JP2019119705A - Oral composition for improving touch feeling including adlay extract - Google Patents

Oral composition for improving touch feeling including adlay extract Download PDF

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JP2019119705A
JP2019119705A JP2017255193A JP2017255193A JP2019119705A JP 2019119705 A JP2019119705 A JP 2019119705A JP 2017255193 A JP2017255193 A JP 2017255193A JP 2017255193 A JP2017255193 A JP 2017255193A JP 2019119705 A JP2019119705 A JP 2019119705A
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skin
extract
oral composition
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友規 井上
Yuki Inoue
友規 井上
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Sunstar Inc
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Abstract

To provide a novel application of adlay extract.SOLUTION: There is provided the oral composition for improving touch feeling including adlay extract.SELECTED DRAWING: None

Description

本発明は、ハトムギエキスを含有する、肌触り感改善用の経口組成物等に関する。   The present invention relates to an oral composition and the like for improving the feel of the skin, which comprises a cottonseed extract.

ハトムギは、通常、脱穀した子実を食用とするが、脱穀時に得られるハトムギの殻、薄皮、渋皮等についても有効利用の検討がなされており、例えば、特許文献1には、ハトムギの殻、薄皮、渋皮等を酵素処理等して得られるエキスが腫瘍等の治療に有効であることが記載されている。また、特許文献1に記載のハトムギエキスの一態様は、ハトムギCRDエキスとして株式会社アグリリンクテクノロジーから市販されている。また、ハトムギエキスを安定に含有する液状組成物についても開発が行われている(特許文献2)。   Hatomugi usually use threshed grains for food, but studies have also been made on effective use of the hut shell, thin skin, astringent skin etc. obtained at the time of threshing. It is described that an extract obtained by enzymatic treatment of thin skin, astringent skin and the like is effective for treatment of a tumor and the like. In addition, one aspect of the adlay extract described in Patent Document 1 is commercially available from Agrilink Technology, Inc. as adlay CRD extract. In addition, development has also been carried out for liquid compositions that contain a stable extract of castor bean extract (Patent Document 2).

特許第3590042号公報Patent No. 3590042 特開2014−090675号公報JP, 2014-090675, A

本発明は、ハトムギエキスの新規用途を提供することを課題とする。   An object of the present invention is to provide a novel use of a mint extract.

本発明者らは、ハトムギエキスを経口摂取することで肌触り感を向上させ、化粧のりも向上させ得ることを見出し、さらに改良を重ねて本発明を完成させるに至った。
本発明は例えば以下の項に記載の主題を包含する。
項1.
ハトムギエキスを含有する、肌触り感改善用経口組成物。
項2.
顔の肌の肌触り感改善用である、項1に記載の経口組成物。
項3.
少なくとも4週間継続投与又は摂取するように用いられる、項1または2いずれか1項に記載の経口組成物。
項4.
液体組成物である、項1〜3のいずれか1項に記載の経口組成物。
項5.
医薬組成物又は食品組成物である、項1〜4のいずれか1項に記載の経口組成物。
The inventors of the present invention found that oral intake of Hatomugi extract can improve the touch feeling and the cosmetic paste, and further improvement has been made to complete the present invention.
The present invention includes, for example, the subject matter described in the following sections.
Item 1.
An oral composition for improving the feeling of touch, which comprises an eggplant extract.
Item 2.
Item 2. The oral composition according to item 1, which is for improving the feel of facial skin.
Item 3.
The oral composition according to any one of Items 1 and 2, which is used for continuous administration or intake for at least 4 weeks.
Item 4.
The oral composition according to any one of Items 1 to 3, which is a liquid composition.
Item 5.
The oral composition according to any one of Items 1 to 4, which is a pharmaceutical composition or a food composition.

本発明に係る肌触り感改善用経口組成物により、肌触り感が改善し、化粧のりが良くなることで化粧がしやすくなる。   With the oral composition for improving the feeling of touch according to the present invention, the feeling of feeling is improved and the cosmetic paste is improved, so that makeup can be facilitated.

