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JP4723738B2 - Deodorant - Google Patents
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JP4723738B2 - Deodorant - Google Patents

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Publication number
JP4723738B2
JP4723738B2 JP2001057137A JP2001057137A JP4723738B2 JP 4723738 B2 JP4723738 B2 JP 4723738B2 JP 2001057137 A JP2001057137 A JP 2001057137A JP 2001057137 A JP2001057137 A JP 2001057137A JP 4723738 B2 JP4723738 B2 JP 4723738B2
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Prior art keywords
glucuronidase
plant
extract
odor
deodorant
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JP2002255776A (en
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正勝 浜
俊一 秋葉
勝俊 荒
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Kao Corp
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Kao Corp
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Description

【0001】
【発明の属する技術分野】
本発明は、ヒトの不快な体臭の発生を抑制するデオドラント剤に関する。
【0002】
【従来の技術及び発明が解決しようとする課題】
ヒトの不快な体臭の防除技術には、制汗機能を有する素材による汗の制御技術、抗菌機能を有する素材による不快臭発生原因菌の増殖の制御技術、発生した不快な体臭を消臭する技術及び香りによるマスキング技術等がある。
【0003】
制汗技術としては比較的強い収斂作用を有するパラフェノールスルホン酸亜鉛やクエン酸、各種のアルミニウムやジルコニウム塩を用いて発汗を抑制する方法が考案され、抗菌技術としては体臭の原因物質を作り出す原因菌(皮膚常在菌を含む)の増殖を抑制する機能を有するトリクロ酸、塩化ベンザルコニウム、塩化ベンゼトニウム、塩酸クロルヘキシジン、ハロカルバン等の抗菌剤を用いて臭気の発生を抑制する方法が考案されている。
【0004】
また、消臭技術としては不快な体臭の原因物質の―つである低級脂肪酸を亜鉛華(酸化亜鉛)などにより金属塩に変えることでその特異的な臭気の発生を抑制する方法やフラボノイドやクロロフィルなど消臭効果を有する素材の配合が考案され、マスキング技術としては、香水やオーデコロンにより程度の弱い体臭をマスキングする方法等が考案されている。
【0005】
しかしながら、従来の制汗技術、消臭技術及びマスキング技術は、効果の持続性という点で充分でなく、また抗菌技術は不快臭の発生原因菌以外に皮膚常在菌をも殺菌することで皮膚の一次バリアー機能を低下させるおそれが示唆されている。
【0006】
本発明は、皮膚の常在菌を殺すことなく、不快な体臭を持続的に抑制できるデオドラント剤を提供することを目的とする。
【0007】
【課題を解決するための手段】
本発明者らは、ヒトの不快な体臭の原因の一つとされる揮発性ステロイド臭の原因物質であるアンドロステ16−エン類に着目し、その生成抑制について検討したところ、特定の植物及び菌類抽出物に優れたβ―グルクロニダーゼ阻害活性があり、皮膚常在菌を殺すことなくアンドロステ16−エン類に由来する不快な体臭の発生を抑制でき、デオドラント剤として有用であることを見出した。
【0008】
すなわち本発明は、オウゴン、ゴバイシ、クチナシ、シコン、シャクヤク、エンメイソウ、カミツレ、ツボクサ、コンフリー、アマチャ、カンゾウ、センブリ、冬虫夏草、チンピ、イラクサ及びハマメリスから選ばれる植物及び菌類又はその抽出物からなるデオドラント剤及びβ−グルクロニダーゼ阻害剤を提供するものである。
【0009】
