NO783111L - Tann- og munnpleiemiddel. - Google Patents

Tann- og munnpleiemiddel.

Info

Publication number: NO783111L
Authority: NO; Norway
Prior art keywords: dental; lysine; ester; oral care; caries
Prior art date: 1977-09-21

Application number

NO783111A

Other languages

English (en)

Norwegian (no)

Inventor

Udo Hoppe

Gerhard Sauermann

Julius Curts

Per-Olof Glantz

Bo Krasse

Kaare Larsson

Boerje Noren

Goeran Odham

Jan Olsson

Original Assignee

Beiersdorf Ag

Priority date (The priority date 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 date listed.)

1977-09-21

Filing date

1978-09-14

Publication date

1979-03-22

1978-09-14 Application filed by Beiersdorf Ag filed Critical Beiersdorf Ag

1979-03-22 Publication of NO783111L publication Critical patent/NO783111L/no

Links

-1 aliphatic alcohols Chemical class 0.000 claims description 16
239000004472 Lysine Substances 0.000 claims description 14
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 14
239000003795 chemical substances by application Substances 0.000 claims description 14
208000002925 dental caries Diseases 0.000 claims description 10
230000002401 inhibitory effect Effects 0.000 claims description 9
150000002148 esters Chemical class 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
235000015218 chewing gum Nutrition 0.000 claims description 6
150000003839 salts Chemical class 0.000 claims description 6
229940112822 chewing gum Drugs 0.000 claims description 5
239000002324 mouth wash Substances 0.000 claims description 5
239000000606 toothpaste Substances 0.000 claims description 5
229940051866 mouthwash Drugs 0.000 claims description 4
239000008375 oral care agent Substances 0.000 claims description 4
239000000843 powder Substances 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
229940034610 toothpaste Drugs 0.000 claims description 4
239000007937 lozenge Substances 0.000 claims description 3
230000003239 periodontal effect Effects 0.000 claims description 3
239000000499 gel Substances 0.000 claims description 2
235000018977 lysine Nutrition 0.000 description 12
239000000243 solution Substances 0.000 description 10
239000013543 active substance Substances 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
239000000126 substance Substances 0.000 description 8
MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 6
230000000845 anti-microbial effect Effects 0.000 description 5
230000010065 bacterial adhesion Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
210000000214 mouth Anatomy 0.000 description 5
239000002953 phosphate buffered saline Substances 0.000 description 5
238000005498 polishing Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
230000001580 bacterial effect Effects 0.000 description 4
230000003385 bacteriostatic effect Effects 0.000 description 4
230000001332 colony forming effect Effects 0.000 description 4
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
238000012360 testing method Methods 0.000 description 4
229920001817 Agar Polymers 0.000 description 3
208000010266 Aggressive Periodontitis Diseases 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
239000008272 agar Substances 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
239000002609 medium Substances 0.000 description 3
201000006727 periodontosis Diseases 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
239000003826 tablet Substances 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 2
208000002064 Dental Plaque Diseases 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
206010044029 Tooth deposit Diseases 0.000 description 2
239000002253 acid Substances 0.000 description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
229960000541 cetyl alcohol Drugs 0.000 description 2
229960003260 chlorhexidine Drugs 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003906 humectant Substances 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
238000011534 incubation Methods 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
238000005259 measurement Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
239000003094 microcapsule Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
238000001179 sorption measurement Methods 0.000 description 2
239000007921 spray Substances 0.000 description 2
HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
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 description 1
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
229920001412 Chicle Polymers 0.000 description 1
OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
UDIPTWFVPPPURJ-UHFFFAOYSA-M Cyclamate Chemical compound [Na+].[O-]S(=O)(=O)NC1CCCCC1 UDIPTWFVPPPURJ-UHFFFAOYSA-M 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
208000006558 Dental Calculus Diseases 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical class F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
239000007836 KH2PO4 Substances 0.000 description 1
BVHLGVCQOALMSV-JEDNCBNOSA-N L-lysine hydrochloride Chemical compound Cl.NCCCC[C@H](N)C(O)=O BVHLGVCQOALMSV-JEDNCBNOSA-N 0.000 description 1
240000001794 Manilkara zapota Species 0.000 description 1