典型的な静動摩擦測定波形の例を示す。An example of a typical static friction measurement waveform is shown. 静摩擦出現距離の測定結果を示す。The measurement result of static friction appearance distance is shown. 静摩擦係数の測定結果を示す。The measurement results of the static friction coefficient are shown. 平均動摩擦係数の測定結果を示す。The measurement results of the average dynamic friction coefficient are shown. 水負荷試験の総水分量の測定結果を示す。The measurement result of the total water content of a water load test is shown. 水負荷試験の水分保持能の測定結果を示す。The measurement result of the water retention ability of a water load test is shown. Cutometerの測定で得られる典型的な波形の例を示す。The example of the typical waveform obtained by the measurement of Cutometer is shown. Cutometerの測定で得られた波形から得られる再変形能力(R1)の結果を示す。The result of the re-deformability (R1) obtained from the waveform obtained by the measurement of the Cutometer is shown. Cutometerの測定で得られた波形から得られる正味の弾力性(R5)の結果を示す。The result of the net elasticity (R5) obtained from the waveform obtained by the measurement of the Cutometer is shown. レプリカの陰影画像から得られた肌のキメ体積率の結果を示す。The result of the skin volume fraction obtained from the shadow image of a replica is shown. レプリカの陰影画像から得られた肌のキメ最大深長の結果を示す。The result of the skin texture maximum depth obtained from the shadow image of the replica is shown. レプリカの陰影画像から得られた肌のキメ最大幅長の結果を示す。The result of the texture maximum width of the skin obtained from the shadow image of the replica is shown. アンケートによる「肌の調子」の集計結果を示す。We show tallying result of "skin condition" by questionnaire. アンケートによる「肌のハリ」の集計結果を示す。We show count result of "skin firmness" by questionnaire. アンケートによる「肌のキメ・なめらかさ」の集計結果を示す。We show tallying result of "skin texture, smoothness" by questionnaire. アンケートによる「肌の手触り感」の集計結果を示す。We show count result of "feel of skin touch" by questionnaire. アンケートによる「化粧のりの良さ」の集計結果を示す。We show tallying result of "goodness of makeup paste" by questionnaire.

以下、本発明の各実施形態について、さらに詳細に説明する。   Hereinafter, each embodiment of the present invention will be described in more detail.

本発明に包含される肌触り感改善用経口組成物は、ハトムギエキスを含有する。   The oral composition for improving the feel included in the present invention contains a mint extract.

本発明に用いるハトムギエキスは、特許文献1(特許第3590042号公報)に記載されるハトムギエキスであり、より詳細には、少なくともハトムギの殻・薄皮・渋皮の酵素処理物を遠心濾過し、得られた上清画分を濃縮し(目的に応じて更に乾燥して)得られるハトムギエキスである。よって、当該ハトムギエキスはハトムギ酵素処理エキスといえる。当該酵素処理に用いる酵素は、該特許文献1に記載の通りであり、ジアスターゼ、タカジアスターゼ、α−アミラーゼ、β−アミラーゼ、グルコアミラーゼ等、ペクチナーゼ、β−ダルコシダーゼ、セルラーゼ、ヘミセルラーゼ、キシラナーゼ等の各種の酵素が挙げられる。つまり、当該酵素処理に用いる酵素は、多糖類(例えばデンプン、セルロース、ペクチンなど)を構成する各糖分子間のα−1,4結合又はα−1,6結合を切断する酵素である。酵素処理時には、例えば水などの適当な溶媒を用いることができる。 なお、本発明に用いるハトムギエキスは、ハトムギの殻、薄皮及び渋皮から選択される少なくとも1種から得られるハトムギ酵素処理エキスが含まれていればよい。よって、その他のハトムギエキスが含まれていてもよく、例えば、ハトムギの殻・薄皮・渋皮以外の部分(例えば子実、茎など)を同様に処理して得られるハトムギ酵素処理エキスが更に含まれていても、あるいはハトムギの熱水抽出エキスが含まれていてもよい。好ましくは、本発明のハトムギエキスは、ハトムギの殻、薄皮及び渋皮から選択される少なくとも1種から得られるハトムギ酵素処理エキスを主に含むものである。上述した本発明に用いるハトムギエキスとしては、市販品を用いることもでき、例えばハトムギCRDエキス(株式会社アグリリンクテクノロジー製)を特に好適に用いることができる。 本発明に係るくすみ改善用経口組成物が含有するハトムギエキスは、特に制限はされないが、乾燥質量換算で、1000〜20000mg程度が好ましく、3000〜15000mg程度がより好ましく、5000〜10000mg程度がさらに好ましい。   The Hatomugi extract used in the present invention is the Hatomugi extract described in Patent Document 1 (Japanese Patent No. 3590042), and more specifically, it is obtained by centrifugally filtering at least the enzyme-treated product of the husk shell, skin and astringent skin. It is a cottonseed extract obtained by concentrating the obtained supernatant fraction (by further drying according to the purpose). Therefore, the Hatomugi extract can be said to be a Hatomugi enzyme-treated extract. The enzymes used for the enzyme treatment are as described in the patent document 1, and include diastase, takadiastase, α-amylase, β-amylase, glucoamylase, etc., pectinase, β-dalcosidase, cellulase, hemicellulase, xylanase etc. Various enzymes are mentioned. That is, the enzyme used for the said enzyme process is an enzyme which cut | disconnects the alpha-1, 4 bond or alpha-1, 6 bond between each sugar molecule which comprises polysaccharides (for example, starch, cellulose, pectin etc.). At the time of enzyme treatment, a suitable solvent such as water can be used, for example. In addition, the cottonseed extract to be used in the present invention may contain a cottonseed extract treated with a cottonseed extract obtained from at least one selected from a hut shell, thin skin and astringent skin. Therefore, other cottonseed extract may be included, for example, a cotton bean enzyme-treated extract obtained by similarly treating other parts (for example, grains, stems, etc.) other than the husk shell, thin skin and astringent skin is further included Or may contain hot water extract of castor bean. Preferably, the cottonseed extract of the present invention mainly comprises a cotton bean enzyme-treated extract obtained from at least one selected from husk shell, thin skin and astringent skin. A commercial item can also be used as a Hatomugi extract used for this invention mentioned above, for example, a Hatomugi CRD extract (made by Agrilink Technology, Inc.) can be used especially suitably. No particular limitation is imposed on the hazemoth extract contained in the oral composition for improving blur according to the present invention, but about 1000 to 20000 mg is preferable, about 3000 to 15000 mg is more preferable, and about 5000 to 10000 mg is more preferable. .

