JP2002068924A - Antimicrobial agent composition for cosmetic and cosmetic containing the same formulated therewith - Google Patents
Antimicrobial agent composition for cosmetic and cosmetic containing the same formulated therewithInfo
- Publication number
- JP2002068924A JP2002068924A JP2000257068A JP2000257068A JP2002068924A JP 2002068924 A JP2002068924 A JP 2002068924A JP 2000257068 A JP2000257068 A JP 2000257068A JP 2000257068 A JP2000257068 A JP 2000257068A JP 2002068924 A JP2002068924 A JP 2002068924A
- Authority
- JP
- Japan
- Prior art keywords
- cosmetic
- water
- agent composition
- parabens
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002537 cosmetic Substances 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims abstract description 14
- 239000004599 antimicrobial Substances 0.000 title abstract description 4
- 235000016639 Syzygium aromaticum Nutrition 0.000 claims abstract description 16
- 244000223014 Syzygium aromaticum Species 0.000 claims abstract description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 7
- 229930195729 fatty acid Natural products 0.000 claims abstract description 7
- 239000000194 fatty acid Substances 0.000 claims abstract description 7
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000003960 organic solvent Substances 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 239000003242 anti bacterial agent Substances 0.000 claims description 2
- 238000004332 deodorization Methods 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- 230000000845 anti-microbial effect Effects 0.000 abstract 3
- 230000001877 deodorizing effect Effects 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 description 20
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 16
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 8
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 8
- 229960002216 methylparaben Drugs 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- -1 etc. Substances 0.000 description 5
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 4
- 206010040880 Skin irritation Diseases 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- 230000036556 skin irritation Effects 0.000 description 4
- 231100000475 skin irritation Toxicity 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- GHBFNMLVSPCDGN-UHFFFAOYSA-N rac-1-monooctanoylglycerol Chemical compound CCCCCCCC(=O)OCC(O)CO GHBFNMLVSPCDGN-UHFFFAOYSA-N 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 2
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 239000004287 Dehydroacetic acid Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 241000191967 Staphylococcus aureus Species 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- FUWUEFKEXZQKKA-UHFFFAOYSA-N beta-thujaplicin Chemical compound CC(C)C=1C=CC=C(O)C(=O)C=1 FUWUEFKEXZQKKA-UHFFFAOYSA-N 0.000 description 2
- 229940067596 butylparaben Drugs 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 235000019258 dehydroacetic acid Nutrition 0.000 description 2
- 229940061632 dehydroacetic acid Drugs 0.000 description 2
- JEQRBTDTEKWZBW-UHFFFAOYSA-N dehydroacetic acid Chemical compound CC(=O)C1=C(O)OC(C)=CC1=O JEQRBTDTEKWZBW-UHFFFAOYSA-N 0.000 description 2
- PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Natural products CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 description 2
- 239000000645 desinfectant Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 229960001617 ethyl hydroxybenzoate Drugs 0.000 description 2
- 235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 description 2
- 239000004403 ethyl p-hydroxybenzoate Substances 0.000 description 2
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 2
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 2
- 229960003415 propylparaben Drugs 0.000 description 2
- 229960004889 salicylic acid Drugs 0.000 description 2
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- IJALWSVNUBBQRA-UHFFFAOYSA-N 4-Isopropyl-3-methylphenol Chemical compound CC(C)C1=CC=C(O)C=C1C IJALWSVNUBBQRA-UHFFFAOYSA-N 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 241000191070 Escherichia coli ATCC 8739 Species 0.000 description 1
- 241000266331 Eugenia Species 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000219926 Myrtaceae Species 0.000 description 1
- 239000005643 Pelargonic acid Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- TUFYVOCKVJOUIR-UHFFFAOYSA-N alpha-Thujaplicin Natural products CC(C)C=1C=CC=CC(=O)C=1O TUFYVOCKVJOUIR-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- 229960001950 benzethonium chloride Drugs 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N isopropylmethylphenol Natural products CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 235000015961 tonic Nutrition 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 229960000716 tonics Drugs 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は化粧用抗菌剤組成物及び
化粧料に関し、特にアルカリ性領域においても優れた抗
菌性を有する化粧料に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antibacterial cosmetic composition and a cosmetic, and more particularly to a cosmetic having excellent antibacterial properties even in an alkaline region.
