JP2000109417A - Cosmetic for improving somber color - Google Patents
Cosmetic for improving somber colorInfo
- Publication number
- JP2000109417A JP2000109417A JP10297640A JP29764098A JP2000109417A JP 2000109417 A JP2000109417 A JP 2000109417A JP 10297640 A JP10297640 A JP 10297640A JP 29764098 A JP29764098 A JP 29764098A JP 2000109417 A JP2000109417 A JP 2000109417A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- essence
- skin
- vitamin
- 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
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- 102000016387 Pancreatic elastase Human genes 0.000 claims abstract description 16
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- KJYGRYJZFWOECQ-UHFFFAOYSA-N [2-hydroxy-3-[2-hydroxy-3-[2-hydroxy-3-(16-methylheptadecanoyloxy)propoxy]propoxy]propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)COCC(O)COC(=O)CCCCCCCCCCCCCCC(C)C KJYGRYJZFWOECQ-UHFFFAOYSA-N 0.000 description 5
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- 235000010323 ascorbic acid Nutrition 0.000 description 4
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- 238000001816 cooling Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
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- 239000011719 vitamin A Substances 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 2
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- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 2
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- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
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- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- VFXZKNGPBLVKPC-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid;sodium Chemical compound [Na].OCCN1CCN(CCS(O)(=O)=O)CC1 VFXZKNGPBLVKPC-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
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Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、くすみ等の加齢変
化に伴うトラブルを改善するのに有用な化粧料等の皮膚
外用組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a composition for external use on the skin such as cosmetics which is useful for improving troubles associated with aging such as dullness.
【0002】[0002]
【従来の技術】肌の美しさは、年と共に変化するもので
あり、中年を過ぎると年と共にシワが増加したり、くす
みが増加したりして昔の美しさは面影もなくなってしま
う。この内、くすみは、その要因としてはメラニンの過
剰生産と皮膚の形態変化の相乗的な結果であると言われ
ている。この様な容貌の加齢変化に対しては人々は、古
来よりこの変化を少なくすべく努力を重ね、数々の技術
を開発してきた。この様な技術としては、レチノール、
レチノイン、ビタミンA酸等のビタミンA類によるシワ
とり技術、燐酸アスコルビン酸マグネシウムなどによる
光ダメージの緩和技術、アミノエチル化合物、ユキノシ
タ科の植物の抽出物等によるコラーゲン架橋抑制剤を用
いた、コラーゲン線維の弾性消失抑制などの技術が挙げ
られる。しかしながら、これらの技術は確かにそこそこ
の効果はあるものの、十分に満足のいくものではなく、
加えてビタミンA類等の場合には過剰症などの好ましく
ない作用などが発現する場合があり、使用量も限られる
欠点があった。即ち、更なる、優れたくすみ改善作用を
有し、かかる加齢変化を抑制する組成物の開発が望まれ
ていた。2. Description of the Related Art The beauty of the skin changes with the age. After the middle age, wrinkles increase and dullness increases with the age, and the beauty of the past disappears. Among them, dullness is said to be a synergistic result of overproduction of melanin and morphological change of skin. In response to such age-related changes in appearance, people have been striving to reduce this change since ancient times and have developed various technologies. Such technologies include retinol,
Wrinkle removal technology using vitamin A such as retinoin and vitamin A acid, light damage mitigation technology using magnesium phosphate ascorbate, collagen fiber using collagen cross-linking inhibitor using aminoethyl compounds, extracts of plants of the family Saxifragaceae, etc. For suppressing the disappearance of elasticity. However, although these techniques do work, they are not quite satisfactory,
In addition, in the case of vitamins A and the like, undesired effects such as excessive symptoms may be exhibited, and the amount of vitamin A used is limited. That is, the development of a composition that has a further excellent dullness-improving effect and suppresses such aging changes has been desired.
【0003】一方、皮膚外用剤に於いて、エラスターゼ
活性抑制剤とメラニン生成抑制剤とを含有させることは
全く知られておらず、更に、この様な成分を含む皮膚外
用剤が優れた整肌作用を有し、加齢変化に対して有効で
あることも全く知られていなかった。On the other hand, it has not been known at all that skin external preparations contain an elastase activity inhibitor and a melanin production inhibitor, and further, a skin external preparation containing such components is excellent in skin conditioning. It had no effect, nor was it known to be effective against age-related changes.
【0004】[0004]
【発明が解決しようとする課題】本発明は、この様な状
況下為されたものであり、優れたくすみ改善作用を有
し、加齢変化に対して有効である、化粧料などの皮膚外
用組成物を提供することを課題とする。SUMMARY OF THE INVENTION The present invention has been made under such circumstances, and has an excellent dullness-improving effect and is effective against aging. It is an object to provide a composition.
【0005】[0005]
【課題の解決手段】本発明者らは、この様な状況に鑑み
て、優れた整肌作用を有し、加齢変化に対して有効であ
る、化粧料などの皮膚外用剤を求めて鋭意研究努力を重
ねた結果、エラスターゼ活性抑制剤とメラニン生成抑制
剤とを含有する皮膚外用剤にこの様な作用を見出し、発
明を完成させるに至った。以下、本発明について、実施
の形態を中心に詳細に説明を加える。In view of such circumstances, the present inventors have sought to provide a skin external preparation such as a cosmetic, which has an excellent skin conditioning effect and is effective against aging. As a result of repeated research efforts, they have found such an effect in an external preparation for skin containing an elastase activity inhibitor and a melanin production inhibitor, and have completed the invention. Hereinafter, the present invention will be described in detail focusing on embodiments.
