JP2006298889A - External aqueous composition for skin - Google Patents

External aqueous composition for skin Download PDF

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Publication number
JP2006298889A
JP2006298889A JP2005150109A JP2005150109A JP2006298889A JP 2006298889 A JP2006298889 A JP 2006298889A JP 2005150109 A JP2005150109 A JP 2005150109A JP 2005150109 A JP2005150109 A JP 2005150109A JP 2006298889 A JP2006298889 A JP 2006298889A
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effect
skin
composition
aqueous
ascorbic acid
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Tadao Miyagi
忠夫 宮城
Shigeaki Yokoi
繁明 横井
Katsuhiro Koyama
且洋 小山
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MMT KK
MMT Co Ltd
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MMT KK
MMT Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an external aqueous composition which is used for the skins, has an excellent skin-bleaching effect, excellent ageing-preventing effects (active oxygen-controlling effect, peroxidized lipid-controlling effect, collagen and elastin production-promoting effect, and the like), an excellent effect for improving wrinkles, and a good effect for holding young beautiful skins, and exhibits excellent functional characteristics, when coated on the skins. <P>SOLUTION: This stable external aqueous composition for the skins contains an ascorbic acid derivative in an amount of 5 to 30 wt.% based on the total amount of the composition, and furthermore contains an α-hydroxy acid. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は皮膚に対する美白効果並びに老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)に優れ、できてしまったシワの改善に優れた効果を有し、皮膚に塗布したときの官能特性に優れた、アスコルビン酸誘導体、α−ヒドロキシ酸を配合してなる皮膚外用水性組成物である。  The present invention is excellent in skin whitening effect and anti-aging effect (active oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect, etc.), and has an excellent effect in improving wrinkles that have been made, It is an aqueous composition for external use on skin, which is excellent in sensory characteristics when applied to the skin, and is formulated with an ascorbic acid derivative and an α-hydroxy acid.

従来、アスコルビン酸は粉体であり水に非常に溶解性が良好であることが良く知られている。しかし、水に溶解したアスコルビン酸は水中の酸素等の影響により極めて短時間でその効力を失うこともまた良く知られる事実である。化粧品等の配合成分としてアスコルビン酸は美白効果の高い成分として使用されることがあるが、前述の如く水中安定性が悪いために、紛体又はタブレットの状態で使用することは可能ではあるものの、いわゆる化粧品として実際の製品に使用することは非常に困難である。従って、皮膚に塗布して美白効果並びに老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)を有する成分としては、安定性も高く、皮膚効果性も高いアスコルビン酸誘導体が化粧品等の皮膚外用水性組成物として広く使用されているが、アスコルビン酸誘導体の水への配合濃度は溶解性等の問題から配合上限が5%前後であり、また経時的に沈殿を生ずる等の問題から、皮膚に対する美白効果並びに老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)としては未だ満足し得るものではない。  Conventionally, it is well known that ascorbic acid is a powder and has very good solubility in water. However, it is also well known that ascorbic acid dissolved in water loses its effectiveness in a very short time due to the influence of oxygen in the water. Ascorbic acid may be used as a component with a high whitening effect as a blending component of cosmetics and the like, but because it has poor underwater stability as described above, it can be used in the form of powder or tablet, but it is so-called It is very difficult to use it in a real product as a cosmetic. Therefore, as a component that is applied to the skin and has a whitening effect and an anti-aging effect (active oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect, etc.), it has high stability and skin effect. Ascorbic acid derivatives are widely used as an external skin composition for cosmetics and the like, but the concentration of the ascorbic acid derivative in water is around 5% due to solubility and other problems. Due to problems such as precipitation, the skin whitening effect and anti-aging effect (active oxygen inhibitory effect, lipid peroxide inhibitory effect, collagen / elastin production promoting effect, etc.) are still unsatisfactory.

