KR20220107992A - Oral composition for preventing and improving sensitive teeth - Google Patents
Oral composition for preventing and improving sensitive teeth Download PDFInfo
- Publication number
- KR20220107992A KR20220107992A KR1020220011695A KR20220011695A KR20220107992A KR 20220107992 A KR20220107992 A KR 20220107992A KR 1020220011695 A KR1020220011695 A KR 1020220011695A KR 20220011695 A KR20220011695 A KR 20220011695A KR 20220107992 A KR20220107992 A KR 20220107992A
- Authority
- KR
- South Korea
- Prior art keywords
- composition
- oral use
- potassium
- use according
- betaine
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 116
- 239000004094 surface-active agent Substances 0.000 claims abstract description 49
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims abstract description 34
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 25
- -1 alkali metal salt Chemical class 0.000 claims abstract description 25
- 229960003237 betaine Drugs 0.000 claims abstract description 17
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 claims abstract description 14
- 229940094506 lauryl betaine Drugs 0.000 claims description 20
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 claims description 20
- 229940079988 potassium cocoyl glycinate Drugs 0.000 claims description 20
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical group [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 14
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 14
- 239000003242 anti bacterial agent Substances 0.000 claims description 12
- 239000001508 potassium citrate Substances 0.000 claims description 10
- 229960002635 potassium citrate Drugs 0.000 claims description 10
- 235000011082 potassium citrates Nutrition 0.000 claims description 10
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 claims description 9
- 239000004386 Erythritol Substances 0.000 claims description 7
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 7
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical group OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 7
- 235000019414 erythritol Nutrition 0.000 claims description 7
- 229940009714 erythritol Drugs 0.000 claims description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 7
- 235000011181 potassium carbonates Nutrition 0.000 claims description 7
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims description 6
- 229940093956 potassium carbonate Drugs 0.000 claims description 4
- 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 claims description 3
- 229930182555 Penicillin Natural products 0.000 claims description 3
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 claims description 3
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 3
- 235000011126 aluminium potassium sulphate Nutrition 0.000 claims description 3
- 229960003260 chlorhexidine Drugs 0.000 claims description 3
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 claims description 3
- 229940073507 cocamidopropyl betaine Drugs 0.000 claims description 3
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 3
- 235000019796 monopotassium phosphate Nutrition 0.000 claims description 3
- 229910000402 monopotassium phosphate Inorganic materials 0.000 claims description 3
- HLERILKGMXJNBU-UHFFFAOYSA-N norvaline betaine Chemical compound CCCC(C([O-])=O)[N+](C)(C)C HLERILKGMXJNBU-UHFFFAOYSA-N 0.000 claims description 3
- 229940049954 penicillin Drugs 0.000 claims description 3
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 claims description 3
- 229940050271 potassium alum Drugs 0.000 claims description 3
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 claims description 3
- 239000011736 potassium bicarbonate Substances 0.000 claims description 3
- 235000015497 potassium bicarbonate Nutrition 0.000 claims description 3
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 3
- 239000001103 potassium chloride Substances 0.000 claims description 3
- 235000011164 potassium chloride Nutrition 0.000 claims description 3
- 229960002816 potassium chloride Drugs 0.000 claims description 3
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 3
- 229940086066 potassium hydrogencarbonate Drugs 0.000 claims description 3
- 239000004323 potassium nitrate Substances 0.000 claims description 3
- 235000010333 potassium nitrate Nutrition 0.000 claims description 3
- 229940093928 potassium nitrate Drugs 0.000 claims description 3
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 3
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 3
- 229940093914 potassium sulfate Drugs 0.000 claims description 3
- 235000011151 potassium sulphates Nutrition 0.000 claims description 3
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 229940065859 sodium cocoyl glycinate Drugs 0.000 claims description 3
- IKGKWKGYFJBGQJ-UHFFFAOYSA-M sodium;2-(dodecanoylamino)acetate Chemical compound [Na+].CCCCCCCCCCCC(=O)NCC([O-])=O IKGKWKGYFJBGQJ-UHFFFAOYSA-M 0.000 claims description 3
- 239000000811 xylitol Substances 0.000 claims description 3
- 235000010447 xylitol Nutrition 0.000 claims description 3
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 3
- 229960002675 xylitol Drugs 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229940060037 fluorine Drugs 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 18
- 230000000694 effects Effects 0.000 description 17
- 239000000341 volatile oil Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- 238000005187 foaming Methods 0.000 description 8
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 8
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- 239000006260 foam Substances 0.000 description 6
- 229940016409 methylsulfonylmethane Drugs 0.000 description 6
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- 239000004475 Arginine Substances 0.000 description 5
- ITJLNEXJUADEMK-UHFFFAOYSA-N Shirin Natural products CCC(C)(O)c1c(Cl)c(OC)c(C)c2OC(=O)c3c(C)c(Cl)c(O)c(Cl)c3Oc12 ITJLNEXJUADEMK-UHFFFAOYSA-N 0.000 description 5
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 5
- 210000000214 mouth Anatomy 0.000 description 5
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 4
- 235000009024 Ceanothus sanguineus Nutrition 0.000 description 4
- 235000005979 Citrus limon Nutrition 0.000 description 4
- 244000131522 Citrus pyriformis Species 0.000 description 4
- 229920000858 Cyclodextrin Polymers 0.000 description 4
- 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 4
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 4
- 240000003553 Leptospermum scoparium Species 0.000 description 4
- 235000015459 Lycium barbarum Nutrition 0.000 description 4
- 244000246386 Mentha pulegium Species 0.000 description 4
- 235000016257 Mentha pulegium Nutrition 0.000 description 4
- 235000004357 Mentha x piperita Nutrition 0.000 description 4
- 239000004376 Sucralose Substances 0.000 description 4
- 235000001050 hortel pimenta Nutrition 0.000 description 4
- 239000001683 mentha spicata herb oil Substances 0.000 description 4
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- 239000011148 porous material Substances 0.000 description 4
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 4
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- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
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- 206010020751 Hypersensitivity Diseases 0.000 description 2
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
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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
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/25—Silicon; Compounds 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- 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
- 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
- A61K8/60—Sugars; Derivatives thereof
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/28—Rubbing or scrubbing compositions; Peeling or abrasive compositions; Containing exfoliants
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Abstract
Description
본 발명은 구강용 조성물에 관한 것이다. 보다 상세하게는 시린이 예방 및 개선 효과가 있는 구강용 조성물에 관한 것이다.The present invention relates to a composition for oral use. More particularly, it relates to a composition for oral cavity which has a preventive and ameliorating effect of shirin.
