JP2011001351A - Antimicrobial agent, composition for oral cavity using the same, and food and drink - Google Patents
Antimicrobial agent, composition for oral cavity using the same, and food and drink Download PDFInfo
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- JP2011001351A JP2011001351A JP2010114027A JP2010114027A JP2011001351A JP 2011001351 A JP2011001351 A JP 2011001351A JP 2010114027 A JP2010114027 A JP 2010114027A JP 2010114027 A JP2010114027 A JP 2010114027A JP 2011001351 A JP2011001351 A JP 2011001351A
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- 210000000214 mouth Anatomy 0.000 title claims abstract description 26
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- 235000013305 food Nutrition 0.000 title abstract description 15
- 239000004599 antimicrobial Substances 0.000 title abstract 4
- 241001148471 unidentified anaerobic bacterium Species 0.000 claims abstract description 32
- -1 fatty acid esters Chemical class 0.000 claims abstract description 25
- 241000894006 Bacteria Species 0.000 claims abstract description 24
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims abstract description 18
- MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 claims abstract description 15
- JOZKFWLRHCDGJA-UHFFFAOYSA-N citronellol acetate Chemical compound CC(=O)OCCC(C)CCC=C(C)C JOZKFWLRHCDGJA-UHFFFAOYSA-N 0.000 claims abstract description 13
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- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 claims abstract description 11
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- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229940117955 isoamyl acetate Drugs 0.000 claims abstract description 8
- YLYBTZIQSIBWLI-UHFFFAOYSA-N octyl acetate Chemical compound CCCCCCCCOC(C)=O YLYBTZIQSIBWLI-UHFFFAOYSA-N 0.000 claims abstract description 8
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 claims abstract description 7
- JOZKFWLRHCDGJA-LLVKDONJSA-N Citronellyl acetate Natural products CC(=O)OCC[C@H](C)CCC=C(C)C JOZKFWLRHCDGJA-LLVKDONJSA-N 0.000 claims abstract description 6
- 229940093499 ethyl acetate Drugs 0.000 claims abstract description 6
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- HIGQPQRQIQDZMP-FLIBITNWSA-N neryl acetate Chemical compound CC(C)=CCC\C(C)=C/COC(C)=O HIGQPQRQIQDZMP-FLIBITNWSA-N 0.000 claims abstract description 6
- MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 claims abstract description 6
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- KGEKLUUHTZCSIP-UHFFFAOYSA-N Isobornyl acetate Natural products C1CC2(C)C(OC(=O)C)CC1C2(C)C KGEKLUUHTZCSIP-UHFFFAOYSA-N 0.000 claims abstract description 4
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- IUSBVFZKQJGVEP-UHFFFAOYSA-N trans-isoeugenol acetate Natural products COC1=CC(C=CC)=CC=C1OC(C)=O IUSBVFZKQJGVEP-UHFFFAOYSA-N 0.000 claims abstract description 4
- QUMXDOLUJCHOAY-UHFFFAOYSA-N alpha-methylbenzyl acetate Natural products CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 claims abstract description 3
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- 239000003242 anti bacterial agent Substances 0.000 claims description 27
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- 241000605986 Fusobacterium nucleatum Species 0.000 description 3
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Landscapes
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Confectionery (AREA)
Abstract
Description
本発明は、複数種の口腔内嫌気性細菌、特に歯周病原因菌に対し、実際の口腔内において、直接的接触と間接的接触のどちらか一方であっても優れた抗菌性を有し、且つ香味良好で日常の連用に適した抗菌剤並びにそれを用いた口腔用組成物及び飲食品に関する。 The present invention has an excellent antibacterial property against a plurality of types of oral anaerobic bacteria, particularly periodontal disease-causing bacteria, in the actual oral cavity, whether it is direct contact or indirect contact. The present invention also relates to an antibacterial agent having a good flavor and suitable for daily use, and an oral composition and food and drink using the same.
近年、精油や香料の機能のひとつに、口腔内疾患である歯周病原因菌に対する抗菌作用があることは広く知られている。
例えば、フソバクテリウム・ヌクレアタム(Fusobacterium nucleatum)、ポルフィロモナス・ジンジバリス(Porphyromonas gingivalis)、プレボテラ・インターメディア(Prevotella intermedia)といった歯周病原因菌に、有効に抑制作用を示す抗菌香料が知られている(例えば、特許文献1参照)。
しかしながら、上記抗菌香料は、口腔内疾患に関与するユーバクテリウム属(Eubacterium sp.)、タンネレラ・フォーサイセンシス(Tannerella forsythensis)、トレポネマ・デンティコラ(Treponema denticola)等の口腔内嫌気性細菌に対する抗菌性の報告はなされておらず、歯周病原因菌を代表する口腔内嫌気性細菌全般に効果を奏するものではなかった。また、上記抗菌香料は、薬品臭、消毒薬臭、スモーク臭、香粧品臭、苦味、渋味、えぐみ等の独特の好ましくない香味をもつため、口中に含むと不快感を引き起こすものが殆どであり、口腔用組成物や飲食品に用いるには、実用性や連用性に劣るという問題点があった。
In recent years, it is widely known that one of the functions of essential oils and fragrances has an antibacterial action against periodontal disease-causing bacteria that are oral diseases.
For example, antibacterial fragrances that are effective in inhibiting periodontal diseases such as Fusobacterium nucleatum, Porphyromonas gingivalis and Prevotella intermedia (Prevotella intermedia) are known. For example, see Patent Document 1).
However, the antibacterial flavor is antibacterial against oral anaerobic bacteria such as Eubacterium sp., Tannerella forsythesis, Treponema denticola, etc., which are involved in oral diseases. No report has been made, and it has not been effective in all oral anaerobic bacteria representing periodontal disease-causing bacteria. In addition, the antibacterial fragrances described above have unique and unfavorable flavors such as chemical odors, disinfectant odors, smoke odors, cosmetic odors, bitterness, astringency, and sardines. Therefore, there is a problem that it is inferior in practicality and continuity for use in oral compositions and foods and drinks.
