JP4473439B2 - Whitening agent - Google Patents

Whitening agent Download PDF

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Publication number
JP4473439B2
JP4473439B2 JP2000313194A JP2000313194A JP4473439B2 JP 4473439 B2 JP4473439 B2 JP 4473439B2 JP 2000313194 A JP2000313194 A JP 2000313194A JP 2000313194 A JP2000313194 A JP 2000313194A JP 4473439 B2 JP4473439 B2 JP 4473439B2
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JP
Japan
Prior art keywords
extract
present
whitening agent
agrasejo
skin
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.)
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JP2000313194A
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Japanese (ja)
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JP2002121125A (en
Inventor
宏行 山羽
和寿 大隅
友則 堅田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Menard Cosmetic Co Ltd
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Nippon Menard Cosmetic Co Ltd
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Priority to JP2000313194A priority Critical patent/JP4473439B2/en
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Description

【0001】
【発明の属する技術分野】
本発明は、特定の植物の抽出物を配合する美白剤に関する。
【0002】
【従来の技術】
一般にシミ、ソバカス、日焼けなどに見られる皮膚の色素沈着は、ホルモンの異常や紫外線の刺激により、皮膚内に存在するメラニン色素生成細胞がメラニン色素を過剰に生成し、これが皮膚内に沈着することが原因と考えられている。このような色素沈着を防ぐ方法の一つに、メラニンの過剰な生成を抑制する方法が知られている。従来、色素沈着の治療にはハイドロキノンやアスコルビン酸(ビタミンC)などを外用する処置が行われてきた。
【0003】
【発明が解決しようとする課題】
美白剤としては、副作用の危険性のあるハイドロキノン等の化学合成品ではなく、安全性の高い天然原料が望まれている。また、アスコルビン酸は不安定であり、製剤化が難しい。
【0004】
以上のことから、安全で安定性に優れた美白剤が望まれている。
【0005】
【課題を解決するための手段】
この様な事情により、本発明者らは鋭意研究を重ねた結果、アグラセホの抽出物が優れたメラニン生成抑制作用をもち、安定性においても優れていることを見出した。さらに、アグラセホの抽出物を含有する美白剤が安全で優れた皮膚の美白作用をもつことを見出し、本発明を完成するに至った。
【0006】
本発明で用いられるアグラセホ(学名:Berberis vulgaris、別名:Agracejo、セイヨウメギ)は、メギ科の低木である。主にヨーロッパから中部アジア、熱帯アメリカに広く分布し、生薬として広く使用されている。
【0007】
本発明で使用するアグラセホの抽出物とは、アグラセホの葉、茎、樹皮、花、実、根等の植物体の一部又は全草から抽出したものである。好ましくは、アグラセホの葉及び茎から抽出して得られるものが良い。その抽出方法は常温抽出したものであって良い。
【0008】
抽出する溶媒としては、水又はエタノールが良い。これらの溶媒を混合して用いても良い。
【0009】
アグラセホの抽出物は、抽出した溶液のまま用いても良く、必要に応じて、濃縮、希釈、濾過等の処理をして用いても良い。更には、抽出した溶液を濃縮乾固、噴霧乾燥、凍結乾燥等の処理を行い、乾燥物として用いても良い。
