toxicity 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 238000001506 fluorescence spectroscopy Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 210000001983 hard palate Anatomy 0.000 description 1
- 208000010501 heavy metal poisoning Diseases 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- 230000005745 host immune response Effects 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000000984 immunochemical effect Effects 0.000 description 1
- 229940088592 immunologic factor Drugs 0.000 description 1
- 239000000367 immunologic factor Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 244000005706 microflora Species 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- YKQOSKADJPQZHB-RGYSVOEGSA-N n-[(2s)-4-amino-1-[[(2s,3r)-1-[[(2s)-4-amino-1-oxo-1-[[(6r,9s,12r,15r,18s,21s)-6,9,18-tris(2-aminoethyl)-3-[(1r)-1-hydroxyethyl]-12,15-bis(2-methylpropyl)-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazacyclotricos-21-yl]amino]butan-2-yl]amino]-3-hydr Chemical compound CCC(C)CCCC(=O)N[C@@H](CCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)C([C@@H](C)O)NC(=O)[C@@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O YKQOSKADJPQZHB-RGYSVOEGSA-N 0.000 description 1
- 239000002417 nutraceutical Substances 0.000 description 1
- 235000021436 nutraceutical agent Nutrition 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 231100000915 pathological change Toxicity 0.000 description 1
- 230000036285 pathological change Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 230000007505 plaque formation Effects 0.000 description 1
- 229940127126 plasminogen activator Drugs 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 235000019419 proteases Nutrition 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009993 protective function Effects 0.000 description 1
- 229940121649 protein inhibitor Drugs 0.000 description 1
- 239000012268 protein inhibitor Substances 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 210000001584 soft palate Anatomy 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 230000008354 tissue degradation Effects 0.000 description 1
- 230000017423 tissue regeneration Effects 0.000 description 1
- 210000003781 tooth socket Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
- 239000000304 virulence factor Substances 0.000 description 1
- 230000007923 virulence factor Effects 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 235000019168 vitamin K Nutrition 0.000 description 1
- 239000011712 vitamin K Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- A61K9/0063—Periodont
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/55—Protease inhibitors
- A61K38/56—Protease inhibitors from plants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/55—Protease inhibitors
- A61K38/57—Protease inhibitors from animals; from humans
-
- 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
Definitions
- composition for the treatment of periodontal diseases is provided.
- the subject of the present invention is a pharmaceutical composition for the treatment of periodontal disease during both walk-in and hospitalized dentistry, as well as in dental surgery.
- Periodontitis does not only concern older persons, but also 20 and 30-year olds, and a number of forms are observed in children as well, and constitute the most common cause of tooth loss.
- Statistical analyses show that inflammatory changes of the gums constitute the most serious cause of tooth loss, and some 60% of the population of the European Union suffers from this problem. This is most often caused by improper oral hygiene and leads to plaque formation, which may be a cause of gingivitis.
- Periodontitis is aided by some genetic factors, smoking, cavities, over or under-bites, poorly set fillings, hormonal disruptions, the activity of certain drugs or heavy metal poisoning.
- teeth are supported by the gum, the periodontium or connective tissue between the tooth and the jaw, as well as the jaw bone.
- the periodontal apparatus is susceptible to inflammation, chiefly due to improper oral hygiene.
- Periodontal disease including gingivitis
- gingivitis leads to a disappearance of tissues around the teeth. In most cases, they disappear and leave the neck of the tooth exposed. The disease develops slowly, and symptoms may include bleeding during brushing or flossing, reddened gums, receding gums or plaque. When these problems are not observed sufficiently early, this leads to osteological changes in periodontium, which is evidenced by its increased mobility. The cause of changes in the gums and the bone surrounding the tooth is inflammation. Bacteria accrue in the periodontal space, which cause inflammation, whence the teeth begin to move and fall out. Inflammation is caused by bacteria which settle on the surface of the root of the tooth, which develop underneath the gum, and the inflammation progresses deeper.