また、他に、フソバクテリウム・ヌクレアタムに有効に抑制作用を示す、上記抗菌香料とは異なる香料成分による抗菌香料組成物が知られている(例えば、特許文献2参照)。
しかしながら、上記抗菌香料組成物とは、ヘキシルアルデヒド等の特定の香料成分であり、酢酸エステルによる抗菌性は開示されていない。また、口腔内疾患に関与するポルフィロモナス・ジンジバリス、ユーバクテリウム属、プレボテラ・インターメディア、タンネレラ・フォーサイセンシス、トレポネマ・デンティコラ等の口腔内嫌気性細菌に対する抗菌性の報告はなかった。更に、上記抗菌香料もまた、薬品臭、消毒薬臭、スモーク臭、香粧品臭、苦味、渋味、えぐみ等の独特の好ましくない香味をもつため、口中に含むと不快感を引き起こすものが殆どであり、口腔用組成物や飲食品に用いるには、実用性や連用性に劣るという問題点があった。
In addition, an antibacterial perfume composition comprising a perfume component different from the above antibacterial perfume that effectively inhibits Fusobacterium nucleatum is known (for example, see Patent Document 2).
However, the antibacterial fragrance composition is a specific fragrance component such as hexyl aldehyde, and the antibacterial property by acetate is not disclosed. In addition, there was no report of antibacterial activity against oral anaerobic bacteria such as Porphyromonas gingivalis, Eubacterium, Prevotella intermedia, Tannerera forseicensis, Treponema denticola, etc. involved in oral diseases. Furthermore, the antibacterial fragrances described above also have unique and unfavorable flavors such as chemical odors, disinfectant odors, smoke odors, cosmetic odors, bitter tastes, astringent tastes, and sardines. In most cases, there is a problem that it is inferior in practicality and continuity for use in oral compositions and foods and drinks.
一方、「香りを発現する」という香料の特性をより発揮できる状態を考慮し、香料の直接的接触だけでなく、気化した蒸気状態における精油や香料の抗菌性について報告されている(例えば、非特許文献1参照)。
しかしながら、該香料等の抗菌性は好気性細菌や真菌類に有効であり、口腔内疾患に関与する上記に挙げたような口腔内嫌気性細菌に対する抗菌性の報告例は皆無であった。また、口腔内嫌気性細菌はもとより、歯周病原因菌だけでも何十種類も存在し、ひとつの原因菌に抗菌性を示すだけでは、口腔疾患改善に不十分である。
On the other hand, in consideration of the state in which the characteristic of a fragrance “expressing a fragrance” can be exhibited more, not only the direct contact of the fragrance but also the antibacterial properties of essential oils and fragrances in a vaporized vapor state have been reported (for example, non- Patent Document 1).
However, the antibacterial properties of the fragrances and the like are effective against aerobic bacteria and fungi, and there have been no reports of antibacterial properties against oral anaerobic bacteria such as those mentioned above that are involved in oral diseases. In addition to the anaerobic bacteria in the oral cavity, there are dozens of types of periodontal disease-causing bacteria alone, and it is insufficient to improve oral diseases if only one causative bacteria exhibits antibacterial properties.
本発明は、以上のような事情に鑑みなされたものであって、その目的とするところは、複数種の口腔内嫌気性細菌、特に歯周病原因菌に対し、実際の口腔内において、直接的及び間接的のどちらか一方の接触であっても優れた抗菌性を有し、且つ香味良好で日常の連用に適した抗菌剤並びにそれを用いた口腔用組成物及び飲食品を提供するにある。 The present invention has been made in view of the circumstances as described above, and the object thereof is to directly against a plurality of types of oral anaerobic bacteria, particularly periodontal disease-causing bacteria, in the actual oral cavity. To provide an antibacterial agent that has excellent antibacterial properties even if it is in contact with either the target or indirect, has a good flavor and is suitable for daily continuous use, and an oral composition and food and drink using the same is there.
本発明は、口腔内嫌気性細菌に対する抗菌性を有する抗菌剤であって、酢酸エステルを含有することを特徴とする抗菌剤により上記目的を達成する。 The present invention achieves the above object with an antibacterial agent having antibacterial properties against anaerobic bacteria in the oral cavity and containing an acetate ester.
好ましくは、酢酸エステルが、酢酸イソアミル、酢酸イソブチル、酢酸ゲラニル、酢酸リナリル、酢酸エチル、酢酸プロピル、酢酸オクチル、酢酸シトロネリル、酢酸ネロール、酢酸ボルニル、酢酸イソボルニル、酢酸テルピニル、酢酸ミルセニル、酢酸ベンジル、酢酸フェニルエチル、酢酸シンナミル、酢酸アニシル及びアセチルイソオイゲノールのうち1種又は2種以上である。
更に好ましくは、口腔内嫌気性細菌に対し、直接的に及び/又は間接的に接触することで抗菌性を有する。
更に、上記抗菌剤を口腔用組成物に含有させることが好ましく、更にまた、上記抗菌剤を飲食品に含有させることが好ましい。
Preferably, the acetate ester is isoamyl acetate, isobutyl acetate, geranyl acetate, linalyl acetate, ethyl acetate, propyl acetate, octyl acetate, citronellyl acetate, nerol acetate, bornyl acetate, isobornyl acetate, terpinyl acetate, milcenyl acetate, benzyl acetate, acetic acid One or more of phenylethyl, cinnamyl acetate, anisyl acetate and acetylisoeugenol.
More preferably, it has antibacterial properties by direct and / or indirect contact with oral anaerobic bacteria.
