JP2017193503A - Deodorizing cosmetic - Google Patents

Deodorizing cosmetic Download PDF

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JP2017193503A
JP2017193503A JP2016084230A JP2016084230A JP2017193503A JP 2017193503 A JP2017193503 A JP 2017193503A JP 2016084230 A JP2016084230 A JP 2016084230A JP 2016084230 A JP2016084230 A JP 2016084230A JP 2017193503 A JP2017193503 A JP 2017193503A
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acid
histidine
component
derivative
salt
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JP6534958B2 (en
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克真 鞍本
Katsumasa Kuramoto
克真 鞍本
佑介 河内
Yusuke Kawachi
佑介 河内
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Naris Cosmetics Co Ltd
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Naris Cosmetics Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a deodorizing cosmetic which improves the phenomenon in which a deodorization effect and stability of L-histidine is significantly deteriorated in the coexistence with a specific compound.SOLUTION: There is provided a cleansing cosmetic which comprises the following components (A) to (C): (A) L-histidine, (B) one or more selected from a pyrosulfite, a sulfite and a hydrogensulfite, (C) one or more selected from glycyrrhizinic acid, a derivative of glycyrrhizinic acid, a salt of glycyrrhizinic acid, glycyrrhetinic acid, a derivative of glycyrrhetinic acid, a salt of glycyrrhetinic acid, ε-aminocaproic acid, a derivative of ε-aminocaproic acid, a salt of ε-aminocaproic acid, gluconic acid, a derivative of gluconic acid, a salt of gluconic acid, allantoin and a derivative of allantoin.EFFECT: A deodorizing cosmetic using L-histidine can effectively prevent the reduction in deodorizing effect and stability of L-histidine when blending the component (C).SELECTED DRAWING: None

Description

本発明は、加齢臭の主な原因物質とされる2−ノネナールを消臭する化粧料に関する。さらに詳しくは、本発明は、高い消臭効果を発揮し、また、消臭効果を損なうことなく安定して発揮することのできる化粧料に関する。
The present invention relates to a cosmetic that deodorizes 2-nonenal, which is a main causative substance of an aging odor. More specifically, the present invention relates to a cosmetic that exhibits a high deodorizing effect and that can be stably exhibited without impairing the deodorizing effect.

近年、加齢に伴い身体や頭部から発生する臭いに対してのケアに注目が集まってきており、それらの臭いを炭などの多孔性物質が吸着することにより除去する技術(特許文献1)や原因となる常在菌の繁殖を抑制する技術(特許文献2)、香料成分などでマスキングする技術、ブドウ糖と特定のアミノ酸で消臭化する技術(特許文献3)などが開発されている。このような加齢に伴った不快な臭いは一般的に加齢臭と呼ばれており、夏場の汗臭などとともに不快なものとされ、解消が求められている。   In recent years, attention has been focused on the care for odors generated from the body and head with aging, and a technique for removing these odors by adsorption of a porous substance such as charcoal (Patent Document 1). In addition, a technique for suppressing the propagation of resident bacteria that cause the disease (Patent Document 2), a technique for masking with a fragrance component, etc., a technique for debromating with glucose and a specific amino acid (Patent Document 3), and the like have been developed. Such an unpleasant odor accompanying aging is generally called an aging odor, and it is considered unpleasant with a sweat odor in summer and is required to be solved.

その一方で、加齢臭の主な原因物質として2−ノネナールが提唱されており、この成分は加齢とともに増大することが示されている。特に加齢臭が発生する年齢とされる40歳以降で顕著に増大することが確認されている。2−ノネナールはω7不飽和脂肪酸の酸化的分解によって発生し、過酸化脂質がその酸化的分解を促進することが示されている。
発生した2−ノネナールを消臭する物質については、L−ヒスチジンに極めて高い2−ノネナールの消臭効果があることが知られている。しかし、L−ヒスチジンは特定の化合物と併用した場合、著しく消臭効果が低減し、安定性も経時的に減少する事が問題点であった。
On the other hand, 2-nonenal has been proposed as a main causative substance of an aging odor, and this component has been shown to increase with aging. In particular, it has been confirmed that it significantly increases after the age of 40, which is the age at which an aging odor occurs. 2-nonenal is generated by oxidative degradation of ω7 unsaturated fatty acids, and lipid peroxide has been shown to promote its oxidative degradation.
Regarding substances that deodorize the generated 2-nonenal, it is known that L-histidine has a very high 2-nonenal deodorizing effect. However, when L-histidine is used in combination with a specific compound, the deodorizing effect is remarkably reduced and the stability is also decreased over time.