また、真皮中の腺維芽細胞の増殖によるコラーゲン・エラスチン・ヒアルロン酸等の生成を促進してシワの改善を促し、皮膚の若さ維持、老化防止効果を有する成分として、α−ヒドロキシ酸が知られているが、アスコルビン酸誘導体との水溶液への共存配合は、それぞれのpH値が相反することによる安定性の問題から困難とされている。  In addition, it promotes the production of collagen, elastin, hyaluronic acid, etc. by the proliferation of glandular fibroblasts in the dermis and promotes the improvement of wrinkles. As is known, coexistence in an aqueous solution with an ascorbic acid derivative is considered to be difficult due to stability problems due to conflicting pH values.

しかし、多くの女性にとって白い肌を手に入れること、シワのない若々しい肌をいつまでも維持することは究極の理想であり、美肌を維持して毎日の生活を自信を持って楽しく過ごすためにも、美白効果、老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)に優れ、できてしまったシワの改善に優れた皮膚外用水性組成物が求められている。  However, for many women, it is the ultimate ideal to have white skin and to keep youthful skin without wrinkles forever. To maintain beautiful skin and enjoy everyday life with confidence and fun. Has an excellent whitening effect, anti-aging effect (reactive oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect, etc.), and an aqueous composition for external use for skin that is excellent in improving wrinkles. It has been.

従って、本発明の目的は、皮膚に対する美白効果、老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)に優れ、シワ改善効果を有して若々しい美肌を保つ効果を有する皮膚外用水性組成物を提供することにある。  Therefore, the object of the present invention is excellent in the skin whitening effect, anti-aging effect (active oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect, etc.), and has a youthful wrinkle improving effect. An object of the present invention is to provide an aqueous composition for external use having the effect of maintaining beautiful skin.

本発明者はこのような実情に鑑み、優れた美白効果、老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)に優れ、シワ改善効果を有する皮膚外用水性組成物について鋭意検討した結果、アスコルビン酸誘導体を組成物の総重量を基準にして5〜30重量%高配合し、かつα−ヒドロキシ酸を共存配合してこれらの効果に優れた安定性の高い皮膚外用水性組成物の発明を完成するに至った。  In view of such circumstances, the present inventor has excellent whitening effect, anti-aging effect (active oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect, etc.), and has an effect of improving wrinkles. As a result of diligent examination of the aqueous composition for use, the ascorbic acid derivative is blended in an amount of 5 to 30% by weight based on the total weight of the composition, and the α-hydroxy acid is blended together and the stability is excellent in these effects. The present invention has been completed.

即ち、本発明は、これまでには困難と考えられていた高濃度である、組成物の総重量を基準にして5〜30重量%のアスコルビン酸誘導体を含有し、かつ、同時にα−ヒドロキシ酸を含有することを特徴とする皮膚外用水性組成物である。  That is, the present invention contains 5 to 30% by weight of ascorbic acid derivative based on the total weight of the composition, which has been considered difficult until now, and at the same time α-hydroxy acid. It is an aqueous | water-based composition for external use of the skin characterized by containing.

本発明の実施の形態Embodiment of the present invention

本発明の皮膚外用水性組成物は、当該組成物の総重量を基準にして、0.1〜20重量%のポリオール類、0.01〜1.0重量%のHLBの範囲が約10.0〜16.0のノニオン界面活性剤、0.01〜1.0重量%のα−ヒドロキシ酸、5〜30重量%のアスコルビン酸誘導体および1〜94.5重量%の水を配合してなるものである。  The aqueous skin composition for external use of the present invention has a range of 0.1 to 20% by weight of polyols and 0.01 to 1.0% by weight of HLB based on the total weight of the composition. 0 to 16.0 nonionic surfactant, 0.01 to 1.0% by weight α-hydroxy acid, 5 to 30% by weight ascorbic acid derivative and 1 to 94.5% by weight water. Is.