구강용 조성물 내에 포함된 계면활성제는 구강 세정 시 물과 반응하여 기포를 생성시켜 구강 내 세정력을 향상시키는 역할을 한다. 구강용 조성물 내에 포함된 알칼리금속염은 세공 내로 침투하여 세공에서의 칼슘 이온 방출을 감소시키는 역할을 한다. 이러한 효과로 인해 시린이 예방 및 치료 효과를 나타낼 수 있다.The surfactant included in the composition for oral use acts to improve oral cleaning power by reacting with water during oral cleaning to generate bubbles. The alkali metal salt contained in the composition for oral cavity penetrates into the pores and serves to reduce the release of calcium ions from the pores. Due to these effects, sirin may have prophylactic and therapeutic effects.
기존 치약 등 구강용 조성물은 시린이 예방 및 치료 효과를 위해 알칼리금속염의 함량을 증가시키는 경우, 구강용 조성물 사용시 거품량이 감소하여 사용자의 거부감이 증가하는 문제점이 있었다.In conventional oral compositions such as toothpaste, when the content of alkali metal salts is increased for a preventive and therapeutic effect, the amount of foam decreases when using the composition for oral use, thereby increasing the user's reluctance.
이러한 문제점으로 알칼리금속염을 포함하면서도 계면활성제를 함께 사용함으로써 거품량을 유지하며, 시린이 질환을 가진 사람 등 구강 내부가 민감한 사람들에 있어서, 상기 구강용 조성물을 사용시 거부감을 낮추는 효과를 갖는 구강용 조성물이 필요하였다.Due to this problem, the amount of foam is maintained by using a surfactant while containing an alkali metal salt, and for people with sensitive oral cavity, such as those with a sore throat, an oral composition having an effect of lowering the objection when using the composition for oral use this was needed
본 발명은 시린이 증상의 예방 및 개선 효과와 우수한 거품성을 가지는 구강용 조성물을 제공하는 것을 목적으로 한다.An object of the present invention is to provide a composition for oral use having an effect of preventing and improving symptoms of shirin and excellent foaming properties.
1. 알칼리금속염, 베타인계 계면활성제 및 글리시네이트계 계면활성제를 포함하는 구강용 조성물.1. An oral composition comprising an alkali metal salt, a betaine-based surfactant and a glycinate-based surfactant.
2. 위 1 에 있어서, 상기 알칼리금속염은 칼륨염인 구강용 조성물.2. The composition for oral use according to the above 1, wherein the alkali metal salt is a potassium salt.
3. 위 2 에 있어서, 상기 칼륨염은 구연산 칼륨, 질산칼륨, 염화칼륨, 인산 2 수소칼륨, 황산칼륨, 탄산칼륨, 탄산수소칼륨 및 명반으로 이루어진 군에서 선택되는 적어도 하나인 구강용 조성물.3. The composition for oral use according to the above 2, wherein the potassium salt is at least one selected from the group consisting of potassium citrate, potassium nitrate, potassium chloride, potassium dihydrogen phosphate, potassium sulfate, potassium carbonate, potassium hydrogen carbonate, and alum.
4. 위 2 에 있어서, 상기 칼륨염은 상기 조성물 전체에 대해 5 중량% 내지 10 중량%로 포함된 구강용 조성물.4. The composition for oral use according to the above 2, wherein the potassium salt is included in an amount of 5 wt% to 10 wt% with respect to the total composition.
5. 위 1 에 있어서, 상기 베타인계 계면활성제는 라우릴베타인, 코코베타인, 코카미도프로필베타인, 라우로미도프로필베타인 및 프로필베타인 중 적어도 하나인 구강용 조성물.5. The composition for oral use according to the above 1, wherein the betaine-based surfactant is at least one of lauryl betaine, coco betaine, cocamidopropyl betaine, lauromidopropyl betaine and propyl betaine.
6. 위 5 에 있어서, 상기 베타인계 계면활성제는 라우릴베타인인 구강용 조성물.6. The composition for oral use according to the above 5, wherein the betaine-based surfactant is lauryl betaine.
7. 위 6 에 있어서, 상기 라우릴베타인은 상기 조성물 전체에 대해 0.5 중량% 내지 2 중량%로 포함된 구강용 조성물.7. The composition for oral use according to the above 6, wherein the lauryl betaine is contained in an amount of 0.5 wt% to 2 wt% based on the total composition.
8. 위 1 에 있어서, 상기 글리시네이트계 계면활성제는 포타슘 코코일글리시네이트 또는 소듐 코코일글리시네이트인 구강용 조성물.8. The composition for oral use according to the above 1, wherein the glycinate-based surfactant is potassium cocoyl glycinate or sodium cocoyl glycinate.
