JP2001048743A - Skin lotion - Google Patents

Skin lotion

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Publication number
JP2001048743A
JP2001048743A JP11223077A JP22307799A JP2001048743A JP 2001048743 A JP2001048743 A JP 2001048743A JP 11223077 A JP11223077 A JP 11223077A JP 22307799 A JP22307799 A JP 22307799A JP 2001048743 A JP2001048743 A JP 2001048743A
Authority
JP
Japan
Prior art keywords
acid
fatty acid
weight
lotion
sucrose
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.)
Pending
Application number
JP11223077A
Other languages
Japanese (ja)
Inventor
Kiyoko Tanabe
聖子 田辺
Satoyuki Kanemitsu
智行 金光
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
QP Corp
Original Assignee
QP Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by QP Corp filed Critical QP Corp
Priority to JP11223077A priority Critical patent/JP2001048743A/en
Publication of JP2001048743A publication Critical patent/JP2001048743A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a skin lotion excellent in preservation stability, especially stability at a low temperature. SOLUTION: This skin lotion contains a lysophospholipid and a fatty acid ester of sucrose, and >=80 wt.% of the fatty acid ester of the sucrose is a monoester. The fatty acid ester of the sucrose is the one obtained by forming an ester bond between one or more hydroxy groups in the sucrose and a saturated or unsaturated fatty acid, and the constituent fatty acid is the one having about 10-24 carbons, concretely, e.g. lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid and behenic acid. The lysophospholipid is any one of monoacyl type phospholipids, e.g. lysophosphatidylcholine, lysophosphatidylethanolamine, lysophosphatidylinositol, lysophosphatidic acid and lysophosphatidylserine, and a mixture thereof can be also used.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、保存安定性に優れ
た化粧水に関する。
[0001] The present invention relates to a lotion having excellent storage stability.

【0002】[0002]

【従来の技術】リゾリン脂質は、卵黄、大豆、細胞等の
動植物に存在するリン脂質をリン脂質分解酵素の一種で
あるホスホリパーゼA2で処理し、1位あるいは2位に
位置するアシル基を選択的に加水分解して水酸基とした
ものである。リゾリン脂質は、このように分子内に水酸
基を有し親水性が高められていることから、優れた乳化
作用と、さらに可溶化作用を有し、近年、色々な分野で
天然由来の界面活性剤として利用されるようになった。
化粧品分野でも、同様であり、安全性及び天然嗜好に伴
い、天然由来の界面活性剤であるリゾリン脂質が注目さ
れるようになり、乳化剤及び可溶化剤としての利用、さ
らにリゾリン脂質が脂質的性質も有することから保湿剤
としても利用されるようになった。
BACKGROUND ART lysophospholipid selected egg yolk, soybeans, an acyl group of phospholipids present in animal and plant cells and the like were treated with phospholipase A 2, which is a kind of phospholipid degrading enzyme, located in the 1-position or 2-position Is hydrolyzed to a hydroxyl group. Since lysophospholipids have a hydroxyl group in the molecule and thus have enhanced hydrophilicity, lysophospholipids have an excellent emulsifying effect and a further solubilizing effect, and in recent years, naturally-derived surfactants have been used in various fields. It came to be used as.
Similarly, in the cosmetics field, lysophospholipids, which are naturally-derived surfactants, have been attracting attention due to their safety and natural taste, and their use as emulsifiers and solubilizers. It has also been used as a humectant because of having the same.

【0003】ところが、リゾリン脂質を用いた化粧料、
特に外観変化が判りやすい化粧水において、該化粧水を
低温で保存した場合、沈殿物やにごりの発生、あるいは
粘度上昇等を生じ、商品価値を損なうという問題があっ
た。そこで、このような問題を解決すべくサポニンを加
配させることで低温での保存安定性を改良した化粧水が
提案されている(特開平2−169507号公報)。し
かしながら、未だ満足できる程の安定性を有したものと
は言い難く、さらなる改善が望まれている。
However, cosmetics using lysophospholipids,
In particular, there is a problem that, when the lotion is stored at a low temperature in a lotion in which the appearance change is easily recognized, a precipitate or a smudge is generated, the viscosity is increased, and the commercial value is impaired. In order to solve such a problem, there has been proposed a lotion in which storage stability at low temperature is improved by adding saponin (Japanese Patent Application Laid-Open No. 2-169507). However, it is still difficult to say that it has a satisfactory degree of stability, and further improvement is desired.