本発明に用いられるポリオールとは、皮膚に対する保湿性の高い多価アルコールであり、例えばグリセリン、ジグリセリン、1,3ブチレングリコール、プロピレングリコール、ペンチレングリコール等をいい、化粧品の保湿成分としての汎用性が高いものである。これはアスコルビン酸誘導体が高濃度の場合、当該皮膚外用水性組成物を肌に塗布して水分が蒸散し肌の乾燥をひきおこす可能性がある為である。尚、上記のポリオール類は一例であり、水溶性で保湿効果の高いもので配合が可能であれば上記に限定されるものではない。また、保湿効果を上げるために、多糖類の配合、例えばヒアルロン酸等のムコ多糖類の使用も効果的である。  The polyol used in the present invention is a polyhydric alcohol having high moisture retention on the skin, such as glycerin, diglycerin, 1,3 butylene glycol, propylene glycol, pentylene glycol, etc. It is highly probable. This is because, when the ascorbic acid derivative is in a high concentration, the skin external aqueous composition may be applied to the skin to cause moisture to evaporate and cause the skin to dry. In addition, said polyol is an example, and if it can mix | blend with what is water-soluble and has a high moisturizing effect, it will not be limited to the above. In order to increase the moisturizing effect, it is also effective to use polysaccharides such as mucopolysaccharides such as hyaluronic acid.

一般的にノニオン界面活性剤は、溶解、分散、乳化等に用いられるが、当該皮膚外用水性組成物においては溶解性を高める目的から、可溶化性のノニオン界面活性剤としてPOE硬化ヒマシ油を使用している。一般的にPOE硬化ヒマシ油は硬化ヒマシ油にポリオキシエチレン鎖を反応させてできた可溶化性能の高い活性剤であり、注射薬の可溶化剤としても使用されている。本発明で用いられるPOE硬化ヒマシ油とは、HLB範囲が約10.0〜16.0、好ましくは12.0〜14.0であり、ポリオキシエチレンが40モル〜60モル付加されたPOE硬化ヒマシ油である。  In general, nonionic surfactants are used for dissolution, dispersion, emulsification, and the like. For the purpose of enhancing the solubility in the aqueous external composition, POE hydrogenated castor oil is used as a solubilizing nonionic surfactant. I use it. In general, POE hydrogenated castor oil is an active agent having high solubilization performance obtained by reacting hydrogenated castor oil with polyoxyethylene chains, and is also used as a solubilizer for injections. POE hydrogenated castor oil used in the present invention has an HLB range of about 10.0 to 16.0, preferably 12.0 to 14.0, and POE cured with 40 to 60 mol of polyoxyethylene added. Castor oil.

本発明に用いられるα−ヒドロキシ酸は一般的にフルーツ等に含まれるクエン酸、りんご酸、酒石酸等であるが、これらの水溶液のpH値は酸性側にあり、本発明の皮膚外用水性組成物はアルカリ側にあることから、多量のα−ヒドロキシ酸を配合した場合は組成物の安定性に影響が出るため、配合濃度は0.01〜1.0重量%、好ましくは0.01〜0.5重量%が適正である。1.0重量%以上の配合になると、アスコルビン酸誘導体の溶解安定性に影響が出て沈殿が生じることがある。本発明においては、アスコルビン酸誘導体の配合量が最大30重量%と高濃度であることから、特にpH依存の安定性が高く、α−ヒドロキシ酸の配合量が多すぎることは禁忌である。上記の内容による成分を配合することにより、皮膚に対する美白効果、老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果)を同時に得ることができ、また皮膚に対して刺激を実質的に与えず、皮膚に対する作用が温和な皮膚外用水性組成物を得ることができる。  The α-hydroxy acid used in the present invention is generally citric acid, malic acid, tartaric acid, etc. contained in fruits and the like, but the pH value of these aqueous solutions is on the acidic side, and the aqueous composition for external use of the skin of the present invention Since the product is on the alkali side, when a large amount of α-hydroxy acid is blended, the stability of the composition is affected, so the blending concentration is 0.01 to 1.0% by weight, preferably 0.01 to 0.5% by weight is appropriate. When the blending amount is 1.0% by weight or more, the dissolution stability of the ascorbic acid derivative is affected and precipitation may occur. In the present invention, since the amount of ascorbic acid derivative is as high as 30% by weight, the pH-dependent stability is particularly high, and it is contraindicated that the amount of α-hydroxy acid is too large. By blending the ingredients according to the above contents, whitening effect on skin, anti-aging effect (reactive oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect) can be obtained at the same time. Thus, it is possible to obtain an aqueous external composition for skin that does not substantially irritate and has a mild effect on the skin.