- Cystatin S in saliva inhibits the development of P. gingivalis as well as the activity of cysteine endopeptidases secreted by periodontal bacteria as well as egg protein inhibitors which inhibit the growth of P. gingivalis in vitro in gingival crevice fluid.
- Bokenvoorde MFJ. Henskens Wim van 't Hot YMC, Amerongen AV N. (1996): Inhibition of the growth and cysteine proteinase activity of porphyromonas gingivalis by human salivary cystatin S and chicken cystatin. Biol. Chern. 377, 847-850).
- Three cystatins have been isolated from human saliva so far, which are produced in the salivary glands.
- a curettage is performed. This consists of scraping off the plaque. Bacteria and diseased tissues are thus removed, and the periodontium can heal and regenerate, thus form new tissue. If the disease has destroyed most of the periodontium, and the teeth are poorly held in the bone, they can be bridged, or stiffened. In this procedure, the teeth are connected to one another using various techniques. This may consist of a ligature, or special wires, or a bridging prosthesis, or splints of a composite material. Such a stiff structure of connected teeth stops them from swinging too much. When the wounds in the gums have healed and the periodontium has regenerated, these may be removed.
- the goal of surgical treatment is to remove disease-altered tissues as well as their regeneration or reformation.
- a periodontologist has in his arsenal several treatment methods including: root-to-crown, controlled tissue regeneration using implantable barrier membranes, bone grafts of human or animal bone or natural or synthetic bioglass.
- new tissue is formed which is a copy of the natural one, both in terms of structure and functionality.
- Of paramount importance is the reconstruction of adhesive function, of the periodontal attachments.
- a novel preparation, emdogain gives some hope. It contains enamel proteins, the so-called hydrophobic proteins, which stimulate the regeneration of tissues.
- cysteine peptidase inhibitors are used in the form of preparations purified from various sources, including egg proteins in a composition with vitamins K and D, and the fundamental goal is to rebuild a degraded periodontium and bony periodontal fragments, including the root degraded during periodontitis ( Takada Y., Atsushi Serizawa A., Hidetoshi Ishikawa H., Tomoe Y.,_ Seiichiro Aoe S. (2003) P USA 420102. Bone resorption suppressing agent. Reynolds EC, Bhogal PS., Slakeski N. (2003): Diagnostics and treatments of periodontal disease. P USA 66330 ).
- Polish patent No. 148352 reveals an agent for the treatment of advanced periodontitis in the form of a cellulose derivative at 3 - 7 % by mass, with a polyhydroxyl alcohol or a polymer thereof at 1 - 5% by mass, with an addition of 0.25 % by mass of Kunitz protease inhibitor and water to 100% by mass.
- This complex is a hydrophilic gel with thixotropic properties and a high flow threshold, due to which it may be considered a pseudoplastic substance, which makes it resistant to the activity of mechanical factors such as the activity of saliva, beverages and food.
- Polish patent No. 164585 reveals a therapeutic agent for use in dental surgery, composed of 10-50% gelatin by mass, 2 - 50 % glycerol by mass, or 1.2-propylene glycol, or polyoxyethylene glycol with a molar mass of 200-15000 as well as 1 - 25% by mass of polyvinylpyrolidone with a molar mass of 160000-360000, or polyvinyl alcohol and water to 100% by mass.
- This substance is dosed into wounds, where it becomes hydrolysed by systemic enzymes, and the hydrolysis products comprising amino acids are resorbed. As the bone becomes replenished, the therapeutic agent diminishes in volume, so it requires no replacement.
- gelatin a substance of animal origin, ensures resorption due to hydrolysis into amino-acids.
- Polyvinyl alcohol and polyvinylpyrolidone are also metabolised in the human.
- the release of therapeutically active substances into the tissues follows a zero-order kinetic process, which ensures a constant concentration of the drug in the tissue.