「肌触り感」とは、特に肌に指の腹を当て、指を滑らせたときに指や肌に感じる感触から受ける触感を意味し、本願で言う「良い肌触り感」とは、均質な感触でかつ引っかかりを感じない滑らかな印象を受ける触感である。肌触りに関与する要因としては、肌表面の凹凸の状態、皮膚表面の水分量や水分保持力の程度、肌の弾性や形状復元力の程度などが挙げられ、それらの複合的な作用は、肌の静摩擦計数や動摩擦計数を測定することにより相対的に評価出来る。一般的には、肌表面の凹凸の程度が少なく、凹凸の存在は均一であり、弾力性に富み、かつ形状復元性が高い皮膚は、肌表面部位における静摩擦計数や動摩擦計数の変動が少なく、その平均値も小さくなることから、「良い肌触り感」を有すると考えられる。また、特に、顔の皮膚において化粧を行なう際に肌の状態の差異を微妙に実感されるが、一般的に良い肌触り感を有する肌は化粧のりが良い。化粧のりの評価としては、たとえば、皮膚表面の凹凸の状態は、特に粉体を含有する化粧品であるファンデーションを塗布する際の化粧品の延ばし易さ、単位面積当たりの皮膚への化粧品組成物の付着量(塗布量)の相違や付着量の均一性に影響を与えやすく、最終的な化粧の完成度に大きな影響を与えやすい。従って、日常化粧を行なう人において、化粧のりの実感は化粧のし易さや化粧の出来栄えを左右することから、非常に気になるポイントとなっており、化粧を日常行なっている女性は、化粧の都度、評価していることから、肌触り感や化粧のりに関して鋭敏な評価ができる人が多い。従って、官能評価は「肌触り感」の総合的な評価として極めて重要である。   "Feeling feel" refers to the touch received from the feel felt by the finger or the skin, especially when the finger is placed on the skin and the finger is slipped, and "good feel" in the present application means a homogeneous feeling. And feel a smooth impression without feeling stuck. Factors involved in the touch include the state of unevenness of the skin surface, the amount of moisture and moisture retention of the skin surface, and the degree of elasticity and shape restoration of the skin, and their combined action is The relative evaluation can be made by measuring the static friction coefficient or the dynamic friction coefficient of the In general, skin with a small degree of unevenness on the skin surface, uniform presence of unevenness, high elasticity, and high shape restoration property has less variation in static friction coefficient and dynamic friction coefficient on the skin surface, Since the average value also decreases, it is considered to have a "good touch feeling". Further, in particular, when makeup is performed on the skin of the face, the difference in skin condition is slightly felt, but in general, the skin having a good touch feeling has a good makeup paste. For the evaluation of makeup paste, for example, the state of unevenness of the skin surface is the spreadability of the cosmetic when applying foundation which is a cosmetic containing a powder in particular, adhesion of the cosmetic composition to the skin per unit area It is easy to affect the difference of the amount (application amount) and the uniformity of the adhesion amount, and it is easy to greatly affect the final cosmetic perfection. Therefore, in people who do daily makeup, the feeling of making up the makeup affects the ease of making up and finishing of the makeup, so it has become a very anxious point, and women who are regularly doing up As we evaluate each time, there are many people who are able to make a quick evaluation regarding the feeling of touch and the paste of makeup. Therefore, sensory evaluation is extremely important as a comprehensive evaluation of "feel".

本発明に係る肌触り感改善用の経口組成物は、特に制限はされないが、一日適量を継続して投与又は摂取されることが好ましい。継続期間としては、少なくとも2週間が好ましく挙げられ、少なくとも4週間がより好ましく挙げられる。本発明に係る肌触り感改善用の経口組成物の、一日の適当な投与又は摂取量としては、特に制限はされないが、例えば成人一日あたり、ハトムギエキスが2000〜40000mg程度含有される量が好ましく、6000〜30000mg程度含有される量がより好ましく、10000〜20000mg程度含有される量がさらに好ましい。本発明に係る肌触り感改善用の経口組成物を継続投与又は摂取することにより、投与又は摂取を中断したとしても、その投与又は摂取中断中でも肌触り改善効果が持続及び/増強され得る。   The oral composition for improving the feeling of touch according to the present invention is not particularly limited, but it is preferable that the daily dosage be continuously administered or taken. The duration is preferably at least 2 weeks, more preferably at least 4 weeks. The appropriate daily administration or intake of the oral composition for improving the feeling of touch according to the present invention is not particularly limited, but for example, an amount containing about 2000 mg to about 40 000 mg of adlay extract per adult day Preferably, an amount of about 6000 to 300000 mg is more preferable, and an amount of about 10000 to 20000 mg is more preferable. By continuing administration or intake of the oral composition for improving the feel according to the present invention, even if administration or intake is interrupted, the skin improvement effect can be sustained and / or enhanced even when administration or intake is interrupted.