以下に、本発明の皮膚外用水性組成物の実施例を示す。これらの実施例は本発明をより詳しく説明するためのものであり、本発明の範囲を限定するものでなく、種々の変更が可能である。尚、実施例中の〔%〕とあるものはいずれも重量%を示す。  Examples of the aqueous skin composition for external use of the present invention are shown below. These examples are for explaining the present invention in more detail, and do not limit the scope of the present invention, and various modifications are possible. In the examples, [%] indicates weight%.

実施例1
配合成分 配合割合〔%〕
(1) クエン酸 0.002
(2) グリコール酸 0.002
(3) リンゴ酸 0.002
(4) 茶エキス 0.002
(5) グルコース 0.002
(6) アスコルビルリン酸Na 20.000
(7) POE硬化ヒマシ油(60E0) 0.010
(8) ペンチレングリコール 3.000
(9) メチルパラベン 0.010
(10)精製水 76.880
合 計 100.000
Example 1
Blending ingredients Blending ratio [%]
(1) Citric acid 0.002
(2) Glycolic acid 0.002
(3) Malic acid 0.002
(4) Tea extract 0.002
(5) Glucose 0.002
(6) Ascorbyl phosphate Na 20.000
(7) POE hydrogenated castor oil (60E0) 0.010
(8) Pentylene glycol 3.000
(9) Methylparaben 0.010
(10) Purified water 76.880
Total 100.000

調整方法
〔1〕(1)〜(6)及び(10)の成分を常温で攪拌溶解する。
〔2〕(7)〜(9)の成分を60℃で加熱溶解する。
〔3〕〔1〕、〔2〕を常温で混合攪拌溶解する。
Preparation method [1] The components of (1) to (6) and (10) are stirred and dissolved at room temperature.
[2] The components (7) to (9) are dissolved by heating at 60 ° C.
[3] [1] and [2] are mixed and dissolved at room temperature.

得られた皮膚外用水性組成物の一部を取り出し、5℃冷却における安定性を確認したところ、90日経過においても、沈殿は生じず安定であった。  A part of the obtained aqueous external composition for skin was taken out and confirmed to be stable at 5 ° C. cooling. As a result, even after 90 days, no precipitation occurred and the composition was stable.

実施例2
実施例1におけるリンゴ酸の変わりに酒石酸を、ペンチレングリコールの代わりに1,3ブチレングリコールを、POE硬化ヒマシ油(60E0)の代わりにPOE硬化ヒマシ油(50E0)を配合し、同様の性状、安定性を得られた。
Example 2
Tartaric acid instead of malic acid in Example 1, 1,3-butylene glycol instead of pentylene glycol, POE hydrogenated castor oil (50E0) instead of POE hydrogenated castor oil (50E0), the same properties, Stability was obtained.

実施例3
配合成分 配合割合〔%〕
(1) ヒアルロン酸Na 0.0500
(2) クエン酸 0.0025
(3) 乳酸 0.0025
(4) リンゴ酸 0.0025
(5) 茶エキス 0.0025
(6) アスコルビルリン酸Na 10.0000
(7) POE硬化ヒマシ油(60E0) 0.0100
(8) ペンチレングリコール 3.0000
(9) メチルパラベン 0.1000
(10)精製水 86.8300
合 計 100.0000
Example 3
Blending ingredients Blending ratio [%]
(1) Hyaluronic acid Na 0.0500
(2) Citric acid 0.0025
(3) Lactic acid 0.0025
(4) Malic acid 0.0025
(5) Tea extract 0.0025
(6) Ascorbyl phosphate Na 10.00000
(7) POE hydrogenated castor oil (60E0) 0.0100
(8) Pentylene glycol 3.0000
(9) Methylparaben 0.1000
(10) Purified water 86.8300
Total 100.000