【0006】[0006]
【発明の実施の形態】(1)本発明の必須成分であるエ
ラスターゼ活性阻害剤 本発明の皮膚外用組成物はエラスターゼ活性阻害剤を必
須成分とする。本発明で言うエラスターゼ活性阻害剤と
は、基質液として2mMエラスターゼサブストレイト、
0.1M HEPES含有0.5M塩化ナトリウム緩衝
液(pH7.5)を0.1ml用い、酵素液としてヒト
・リューコサイト・エラスターゼ(シグマ社製、1ユニ
ット)を50mlのHEPES塩化ナトリウム緩衝液
(pH7.5)に溶かしたものを1.8ml用い、これ
に0.1mlの検体を加え、室温で1時間放置後エラス
ターゼ活性を405nmの吸光度として測定する試験系
に於いて、エラスターゼ阻害発現濃度が0.05%以下
であり、且つ、50%阻止濃度が0.5%以下である物
質群を意味し、この様なものとしては、例えば阻害発現
濃度が0.01%であり、50%阻止濃度が0.1%で
ある大豆蛋白(エルヒビン;ペンタファーム社製)や阻
害発現濃度が0.001%であり、50%阻止濃度が
0.01%であるコウキのエッセンスであるコウキ抽出
液BG(コウキの葉の1,3−ブタンジオール抽出液;
丸善製薬製)等が好ましく例示できる。尚、本発明で言
うエッセンスとは、植物体それ自身、植物体を乾燥、粉
砕などした加工物、植物体やその加工物にアルコール
類、エステル類、ハロゲン化炭化水素類、多価アルコー
ル類、ケトン類、水等の溶媒を加え抽出をした抽出物、
抽出物より溶媒を除去した抽出物の溶媒除去物、これを
分画した分画物の総称である。本発明の皮膚外用組成物
では、これらエラスターゼ活性阻害剤をただ一種或いは
数種を組み合わせて含有させることが出来る。本発明の
皮膚外用組成物に於ける、これらエラスターゼ活性阻害
剤の好ましい含有量は、0.01〜10重量%であり、
更に好ましくは0.05〜5重量%である。DESCRIPTION OF THE PREFERRED EMBODIMENTS (1) Elastase activity inhibitor which is an essential component of the present invention The external composition for skin of the present invention contains an elastase activity inhibitor as an essential component. The elastase activity inhibitor referred to in the present invention is 2 mM elastase substrate as a substrate solution,
0.1 ml of a 0.5 M sodium chloride buffer (pH 7.5) containing 0.1 M HEPES was used, and 50 ml of a human leucocyte elastase (Sigma, 1 unit) was used as an enzyme solution in a 50 ml HEPES sodium chloride buffer (pH 7). 1.8 ml of the solution dissolved in .5), 0.1 ml of the sample was added thereto, and after standing at room temperature for 1 hour, elastase activity was measured as an absorbance at 405 nm. 0.05% or less and a 50% inhibitory concentration of 0.5% or less, such as an inhibitory expression concentration of 0.01% and a 50% inhibitory concentration. Is 0.1% soybean protein (Elhibin; manufactured by Pentafarm Co., Ltd.) and Kouki having an inhibitory expression concentration of 0.001% and a 50% inhibitory concentration of 0.01% Kouki Extract BG (1,3-butanediol extract of leaves of Kouki;
(Maruzen Pharmaceutical Co., Ltd.) can be preferably exemplified. The essence referred to in the present invention is a plant itself, a processed product obtained by drying and pulverizing the plant, an alcohol, an ester, a halogenated hydrocarbon, a polyhydric alcohol, Extracts obtained by adding solvents such as ketones and water,
This is a generic term for the solvent-extracted product of the extract obtained by removing the solvent from the extract, and the fractionated product thereof. In the external composition for skin of the present invention, these elastase activity inhibitors can be contained alone or in combination of several kinds. The preferred content of these elastase activity inhibitors in the skin external composition of the present invention is 0.01 to 10% by weight,
More preferably, it is 0.05 to 5% by weight.