- Polish patent No. 311322 releases a dental gel containing 70-90% by mass of a carrier, composed of water physiological saline and a moisturizer, preferentially hydroxyethylcellulose, a plant extract containing tannins and 0.1-5% by mass of sweeteners and aromas.
- This gel also contains a composition comprising antibiotics such as dethreomycine, colistine, clindamycine in a mass percentage ratio of 1:0.23:5, a steroid anti-inflammatory substance, particularly hydrocortisone at 0.02-1% by mass as well as a plant extract, preferentially of Bergenia, at 1-5 % by mass.
- the dental gel according to the application in question is useful in the treatment of periodontitis.
- the present invention relaters to a pharmaceutical composition for the treatment of periodontitis containing at least gel-forming substances.
- the active substance of the composition is a cysteine protease inhibitor from egg proteins, urine, human and animal amniotic fluid, human and animal placentae, and from plants, which is suspended in 50 g of a polyhydroxyl alcohol, preferentially glycerol, and 50 g of a 0.05 M phosphate buffer solution , pH 6.0 to 7.5, which constitutes a base for the composition in an amount from 20 to 50% by mass, whereas the carrier comprises gelling substances at 7 to 20 % by mass as well as water to 100 % by mass.
- the gelling substances comprise methylcellulose, hydroxypropylmethylcellulose, carboxymethylcellulose sodium salt, gelatin, apple- citrus pectin, dextran or a mixture thereof.
- the composition contains additives in the form of polyhydroxyl alcohols such as glycerol, polyvinylpirolidone K-30 or K-90, polyoxyethylene glycol-200 or glycol propylene-1,2 at 5 to 25 % by mass.
- polyhydroxyl alcohols such as glycerol, polyvinylpirolidone K-30 or K-90, polyoxyethylene glycol-200 or glycol propylene-1,2 at 5 to 25 % by mass.
- a preservative is included in the composition, preferentially in the form of Nipagin.
- compositions in the example sets were used in tests of their ability to treat periodentosis.
- the observation showed that the activity of cysteine proteases was inhibited in the gingival crevices by specific inhibitors obtained from chicken eggs.
- the determinations were made on a 30-patient group at the Facial and Jaw clinic of the Medical Academy of Wroclaw. Gingival crevice fluid was collected from two distant crevices from a patient, and then cysteine peptidase activity was quantified, and then inhibited with cystein protease inhibitors. The inhibition exceeded 90%.
- these inhibitors are suitable for treatment of periodontal inflammations by using appropriate compositions thereof administered directly into periodontal crevices and in mouthwashes for periodontitis patients.
- compositions using cysteine peptidase inhibitors are easily obtained and inexpensive.
- the research also indicates the possibility of using other sources of inhibitors in novel drugs, provided that they are not toxic to the human.
- the research was performed in vitro in fluid collected from the periodontal crevices of patients with diagnosed periodontitis.
- the base which is also an active substance of the composition, composed of the cysteine peptidase inhibitor, polyhydroxyl alcohol and phosphate buffer solution of an appropriate pH may be maintained at 4°C for up to 12 months.
- compositions according to the invention are suitable for both prophylaxis as well as in curettage or surgical treatment as a supplemental treatment.
- the subject of the present invention is shown in example embodiments.
- BASE cysteine peptidase inhibitor, 1-50 activity units suspended in 50 g glycerol, and 50 g 0.05 M phosphate buffer solution pH 6.0 to 7.5 30.0
- Nipagin (Aseptins, Parabens) 0.1 Water 48.
- composition base is prepared by mixing the planned quantities of its components, meaning an appropriate number of units of the cysteine peptidase inhibitor with the polyhydroxyl alcohol and 0.05M phosphate buffer solution with a selected pH. in the range of 6.0 to 7.5.
- the base is apportioned into plastic or glass containers, and stored, preferentially at 4°C.
- the measured quantity of base is supplemented with the given quantities of the remaining components and mixed until homogeneity.