9. 위 8 에 있어서, 상기 글리시네이트계 계면활성제는 포타슘 코코일글리시네이트인 구강용 조성물.9. The composition for oral use according to 8 above, wherein the glycinate-based surfactant is potassium cocoyl glycinate.
10. 위 8 에 있어서, 상기 포타슘 코코일글리시네이트는 상기 조성물 전체에 대해 1 중량% 내지 3 중량%로 포함된 구강용 조성물.10. The composition for oral use according to the above 8, wherein the potassium cocoyl glycinate is included in an amount of 1% to 3% by weight based on the total composition.
11. 위 1 에 있어서, 베타인계 계면활성제인 라우릴 베타인 및 글리시네이트계 계면활성제인 포타슘 코코일 글리시네이트를 1:3 내지 3:1 의 중량비로 포함하는 구강용 조성물.11. The composition for oral use according to the above 1, comprising lauryl betaine as a betaine-based surfactant and potassium cocoyl glycinate as a glycinate-based surfactant in a weight ratio of 1:3 to 3:1.
12. 위 1 에 있어서, 연마제 또는 항균제를 더 포함하는 구강용 조성물.12. The composition for oral use according to the above 1, further comprising an abrasive or an antibacterial agent.
13. 위 12 에 있어서, 상기 연마제는 에리스리톨 또는 실리카인 구강용 조성물.13. The composition for oral use according to the above 12, wherein the abrasive is erythritol or silica.
14. 위 12 에 있어서, 상기 연마제는 상기 조성물 전체에 대해 20 중량% 내지 35 중량%로 포함된 구강용 조성물.14. The composition for oral use according to the above 12, wherein the abrasive is included in an amount of 20 wt% to 35 wt% with respect to the total composition.
15. 위 12 에 있어서, 상기 항균제는 불소, 클로르헥시딘, 자일리톨 및 페니실린으로 이루어진 군에서 선택된 하나 이상인 구강용 조성물.15. The composition for oral use according to the above 12, wherein the antibacterial agent is at least one selected from the group consisting of fluorine, chlorhexidine, xylitol and penicillin.
16. 위 12 에 있어서, 상기 항균제는 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함된 구강용 조성물.16. The composition for oral use according to the above 12, wherein the antibacterial agent is included in an amount of 0.01 wt% to 3 wt% with respect to the total composition.
본 발명의 구강용 조성물은 알칼리금속염을 포함하여 시린이 억제 효과를 보일 수 있다.The composition for oral use of the present invention may contain an alkali metal salt, thereby exhibiting an anti-inflammatory effect.
본 발명의 구강용 조성물은 특정 계면활성제를 포함하여 알칼리금속염의 침투를 저감하지 않으면서도 우수한 거품성을 보일 수 있다.The composition for oral use of the present invention can show excellent foaming properties without reducing the penetration of alkali metal salts, including specific surfactants.
이하 본 발명을 상세히 설명한다. 특별한 정의가 없는 한 본 명세서의 모든 용어는 본 발명이 속하는 기술분야의 통상의 지식을 가진 기술자가 이해하는 당해 용어의 일반적인 의미와 동일하고 만약 본 명세서에 사용된 용어의 의미와 충돌하는 경우에는 본 명세서에 사용된 의미를 따른다.Hereinafter, the present invention will be described in detail. Unless otherwise defined, all terms in this specification have the same general meaning as understood by those of ordinary skill in the art to which the present invention belongs, and in case of conflict with the meaning of the terms used in this specification, the The meaning used in the specification is followed.
본 발명은 알칼리금속염과 베타인계 계면활성제 및 글리시네이트계 계면활성제를 포함하는 구강용 조성물에 관한 것이다.The present invention relates to an oral composition comprising an alkali metal salt, a betaine-based surfactant and a glycinate-based surfactant.
본 발명의 구강용 조성물은 알칼리금속염과 특정한 계면활성제를 함께 사용함으로써 거품량을 유지하여, 알칼리금속염에 의한 시린이 예방 및 치료 효과와 함께 상기 구강용 조성물을 사용시 거부감 및 지각과민을 감소시키는 효과를 가질 수 있다. 따라서 시린이 질환을 가진 사람 등, 구강 내부가 민감한 사람들이 상기 구강용 조성물을 사용시 거부감을 적게 느낄 수 있다.The composition for oral use of the present invention maintains the amount of foam by using an alkali metal salt and a specific surfactant together, thereby preventing and treating irritation caused by alkali metal salts and reducing the feeling of rejection and hypersensitivity when using the composition for oral use. can have Therefore, people with sensitive oral cavity, such as those with a sore throat disease, may feel less reluctance when using the composition for oral use.
본 발명에서 상기 알칼리금속염이 치아의 세공으로 침투하여 지각과민을 완화시킬 수 있으며, 시린이 증상을 완화시킬 수 있다.In the present invention, the alkali metal salt penetrates into the pores of the tooth to relieve hypersensitivity, and pain can relieve symptoms.
본 발명에서 알칼리금속염은 구강용 조성물에 사용될 수 있는 것이라면 제한 없이 사용될 수 있으며, 예를 들어 상기 알칼리금속염은 칼륨염일 수 있다.In the present invention, the alkali metal salt may be used without limitation as long as it can be used in the oral composition, for example, the alkali metal salt may be a potassium salt.
본 발명에서 칼륨염은 치아의 칼슘 균형 유지에 도움을 준다. 또한, 칼슘 이온이 치아 세공으로 침투하여 시린이 방지 효과를 줄 수 있다.In the present invention, the potassium salt helps to maintain the calcium balance of teeth. In addition, calcium ions may penetrate into the pores of the tooth to provide an anti-irritation effect.
