JP2009023912A - Demulcent for dryness and itch of skin - Google Patents
Demulcent for dryness and itch of skin Download PDFInfo
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- JP2009023912A JP2009023912A JP2007185249A JP2007185249A JP2009023912A JP 2009023912 A JP2009023912 A JP 2009023912A JP 2007185249 A JP2007185249 A JP 2007185249A JP 2007185249 A JP2007185249 A JP 2007185249A JP 2009023912 A JP2009023912 A JP 2009023912A
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Abstract
Description
本発明は、低分子ペクチンを有効成分として含有する肌の乾燥・かゆみ緩和剤に関する。 The present invention relates to a skin dry / itch relieving agent containing low molecular weight pectin as an active ingredient.
かゆみを伴う疾患のひとつとして、乾燥からおこる乾皮症があげられる。この症状は掻くことにより乾燥を増幅させ症状の悪化を招く。この症状を処置すべくさまざまな外用剤が提案されている。たとえば、皮膚の角質層に存在する天然成分の尿素は保湿剤、クロタミトンという成分は皮膚に軽い刺激を与えそれによりかゆみを抑える鎮痒剤として知られ、市販の皮膚外用剤はこれらの成分を複数配合している。しかしながら、従来の保湿剤・鎮痒剤には、抗ヒスタミン剤などが用いられているが、皮膚に刺激を与えるため、アトピー性皮膚炎などの痒みを伴う乾燥肌のように刺激に弱い皮膚には使用することができない、という問題があった。
One of the diseases accompanied by itching is xeroderma caused by dryness. This symptom increases the dryness by scratching and causes the symptom to worsen. Various external preparations have been proposed to treat this symptom. For example, the natural ingredient urea that exists in the stratum corneum of the skin is known as a moisturizer, and the ingredient crotamiton is known as an antipruritic agent that gives mild irritation to the skin and thereby suppresses itching. is doing. However, anti-histamines are used in conventional moisturizers and antipruritic agents, but they are used for skin that is sensitive to irritation such as dry skin with itching such as atopic dermatitis to irritate the skin. There was a problem that it was not possible.
一方、ペクチンは植物の細胞壁に存在しているガラクツロン酸を主体とした酸性多糖類であり、ゲル化剤やタンパク質の安定剤として広く用いられている。主鎖はα−D−ガラクツロン酸がα−1,4結合しており、不均一にラムノース、アラビノース等の中性糖が入り込む形でラムノガラクツロナン鎖を形成している。さらに、分枝してガラクツロン酸や中性糖からなる側鎖を持つと考えられており、平均重合度は200から1000といわれている。 On the other hand, pectin is an acidic polysaccharide mainly composed of galacturonic acid present in plant cell walls, and is widely used as a gelling agent and a protein stabilizer. Α-D-galacturonic acid is α-1,4 linked to the main chain, and a rhamnogalacturonan chain is formed in a form in which neutral sugars such as rhamnose and arabinose enter heterogeneously. Furthermore, it is considered to have side chains consisting of galacturonic acid and neutral sugars, and the average degree of polymerization is said to be 200 to 1000.
また、平均重合度が300以下の低分子ペクチンには乳化作用、平均重合度が10以下の低分子ペクチンには抗菌作用、また、食物繊維としての整腸作用などを有することが知られている。 It is also known that low molecular weight pectin with an average degree of polymerization of 300 or less has an emulsifying action, low molecular weight pectin with an average degree of polymerization of 10 or less has an antibacterial action, and an intestinal action as a dietary fiber. .
しかしながら、低分子ペクチンが肌に及ぼす影響に関しては、特許文献1に記載の美白効果が公知であるが、乾燥やかゆみを緩和する効果があることは知られていなかった。
以上のような問題点を鑑み、本発明の目的は、皮膚の保湿、保護および鎮痒効果に優れ、しかも低刺激でアトピー性皮膚炎などの痒みを伴う乾燥肌に対して有用性の高い皮膚塗布剤組成物を提供することにある。 In view of the above problems, the object of the present invention is to provide a skin application that is excellent in moisturizing, protecting and antipruritic effects of the skin, and is highly useful for dry skin accompanied by itching such as atopic dermatitis. It is to provide an agent composition.