【0010】
本発明の美白剤には、上記抽出物をそのまま使用しても良く、アグラセホの抽出物の効果を損なわない範囲内で、通常の外用剤に用いられる成分である油脂類、ロウ類、炭化水素類、脂肪酸類、アルコール類、エステル類、界面活性剤、金属石鹸、pH調整剤、防腐剤、香料、保湿剤、粉体、紫外線吸収剤、増粘剤、色素、酸化防止剤、美白剤、キレート剤等の成分を配合することもできる。
【0011】
本発明の美白剤は、化粧品、医薬部外品及び医薬品のいずれにも用いることができ、その剤型としては、例えば、化粧水、クリーム、乳液、ゲル剤、エアゾール剤、軟膏、パップ剤、エッセンス、パック、洗浄剤、浴用剤、ファンデーション、打粉、口紅等の皮膚に適用されるものが挙げられる。
【0012】
本発明に用いるアグラセホの抽出物の配合量は、配合する製剤全量に対し、固形物に換算して0.0001重量%以上、好ましくは 0.001〜10重量%が良い。0.0001重量%未満では十分な効果は発揮されにくい。10重量%を越えて配合した場合、効果の増強はみられにくく不経済である。また、添加の方法については、予め加えておいても、製造途中で添加しても良く、作業性を考えて適宜選択すれば良い。
【0013】
【実施例】
次に本発明を詳細に説明するため、実施例として本発明に用いる抽出物の製造例、本発明の処方例及び実験例を挙げるが、本発明はこれに限定されるものではない。実施例に示す配合量の部とは重量部を示し、%は重量%を示す。
【0014】
製造例1 アグラセホの50%エタノール抽出物
アグラセホの葉及び茎の乾燥物100gに精製水1L及びエタノール1Lを加え、常温で7日間抽出した後、濾過し、その濾液を濃縮乾固して、アグラセホのエタノール抽出物を21g得た。
【0015】
実施例1 化粧水
処方 配合量
1. アグラセホの50%エタノール抽出物(製造例1) 0.1部
2. 1,3−ブチレングリコール 8.0
3. グリセリン 2.0
4. キサンタンガム 0.02
5. クエン酸 0.01
6. クエン酸ナトリウム 0.1
7. エタノール 5.0
8. パラオキシ安息香酸メチル 0.1
9. ポリオキシエチレン硬化ヒマシ油(40E.O.) 0.1
10. 香料 適量
11. 精製水にて全量を100とする
[製造方法]成分1〜6及び11と、成分7〜10をそれぞれ均一に溶解し、両者を混合し濾過して製品とする。
【0016】
実施例2 乳液
処方 配合量
1. アグラセホの50%エタノール抽出物(製造例1) 0.5部
2. スクワラン 5.0
3. オリーブ油 5.0
4. ホホバ油 5.0
5. セタノール 1.5
6. モノステアリン酸グリセリン 2.0
7. ポリオキシエチレンセチルエーテル(20E.O.) 3.0
8. ポリオキシエチレンソルビタンモノオレエート(20E.O.)2.0
9. 香料 0.1
10. プロピレングリコール 1.0
11. グリセリン 2.0
12. パラオキシ安息香酸メチル 0.2
13. 精製水にて全量を100とする
[製造方法]成分2〜8を加熱溶解して混合し、70℃に保ち油相とする。成分 1及び10〜13を加熱溶解して混合し、75℃に保ち水相とする。油相に水相を加えて乳化して、かき混ぜながら冷却し、45℃で成分9を加え、更に30℃まで冷却して製品とする。
【0017】
次に、本発明の効果を詳細に説明するため、実験例を挙げる。
【0018】
実験例1 B16マウスメラノーマを用いたメラニン生成抑制試験(美白作用)
対数増殖期にあるメラノーマをφ60mm dishに3×104細胞播種し、各種の濃度のアグラセホの50%エタノール抽出物あるいは陽性対照であるアスコルビン酸を含むEagles’ MEM(10%牛胎児血清含有)を加え、37℃、5%CO条件下にて培養した。また、試料の安定性を確認するために、試料の水溶液を24時間室温で放置した液を使用して同様に評価を行った。培養5日後に細胞をdishから剥離し、細胞を超音波破砕した後に、2N水酸化ナトリウム水溶液を加え60℃で2時間の処理を行い、分光光度計でO.D.475nmを測定した。尚、超音波処理後の細胞破砕液をLowryの方法(J.Biol.Chem.,193,265−275,1951)でタンパク定量し、タンパク量当りのメラニン量を比較することによって、メラニン生成抑制作用の指標とした。
【0019】
これらの試験結果を表1に示した。また、アスコルビン酸は24時間放置すると、メラニン生成抑制作用は減少したが、アグラセホの抽出物は作用に変化はなかった。その結果、アグラセホの抽出物は、安定で優れたメラニン生成抑制作用を有していることが認められた。
【0020】
【表1】