235000011339 Manilkara zapota Nutrition 0.000 description 1
229930195725 Mannitol Natural products 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
240000004760 Pimpinella anisum Species 0.000 description 1
235000012550 Pimpinella anisum Nutrition 0.000 description 1
241000194019 Streptococcus mutans Species 0.000 description 1
241000194024 Streptococcus salivarius Species 0.000 description 1
241000194023 Streptococcus sanguinis Species 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000001412 amines Chemical group 0.000 description 1
239000006161 blood agar Substances 0.000 description 1
230000005587 bubbling Effects 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229960003563 calcium carbonate Drugs 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
JUNWLZAGQLJVLR-UHFFFAOYSA-J calcium diphosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O JUNWLZAGQLJVLR-UHFFFAOYSA-J 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229940043256 calcium pyrophosphate Drugs 0.000 description 1
238000000160 carbon, hydrogen and nitrogen elemental analysis Methods 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
229940109275 cyclamate Drugs 0.000 description 1
210000003298 dental enamel Anatomy 0.000 description 1
239000000551 dentifrice Substances 0.000 description 1
210000004268 dentin Anatomy 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
235000019821 dicalcium diphosphate Nutrition 0.000 description 1
229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 1
239000005454 flavour additive Substances 0.000 description 1
150000002222 fluorine compounds Chemical class 0.000 description 1
235000013355 food flavoring agent Nutrition 0.000 description 1
239000003349 gelling agent Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
SXZCBVCQHOJXDR-ILKKLZGPSA-N hydron;methyl (2s)-2,6-diaminohexanoate;dichloride Chemical compound Cl.Cl.COC(=O)[C@@H](N)CCCCN SXZCBVCQHOJXDR-ILKKLZGPSA-N 0.000 description 1
229920001477 hydrophilic polymer Polymers 0.000 description 1
229920001600 hydrophobic polymer Polymers 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229940035429 isobutyl alcohol Drugs 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
238000001819 mass spectrum Methods 0.000 description 1
239000001525 mentha piperita l. herb oil Substances 0.000 description 1
239000001683 mentha spicata herb oil Substances 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
235000019796 monopotassium phosphate Nutrition 0.000 description 1
229940043348 myristyl alcohol Drugs 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
229940041678 oral spray Drugs 0.000 description 1
239000000668 oral spray Substances 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000019477 peppermint oil Nutrition 0.000 description 1
208000028169 periodontal disease Diseases 0.000 description 1
201000001245 periodontitis Diseases 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
239000006187 pill Substances 0.000 description 1
229940068196 placebo Drugs 0.000 description 1
239000000902 placebo Substances 0.000 description 1
230000007505 plaque formation Effects 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
235000003270 potassium fluoride Nutrition 0.000 description 1
239000011698 potassium fluoride Substances 0.000 description 1
239000008057 potassium phosphate buffer Substances 0.000 description 1
230000002265 prevention Effects 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
229940081974 saccharin Drugs 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
235000019204 saccharin Nutrition 0.000 description 1
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
229940085605 saccharin sodium Drugs 0.000 description 1
210000003296 saliva Anatomy 0.000 description 1
239000012488 sample solution Substances 0.000 description 1
239000012047 saturated solution Substances 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000013024 sodium fluoride Nutrition 0.000 description 1
239000011775 sodium fluoride Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
235000010356 sorbitol Nutrition 0.000 description 1
235000019721 spearmint oil Nutrition 0.000 description 1
229940012831 stearyl alcohol Drugs 0.000 description 1
229960004793 sucrose Drugs 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 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
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/20—Halogens; Compounds thereof
- A61K8/21—Fluorides; Derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Epidemiology (AREA)
Birds (AREA)
Chemical & Material Sciences (AREA)
Inorganic Chemistry (AREA)
Oral & Maxillofacial Surgery (AREA)
Cosmetics (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

NO783111A 1977-09-21 1978-09-14 Tann- og munnpleiemiddel. NO783111L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2742411A DE2742411B1 (de)	1977-09-21	1977-09-21	Zahn- und Mundpflegemittel

Publications (1)

Publication Number	Publication Date
NO783111L true NO783111L (no)	1979-03-22

Family

ID=6019476

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO783111A NO783111L (no)	1977-09-21	1978-09-14	Tann- og munnpleiemiddel.