【0007】(2)本発明の必須成分であるメラニン産
生抑制剤 本発明で言うメラニン産生抑制剤とは、大きな細胞毒性
を有さず、メラニンの産生を抑制する物質のことを意味
し、好ましくは、メラノーマB16細胞を用いたスクリ
ーニングに於いて、検体の濃度が終濃度で0.1%以下
に於いて、対照と有意差がない程度に細胞毒性が低く、
有意にメラニンの産生を抑制する物質を意味する。この
様な物質としては、例えば、アルブチン、配糖体、塩な
どのその誘導体、ビタミンC、エステル、エーテル、配
糖体、塩等のその誘導体、ロイヤルゼリーのエッセンス
及びソウハクヒのエッセンス、シラカバのエッセンス、
タンニン、レゾルシン等のフェノール性物質とその誘導
体等が例示できる。これらの内、特に好ましいものは、
アルブチン、ビタミンC、ビタミンCの誘導体、ロイヤ
ルゼリーのエッセンス及びソウハクヒのエッセンスから
選ばれる1種乃至は2種以上である。これは、この様な
物質が、特にくすみなどに関与するメラニン産生を良く
抑制するからである。本発明の皮膚外用組成物に於け
る、メラニン産生抑制剤の好ましい含有量は、0.01
〜10重量%であり、更に好ましくは0.05〜5重量
%である。(2) Melanin production inhibitor which is an essential component of the present invention The melanin production inhibitor referred to in the present invention means a substance which has no significant cytotoxicity and suppresses the production of melanin. Shows that in screening using melanoma B16 cells, when the concentration of the sample is 0.1% or less in final concentration, the cytotoxicity is so low that it is not significantly different from the control,
It means a substance that significantly suppresses the production of melanin. Such substances include, for example, derivatives thereof such as arbutin, glycosides and salts, derivatives thereof such as vitamin C, esters, ethers, glycosides and salts, essence of royal jelly and essence of soybean, and essence of birch ,
Examples thereof include phenolic substances such as tannin and resorcin and derivatives thereof. Of these, particularly preferred are:
One or more selected from arbutin, vitamin C, a derivative of vitamin C, royal jelly essence and soybean essence. This is because such a substance well suppresses the production of melanin, which is particularly involved in dullness and the like. In the skin external composition of the present invention, the preferred content of the melanin production inhibitor is 0.01
10 to 10% by weight, more preferably 0.05 to 5% by weight.
【0008】(3)本発明の皮膚外用組成物 本発明の皮膚外用組成物は、上記エラスターゼ活性阻害
剤とメラニン産生抑制剤とを含有することを特徴とす
る。本発明の皮膚外用組成物としては、化粧料や抗真菌
剤、抗炎症剤、ステロイド剤等の皮膚外用医薬等が例示
でき、この中では化粧料に適用するのが特に好ましく、
中でも柔軟性の低下のような加齢変化による皮膚の変化
を抑制し、老化によるくすみを改善し、肌をくすみなく
美しく保つことが出来ることから、くすみの改善と悪化
の抑制を目指した、くすみ用の化粧料として用いるのが
特に好ましい。本発明の皮膚外用組成物では、上記必須
成分以外に通常皮膚外用組成物で使用される任意成分を
含有することが出来る。かかる任意成分としては、例え
ば、ワセリンやマイクロクリスタリンワックス等のよう
な炭化水素類、ホホバ油やゲイロウ等のエステル類、牛
脂、オリーブ油等のトリグリセライド類、セタノール、
オレイルアルコール等の高級アルコール類、ステアリン
酸、オレイン酸等の脂肪酸、グリセリンや1,3−ブタ
ンジオール等の多価アルコール類、非イオン界面活性
剤、アニオン界面活性剤、カチオン界面活性剤、両性界
面活性剤、エタノール、カーボポール等の増粘剤、防腐
剤、紫外線吸収剤、抗酸化剤、色素、粉体類等が好まし
く例示できる。これら任意成分の中で特に好ましいもの
は、プラセンターエキス、ローヤルゼリー、グリコーゲ
ン等の細胞を賦活する作用を有する物質や硫酸化アルギ
ン酸とその生理的に許容される塩やバクガの根部のエッ
センス等のコラーゲン合成を促進する成分、或いは、ミ
ントのエッセンス、セージのエッセンス、ローズマリー
のエッセンス、ジンセンのエッセンス、オウゴンのエッ
センス等の過酸化物生成抑制剤である。これら細胞賦活
成分やコラーゲン合成促進剤、過酸化物生成抑制剤はそ
れぞれ総量で0.01〜1重量%程度含有することが好
ましい。これらの成分を常法に従って処理することによ
り、本発明の皮膚外用組成物を製造することが出来る。(3) The composition for external use of the skin of the present invention The composition for external use of the skin of the present invention is characterized by containing the above elastase activity inhibitor and melanin production inhibitor. Examples of the composition for external use of the skin of the present invention include cosmetics and antifungal agents, anti-inflammatory agents, external dermatological drugs such as steroid agents, and among them, it is particularly preferable to apply the composition to cosmetics.
Above all, because it can suppress skin changes due to aging changes such as loss of flexibility, improve dullness due to aging, and keep skin beautiful without dullness, dullness aimed at improving dullness and suppressing deterioration It is particularly preferable to use as cosmetics for cosmetics. The composition for external use on the skin of the present invention may contain, in addition to the above essential components, optional components usually used in the composition for external use on the skin. Such optional components include, for example, hydrocarbons such as petrolatum and microcrystalline wax, esters such as jojoba oil and gay wax, tallow, triglycerides such as olive oil, cetanol,
Higher alcohols such as oleyl alcohol, fatty acids such as stearic acid and oleic acid, polyhydric alcohols such as glycerin and 1,3-butanediol, nonionic surfactants, anionic surfactants, cationic surfactants and amphoteric interfaces Activators, thickeners such as ethanol and carbopol, preservatives, ultraviolet absorbers, antioxidants, pigments, powders and the like can be preferably exemplified. Among these optional components, particularly preferred are substances such as placenta extract, royal jelly, glycogen and the like which activate cells, sulfated alginic acid and physiologically acceptable salts thereof, and collagen such as essence of the root of Bacuga. It is a component that promotes synthesis, or a peroxide generation inhibitor such as mint essence, sage essence, rosemary essence, ginseng essence, and gougon essence. These cell activating components, collagen synthesis promoters, and peroxide production inhibitors are preferably contained in a total amount of about 0.01 to 1% by weight. By treating these components according to a conventional method, the composition for external use on skin of the present invention can be produced.