【0004】[0004]

【発明が解決しようとする課題】そこで本発明の目的
は、保存安定性、特に、低温での安定性に優れた化粧水
を提供することである。
SUMMARY OF THE INVENTION An object of the present invention is to provide a lotion having excellent storage stability, especially at low temperatures.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記の目
的を達成すべく鋭意研究を重ねた結果、約80重量%以
上がモノエステルであるショ糖脂肪酸エステルを含有さ
せることにより意外にも低温で保存したとしても沈殿物
やにごりの発生、あるいは粘度上昇等を生じ難いことを
見出し、本発明を完成するに至った。すなわち、本発明
は、リゾリン脂質とショ糖脂肪酸エステルとを含有した
化粧水であって、該ショ糖脂肪酸エステルの約80重量
%以上がモノエステルであることを特徴とする化粧水、
を提供することである。
Means for Solving the Problems The inventors of the present invention have conducted intensive studies to achieve the above object, and as a result, surprisingly, the sucrose fatty acid ester, which is a monoester, is contained in an amount of about 80% by weight or more. It was also found that even when stored at a low temperature, it was difficult to cause generation of precipitates and dust, or increase in viscosity, and the present invention was completed. That is, the present invention provides a lotion containing a lysophospholipid and a sucrose fatty acid ester, wherein about 80% by weight or more of the sucrose fatty acid ester is a monoester.
It is to provide.

【0006】[0006]

【発明の実施の形態】以下本発明を説明する。本発明に
おいて「化粧水」とは、660nmの波長における透過
率が80%以上を有し水をベースとした化粧料であれば
いずれでもよく、このような化粧料としては、一般的に
「ローション」と称されるが、本発明においては、各種
エキス剤、ヒアルロン酸等の保湿剤、アスコルビン酸リ
ン酸エステル等の美白剤等の生理活性物質を比較的高濃
度含有した美容液等も含まれる。また、本発明の化粧水
は、皮膚ばかりでなく、頭皮あるいは頭髪等にも用いら
れるものであってもよい。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below. In the present invention, the “lotion” may be any water-based cosmetic having a transmittance at a wavelength of 660 nm of 80% or more and is generally a lotion. In the present invention, various extracts, humectants such as hyaluronic acid, and serums containing relatively high concentrations of physiologically active substances such as whitening agents such as ascorbic acid phosphate are also included. . Further, the lotion of the present invention may be used not only on the skin but also on the scalp or hair.

【0007】本発明に含有されているショ糖脂肪酸エス
テルとは、ショ糖中の1個あるいは2個以上の水酸基と
飽和あるいは不飽和の脂肪酸とがエステル結合したもの
であり、その構成脂肪酸としては、通常、炭素数が10
〜24くらいのもの、具体的には、例えば、ラウリン
酸、ミリスチン酸、パルミチン酸、ステアリン酸、オレ
イン酸、リノール酸、ベヘニン酸等が用いられている。
一般的に市販されているショ糖脂肪酸エステルは、ショ
糖中の水酸基と脂肪酸とが1個エステル結合したモノエ
ステル、2個エステル結合したジエステル、3個エステ
ル結合したトリエステル等の混合物であるが、本発明に
用いるショ糖脂肪酸エステルは、その約80重量%以上
がモノエステルである。後述の試験例に示すようにモノ
エステルの含有量が80重量%より低いと低温での保存
安定性に優れた化粧水が得られず好ましくない。ショ糖
脂肪酸エステルの含有量は、リゾリン脂質50重量部に
対し少なくとも1重量部以上、好ましくは5重量部以上
がよく、また、上限は、それ以上の効果が期待できず経
済的でないことから、リゾリン脂質1重量部に対しショ
糖脂肪酸エステルを100重量部以下とすることが望ま
しい。
The sucrose fatty acid ester contained in the present invention is a sucrose having one or more hydroxyl groups and a saturated or unsaturated fatty acid in an ester bond. Usually 10 carbon atoms
Up to about 24, specifically, for example, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, behenic acid and the like are used.
Generally, commercially available sucrose fatty acid esters are a mixture of a monoester in which one hydroxyl group and a fatty acid in sucrose are ester-bonded, a diester in which two ester bonds are bonded, and a triester in which three ester bonds are bonded. About 80% by weight or more of the sucrose fatty acid ester used in the present invention is a monoester. If the content of the monoester is lower than 80% by weight as shown in the test examples described later, a lotion having excellent storage stability at low temperatures cannot be obtained, which is not preferable. The content of the sucrose fatty acid ester is at least 1 part by weight, preferably 5 parts by weight or more based on 50 parts by weight of the lysophospholipid, and the upper limit is not economical because no further effect can be expected. It is desirable that the amount of the sucrose fatty acid ester be 100 parts by weight or less based on 1 part by weight of the lysophospholipid.