【0002】[0002]
【従来の技術】従来より化粧品や医薬部外品には、防腐
殺菌剤としてメチルパラベン、エチルパラベン、プロピ
ルパラベン、ブチルパラベン等のパラベン類、安息香酸
及びその塩、サリチル酸及びその塩、デヒドロ酢酸及び
その塩、等が用いられており、特にパラベンは最も汎用
されている。2. Description of the Related Art Conventionally, cosmetics and quasi-drugs have been used as preservatives and bactericides such as parabens such as methylparaben, ethylparaben, propylparaben and butylparaben, benzoic acid and its salts, salicylic acid and its salts, dehydroacetic acid and its derivatives. Salt and the like are used, and paraben is most widely used.
【0003】しかしながら、パラベン類はアルカリ性領
域でその抗菌性は低下することが知られている。例えば
ジョン・J・カバラの「香粧品 医薬品 防腐・殺菌剤
の科学」(フレグランスジャーナル社)には、パラベン
類はpHが8以上に上昇すると分子が解離し、pH8.
5ではその50%が解離しているので、抗菌活性のかな
りのロスが起こると記載されている。またJ.Soc.Cosme
t.Chem.,38,83-98(1987)には、メチルパラベンはpH
8.3以上になるとフェノール性水酸基の解離が起こ
り、その結果色素や顔料を含む化粧料では抗菌活性が低
下することが記載されている。このようにパラベン類は
酸性〜中性領域での化粧料では優れた抗菌性を有するも
のの、アルカリ性領域においては必ずしもその抗菌性は
満足できるものではない。[0003] However, it is known that antibacterial properties of parabens decrease in an alkaline region. For example, John J. Kabbalah's "Science of Cosmetics, Pharmaceuticals, Preservatives and Disinfectants" (Fragrance Journal) states that molecules of parabens are dissociated when the pH rises to 8 or more, and the pH 8.
In No. 5, it is described that a considerable loss of antibacterial activity occurs because 50% of them are dissociated. Also J.Soc.Cosme
t. Chem. , 38, 83-98 (1987) states that methyl paraben
It is described that when it is 8.3 or more, phenolic hydroxyl groups are dissociated, and as a result, the antibacterial activity of a cosmetic containing a dye or a pigment is reduced. Thus, parabens have excellent antibacterial properties in cosmetics in the acidic to neutral range, but their antibacterial properties are not always satisfactory in the alkaline range.
【0004】また、これら抗菌性の低下を加味してパラ
ベン類を大量に配合すればアルカリ性領域での化粧料に
おいても抗菌性は維持することができるが、近年、パラ
ベン類の皮膚刺激性が問題となっており、安全性の面か
らもできる限り少ない配合量での使用が望まれている。[0004] In addition, if a large amount of parabens is added in consideration of these reductions in antibacterial properties, antibacterial properties can be maintained even in cosmetics in the alkaline range, but in recent years, skin irritation of parabens has become a problem. Therefore, from the viewpoint of safety, it is desired to use a compounding amount as small as possible.
【0005】一般にローションやクリームなどの基礎化
粧品は弱酸性のものが多いが、薬剤成分の安定性を維持
する目的で弱アルカリ性に調製された化粧料、石けんを
乳化剤として使用する場合の化粧料、石けんを主成分と
する洗浄料などにおいてはアルカリ性領域の化粧料も多
く見られる。[0005] In general, many basic cosmetics such as lotions and creams are weakly acidic. However, cosmetics prepared to be weakly alkaline for the purpose of maintaining the stability of drug components, cosmetics when soap is used as an emulsifier, In the case of detergents containing soap as a main component, cosmetics in the alkaline region are often found.