【0009】[0009]
【実施例】以下に、実施例を挙げて本発明について更に
詳細に説明を加えるが、本発明がこれら実施例にのみ限
定を受けないことは言うまでもない。EXAMPLES Hereinafter, the present invention will be described in more detail with reference to Examples, but it goes without saying that the present invention is not limited to only these Examples.
【0010】<実施例1〜6>下記に示す処方に従っ
て、化粧水を作成した。即ち、処方成分を室温で攪拌
し、可溶化して化粧水を得た。 1,3−ブタンジオール 5 重量部 グリセリン 3 重量部 エタノール 10 重量部 メラニン生成抑制剤* 1 重量部 エラスターゼ活性阻害剤* 1 重量部 メチルパラベン 0.2重量部 POE(60)硬化ひまし油 0.1重量部 水 79.7重量部 *詳細は表1に記載<Examples 1 to 6> Lotions were prepared according to the following formulations. That is, the ingredients were stirred at room temperature and solubilized to obtain a lotion. 1,3-butanediol 5 parts by weight Glycerin 3 parts by weight Ethanol 10 parts by weight Melanin production inhibitor * 1 part by weight Elastase activity inhibitor * 1 part by weight Methyl paraben 0.2 part by weight POE (60) hardened castor oil 0.1 part by weight 79.7 parts by weight of water * See Table 1 for details
【0011】[0011]
【表1】 [Table 1]
【0012】<実施例7>茶色モルモット(30週齢)
を用いたくすみモデルを用いて、実施例1〜6の化粧水
のくすみ改善を調べた。即ち、茶色モルモット1群3匹
の背部を剃毛し、これに0.5×MED(最小紅斑濃
度)の紫外線を5日間あててくすみモデルを作成した。
このものの背部2cm×2cmの投与部位を設け、検体
を0.01ml/回/日、これを5回/週で8週間投与
した。比較例1として、実施例1のエルヒビンを水に置
換したもの、比較例2として、実施例1のソウハクヒの
エッセンスを水に置換したもの、比較例3として、実施
例2のソウハクヒのエッセンスを水に置換したもの、比
較例4として実施例3のエルヒビンを水に置換したも
の、比較例5として実施例5のエルヒビンを水に置換し
たものを用いた。又、対照例は実施例1のエルヒビンと
ソウハクヒのエッセンスを水に置換したものを用いた。
くすみ改善効果は、最後の投与の24時間後に対照群の
平均のくすみ具合と比較して、++:著しく改善、+:
明らかに改善、±:僅かに改善、−:改善せずの基準で
各動物毎に判定した。結果を出現例数として、表2に示
す。これより、本発明の皮膚外用組成物である、化粧水
はくすみを改善する効果に優れることがわかる。<Example 7> Brown guinea pig (30 weeks old)
The dullness improvement of the lotions of Examples 1 to 6 was examined using a dullness model using. That is, the back of a group of three brown guinea pigs was shaved and exposed to ultraviolet rays of 0.5 × MED (minimum erythema concentration) for 5 days to prepare a dull model.
An administration site of 2 cm × 2 cm on the back was provided, and the sample was administered at 0.01 ml / time / day, 5 times / week for 8 weeks. Comparative Example 1 was obtained by substituting erhibin of Example 1 with water, Comparative Example 2 was obtained by substituting the essence of Sohakuhumi of Example 1 with water, and Comparative Example 3 was obtained by replacing the essence of Souhakuhhi of Example 2 with water. Comparative Example 4 was obtained by replacing erhibin of Example 3 with water, and Comparative Example 5 was obtained by replacing erhibin of Example 5 with water. In the control example, the essence of Elhibin and Sour pork in Example 1 was replaced with water.
The effect of improving dullness was as follows: 24 hours after the last administration, ++: markedly improved, +:
Clear improvement, ±: slight improvement,-: judgment was made for each animal on the basis of no improvement. Table 2 shows the results as the number of appearance cases. This shows that the lotion, which is a composition for external use on the skin of the present invention, has an excellent effect of improving dullness.
