JP2589761B2 - Cosmetic additives - Google Patents
Cosmetic additivesInfo
- Publication number
- JP2589761B2 JP2589761B2 JP63133891A JP13389188A JP2589761B2 JP 2589761 B2 JP2589761 B2 JP 2589761B2 JP 63133891 A JP63133891 A JP 63133891A JP 13389188 A JP13389188 A JP 13389188A JP 2589761 B2 JP2589761 B2 JP 2589761B2
- Authority
- JP
- Japan
- Prior art keywords
- cosmetics
- prepared
- ascorbic acid
- cream
- emulsion
- 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.)
- Expired - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/738—Cyclodextrins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/67—Vitamins
- A61K8/676—Ascorbic acid, i.e. vitamin C
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/02—Preparations for care of the skin for chemically bleaching or whitening the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は安定なアスコルビン酸の誘導体を有効成分と
する化粧品添加物に関するものである。The present invention relates to a cosmetic additive containing a stable ascorbic acid derivative as an active ingredient.
アスコルビン酸の有効性は種々知られているが、肌に
対する作用として、コラーゲンの生合成に関与して(Ha
ns Von Eulerら、レダクトン化学の基礎とビタミンCの
生化学的成果、内田老鶴圃新社(1960)及び末松俊彦、
ビタミンCの効用、ヘルス研究所(1987))ハリのある
みずみずしい状態を維持するとともに、シミ、ソバカス
の原因となるメラニン色素の生成を抑制し、(末松俊
彦、ビタミンCの効用、ヘルス研究所(1987)及び市川
ら、臨皮、3月号、372(1969))美しい肌状態を維持
する効果が知られ、化粧品分野の薬効剤として好適であ
る。しかし、アスコルビン酸は強い還元性物質ゆえ非常
に不安定であり、その安定化を求めて種々のアスコルビ
ン酸誘導体が開発されたが、その中でもL−アスコルビ
ン酸−2−リン酸エステルまたはその塩類(以降APと称
す)が安定性、安全性および肌に対する作用効果等の点
で最も優れたアスコルビン酸誘導体であり、今日ローシ
ョン、エッセンス、パック等の水系の化粧品に配合され
るに至っている。しかし、このAPを乳液、クリーム等の
乳化系化粧品に配合すると、油相、水相に分離したり、
また逆に固くしまったり等化粧品としての機能性と安定
性が損われ、乳化系化粧品への応用は極めて困難であっ
た。Although various effects of ascorbic acid are known, it is involved in collagen biosynthesis as an effect on the skin (Ha
ns Von Euler et al., Basics of Reductone Chemistry and Biochemical Results of Vitamin C, Uchida Lao Tsuruho Shinsha (1960) and Toshihiko Suematsu,
Vitamin C Utility, Health Research Institute (1987) Maintains a firm and fresh state and suppresses the production of melanin pigments that cause spots and freckles. (Suematsu Toshihiko, Vitamin C Utility 1987) and Ichikawa et al., Shinkin, March Issue, 372 (1969)) are known to have an effect of maintaining a beautiful skin condition, and are suitable as medicinal agents in the cosmetics field. However, ascorbic acid is very unstable due to a strong reducing substance, and various ascorbic acid derivatives have been developed for stabilization. Among them, L-ascorbic acid-2-phosphate or a salt thereof ( (Hereinafter referred to as AP) is the most excellent ascorbic acid derivative in terms of stability, safety and action effect on the skin, etc., and has been used in aqueous cosmetics such as lotions, essences and packs today. However, when this AP is incorporated into emulsified cosmetics such as milky lotions and creams, it may separate into an oil phase and an aqueous phase,
Conversely, the functionality and stability of cosmetics such as hardening and the like are impaired, and application to emulsified cosmetics is extremely difficult.
このような事情から、本発明者らはアスコルビン酸誘
導体を安定に配合した乳化組成物を得るべく鋭意研究を
重ねた結果、APとサクロデキストリン(以降CDと称す)
を配合した乳化組成物が化粧品としての機能性と安定性
を満足することを見い出し本発明に至った。Under these circumstances, the present inventors have conducted intensive studies to obtain an emulsified composition in which an ascorbic acid derivative is stably blended. As a result, AP and saclodextrin (hereinafter referred to as CD) were obtained.
It has been found that an emulsified composition containing satisfies the functionality and stability as cosmetics, and has led to the present invention.
すなわち本発明は、APとCDを配合してなる乳化系化粧
品への添加物を提供するものである。That is, the present invention provides an additive to an emulsified cosmetic product comprising AP and CD.
このAPとCDを配合した乳化組成物はきわめて安定でか
つ使用感も良く、化粧品としての機能性も充分満足し、
更にアスコルビン酸が持つ肌に対する有効性から肌の美
化にきわめて良好な効果を発揮する。The emulsified composition containing this AP and CD is extremely stable and has a good feeling of use, and fully satisfies the functionality as cosmetics.