本発明に係る肌触り感改善用の経口組成物は、固体組成物であっても液体組成物であってもよいが、液体組成物であることが好ましい。液体組成物とする場合には、特許文献2(特開2014−090675号公報)の記載を参考にすることで、液体組成物中でハトムギエキスを安定に含有させることができる。   The oral composition for improving the feeling of touch according to the present invention may be a solid composition or a liquid composition, but is preferably a liquid composition. When it is set as a liquid composition, a poplar bean extract can be stably contained in a liquid composition by referring the description of patent document 2 (Unexamined-Japanese-Patent No. 2014-090675).

また、本発明に係る肌触り感改善用の経口組成物には、本発明の効果を損なわない範囲で、ハトムギエキス以外の他の成分を含ませてもよい。他の成分としては、例えば、通常医薬、食品添加剤又は食品に用いられる基剤、担体、添加物等が挙げられる。また、上述した、特許文献2(特開2014−090675号公報)に記載の成分が好ましく挙げられる。     In addition, the oral composition for improving the feeling of touch according to the present invention may contain other components other than the poplar extract, as long as the effects of the present invention are not impaired. Other components include, for example, bases, carriers, additives, etc. which are usually used for pharmaceuticals, food additives or foods. Moreover, the component as described in the patent document 2 (Unexamined-Japanese-Patent No. 2014-090675) mentioned above is mentioned preferably.

本発明の肌触り感改善用の経口組成物は、例えば医薬組成物又は食品組成物として好適に用いることができる。   The oral composition for improving touch feeling of the present invention can be suitably used, for example, as a pharmaceutical composition or a food composition.

本発明に係る肌触り感改善用の経口組成物を医薬組成物として用いる場合、他の成分としては、薬学的に許容される基剤、担体、及び/又は添加剤(例えば溶剤、分散剤、乳化剤、緩衝剤、安定剤、賦形剤、結合剤、崩壊剤、滑沢剤等)等が例示できる。投与形態は経皮投与又は経口投与が好ましく、経口投与がより好ましい。当該医薬組成物は常法により調製することができる。   When the oral composition for improving the feeling of touch according to the present invention is used as a pharmaceutical composition, other ingredients include pharmaceutically acceptable carriers, carriers, and / or additives (eg, solvents, dispersants, emulsifiers) , Buffers, stabilizers, excipients, binders, binders, disintegrants, lubricants, etc.). The administration mode is preferably transdermal administration or oral administration, and more preferably oral administration. The said pharmaceutical composition can be prepared by a conventional method.

本発明に係る肌触り感改善用の経口組成物を食品組成物として用いる場合、他の成分としては、食品衛生学上許容される基剤、担体、添加剤や、その他食品として利用され得る成分・材料が例示できる。例えば、フレーバーや、保存剤、香味剤、甘味剤等が挙げられ、より具体的には、例えば香味剤や甘味剤としては、クエン酸やアスコルビン酸、エリソルビン酸、ビタミンEおよびその誘導体、レモンなどの柑橘果実の搾汁、クエン酸などの有機酸やその塩、エリスリトール、キシリトール、ブドウ糖、ショ糖、異性化糖、甘草エキス、アスパルテーム、スクロース、アセスルファムカム、などが挙げられる。また、当該くすみ改善用経口組成物の形態も特に制限されず、例えば飲料として用いることができ、より具体的には例えば加工食品、健康食品(栄養機能食品、機能性表示食品、特定保健用食品等)、サプリメント、病者用食品(病院食、病人食又は介護食等も含む)等として用いることができる。これらは常法により調製することができる。特に、健康食品(栄養機能食品、機能性表示食品、特定保健用食品等)、又はサプリメントとして調製する場合は、継続的な摂取が行いやすいように、例えばドリンク剤等の形態で調製することが好ましいが、特にこれらに限定されるものではない。   When the oral composition for improving the feeling of touch according to the present invention is used as a food composition, as other ingredients, food hygiene acceptable bases, carriers, additives, and other ingredients that can be used as food Materials can be exemplified. For example, flavors, preservatives, flavoring agents, sweetening agents and the like can be mentioned, and more specifically, for example, as flavoring agents and sweetening agents, citric acid, ascorbic acid, erythorbic acid, vitamin E and its derivatives, lemon, etc. And citrus fruits, organic acids such as citric acid and salts thereof, erythritol, xylitol, glucose, sucrose, isomerized sugar, licorice extract, aspartame, sucrose, acesulfame cam, and the like. In addition, the form of the oral composition for improving darkness is not particularly limited, and can be used, for example, as a beverage, and more specifically, for example, processed foods, health foods (nutrition functional foods, functional display foods, foods for specified health use Etc.), supplements, food for the sick (including hospital food, sick food, nursing care food, etc.) and the like. These can be prepared by conventional methods. In particular, when prepared as a health food (a nutritive function food, a functional indication food, a food for specified health, etc.) or a supplement, it may be prepared, for example, in the form of a drink to facilitate continuous intake. Although preferred, it is not particularly limited thereto.