【0013】[0013]
【表2】 [Table 2]
【0014】<実施例8>下記に示す処方に従って、化
粧水を作成した。即ち、処方成分を室温で攪拌し、可溶
化して化粧水を得た。 1,3−ブタンジオール 5 重量部 グリセリン 3 重量部 エタノール 10 重量部 硫酸化アルギン酸ナトリウム 0.1重量部 バクガコンのエッセンス 0.1重量部 エルヒビン 0.5重量部 コウキ抽出物BG 0.5重量部 プラセンターエキス 0.1重量部 ソウハクヒのエッセンス 0.5重量部 グリコーゲン 0.1重量部 ローヤルゼリー 0.5重量部 メチルパラベン 0.2重量部 POE(60)硬化ひまし油 0.1重量部 オウゴンのエッセンス 0.1重量部 ジンセンのエッセンス 0.1重量部 シラカバのエッセンス 0.1重量部 水 79 重量部Example 8 A lotion was prepared according to the following formulation. That is, the ingredients were stirred at room temperature and solubilized to obtain a lotion. 1,3-butanediol 5 parts by weight Glycerin 3 parts by weight Ethanol 10 parts by weight Sulfated sodium alginate 0.1 part by weight Bakgacon essence 0.1 parts by weight Elhibin 0.5 parts by weight Kouki extract BG 0.5 parts by weight Plastic Center extract 0.1 parts by weight Sour bean essence 0.5 parts by weight Glycogen 0.1 parts by weight Royal jelly 0.5 parts by weight Methyl paraben 0.2 parts by weight POE (60) hardened castor oil 0.1 parts by weight Parts by weight Ginseng essence 0.1 parts by weight Birch essence 0.1 parts by weight Water 79 parts by weight
【0015】<実施例9>50歳以上の女性であって、
肌のくすみに悩むパネラー1群10名、計30名を集
め、上記実施例6の化粧水、実施例8の化粧水のソウハ
クヒのエッセンスとローヤルゼリーを水に置換した比較
例6の化粧水、実施例8の化粧水のエルヒビンとコウキ
抽出物BGを水に置換した比較例7について、そのくす
み改善作用を評価してもらった。これらの化粧水は1日
朝・晩2回、8週間使用してもらい、肌のくすみの改善
を、++:著しい改善、+:明らかな改善、±:僅かな
改善、−:改善せずの基準で評価してもらった。結果を
表3に出現例数とした示す。これより、本発明の化粧料
は、加齢変化によってくすみが蓄積した肌に、そのくす
み改善作用によって、くすみを改善し、健康な肌とする
作用に優れることがわかる。<Example 9> A woman over 50 years old,
A total of 30 panelists, a group of panelists suffering from dull skin, gathered a total of 30 persons, and applied the lotion of Comparative Example 6 in which the essence of Souhakuh and the royal jelly of the lotion of Example 6 and Example 8 were replaced with water. Comparative Example 7 in which Elhibin and Kouki Extract BG in Example 8 were replaced with water was evaluated for its dullness-improving effect. These lotions are used twice a day, morning and evening for 8 weeks, and the improvement of dullness of the skin is ++: marked improvement, +: obvious improvement, ±: slight improvement,-: standard without improvement I was evaluated. The results are shown in Table 3 as the number of appearance cases. This shows that the cosmetics of the present invention are excellent in the effect of improving dullness and making the skin healthy by improving the dullness on the skin in which dullness has accumulated due to aging changes.
【0016】[0016]
【表3】 [Table 3]
【0017】<実施例10>下記に示す処方に従って、
クリームを作成した。即ち、イ、ロ、ハ、ニのそれぞれ
の成分を70℃に加熱し、イとロを混合し、良く混練り
し、これをハを加えて希釈し、これにニを徐々に加え乳
化し、攪拌冷却し、クリームを得た。 イ 70%マルチトース水溶液 5 重量部 グリセリン 3 重量部 1,3−ブタンジオール 5 重量部 メチルパラベン 0.2重量部 ロ トリグリセリンジイソステアレート 4 重量部 ソルビタンセスキオレート 0.5重量部 ハ 軽質イソパラフィン 10 重量部 流動パラフィン 10 重量部 グリセリルトリイソオクタネート 5 重量部 ニ 水 55.3重量部 硫酸化アルギン酸ナトリウム 0.1重量部 バクガコンのエッセンス 0.1重量部 エルヒビン 0.5重量部 コウキ抽出物BG 0.1重量部 プラセンターエキス 0.1重量部 グリコーゲン 0.1重量部 ローヤルゼリー 0.5重量部 ジンセンのエッセンス 0.1重量部 オウゴンのエッセンス 0.1重量部 シラカバのエッセンス 0.1重量部 ソウハクヒのエッセンス 0.1重量部 アルブチン 0.1重量部Example 10 According to the following formulation,
A cream was made. That is, each of the components (a), (b), (c), and (d) are heated to 70 ° C., (a) and (b) are mixed, kneaded well, and the mixture is diluted by adding (c), and gradually added and emulsified. After stirring and cooling, a cream was obtained. A 70% maltose aqueous solution 5 parts by weight Glycerin 3 parts by weight 1,3-butanediol 5 parts by weight Methyl paraben 0.2 parts by weight b Triglycerin diisostearate 4 parts by weight Sorbitan sesquiolate 0.5 parts by weight C Light isoparaffin 10 parts by weight Liquid paraffin 10 parts by weight Glyceryl triisooctanoate 5 parts by weight D water 55.3 parts by weight Sulfated sodium alginate 0.1 part by weight Essence of bacgacone 0.1 part by weight Elhibin 0.5 part by weight Kouki extract BG 0. 1 part by weight Placenta extract 0.1 part by weight Glycogen 0.1 part by weight Royal jelly 0.5 part by weight Ginseng essence 0.1 part by weight Ougon essence 0.1 part by weight Birch essence 0.1 part by weight Sohakuhi essence 0.1 parts by weight Butyne 0.1 part by weight