【0006】[0006]
【発明が解決しようとしている課題】そこでアルカリ性
領域においても優れた抗菌性を有し、且つ安全性や使用
性の優れた化粧料を提供できれば、その意義はきわめて
大きいものとなる。本発明は従来のアルカリ性領域での
化粧料における問題点を解決しつつ、微生物による品質
劣化を充分に防ぐことのできる化粧料を提供することを
目的とする。Therefore, if a cosmetic having excellent antibacterial properties even in an alkaline region and excellent in safety and usability can be provided, its significance will be extremely large. SUMMARY OF THE INVENTION An object of the present invention is to provide a cosmetic that can sufficiently prevent quality deterioration by microorganisms while solving the problems of conventional cosmetics in the alkaline region.
【0007】[0007]
【課題を解決するための手段】本発明者らは、鋭意研究
を重ねた結果、パラベン類のうちの少なくとも1種と、
クローブより有機溶剤等を用いて抽出し、抽出液に水を
添加して析出した非水溶性成分を除去し、水を留去する
ことにより精油成分を除去して得られた水溶性成分と、
炭素数8〜12の脂肪酸モノグリセライドとを組み合わ
せて配合することにより、アルカリ性領域においても幅
広い微生物に対して優れた抗菌性を発揮することを見出
し、本発明を完成するに至った。Means for Solving the Problems As a result of intensive studies, the present inventors have found that at least one of parabens and
Extracted from the clove using an organic solvent, etc., water was added to the extract to remove precipitated water-insoluble components, and water-soluble components obtained by removing essential oil components by distilling off water,
It has been found that, by combining with a fatty acid monoglyceride having 8 to 12 carbon atoms, the composition exhibits excellent antibacterial properties against a wide range of microorganisms even in an alkaline region, and has completed the present invention.
【0008】以下本発明を詳細に説明する。本発明に用
いられるパラベン類としては、特にメチルパラベン、エ
チルパラベン、プロピルパラベン、ブチルパラベンの4
種であり、これらは化粧料の防腐殺菌剤として従来より
広く用いられている。本発明においても、上記4種のパ
ラベン類の1種以上が用いられ、これらの配合量として
は0.01〜1重量%、特に0.05〜0.2重量%が
好ましい。0.2重量%以上の配合量は皮膚刺激性の面
からあまり好ましくない。Hereinafter, the present invention will be described in detail. The parabens used in the present invention include, in particular, methyl paraben, ethyl paraben, propyl paraben and butyl paraben.
These are seeds, which have been widely used as antiseptic and disinfecting agents for cosmetics. In the present invention, one or more of the above-mentioned four types of parabens are used, and the blending amount thereof is preferably 0.01 to 1% by weight, particularly preferably 0.05 to 0.2% by weight. A blending amount of 0.2% by weight or more is not so preferable from the viewpoint of skin irritation.
【0009】本発明に用いられるクローブは、フトモモ
科の植物であるチョウジ(学名eugenia caryophyllat
a)の花蕾、葉、茎などがあげられるが、特に花蕾が好
ましい。本発明におけるクローブの水溶性成分は、クロ
ーブを有機溶剤等で抽出し、得られた抽出液に水を加え
て析出した非水溶性成分を除去し、水を留去すると同時
に精油成分を除去することにより得られる。このクロー
ブより得られた水溶性成分の配合量は0.001〜1重
量%、特に0.002〜0.5重量%が好ましい。The clove used in the present invention is a clove ( eugenia caryophyllat) , a plant belonging to the family Myrtaceae.
a ) Flower buds, leaves, stems and the like are mentioned, and flower buds are particularly preferred. The water-soluble component of the clove in the present invention is obtained by extracting the clove with an organic solvent or the like, removing water-insoluble components precipitated by adding water to the obtained extract, and removing essential oil components while distilling off water. It can be obtained by: The amount of the water-soluble component obtained from this clove is preferably 0.001 to 1% by weight, particularly preferably 0.002 to 0.5% by weight.
