JPH06263623A - Natural ultraviolet absorber and cosmetic containing it - Google Patents
Natural ultraviolet absorber and cosmetic containing itInfo
- Publication number
- JPH06263623A JPH06263623A JP5078670A JP7867093A JPH06263623A JP H06263623 A JPH06263623 A JP H06263623A JP 5078670 A JP5078670 A JP 5078670A JP 7867093 A JP7867093 A JP 7867093A JP H06263623 A JPH06263623 A JP H06263623A
- Authority
- JP
- Japan
- Prior art keywords
- natural
- ultraviolet absorbing
- ultraviolet
- absorbing substance
- 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.)
- Granted
Links
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】この発明は海藻または陸生植物か
ら抽出した天然紫外線吸収物質およびこれを含む化粧品
に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a natural ultraviolet absorbing substance extracted from seaweed or terrestrial plants and cosmetics containing the same.
【0002】[0002]
【従来の技術及びその背景】従来紫外線は皮膚に多くの
影響を与えることが知られている。例えば急激な影響は
日焼けがあり、長期的には、しみ、しわ等の皮膚の老化
(光老化)や、皮膚癌と密接な関係があるといわれてい
る。2. Description of the Related Art Ultraviolet rays are known to have many effects on the skin. For example, it is said that the acute effect is sunburn, and in the long term, it is closely related to skin aging (photoaging) such as spots and wrinkles, and skin cancer.
【0003】一般に日焼けには、サンバーンとサンタン
がある。サンバーンとは、主にUVB(290〜320
nm)といわれる中波紫外線によって発生する皮膚の赤い
炎症(一種のやけど状態、紅斑と言われる)で、数日後
サンバーンがサンタンに移行する。サンタンとは、紫外
線にあたる事によってメラニンが活性化し、皮膚が黒く
なる。サンタンは肌を黒くすることによって紫外線を遮
断しようとする生体防衛反応である。サンタンには、U
VA(320〜400nm)による一時黒化と、サンバー
ンから移行する二次黒化がる。Generally, sunburn includes sunburn and suntan. Sunburn is mainly UVB (290-320
The red inflammation of the skin (a kind of burn condition, called erythema) caused by medium-wave ultraviolet rays, which is called "nm"), causes sunburn to transfer to suntan after a few days. Suntan activates melanin by exposing it to ultraviolet rays, which makes the skin black. Suntan is a biological defense reaction that seeks to block UV rays by blackening the skin. U on the suntan
There is temporary blackening due to VA (320 to 400 nm) and secondary blackening shifting from sunburn.
【0004】従って紫外線による皮膚の老化は、メラニ
ンの沈着によるしみ、そばかすや真皮層の繊維組織が破
壊される事によるしわ、たるみ等があり、UVAとUV
Bの両方が原因になっているとされている。一方皮膚癌
は、露出部、赤道に近い日光の強い地域、戸外で働く
人、肌の色が白い(紫外線を防衛するメラニンが少な
い)人に発生し易く、紫外線が皮膚癌の原因になること
は動物実験で実証されている。また紫外線が、DNAに
損傷を与えることおよび免疫力を低下させることが原因
ともいわれている。Therefore, the aging of the skin due to ultraviolet rays includes spots due to the deposition of melanin, wrinkles and sagging due to the destruction of the freckles and the fibrous tissue of the dermis layer, and UVA and UV.
Both B are said to be the cause. On the other hand, skin cancer is more likely to occur in exposed areas, areas with strong sunlight near the equator, people who work outdoors, and people with white skin (low melanin that protects from UV rays), and UV rays can cause skin cancer. Has been demonstrated in animal studies. It is also said that ultraviolet rays cause damage to DNA and decrease immunity.
【0005】近年、オゾン層の破壊により、今までは地
表に届くことの無かった、紫外線の中で最も有害性の高
いUVC(200〜290nm)が地上にも届くように
なり、問題となっている。UVBが地表に届く量も多く
なってきている。In recent years, due to the destruction of the ozone layer, UVC (200 to 290 nm), which is the most harmful of the ultraviolet rays, which has never reached the surface of the earth, reaches the surface, which is a problem. There is. The amount of UVB reaching the surface is also increasing.