Further, the antibacterial agent is preferably contained in the oral composition, and the antibacterial agent is preferably contained in the food or drink.
すなわち、本発明者らは、従来のように香味が悪く、服用しづらい殺菌剤や抗菌香料に替わり得る香料成分を探索するため、ヒトにとって香味良好なフルーツや嗜好品に含有される或いは用いられる精油、香料及び香料成分に注目し、歯周病原因菌等の口腔内嫌気性細菌に対する抗菌性の有無について、まずスクリーニング試験を行った。
その結果、直接的接触法において、カモミール精油、スペアミント香料、シソ香料、バナナ香料、ベルガモット香料、ココナッツ香料、グレープフルーツ香料、カルダモン香料、ウィンターグリーン香料、シトラール、ネロリドール、リナロール、ゲラニオール、メントール及びシネオールに抗菌性があることを見出した。
更に、上記香料等を含有する口腔用組成物や飲食品によって、実際に口腔内で抗菌性を発揮させることを考慮して、間接的接触法における抗菌性を検討した。従来より、抗菌性を有する香料成分としては、フェノール類やモノテルペンアルコール類が一般的に知られているため、それらを多く含有するウィンターグリーン香料やモノテルペンアルコールそのものであるリナロール、ゲラニオール等が強い抗菌性を有すると予想していた。しかしながら、検討の結果、驚くべきことに、バナナ香料及びベルガモット香料が、直接的接触法と間接的接触法の両方において、複数の異なる口腔内嫌気性細菌に対して抗菌性を示し、総合的に最も汎用性が高く、有効であることを見出した。
そこで、更にバナナ香料及びベルガモット香料の含有成分について検討したところ、主成分である酢酸エステルが口腔内嫌気性細菌に対し抗菌性を有し、且つ口中に含んでも香味良好であることを見出した。
すなわち、本発明者らは、酢酸エステルが口腔内嫌気性細菌の細胞膜自体や膜透過性に対し障害を与える、又は菌体内に取り込まれた後の代謝産物であるアルコール類の抗菌効果により、口腔内嫌気性細菌に対して抗菌性を有するのではないかと考え、本発明に到達した。
That is, the present inventors search for a perfume ingredient that has a poor flavor and is difficult to take and can be replaced with a fungicide or antibacterial perfume as in the prior art. Focusing on essential oils, fragrances, and fragrance components, screening tests were first conducted for the presence or absence of antibacterial activity against oral anaerobic bacteria such as periodontal disease-causing bacteria.
As a result, in the direct contact method, chamomile essential oil, spearmint flavor, perilla flavor, banana flavor, bergamot flavor, coconut flavor, grapefruit flavor, cardamom flavor, winter green flavor, citral, nerolidol, linalool, geraniol, menthol and cineole. It was found that it has antibacterial properties.
Furthermore, the antibacterial property in the indirect contact method was examined in consideration of the fact that the antibacterial property was actually exhibited in the oral cavity by the oral composition containing the fragrance and the like. Conventionally, phenols and monoterpene alcohols are generally known as perfume ingredients having antibacterial properties. Therefore, wintergreen fragrances containing a large amount of them and monoterpene alcohols themselves such as linalool and geraniol are strong. Expected to have antibacterial properties. However, as a result of the study, surprisingly, banana flavor and bergamot flavor showed antibacterial properties against a plurality of different oral anaerobic bacteria in both direct contact method and indirect contact method. It was found to be the most versatile and effective.
Then, when the content component of a banana fragrance | flavor and a bergamot fragrance | flavor was further examined, it discovered that the acetic acid ester which is a main component has antibacterial property with respect to anaerobic bacteria in the oral cavity, and has a favorable flavor even if it contains it in the mouth.
That is, the present inventors have found that the acetate ester has an obstacle to the cell membrane itself and membrane permeability of oral anaerobic bacteria, or the antibacterial effect of alcohols that are metabolites after being taken into the cells, The present inventors reached the present invention because they thought that they had antibacterial properties against internal anaerobic bacteria.
本発明の抗菌剤は、口腔内嫌気性細菌に対し抗菌性を有する。
本発明の抗菌剤は、直接的に接触するか、間接的に接触するかのどちらか一方であって
も、複数の異なる口腔内嫌気性細菌に対し抗菌性を有するため、間接的接触により抗菌効果を奏するものは、口腔内の病変部位に直接塗布する必要がなく、これを用いた口腔用組成物や飲食品を、口腔内に滞留するだけで有効に抗菌効果を得ることができる。
本発明の抗菌剤を用いた口腔用組成物や飲食品は、薬品臭、消毒薬臭、スモーク臭、香粧品臭、苦味、渋味、えぐみ等の独特の好ましくない香味をもつ従来の殺菌剤や抗菌剤とは異なり、香味良好で実用性や連用性に優れる。
また、本発明の抗菌効果は、複数の異なる口腔内嫌気性細菌に対して発揮されるので、口腔内疾患のうちでも代表的な歯周病を予防・防止する、ひいては口臭防止の口腔衛生効果も期待できる。
The antibacterial agent of the present invention has antibacterial properties against oral anaerobic bacteria.
The antibacterial agent of the present invention has antibacterial properties against a plurality of different anaerobic bacteria in the oral cavity, whether it is in direct contact or indirect contact. What has an effect does not need to be directly applied to a lesion site in the oral cavity, and an antibacterial effect can be effectively obtained simply by retaining an oral composition or food or drink using the same in the oral cavity.
Oral compositions and foods and drinks using the antibacterial agent of the present invention are conventional sterilizations having unique unfavorable flavors such as chemical odor, disinfectant odor, smoke odor, cosmetic odor, bitterness, astringency, and sardine. Unlike agents and antibacterial agents, it has a good flavor and excellent utility and continuity.