本発明者らは、鋭意検討した結果、低分子ペクチンが肌に対する刺激が少なく安全性に優れ、しかも肌の乾燥の緩和する効果と乾燥によるかゆみが軽減する効果を示すことを見出し、本発明に到達した。即ち、本発明は低分子ペクチンを有効成分として含有することを特徴とする肌の乾燥・かゆみ緩和剤である。 As a result of intensive studies, the present inventors have found that low molecular weight pectin is excellent in safety with little irritation to the skin, and also has an effect of alleviating dryness of the skin and an effect of reducing itching due to dryness. Reached. That is, the present invention is a skin dryness / itchiness alleviating agent characterized by containing a low molecular weight pectin as an active ingredient.
本発明に用いる低分子ペクチンとは、平均重合度が300以下のものをいい、好ましくは平均重合度が3から50のものである。本発明の低分子ペクチンは、公知の方法、例えばペクチンの加水分解や酵素分解によって得られる。 The low molecular weight pectin used in the present invention refers to those having an average degree of polymerization of 300 or less, preferably those having an average degree of polymerization of 3 to 50. The low molecular weight pectin of the present invention can be obtained by a known method, for example, hydrolysis or enzymatic degradation of pectin.
本発明の肌の乾燥・かゆみ緩和剤の剤形は、有効成分として低分子ペクチンを含有する限り、特に限定されるものではなく、軟膏、乳化剤、クリーム、ローション、ジェル、パウダー、シート剤、貼付剤等任意の製剤として提供できる。 The dosage form of the skin dryness / itchiness relieving agent of the present invention is not particularly limited as long as it contains low molecular weight pectin as an active ingredient, and is not an ointment, emulsifier, cream, lotion, gel, powder, sheet, patch It can be provided as an arbitrary preparation such as an agent.
また、本発明の効果を損なわない範囲において、通常用いられる基材(例:ワセリン、ポリエチレングリコール等)、溶剤(例:水、エタノール等)、界面活性剤、香料等の成分を適宜配合することができる。 Moreover, within the range which does not impair the effect of this invention, it mix | blends components, such as a normally used base material (example: petrolatum, polyethyleneglycol, etc.), a solvent (example: water, ethanol, etc.), surfactant, a fragrance | flavor suitably. Can do.
本発明の肌の乾燥・かゆみ緩和剤において低分子ペクチンの含有量は、剤形にもよるが通常1〜50重量%程度が好ましい。 In the skin dryness / itchiness relieving agent of the present invention, the content of low molecular weight pectin is usually preferably about 1 to 50% by weight, although it depends on the dosage form.
<低分子ペクチンの生成(1)>
ペクチン(UNIPECTINE SS ND:Cargill社製)300gを水3kgに分散させ、オートクレーブ(HIRAYAMA HA-240M)で121℃135分間加圧加熱を行い、低分子ペクチン溶液2453gを得た。この低分子ペクチンの重合度を測定した結果、12であった。
低分子ペクチンは食品、化粧品、医薬品等の成分として用いることができる。得られる低分子ペクチンは水溶液として得られるが、これにエタノールやイソプロパノールを加えて沈殿させたり、減圧濃縮を行うことにより、さらに濃い溶液あるいは粉末として利用することも可能である。
重合度は低分子ペクチンのウロン酸量と還元末端量を定量し、下記式により求めた。ウロン酸量測定方法は、Z. Dische, J. Biol. Chem., 167, 189 (1947)に、還元末端量測定方法は、Y. Milner, G. Avigad, Carbohyd. Res., 4, 359-361 (1967)に、記載される方法によった。
<Production of low molecular weight pectin (1)>
300 g of pectin (UNIPECTINE SS ND: manufactured by Cargill) was dispersed in 3 kg of water and heated under pressure in an autoclave (HIRAYAMA HA-240M) at 121 ° C. for 135 minutes to obtain 2453 g of a low molecular weight pectin solution. The degree of polymerization of this low molecular weight pectin was measured and found to be 12.
Low molecular weight pectin can be used as a component of food, cosmetics, pharmaceuticals and the like. The resulting low molecular weight pectin can be obtained as an aqueous solution, but it can also be used as a thicker solution or powder by adding ethanol or isopropanol to this and precipitating it or concentrating under reduced pressure.
The degree of polymerization was determined by quantifying the amount of uronic acid and the amount of reducing end of low molecular weight pectin, and using the following formula. The method for measuring the amount of uronic acid is Z. Dische, J. Biol. Chem., 167, 189 (1947), and the method for measuring the amount of reducing end is Y. Milner, G. Avigad, Carbohyd. Res., 4, 359- 361 (1967).