【0006】前記のように紫外線が肌に与える影響は種
々あり、その紫外線を防衛する必要性は十分にある。現
にスキンケア化粧品が出回っているが、これらの紫外線
防衛能は合成品により与えられている。[0006] As described above, there are various effects of ultraviolet rays on the skin, and there is a sufficient need to protect the ultraviolet rays. Actually, skin care cosmetics are available on the market, but their UV protection ability is provided by synthetic products.
【0007】[0007]
【発明により解決すべき課題】前記従来の紫外線防衛化
粧品には、合成品よりなる紫外線吸収物質が添加されて
いるので、酸化され易く、変質して皮膚に悪影響を及ぼ
すおそれがあった。SUMMARY OF THE INVENTION Since the conventional ultraviolet ray protective cosmetics contain a synthetic ultraviolet ray absorbing substance, they may be easily oxidized and deteriorated to adversely affect the skin.
【0008】然して酸化防止の為に添加される酸化防止
剤も化学品である為に、これも皮膚に悪影響を及ぼすな
どの問題点があった。However, since the antioxidant added to prevent oxidation is also a chemical product, there is a problem in that it also adversely affects the skin.
【0009】[0009]
【課題を解決するための手段】然るにこの発明は、海藻
類または陸生植物の抽出物よりなる紫外線吸収物質を化
粧料へ混入するので、当該抽出物が酸化防止機能を有す
るのみならず、紫外線吸収防衛能もあるので、前記従来
の問題点を解決したのである。SUMMARY OF THE INVENTION However, according to the present invention, since an ultraviolet absorbing substance composed of an extract of seaweed or a terrestrial plant is mixed into cosmetics, the extract not only has an antioxidant function but also absorbs ultraviolet rays. Since it also has a defense ability, it solves the above-mentioned conventional problems.
【0010】この発明の紫外線吸収物質は、試料を適当
な溶媒により抽出することにより得られる。The ultraviolet absorbing substance of the present invention can be obtained by extracting a sample with a suitable solvent.
【0011】尚、抽出溶媒としては、水、アルコール
類、アセトン等水に可溶な有機溶媒の他、ベンゼン、ト
ルエン等の芳香族炭化水素やクロロホルム、四塩化炭素
等の脂肪族炭化水素のハロゲン化化合物などが挙げられ
る。また、エーテル、エステル、ケトン等が使用され
る。As the extraction solvent, in addition to water, organic solvents such as alcohols and acetone, which are soluble in water, aromatic hydrocarbons such as benzene and toluene, and halogens of aliphatic hydrocarbons such as chloroform and carbon tetrachloride. Compound and the like. Further, ethers, esters, ketones and the like are used.
【0012】発明による化粧品は、クリーム、ローショ
ン、オイル、ファンデーション(日焼け、日焼け止め両
方)また、ヘアケア用として利用される。The cosmetics according to the invention are used for creams, lotions, oils, foundations (both sunburns and sunscreens) and for hair care.
【0013】即ち紫外線吸収物質の発明は海藻または陸
生植物から抽出した複数種よりなることを特徴とした天
然紫外線吸収物質である。また他の発明は海藻を緑藻
類、褐藻類および紅藻類としたものであり、陸生植物を
γ−オリザノールおよび甘草としたものである。次に化
粧品の発明は海藻または陸生植物から抽出した一種又は
複数種の紫外線吸収物質を化粧料に混入させ、SPF2
以上としたことを特徴とする天然紫外線吸収物質を含む
化粧品であり、他の発明は海藻または陸生植物から抽出
した一種又は複数種の紫外線吸収物質と合成紫外線吸収
物質を混入させ、SPF2以上としたことを特徴とする
天然紫外線吸収物質を含む化粧品である。That is, the invention of the ultraviolet absorbing substance is a natural ultraviolet absorbing substance characterized by comprising a plurality of species extracted from seaweed or terrestrial plants. In another invention, seaweeds are green algae, brown algae and red algae, and terrestrial plants are γ-oryzanol and licorice. Next, in the invention of cosmetics, one or more kinds of ultraviolet absorbing substances extracted from seaweed or terrestrial plants are mixed into cosmetics to obtain SPF2.