なお、本明細書において「含む」とは、「本質的にからなる」と、「からなる」をも包含する(The term "comprising" includes "consisting essentially of” and "consisting of.")。   In the present specification, the term "comprising" also includes "consisting essentially of" and "consisting of" (The term "comprising" includes "consisting essentially of" and "consisting of.").

以下、本発明をより具体的に説明するが、本発明は下記の例に限定されるものではない。   Hereinafter, the present invention will be described more specifically, but the present invention is not limited to the following examples.

試験用経口組成物(被験組成物)の調製
高圧ホモジナイザーを用い、水と増粘性剤を攪拌し適度な粘度に施した調整液に、ハトムギCRDエキス、クエン酸、フレーバー等を投入し、再びホモミキサーにより混合して均一に分散させ、30mlあたり当該ハトムギエキス8000mgが含まれる液体組成物を調製した。ビン1本あたり当該液体組成物30mlを充填し、被験組成物として、以下の検討に用いた。
Preparation of test oral composition (test composition) To the adjustment solution prepared by stirring water and thickening agent using a high-pressure homogenizer and applying an appropriate viscosity, castwood CRD extract, citric acid, flavor etc. are added again and homo The mixture was mixed and dispersed uniformly by a mixer to prepare a liquid composition containing 8000 mg of the wax extract per 30 ml. Each bottle was filled with 30 ml of the liquid composition, and used as a test composition in the following study.

試験用経口組成物(被験組成物)の飲用試験
被験者(27〜43歳の女性22名)に、被験組成物を1日1本4週間飲用した。試験デザインは単盲検試験とし、飲用直前と飲用終了時(4週間飲用直後)の各時点(0w、4wと標記する場合がある)で各種試験を実施した。なお、実施期間が7月下旬から8月下旬であったことから、試験期間中、各人の日常生活の状態をできる限り維持し、海水浴や野外活動など、過度な日焼けをする状況は避けること、エステティックなどを被験者としての条件とした。評価部位は左右の前腕内側部で、評価試験としては、摩擦計数測定(静的、動的)、水負荷測定、弾力性測定、レプリカ採取による二次元画像解析、及びアンケートとした。統計解析としては、正規分布に従っているデータは、反復測定分散分析の後にDunnettの多重比較検定を採用し、正規分布に従っていないデータは、Wilcoxonの符号付順位検定の後、Bonferroni補正を行ない、飲用直前と飲用終了時(4週間飲用直後)の有意差検定を採用した。なお、Bonferroni補正では、有意水準を比較するペアの数で割った数値(今回は0.016)を補正有意水準とした。また、統計解析には統計ソフト「SPSS version18.0 for Windows(SPSS japan Inc.)」を用いた。
Drinking test test oral composition (test composition) The test composition was consumed once a day for four weeks to 22 test subjects (22 women aged 27 to 43). The test design was a single-blind test, and various tests were carried out immediately before and at the end of drinking (4 weeks after drinking), which may be described as 0 w and 4 w. In addition, since the implementation period was from the end of July to the end of August, maintain the condition of each person's daily life as much as possible during the test period, and avoid excessive sunburn such as sea bathing and outdoor activities. And esthetics were the conditions for the subjects. The evaluation site was the inner part of the left and right forearm, and the evaluation test was friction count measurement (static, dynamic), water load measurement, elasticity measurement, two-dimensional image analysis by replica collection, and questionnaire. As statistical analysis, data following normal distribution adopts Dunnett's multiple comparison test after repeated measures analysis of variance, and data not following normal distribution is subjected to Bonferroni correction after Wilcoxon's signed rank test, just before drinking And a test of significant difference at the end of drinking (immediately after 4 weeks drinking) was adopted. In Bonferroni's correction, the value obtained by dividing the significance level by the number of pairs to be compared (this time 0.016) was used as the correction significance level. For statistical analysis, statistical software "SPSS version 18.0 for Windows (SPSS Japan Inc.)" was used.