【発明の実施の形態】
本発明のオウゴンはシソ科(Labiatae)のコガネバナScutellaria baicalensis Georgiの周皮を除いた根を、ゴバイシはウルシ科(Anacardiaceae)のヌルデRhus javanica L.の葉につくヌルデノシロアブラムシが寄生した虫えい(虫コブ)を、シコンはムラサキ科(Boraginaceae)のムラサキLithospermum erythrorhizon Siebold et Zuccariniの根を、シャクヤクはキンポウゲ科(Ranunculaceae)のシャクヤクPaeonia lactinora PALL.の根を、エンメイソウはシソ科(Labiatae)のヒキオコシIsodon japonicus Haraの茎葉を、アマチャはユキノシタ科(Saxifragaceae)のアマチャHydrandea serrata Seringe var. thunbergii Makinoの葉及び枝先を、チョウジはフトモモ科(Myrtaceae)のSyzygium aromaticum Merrill et Perryのつぼみを、カンゾウはマメ科(Leguminosae)のGlycyrrhiza uralensis Fischer, Glycyrrhiza glabra L.又はその他同属植物の根およびストロンを、センブリはリンドウ科(Gentianaceae)のセンブリSwertia japonica Makinoの開花期の全草を、チンピはミカン科(Rutaceae)ウンシュウミカンCitrus unshiu Markovich又はその他近縁植物の成熟した果皮をそれぞれ意味する。
【0010】
クチナシはアカネ科(Rubiaceae)のクチナシGardenia jasminoides Elliであり、主としてその花及び果実が用いられ、カミツレはキク科(Compositae)のMatricaria chamomilla L.であり、主としてその開花期の花弁が用いられ、ツボクサはセリ科(Umblliferae)のツボクサCentella asiatica (L. ) RUBANであり、主としてその全草が用いられ、コンフリーはムラサキ科(Boraginaceae)のヒレハリソウSymphytum officinale L.であり、主としてその葉及び根が用いられ、イラクサはイラクサ科(Urtiaceae)のイラクサ(U.thumbergiana)であり、主としてその全草が用いられ、ハマメリスはマンサク科(Hamamelidsceae)アメリカマンサクHamamelis virginianaであり、主としてその葉及び樹皮が用いられる。
冬虫夏草は、バッカクキン科(Clavicipitaceae)の菌が昆虫に寄生したキノコである。
【0011】
斯かる植物又はその抽出物は、β−グルクロニダーゼ阻害活性を有し、皮膚上でのアンドロステ16−エン類の生成を抑制する(後記実施例1)。ここで、アンドロステ16−エン類はヒトの体臭、主に腺臭の原因臭とされる揮発性ステロイドであり、グルクロン酸包合されて可溶性を増すことによって汗中に分泌され、皮膚に生息する細菌(アクネ菌(Propionibacterium acne)の代謝を介して生成される。従って、グルクロン酸包合された前駆物質の代謝に関わるβ−グルクロニダーゼを阻害すればアンドロステ16−エン類の生成が抑制され不快な体臭の発生を抑制できることから、デオドランド剤として有用である。
また、デオドラント剤としては、皮膚のバリヤー機能の維持に関与する皮膚常在菌に対して抗菌性、望ましくは殺菌性を示さないものが好ましいが、斯かる点においても上記植物及び菌類抽出物は皮膚常在菌を殺すことがなく有用性が高い(図1)。
尚、ここでいう殺菌性を示さないとは、Tween80を0.5%含むSCD培地に、被験物質を添加したものに皮膚常在菌を接種し、37℃、24時間反応後に、胞子形成菌(Bacillus subtilis)はコントロールに対し菌数が1/10以下に減少せず、通常細菌(Staphylococcus epidermidis)はコントロールに対し1/100以下に減少しないことをいう。
【0012】
本発明のデオドラント剤及びβ−グルクロニダーゼ阻害剤の有効成分である上記植物及び菌類は、その植物の全草又は葉、根、根茎、果実、種子、花及び菌類のうちの1以上をそのまま又は粉砕して用いる。また、本発明において抽出物とは、更にこれを常温又は加温下にて抽出するか又はソックスレー抽出器等の抽出器具を用いて抽出することにより得られる各種溶剤抽出液、その希釈液、その濃縮液又はその乾燥末を意味するものである。ここで抽出物は、2種以上の植物から得られた混合物であってもよい。
【0013】