The present invention is a cosmetic containing a natural UV absorbing substance characterized by the above, and another invention is one in which one or more kinds of UV absorbing substances extracted from seaweed or terrestrial plants and a synthetic UV absorbing substance are mixed to obtain SPF 2 or more. The present invention is a cosmetic containing a natural ultraviolet absorbing substance.
【0014】前記における海藻としては緑藻類(例えば
ミル、アオサ、アオノリ)、褐藻類(例えばエゾイシ
ゲ、コンブ、ワカメ、ヒジキ、ホンダワラ、イソモク)
および紅藻類(例えばアサクサのり、テングサ、アカハ
ギンナンソウ、ベンモズク、ウシケノリ)がある。As the seaweed in the above, green algae (for example, mill, sea lettuce, sea squirrel), brown algae (for example, Ezo shige, kelp, wakame, hijiki, hondawara, isomoku)
And red algae (for example, Prickly Pear paste, Agar beetle, Red pearl hemlock, Benmozuku, Ushikenori).
【0015】また陸生植物としては、γ−オリザノー
ル、アロエ、カミツレ、甘草などがある。The land plants include γ-oryzanol, aloe, chamomile, licorice and the like.
【0016】前記におけるSPF値とは、炎症の原因と
なる中波長領域(UVB)をカットする能力を示し、数
字が大きい程強力にUVBをカットすることになる。ま
た、数字は、化粧品を使用して炎症が起きる時間を素肌
の場合と比べた倍率であるから、素肌の時20分間で炎
症が起きた場合、化粧品を使用して40分までのびれ
ば、SPF2ということになる。The SPF value in the above means the ability to cut the medium wavelength region (UVB) which causes inflammation, and the larger the number, the stronger the UVB cutting. In addition, the number is the magnification of the time that inflammation occurs using cosmetics compared to the case of bare skin, so if inflammation occurs in 20 minutes with bare skin, if you use cosmetics and reach up to 40 minutes, It means SPF2.
【0017】[0017]
【実施例1】乾燥エゾイシゲ1kgに50%エタノール1
0lを加え14日間抽出を行う。得られた抽出液は、減
圧濃縮し濃縮液200g を得る。濃縮液をエタノールで
0.02%に希釈し紫外吸収を調べた。Example 1 1 kg of 50% ethanol to 1 kg of dried Eishige
Add 0 l and perform extraction for 14 days. The obtained extract is concentrated under reduced pressure to obtain 200 g of a concentrate. The concentrated solution was diluted with ethanol to 0.02% and the ultraviolet absorption was examined.
【0018】230nm付近に吸収極大を示す物質が確認
された。濃縮液0.02%が、パラジメチルアミノ安息
香酸−2−エチルヘキシルの0.02%希釈液に相当す
る吸収が確認された(図1)。A substance having an absorption maximum around 230 nm was confirmed. It was confirmed that 0.02% of the concentrated liquid had an absorption corresponding to a 0.02% diluted liquid of 2-ethylhexyl paradimethylaminobenzoate (FIG. 1).
【0019】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルと等量使用すればよい
ことになる。That is, when it is used, it may be used in an amount equal to that of 2-ethylhexyl paradimethylaminobenzoate.
【0020】[0020]
【実施例2】乾燥アカハギンナンソウ1kgに50%エタ
ノール10lを加え14日間抽出を行う。得られた抽出
液は、減圧濃縮し、濃縮液200g を得る。濃縮液をエ
タノールで0.02%に希釈し、紫外吸収を調べた。[Example 2] 10 kg of 50% ethanol was added to 1 kg of dried red scallions and extraction was carried out for 14 days. The obtained extract is concentrated under reduced pressure to obtain 200 g of a concentrate. The concentrated solution was diluted with ethanol to 0.02% and examined for ultraviolet absorption.