【0018】<実施例11>下記に示す処方に従って、
クリームを作成した。即ち、イ、ロ、ハ、ニのそれぞれ
の成分を70℃に加熱し、イとロを混合し、良く混練り
し、これをハを加えて希釈し、これにニを徐々に加え乳
化し、攪拌冷却し、クリームを得た。 イ 70%マルチトース水溶液 5 重量部 グリセリン 3 重量部 1,3−ブタンジオール 5 重量部 メチルパラベン 0.2重量部 ロ トリグリセリンジイソステアレート 4 重量部 ソルビタンセスキオレート 0.5重量部 ハ 軽質イソパラフィン 10 重量部 流動パラフィン 10 重量部 グリセリルトリイソオクタネート 5 重量部 ニ 水 56.1重量部 硫酸化アルギン酸ナトリウム 0.1重量部 バクガコンのエッセンス 0.1重量部 エルヒビン 0.1重量部 コウキ抽出物BG 0.1重量部 プラセンターエキス 0.1重量部 グリコーゲン 0.1重量部 ローヤルゼリー 0.1重量部 ジンセンのエッセンス 0.1重量部 オウゴンのエッセンス 0.1重量部 シラカバのエッセンス 0.1重量部 アスコルビン酸燐酸マグネシウム 0.1重量部 アルブチン 0.1重量部<Example 11> According to the following formulation,
A cream was made. That is, each of the components (a), (b), (c), and (d) are heated to 70 ° C., (a) and (b) are mixed, kneaded well, and the mixture is diluted by adding (c), and gradually added and emulsified. After stirring and cooling, a cream was obtained. A 70% maltose aqueous solution 5 parts by weight Glycerin 3 parts by weight 1,3-butanediol 5 parts by weight Methyl paraben 0.2 parts by weight b Triglycerin diisostearate 4 parts by weight Sorbitan sesquiolate 0.5 parts by weight C Light isoparaffin 10 parts by weight Liquid paraffin 10 parts by weight Glyceryl triisooctate 5 parts by weight D. water 56.1 parts by weight Sulfated sodium alginate 0.1 part by weight Bacgacone essence 0.1 part by weight Elhibin 0.1 part by weight Kouki extract BG 0. 1 part by weight Placenta extract 0.1 part by weight Glycogen 0.1 part by weight Royal jelly 0.1 part by weight Ginseng essence 0.1 part by weight Ougon essence 0.1 part by weight Birch essence 0.1 part by weight ascorbic acid phosphoric acid Magnesium 0.1 weight Amount 0.1 parts by weight of arbutin
【0019】<実施例12>下記に示す処方に従って、
皮膚外用医薬である抗炎症用クリームを作成した。即
ち、イ、ロ、ハ、ニのそれぞれの成分を70℃に加熱
し、イとロを混合し、良く混練りし、これをハを加えて
希釈し、これにニを徐々に加え乳化し、攪拌冷却し、ク
リームを得た。 イ 70%マルチトース水溶液 5 重量部 グリセリン 3 重量部 1,3−ブタンジオール 5 重量部 メチルパラベン 0.2重量部 インドメタシン 1 重量部 ロ トリグリセリンジイソステアレート 4 重量部 ソルビタンセスキオレート 0.5重量部 ハ 軽質イソパラフィン 10 重量部 流動パラフィン 10 重量部 グリセリルトリイソオクタネート 5 重量部 ニ 水 57.1重量部 硫酸化アルギン酸ナトリウム 0.1重量部 バクガコンのエッセンス 0.1重量部 エルヒビン 0.1重量部 コウキ抽出物BG 0.1重量部 プラセンターエキス 0.1重量部 グリコーゲン 0.1重量部 ローヤルゼリー 0.1重量部 ジンセンのエッセンス 0.1重量部 オウゴンのエッセンス 0.1重量部 シラカバのエッセンス 0.1重量部 アスコルビン酸燐酸マグネシウム 0.1重量部 アルブチン 0.1重量部Example 12 According to the following formulation,
An anti-inflammatory cream, a skin external medicine, was prepared. That is, each of the components (a), (b), (c), and (d) are heated to 70 ° C., (a) and (b) are mixed, kneaded well, and the mixture is diluted by adding (c), and gradually added and emulsified. After stirring and cooling, a cream was obtained. A 70% maltose aqueous solution 5 parts by weight Glycerin 3 parts by weight 1,3-butanediol 5 parts by weight Methyl paraben 0.2 parts by weight Indomethacin 1 part by weight b Triglycerin diisostearate 4 parts by weight Sorbitan sesquiolate 0.5 parts by weight C Light isoparaffin 10 parts by weight Liquid paraffin 10 parts by weight Glyceryl triisooctanoate 5 parts by weight D. water 57.1 parts by weight Sulfated sodium alginate 0.1 part by weight Bacgacone essence 0.1 parts by weight Elhibin 0.1 parts by weight Kouki extraction Material BG 0.1 part by weight Placenta extract 0.1 part by weight Glycogen 0.1 part by weight Royal jelly 0.1 part by weight Ginseng essence 0.1 part by weight Ougon essence 0.1 part by weight Birch essence 0.1 part by weight Part ascorbic acid Magnesium acid 0.1 parts by weight arbutin 0.1 part by weight
【0020】<実施例13>下記に示す処方に従って、
皮膚外用医薬であるステロイドクリームを作成した。即
ち、イ、ロ、ハ、ニのそれぞれの成分を70℃に加熱
し、イとロを混合し、良く混練りし、これをハを加えて
希釈し、これにニを徐々に加え乳化し、攪拌冷却し、ク
リームを得た。 イ 70%マルチトース水溶液 5 重量部 グリセリン 3 重量部 1,3−ブタンジオール 5 重量部 メチルパラベン 0.2重量部 エストラジオール 1 重量部 ロ トリグリセリンジイソステアレート 4 重量部 ソルビタンセスキオレート 0.5重量部 ハ 軽質イソパラフィン 10 重量部 流動パラフィン 10 重量部 グリセリルトリイソオクタネート 5 重量部 ニ 水 57.1重量部 硫酸化アルギン酸ナトリウム 0.1重量部 バクガコンのエッセンス 0.1重量部 エルヒビン 0.1重量部 コウキ抽出物BG 0.1重量部 プラセンターエキス 0.1重量部 グリコーゲン 0.1重量部 ローヤルゼリー 0.1重量部 ジンセンのエッセンス 0.1重量部 オウゴンのエッセンス 0.1重量部 シラカバのエッセンス 0.1重量部 アスコルビン酸燐酸マグネシウム 0.1重量部 アルブチン 0.1重量部Example 13 According to the following formulation,