調整方法
〔1〕(1)〜(6)及び(10)の成分を常温で攪拌溶解する。
〔2〕(7)〜(9)の成分を60℃で加熱溶解する。
〔3〕〔1〕、〔2〕を常温で混合攪拌溶解する。
Preparation method [1] The components of (1) to (6) and (10) are stirred and dissolved at room temperature.
[2] The components (7) to (9) are dissolved by heating at 60 ° C.
[3] [1] and [2] are mixed and dissolved at room temperature.

得られた皮膚外用水性組成物の一部を取り出し、5℃冷却における安定性を確認したところ、90日経過においても、沈殿は生じず安定であった。  A part of the obtained aqueous external composition for skin was taken out and confirmed to be stable at 5 ° C. cooling. As a result, even after 90 days, no precipitation occurred and the composition was stable.

実施例4
実施例3における茶エキスの変わりに酒石酸を、ペンチレングリコールの代わりに1、3ブチレングリコールを、POE硬化ヒマシ油(60E0)の代わりにPOE硬化ヒマシ油(50E0)を配合し、同様の性状、安定性を得られた。
Example 4
Tartaric acid instead of tea extract in Example 3, 1,3 butylene glycol instead of pentylene glycol, POE hydrogenated castor oil (50E0) instead of POE hydrogenated castor oil (50E0), the same properties, Stability was obtained.

実施例5
配合成分 配合割合〔%〕
(1) ヒアルロン酸Na 0.05
(2) クエン酸 0.002
(3) グリコール酸 0.002
(4) 乳酸 0.002
(5) リンゴ酸 0.002
(6) 酒石酸 0.002
(7) 茶エキス 0.002
(8) グルコース 0.002
(9) アスコルビルリン酸Na 30.000
(10)グリセリン 2.000
(11)POE硬化ヒマシ油(60E0) 0.010
(12)ペンチレングリコール 3.000
(13)メチルパラベン 0.100
(14)精製水 64.826
合計 100.000
Example 5
Blending ingredients Blending ratio [%]
(1) Hyaluronic acid Na 0.05
(2) Citric acid 0.002
(3) Glycolic acid 0.002
(4) Lactic acid 0.002
(5) Malic acid 0.002
(6) Tartaric acid 0.002
(7) Tea extract 0.002
(8) Glucose 0.002
(9) Ascorbyl phosphate Na 30.000
(10) Glycerol 2.000
(11) POE hydrogenated castor oil (60E0) 0.010
(12) Pentylene glycol 3000
(13) Methylparaben 0.100
(14) Purified water 64.826
Total 100.000

調整方法
〔1〕(1)〜(10)及び(14)の成分を常温で攪拌溶解する。
〔2〕(11)〜(13)の成分を60℃で加熱溶解する。
〔3〕〔1〕、〔2〕を常温で混合攪拌溶解する。
Preparation method [1] The components of (1) to (10) and (14) are stirred and dissolved at room temperature.
[2] The components (11) to (13) are dissolved by heating at 60 ° C.
[3] [1] and [2] are mixed and dissolved at room temperature.

得られた皮膚外用水性組成物の一部を取り出し、5℃冷却における安定性を確認したところ、90日経過においても、沈殿は生じず安定であった。  A part of the obtained aqueous external composition for skin was taken out and confirmed to be stable at 5 ° C. cooling. As a result, even after 90 days, no precipitation occurred and the composition was stable.