【0021】230nm付近に吸収極大を示す物質と、3
10〜330nm付近に吸収極大を示す物質が確認され
た。濃縮液0.02%が、パラジメチルアミノ安息香酸
−2−エチルヘキシルの0.02%希釈液に相当する吸
収が確認された(図2)。A substance having an absorption maximum around 230 nm and 3
A substance having an absorption maximum around 10 to 330 nm was confirmed. It was confirmed that 0.02% of the concentrated solution had an absorption corresponding to a 0.02% diluted solution of 2-ethylhexyl paradimethylaminobenzoate (FIG. 2).
【0022】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルと等量使用すればよい
ことになる。That is, when it is used, it should be used in an amount equal to that of 2-ethylhexyl paradimethylaminobenzoate.
【0023】[0023]
【実施例3】米糠油1kgから分離精製したγ−オリザノ
ール(白色結晶粉体)をエタノールで0.03%に希釈
し、紫外吸収を調べた。Example 3 γ-Oryzanol (white crystal powder) separated and purified from 1 kg of rice bran oil was diluted to 0.03% with ethanol, and the ultraviolet absorption was examined.
【0024】290nmと330nm付近に主な吸収極大を
示すが、広い範囲において吸収を示す物質が確認され
た。γ−オリザノール0.03%希釈液が、パラジメチ
ルアミノ安息香酸−2−エチルヘキシルの0.02%希
釈液に相当する吸収が確認された(図3)。A substance showing an absorption maximum in the vicinity of 290 nm and 330 nm but showing absorption in a wide range was confirmed. It was confirmed that the 0.03% diluted solution of γ-oryzanol absorbed the 0.02% diluted solution of 2-ethylhexyl paradimethylaminobenzoate (FIG. 3).
【0025】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルの1.5倍量使用すれ
ばよいことになる。That is, when used, it is sufficient to use 1.5 times the amount of 2-ethylhexyl paradimethylaminobenzoate.
【0026】[0026]
【実施例4】甘草の乾燥根1kgにエタノール10lを加
え、還流下で5時間抽出を行う。抽出液を減圧濃縮し、
乾燥粉砕後、粉末30g を得る。精製された甘草抽出物
をエタノールで0.06%に希釈し、紫外吸収を調べ
た。Example 4 To 1 kg of dried licorice root, 10 l of ethanol was added, and extraction was carried out under reflux for 5 hours. Concentrate the extract under reduced pressure,
After dry grinding, 30 g of powder are obtained. The purified licorice extract was diluted with ethanol to 0.06%, and the ultraviolet absorption was examined.
【0027】380nm付近に主な吸収極大を示すが、広
い範囲において吸収を示す物質が確認された。甘草抽出
物0.06%希釈液が、パラジメチルアミノ安息香酸−
2−エチルヘキシルの0.02%希釈液に相当する吸収
が確認された(図4)。A substance having a main absorption maximum around 380 nm, but absorbing in a wide range was confirmed. Licorice extract 0.06% dilution is paradimethylaminobenzoic acid-
Absorption corresponding to a 0.02% dilution of 2-ethylhexyl was confirmed (Fig. 4).
【0028】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルの3倍量使用すればよ
いことになる。That is, when used, it is sufficient to use 3 times the amount of 2-ethylhexyl paradimethylaminobenzoate.
【0029】[0029]
【実施例5】前記実施例1より得たエゾイシゲ抽出液と
実施例3より得たγ−オリザノールを2:3の比で混合
し、それをエタノールで0.04%に希釈し、紫外吸収
を調べた。Example 5 The Ezoishige extract obtained in Example 1 and γ-oryzanol obtained in Example 3 were mixed in a ratio of 2: 3, and the mixture was diluted to 0.04% with ethanol to absorb ultraviolet rays. Examined.