【0010】また本発明に用いられる炭素数8〜12の
脂肪酸モノグリセライドとしては、カプリル酸、ペラル
ゴン酸、カプリン酸、ウンデシル酸、ラウリン酸等のモ
ノグリセライドが挙げられる。ジグリセライド、トリグ
リセライドも若干の抗菌効果を有するが、モノグリセラ
イドが最も効果が大きい。炭素数7以下、または炭素数
13を越える脂肪酸モノグリセライドも効果を有する
が、臭気や溶解性の面から実用的には炭素数8〜12の
脂肪酸モノグリセライドに限られる。これらの配合量と
しては0.01〜1重量%、特に0.05〜0.5重量
%が好ましい。The fatty acid monoglycerides having 8 to 12 carbon atoms used in the present invention include monoglycerides such as caprylic acid, pelargonic acid, capric acid, undecylic acid and lauric acid. Diglycerides and triglycerides also have some antibacterial effects, but monoglycerides are the most effective. Fatty acid monoglycerides having 7 or less carbon atoms or having more than 13 carbon atoms also have an effect, but are practically limited to fatty acid monoglycerides having 8 to 12 carbon atoms in terms of odor and solubility. The amount of these components is preferably 0.01 to 1% by weight, particularly preferably 0.05 to 0.5% by weight.
【0011】パラベン類に、上記のクローブより得られ
た水溶性成分と、脂肪酸モノグリセライドとを組み合わ
せることにより、パラベン類の配合量を増量することな
く少ない使用量でアルカリ性領域においても優れた抗菌
性を発揮させることができる。By combining parabens with the water-soluble component obtained from the above cloves and fatty acid monoglyceride, excellent antibacterial properties can be obtained even in an alkaline region with a small amount of use without increasing the amount of parabens. Can be demonstrated.
【0012】また上記の抗菌剤組成物に皮膚刺激や安全
性、使用性の影響を伴わない範囲でパラベン類以外の他
の防腐殺菌剤を併用することもできる。このような防腐
殺菌剤としてはイソプロピルメチルフェノール、ヒノキ
チオール、フェノキシエタノール等のフェノール類、安
息香酸及びその塩、サリチル酸及びその塩、デヒドロ酢
酸及びその塩、ソルビン酸及びその塩等の酸類、塩化ベ
ンザルコニウム、塩化ベンゼトニウム、塩化アルキルト
リメチルアンモニウム等の第4級アンモニウム類、塩酸
アルキルアミノエチルグリシン、塩化ステアリルヒドロ
キシエチルベタインナトリウム等両性活性剤、感光素等
が挙げられる。Further, other antiseptic and fungicides other than parabens can be used in combination with the above antibacterial agent composition as long as they do not affect skin irritation, safety and usability. Examples of such preservatives include phenols such as isopropylmethylphenol, hinokitiol, and phenoxyethanol; benzoic acid and its salts; salicylic acid and its salts; dehydroacetic acid and its salts; sorbic acid and its salts; and acids such as benzalkonium chloride. And quaternary ammoniums such as benzethonium chloride and alkyltrimethylammonium chloride; amphoteric activators such as alkylaminoethylglycine hydrochloride and sodium stearylhydroxyethylbetaine chloride; and photosensitizers.
【0013】本発明における化粧料は、クリーム、乳
液、化粧水、美容液等の基礎化粧品、石鹸、洗顔料、シ
ャンプー、リンス等の清浄用化粧品、ヘアトニック、整
髪料等の頭髪用化粧品、ファンデーション、アイライナ
ー、マスカラ、口紅等のメイクアップ化粧品、歯磨き等
の口腔化粧品、浴用化粧品等に適用される。The cosmetics of the present invention include basic cosmetics such as creams, milky lotions, lotions, and essences; cleaning cosmetics such as soaps, facial cleansers, shampoos, and rinses; hair cosmetics such as hair tonics and hair styling products; , Eyeliner, mascara, lipstick, etc., cosmetics such as toothpaste, bath cosmetics, etc.