본 발명에서 칼륨염은 유기산과 무기산 중 적어도 하나의 칼륨염일 수 있다.In the present invention, the potassium salt may be a potassium salt of at least one of an organic acid and an inorganic acid.
본 발명에서 유기산은 구연산, 초산, 젖산, 주석산, 말레인산, 푸마르산, 포름산, 프로피온산, 옥살산, 트리플로오로아세트산, 벤조산, 글루콘산, 메타술폰산, 글리콜산, 숙신산, 4-톨루엔술폰산, 글루탐산 및 아스파르트산 일 수 있다. In the present invention, organic acids include citric acid, acetic acid, lactic acid, tartaric acid, maleic acid, fumaric acid, formic acid, propionic acid, oxalic acid, trifluoroacetic acid, benzoic acid, gluconic acid, metasulfonic acid, glycolic acid, succinic acid, 4-toluenesulfonic acid, glutamic acid and aspartic acid. can be
본 발명의 일 실시예에서, 유기산은 구연산일 수 있다. 또한, 본 발명에서 무기산은 염산, 브롬산, 황산 또는 인산일 수 있다. 다만, 이에 제한되지 않는다.In one embodiment of the present invention, the organic acid may be citric acid. In addition, in the present invention, the inorganic acid may be hydrochloric acid, hydrobromic acid, sulfuric acid or phosphoric acid. However, the present invention is not limited thereto.
본 발명의 일 실시예에 있어서, 칼륨염의 예시로는, 구연산 칼륨, 질산칼륨, 염화칼륨, 인산 2 수소칼륨, 황산칼륨, 탄산칼륨, 탄산수소칼륨, 또는 명반일 수 있으며, 구체적으로 구연산칼륨일 수 있다(화학식 1 참조). 다만 이에 제한되지 않는다.In one embodiment of the present invention, examples of the potassium salt may be potassium citrate, potassium nitrate, potassium chloride, potassium dihydrogen phosphate, potassium sulfate, potassium carbonate, potassium hydrogen carbonate, or alum, specifically potassium citrate There is (see Formula 1). However, the present invention is not limited thereto.
[화학식 1][Formula 1]
구연산칼륨(Potassium citrate)Potassium citrate
본 발명에서 칼륨염은 상기 조성물 전체에 대해 1 중량% 내지 20 중량%로 포함될 수 있으며, 예를 들어 1 중량% 내지 15 중량%, 3 중량% 내지 13 중량% 또는 5 중량% 내지 10 중량%로 포함될 수 있다.In the present invention, the potassium salt may be included in an amount of 1 wt% to 20 wt%, for example, 1 wt% to 15 wt%, 3 wt% to 13 wt%, or 5 wt% to 10 wt% with respect to the entire composition may be included.
본 발명에서 계면활성제는 베타인계 계면활성제 및 글리시네이트계 계면활성제가 사용된다.In the present invention, a betaine-based surfactant and a glycinate-based surfactant are used as the surfactant.
본 발명의 일 실시예에 있어서, 베타인계 계면활성제로는 라우릴베타인, 코코베타인, 코카미도프로필베타인, 라우로미도프로필베타인 또는 프로필베타인 등이 각각 단독으로 또는 2 종 이상 혼합되어 사용될 수 있다.In one embodiment of the present invention, as the betaine-based surfactant, lauryl betaine, cocobetaine, cocamidopropyl betaine, lauromidopropyl betaine or propyl betaine, etc. are each alone or a mixture of two or more and can be used
본 발명의 일 실시예에 있어서, 글리시네이트계 계면활성제로는 포타슘 코코일글리시네이트 또는 소듐 코코일글리시네이트 등이 각각 단독으로 또는 2 종 이상 혼합되어 사용될 수 있다.In one embodiment of the present invention, as the glycinate-based surfactant, potassium cocoyl glycinate or sodium cocoyl glycinate may be used alone or in combination of two or more.
예시적인 실시예로서, 본 발명의 구강용 조성물은 계면활성제로 라우릴베타인과 포타슘 코코일글리시네이트를 포함할 수 있다.As an exemplary embodiment, the composition for oral use of the present invention may include lauryl betaine and potassium cocoyl glycinate as surfactants.
본 발명에서 계면활성제는 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.5 중량% 내지 10 중량%, 0.5 중량% 내지 7 중량% 또는 1 중량% 내지 5 중량%로 포함될 수 있다.In the present invention, the surfactant may be included in an amount of 0.1 wt% to 10 wt% with respect to the entire composition, for example, 0.5 wt% to 10 wt%, 0.5 wt% to 7 wt%, or 1 wt% to 5 wt% may be included.
본 발명에서 상기 계면활성제는 베타인계 계면활성제인 라우릴베타인일 수 있으며, 상기 라우릴베타인은 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.1 중량% 내지 5 중량%, 0.1 중량% 내지 3 중량% 또는 0.5 중량% 내지 2 중량%로 포함될 수 있다.In the present invention, the surfactant may be lauryl betaine, which is a betaine-based surfactant, and the lauryl betaine may be included in an amount of 0.1 wt% to 10 wt% based on the total composition, for example, 0.1 wt% to 5 wt% %, 0.1 wt% to 3 wt% or 0.5 wt% to 2 wt% may be included.