【0030】200〜340nmの広い範囲において吸収
を示す物質が確認された。この混合物0.04%希釈液
が、パラジメチルアミノ安息香酸−2−エチルヘキシル
の0.02%希釈液に相当する吸収が確認された(図
5)。Materials having absorption in a wide range of 200 to 340 nm were confirmed. It was confirmed that the 0.04% diluted solution of this mixture had an absorption corresponding to a 0.02% diluted solution of 2-ethylhexyl paradimethylaminobenzoate (FIG. 5).
【0031】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルの2倍量使用すればよ
いことになる。That is, when used, it is sufficient to use twice the amount of 2-ethylhexyl paradimethylaminobenzoate.
【0032】更に本混合物は、紫外線吸収力以外に消炎
等の薬理効果や酸化防止力を備えた有用性の高い物質で
ある。Further, this mixture is a highly useful substance having a pharmacological effect such as anti-inflammatory and an antioxidant, in addition to the ability to absorb ultraviolet rays.
【0033】[0033]
【実施例6】前記実施例4より得た甘草エキスとパラジ
メチルアミノ安息香酸−2−エチルヘキシルを3:1の
比で混合し、それをエタノールで0.04%に希釈し、
紫外吸収を調べた。Example 6 The licorice extract obtained in Example 4 and 2-ethylhexyl paradimethylaminobenzoate were mixed at a ratio of 3: 1 and diluted with ethanol to 0.04%.
The ultraviolet absorption was examined.
【0034】200〜380nmの広い範囲において吸収
を示す物質が確認された。この混合物0.04%希釈液
が、パラジメチルアミノ安息香酸−2−エチルヘキシル
の0.02%希釈液に相当する吸収が確認された(図
6)。Materials having absorption in a wide range of 200 to 380 nm were confirmed. It was confirmed that the 0.04% diluted solution of this mixture had an absorption corresponding to the 0.02% diluted solution of 2-ethylhexyl paradimethylaminobenzoate (FIG. 6).
【0035】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルの2倍量使用すればよ
いことになる。That is, when used, it is sufficient to use twice the amount of 2-ethylhexyl paradimethylaminobenzoate.
【0036】更に合成紫外線吸収剤は、酸化されやすく
安全性に対して問題が有るが、甘草抽出液を用いること
により、合成品の使用量を抑えることができ、消炎効果
により皮膚の炎症を鎮める。Further, synthetic ultraviolet absorbers are easily oxidized and have a problem in safety. However, by using a licorice extract, the amount of the synthetic product used can be suppressed and the inflammation of the skin is suppressed by the anti-inflammatory effect. .
【0037】[0037]
【実施例7】前記実施例2より得たアカハギンナンソウ
抽出液とパラジメチルアミノ安息香酸−2−エチルヘキ
シルを1:1の比で混合し、それをエタノールで0.0
2%に希釈し、紫外吸収を調べた。[Example 7] The red peach extract obtained in Example 2 and 2-ethylhexyl paradimethylaminobenzoate were mixed at a ratio of 1: 1 and the mixture was mixed with ethanol to give 0.0.
Diluted to 2% and examined for UV absorption.
【0038】200〜340nmの広い範囲において吸収
を示す物質が確認された。この混合物0.02%希釈液
が、パラジメチルアミノ安息香酸−2−エチルヘキシル
の0.02%希釈液に相当する吸収が確認された(図
7)。Materials having absorption in a wide range of 200 to 340 nm were confirmed. It was confirmed that the 0.02% diluted solution of this mixture had an absorption corresponding to the 0.02% diluted solution of 2-ethylhexyl paradimethylaminobenzoate (FIG. 7).
【0039】即ち、使用する場合は、パラジメチルアミ
ノ安息香酸−2−エチルヘキシルと等量使用すればよい
ことになる。That is, when it is used, it may be used in the same amount as that of 2-ethylhexyl paradimethylaminobenzoate.