【0014】以下実施例及び比較例により、本発明をよ
り詳細に説明するが、本発明はこれらの実施例によって
限定されるものではない。Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
【0015】[製造例]クローブより水溶性成分の抽出 クローブの乾燥した花蕾150gに80%含水エタノー
ル300gを加え、常温にて24時間抽出し、減圧濾過
により抽出液を得た。抽出液に水600gを加えると非
水溶性成分が析出した。この溶液を遠心分離(10,000rp
m、10分間)により析出物を分離し、上澄液を採取
後、300gまで減圧濃縮した。更にこの濃縮液に、水
を600g加え、300gになるまで減圧濃縮すること
により、水溶性成分のみを含むクローブ抽出液を得た。[Preparation Example] Extraction of water-soluble components from cloves 150 g of dried flower buds of clove were added with 300 g of 80% aqueous ethanol, extracted at normal temperature for 24 hours, and filtered to obtain an extract under reduced pressure. When 600 g of water was added to the extract, a water-insoluble component was precipitated. Centrifuge this solution (10,000 rp)
(10 minutes), the precipitate was separated, and the supernatant was collected and concentrated under reduced pressure to 300 g. Further, 600 g of water was added to this concentrated solution, and the mixture was concentrated under reduced pressure until the concentration became 300 g, thereby obtaining a clove extract containing only a water-soluble component.
【0016】[抗菌性評価方法] 下記A〜Eの試験菌株を使用した。 A:黄色ブドウ球菌(Staphylococcus aureus ATCC 653
8) B:大腸菌(Escherichia coli ATCC 8739) C:緑膿菌(Pseudomonas aeruginosa ATCC 9627) D:カンジダ酵母(Candida albicans ATCC 10231) E:黒麹カビ(Asperugillus niger ATCC 16404) 試料1gあたり、細菌(A〜C)は106個、真菌
(D、E)は105個を植菌し、37℃、及び25℃に
てそれぞれ培養して、接種直後、7日目、14日目、2
1日目、28日目の生菌数を測定し、下記基準で抗菌性
を評価した。[Method for evaluating antibacterial activity] The following test strains A to E were used. A: Staphylococcus aureus ATCC 653
8) B: Escherichia coli ATCC 8739 C: Pseudomonas aeruginosa ATCC 9627 D: Candida albicans ATCC 10231 E: Asperugillus niger ATCC 16404 Bacteria (A) per 1 g of sample To C) were inoculated with 10 6 fungi and the fungi (D and E) were inoculated with 10 5 and cultured at 37 ° C. and 25 ° C., respectively.
The viable cell count was measured on the 1st and 28th days, and the antibacterial property was evaluated based on the following criteria.
【0017】[抗菌性の評価基準] 細菌試料の場合:接種した細菌が、14日以内に初発菌
数の0.1%以下に減少し、残りの14日間でそれ以前
のレベルを維持、あるいはそれ以下に減少する。 真菌試料の場合:接種した真菌が、14日以内に初発菌
数の10%以下に減少し、残りの14日間でそれ以前の
レベルを維持、あるいはそれ以下に減少する。なお試験
結果は、合格したものを「○」、不合格のものを「×」
として表示した。[Evaluation Criteria for Antibacterial Activity] In the case of a bacterial sample: the inoculated bacteria decrease to 0.1% or less of the initial number of bacteria within 14 days, and maintain the level before that in the remaining 14 days, or It decreases below that. For fungal samples: the inoculated fungus decreases to less than 10% of the initial number of bacteria within 14 days and maintains or decreases to the previous level in the remaining 14 days. The test results are shown as "○" for those that passed and "X" for those that failed.
Displayed as
【0018】[実施例、比較例1〜4]<1>〜<10>の
各成分を混合して、第1表に示す組成におけるローショ
ンを作成した。尚、配合量は重量%であり、組成全体で
100重量%となるようにした。又、前述の評価方法、
評価基準にて、それぞれの抗菌性を評価した。[Examples and Comparative Examples 1 to 4] Each component of <1> to <10> was mixed to prepare a lotion having the composition shown in Table 1. The blending amount was% by weight, and the total composition was 100% by weight. Also, the evaluation method described above,
Each antibacterial property was evaluated based on the evaluation criteria.