Country Status (17)

Country	Link
US (1)	US4296095A (de)
JP (1)	JPS5452735A (de)
AT (1)	AT363192B (de)
AU (1)	AU518717B2 (de)
BE (1)	BE870659A (de)
CA (1)	CA1099646A (de)
CH (1)	CH636008A5 (de)
DE (1)	DE2742411B1 (de)
DK (1)	DK414478A (de)
FI (1)	FI782881A7 (de)
FR (1)	FR2403796A1 (de)
GB (1)	GB2004463B (de)
IT (1)	IT1098866B (de)
NL (1)	NL7809314A (de)
NO (1)	NO783111L (de)
PT (1)	PT68572A (de)
SE (1)	SE437121B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4749694A (en) *	1984-04-26	1988-06-07	Merck & Co., Inc.	Novel lysine esters used as absorption
US5064640A (en) *	1986-12-02	1991-11-12	Purdue Research Foundation	Anticariogenic compositions
US5188819A (en) *	1992-02-21	1993-02-23	Purdue Research Foundation	Manufacture of aluminum-based anticariogenic compositions
US20020153508A1 (en) *	2000-06-29	2002-10-24	Lynch Matthew Lawrence	Cubic liquid crystalline compositions and methods for their preparation
DE50114021D1 (de) *	2001-01-08	2008-07-24	Csl Behring Gmbh	Stabilisierte Flüssigzubereitung der den Blutgerinnungsfaktor VII aktivierenden Protease oder ihres Proenzyms
BRPI0721019A2 (pt) *	2007-02-07	2012-12-25	Miret Lab	combinaÇço de conservantes catiânicos com componentes de mascaraÇço de sabor

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH448122A (de) *	1963-10-14	1967-12-15	Hoffmann La Roche	Verfahren zur Herstellung von Estern
FR2057739A5 (de) *	1969-08-25	1971-05-21	Allied Chem
GB1356873A (en) *	1971-01-23	1974-06-19	Ajinomoto Kk	Fungicidal compositions and their use
GB1372932A (en) *	1971-03-15	1974-11-06	Gen Foods Corp	Anti-caries compositions
US3821403A (en) *	1972-01-20	1974-06-28	Rikagaku Kenkyusho	Method of combatting bacteria or fungi on plants using amino acid higher alkyl esters
US3899585A (en) *	1972-01-20	1975-08-12	Rikagaku Kenkyusho	Fungicidal method for protecting a plant

1977
- 1977-09-21 DE DE2742411A patent/DE2742411B1/de not_active Ceased
1978
- 1978-09-13 SE SE7809634A patent/SE437121B/sv unknown
- 1978-09-13 NL NL7809314A patent/NL7809314A/xx not_active Application Discontinuation
- 1978-09-14 CH CH960478A patent/CH636008A5/de not_active IP Right Cessation
- 1978-09-14 NO NO783111A patent/NO783111L/no unknown
- 1978-09-15 AU AU39905/78A patent/AU518717B2/en not_active Expired
- 1978-09-18 PT PT68572A patent/PT68572A/de unknown
- 1978-09-18 CA CA311,515A patent/CA1099646A/en not_active Expired
- 1978-09-19 JP JP11418378A patent/JPS5452735A/ja active Pending
- 1978-09-19 DK DK414478A patent/DK414478A/da unknown
- 1978-09-20 IT IT27872/78A patent/IT1098866B/it active
- 1978-09-20 FR FR7826925A patent/FR2403796A1/fr active Granted
- 1978-09-20 AT AT0678278A patent/AT363192B/de not_active IP Right Cessation
- 1978-09-20 US US05/944,195 patent/US4296095A/en not_active Expired - Lifetime
- 1978-09-21 GB GB7837663A patent/GB2004463B/en not_active Expired
- 1978-09-21 FI FI782881A patent/FI782881A7/fi unknown
- 1978-09-21 BE BE190626A patent/BE870659A/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
JPS5452735A (en)	1979-04-25
AU518717B2 (en)	1981-10-15
FR2403796B1 (de)	1980-07-04
SE7809634L (sv)	1979-03-22
DK414478A (da)	1979-03-22
FI782881A7 (fi)	1979-03-22
ATA678278A (de)	1980-12-15
GB2004463B (en)	1982-05-26
CA1099646A (en)	1981-04-21
BE870659A (fr)	1979-01-15
NL7809314A (nl)	1979-03-23
IT1098866B (it)	1985-09-18
AU3990578A (en)	1980-03-20
PT68572A (de)	1978-10-01
SE437121B (sv)	1985-02-11
AT363192B (de)	1981-07-10
CH636008A5 (de)	1983-05-13
DE2742411B1 (de)	1979-01-18
GB2004463A (en)	1979-04-04
US4296095A (en)	1981-10-20
FR2403796A1 (fr)	1979-04-20
IT7827872A0 (it)	1978-09-20

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