본 발명에서 상기 계면활성제는 글리시네이트계 계면활성제인 포타슘 코코일글리시네이트일 수 있으며, 상기 포타슘 코코일글리시네이트는 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.1 중량% 내지 5 중량%, 0.1 중량% 내지 3 중량% 또는 1 중량% 내지 3 중량%로 포함될 수 있다.In the present invention, the surfactant may be potassium cocoyl glycinate, which is a glycinate-based surfactant, and the potassium cocoyl glycinate may be included in an amount of 0.1 wt% to 10 wt% with respect to the entire composition, for example For example, it may be included in 0.1 wt% to 5 wt%, 0.1 wt% to 3 wt%, or 1 wt% to 3 wt%.
본 발명에서 구강용 조성물은 베타인계 계면활성제인 라우릴베타인 및 글리시네이트계 계면활성제인 포타슘 코코일 글리시네이트를 1:10 내지 10:1 의 중량비로 포함할 수 있으며, 예를 들어 1:5 내지 5:1 의 중량비, 1:3 내지 3:1 의 중량비 또는 2:3 내지 3:2 의 중량비로 포함할 수 있다.In the present invention, the composition for oral use may include lauryl betaine, a betaine-based surfactant, and potassium cocoyl glycinate, a glycinate-based surfactant, in a weight ratio of 1:10 to 10:1, for example, 1 It may be included in a weight ratio of :5 to 5:1, a weight ratio of 1:3 to 3:1, or a weight ratio of 2:3 to 3:2.
본 발명의 구강용 조성물은 구강용 조성물의 제조에 통상적으로 사용하는 적절한 연마제, 항균제, 용매를 더 포함할 수 있다.The composition for oral use of the present invention may further include an appropriate abrasive, antibacterial agent, and solvent commonly used in the preparation of oral compositions.
본 발명에서 상기 연마제는 구강용 조성물에 사용될 수 있는 것이라면 제한 없이 사용될 수 있다. 예를 들어 상기 연마제는 에리스리톨 또는 실리카일 수 있다.In the present invention, the abrasive may be used without limitation as long as it can be used in the oral composition. For example, the abrasive may be erythritol or silica.
본 발명에서 상기 연마제는 상기 조성물 전체에 대해 20 중량% 내지 35 중량%로 포함될 수 있으며, 예를 들어 25 중량% 내지 35 중량% 또는 25 중량% 내지 30 중량%로 포함될 수 있다.In the present invention, the abrasive may be included in an amount of 20 wt% to 35 wt%, for example, 25 wt% to 35 wt% or 25 wt% to 30 wt% with respect to the entire composition.
본 발명에서 상기 항균제는 천연 향균제, 화학적 향균제 등을 포함할 수 있다. 구체적으로, 불소 화합물, 클로르헥시딘, 자일리톨 및 페니실린과 같은 화학적 항균제를 포함할 수 있다. 다만, 이에 제한되지 않는다.In the present invention, the antibacterial agent may include a natural antibacterial agent, a chemical antibacterial agent, and the like. Specifically, it may include chemical antibacterial agents such as fluorine compounds, chlorhexidine, xylitol and penicillin. However, the present invention is not limited thereto.
본 발명에서 상기 항균제는 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 0.5 중량%로 포함될 수 있다.In the present invention, the antibacterial agent may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt% or 0.05 wt% to 0.5 wt% with respect to the entire composition.
본 발명의 구강용 조성물은 시린이 방지를 위해 아르기닌, MSM(Methylsulfonylmethane) 등을 더 포함할 수 있다.The composition for oral use of the present invention may further include arginine, MSM (Methylsulfonylmethane), and the like to prevent sore throat.
또한 본 발명의 구강용 조성물은 추가적인 첨가제로 방부제, 습윤제 또는 방향제 등을 추가로 포함할 수 있다.In addition, the composition for oral use of the present invention may further include a preservative, a wetting agent, or a fragrance as an additional additive.
본 발명의 구강용 조성물은 치약, 구강용 세정제, 구강 청정제, 구강 스프레이 또는 구강 양치액 제형을 포함할 수 있다. 다만, 이에 제한되지 않는다.The composition for oral use of the present invention may include a toothpaste, mouthwash, mouthwash, oral spray, or mouthwash formulation. However, the present invention is not limited thereto.
본 발명의 일 실시예에서 구강용 조성물은 탄산칼륨, 구연산, 라우릴베타인, 포타슘 코코일글리시네이트, MSM, 아르기닌, 멘톨, 불화나트륨, 에리스리톨, 사이클로덱스트린, 레몬 에센셜오일, 스피아민트 오일, 페퍼민트 에센셜오일, 티트리 에센셜오일, 수크랄로스, 폴리비닐피롤리돈, 잔탄검 및 잔량의 솔비톨를 포함할 수 있다.In an embodiment of the present invention, the composition for oral use includes potassium carbonate, citric acid, lauryl betaine, potassium cocoyl glycinate, MSM, arginine, menthol, sodium fluoride, erythritol, cyclodextrin, lemon essential oil, spearmint oil, It may contain peppermint essential oil, tea tree essential oil, sucralose, polyvinylpyrrolidone, xanthan gum and the balance of sorbitol.
상기 탄산칼륨은 상기 구강용 조성물 전체에 대해 0.1 중량% 내지 20.0 중량%로 포함될 수 있다. 본 발명의 일 실시예에서, 상기 칼륨염은 1.0 중량% 내지 10.0 중량%로 포함될 수 있다.The potassium carbonate may be included in an amount of 0.1 wt% to 20.0 wt% with respect to the total composition for oral use. In an embodiment of the present invention, the potassium salt may be included in an amount of 1.0 wt% to 10.0 wt%.