特開2002−145747JP2002-145747 特開2008−110999JP 2008-110999 A 特開2010−013418JP2010-013418A

本発明は、L−ヒスチジンの消臭効果および安定性が特定の化合物:成分(C)との共存時に著しく低下する現象に対し、これを改善した化粧料を提供することを目的とする。
An object of the present invention is to provide a cosmetic that improves the deodorizing effect and stability of L-histidine against a phenomenon in which the deodorizing effect and stability of the L-histidine are significantly reduced when coexisting with a specific compound: component (C).

以上の問題を解決するため、本発明者が鋭意検討した結果、L−ヒスチジンの成分(C)による消臭効果および安定性の低下が、ピロ亜硫酸塩、亜硫酸塩、亜硫酸水素塩を用いることで改善することを見出した。さらにこれら3成分を組み合わせることによって、製剤の経時安定化についても相乗的に効果が上昇することが判明した。
As a result of intensive studies by the present inventors in order to solve the above problems, the deodorizing effect and the stability decrease due to the component (C) of L-histidine are reduced by using pyrosulfite, sulfite, and bisulfite. Found to improve. Furthermore, it has been found that combining these three components synergistically increases the stability of the formulation over time.

すなわち本発明は
次の成分(A)〜(C)、
(A)L−ヒスチジン
(B)ピロ亜硫酸塩、亜硫酸塩、亜硫酸水素塩から選択される1種又は2種以上
(C)グリチルリチン酸、グリチルリチン酸の誘導体、及びグリチルリチン酸の塩、グリチルレチン酸、グリチルレチン酸の誘導体、及びグリチルレチン酸の塩、ε−アミノカプロン酸、ε−アミノカプロン酸の誘導体、及びε−アミノカプロン酸の塩、グルコン酸、グルコン酸の誘導体、及びグルコン酸の塩、アラントイン及びアラントインの誘導体から選択される1種又は2種以上
を含有する化粧料である。
That is, the present invention includes the following components (A) to (C),
(A) L-histidine (B) one or more selected from pyrosulfite, sulfite, bisulfite (C) glycyrrhizic acid, a derivative of glycyrrhizic acid, and a salt of glycyrrhizic acid, glycyrrhetinic acid, glycyrrhetin Derivatives of acids, and salts of glycyrrhetinic acid, ε-aminocaproic acid, ε-aminocaproic acid, and ε-aminocaproic acid, gluconic acid, gluconic acid, and gluconic acid salts, allantoin and allantoin derivatives It is a cosmetic containing one or more selected.

本発明によれば、L−ヒスチジンを用いた消臭化粧料について、L−ヒスチジンの消臭効果および安定性が特定の成分、成分(C)の配合時に低下するのを、効果的に防ぐことが可能となる。 According to the present invention, for deodorant cosmetics using L-histidine, the deodorizing effect and stability of L-histidine are effectively prevented from decreasing when the specific component, component (C) is blended. Is possible.

以下、本発明について更に詳しく説明する。   Hereinafter, the present invention will be described in more detail.

本発明に用いられる成分(A)L−ヒスチジンは、本発明において2−ノネナールを消臭するために配合している。 Component (A) L-histidine used in the present invention is blended in the present invention to deodorize 2-nonenal.

本発明に用いられる成分(A)L−ヒスチジンは望ましくは0.01%〜5%が望ましい。さらに望ましくは0.1%〜3%が望ましい。 Component (A) L-histidine used in the present invention is desirably 0.01% to 5%. More preferably, the content is 0.1% to 3%.