Figure 0004473439
【0021】
実験例2 使用試験
実施例1の化粧水及び実施例2の乳液を用いて、各々女性30人(30〜45才)を対象に1ヶ月間の使用試験を行った。使用後、肌のしみ、そばかす及び透明感の改善に関するアンケート調査により皮膚の美白作用を判定した。その結果、実施例1の化粧水及び実施例2の乳液は、安全で優れた皮膚の美白作用を示した。
【0022】
【発明の効果】
以上のことから、本発明のアグラセホの抽出物は優れたメラニン生成抑制作用をもち、優れた安定性を示した。さらに、アグラセホの抽出物は安全で優れた皮膚の美白作用を示した。 [0001]
BACKGROUND OF THE INVENTION
The present invention relates to a whitening agent containing an extract of a specific plant.
[0002]
[Prior art]
Skin pigmentation commonly found in spots, buckwheat, sunburn, etc., is caused by excessive melanin pigment formation in the skin by melanin-producing cells present in the skin due to hormonal abnormalities or stimulation of ultraviolet rays. Is considered to be the cause. As one method for preventing such pigmentation, a method for suppressing excessive production of melanin is known. Conventionally, hydroquinone, ascorbic acid (vitamin C), and the like have been used for the treatment of pigmentation.
[0003]
[Problems to be solved by the invention]
As a whitening agent, a highly safe natural raw material is desired rather than a chemically synthesized product such as hydroquinone which has a risk of side effects. Moreover, ascorbic acid is unstable and difficult to formulate.
[0004]
From the above, a whitening agent that is safe and excellent in stability is desired.
[0005]
[Means for Solving the Problems]
Under such circumstances, as a result of intensive studies, the present inventors have found that an extract of aglacefo has an excellent melanin production inhibitory effect and is also excellent in stability. Furthermore, the present inventors have found that a whitening agent containing an extract of agrasejo has a safe and excellent skin whitening action, and have completed the present invention.
[0006]
Agrasejo (scientific name: Berberis vulgaris, also known as: Gracejo, barberry) used in the present invention is a shrub of the Barberry family. It is widely distributed mainly in Europe, Central Asia and tropical America, and is widely used as a crude drug.
[0007]
The extract of aglacejo used in the present invention is extracted from a part of a plant body such as agrasefo leaves, stems, bark, flowers, fruits, roots or the whole plant. Preferably, those obtained by extraction from the leaves and stems of Agrasejo are good. The extraction method may be a room temperature extraction.
[0008]
As the solvent to be extracted, water or ethanol is preferable . A mixture of these solvents may be used.
[0009]
The Agrasejo extract may be used as it is, or may be used after concentration, dilution, filtration, or the like, if necessary. Further, the extracted solution may be subjected to a treatment such as concentration to dryness, spray drying, freeze drying, etc., and used as a dried product.
[0010]
In the whitening agent of the present invention, the above-mentioned extract may be used as it is, and within the range not impairing the effect of the extract of Agraceho, oils and fats, waxes, hydrocarbons which are components used in ordinary external preparations , Fatty acids, alcohols, esters, surfactants, metal soaps, pH adjusters, preservatives, fragrances, moisturizers, powders, UV absorbers, thickeners, pigments, antioxidants, whitening agents, Components such as chelating agents can also be blended.
[0011]
The whitening agent of the present invention can be used in any of cosmetics, quasi-drugs, and pharmaceuticals. Examples of the dosage form include lotions, creams, emulsions, gels, aerosols, ointments, poultices, Examples include essences, packs, cleaning agents, bath preparations, foundations, dusting powders, lipsticks, and the like applied to the skin.
[0012]
The blending amount of the extract of agrasefo used in the present invention is 0.0001% by weight or more, preferably 0.001 to 10% by weight, in terms of solid matter, with respect to the total amount of the preparation to be blended . If it is less than 0.0001% by weight, sufficient effects are hardly exhibited. When it exceeds 10% by weight, the effect is hardly increased, which is uneconomical. In addition, the addition method may be added in advance or during the production, and may be appropriately selected in consideration of workability.
[0013]
【Example】
Next, in order to describe the present invention in detail, examples of producing the extract used in the present invention, formulation examples and experimental examples of the present invention will be given as examples, but the present invention is not limited thereto. The part of the amount shown in the examples indicates part by weight, and% indicates% by weight.