In addition, since the antibacterial effect of the present invention is exerted against a plurality of different oral anaerobic bacteria, it prevents or prevents typical periodontal disease among oral diseases, and thus oral hygiene effect of preventing bad breath Can also be expected.
次に、本発明を詳しく説明する。
本発明の抗菌剤は、口腔内嫌気性細菌に対する抗菌性を有する抗菌剤であって、酢酸エステルを含有する。
Next, the present invention will be described in detail.
The antibacterial agent of the present invention is an antibacterial agent having antibacterial properties against anaerobic bacteria in the oral cavity and contains an acetate ester.
まず、本発明に係る口腔内嫌気性細菌とは、口腔内疾患すなわち歯周病原因菌等を指し、例えば、ポルフィロモナス・ジンジバリス、フソバクテリウム・ヌクレアタム、ユーバクテリウム属、プレボテラ・インターメディア、タンネレラ・フォーサイセンシス、トレポネマ・デンティコラ等の歯周病菌が挙げられる。これらの中でも特に、ポルフィロモナス・ジンジバリス、フソバクテリウム・ヌクレアタム及びユーバクテリウム属に対して、本発明の抗菌剤は、抗菌性を有効に発揮する。 First, the oral anaerobic bacteria according to the present invention refer to oral diseases, ie periodontal disease causative bacteria, etc. -Periodontal disease bacteria such as Forsycensis, Treponema denticola and the like. Among these, the antibacterial agent of the present invention effectively exhibits antibacterial activity against Porphyromonas gingivalis, Fusobacterium nucleatum and Eubacterium.
本発明における酢酸エステルとは、一般に下記の化学式(1)で表される化合物で、特に花卉や果実類の香気成分に含まれる芳香のある液体又は結晶である。例えば、酢酸イソアミル、酢酸イソブチル、酢酸ゲラニル、酢酸リナリル、酢酸エチル、酢酸プロピル、酢酸オクチル、酢酸シトロネリル、酢酸ネロール、酢酸ボルニル、酢酸イソボルニル、酢酸テルピニル、酢酸ミルセニル、酢酸ベンジル、酢酸フェニルエチル、酢酸シンナミル、酢酸アニシル及びアセチルイソオイゲノール等が挙げられ、これらは単独あるいは2種以上混合してもよい。この中でも特に、各口腔内嫌気性細菌に対し有効に抗菌性を示し、香味が良好である点で、酢酸イソアミル、酢酸イソブチル、酢酸ゲラニル、酢酸リナリル、酢酸エチル、酢酸プロピル、酢酸シトロネリル、酢酸ネロール、酢酸テルピニルが好適である。 The acetate ester in the present invention is a compound generally represented by the following chemical formula (1), and is particularly a liquid or crystal having an fragrance contained in aroma components of florets and fruits. For example, isoamyl acetate, isobutyl acetate, geranyl acetate, linalyl acetate, ethyl acetate, propyl acetate, octyl acetate, citronellyl acetate, nerol acetate, bornyl acetate, isobornyl acetate, terpinyl acetate, myrcenyl acetate, benzyl acetate, phenylethyl acetate, cinnamyl acetate , Anisyl acetate, acetylisoeugenol, and the like. These may be used alone or in combination of two or more. Among them, isoamyl acetate, isobutyl acetate, geranyl acetate, linalyl acetate, ethyl acetate, propyl acetate, citronellyl acetate, nerol acetate are particularly effective in showing antibacterial activity against each oral anaerobic bacterium. Terpinyl acetate is preferred.
また、本発明の抗菌剤は、口腔内嫌気性細菌に対して直接的か間接的のどちらか一方の接触のみで、抗菌効果を発揮する。ここで間接的に接触するとは、酢酸エステルが揮発し蒸気状態で口腔内嫌気性細菌に接触することを指す。
すなわち、間接的に接触することで抗菌性を有する場合、口腔内の嫌気性細菌による病変部位に直接塗布する必要がなく、本発明の抗菌剤を用いた口腔用組成物や飲食品を、口腔内に滞留するだけで有効に抗菌効果を得ることができる点で好適である。
In addition, the antibacterial agent of the present invention exerts an antibacterial effect only by direct or indirect contact with oral anaerobic bacteria. Here, indirect contact means that the acetate ester volatilizes and contacts the oral anaerobic bacteria in the vapor state.
That is, when it has antibacterial properties by contact indirectly, it is not necessary to apply directly to the lesion site due to anaerobic bacteria in the oral cavity, and the oral composition or food and drink using the antibacterial agent of the present invention It is preferable in that an antibacterial effect can be obtained effectively only by staying inside.
本発明の抗菌剤は、上記酢酸エステルを単独で、あるいは2種以上混合して用いられ、例えば、各種の口腔用組成物や飲食品に添加し、従来の公知の方法により、各種の製品形態にして使用される。
添加方法は、上記酢酸エステルを含有する香料として、あるいは酢酸エステルそのものを添加する等が挙げられる。
口腔用組成物全体重量中、又は飲食品全体重量中の含有量は、酢酸エステルとして、0.005重量%以上であることが抗菌性を発揮する点で好ましい。
The antibacterial agent of the present invention is used alone or in combination of two or more of the above-mentioned acetate esters. For example, various antibacterial agents can be added to various oral compositions and foods and drinks, and various product forms can be obtained by conventional methods. Used.
Examples of the addition method include adding the acetate ester itself as a fragrance containing the acetate ester.
The content in the total weight of the oral composition or in the total weight of the food and drink is preferably 0.005% by weight or more as an acetate ester in terms of exhibiting antibacterial properties.