【0040】更に合成紫外線吸収剤は酸化し易いが、海
藻を加えることにより紫外線吸収力が増強される。ま
た、その酸化防止効果により酸化されにくい物質が得ら
れる。Further, the synthetic ultraviolet absorber is easily oxidized, but the ultraviolet absorbing power is enhanced by adding seaweed. In addition, a substance that is difficult to oxidize can be obtained due to its antioxidant effect.
【0041】[0041]
【実施例8】一般処方のスキンクリームに、実施例2記
載のアカハギンナンソウ抽出液を5%を配合すると、S
PF6に相当する日焼け止めスキンクリームができる。[Embodiment 8] When 5% of the red velvet extract as described in Embodiment 2 is added to the skin cream of the general formula, S
A sunscreen skin cream equivalent to PF6 is produced.
【0042】パラジメチルアミノ安息香酸−2−エチル
ヘキシルを化粧品に配合する場合の目安は、3%を配合
するとSPF4(日焼け用化粧品)程度であり、5%を
配合するとSPF6(日焼け止め化粧品)程度である。When 2-ethylhexyl paradimethylaminobenzoate is mixed in cosmetics, the standard is about 3% SPF4 (sunscreen cosmetics), and 5% is SPF6 (sunscreen cosmetics). is there.
【0043】[0043]
【実施例9】一般処方のローションに、実施例4記載の
甘草抽出物を6%を配合すると、SPF3に相当する日
焼け用ローションができる。[Example 9] By adding 6% of the licorice extract described in Example 4 to a lotion having a general formulation, a suntan lotion corresponding to SPF3 can be obtained.
【0044】[0044]
【実施例10】一般処方のスキンオイルに、実施例3記
載のγ−オリザノールを3%を配合すると、SPF3に
相当する日焼け用オイルができる。Example 10 If 3% of γ-oryzanol described in Example 3 is mixed with a skin oil having a general formulation, a suntan oil corresponding to SPF3 can be obtained.
【0045】[0045]
【実施例11】一般処方のクリームに、実施例7記載の
混合物を5%を配合すると、SPF6に相当する日焼け
止めクリームができる。[Example 11] By adding 5% of the mixture described in Example 7 to a cream having a general formulation, a sunscreen cream corresponding to SPF6 can be obtained.
【0046】[0046]
【発明の効果】この発明によれば、天然抽出物を使用し
たので、合成紫外線吸収物質を使用した場合の問題点が
なくなった。また天然抽出物に含まれる紫外線吸収物質
は、酸化防止能があり比較的安定であり、各々吸収能に
特性があるので(或範囲に吸収能の極大部がある)、適
宜複合使用することにより、全波長に平均的効果を奏す
る化粧品又は選択的波長に特性を有する化粧品を得るこ
とができる。また合成紫外線吸収物質と併用すれば、合
成紫外線吸収物質の使用量が抑えられ、合成酸化防止剤
の添加が不必要となると共に吸収能を助長することがで
きる。According to the present invention, since the natural extract is used, the problem when using the synthetic ultraviolet absorbing substance is eliminated. In addition, the ultraviolet absorbing substances contained in the natural extract have antioxidant ability and are relatively stable, and each has a characteristic of absorbing ability (there is a maximum absorbing ability in a certain range). Thus, it is possible to obtain a cosmetic having an average effect over all wavelengths or a cosmetic having characteristics at a selective wavelength. When used in combination with a synthetic ultraviolet absorbing substance, the amount of the synthetic ultraviolet absorbing substance used can be suppressed, the addition of a synthetic antioxidant becomes unnecessary, and the absorbing ability can be promoted.
【0047】更に合成紫外線吸収物質の使用に比し、皮
膚に対しての安全性が高くなり、合成紫外線吸収物質に
よる炎症刺激を防止などの諸効果がある。Further, as compared with the use of the synthetic ultraviolet absorbing substance, the safety to the skin is enhanced, and various effects such as prevention of inflammatory stimulation due to the synthetic ultraviolet absorbing substance are obtained.