【0008】本発明に含有されているリゾリン脂質は、
モノアシル型リン脂質であればいずれでもよく、例え
ば、リゾホスファチジルコリン、リゾホスファチジルエ
タノールアミン、リゾホスファチジルイノシトール、リ
ゾホスファチジン酸、リゾホスファチジルセリン等が挙
げられ、これらの混合物であってもよい。また、リゾリ
ン脂質は、例えば、卵黄、大豆、細胞等の動植物に存在
するリン脂質をリン脂質分解酵素の一種であるホスホリ
パーゼA2で処理することにより得られる。特に、卵黄
由来のリゾホスファチジルコリンは、アシル基が殆ど飽
和脂肪酸より構成されていることから酸化安定性に優
れ、また水に透明に溶解しやすいことから、化粧水の原
料と好ましい。リゾリン脂質の含有量としては、特に限
定するものではないが、化粧水全体に対し0.0001
〜5.0重量%含有させるとよい。
The lysophospholipid contained in the present invention comprises:
Any monoacyl type phospholipid may be used, and examples thereof include lysophosphatidylcholine, lysophosphatidylethanolamine, lysophosphatidylinositol, lysophosphatidic acid, and lysophosphatidylserine, and a mixture thereof. Moreover, lysophospholipids, for example, egg yolk, soybeans, obtained by the phospholipids present in animal and plant cells and the like are treated with phospholipase A 2, which is a kind of phospholipid degrading enzyme. In particular, lysophosphatidylcholine derived from egg yolk is preferable as a raw material for lotion because it has excellent oxidative stability because the acyl group is almost entirely composed of saturated fatty acids, and is easily transparently dissolved in water. The content of the lysophospholipid is not particularly limited, but may be 0.0001 to the total lotion.
It is good to make it contain -5.0 weight%.

【0009】本発明の化粧水の製造は、特に限定するも
のではないが、一般的に化粧水の原料として使用されて
いる、例えば、ヒアルロン酸、コラーゲン、多価アルコ
ール等の保湿剤、動植物あるいは合成の油脂類、エラス
チン等の各種エキス剤、アスコルビン酸リン酸エステル
等の美白剤、香料、防腐剤、着色剤、アルコール類、界
面活性剤等を本発明の効果を損なわない範囲で適宜選択
し、これらの原料とリゾリン脂質及びショ糖脂肪酸エス
テルを精製水に溶解あるいは分散させることにより本発
明の化粧水が得られる。なお、リゾリン脂質及びショ糖
脂肪酸エステルは加温した精製水、あるいは分散させた
後、加温することにより透明に溶解しやすいことから、
このような方法で化粧水を製造することが好ましい。
The production of the lotion of the present invention is not particularly limited, but is generally used as a raw material of the lotion, for example, a humectant such as hyaluronic acid, collagen, polyhydric alcohol, animals and plants, or Synthetic oils and fats, various extractants such as elastin, whitening agents such as ascorbic acid phosphate, fragrances, preservatives, coloring agents, alcohols, surfactants and the like are appropriately selected within a range that does not impair the effects of the present invention. By dissolving or dispersing these raw materials, lysophospholipid and sucrose fatty acid ester in purified water, the lotion of the present invention can be obtained. In addition, since lysophospholipids and sucrose fatty acid esters are heated and purified water, or after being dispersed, they are easily transparently dissolved by heating,
It is preferable to produce a lotion by such a method.

【0010】次に、本発明を実施例及び試験例に基づ
き、さらに詳細に説明する。
Next, the present invention will be described in more detail based on examples and test examples.