摩擦計数測定(静的、動的)
測定部位は、左腕前腕内側部で手首側から肘方向に向けて約3分の1の距離の部位とした。測定機器としては、静動摩擦測定装置TL−201((株)トリニティラボ社製)を使用し、測定条件として、荷重(20g)、測定速度(10mm/秒)、測定距離(20mm)、測定回数(1回)を採用した。測定結果として得られる典型的な波形を図1に示す。静摩擦計数は図1のグラフの最初に表れる大きなピークに現れ、このピークが出現するまでの距離が皮膚の粘弾性と関連し、いわゆる「肌のハリ」と関連する指標といわれている。また平均動摩擦計数は、今回、プレ試験により最も計測値が安定していた部位(測定範囲0〜20mmのうち、10〜12mm)において測定された動摩擦計数の平均値を用いた。得られた結果は、静摩擦の出現距離を図2、静摩擦計数を図3及び平均動摩擦計数を図4に示す。
Friction count measurement (static, dynamic)
The measurement site was a site at a distance of about one third from the wrist side toward the elbow direction at the inner side of the left forearm. As a measuring instrument, a static friction measuring apparatus TL-201 (manufactured by Trinity Lab Co., Ltd.) is used, and as a measuring condition, load (20 g), measuring speed (10 mm / sec), measuring distance (20 mm), number of times of measurement (1 time) was adopted. A typical waveform obtained as a measurement result is shown in FIG. The static friction coefficient appears at a large peak appearing at the beginning of the graph of FIG. 1, and the distance until this peak appears is related to the viscoelasticity of the skin and is said to be an index related to so-called "skin firmness". Moreover, the average dynamic friction count used the average value of the dynamic friction count currently measured in the site | part (10-12 mm of 0-20 mm of measurement ranges) most measured value was stable by the pre test. The obtained results are shown in FIG. 2, the static friction count in FIG. 3, and the average dynamic friction count in FIG.

図2に示されるとおり、試験群では有意に距離が短くなっているのに対して、プラセボ群ではほぼ同じ値を示した。図3において示されるとおり、試験群ではほぼ同じ静摩擦計数を示しているのみ対してプラセボ群では大きく増加していた。また図4に示されるとおり、平均動摩擦計数は試験群では若干減少傾向にあるのに対して、プラセボ群では増加傾向を示した。これらから、日常生活で日光の影響を受けやすい夏場での試験を考慮すると、試験群では肌のハリが回復傾向にあり、摩擦計数はプラセボが増加傾向にあるのに対して、試験群ではほぼ同水準であることから、被検組成物の4週間の継続飲用は肌のすべり特性の悪化防止効果を示していることがわかった。   As shown in FIG. 2, while the distance was significantly shortened in the test group, the placebo group showed almost the same value. As shown in FIG. 3, the test group had a large increase whereas the placebo group only showed approximately the same static friction count. Also, as shown in FIG. 4, the mean kinetic friction coefficient tended to decrease slightly in the test group, while it tended to increase in the placebo group. From the above, considering the summer test that is susceptible to sunlight in daily life, the skin tension tends to recover in the test group, and the friction coefficient tends to increase in the placebo, while it is almost the same in the test group. From the same level, it was found that continuous drinking of the test composition for 4 weeks shows the effect of preventing the deterioration of the skin's slip characteristics.

水負荷測定
測定部位は、左腕前腕内側部で手首側から肘方向に向けて約3分の1の距離の部位とした。測定機器としては、CorneoMeter CM−825(Courage+Khazaka electronic GmbH社製)を使用した。測定方法は、先ず測定部位の水分測定を行なった後に、測定部位に20μlのイオン交換水を滴下し、10秒放置後に綿花を軽く押し当てて水分を除去し、綿花を取り除いた直後の水分測定を行なった。更に、直後の測定時から30秒ごとに120秒までの間、水分測定を繰り返し実施した(計5回の測定)。測定結果は、測定部位に与えた総水分量とその水分の変化量(水分保持能)を求めることで表した。測定部位に与えた総水分量は、綿花除去直後の皮膚水分量測定値から水滴下前の皮膚水分量測定値を差し引いた値で表し、水分の変化量(水分保持能)は、繰り返し測定した綿花除去後30秒後から120秒後の4回の皮膚水分量測定値の平均値を綿花除去直後の皮膚水分量測定値で除した百分率で表した。得られた結果は、総水分量を図5、水分保持能を図6に示す。
The water loading measurement site was a site at a distance of about one third from the wrist side toward the elbow direction at the inner side of the left forearm. As a measuring instrument, CorneoMeter CM-825 (made by Courage + Khazaka electronic GmbH) was used. The measurement method first measures the moisture of the measurement site, then drops 20 μl of ion-exchanged water on the measurement site, and after leaving for 10 seconds, gently presses the cotton to remove moisture and measures the moisture immediately after removing the cotton Did. Furthermore, moisture measurement was repeatedly performed for up to 120 seconds every 30 seconds from the measurement immediately after (total 5 times measurement). The measurement results were expressed by determining the total amount of water given to the measurement site and the amount of change of the water (water holding ability). The total water content given to the measurement site was expressed as a value obtained by subtracting the skin water content measurement value before dripping of water from the skin water content measurement value immediately after cotton removal, and the change amount of water (water retention capacity) was measured repeatedly. The average value of the four skin moisture content measurement values after 30 seconds after cotton removal and 120 seconds after was expressed as a percentage divided by the skin moisture content measurement value immediately after cotton removal. The obtained results are shown in FIG. 5 for the total water content and in FIG. 6 for the water retention ability.