A steroid cream for external use on the skin was prepared. That is, each of the components (a), (b), (c), and (d) are heated to 70 ° C., (a) and (b) are mixed, kneaded well, and the mixture is diluted by adding (c), and gradually added and emulsified. After stirring and cooling, a cream was obtained. A 70% maltose aqueous solution 5 parts by weight glycerin 3 parts by weight 1,3-butanediol 5 parts by weight methyl paraben 0.2 parts by weight estradiol 1 part by weight b triglycerin diisostearate 4 parts by weight sorbitan sesquiolate 0.5 parts by weight c Light isoparaffin 10 parts by weight Liquid paraffin 10 parts by weight Glyceryl triisooctanoate 5 parts by weight D. water 57.1 parts by weight Sulfated sodium alginate 0.1 part by weight Bacgacone essence 0.1 parts by weight Elhibin 0.1 parts by weight Kouki extraction Material BG 0.1 part by weight Placenta extract 0.1 part by weight Glycogen 0.1 part by weight Royal jelly 0.1 part by weight Ginseng essence 0.1 part by weight Ougon essence 0.1 part by weight Birch essence 0.1 part by weight Department Ascorbin Magnesium phosphate 0.1 part by weight arbutin 0.1 part by weight
【0021】<実施例14>下記に示す処方に従って、
皮膚外用医薬である抗真菌クリームを作成した。即ち、
イ、ロ、ハ、ニのそれぞれの成分を70℃に加熱し、イ
とロを混合し、良く混練りし、これをハを加えて希釈
し、これにニを徐々に加え乳化し、攪拌冷却し、クリー
ムを得た。 イ 70%マルチトース水溶液 5 重量部 グリセリン 3 重量部 1,3−ブタンジオール 5 重量部 メチルパラベン 0.2重量部 ビフォナゾール 1 重量部 ロ トリグリセリンジイソステアレート 4 重量部 ソルビタンセスキオレート 0.5重量部 ハ 軽質イソパラフィン 10 重量部 流動パラフィン 10 重量部 グリセリルトリイソオクタネート 5 重量部 ニ 水 57.1重量部 硫酸化アルギン酸ナトリウム 0.1重量部 バクガコンのエッセンス 0.1重量部 エルヒビン 0.1重量部 コウキ抽出物BG 0.1重量部 プラセンターエキス 0.1重量部 グリコーゲン 0.1重量部 ローヤルゼリー 0.1重量部 ジンセンのエッセンス 0.1重量部 オウゴンのエッセンス 0.1重量部 シラカバのエッセンス 0.1重量部 アスコルビン酸燐酸マグネシウム 0.1重量部 アルブチン 0.1重量部Example 14 According to the following formulation,
An antifungal cream, a skin external medicine, was prepared. That is,
Heat each component of b, b, c and d to 70 ° C, mix a and b, knead well, dilute by adding c, add d slowly to this, emulsify and stir Cool to obtain a cream. A 70% maltose aqueous solution 5 parts by weight Glycerin 3 parts by weight 1,3-butanediol 5 parts by weight Methylparaben 0.2 parts by weight Bifonazole 1 part by weight b Triglycerin diisostearate 4 parts by weight Sorbitan sesquiolate 0.5 parts by weight C Light isoparaffin 10 parts by weight Liquid paraffin 10 parts by weight Glyceryl triisooctanoate 5 parts by weight D. water 57.1 parts by weight Sulfated sodium alginate 0.1 part by weight Bacgacone essence 0.1 parts by weight Elhibin 0.1 parts by weight Kouki extraction Material BG 0.1 part by weight Placenta extract 0.1 part by weight Glycogen 0.1 part by weight Royal jelly 0.1 part by weight Ginseng essence 0.1 part by weight Ougon essence 0.1 part by weight Birch essence 0.1 part by weight Part ascorbic acid Magnesium acid 0.1 parts by weight arbutin 0.1 part by weight
【0022】[0022]
【発明の効果】本発明によれば、優れたくすみ改善作用
を有し、加齢変化に対して有効である、化粧料などの皮
膚外用組成物を提供することができる。According to the present invention, it is possible to provide a skin external composition such as a cosmetic, which has an excellent dulling effect and is effective against aging.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 7/00 A61K 7/00 W A61P 17/00 31/00 617 Fターム(参考) 4C083 AA011 AA012 AA071 AA072 AA111 AA112 AC012 AC022 AC102 AC122 AC132 AC422 AC432 AC442 AC482 AC852 AD302 AD391 AD392 AD411 AD412 AD492 AD592 AD641 AD642 BB51 CC01 CC02 CC04 CC05 DD22 DD23 DD27 DD31 EE12 EE16 ──────────────────────────────────────────────────の Continuation of the front page (51) Int.Cl. 7 Identification symbol FI theme coat ゛ (reference) A61K 7/00 A61K 7/00 W A61P 17/00 31/00 617 F term (reference) 4C083 AA011 AA012 AA071 AA072 AA111 AA112 AC012 AC022 AC102 AC122 AC132 AC422 AC432 AC442 AC482 AC852 AD302 AD391 AD392 AD411 AD412 AD492 AD592 AD641 AD642 BB51 CC01 CC02 CC04 CC05 DD22 DD23 DD27 DD31 EE12 EE16
Claims (7)
抑制剤とを含有する、皮膚外用組成物。1. A composition for external use on the skin, comprising an elastase activity inhibitor and a melanin production inhibitor.