【0011】[0011]

【実施例】 実施例1 <処方> ・卵黄リゾホスファチジルコリン(キユーピー(株)製、 商品名「卵黄レシチンLC-100」) 1.0重量% ・ショ糖ラウリン酸エステル (三菱化学フーズ(株)製、商品名「リョートーシュガー エステルL-1695(モノエステル:約80重量%)」) 1.0重量% ・ヒアルロン酸ナトリウム水溶液(1重量%)(キユーピー(株)、 商品名「ヒアルロンサンHA-Q1」) 1.0重量% ・グリセリン 5.0重量% ・メチルパラベン 0.1重量% ・精製水 91.9重量% <製造方法>精製水を70℃に加温後、卵黄リゾホスフ
ァチジルコリン、ショ糖脂肪酸エステル、グリセリン及
びメチルパラベンを溶解させた。この溶液を室温まで冷
却後、ヒアルロン酸ナトリウム水溶液を添加・均一と
し、透明な化粧水を得た。得られた化粧水を4℃で1ヶ
月間保存しても、沈殿物及びにごりの発生、また粘度変
化もなく安定であった。
Example 1 Example 1 <Prescription>-Egg yolk lysophosphatidylcholine (manufactured by Kewpie Co., Ltd., trade name "Egg yolk lecithin LC-100") 1.0% by weight-Sucrose laurate ester (manufactured by Mitsubishi Chemical Foods Corporation) , Brand name "Ryoto Sugar Ester L-1695 (monoester: about 80% by weight)") 1.0% by weight ・ Sodium hyaluronate aqueous solution (1% by weight) (Kewpie Co., Ltd., brand name "Hyaluron Sun HA-Q1" 1.0% by weight-Glycerin 5.0% by weight-Methylparaben 0.1% by weight-Purified water 91.9% by weight <Production method> After heating purified water to 70 ° C, egg yolk lysophosphatidylcholine, sucrose fatty acid The ester, glycerin and methyl paraben were dissolved. After the solution was cooled to room temperature, an aqueous solution of sodium hyaluronate was added to make the solution uniform, and a clear lotion was obtained. Even when the obtained lotion was stored at 4 ° C. for one month, the lotion was stable without generation of precipitates and mist, and no change in viscosity.

【0012】 実施例2 <処方> ・卵黄リゾホスファチジルコリン(キユーピー(株)製、 商品名「卵黄レシチンLC-100」) 1.0重量% ・ショ糖ラウリン酸エステル (三菱化学フーズ(株)製、商品名「リョートーシュガー エステルL-1695(モノエステル:約80重量%)」) 0.2重量% ・POE(60)硬化ヒマシ油 0.1重量% ・α−トコフェロール 0.05重量% ・可溶性卵殻膜(キユーピー(株)製、商品名 「EMプロテイン−P」) 0.05重量% ・ジプロピレングリコール 10.0重量% ・メチルパラベン 0.1重量% ・精製水 88.5重量% <製造方法>70℃に加温した精製水にショ糖脂肪酸エ
ステル及びメチルパラベンを溶解させた。一方、70℃
に加温したジプロピレングリコールに卵黄ホスファチジ
ルコリン、POE(60)硬化ヒマシ油及びα−トコフ
ェロールを均一に分散させ、この分散液を攪拌させなが
ら前記水溶液を注加し均一とした。次に、可溶性卵殻膜
を溶解させ、室温まで冷却し、透明な化粧水を得た。得
られた化粧水を4℃で1ヶ月間保存しても、沈殿物及び
にごりの発生、また粘度変化もなく安定であった。
Example 2 <Formulation> Egg yolk lysophosphatidylcholine (manufactured by Kewpie Co., Ltd., trade name “yolk lecithin LC-100”) 1.0% by weight ・ Sucrose laurate ester (manufactured by Mitsubishi Chemical Foods Corporation) Trade name "Ryoto Sugar Ester L-1695 (monoester: about 80% by weight)") 0.2% by weight ・ POE (60) hydrogenated castor oil 0.1% by weight ・ α-tocopherol 0.05% by weight ・ Soluble Eggshell membrane (manufactured by KUP Co., Ltd., trade name "EM Protein-P") 0.05% by weight ・ Dipropylene glycol 10.0% by weight ・ Methylparaben 0.1% by weight ・ Purified water 88.5% by weight <Production method Sucrose fatty acid ester and methyl paraben were dissolved in purified water heated to> 70 ° C. On the other hand, 70 ° C
The yolk phosphatidylcholine, POE (60) hydrogenated castor oil and α-tocopherol were uniformly dispersed in the heated dipropylene glycol, and the aqueous solution was poured while stirring this dispersion to make it uniform. Next, the soluble eggshell membrane was dissolved and cooled to room temperature to obtain a clear lotion. Even when the obtained lotion was stored at 4 ° C. for one month, the lotion was stable without generation of precipitates and mist, and no change in viscosity.