抽出に用いる溶剤としては水;メタノール、エタノール、プロパノール、ブタノール等のアルコール類;プロピレングリコール、ブチレングリコール等の多価アルコール;アセトン、メチルエチルケトン等のケトン類;酢酸メチル、酢酸エチル等のエステル類;テトラヒドロフラン、ジエチルエーテル等の鎖状及び環状エーテル類;ジクロロメタン、クロロホルム、四塩化炭素等のハロゲン化水素類;ヘキサン、シクロヘキサン、石油エーテル等の炭化水素類;ベンゼン、トルエン等の芳香族炭化水素類;ポリエチレングリコール等のポリエーテル類;ピリジン類などが挙げられ、これらを単独又は混合物として用いることができる。
【0014】
また、液々分配等の技術により、上記抽出物から不活性な爽雑物を除去して用いることもでき、本発明においてはこのようなものを用いることが好ましい。これらは、必要により公知の方法で脱臭、脱色等の処理を施してから用いてもよい。
【0015】
当該植物及び菌類又はその抽出物は、本発明のデオドラント剤及びβ−グルクロニダーゼ阻害剤としてそのまま用いることもできるが、当該抽出物を希釈調製して又は濃縮若しくは凍結乾燥した後、粉末又はペースト状に調製して用いることもできる。
【0016】
本発明のデオドランド剤及びβ−グルクロニダーゼ阻害剤は、化粧料、外用医薬品又は医薬部外品等の製剤、例えばクリーム、乳液、ローション、パウダー、スプレー、スティック等として用いることができ、またいくつかの使用方法を併用することも可能である。
【0017】
化粧料、外用医薬品又は医薬部外品として用いる場合のデオドランド剤又はβ−グルクロニダーゼ阻害剤の含有量は、一般的に0.1〜20重量%とするのが好ましく、特に0.5〜10重量%とするのが好ましい。また、植物抽出物としての含有量は、一般的に固形分換算で0.0001〜10重量%とするのが好ましく、特に0.001〜5重量%とするのが好ましい。
【0018】
これらの化粧料、外用医薬品又は医薬部外品には、通常用いられる各種成分、例えば化粧料成分として一般的に使用される油分、界面活性剤、アルコール類、キレート剤、pH調整剤、防腐剤、増粘剤、色素類、香料等の他、紫外線吸収剤、美白剤、しわ改善剤、保湿剤、皮脂分泌抑制剤、柔軟剤、角質保護剤、薬効剤、酸化防止剤、溶剤等の成分を任意に組み合わせ配合して製剤化することができる。
【0019】
本発明のデオドランド剤及びβ−グルクロニダーゼ阻害剤は、足、腋、頭部、陰部等不快臭の発生しやすい箇所に局所的に適用することにより、不快臭の発生を制御することができる。斯かる場合の製剤の使用量は、有効成分の含有量により異なるが例えば液状製剤の場合皮膚面1cm2当たり1〜20mg、固形状の製剤の場合、同じく1〜50mgとするのが好ましい。
【0020】
【実施例】
植物及び菌類抽出物は、いずれも化粧品原料基準に適合した下記の市販品を使用した。
【0021】
【表1】

Figure 0004723738
【0022】
実施例1 β−グルクロニダーゼ阻害活性
0.1mol/L酢酸ナトリウム緩衝液(pH5.0)0.4mL、0.06%フェノールフタレイン−β−D−グルクロニドナトリウム0.4mL及び10%に希釈した植物抽出物0.1mLを試験管に入れ、37℃で予備加温する(Blankも同じ)。0.2%塩化ナトリウム溶液で250units/mLに希釈したβ−グルクロニダーゼ(和光純薬工業株式会社,ウシ肝臓製)を0.1mL入れ(Blankには入れない)、反応を開始する。37℃で正確に30分間加温し、5%トリクロロ酢酸溶液0.1mLを加え反応を停止する(Blankにも入れる)。Blankに0.2%塩化ナトリウム溶液で250units/mLに希釈したβ−グルクロニダーゼ(和光純薬工業株式会社,ウシ肝臓製)を0.1mL入れた後、0.2mol/lグリシン溶液(pH10.4)を3mL加え発色させる。吸収セル10mmを用い、540nmにおける吸光度をBlankを対照液として測定する。サンプル(10%に希釈した植物抽出物)の代わりに蒸留水0.1mを入れた物をコントロールとし、コントロールの吸光度とサンプルの吸光度から、下記式に基づきサンプル(1%植物抽出物)のβ−グルクロニダーゼ活性阻害率を計算した。
【0023】
β−グルクロニダーゼ活性阻害(%)=(1−(サンプルの吸光度/コントロールの吸光度))×100
【0024】
また、0.1%植物抽出物及び0.01%植物抽出物についても、それぞれ1%及び0.1%に希釈した植物抽出物をサンプルとし、1%植物抽出物と同様にβ−グルクロニダーゼ活性阻害率を測定した。結果を図2に示す。
【0025】
実施例2 臭い発生抑制効果
(1)β−グルクロニダーゼ処理による臭い発生の確認