- the gel produced, with a viscosity of 337.53 mPa*s is apportioned into 20 or 50 ml containers.
- the example composition is meant for rinsing the jaw pocket.
- Example composition is produced as in Example 1, by first selecting the components, and then apportioning in the same way.
- the example composition is produced as in Example 1, by first selecting the components, and then apportioning in the same way.
- the example composition is produced as in Example 1, by first selecting the components, and then apportioning in the same way.
- the example composition is produced as in Example 1, by first selecting the components, and then apportioning in the same way.
- the example composition is produced as in Example 1, by first selecting the components, and then apportioning in the same way.
- Table 1 Inhibition of cysteine peptidases in the gingival crevice fluid by egg protein cystatins using a colorimetric method.
- Table 2 Inhibition of cysteine peptidases in gingival crevice fluid by egg protein cystatins (5 ⁇ g ). Inhibitor activity (180 imEU/mg protein) using spectrofluorometry.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nutrition Science (AREA)
- Zoology (AREA)
- Physiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Botany (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL385972A PL219098B1 (pl) | 2008-08-28 | 2008-08-28 | Kompozycja farmaceutyczna do leczenia chorób przyzębia |
| PCT/PL2009/050024 WO2010024702A2 (en) | 2008-08-28 | 2009-08-28 | Pharmaceutical composition for the treatment of periodontal diseases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2349199A2 true EP2349199A2 (en) | 2011-08-03 |
Family
ID=41343718
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09737192A Withdrawn EP2349199A2 (en) | 2008-08-28 | 2009-08-28 | Pharmaceutical composition for the treatment of periodontal diseases |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP2349199A2 (pl) |
| PL (1) | PL219098B1 (pl) |
| WO (1) | WO2010024702A2 (pl) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012113037A1 (en) * | 2011-02-25 | 2012-08-30 | The University Of Melbourne | Method for inhibiting proteins |
| RU2606040C2 (ru) * | 2015-04-01 | 2017-01-10 | Ирина Николаевна Усманова | Способ лечения хронического воспаления тканей пародонта и слизистой оболочки с элементами гиперкератоза у лиц молодого возраста |
| RU2637413C1 (ru) * | 2016-07-04 | 2017-12-04 | Ирина Николаевна Усманова | Способ лечения хронического воспаления слизистой оболочки рта с элементами гиперкератоза у лиц молодого возраста |
| PL239917B1 (pl) * | 2018-11-28 | 2022-01-24 | Univ Medyczny Im Piastow Slaskich We Wroclawiu | Kompozycja zawierająca cystatynę oraz jej zastosowanie w implantologii kostnej |
| WO2020167152A1 (en) * | 2019-02-15 | 2020-08-20 | RAPAK, Andrzej Marek | Inhibitors of cysteine peptidases isolated from natural raw materials and use of the inhibitors in medicine and veterinary medicine |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4592127B2 (ja) * | 1999-03-30 | 2010-12-01 | 雪印乳業株式会社 | 骨吸収抑制剤 |
| PL190404B1 (pl) * | 1999-08-02 | 2005-12-30 | Akad Medyczna | Środek farmaceutyczny działający przeciwko nowotworom, mikroorganizmom chorobotwórczym i chorobom inwazyjnym |
| PL195665B1 (pl) * | 2000-06-13 | 2007-10-31 | Przed Farmaceutyczne Jelfa Sa | Środek farmaceutyczny w postaci żelu do stosowania miejscowego w leczeniu chorób przyzębia |
| US8283135B2 (en) * | 2000-06-30 | 2012-10-09 | The Procter & Gamble Company | Oral care compositions containing combinations of anti-bacterial and host-response modulating agents |
-
2008
- 2008-08-28 PL PL385972A patent/PL219098B1/pl unknown
-
2009
- 2009-08-28 WO PCT/PL2009/050024 patent/WO2010024702A2/en not_active Ceased