【0019】[0019]
【表1】 [Table 1]
【0020】第1表の結果から、メチルパラベンとクロ
ーブ抽出液とグリセリンモノカプリル酸エステルとを併
用した実施例では、メチルパラベンの少ない配合量で全
ての試験菌株に対して良好な抗菌性を示した。一方、メ
チルパラベンのみを配合した比較例1ではグラム陽性細
菌である黄色ブドウ球菌、及びカンジダ酵母に対して判
定基準に不合格となった。またクローブ抽出液とグリセ
リンモノカプリル酸エステルのみを併用した比較例2で
は、グラム陰性細菌である緑膿菌と大腸菌に対して、メ
チルパラベンとクローブ抽出液のみを併用した比較例3
では、カンジダ酵母に対して、メチルパラベンとグリセ
リンモノカプリル酸エステルのみを併用した比較例4で
は黄色ブドウ球菌に対して判定基準に不合格となった。From the results shown in Table 1, in Examples in which methylparaben, clove extract and glycerin monocaprylate were used in combination, good antibacterial properties were exhibited against all the test strains with a small amount of methylparaben. On the other hand, in Comparative Example 1 in which only methylparaben was blended, the criterion was rejected for gram-positive bacteria S. aureus and Candida yeast. In Comparative Example 2 using only clove extract and glycerin monocaprylate, Comparative Example 3 using only methylparaben and clove extract against Pseudomonas aeruginosa and Escherichia coli, which are gram-negative bacteria.
In Comparative Example 4, in which only methylparaben and glycerin monocaprylate were used in combination for Candida yeast, the criterion was rejected for Staphylococcus aureus.
【0021】[0021]
【発明の効果】本発明の化粧料においては、パラベン類
の少なくとも1種と、クローブより抽出した水溶性成分
と、炭素数8〜12のモノグリセライドとを組み合わせ
て配合することにより、パラベン類の少ない配合量で皮
膚刺激等の問題点を解消しつつ、アルカリ性領域の化粧
料においても良好な抗菌性を有するものとなる。According to the cosmetic of the present invention, at least one kind of parabens, a water-soluble component extracted from clove, and a monoglyceride having 8 to 12 carbon atoms are combined and blended to reduce the amount of parabens. The amount of the compound eliminates problems such as skin irritation and has good antibacterial properties even in cosmetics in the alkaline region.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4C083 AA111 AA112 AB032 AC122 AC302 AC422 AC432 AC481 AC482 AD042 BB48 CC01 CC06 DD23 EE01 EE05 EE10 FF01 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4C083 AA111 AA112 AB032 AC122 AC302 AC422 AC432 AC481 AC482 AD042 BB48 CC01 CC06 DD23 EE01 EE05 EE10 FF01
Claims (2)
ローブより有機溶剤等で抽出して得られた抽出物より非
水溶性成分を分別後、脱臭、精製して得られた水溶性成
分0.001〜1重量%と、炭素数8〜12の脂肪酸モ
ノグリセライド0.01〜1重量%とが組み合わせてな
ることを特徴とする化粧用抗菌剤組成物。1. A water-soluble component obtained by separating at least one of parabens and a water-insoluble component from an extract obtained by extracting a clove with an organic solvent or the like, followed by deodorization and purification. 0.001 to 1% by weight and a fatty acid monoglyceride having 8 to 12 carbon atoms in a combination of 0.01 to 1% by weight.
Hが7〜12であることを特徴とする化粧料。2. A composition comprising the antibacterial agent composition according to claim 1 and
H is 7-12, The cosmetics characterized by the above-mentioned.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000257068A JP2002068924A (en) | 2000-08-28 | 2000-08-28 | Antimicrobial agent composition for cosmetic and cosmetic containing the same formulated therewith |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000257068A JP2002068924A (en) | 2000-08-28 | 2000-08-28 | Antimicrobial agent composition for cosmetic and cosmetic containing the same formulated therewith |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002068924A true JP2002068924A (en) | 2002-03-08 |
Family
ID=18745591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000257068A Pending JP2002068924A (en) | 2000-08-28 | 2000-08-28 | Antimicrobial agent composition for cosmetic and cosmetic containing the same formulated therewith |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002068924A (en) |
-
2000
- 2000-08-28 JP JP2000257068A patent/JP2002068924A/en active Pending
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