In addition, ascorbic acid exerts a very good effect on skin beautification due to its effectiveness on the skin.
本発明に使用されるAP塩類はNa、K、MgまたはCa塩等
であり、また、CDはα,βおよびγタイプのいずれを使
用しても良いが、その中でもβタイプが最も好ましい。
AP:CDの比については特に厳密な規定はないが、一般にA
P1重量部に対しCD0.3〜2重量部が適当である。The AP salts used in the present invention are Na, K, Mg or Ca salts, and any of α, β and γ types of CD may be used. Among them, β type is most preferable.
Although there is no strict regulation on the ratio of AP: CD,
0.3 to 2 parts by weight of CD is appropriate for 1 part by weight of P.
化粧品への添加量は、対象により異なり、必ずしも一
概には規定し得ないが、例えば、乳化組成物の処方中、
CDとして0.1〜10重量%であり、好ましくは1〜5重量
%である。The amount added to cosmetics varies depending on the subject, and cannot always be specified unconditionally, for example, during the formulation of an emulsion composition,
It is 0.1 to 10% by weight as CD, preferably 1 to 5% by weight.
以下に代表的な実施例を示すが、これらのみに制限さ
れるものではない。Hereinafter, typical examples will be described, but the present invention is not limited to these examples.
・実施例1(クリーム) 上記(A)成分および(B)成分をそれぞれ80℃に加
熱した後、混合し、攪拌する。50℃まで冷却後(C)成
分を加えて更に攪拌混合し、均一なクリームを調製し
た。-Example 1 (cream) The above components (A) and (B) are each heated to 80 ° C., then mixed and stirred. After cooling to 50 ° C., the component (C) was added and further stirred and mixed to prepare a uniform cream.
注 *は共栄化学工業株式会社製、以下同様 ・実施例2(乳液) 上記(A)成分および(B)成分をそれぞれ80℃に加
熱した後、混合し攪拌する。50℃まで冷却後(C)成分
を加えて更に攪拌混合し、均一な乳液を調製した。Note *: Kyoei Chemical Industry Co., Ltd., same as below. ・ Example 2 (Emulsion) The above components (A) and (B) are each heated to 80 ° C., then mixed and stirred. After cooling to 50 ° C., the component (C) was added and further stirred and mixed to prepare a uniform emulsion.
次に、APを配合した乳化系組成物の実施例1および2
の化粧品としての安定性および機能性について、後述の
比較実施例によって調製したクリーム、乳液を用いて比
較試験を実施した。Next, Examples 1 and 2 of emulsified compositions containing AP
A comparative test was carried out on the stability and functionality as a cosmetic using the creams and emulsions prepared in Comparative Examples described below.
(1)安定性試験 実施例1、2で調製したクリーム、乳液の化粧品とし
ての安定性について以下の比較実施例1、2で調製した
CDを配合しないクリーム、乳液を調製し40℃(恒温)で
2週間経過後の外観を比較観察した。(1) Stability test The stability of the creams and emulsions prepared in Examples 1 and 2 as cosmetics was prepared in Comparative Examples 1 and 2 below.
Creams and emulsions containing no CD were prepared, and the appearance after two weeks at 40 ° C. (constant temperature) was compared and observed.
結果を第1表に示す。 The results are shown in Table 1.
・比較例1(クリーム) CD(β−タイプ)の代わりにグリセリルモノステアレ
ートを配合したほかは、実施例1と同様にしてクリーム
を調製した。Comparative Example 1 (Cream) A cream was prepared in the same manner as in Example 1 except that glyceryl monostearate was used instead of CD (β-type).
・比較例2(乳液) CD(β−タイプ)の代わりにグリセリルモノステアレ
ートを配合したほかは、実施例2と同様にして乳液を調
製した。Comparative Example 2 (Emulsion) An emulsion was prepared in the same manner as in Example 2 except that glyceryl monostearate was used instead of CD (β-type).
(2)機能性試験 実施例1、2で調製したクリーム、乳液の化粧品とし
ての機能性についてCDを配合せずに界面活性剤のみで乳
化系を安定化した以下の比較実施例3、4のクリーム乳
液を調製し、以下についてのモニターテストを実施し
た。(2) Functionality test Regarding the functionalities of the creams and emulsions prepared in Examples 1 and 2 as cosmetics, the following Comparative Examples 3 and 4 in which the emulsification system was stabilized only with a surfactant without adding CD. A cream emulsion was prepared and monitored for the following:
・比較例3(クリーム) 上記(A)成分および(B)成分をそれぞれ80℃に加
熱した後、混合し攪拌する。50℃まで冷却後(C)成分
を加えて更に攪拌混合し、均一なクリームを調製した。-Comparative example 3 (cream) The above components (A) and (B) are each heated to 80 ° C., then mixed and stirred. After cooling to 50 ° C., the component (C) was added and further stirred and mixed to prepare a uniform cream.