また、本発明の口腔用組成物としては、歯磨き剤、洗口剤、歯間ブラシ、舌ブラシ、フィルム剤、パッチ剤等が挙げられ、飲食品としては、飲料(茶類、アイソトニック飲料等)、チューインガム、ソフトキャンディ、グミキャンディ、ハードキャンディ、錠菓、マイクロカプセル等が挙げられ、研磨、洗浄、含嗽、拭付、貼付、咀嚼、舐める、飲食による口中滞留等によって口腔内で長く滞留させ、抗菌性を有効に発揮できる点で好適である。 In addition, examples of the oral composition of the present invention include dentifrices, mouthwashes, interdental brushes, tongue brushes, films, patches, and the like, and foods and beverages include beverages (teas, isotonic beverages, etc.). , Chewing gum, soft candy, gummy candy, hard candy, tablet candy, microcapsule, etc., polishing, washing, gargle, wiping, sticking, chewing, licking, etc. This is preferable in that it can effectively exhibit antibacterial properties.
本発明の口腔用組成物は、上記抗菌剤と各種口腔用組成物原料と混合し、得られた混合物を用いて、従来公知の製造方法に従うことにより得られる。
例えば、歯磨き剤の場合は、上記抗菌剤と界面活性剤、発泡剤、湿潤剤、粘結剤、抗炎症剤、収斂剤、保存料、香料、甘味料等を混合して製造される。
このようにして得られた歯磨き剤は、口中に含み、歯と歯ぐきを研磨、洗浄することにより病変部位近辺に存在する口腔内嫌気性細菌に、酢酸エステルが直接的及び/又は揮発し蒸気状態で間接的に接触し、効果的に抗菌性を発揮することができる。また、香味良好で日常の連用に適している点で好ましい。
The oral composition of the present invention is obtained by mixing the antibacterial agent and various oral composition raw materials, and using the resulting mixture according to a conventionally known production method.
For example, a dentifrice is produced by mixing the antibacterial agent with a surfactant, a foaming agent, a wetting agent, a binder, an anti-inflammatory agent, an astringent, a preservative, a fragrance, a sweetener and the like.
The dentifrice obtained in this way is contained in the mouth, and by polishing and washing the teeth and gums, acetate is directly and / or volatilized into the anaerobic bacteria in the oral cavity existing in the vicinity of the lesion. Indirect contact with can effectively exhibit antibacterial properties. Moreover, it is preferable in terms of good flavor and suitable for daily continuous use.
本発明の飲食品は、例えば、チューインガムの場合は、まず、ニーダー中に通常のガムベース用原料を投入して溶融混合し、ガムベースを作製する。次に、上記ガムベースに対し糖類、色素等を添加して混合し、更に上記抗菌剤、香料等を添加して混合する。そして、得られた混合物を適宜の形状に成形することにより抗菌剤含有チューインガムが得られる。
このようにして得られたチューインガムは、口中で咀嚼することにより、病変部位近辺に存在する口腔内嫌気性細菌に、酢酸エステルが直接的、或いは揮発し蒸気状態で間接的に接触し、効果的に抗菌性を発揮することができる。また、一般的な嗜好性チューインガムと香味上大差なく、連用が容易となる点で好ましい。
For example, in the case of a chewing gum, the food or drink of the present invention is prepared by first putting a normal raw material for gum base into a kneader and melt-mixing it to produce a gum base. Next, saccharides, pigments, and the like are added to and mixed with the gum base, and the antibacterial agent, fragrance, and the like are further added and mixed. And the antibacterial agent containing chewing gum is obtained by shape | molding the obtained mixture in a suitable shape.
The chewing gum obtained in this way is effective by chewing in the mouth, and directly contacting the anaerobic bacteria in the mouth near the lesion site or directly in the vapor state by evaporation of acetate. Can exhibit antibacterial properties. Moreover, it is preferable at the point which is easy to use continuously, without a great difference in flavor with general preference chewing gum.
以下に、本発明の実施例を用いて例示する。
<精油、香料及び香料成分のスクリーニング>
口腔内嫌気性細菌に対する抗菌性の有無について、フルーツに含有される、或いは嗜好品に用いられる精油、香料及び香料成分のスクリーニングを行った。スクリーニングに用いた口腔内嫌気性細菌の試験菌株名を表1に示す。以下本文中では、口腔内嫌気性細菌名を表1中の略号で記載する。また、Pg−1及びElは理化学研究所より、Pg−2は岐阜大学生命科学総合研究支援センターより、Fnは住商ファーマインターナショナル(株)より入手した。なお、抗菌性測定は、直接的接触法及び間接的接触法の両方について実施した。
In the following, examples of the present invention are used to illustrate.
<Screening of essential oils, fragrances and fragrance ingredients>
About the presence or absence of the antibacterial property with respect to an anaerobic bacterium in an oral cavity, the essential oil contained in a fruit or used for a favorite item, the fragrance | flavor, and the fragrance | flavor component were screened. Table 1 shows the names of test strains of oral anaerobic bacteria used for screening. Hereinafter, in the text, oral anaerobic bacteria are indicated by abbreviations in Table 1. Pg-1 and El were obtained from RIKEN, Pg-2 from Gifu University Life Sciences Research Support Center, and Fn from Sumisho Pharma International Co., Ltd. In addition, the antibacterial measurement was implemented about both the direct contact method and the indirect contact method.
<抗菌性測定用培地の作成>
ブルセラHK寒天培地(極東製薬工業(株)製)に、5%の兎無菌脱繊血((株)日本生物材料センター製)を添加した平板培地を用いた。
<試験菌液の調製>
各口腔内嫌気性細菌の試験菌液は以下のようにして調製した。
まず、表1の試験菌を上記抗菌性測定用培地で培養した。培養した試験菌を、Difco Anaerobe Broth MIC(Becton,Dickinson and Company製)による液体培地に分散させ、試験菌液の原液とした。抗菌性測定には、抗菌性測定用培地に試験菌液を100μl塗抹した時に、30〜300個のコロニーが生える程度の濃度になるよう、上記液体培地で更に希釈したものを用いた。
<Creation of antibacterial measurement medium>
A flat plate medium in which 5% sterilized defibrillated blood (manufactured by Japan Biomaterials Center) was added to Brucella HK agar medium (manufactured by Kyokuto Pharmaceutical Co., Ltd.) was used.