本発明に用いられる成分(B)ピロ亜硫酸塩、亜硫酸塩、亜硫酸水素塩は、これらに成分(A)と成分(C)とを共に配合することで、偶然にも成分(A)の消臭効果が効果的に保持できた。塩の種類は特に限定されず、成分(B)は還元能を有する成分であることが望ましい。 The component (B) pyrosulfite, sulfite, and hydrogen sulfite used in the present invention, together with the component (A) and the component (C), accidentally deodorizes the component (A). The effect could be maintained effectively. The kind of salt is not particularly limited, and component (B) is preferably a component having reducing ability.

本発明に用いられる成分(B)は望ましくは0.001%〜1%が望ましい。さらに望ましくは0.01%〜0.1%が望ましい。 The component (B) used in the present invention is desirably 0.001% to 1%. More desirably, the content is 0.01% to 0.1%.

本発明に用いられる成分(C)に挙げた成分は化粧品添加物として、医薬部外品の有効成分、添加物として一般的に汎用されている成分であり、抗炎症効果や肌荒れ防止効果などを目的にスキンケア、トイレタリー製品などに幅広く配合される。 Ingredients (C) used in the present invention are ingredients that are commonly used as cosmetic additives, quasi-drug active ingredients, and additives, and have anti-inflammatory effects and rough skin prevention effects. Widely used in skin care and toiletry products for purposes.

成分(C)の塩の種類、誘導体の種類は特に限定されず、成分の母体構造が共通していれば成分(A)の消臭効果及び安定性を損ない、損なわれた効果や安定性が成分(B)の存在時に改善した。 The kind of the salt of component (C) and the kind of derivative are not particularly limited. If the matrix structure of the component is common, the deodorizing effect and stability of component (A) are impaired, and the impaired effect and stability are reduced. Improved in the presence of component (B).

本発明の皮膚洗浄用組成物は液状、ペースト状、クリーム状、およびジェル状など剤型には寄らず適用することができる。
The skin cleansing composition of the present invention can be applied regardless of the dosage form such as liquid, paste, cream, and gel.

以下に実施例を挙げて、本発明を更に説明する。なお、これらは本発明を何ら限定するものではない。配合量は組成物全量に対する質量%である。 The following examples further illustrate the present invention. In addition, these do not limit this invention at all. A compounding quantity is the mass% with respect to the composition whole quantity.

本実施例で用いた評価項目について説明する。
1.「消臭効果(分析)」
「評価方法」
2−ノネナール除去能の評価は、HPLCを利用した測定方法(分析化学, 46(1) , 31-36, 1997)を改変して2−ノネナールの量を測定することにより行った。
Evaluation items used in this example will be described.
1. "Deodorizing effect (analysis)"
"Evaluation method"
Evaluation of 2-nonenal removal ability was performed by measuring the amount of 2-nonenal by modifying a measurement method using HPLC (Analytical Chemistry, 46 (1), 31-36, 1997).

実施例もしくは比較例の化粧料を、95%エタノール水溶液を溶媒として50%溶液として試料とした。
陽性対象には、2−ノネナールの除去効果が知られているL−リジン(特開2011−1
56227)と、同じ塩基性アミノ酸のL−ヒスチジンを用いた。L−リジンは50%エ
タノール水溶液を溶媒として1%溶液とし、L−ヒスチジンは1%水溶液を調整し、試験に用いた。
The cosmetics of Examples or Comparative Examples were used as samples with a 95% ethanol aqueous solution as a solvent and a 50% solution.
For positive subjects, L-lysine (Japanese Unexamined Patent Publication No. 2011-1), which is known to have a removal effect of 2-nonenal.
56227) and the same basic amino acid L-histidine was used. L-lysine was prepared as a 1% solution using a 50% ethanol aqueous solution as a solvent, and L-histidine was used in the test after preparing a 1% aqueous solution.