図5に示されるとおり、測定部位の皮膚に与えた総水分量は、両群でほぼ同水準であり、水分保持能も絶対値に差は見られるものの、経時的な水分保持能の変化率はほぼ同程度であった。   As shown in FIG. 5, the total amount of water given to the skin at the measurement site is almost the same in both groups, and although the water holding ability shows a difference in absolute value, the change rate of water holding ability over time Were almost the same.

弾力性測定
測定部位は、左腕前腕内側部で手首側から肘方向に向けて約3分の1の距離の部位で、水負荷試験の位置より約2cm肩方向にずらした部位とした。測定機器としては、Cuto Meter MPA−580(Courage+Khazaka electronic GmbH社製)を使用した。測定条件は、吸引圧200hPa、吸引時間5秒、開放時間2秒、吸引回数1回で実施した。測定は、部位が重ならないようにずらして計4回行ない、その平均値を測定値とした。測定結果として得られる典型的な波形を図7に示す。図7において、R1及びR5で示した位置に相当する縦軸の数値を、各々R1パラメータ及びR5パラメータとした。R1パラメータは、吸引により変化した形状を吸引前の形状に戻す能力(再変形能力)を表し、R5パラメータは弾力性を表す(1.0に近い値ほど高い弾力性を示す)。得られた結果は、R1パラメータを図8、R5パラメータを図9に示す。
The elasticity measurement measurement site was a site at a distance of about one third from the wrist side toward the elbow direction on the inner side of the left forearm and a site shifted about 2 cm in the shoulder direction from the position of the water load test. As a measuring instrument, Cuto Meter MPA-580 (made by Courage + Khazaka electronic GmbH) was used. The measurement conditions were a suction pressure of 200 hPa, a suction time of 5 seconds, an open time of 2 seconds, and a suction number of once. The measurement was carried out a total of four times with shifting so that the portions do not overlap, and the average value was taken as the measured value. A typical waveform obtained as a measurement result is shown in FIG. In FIG. 7, numerical values on the vertical axis corresponding to positions indicated by R1 and R5 are respectively set as an R1 parameter and an R5 parameter. The R1 parameter represents the ability to reshape the shape changed by suction to the shape before suction (re-deformability), and the R5 parameter represents elasticity (a value closer to 1.0 indicates higher elasticity). The obtained results are shown in FIG. 8 for the R1 parameter and in FIG. 9 for the R5 parameter.

図8に示されるとおり、皮膚の再変形能力は、プラセボでは変化が無かったが、試験群では向上傾向にあった。また、図9に示されるとおり、皮膚の弾力性は、プラセボでは変化が無かったが、試験群では減少する傾向が示された。   As shown in FIG. 8, the re-deformability of the skin was unchanged with the placebo, but tended to improve in the test group. Also, as shown in FIG. 9, the elasticity of the skin did not change with the placebo, but showed a tendency to decrease in the test group.

レプリカ採取による二次元画像解析Two-dimensional image analysis by replica collection

レプリカ採取部位は、右腕前腕内側部で手首側から肘方向に向けて約3分の1の距離の部位とした。測定機器としては、ASA−03RXD(アサヒバイオメッド社製)を使用した。レプリカは、測定部位にシリコーンを塗布し、乾燥後に剥離することで採取した。評価に使用したレプリカの範囲は5mm×5mmの領域とした。採取したレプリカの評価部位に対して斜め方向30°から光を照射した時にレプリカ上に現れる陰影を180°回転させた2方向から各々撮影し、2枚の陰影画像を得た。この2枚の陰影画像の解析から得られた一部に130μm以下の深長を有する凹部(溝様構造)を「キメ」と定義し、この陰影画像における各種パラメータの数値を測定した。「キメ」
として認識された溝の体積の総和、最大深長と最大幅長について、各々図10、図11および図12に示す。
The replica collection site was a site at a distance of about one third from the wrist side toward the elbow direction on the inner side of the right forearm. As a measurement instrument, ASA-03 RXD (manufactured by Asahi BioMed) was used. The replica was collected by applying silicone to the measurement site and peeling after drying. The range of the replica used for evaluation was an area of 5 mm × 5 mm. When light was irradiated from an oblique direction of 30 ° to the evaluation part of the collected replica, the shadows appearing on the replica were photographed 180 ° from each of which were photographed from two directions to obtain two shadow images. A recess (groove-like structure) having a depth of 130 μm or less was defined as “Ki” in a part obtained from the analysis of these two shadow images, and the numerical values of various parameters in this shadow image were measured. "Kime"
The sum of the volume of the groove recognized as H, the maximum depth and the maximum width are shown in FIG. 10, FIG. 11 and FIG. 12 respectively.