[0014]
Production Example 1 50% ethanol extract of Aglacejo 1 L of purified water and 1 L of ethanol were added to 100 g of dried Agrasefo leaves and stems, extracted for 7 days at room temperature, filtered, and the filtrate was concentrated to dryness. 21 g of ethanol extract was obtained.
[0015]
Example 1 lotion formulation 1. 50 parts ethanol extract of Agrasejo ( Production Example 1 ) 0.1 part 1,3-butylene glycol 8.0
3. Glycerin 2.0
4). Xanthan gum 0.02
5). Citric acid 0.01
6). Sodium citrate 0.1
7). Ethanol 5.0
8). Methyl paraoxybenzoate 0.1
9. Polyoxyethylene hydrogenated castor oil (40E.O.) 0.1
10. Perfume proper amount11. [Manufacturing method] Components 1 to 6 and 11 and components 7 to 10 are uniformly dissolved in purified water, and both are mixed and filtered to obtain a product.
[0016]
Example 2 Emulsion Formulation Amount 0.5 parts of Agrasejo 50% ethanol extract ( Production Example 1 ) Squalane 5.0
3. Olive oil 5.0
4). Jojoba oil 5.0
5). Cetanol 1.5
6). Glycerol monostearate 2.0
7). Polyoxyethylene cetyl ether (20E.O.) 3.0
8). Polyoxyethylene sorbitan monooleate (20E.O.) 2.0
9. Fragrance 0.1
10. Propylene glycol 1.0
11. Glycerin 2.0
12 Methyl paraoxybenzoate 0.2
13. [Manufacturing method] Components 2 to 8 are heated and dissolved and mixed with purified water to a total amount of 100, and kept at 70 ° C to obtain an oil phase. Ingredients 1 and 10-13 are dissolved by heating and mixed, and kept at 75 ° C. to form an aqueous phase. The aqueous phase is added to the oil phase to emulsify, and the mixture is cooled while stirring.
[0017]
Next, experimental examples will be given to explain the effects of the present invention in detail.
[0018]
Experimental Example 1 Melanin production inhibition test using B16 mouse melanoma (whitening effect)
Logarithmically growing melanoma is seeded at 3 × 10 4 cells in a 60 mm dish and added with 50% ethanol extract of various concentrations of Aglaceho or Eagles' MEM (containing 10% fetal calf serum) containing ascorbic acid as a positive control. The cells were cultured at 37 ° C. under 5% CO 2 conditions. Further, in order to confirm the stability of the sample, the same evaluation was performed using a solution in which the aqueous solution of the sample was allowed to stand at room temperature for 24 hours. After 5 days of culture, the cells were detached from the dish, and the cells were sonicated, and then treated with 2N aqueous sodium hydroxide at 60 ° C. for 2 hours. D. 475 nm was measured. In addition, the protein quantification is performed for the cell lysate after sonication by Lowry's method (J. Biol. Chem., 193, 265-275, 1951), and the amount of melanin per amount of protein is compared to suppress melanin production. It was used as an index of action.
[0019]
The test results are shown in Table 1. In addition, when ascorbic acid was allowed to stand for 24 hours, the inhibitory action on melanin production decreased, but the action of the extract of aglacefo did not change. As a result, it was confirmed that the extract of aglacefo had a stable and excellent melanin production inhibitory action.
[0020]
[Table 1]
Figure 0004473439
[0021]
Experiment 2 Usage test
Using the lotion of Example 1 and the emulsion of Example 2, a use test for one month was conducted for 30 women (30 to 45 years old). After use, the skin whitening effect was determined by a questionnaire survey on the improvement of skin spots, freckles and transparency. As a result, the lotion of Example 1 and the emulsion of Example 2 showed a safe and excellent skin whitening effect.
[0022]
【The invention's effect】
From the above, the extract of aglacefo of the present invention had an excellent melanin production inhibitory action and showed excellent stability. In addition, Agrasejo extract showed a safe and excellent skin whitening effect.

Claims (1)

アグラセホの水及び/又はエタノールによる抽出物であって、抽出法が常温抽出である抽出物を含有することを特徴とする美白剤。A whitening agent comprising an extract of water and / or ethanol of Agrasejo, wherein the extraction method is extraction at room temperature.
JP2000313194A 2000-10-13 2000-10-13 Whitening agent Expired - Lifetime JP4473439B2 (en)

Priority Applications (1)

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Application Number Priority Date Filing Date Title
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JP4473439B2 true JP4473439B2 (en) 2010-06-02

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011088845A (en) * 2009-10-21 2011-05-06 Kao Corp Involucrin expression inhibitor

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