상기 구연산은 상기 구강용 조성물 전체에 대해 0.1 중량% 내지 20.0 중량%로 포함될 수 있다. 본 발명의 일 실시예에서, 상기 칼륨염은 1.0 중량% 내지 10.0 중량%로 포함될 수 있다.The citric acid may be included in an amount of 0.1 wt% to 20.0 wt% with respect to the entire composition for oral use. In an embodiment of the present invention, the potassium salt may be included in an amount of 1.0 wt% to 10.0 wt%.
상기 MSM 은 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.1 중량% 내지 5 중량% 또는 0.5 중량% 내지 5 중량%로 포함될 수 있다.The MSM may be included in an amount of 0.1 wt% to 10 wt%, for example, 0.1 wt% to 5 wt%, or 0.5 wt% to 5 wt%, based on the total weight of the composition.
상기 아르기닌은 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.1 중량% 내지 5 중량% 또는 0.5 중량% 내지 5 중량%로 포함될 수 있다.The arginine may be included in an amount of 0.1 wt% to 10 wt%, for example, 0.1 wt% to 5 wt% or 0.5 wt% to 5 wt% with respect to the entire composition.
상기 멘톨은 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.1 중량% 내지 5 중량% 또는 0.1 중량% 내지 3 중량%로 포함될 수 있다.The menthol may be included in an amount of 0.1 wt% to 10 wt%, for example, 0.1 wt% to 5 wt% or 0.1 wt% to 3 wt% with respect to the total composition.
상기 불화나트륨은 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 0.5 중량%로 포함될 수 있다.The sodium fluoride may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt% or 0.05 wt% to 0.5 wt% based on the total weight of the composition.
상기 솔비톨은 상기 조성물 전체에 대해 30 중량% 내지 40 중량%로 포함될 수 있으며, 예를 들어 33 중량% 내지 38 중량% 또는 34 중량% 내지 36 중량%로 포함될 수 있다.The sorbitol may be included in an amount of 30 wt% to 40 wt%, for example, in an amount of 33 wt% to 38 wt% or 34 wt% to 36 wt% with respect to the entire composition.
상기 에리스리톨은 상기 조성물 전체에 대해 20 중량% 내지 40 중량%로 포함될 수 있으며, 예를 들어 20 중량% 내지 35 중량% 또는 23 중량% 내지 33 중량%로 포함될 수 있다.The erythritol may be included in an amount of 20 wt% to 40 wt%, for example, 20 wt% to 35 wt% or 23 wt% to 33 wt% with respect to the entire composition.
상기 사이클로덱스트린은 상기 조성물 전체에 대해 1 중량% 내지 20 중량%로 포함될 수 있으며, 예를 들어 5 중량% 내지 15 중량% 또는 7 중량% 내지 13 중량%로 포함될 수 있다.The cyclodextrin may be included in an amount of 1% to 20% by weight, for example, 5% to 15% by weight or 7% to 13% by weight based on the total weight of the composition.
상기 레몬 에센셜오일은 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 0.5 중량%로 포함될 수 있다.The lemon essential oil may be included in an amount of 0.01% to 3% by weight, for example, 0.01% to 1% by weight or 0.05% to 0.5% by weight based on the total weight of the composition.
상기 스피아민트 오일은 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 1.0 중량%로 포함될 수 있다.The spearmint oil may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt%, or 0.05 wt% to 1.0 wt%, based on the entire composition.
상기 페퍼민트 에센셜오일은 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 0.5 중량%로 포함될 수 있다.The peppermint essential oil may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt% or 0.05 wt% to 0.5 wt%, based on the total weight of the composition.
상기 티트리 에센셜오일은 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 0.5 중량%로 포함될 수 있다.The tea tree essential oil may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt% or 0.05 wt% to 0.5 wt%, based on the total weight of the composition.
상기 수크랄로스는 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.01 중량% 내지 0.5 중량%로 포함될 수 있다.The sucralose may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt%, or 0.01 wt% to 0.5 wt%, based on the total weight of the composition.
상기 폴리비닐피롤리돈은 상기 조성물 전체에 대해 0.1 중량% 내지 10 중량%로 포함될 수 있으며, 예를 들어 0.1 중량% 내지 5 중량% 또는 0.1 중량% 내지 3 중량%로 포함될 수 있다.The polyvinylpyrrolidone may be included in an amount of 0.1 wt% to 10 wt%, for example, 0.1 wt% to 5 wt% or 0.1 wt% to 3 wt% with respect to the entire composition.
상기 잔탄검은 상기 조성물 전체에 대해 0.01 중량% 내지 3 중량%로 포함될 수 있으며, 예를 들어 0.01 중량% 내지 1 중량% 또는 0.05 중량% 내지 1.0 중량%로 포함될 수 있다.The xanthan gum may be included in an amount of 0.01 wt% to 3 wt%, for example, 0.01 wt% to 1 wt% or 0.05 wt% to 1.0 wt%, based on the total weight of the composition.
본 발명의 구강용 조성물은 치주 질환의 예방 또는 치료 보조 효과를 가질 수 있다. 구체적으로, 상기 치주질환은 시린이, 치아우식증, 치은염, 치주염, 치조골 파손, 치조골 골다공증, 치조골 연화증, 치조골 감소증, 치조골 재형성 장애 및 구취 등을 포함할 수 있다. 다만, 이에 제한되지 않는다.The composition for oral use of the present invention may have a preventive or therapeutic auxiliary effect of periodontal disease. Specifically, the periodontal disease may include toothache, dental caries, gingivitis, periodontitis, alveolar bone damage, alveolar osteoporosis, alveolar osteomalacia, alveolar osteopenia, alveolar bone remodeling disorder, and bad breath. However, the present invention is not limited thereto.