上記試料又は陽性対照であるL−リジン溶液、又はL‐ヒスチジン溶液を500μLと、95%エタノールを溶媒として調製した5μM2‐ノネナール溶液500μLとを混合後、32℃の恒温槽で8時間温めた。Controlには試料の代わりに95%エタノール水溶液を用いた。その後DNPA液500μLを混合後、45℃の恒温槽で30min反応させた(反応液)。DNPA液とは、DNPH(2,4‐Dinitrophenyl hydrazine Hydrochloride) 25mg, 99.5%エタノール45mL, 濃塩酸1mL, 蒸留水 4mLの混合液を指す。反応液は 氷水で約10min冷却し、反応を停止させた。反応を停止させた反応液はろ過後、HPLCにて解析を行った。2-ノネナールの検出はリテンションタイム11.5minに確認された。体臭成分である2‐ノネナールの除去率は、以下の式に従いピーク面積から求めた。 500 μL of the L-lysine solution or L-histidine solution, which is the sample or the positive control, was mixed with 500 μL of a 5 μM 2-nonenal solution prepared using 95% ethanol as a solvent, and then heated in a constant temperature bath at 32 ° C. for 8 hours. A 95% ethanol aqueous solution was used for Control instead of the sample. Thereafter, 500 μL of DNPA solution was mixed and reacted in a 45 ° C. constant temperature bath for 30 min (reaction solution). The DNPA liquid refers to a mixed solution of 25 mg of DNPH (2,4-dinitrophenyl hydride), 45 mL of 99.5% ethanol, 1 mL of concentrated hydrochloric acid, and 4 mL of distilled water. The reaction solution was cooled with ice water for about 10 minutes to stop the reaction. The reaction solution whose reaction was stopped was filtered and analyzed by HPLC. The detection of 2-nonenal was confirmed at a retention time of 11.5 min. The removal rate of 2-nonenal, which is a body odor component, was determined from the peak area according to the following formula.

<式1>

Figure 2017193503
<Formula 1>
Figure 2017193503

<HPLC 条件>
カラム; CHEMCOBOND 5−ODS−W size6.0×150 (6A)
流速 ; 1.5 mL/min
カラム温度 ; 50 ℃
移動相 ; CH3CN:H2O = 80:20( V/V)
検出器/測定波長 ;紫外可視検出器/365 nm
<HPLC conditions>
Column; CHEMCOBOND 5-ODS-W size 6.0 × 150 (6A)
Flow rate: 1.5 mL / min
Column temperature: 50 ° C
Mobile phase: CH3CN: H2O = 80: 20 (V / V)
Detector / measurement wavelength: UV-visible detector / 365 nm

「評価基準」
上記方法でL−ヒスチジンの2−ノネナールの除去率によって以下のように評価した。
○:除去率80%以上
△:除去率40%以上、80%未満
×:除去率1%以上、40%未満
××:除去率1%未満
"Evaluation criteria"
According to the above method, the removal rate of L-histidine 2-nonenal was evaluated as follows.
○: Removal rate 80% or more Δ: Removal rate 40% or more, less than 80% ×: Removal rate 1% or more, less than 40% XX: Removal rate less than 1%

2.「消臭効果(官能)」
「評価方法」
実施例もしくは比較例の化粧料を、水を溶媒として50%溶液として試料とした。陰性対照として水を用いた。10μM2−ノネナール溶液と試料を1:1の割合で混合し、10分後のにおいを評価することによって確認した。なお、評価は熟練の評価者5名で行った。
「評価基準」
上記試験結果から、各試料と混合した溶液のにおいに以下のようにスコアをつけた。
5点:においなし
4点:ほとんどにおいなし
3点:においは低減しているが残っている
2点:わずかににおいが減っている
1点:変化なし
続いて評価者5名の平均スコアを算出し、以下のように評価を行った。
○:4点以上
△:2点以上4点未満
×:2点未満
2. "Deodorizing effect (sensory)"
"Evaluation method"
The cosmetics of Examples or Comparative Examples were used as samples in a 50% solution using water as a solvent. Water was used as a negative control. It confirmed by mixing 10 micromol 2-nonenal solution and a sample by the ratio of 1: 1, and evaluating the smell after 10 minutes. The evaluation was performed by five skilled evaluators.
"Evaluation criteria"
From the test results, the odor of the solution mixed with each sample was scored as follows.
5 points: No odor 4 points: Almost no odor 3 points: Odor is reduced but remaining 2 points: Slightly reduced odor 1 point: No change Subsequently, average score of 5 evaluators is calculated Then, evaluation was performed as follows.
○: 4 points or more Δ: 2 points or more and less than 4 points ×: Less than 2 points