- 2009-08-28 EP EP09737192A patent/EP2349199A2/en not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2010024702A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010024702A2 (en) | 2010-03-04 |
| WO2010024702A3 (en) | 2011-06-03 |
| PL385972A1 (pl) | 2010-03-01 |
| PL219098B1 (pl) | 2015-03-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chen et al. | Dental implants: Maintenance, care and treatment of peri‐implant infection | |
| US7115252B2 (en) | Therapeutic compositions and methods of use thereof | |
| TWI899058B (zh) | 用於治療牙周病之化合物 | |
| EP2349199A2 (en) | Pharmaceutical composition for the treatment of periodontal diseases | |
| EP1292325B1 (en) | Matrix protein compositions for dentin regeneration | |
| US10016492B2 (en) | Methods for extracting a tooth | |
| US7304030B2 (en) | Matrix protein composition for dentin regeneration | |
| KR102913837B1 (ko) | 치주염 치료 및 치간 유두 재생용 조성물 | |
| Çiçek et al. | Streptococcal gingivitis: A report of case with a description of a unique gingival prothesis | |
| KR20220143012A (ko) | 치주염 또는 치은염에 대한 활성 물질로서의 콜라겐 가수분해물 | |
| Gamal et al. | Guided creeping technique (GCT) as a novel minimally invasive approach in treating limited gingival recession–Case series | |
| RU2821775C1 (ru) | Способ поддерживающей терапии при воспалительных заболеваниях пародонта у пациентов пожилого и старческого возраста | |
| Komara et al. | Application of Apatite Carbonate Membrane Effect to Bleeding on Probing after Scaling and Root Planing | |
| RU2808463C2 (ru) | Композиция для лечения пародонтита и регенерации межзубных сосочков | |
| Henderson | Root coverage using Alloderm® acellular dermal graft material | |
| US20070020200A1 (en) | Therapeutic compositions and methods of use thereof | |
| Awad et al. | Evaluation of The Effect of Socket Shield Technique on The Success of Immediate Dental Implant | |
| Vinogradova et al. | The practical usage of the remedy containing an aldehyde group of formaldehyde in vital amputation of the temporary molars | |
| HK40049113A (en) | A composition for the treatment of periodontitis and regeneration of interdental papilla | |
| Argento et al. | Flapless Technique for Periodontal Bone Grafts in Treatment of Severe Periodontitis. Presentation and Long-Term Retrospective Study. J Microbial Biochem Technol 2: 107-110. doi: 10.4172/1948-5948.1000033 | |
| Held | The period between 1970 and 1980 | |
| EA046983B1 (ru) | Кремниевая кислота для применения в лечении периодонтита | |
| EA042241B1 (ru) | Лечение гингивита |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR |
|
| AX | Request for extension of the european patent |
Extension state: AL BA RS |
|
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: TRZISZKA, TADEUSZ Inventor name: BRYJAK, MAREK Inventor name: SEBZDA, TADEUSZ Inventor name: NIENARTOWICZ, JAN Inventor name: MALOLEPSZA-JARMOLOWSKA, KATARZYNA Inventor name: WNUKIEWICZ, BEATA Inventor name: WNUKIEWICZ, JAN Inventor name: SIEWINSKI, MACIEJ |
|
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: TRZISZKA, TADEUSZ Inventor name: BRYJAK, MAREK Inventor name: SEBZDA, TADEUSZ Inventor name: NIENARTOWICZ, JAN Inventor name: MALOLEPSZA-JARMOLOWSKA, KATARZYNA Inventor name: WNUKIEWICZ, BEATA Inventor name: WNUKIEWICZ, JAN Inventor name: SIEWINSKI, MACIEJ |
|
| 17P | Request for examination filed |
Effective date: 20111205 |
|
| RBV | Designated contracting states (corrected) |
Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR |
|
| DAX | Request for extension of the european patent (deleted) | ||
| 17Q | First examination report despatched |
Effective date: 20120522 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 20160301 |