본 발명에 따른 구강용 조성물은 개별 사용하거나 다른 구강용 치료제와 병용하여 사용될 수 있고 종래의 치료제 등과 순차적 또는 동시에 사용될 수 있으며, 단일 또는 다중 사용될 수 있다. 상기한 요소들을 모두 고려하여 부작용 없이 최소한의 양으로 최대 효과를 얻을 수 있는 양을 사용하는 것이 중요하며, 이는 통상의 기술자에 의해 용이하게 결정될 수 있다.The oral composition according to the present invention may be used individually or in combination with other oral therapeutic agents, may be used sequentially or simultaneously with conventional therapeutic agents, and may be used singly or multiple times. In consideration of all of the above factors, it is important to use an amount that can obtain the maximum effect with a minimum amount without side effects, which can be easily determined by a person skilled in the art.
구체적으로 본 발명의 구강용 조성물의 유효량은 환자의 연령, 성별, 상태, 체중, 체내에 활성 성분의 흡수도, 불활성율 및 배설속도, 질병종류, 병용되는 약물에 따라 달라질 수 있다. 다만, 사용하는 환자의 조건에 따라 달라질 수 있으므로, 특정 유효량에 제한되지 않는다.Specifically, the effective amount of the composition for oral use of the present invention may vary depending on the patient's age, sex, condition, weight, absorption of the active ingredient into the body, inactivation rate and excretion rate, disease type, and drugs used in combination. However, since it may vary depending on the conditions of the patient to be used, it is not limited to a specific effective amount.
이하, 본 발명을 구체적으로 설명하기 위해 실시예 및 실험예를 들어 상세하게 설명하기로 한다.Hereinafter, examples and experimental examples will be described in detail to explain the present invention in detail.
실시예 1. 구강용 조성물의 제조Example 1. Preparation of composition for oral use
탄산칼륨 8.0 중량%, 구연산 8.0 중량% 및 계면활성제 3.0 중량%, 메틸설포닐메탄 3.1 중량%, 아르기닌 1.9 중량%, 멘톨 0.7 중량%, 불화나트륨 0.3 중량%, 에리스리톨 27.0 중량%, 사이클로덱스트린 10.3 중량%, 레몬 에센셜오일 0.2 중량%, 스피아민트 오일 0.4 중량%, 페퍼민트 에센셜오일 0.2 중량%, 티트리 에센셜오일 0.2 중량%, 수크랄로스 0.2 중량%, 폴리비닐피롤리돈 0.9 중량%, 잔탄검 0.4 중량% 및 잔량의 솔비톨를 혼합하여 하기 표 1의 구강용 조성물을 제조하였다.Potassium carbonate 8.0% by weight, citric acid 8.0% by weight and surfactant 3.0% by weight, methylsulfonylmethane 3.1% by weight, arginine 1.9% by weight, menthol 0.7% by weight, sodium fluoride 0.3% by weight, erythritol 27.0% by weight, cyclodextrin 10.3% by weight %, lemon essential oil 0.2 wt%, spearmint oil 0.4 wt%, peppermint essential oil 0.2 wt%, tea tree essential oil 0.2 wt%, sucralose 0.2 wt%, polyvinylpyrrolidone 0.9 wt%, xanthan gum 0.4 wt% And the remaining amount of sorbitol was mixed to prepare a composition for oral use in Table 1 below.
상기 계면활성제로 라우릴베타인 및 포타슘 코코일글리시네이트의 조성을 달리하여 하기 표 2의 실시예 1 내지 3 의 구강용 조성물을 제조하고, 비교를 위해 하기 표 3의 알칼리금속염을 포함하지 않은 구강용 조성물인 비교예 1, 계면활성제를 포함하지 않은 비교예 2를 제조하였다.By varying the composition of lauryl betaine and potassium cocoyl glycinate as the surfactant, the oral compositions of Examples 1 to 3 of Table 2 below were prepared, and for comparison, the oral cavity without alkali metal salts of Table 3 Comparative Example 1, which is a composition for use, and Comparative Example 2, which does not contain a surfactant, were prepared.
8.0중량%Potassium Citrate
8.0% by weight
8.0중량%Potassium Citrate
8.0% by weight
8.0%중량Potassium Citrate
8.0% by weight
0.5 중량%lauryl betaine
0.5% by weight
1.2 중량%lauryl betaine
1.2 wt%
1.9 중량%lauryl betaine
1.9 wt%
2.5 중량%Potassium Cocoyl Glycinate
2.5% by weight
1.8 중량%Potassium Cocoyl Glycinate
1.8 wt%
1.1 중량%Potassium Cocoyl Glycinate
1.1 wt%
8.0% 중량Potassium Citrate
8.0% by weight
1.2 중량%lauryl betaine
1.2 wt%
1.8 중량%Potassium Cocoyl Glycinate
1.8 wt%
비교예에서 알칼리금속염이나 계면활성제를 첨가하지 않은 경우에는 동량의 정제수를 첨가하였다.In Comparative Example, when no alkali metal salt or surfactant was added, the same amount of purified water was added.
실험예 1. 구강용 조성물의 거품생성능 비교Experimental Example 1. Comparison of foaming performance of oral compositions
상기 실시예 1에서 제조한 구강용 조성물 5종의 거품량 확인을 위하여, 다음과 같은 방법으로 거품생성능을 비교하였다.In order to confirm the amount of foam of the five oral compositions prepared in Example 1, the foaming performance was compared in the following way.