3.「安定性」
「評価方法」
実施例および比較例の化粧料を60℃下に1週間静置し、熟練の評価者が外観の経時変化を目視により確認することで評価を行った。
「評価基準」
上記方法により経時変化を確認し、経時変化の度合いにより以下のように評価を行った。
○:変化なし
×:黄色に変色している。
3. “Stability”
"Evaluation method"
The cosmetics of the examples and comparative examples were allowed to stand at 60 ° C. for 1 week, and evaluation was performed by a skilled evaluator confirming the appearance change with time by visual observation.
"Evaluation criteria"
The change with time was confirmed by the above method, and evaluation was performed as follows according to the degree of change with time.
○: No change ×: Discolored to yellow.

Figure 2017193503
Figure 2017193503

Figure 2017193503
Figure 2017193503

比較例2、3、および7〜9を参照すると、成分(A)と成分(C)が共存することにより、消臭効果、安定性共に非常に悪いことが伺える。これに対し、実施例を参照すると、成分(B)が配合された場合、消臭効果、安定性共に非常に良好である。 Referring to Comparative Examples 2, 3, and 7 to 9, it can be seen that the component (A) and the component (C) coexist so that both the deodorizing effect and the stability are very poor. On the other hand, when an Example is referred, when a component (B) is mix | blended, both a deodorizing effect and stability are very favorable.

実施例1、2、3では成分Bの配合量を変化させているが、0.001%でも十分な効果が得られていることが分かる。また、実施例4に示したとおり成分Aの配合量が0.01%でも十分な消臭効果が得られていることが分かる。 In Examples 1, 2, and 3, although the compounding quantity of the component B was changed, it turns out that sufficient effect is acquired even if it is 0.001%. Further, as shown in Example 4, it can be seen that a sufficient deodorizing effect is obtained even when the blending amount of Component A is 0.01%.

なお、安定性の評価において色調の変化が起こっているものは、使用感にも変動が起きている傾向があり、成分(A)、成分(B)及び成分(C)が共存することにより、使用感の変化を抑える利点も確認された。 In addition, in the evaluation of stability, the change in color tone tends to have a change in the feeling of use, and when the component (A), the component (B) and the component (C) coexist, The advantage of suppressing changes in the feeling of use was also confirmed.

以上の結果から、処方に成分(C)を配合する際に、成分(A)を用いて消臭効果を付与したい場合は、成分(B)を組み合わせて配合することで、より高い消臭効果と安定性を付与することができる。 From the above results, when blending the component (C) in the prescription, if it is desired to impart a deodorizing effect using the component (A), a higher deodorizing effect can be obtained by combining the components (B). And stability can be imparted.

常法にて、各処方の組成物を作製した。いずれの処方においても本発明の効果を奏することが確認された。
(1)シャンプー
配合成分 配合量(%)
水 残量
L−ヒスチジン 0.3
亜硫酸Na 0.05
グリチルリチン酸2K 0.10
塩化Na 適量
pH調整剤 適量
防腐剤 適量
グリセリン 8.00
エデト酸塩 0.05
ラウレス硫酸Na 12.00
PPG−2コカミド 2.00
ラウリルヒドロキシスルタイン 3.00
ポリクオタニウムー10 0.05
合計(%) 100.00