<Preparation of test bacterial solution>
A test bacterial solution for each oral anaerobic bacterium was prepared as follows.
First, the test bacteria in Table 1 were cultured in the antibacterial measurement medium. The cultured test bacteria were dispersed in a liquid medium using Difco Anarobe Broth MIC (manufactured by Becton, Dickinson and Company) to obtain a stock solution of the test bacterial solution. For the antibacterial measurement, a solution further diluted with the above liquid medium was used so that the concentration was such that 30 to 300 colonies would grow when 100 μl of the test bacterial solution was smeared on the antibacterial measurement medium.
<スクリーニング−直接的接触法>
上記抗菌性測定用培地に、表2に記載の精油、香料及び香料成分を400μl塗抹し、その上から表1の試験菌液100μlを塗抹したものを、アネロパック・ケンキ(三菱ガス化学(株)製)を用いて、37℃で嫌気培養した。なお、抗菌性の有無は、精油、香料及び香料成分の代わりにオリーブ油400μlを塗抹したコントロールにコロニーが発生した時点で、試験菌の生育を目視確認し、試験菌のコロニー未発生のものを抗菌性あり、発生したものを抗菌性なしと評価し、表2に示した。
<スクリーニング−間接的接触法>
表2に記載の精油、香料及び香料成分8mlを乾熱滅菌した脱脂綿に染み込ませ、空のシャーレに入れた。別に、表1の試験菌液100μlを塗抹した抗菌性測定用培地を準備した。両者を同じパウチ袋に入れ、アネロパック・ケンキを用いて、37℃で嫌気培養した。なお、抗菌性の有無は、精油、香料及び香料成分の代わりに蒸留水8mlを乾熱滅菌した脱脂綿に染み込ませたものと、試験菌液塗抹培地を一緒に嫌気培養したものをコントロールとし、コントロールにコロニーが発生した時点で、試験菌の生育を目視確認し、直接的接触法と同様に評価した。
<Screening-direct contact method>
The above-mentioned antibacterial measurement medium was smeared with 400 μl of the essential oils, fragrances and fragrance ingredients listed in Table 2, and 100 μl of the test bacterial solution in Table 1 was smeared thereon. Aneropack Kenki (Mitsubishi Gas Chemical Co., Ltd.) And anaerobic culture at 37 ° C. In addition, the presence or absence of antibacterial properties is determined by visually checking the growth of the test bacteria when colonies are generated in the control smeared with 400 μl of olive oil instead of essential oil, fragrance, and fragrance ingredients, Those that occurred were evaluated as having no antibacterial properties and are shown in Table 2.
<Screening-Indirect contact method>
The essential oils, fragrances and fragrance components listed in Table 2 were soaked in absorbent cotton sterilized by dry heat and placed in an empty petri dish. Separately, an antibacterial assay medium smeared with 100 μl of the test bacterial solution shown in Table 1 was prepared. Both were placed in the same pouch bag and anaerobically cultured at 37 ° C. using Aneropack Kenki. In addition, the presence or absence of antibacterial properties is controlled by controlling the essential oil, perfume and perfume ingredients soaked in absorbent cotton sterilized with dry heat and 8 ml of distilled water and anaerobically cultivating the test bacterial solution smear medium. At the time when colonies were generated, the growth of the test bacteria was visually confirmed and evaluated in the same manner as in the direct contact method.
スクリーニングの結果、直接的接触法では、カモミール精油、スペアミント香料、バナナ香料、ベルガモット香料、ココナッツ香料、グレープフルーツ香料、カルダモン香料、ウィンターグリーン香料、シトラール、ネロリドール、リナロール、ゲラニオール、メントール及びシネオールが、すべての口腔内嫌気性細菌に対し抗菌性を示した。
また、間接的接触法では、バナナ香料及びベルガモット香料が最も有効に、抗菌性を示した。
As a result of screening, in the direct contact method, chamomile essential oil, spearmint flavor, banana flavor, bergamot flavor, coconut flavor, grapefruit flavor, cardamom flavor, wintergreen flavor, citral, nerolidol, linalool, geraniol, menthol and cineole are all Antibacterial activity against oral anaerobic bacteria.
In the indirect contact method, the banana flavor and the bergamot flavor showed the most effective antibacterial properties.
スクリーニングによる直接的及び間接的接触法の両方に抗菌性を示した、バナナ香料及びベルガモット香料の含有成分を検討したところ、共通して含有量の多い成分は、酢酸エステルであることから、酢酸エステルとその関連香料成分の抗菌性の強度を、以下の方法を用いて確認した。なお、この抗菌性強度測定も、直接的、間接的接触法の両方について行った。 When we examined the ingredients of banana flavor and bergamot flavor that showed antibacterial properties in both direct and indirect contact methods by screening, the most common component is acetate ester. And the antibacterial strength of the related perfume ingredients were confirmed using the following method. This antibacterial strength measurement was also performed for both direct and indirect contact methods.