/又はコウキのエッセンスである、請求項1に記載の皮
膚外用組成物。2. The composition for external use on skin according to claim 1, wherein the elastase activity inhibitor is an essence of soybean protein and / or kouki.
タミンC、ビタミンCの誘導体、ロイヤルゼリーのエッ
センス及びソウハクヒのエッセンスから選ばれる1種乃
至は2種以上である、請求項1又は2に記載の皮膚外用
組成物。3. The method according to claim 1, wherein the melanin production inhibitor is one or more selected from arbutin, vitamin C, a derivative of vitamin C, royal jelly essence and soybean essence. External composition for skin.
項に記載の皮膚外用組成物。4. The composition for external use on the skin according to any one of claims 1 to 3, which is a cosmetic.
請求項1〜4の何れか一項に記載の皮膚外用組成物。5. It is for improving dullness,
The composition for external use on the skin according to any one of claims 1 to 4.
とアルブチン、ビタミンC、ビタミンCの誘導体、ロイ
ヤルゼリーのエッセンス及びソウハクヒのエッセンスか
ら選ばれる1種乃至は2種以上とを含有する化粧料。6. A cosmetic containing soybean protein and / or kouki essence and one or more selected from arbutin, vitamin C, vitamin C derivative, royal jelly essence and soybean essence.
請求項6に記載の化粧料。7. It is for improving dullness,
The cosmetic according to claim 6.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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JP10297640A JP2000109417A (en) | 1998-10-05 | 1998-10-05 | Cosmetic for improving somber color |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10297640A JP2000109417A (en) | 1998-10-05 | 1998-10-05 | Cosmetic for improving somber color |
Publications (2)
Publication Number | Publication Date |
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JP2000109417A true JP2000109417A (en) | 2000-04-18 |
JP2000109417A5 JP2000109417A5 (en) | 2005-10-27 |
Family
ID=17849206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10297640A Pending JP2000109417A (en) | 1998-10-05 | 1998-10-05 | Cosmetic for improving somber color |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2000109417A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001072567A (en) * | 1999-09-07 | 2001-03-21 | Sunstar Inc | Skin cosmetic |
WO2003028744A1 (en) * | 2001-09-27 | 2003-04-10 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Process for producing collagen production enhancers and use thereof |
JP2006241033A (en) * | 2005-03-02 | 2006-09-14 | Dhc Co | Skin care preparation for external use for amelioration of skin somberness |
JP2006273809A (en) * | 2005-03-30 | 2006-10-12 | Naris Cosmetics Co Ltd | Vegetable trypsin inhibitor |
JP2011241165A (en) * | 2010-05-18 | 2011-12-01 | Pola Chemical Industries Inc | Composition |
JP2012001519A (en) * | 2010-06-21 | 2012-01-05 | Pola Chemical Industries Inc | Composition |
JP2014037448A (en) * | 2013-11-29 | 2014-02-27 | Pola Chem Ind Inc | Production method of skin external agent against aging |
CN105581940A (en) * | 2015-12-21 | 2016-05-18 | 太仓张根木生物科技有限公司 | Relieving and allergy-preventing calendula officinalis flower moisturizing lotion |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001072567A (en) * | 1999-09-07 | 2001-03-21 | Sunstar Inc | Skin cosmetic |
WO2003028744A1 (en) * | 2001-09-27 | 2003-04-10 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Process for producing collagen production enhancers and use thereof |
JP2006241033A (en) * | 2005-03-02 | 2006-09-14 | Dhc Co | Skin care preparation for external use for amelioration of skin somberness |
JP2006273809A (en) * | 2005-03-30 | 2006-10-12 | Naris Cosmetics Co Ltd | Vegetable trypsin inhibitor |
JP2011241165A (en) * | 2010-05-18 | 2011-12-01 | Pola Chemical Industries Inc | Composition |
JP2012001519A (en) * | 2010-06-21 | 2012-01-05 | Pola Chemical Industries Inc | Composition |
JP2014037448A (en) * | 2013-11-29 | 2014-02-27 | Pola Chem Ind Inc | Production method of skin external agent against aging |
CN105581940A (en) * | 2015-12-21 | 2016-05-18 | 太仓张根木生物科技有限公司 | Relieving and allergy-preventing calendula officinalis flower moisturizing lotion |
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