滅菌処理した秤量ビンに、以下に示す方法により採取し、濾過滅菌した汗を5mL入れ、0.2%塩化ナトリウム溶液で900units/mLに希釈したβ−グルクロニダーゼ(和光純薬工業株式会社,ウシ肝臓製)を0.5mL入れ(対照は0.2%塩化ナトリウム溶液0.5mL入れた)37℃で24時間インキュベートし、官能評価をした。結果を図3に示す。
【0026】
(汗の採取法)
一般男性26人の脇の下を、蒸留水1.5mLを湿らせた脱脂綿で拭き取った。
脱脂綿を絞り、回収した物(50mL)を0.45μmのフィルターで濾過した後、MILLIPOREのセントリプレップYM−10で濾過し、凍結乾燥をした。これに50mMクエン酸緩衝液(pH5.0)10mLを入れ汗とする。
【0027】
(2)臭い発生抑制効果
滅菌処理した秤量ビンに、以下に示す方法により採取し、濾過滅菌した汗を2mL、濾過滅菌した1%ハマメリスエキスを0.2mL入れ(対照は、蒸留水0.2mL入れ)、0.2% 塩化ナトリウム溶液で900units/mLに希釈したβ−グルクロニダーゼ(和光純薬工業株式会社,ウシ肝臓製)を0.2mL入れ37℃で24時間インキュベートし、官能評価をした。結果を図4に示す。
【0028】
(汗の採取法)
一般男性25人の脇の下を、蒸留水1.5mLを湿らせた脱脂綿で拭き取った。脱脂綿を絞り、回収した物(50mL)を0.45μmのフィルターで濾過した後、MILLIPOREのセントリプレップYM−10で濾過をし、凍結乾燥をした。これに50mMクエン酸緩衝液(pH5.0)10mLを入れ汗とした。
【0029】
【発明の効果】
本発明のデオドラント剤及びβ−グルクロニダーゼ阻害剤は、皮膚の常在菌を殺すことなく、不快な体臭の発生を持続的に抑制できることから、優れた消臭効果と高い安全性を有する化粧料、外用医薬品又は医薬部外品として有用である。
【図面の簡単な説明】
【図1】植物及び菌類抽出物の皮膚常在菌に対する影響を示す図である。
【図2】植物及び菌類抽出物のβ−グルクロニダーゼ活性阻害率を示す図である。
【図3】β−グルクロニダーゼによる汗臭の変化を示す図である。
【図4】β−グルクロニダーゼ阻害による汗臭生成抑制効果を示す図である。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a deodorant agent that suppresses the generation of unpleasant body odors in humans.
[0002]
[Prior art and problems to be solved by the invention]
Control technology for unpleasant human body odors includes sweat control technology using antiperspirant materials, control technology for the growth of germs causing unpleasant odors using antibacterial materials, and technology for deodorizing unpleasant body odors. And masking technology by fragrance.
[0003]
Antiperspirant technology has been devised to suppress sweating using zinc paraphenol sulfonate, citric acid, various aluminum and zirconium salts, which have a relatively strong astringent action, and antibacterial technology is the cause of creating substances that cause body odor A method has been devised to suppress the generation of odors using antibacterial agents such as trichloric acid, benzalkonium chloride, benzethonium chloride, chlorhexidine hydrochloride, and halocarban, which have the function of suppressing the growth of fungi (including skin resident bacteria). ing.