<抗菌性強度−直接的接触法>
表3に示す酢酸エステル及び香料成分を、100μl/100μlから6.25μl/100μlになるよう、半量ずつ段階的にオリーブ油で希釈した各溶液100μlを、抗菌性測定用培地に塗抹した。その上から表1の試験菌液100μlを塗抹したものを、アネロパック・ケンキを用いて、37℃で嫌気培養した。なお、抗菌性の強度評価は、酢酸
エステルや香料成分の代わりにオリーブ油100μlを塗抹したコントロールにコロニーが発生した時点でそれぞれの試験菌の生育を目視確認し、試験菌の発育の見られない濃度を表3に示した。
<Antimicrobial strength-direct contact method>
100 μl of each solution obtained by gradually diluting the acetate ester and the fragrance component shown in Table 3 with olive oil stepwise from 100 μl / 100 μl to 6.25 μl / 100 μl was smeared on the antibacterial measurement medium. From this, 100 μl of the test bacterial solution in Table 1 was smeared and anaerobically cultured at 37 ° C. using Aneropack Kenki. In addition, the antibacterial strength evaluation was performed by visually checking the growth of each test bacterium when colonies were generated in a control smeared with 100 μl of olive oil instead of acetate or a fragrance component, and the concentration at which the growth of the test bacterium was not observed. Are shown in Table 3.
<抗菌性強度−間接的接触法>
表4に示す酢酸エステル及び香料成分を、8ml/8mlから1ml/8mlになるよう、半量ずつ段階的にオリーブ油で希釈した各溶液8mlを、乾熱滅菌した脱脂綿に染み込ませ、空のシャーレに入れた。別に、表1の試験菌液100μlを塗抹した抗菌性測定用培地を準備した。両者を同じパウチ袋に入れ、アネロパック・ケンキを用いて、37℃で嫌気培養した。抗菌性の強度評価は、酢酸エステル及び香料成分の代わりに蒸留水8mlを乾熱滅菌した脱脂綿に染み込ませたものと、試験菌液塗抹培地を一緒に嫌気培養したものをコントロールとし、コントロールにコロニーが発生した時点でそれぞれの試験菌の生育を目視確認し、試験菌の発育の見られない濃度を表4に示した。
<Antimicrobial strength-indirect contact method>
8 ml of each solution diluted with olive oil stepwise by half so that the acetate and fragrance ingredients shown in Table 4 are reduced from 8 ml / 8 ml to 1 ml / 8 ml are soaked in absorbent cotton sterilized by dry heat and placed in an empty petri dish. It was. Separately, an antibacterial assay medium smeared with 100 μl of the test bacterial solution shown in Table 1 was prepared. Both were placed in the same pouch bag and anaerobically cultured at 37 ° C. using Aneropack Kenki. The antibacterial strength was evaluated by using 8 ml of distilled water soaked in dry heat sterilized cotton instead of acetate and perfume ingredients and anaerobically cultivating the test bacterial solution smear medium together as a control. At the time of occurrence, the growth of each test bacterium was visually confirmed, and the concentrations at which no growth of the test bacterium was observed are shown in Table 4.
表3、4の結果から、直接的接触法では酢酸エステルである酢酸イソアミル、酢酸リナリルは、Pg−1及びPg−2に対し特に抗菌性を示したが、該酢酸エステルの分解物であるイソプロピルアルコールや酢酸イオン(酢酸ナトリウム)は抗菌性を示さなかった。これは、酢酸エステルの抗菌効果が、口腔内嫌気性細菌の細胞内に侵入した後の酢酸エス
テルの分解物による効果でなく、酢酸エステルそのものに起因することを示している。
また、間接的接触法では、酢酸エステルである酢酸イソアミルと酢酸イソブチルは、Pg−1、Pg−2、Fn、Elに対し強い抗菌性を示したものの、香料成分(シトラール、ネロリドール、リナロール、メントール、シネオール)は、抗菌性を示さなかった。
なお、「>」は記載した濃度では試験菌の発育を阻止していないことを示す。
From the results of Tables 3 and 4, in the direct contact method, isoamyl acetate and linalyl acetate, which are acetate esters, showed particularly antibacterial properties against Pg-1 and Pg-2, but isopropyl, which is a decomposition product of the acetate ester. Alcohol and acetate ions (sodium acetate) did not show antibacterial properties. This indicates that the antibacterial effect of the acetate ester is not due to the degradation product of the acetate ester after entering the cells of the oral anaerobic bacteria but the acetate ester itself.
In the indirect contact method, the acetic acid esters isoamyl acetate and isobutyl acetate showed strong antibacterial properties against Pg-1, Pg-2, Fn, and El, but fragrance components (citral, nerolidol, linalool, Menthol, cineole) did not show antibacterial properties.
“>” Indicates that the described concentration does not inhibit the growth of the test bacteria.
更に、表5に示す酢酸エステルの抗菌性強度について、上述の直接的接触法及び間接的接触法を用いて評価した。 Furthermore, the antibacterial strength of the acetate ester shown in Table 5 was evaluated using the direct contact method and the indirect contact method described above.
表5の結果から、全ての酢酸エステルにおいて、直接的接触と間接的接触のどちらか一方或いは両方に優れた抗菌性を有した。また、供した4種類全ての試験菌に対し、少なくとも直接的接触と間接的接触のどちらか一方に抗菌性を示したのは、酢酸イソアミル、酢酸イソブチル、酢酸ゲラニル、酢酸エチル、酢酸プロピル、酢酸シトロネリル、酢酸ネロール、酢酸テルピニルであった。特に、酢酸ゲラニル、酢酸シトロネリルは直接的接触と間接的接触の両方において優れた抗菌性を示した。 From the results of Table 5, all acetate esters had excellent antibacterial properties for either direct contact or indirect contact or both. In addition, for all four types of test bacteria provided, at least one of direct contact and indirect contact showed antibacterial properties: isoamyl acetate, isobutyl acetate, geranyl acetate, ethyl acetate, propyl acetate, acetic acid Citronellyl, nerol acetate, and terpinyl acetate. In particular, geranyl acetate and citronellyl acetate showed excellent antibacterial properties in both direct contact and indirect contact.