・比較例4(乳液) 上記(A)成分および(B)成分をそれぞれ80℃まで
に加熱した後、混合し、攪拌する。50℃まで冷却後
(C)成分を加えて更に攪拌混合し、均一な乳液を調製
した。-Comparative example 4 (emulsion) The above components (A) and (B) are each heated to 80 ° C., then mixed and stirred. After cooling to 50 ° C., the component (C) was added and further stirred and mixed to prepare a uniform emulsion.
テストモニターは無作為に抽出した年令18〜53才の女
性50人を対象に選び実施した。結果を第2表に示す。The test monitor was selected from 50 randomly selected women aged 18 to 53 years. The results are shown in Table 2.
(使用時ののび) (肌へのなじみ) A:非常に良い E:非常によい B:良い F:良い C:普通 G:普通 D:悪い H:悪い (使用後のベタツキ感) I:全く感じない J:あまり感じない K:普通 L:非常に感じる 尚、モニターテストの経過、皮膚に異常を訴えた者は
いなかった。(Expansion at the time of use) (skin familiarity) A: very good E: very good B: good F: good C: normal G: normal D: bad H: bad (stickiness after use) I: totally I do not feel it J: I do not feel much K: Normal L: I feel very much In the course of the monitor test, no one complained of abnormalities on the skin.
(3)顕微鏡観察 実施例1および比較実施例3で調製したクリームにつ
いてエマルジョン形式の状態を比較観察するため、それ
ぞれのクリームをスライドガラスに少量とりカバーガラ
スをかぶせた後軽く押えつけて位相差顕微鏡(600倍)
で観察した。結果を第3表に示す。(3) Microscopy Observation In order to compare and observe the emulsions of the creams prepared in Example 1 and Comparative Example 3, a small amount of each cream was placed on a slide glass, covered with a cover glass, and gently pressed down. (600 times)
Was observed. The results are shown in Table 3.
以上の結果から、本発明に係るAPとCDを配合した乳化
組成物は、従来の界面活性剤のみで調製したAP配合乳化
組成物よりも化粧品としての安定性および機能性にすぐ
れていることを見い出した。またこれらのことは顕微鏡
観察の結果からも確認できた。更に従来から困難とされ
ているAP配合乳化組成物を容易に調製し得ることを見い
出し本発明に至った。 From the above results, it can be seen that the emulsified composition containing the AP and the CD according to the present invention is more excellent in stability and functionality as a cosmetic than the AP-containing emulsified composition prepared only with a conventional surfactant. I found it. These facts could also be confirmed from the results of microscopic observation. Further, they have found that it is possible to easily prepare an emulsified composition containing AP, which has been conventionally difficult, and reached the present invention.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭55−64511(JP,A) ──────────────────────────────────────────────────続 き Continuation of front page (56) References JP-A-55-64511 (JP, A)
Claims (1)
またはその塩とサイクロデキストリンを有効成分とする
化粧品添加物。1. A cosmetic additive comprising L-ascorbic acid-2-phosphate or a salt thereof and cyclodextrin as active ingredients.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63133891A JP2589761B2 (en) | 1988-05-31 | 1988-05-31 | Cosmetic additives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63133891A JP2589761B2 (en) | 1988-05-31 | 1988-05-31 | Cosmetic additives |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01305009A JPH01305009A (en) | 1989-12-08 |
JP2589761B2 true JP2589761B2 (en) | 1997-03-12 |
Family
ID=15115518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63133891A Expired - Lifetime JP2589761B2 (en) | 1988-05-31 | 1988-05-31 | Cosmetic additives |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2589761B2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4767627B2 (en) * | 2005-08-25 | 2011-09-07 | 共栄化学工業株式会社 | Ascorbic acid-2-magnesium phosphate composition and cosmetics containing the same. |
JP6237286B2 (en) * | 2014-02-04 | 2017-11-29 | ライオン株式会社 | Oral composition and oxidative stress inhibitor |
CN109846808A (en) * | 2019-03-20 | 2019-06-07 | 广州纳丽生物科技有限公司 | Crystallite injection liquid cosmetics, preparation method and skin makeup rifle with spot-removing function |
CN109846785A (en) * | 2019-03-20 | 2019-06-07 | 广州纳丽生物科技有限公司 | A kind of solvable micropin and preparation method thereof with spot-removing function |
CN109758379A (en) * | 2019-03-20 | 2019-05-17 | 广州纳丽生物科技有限公司 | A kind of compound blood coagulation acid composition and preparation method thereof, product |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5564511A (en) * | 1978-11-07 | 1980-05-15 | Kanebo Ltd | Cosmetic |
JPS62298508A (en) * | 1986-06-16 | 1987-12-25 | Kanebo Ltd | Skin cosmetic |
-
1988
- 1988-05-31 JP JP63133891A patent/JP2589761B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH01305009A (en) | 1989-12-08 |
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