시험 대상자는 치아 우식이 없고, 치열이 고른 40대 남녀 40명을 시험대상자로 선정하고, 상기 실시예 1에서 제조한 구강용 조성물 5종으로 칫솔질 한 후, 구강용 조성물의 사용 중에 거품 생성 정도에 대해 0점에서 10점을 부여하는 방식으로 관능성 평가를 진행하였다. 10점에 가까울수록 거품 생성능이 우수한 것으로 판단할 수 있다.The test subject did not have dental caries, and 40 men and women in their 40s with even teeth were selected as test subjects, and after brushing with 5 types of oral compositions prepared in Example 1, the degree of foam generation during use of the oral compositions was evaluated. The sensory evaluation was conducted in a manner that gave 0 to 10 points for the It can be judged that the closer to 10 points, the better the foaming ability.
실험예 2. 구강용 조성물의 시린이 개선효과 비교Experimental Example 2. Comparison of the improvement effect of the composition for oral use
상기 실시예 1에서 제조한 구강용 조성물 5종의 시린이 개선효과 판단을 위하여 다음과 같은 방법으로 시린이 개선효과를 비교하였다.In order to determine the improvement effect of the five oral compositions prepared in Example 1, the improvement effect of the five oral compositions was compared in the following way.
시험 대상자는 시린이 증상을 가지고 있는 시린이 유증상 군 40명으로 선정하고, 상기 실시예 1에서 제조한 구강용 조성물 5종으로 2 주간, 3회/일로 칫솔질 한 후, 이의 시린 정도에 대해 0점에서 10점을 부여하는 방식으로 관능성 평가를 진행하였다. 10점에 가까울수록 시린이 증상이 개선되는 것으로서 시린이 개선에 우수한 효과를 보이는 것으로 판단할 수 있다.The test subjects were selected from the group of 40 patients with symptoms of shirin, and after brushing with 5 oral compositions prepared in Example 1 for 2 weeks, 3 times/day, the degree of numbness was 0 The sensory evaluation was carried out in a way that 10 points were given at the points. As the score is closer to 10, it can be judged that the symptoms of shirin are improved, and it can be judged that shirin has an excellent effect on improvement.
표 4에 따르면, 알칼리금속염으로 구연산 칼륨을 포함하고, 계면활성제로서 라우릴베타인, 포타슘 코코일글리시네이트를 혼합하여 사용한 실시예 1 내지 3 모두 우수한 거품 발생 여부를 보이고, 시린이 개선 효과가 우수한 것으로 확인되었다. According to Table 4, Examples 1 to 3 containing potassium citrate as an alkali metal salt and lauryl betaine and potassium cocoyl glycinate mixed as surfactants all showed excellent foaming, and the improvement effect was improved. was found to be excellent.
이와 달리, 계면활성제만을 포함하는 비교예 1의 경우, 거품의 생성능은 실시예의 구성물과 유사하나, 시린이 개선 효과가 거의 나타나지 않은 것을 알 수 있고, 알칼리 금속염만을 포함하는 비교예 2의 경우, 거품 생성능이 거의 없고, 시린이 개선효과도 크게 나타나지 않는 것으로 확인되었다.On the contrary, in the case of Comparative Example 1 containing only the surfactant, the foaming ability is similar to the composition of the Example, but it can be seen that the improvement effect of the sirin is hardly shown, and in the case of Comparative Example 2 containing only the alkali metal salt, the foam It was confirmed that there was little production ability, and the improvement effect of Sirin did not show much.
Claims (16)
An oral composition comprising an alkali metal salt, a betaine-based surfactant and a glycinate-based surfactant.
The composition for oral use according to claim 1, wherein the alkali metal salt is a potassium salt.
The composition for oral use according to claim 2, wherein the potassium salt is at least one selected from the group consisting of potassium citrate, potassium nitrate, potassium chloride, potassium dihydrogen phosphate, potassium sulfate, potassium carbonate, potassium hydrogen carbonate, and alum.
The composition for oral use according to claim 2, wherein the potassium salt is included in an amount of 5 wt% to 10 wt% with respect to the total composition.
The composition for oral use according to claim 1, wherein the betaine-based surfactant is at least one of lauryl betaine, coco betaine, cocamidopropyl betaine, lauromidopropyl betaine, and propyl betaine.
The composition for oral use according to claim 5, wherein the betaine-based surfactant is lauryl betaine.
The composition for oral use according to claim 6, wherein the lauryl betaine is included in an amount of 0.5% to 2% by weight based on the total amount of the composition.
The composition for oral use according to claim 1, wherein the glycinate-based surfactant is potassium cocoyl glycinate or sodium cocoyl glycinate.
The composition for oral use according to claim 8, wherein the glycinate-based surfactant is potassium cocoyl glycinate.
The composition for oral use according to claim 8, wherein the potassium cocoyl glycinate is included in an amount of 1 wt% to 3 wt% with respect to the total composition.
The composition for oral use according to claim 1, comprising lauryl betaine as a betaine-based surfactant and potassium cocoyl glycinate as a glycinate-based surfactant in a weight ratio of 1:3 to 3:1.
The composition for oral use according to claim 1, further comprising an abrasive or an antibacterial agent.
The composition for oral use according to claim 12, wherein the abrasive is erythritol or silica.
The composition for oral use according to claim 12, wherein the abrasive is included in an amount of 20 wt% to 35 wt% with respect to the total composition.
The composition for oral use according to claim 12, wherein the antibacterial agent is at least one selected from the group consisting of fluorine, chlorhexidine, xylitol and penicillin.
The composition for oral use according to claim 12, wherein the antibacterial agent is included in an amount of 0.01 wt% to 3 wt% with respect to the total composition.
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