実施例6
実施例5におけるペンチレングリコールの代わりに1,3ブチレングリコールを、POE硬化ヒマシ油(60E0)の代わりにPOE硬化ヒマシ油(50E0)を配合し、同様の性状、安定性を得られた。

Figure 2006298889
Figure 2006298889
Example 6
The same properties and stability were obtained by blending 1,3 butylene glycol in place of pentylene glycol in Example 5 and POE hydrogenated castor oil (50E0) in place of POE hydrogenated castor oil (60E0).
Figure 2006298889
Figure 2006298889

実施例1の本発明の皮膚外用水性組成物は、人の上腕部内側を用いて人工紫外線照射によりメラニン色素を生成させた後、アスコルビン酸誘導体未配合の水溶液をコントロールとして、30日間塗布比較を行った結果、実施例1の皮膚外用水性組成物を塗布した部位が明らかにメラニン色素の消失が早く、美白効果が優れていることが証明された。  The aqueous composition for external application of the skin of Example 1 of the present invention was applied for 30 days using an aqueous solution containing no ascorbic acid derivative as a control after producing melanin pigment by artificial ultraviolet irradiation using the inner side of the upper arm of a person. As a result, it was proved that the site where the aqueous composition for external application of Example 1 was applied clearly lost melanin quickly and had an excellent whitening effect.

シワの改善効果においては70日間の塗布により、しわの深さが浅くなったことが確認された。(輝度陰影法)  In the wrinkle improvement effect, it was confirmed that the wrinkle depth became shallow after 70 days of application. (Luminance shading method)

また、塗布使用性にも優れ、肌がしっとりするとの評価であった。  Moreover, it was evaluation that it was excellent also in application | use usability and skin was moist.

発明の効果The invention's effect

本発明により、皮膚に対する美白効果並びに老化防止効果(活性酸素抑制効果、過酸化脂質抑制効果、コラーゲン・エラスチンの生成促進効果等)に優れ、できてしまったシワの改善に対する優れた効果を有し、皮膚に塗布したときの官能特性に優れていることから、今後予測される高齢化社会への朗報となるとともに、多くの女性に夢と希望を与えられる化粧料等に応用・提供することができる。  According to the present invention, it has excellent whitening effect on skin and anti-aging effect (active oxygen suppression effect, lipid peroxide suppression effect, collagen / elastin production promotion effect, etc.), and has an excellent effect on improving wrinkles that have been made. Excellent sensory characteristics when applied to the skin, it will be a good news for the future aging society, and it can be applied to and provided in cosmetics that give dreams and hope to many women. it can.

Claims (3)

ポリオール類及びノニオン界面活性剤を必須成分とし、組成物の総重量を基準にして0.1%〜20重量%のポリオール類、0.01〜1.0重量%のノニオン界面活性剤を溶解した水溶液にアスコルビン酸誘導体を配合して安定なる、高濃度アスコルビン酸誘導体配合の皮膚外用水性組成物。  Polyols and nonionic surfactants are essential components, and 0.1% to 20% by weight of polyols and 0.01% to 1.0% by weight of nonionic surfactants were dissolved based on the total weight of the composition. An aqueous composition for external application of skin containing a high-concentration ascorbic acid derivative, which is stabilized by adding an ascorbic acid derivative to an aqueous solution. 水溶液に含まれるアスコルビン酸誘導体の含有量が当該組成物の総重量を基準にして5%〜30重量%である請求項1記載の皮膚外用水性組成物。  The aqueous skin composition for external use according to claim 1, wherein the content of the ascorbic acid derivative contained in the aqueous solution is 5% to 30% by weight based on the total weight of the composition. α−ヒドロキシ酸が一種または二種以上の混合物からなり、pHの範囲が約7.5〜9.0である請求項1記載の皮膚外用水性組成物。  The aqueous external composition for skin according to claim 1, wherein the α-hydroxy acid is composed of one kind or a mixture of two or more kinds and has a pH range of about 7.5 to 9.0.
JP2005150109A 2005-04-20 2005-04-20 External aqueous composition for skin Pending JP2006298889A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009149537A (en) * 2007-12-19 2009-07-09 Lion Corp Oral composition
JP2010248128A (en) * 2009-04-16 2010-11-04 Fancl Corp Oil-in-water type emulsion composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009149537A (en) * 2007-12-19 2009-07-09 Lion Corp Oral composition
JP2010248128A (en) * 2009-04-16 2010-11-04 Fancl Corp Oil-in-water type emulsion composition

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