[0004]
In addition, as a deodorizing technique, a method for suppressing the generation of specific odors by changing lower fatty acids, which are one of the causes of unpleasant body odors, into metal salts with zinc white (zinc oxide), flavonoids and chlorophylls. As a masking technique, a method of masking a weak body odor with a perfume or a cologne has been devised.
[0005]
However, conventional antiperspirant technology, deodorant technology and masking technology are not sufficient in terms of sustainability of the effect, and antibacterial technology is effective by disinfecting skin resident bacteria in addition to the cause of unpleasant odor. There is a suggestion that the primary barrier function may be reduced.
[0006]
An object of this invention is to provide the deodorant agent which can suppress unpleasant body odor continuously without killing the resident bacteria of skin.
[0007]
[Means for Solving the Problems]
The present inventors focused on androste 16-enes, which are causative substances of volatile steroid odor, which is one of the causes of unpleasant body odors in humans. It has been found that the extract has an excellent β-glucuronidase inhibitory activity, can suppress the generation of unpleasant body odor derived from androste 16-enes without killing skin resident bacteria, and is useful as a deodorant agent.
[0008]
That is, the present invention is a deodorant comprising a plant and fungi or an extract thereof selected from the following: And a β-glucuronidase inhibitor are provided.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
Ougon of the present invention is the root of the Labiatae Scutellaria baicalensis Georgi excluding the pericy, and Gobaishi is an insect parasite of the aphids of the aphids on the leaves of the Nurde Rhus javanica L. of the Anacardiaceae ( Insects are the roots of Lithospermum erythrorhizon Siebold et Zuccarini in Boraginaceae, peonies are the roots of Ranunculaceae, and the roots of Paeonia lactinora PALL. japonicus Hara stems and leaves, saxifragaceae armchairs Hydrandea serrata Seringe var. thunbergii Makino leaves and branch tips, clove is myrtaceae Syzygium aromaticum Merrill et Perry buds, legumes legumes (Leguminosae) Glycyrrhiza uralensis Fischer, Glycyrrhiza glabra L. or other genus plants Ron, assembly is the whole plant of the flowering stage of assembly Swertia japonica Makino of gentianaceae (Gentianaceae), citrus unshiu peel means Rutaceae (Rutaceae) of satsuma mandarin Citrus unshiu Markovich, or other closely related plants mature pericarp, respectively.
[0010]
Gardenia jasminoides Elli (Rubiaceae) is mainly used for its flowers and fruits, and chamomile is Matricaria chamomilla L. (Compositae), mainly for its flowering petals. Is Umblliferae's Centella asiatica (L.) RUBAN, mainly using its whole plant, Comfrey is Boraginaceae's spinach Symphytum officinale L., mainly using its leaves and roots The nettle is the nettle (U. thumbergiana) of the Urtiaceae family, and its whole grass is mainly used, and the Hamelis is the American seaweed Hamamelis virginiana, mainly using its leaves and bark.
Cordyceps is a mushroom infested with insects of the Clavicipitaceae family.
[0011]
Such a plant or an extract thereof has β-glucuronidase inhibitory activity, and suppresses the production of androste 16-enes on the skin (Example 1 described later). Here, Androste 16-enes are volatile steroids that are the cause of human body odor, mainly glandular odor, and are secreted into sweat by glucuronic acid inclusion and increase in solubility, and inhabit the skin. Inhibiting β-glucuronidase, which is involved in the metabolism of glucuronic acid-encapsulated precursors, suppresses the production of androste 16-enes. Since it can suppress the generation of unpleasant body odor, it is useful as a deodorant agent.
Further, as the deodorant agent, those that do not exhibit antibacterial activity, desirably bactericidal properties against the skin resident bacteria involved in maintaining the barrier function of the skin are preferable, but also in this respect, the plant and fungal extracts are It is highly useful without killing skin resident bacteria (FIG. 1).
The term "not showing bactericidal properties" as used herein means that a resident bacterium is inoculated into an SCD medium containing 0.5% Tween 80, to which a test substance is added, and after reacting at 37 ° C for 24 hours, (Bacillus subtilis) means that the number of bacteria does not decrease to 1/10 or less of the control, and normal bacteria (Staphylococcus epidermidis) do not decrease to 1/100 or less of the control.