【図1】この発明の実施例1のエゾイシゲの吸光度のグ
ラフ(0.02%溶液)。FIG. 1 is a graph of the absorbance of Ezo shige (Example 2) of the present invention (0.02% solution).
【図2】同じく実施例2のアカハギンナンソウの吸光度
のグラフ(0.02%溶液)。FIG. 2 is a graph (0.02% solution) of the absorbance of the red bud plant of Example 2 as well.
【図3】同じく実施例3のγ−オリザノールの吸光度の
グラフ(0.03%溶液)。FIG. 3 is a graph of the absorbance of γ-oryzanol of Example 3 (0.03% solution).
【図4】同じく実施例4の甘草の吸光度のグラフ(0.
06%溶液)。FIG. 4 is a graph showing the absorbance of licorice of Example 4 (0.
06% solution).
【図5】同じく実施例5の混合物の吸光度のグラフ
(0.04%溶液)。FIG. 5 is a graph of the absorbance of the mixture of Example 5 (0.04% solution).
【図6】同じく実施例6の混合物の吸収光度のグラフ
(0.04%溶液)。FIG. 6 is a graph of absorption luminosity of the mixture of Example 6 (0.04% solution).
【図7】同じく実施例7の混合物の吸光度のグラフ
(0.02%溶液)。FIG. 7 is a graph of the absorbance of the mixture of Example 7 (0.02% solution).
【図8】従来知られているパラジメチルアミノ安息香酸
2−エチルヘキシルの吸光度のグラフ(0.02%溶
液)。FIG. 8 is a graph of the absorbance of a conventionally known 2-ethylhexyl paradimethylaminobenzoate (0.02% solution).
Claims (5)
よりなることを特徴とした天然紫外線吸収物質。1. A natural ultraviolet absorbing substance comprising a plurality of species extracted from seaweed or terrestrial plants.
た請求項1記載の天然紫外線吸収物質。2. The natural ultraviolet absorbing substance according to claim 1, wherein the seaweed is green algae, brown algae or red algae.
カミツレおよび甘草とした請求項1記載の天然紫外線吸
収物質。3. A terrestrial plant comprising γ-oryzanol, aloe,
The natural ultraviolet absorbing substance according to claim 1, which is chamomile or licorice.
は複数種の紫外線吸収物質を化粧料に混入させ、SPF
2以上としたことを特徴とする天然紫外線吸収物質を含
む化粧品。4. An SPF containing one or more kinds of ultraviolet absorbing substances extracted from seaweed or terrestrial plants in a cosmetic composition.
A cosmetic containing a natural ultraviolet-absorbing substance, characterized in that the number is 2 or more.
は複数種の紫外線吸収物質と合成紫外線吸収物質を混入
させ、SPF2以上としたことを特徴とする天然紫外線
吸収物質を含む化粧品。5. A cosmetic containing a natural ultraviolet absorbing substance, wherein one or more kinds of ultraviolet absorbing substances extracted from seaweed or terrestrial plants and a synthetic ultraviolet absorbing substance are mixed to obtain SPF of 2 or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5078670A JP2700601B2 (en) | 1993-03-12 | 1993-03-12 | Natural UV absorbers and cosmetics containing them |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5078670A JP2700601B2 (en) | 1993-03-12 | 1993-03-12 | Natural UV absorbers and cosmetics containing them |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7255406A Division JPH08188521A (en) | 1995-10-02 | 1995-10-02 | Cosmetic containing natural ultraviolet light absorbing substance |
JP9132367A Division JPH1053514A (en) | 1997-05-22 | 1997-05-22 | Natural ultraviolet light absorber and cosmetic comprising the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06263623A true JPH06263623A (en) | 1994-09-20 |
JP2700601B2 JP2700601B2 (en) | 1998-01-21 |
Family
ID=13668309
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5078670A Expired - Lifetime JP2700601B2 (en) | 1993-03-12 | 1993-03-12 | Natural UV absorbers and cosmetics containing them |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2700601B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2803200A1 (en) * | 1999-12-30 | 2001-07-06 | Brev Licences Et Commercialisa | Topical cosmetic composition, useful for protecting skin and hair against sunlight, contains an extract from the red alga Polysiphonia lanosa |