<低分子ペクチンの生成(2)>
ペクチン(UNIPECTINE SS ND:Cargill社製)300gを水3kgに分散させ、オートクレーブ(HIRAYAMA HA-240M)で121℃300分間加圧加熱を行い、低分子ペクチン溶液2453gを得た。この低分子ペクチンの重合度を測定した結果、4であった。
<Production of low molecular weight pectin (2)>
300 g of pectin (UNIPECTINE SS ND: manufactured by Cargill) was dispersed in 3 kg of water and heated under pressure in an autoclave (HIRAYAMA HA-240M) at 121 ° C. for 300 minutes to obtain 2453 g of a low molecular weight pectin solution. The degree of polymerization of this low molecular weight pectin was measured and found to be 4.
<低分子ペクチンの生成3>
ペクチン(UNIPECTINE SS ND:Cargill社製)0.5kgを水10kgに分散した溶液を調製し、ペクチナーゼ300ppmを添加して35℃で15時間反応させて低分子化した。この溶液を濾過、濃縮、乾燥することで低分子ペクチン350gを得た。この低分子ペクチンの重合度を測定した結果、3であった。
<Generation of low molecular weight pectin 3>
A solution in which 0.5 kg of pectin (UNIPECTINE SS ND: Cargill) was dispersed in 10 kg of water was prepared, and 300 ppm of pectinase was added and reacted at 35 ° C. for 15 hours to reduce the molecular weight. This solution was filtered, concentrated and dried to obtain 350 g of low molecular weight pectin. The degree of polymerization of this low molecular weight pectin was measured and found to be 3.
<低分子ペクチンの安全性確認>
実施例1および実施例3で得られた各溶液をサンプルとし、それぞれ各15名、合計30名の被験者で皮膚塗布試験を行った。上腕部内側にスポイト3滴分のサンプルを1日2回1週間皮膚に塗布してもらい、経時変化を見た。その結果皮膚に炎症や痛み等の弊害が出た被験者はなく、低分子ペクチンが安全であることが確認された。
<Safety confirmation of low molecular weight pectin>
Each solution obtained in Example 1 and Example 3 was used as a sample, and a skin application test was performed with 15 subjects each, a total of 30 subjects. A sample of 3 drops of dropper was applied to the skin on the inner side of the upper arm twice a day for 1 week, and the change with time was observed. As a result, there was no subject who suffered from adverse effects such as inflammation and pain on the skin, and it was confirmed that low molecular weight pectin was safe.
<低分子ペクチンの皮膚の乾燥・かゆみ緩和の効果確認>
実施例1および実施例3で得られた溶液をサンプルとし、30名の被験者に皮膚塗布試験を行った。乾燥の気になる部分に患部を覆う程度に1日2回1週間塗布を行ってもらい、経時変化を見た。その結果、30名中7名が、かゆみがおさまったと回答し、30名中3名が、皮膚の乾燥が緩和されたと回答した。
<Confirmation of the effect of low molecular weight pectin on skin dryness and itching relief>
Using the solutions obtained in Example 1 and Example 3 as samples, a skin application test was performed on 30 subjects. The application was performed twice a day for 1 week to cover the affected area in the part that was worried about drying, and the change with time was observed. As a result, 7 out of 30 responded that itching had subsided, and 3 out of 30 responded that skin dryness had been alleviated.
この塗布試験を実施した被験者のその他の感想として、
・指の皮がむけていたのが改善された
・肌の乾燥が減った
・アトピー性の赤くなった状態が良くなった
・髭剃り後に塗布すると効果があった
・虫刺されによる痒み低減に効果があった
・手のアカギレが治った
などがあり、低分子ペクチンの皮膚保護作用の有効性が確認された。
As other impressions of the subject who performed this application test,
・ Improved that the skin of the finger was peeled off ・ Dry skin was reduced ・ Reddish atopic condition improved ・ It was effective when applied after shaving ・ Effective in reducing itching due to insect bites There was a cure for rusting of the hands, and the effectiveness of the low molecular weight pectin for skin protection was confirmed.
<軟膏の調製>
<Preparation of ointment>
Claims (2)
The skin dry / itch relieving agent according to claim 1, wherein the low molecular weight pectin has an average degree of polymerization of 3 to 50.
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JP2007185249A JP2009023912A (en) | 2007-07-17 | 2007-07-17 | Demulcent for dryness and itch of skin |
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JP2007185249A JP2009023912A (en) | 2007-07-17 | 2007-07-17 | Demulcent for dryness and itch of skin |
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JP2004107295A (en) * | 2002-09-20 | 2004-04-08 | National Agriculture & Bio-Oriented Research Organization | Histamine release inhibitor |
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JP2004107295A (en) * | 2002-09-20 | 2004-04-08 | National Agriculture & Bio-Oriented Research Organization | Histamine release inhibitor |
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