[0012]
The plant and fungi which are the active ingredients of the deodorant agent and β-glucuronidase inhibitor of the present invention are the whole plant or leaves, roots, rhizomes, fruits, seeds, flowers and fungi of the plant as it is or ground. And use. Further, in the present invention, the extract is further extracted at room temperature or under heating, or extracted by using an extractor such as a Soxhlet extractor, a dilute solution thereof, It means a concentrated liquid or its dry powder. Here, the extract may be a mixture obtained from two or more kinds of plants.
[0013]
As a solvent used for extraction, water; alcohols such as methanol, ethanol, propanol and butanol; polyhydric alcohols such as propylene glycol and butylene glycol; ketones such as acetone and methyl ethyl ketone; esters such as methyl acetate and ethyl acetate; tetrahydrofuran Linear and cyclic ethers such as diethyl ether; hydrogen halides such as dichloromethane, chloroform and carbon tetrachloride; hydrocarbons such as hexane, cyclohexane and petroleum ether; aromatic hydrocarbons such as benzene and toluene; polyethylene Polyethers such as glycol; pyridines and the like can be mentioned, and these can be used alone or as a mixture.
[0014]
In addition, it is possible to remove inactive contaminants from the extract by a technique such as liquid-liquid distribution, and it is preferable to use such an extract in the present invention. These may be used after performing treatments such as deodorization and decolorization by a known method if necessary.
[0015]
The plant and fungi or the extract thereof can be used as they are as the deodorant agent and β-glucuronidase inhibitor of the present invention, but after the extract is diluted, concentrated or freeze-dried, it is made into a powder or paste. It can also be prepared and used.
[0016]
The deodorant and β-glucuronidase inhibitor of the present invention can be used as a preparation such as a cosmetic, an external medicine or a quasi-drug, such as a cream, emulsion, lotion, powder, spray, stick, etc. It is also possible to use the methods in combination.
[0017]
When used as a cosmetic, topical medicine or quasi-drug, the content of deodorant or β-glucuronidase inhibitor is generally preferably 0.1 to 20% by weight, particularly 0.5 to 10% by weight. % Is preferable. Further, the content as a plant extract is generally preferably 0.0001 to 10% by weight, particularly preferably 0.001 to 5% by weight in terms of solid content.
[0018]
These cosmetics, external medicines or quasi drugs include various commonly used components such as oils, surfactants, alcohols, chelating agents, pH adjusters, preservatives commonly used as cosmetic ingredients. , UV absorbers, whitening agents, wrinkle improvers, moisturizers, sebum secretion inhibitors, softeners, keratin protective agents, medicinal agents, antioxidants, solvents, etc. Can be formulated in any combination.
[0019]
The deodorant agent and β-glucuronidase inhibitor of the present invention can control the generation of an unpleasant odor by applying them locally to a place where an unpleasant odor is likely to occur, such as a foot, a heel, a head, or a genital region. In such a case, the amount of the preparation to be used varies depending on the content of the active ingredient. For example, in the case of a liquid preparation, 1-20 mg per 1 cm 2 of the skin surface, and in the case of a solid preparation, it is preferably 1-50 mg.
[0020]
【Example】
As the plant and fungal extracts, the following commercial products conforming to the cosmetic raw material standards were used.
[0021]
[Table 1]
Figure 0004723738
[0022]
Example 1 β-glucuronidase inhibitory activity 0.1 mol / L sodium acetate buffer (pH 5.0) 0.4 mL, 0.06% phenolphthalein-β-D-glucuronide sodium 0.4 mL and a plant diluted to 10% Place 0.1 mL of extract in a test tube and pre-warm at 37 ° C. (same for Blank). 0.1 mL of β-glucuronidase (Wako Pure Chemical Industries, Ltd., manufactured by Bovine Liver) diluted to 250 units / mL with 0.2% sodium chloride solution is added (not added to Blank) to start the reaction. Warm exactly 30 minutes at 37 ° C., and stop the reaction by adding 0.1 mL of 5% trichloroacetic acid solution (also put into Blank). After adding 0.1 mL of β-glucuronidase (Wako Pure Chemical Industries, Ltd., manufactured by Bovine Liver) diluted to 250 units / mL with 0.2% sodium chloride solution in Blank, 0.2 mol / l glycine solution (pH 10.4) Add 3 mL) to develop color. Using an absorption cell of 10 mm, the absorbance at 540 nm is measured using Blank as a control solution. Instead of the sample (plant extract diluted to 10%), the one containing 0.1m of distilled water was used as a control. From the absorbance of the control and the absorbance of the sample, the β of the sample (1% plant extract) was calculated based on the following formula. -The glucuronidase activity inhibition rate was calculated.