図10に示したとおり試験群では総体積が増加していたが、プラセボ群では変化が見られなかった。一方、キメ構造の変化として、図11や図12に示したとおり、プラセボ群では最大深長と最大幅長が共に約2μm増加していたが、試験群では約7−8μmの増加に抑えられていた。これらの結果から、プラセボ群では、キメの溝が大きく且つ深くなる傾向にあると共に、総体積が変化していないことからキメの数が減少している。一方、試験群ではキメの幅と深さの変化がプラセボに比べて抑制されていると共に、総体積が増加していることから、キメの数は維持若しくは減少が大幅に抑えられ、いわゆる「キメの細かさ」が維持されていることがわかった。   As shown in FIG. 10, the total volume was increased in the test group, but no change was observed in the placebo group. On the other hand, as changes in texture, as shown in FIGS. 11 and 12, both the maximum depth and the maximum width increased by about 2 μm in the placebo group, but were suppressed to about 7-8 μm in the test group The From these results, in the placebo group, the texture groove tends to be large and deep, and the number of textures is reduced because the total volume is not changed. On the other hand, in the test group, changes in the width and depth of the texture are suppressed as compared to the placebo, and the total volume is increased, so that the number of textures is significantly reduced or not maintained. It was found that “fineness” was maintained.

アンケート
4週間の飲用後の被験者に対してアンケートによる皮膚状態の実感調査を実施した。評価項目は、「肌の調子」、「肌のハリ」、「肌のキメ・なめらかさ」、「肌の手触り」、及び「化粧のり」の4項目で、0を「最も状態が悪い」、10を「最も状態が良い」の10段階評価で行った。その結果を、図13〜16に示した。4週間の継続飲用で全ての評価項目において改善が見られた。特に、試験群では「肌の調子」、「肌のハリ」および「肌のキメ・なめらかさ」では有意差を、「肌の手触り」では有意な傾向を確認したが、プラセボ群では何れの項目も有意な傾向も見られなかった。
Questionnaire survey was conducted on the actual condition of skin condition for subjects after drinking for 4 weeks. The evaluation items are "skin condition", "skin firmness", "skin texture / smoothness", "skin feel" and "makeup paste", and 0 is "the worst condition", 0 We performed 10 in 10 steps of "the best condition" evaluation. The results are shown in FIGS. Improvement was seen in all evaluation items after 4 weeks of continuous drinking. In particular, significant differences were found in the "skin tone", "skin firmness" and "skin texture / smoothness" in the test group, and significant tendencies in the "skin feel", but any item in the placebo group There was no significant trend either.

Claims (5)

ハトムギエキスを含有する、肌触り感改善用経口組成物。 An oral composition for improving the feeling of touch, which comprises an eggplant extract. 顔の肌の肌触り感改善用である、項1に記載の経口組成物。 Item 2. The oral composition according to item 1, which is for improving the feel of facial skin. 少なくとも4週間継続投与又は摂取するように用いられる、項1または2いずれか1項に記載の経口組成物。 The oral composition according to any one of Items 1 and 2, which is used for continuous administration or intake for at least 4 weeks. 液体組成物である、項1〜3のいずれか1項に記載の経口組成物。 The oral composition according to any one of Items 1 to 3, which is a liquid composition. 医薬組成物又は食品組成物である、項1〜4のいずれか1項に記載の経口組成物。

The oral composition according to any one of Items 1 to 4, which is a pharmaceutical composition or a food composition.

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07274914A (en) * 1994-04-13 1995-10-24 Shikoku Sogo Kenkyusho:Kk Extraction of adlay extract, adlay extract obtained by the extraction and skin-improving article containing the adlay extract
WO2002072123A1 (en) * 2001-03-02 2002-09-19 Beppu, Kunihide Preventives or remedies for tumor or papillomaviral diseases
JP2008048723A (en) * 2006-07-24 2008-03-06 Fine Co Ltd Method for producing adlay extract, and adlay extract
JP2017001994A (en) * 2015-06-12 2017-01-05 株式会社コーセー Skin quality improving agent

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07274914A (en) * 1994-04-13 1995-10-24 Shikoku Sogo Kenkyusho:Kk Extraction of adlay extract, adlay extract obtained by the extraction and skin-improving article containing the adlay extract
WO2002072123A1 (en) * 2001-03-02 2002-09-19 Beppu, Kunihide Preventives or remedies for tumor or papillomaviral diseases
JP2008048723A (en) * 2006-07-24 2008-03-06 Fine Co Ltd Method for producing adlay extract, and adlay extract
JP2017001994A (en) * 2015-06-12 2017-01-05 株式会社コーセー Skin quality improving agent

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