FR2803201A1 (en) * | 1999-12-30 | 2001-07-06 | Gelyma | Algal extracts containing amino acid analogs of mycosporin are useful as dermatological protecting agents against ultraviolet radiation |
EP1123083A1 (en) * | 1998-10-23 | 2001-08-16 | Norman Huner | Solar radiation protection compositions |
FR2832629A1 (en) * | 2001-11-14 | 2003-05-30 | Larena | A PRODUCT CONTAINING AN EXTRACT OF RED ALGAE OF THE PORPHYRA GENUS AND ITS USES TO PROTECT CELLS |
KR20030069659A (en) * | 2002-02-22 | 2003-08-27 | 박영호 | Preparation of Body Nutritional Cream Prepared by Natural Herb and Seaweeds |
JP2004238519A (en) * | 2003-02-06 | 2004-08-26 | Microalgae Corporation | Extract having antioxidant activity and ultraviolet-absorbing activity, external preparation for skin, and food |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5742621A (en) * | 1980-08-29 | 1982-03-10 | Zenyaku Kogyo Kk | Composition for oryzanol external pharmaceutical |
JPS6013709A (en) * | 1983-07-01 | 1985-01-24 | Nippon Carbide Ind Co Ltd | Novel additive for cosmetic |
JPH01157909A (en) * | 1987-12-15 | 1989-06-21 | Maruzen Kasei Co Ltd | Ultraviolet ray absorber |
-
1993
- 1993-03-12 JP JP5078670A patent/JP2700601B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5742621A (en) * | 1980-08-29 | 1982-03-10 | Zenyaku Kogyo Kk | Composition for oryzanol external pharmaceutical |
JPS6013709A (en) * | 1983-07-01 | 1985-01-24 | Nippon Carbide Ind Co Ltd | Novel additive for cosmetic |
JPH01157909A (en) * | 1987-12-15 | 1989-06-21 | Maruzen Kasei Co Ltd | Ultraviolet ray absorber |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1123083A1 (en) * | 1998-10-23 | 2001-08-16 | Norman Huner | Solar radiation protection compositions |
FR2803200A1 (en) * | 1999-12-30 | 2001-07-06 | Brev Licences Et Commercialisa | Topical cosmetic composition, useful for protecting skin and hair against sunlight, contains an extract from the red alga Polysiphonia lanosa |
FR2803201A1 (en) * | 1999-12-30 | 2001-07-06 | Gelyma | Algal extracts containing amino acid analogs of mycosporin are useful as dermatological protecting agents against ultraviolet radiation |
FR2832629A1 (en) * | 2001-11-14 | 2003-05-30 | Larena | A PRODUCT CONTAINING AN EXTRACT OF RED ALGAE OF THE PORPHYRA GENUS AND ITS USES TO PROTECT CELLS |
WO2003041679A3 (en) * | 2001-11-14 | 2003-10-16 | Larena | Product containing a red alga extract of the genus porphyra and uses thereof for protecting cells |
US7128914B2 (en) | 2001-11-14 | 2006-10-31 | Larena | Product containing an extract of red algae of the genus Porphyra and methods for protecting cells |
KR20030069659A (en) * | 2002-02-22 | 2003-08-27 | 박영호 | Preparation of Body Nutritional Cream Prepared by Natural Herb and Seaweeds |
JP2004238519A (en) * | 2003-02-06 | 2004-08-26 | Microalgae Corporation | Extract having antioxidant activity and ultraviolet-absorbing activity, external preparation for skin, and food |
Also Published As
Publication number | Publication date |
---|---|
JP2700601B2 (en) | 1998-01-21 |
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