[0023]
β-glucuronidase activity inhibition (%) = (1− (absorbance of sample / absorbance of control)) × 100
[0024]
In addition, with respect to 0.1% plant extract and 0.01% plant extract, the plant extract diluted to 1% and 0.1%, respectively, was used as a sample, and β-glucuronidase activity was obtained as in the case of 1% plant extract The inhibition rate was measured. The results are shown in FIG.
[0025]
Example 2 Odor Occurrence Suppressing Effect (1) Confirmation of Odor Occurrence by β-Glucuronidase Treatment Into a sterilized weighing bottle, 5 mL of sweat sterilized by filtration and sterilized by filtration is placed in a 0.2% sodium chloride solution. 0.5 mL of β-glucuronidase (Wako Pure Chemical Industries, manufactured by Bovine Liver) diluted to 900 units / mL was added (control was 0.5 mL of 0.2% sodium chloride solution) and incubated at 37 ° C. for 24 hours. Sensory evaluation was performed. The results are shown in FIG.
[0026]
(How to collect sweat)
The armpits of 26 ordinary men were wiped with absorbent cotton moistened with 1.5 mL of distilled water.
Absorbent cotton was squeezed, and the collected product (50 mL) was filtered through a 0.45 μm filter, then filtered through MILLIPORE Centriprep YM-10, and lyophilized. 10 mL of 50 mM citrate buffer (pH 5.0) is added to this to make sweat.
[0027]
(2) Odor generation suppression effect In a sterilized weighing bottle, 2 mL of sweat sterilized by filtration and 0.2 mL of 1% Hamamelis extract sterilized by filtration are added (control is 0.2 mL of distilled water). Put), 0.2 mL of β-glucuronidase (Wako Pure Chemical Industries, Ltd., manufactured by Bovine Liver) diluted to 900 units / mL with 0.2% sodium chloride solution was added and incubated at 37 ° C. for 24 hours for sensory evaluation. The results are shown in FIG.
[0028]
(How to collect sweat)
The armpits of 25 general men were wiped with absorbent cotton moistened with 1.5 mL of distilled water. Absorbent cotton was squeezed, and the collected product (50 mL) was filtered through a 0.45 μm filter, then filtered through MILLIPORE Centriprep YM-10, and lyophilized. To this was added 10 mL of 50 mM citrate buffer (pH 5.0) to make sweat.
[0029]
【The invention's effect】
Since the deodorant agent and β-glucuronidase inhibitor of the present invention can continuously suppress the generation of unpleasant body odor without killing resident bacteria of the skin, a cosmetic having an excellent deodorizing effect and high safety, It is useful as a topical medicine or quasi-drug.
[Brief description of the drawings]
FIG. 1 is a diagram showing the influence of plant and fungal extracts on skin resident bacteria.
FIG. 2 is a graph showing the β-glucuronidase activity inhibition rate of plant and fungal extracts.
FIG. 3 is a diagram showing changes in sweat odor caused by β-glucuronidase.
FIG. 4 is a diagram showing an effect of inhibiting sweat odor production by β-glucuronidase inhibition.

Claims (1)

クチナシ、ツボクサ、コンフリー、センブリ、冬虫夏草及びイラクサから選ばれる植物並びに菌類、又はそれらの抽出物からなるβ−グルクロニダーゼ阻害剤。 Gardenia, Tsu boxer, comfrey, Se Nburi, Cordyceps and Iraq Sa or al plants and fungi are selected, or consists of extracts β- glucuronidase inhibitor.
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