The composition of each prescription was produced by the conventional method. It was confirmed that the effects of the present invention were achieved in any prescription.
(1) Shampoo compounding ingredients Compounding amount (%)
Water remaining L-histidine 0.3
Sulfite Na 0.05
Glycyrrhizic acid 2K 0.10
Sodium chloride appropriate amount pH adjuster appropriate amount preservative appropriate amount glycerin 8.00
Edetate 0.05
Laureth sulfate Na 12.00
PPG-2 cocamide 2.00
Lauryl hydroxysultain 3.00
Polyquaternium-10 0.05
Total (%) 100.00

(2)化粧水
配合成分 配合量(%)
水 残量
L−ヒスチジン 0.15
亜硫酸Na 0.05
グリチルリチン酸2K 0.10
エタノール 40.00
pH調整剤 適量
防腐剤 適量
1,3−BG 8.00
エデト酸塩 0.01
L−メントール 0.20
合計(%) 100.00
(2) Toner lotion ingredients Amount (%)
Water remaining L-histidine 0.15
Sulfite Na 0.05
Glycyrrhizic acid 2K 0.10
Ethanol 40.00
pH adjuster appropriate amount preservative appropriate amount 1,3-BG 8.00
Edetate 0.01
L-Menthol 0.20
Total (%) 100.00

Claims (3)

次の成分(A)〜(C)、
(A)L−ヒスチジン
(B)ピロ亜硫酸塩、亜硫酸塩、亜硫酸水素塩から選択される1種又は2種以上
(C)グリチルリチン酸、グリチルリチン酸の誘導体、及びグリチルリチン酸の塩、グリチルレチン酸、グリチルレチン酸の誘導体、及びグリチルレチン酸の塩、ε−アミノカプロン酸、ε−アミノカプロン酸の誘導体、及びε−アミノカプロン酸の塩、グルコン酸、グルコン酸の誘導体、及びグルコン酸の塩、アラントイン及びアラントインの誘導体から選択される1種又は2種以上
を含有する化粧料。
The following components (A) to (C),
(A) L-histidine (B) one or more selected from pyrosulfite, sulfite, bisulfite (C) glycyrrhizic acid, a derivative of glycyrrhizic acid, and a salt of glycyrrhizic acid, glycyrrhetinic acid, glycyrrhetin Derivatives of acids, and salts of glycyrrhetinic acid, ε-aminocaproic acid, ε-aminocaproic acid, and ε-aminocaproic acid, gluconic acid, gluconic acid, and gluconic acid salts, allantoin and allantoin derivatives Cosmetics containing one or more selected.
次の成分(A)〜(C)、
成分(A)L−ヒスチジンの配合量が0.01%〜5%
成分(B)の配合量が0.001%〜1%
である請求項1記載の化粧料。
The following components (A) to (C),
Component (A) L-histidine content is 0.01% to 5%
Component (B) content is 0.001% to 1%
The cosmetic according to claim 1, wherein
洗浄用化粧料である請求項1又は2に記載の化粧料。
The cosmetic according to claim 1, which is a cleaning cosmetic.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017193502A (en) * 2016-04-20 2017-10-26 株式会社ナリス化粧品 Deodorizing cosmetic
JP2017193504A (en) * 2016-04-20 2017-10-26 株式会社ナリス化粧品 Deodorizing cosmetic

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014193254A (en) * 2013-03-29 2014-10-09 Kagawa Univ Washing method for fiber product
JP2015168615A (en) * 2014-03-04 2015-09-28 持田製薬株式会社 Composition for cleaning

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014193254A (en) * 2013-03-29 2014-10-09 Kagawa Univ Washing method for fiber product
JP2015168615A (en) * 2014-03-04 2015-09-28 持田製薬株式会社 Composition for cleaning

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017193502A (en) * 2016-04-20 2017-10-26 株式会社ナリス化粧品 Deodorizing cosmetic
JP2017193504A (en) * 2016-04-20 2017-10-26 株式会社ナリス化粧品 Deodorizing cosmetic

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