<実施例1〜3>
上記抗菌性強度測定において、口腔内嫌気性細菌に対し抗菌性を示した酢酸エステル及び香料成分を用いて、各抗菌香料を調製した。
<Examples 1-3>
In the above antibacterial strength measurement, each antibacterial perfume was prepared using an acetate ester and a perfume component that showed antibacterial properties against anaerobic bacteria in the oral cavity.
<比較例1>バナナ様香料
上記抗菌性強度測定において、以下の香料成分を用いてバナナ様香料を調製した(比較例評価のため、酢酸エステルの含有されていないバナナ様の香味を有するバナナ様香料を調製した)。
<Comparative Example 1> Banana-like fragrance In the above antibacterial strength measurement, a banana-like fragrance was prepared using the following fragrance ingredients (for comparative example evaluation, a banana-like flavor that does not contain acetate ester) A fragrance was prepared).
<比較例2>ティーツリー香料
一般的に抗菌性を有する精油成分として知られているテルピネン−4−オールを用いて、ティーツリー香料を調製した。
<Comparative example 2> Tea tree flavor The tea tree flavor was prepared using terpinen-4-ol generally known as an essential oil component having antibacterial properties.
<実施例4>歯磨き剤
実施例1のバナナ香料1を用いて、表11に示した配合にて、抗菌剤含有口腔用組成物として歯磨き剤を調製した。
<Example 4> Dentifrice Using the banana flavor 1 of Example 1, a dentifrice was prepared as an antibacterial agent-containing oral composition with the formulation shown in Table 11.
<実施例5〜7、比較例3〜4>
実施例2〜3、比較例1〜2の各香料及び酢酸エステル(酢酸イソブチル)を用いて、チューインガムを調製した。
表12に示す組成に従い、チューインガム原料を40〜50℃以下に保ちながら、保温ニーダーで加熱混合して均質化し、冷却した後、エクストルーダーを用いて押し出し成形を行い、各チューインガムを得た。
<Examples 5-7, Comparative Examples 3-4>
Chewing gum was prepared using each fragrance | flavor of Examples 2-3 and Comparative Examples 1-2, and acetate ester (isobutyl acetate).
According to the composition shown in Table 12, while keeping the chewing gum raw material at 40 to 50 ° C. or less, it was heated and mixed with a heat insulating kneader to be homogenized and cooled, and then extruded using an extruder to obtain each chewing gum.
以上のようにして得られた実施例及び比較例品について、まず、実施例1〜3及び比較例1〜2の香料と、酢酸イソブチルの抗菌性評価を、Pg−1に対する間接的接触法による抗菌性強度測定で評価した。その結果を表11及び12の抗菌性の評価欄に示す。
更に、実施例4の歯磨き剤と、実施例5〜7及び比較例3〜4のチューインガムについて、専門パネラー10名による香味評価を行った。その結果を表11及び12の香味の評価欄に示す。
About the Example and comparative example goods obtained as mentioned above, first, the perfume of Examples 1-3 and Comparative Examples 1-2, and the antibacterial evaluation of isobutyl acetate are based on the indirect contact method with respect to Pg-1. Evaluation was made by measuring the antibacterial strength. The results are shown in the antibacterial evaluation column of Tables 11 and 12.
Furthermore, about the dentifrice of Example 4, and the chewing gum of Examples 5-7 and Comparative Examples 3-4, the flavor evaluation by 10 professional panelists was performed. The results are shown in the flavor evaluation columns of Tables 11 and 12.
抗菌性評価の結果、実施例1〜3の香料、酢酸イソブチル及び比較例2の香料は、口腔内嫌気性細菌に対して強い抗菌性を示したが、比較例1の香料は抗菌性を示さなかった。
香味については、実施例4の歯磨き剤は薬品臭や収斂味のない良好な香味であり、実施例5〜6のチューインガムも香味が大変良好であって、実施例4〜6は共に日常の連用性にも極めて優れたものであった。実施例7及び比較例3のチューインガムは、香味は優れるものの、実施例5〜6のチューインガムに比べて若干嗜好性に劣るものであった。特に実施例7のチューインガムは単独の香料成分(酢酸イソブチル)しか含有しないため、その香味がやや単調であった。比較例4のチューインガムは、薬品臭が強いためチューイン
ガムとして喫食するには不良であり、日常の連用には適さなかった。
全体としてみると、実施例4の歯磨き剤及び実施例5〜6のチューインガムは、抗菌性が強く、香味も極めて優れるため、本発明の効果が顕著にあらわされた大変良好なものであった。実施例7も、実施例5〜6とほぼ同等な良好品であった。それに対し、比較例3及び4は、抗菌性と香味のどちらか一方において全く効果を奏することがなく、本発明には適さないものであった。
As a result of the antibacterial evaluation, the fragrances of Examples 1 to 3, isobutyl acetate and the fragrance of Comparative Example 2 showed strong antibacterial properties against oral anaerobic bacteria, but the fragrance of Comparative Example 1 showed antibacterial properties. There wasn't.
As for the flavor, the dentifrice of Example 4 has a good flavor without chemical odor and astringency, and the chewing gums of Examples 5 to 6 have a very good flavor. It was also extremely excellent in properties. Although the chewing gum of Example 7 and Comparative Example 3 was excellent in flavor, it was slightly inferior to the chewing gum of Examples 5-6. In particular, the chewing gum of Example 7 contained only a single perfume component (isobutyl acetate), so that the flavor was slightly monotonous. The chewing gum of Comparative Example 4 had a strong chemical odor and was unsatisfactory for eating as a chewing gum and was not suitable for daily continuous use.
As a whole, the dentifrice of Example 4 and the chewing gums of Examples 5 to 6 were very good in that the effects of the present invention were remarkably exhibited because of strong antibacterial properties and extremely excellent flavor. Example 7 was also a good product substantially equivalent to Examples 5-6. On the other hand, Comparative Examples 3 and 4 did not show any effect in either antibacterial property or flavor and were not suitable for the present invention.
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