【0013】[0013]

【試験例】表1に示す安定化剤を含有させた化粧水を下
記の処方及び製造方法に準じて製造した。得られた化粧
水を4℃で1ヶ月間保存し、保存後の沈殿物、あるいは
にごりの発生の有無、また粘度変化について観察した。
なお、いずれのサンプルも保存前は殆ど粘性がない透明
溶液であった。 <処方> ・リゾリン脂質(キユーピー(株)製、商品名 「卵黄レシチンLC-100」) 1.0重量% ・安定化剤 1.0重量% ・メチルパラベン 0.1重量% ・精製水 97.9重量% <製造方法>精製水を70℃に加温後、リゾリン脂質、
安定化剤及びメチルパラベンを溶解させ、化粧水を得
た。得られた化粧水をねじ口瓶に充填し、4℃の低温室
に静置させた。
Test Example A lotion containing a stabilizer shown in Table 1 was produced according to the following formulation and production method. The obtained lotion was stored at 4 ° C. for one month, and after the storage, the presence or absence of a precipitate or a stain was observed, and the change in viscosity was observed.
In addition, all the samples were transparent solutions having almost no viscosity before storage. <Prescription>-Lysophospholipid (QP Corporation, trade name "Egg Yolk Lecithin LC-100") 1.0% by weight-Stabilizer 1.0% by weight-Methylparaben 0.1% by weight-Purified water 97.9 % By weight <Production method> After heating purified water to 70 ° C, lysophospholipid,
The stabilizer and methyl paraben were dissolved to obtain a lotion. The obtained lotion was filled into a screw-mouth bottle and allowed to stand in a low-temperature room at 4 ° C.

【0014】[0014]

【表1】 [Table 1]

【0015】表中の総合評価の記号は下記のとおりであ
る。 ◎:沈殿物及びにごりの発生もなく、粘度変化も殆ど観
察されなかった。 ○:やや粘度が上昇しているものの、沈殿物及びにごり
の発生はなかった。 △:にごりの発生、及びやや粘度上昇がみられるもの
の、沈殿物の発生はなかった。 ×:沈殿物が発生していた。
The symbols for overall evaluation in the table are as follows. :: No precipitate and no smear were generated, and almost no change in viscosity was observed. :: Although the viscosity was slightly increased, no precipitate and no smell were generated. Δ: Smearing and slight increase in viscosity were observed, but no precipitate was generated. ×: A precipitate was generated.

【0016】表1より、リゾリン脂質を含有した化粧水
において、モノエステルが80重量%以上のショ糖脂肪
酸エステルを含有させることにより、低温での安定性に
優れた化粧水が得られることが理解される。
From Table 1, it is understood that a lotion having excellent stability at low temperature can be obtained by adding a sucrose fatty acid ester containing 80% by weight or more of a monoester to a lotion containing lysophospholipid. Is done.

【0017】以上述べたように、本発明の化粧水は、低
温での安定性に優れたものであることから、化粧料とし
て好まい品位を有し更なる需要の拡大が期待される。
As described above, the lotion of the present invention has excellent stability at low temperatures, and therefore has a favorable quality as a cosmetic and is expected to further expand demand.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 リゾリン脂質とショ糖脂肪酸エステルと
を含有した化粧水であって、該ショ糖脂肪酸エステルの
約80重量%以上がモノエステルであることを特徴とす
る化粧水。
1. A lotion containing a lysophospholipid and a sucrose fatty acid ester, wherein about 80% by weight or more of the sucrose fatty acid ester is a monoester.
JP11223077A 1999-08-05 1999-08-05 Skin lotion Pending JP2001048743A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11223077A JP2001048743A (en) 1999-08-05 1999-08-05 Skin lotion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11223077A JP2001048743A (en) 1999-08-05 1999-08-05 Skin lotion

Publications (1)

Publication Number Publication Date
JP2001048743A true JP2001048743A (en) 2001-02-20

Family

ID=16792488

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11223077A Pending JP2001048743A (en) 1999-08-05 1999-08-05 Skin lotion

Country Status (1)

Country Link
JP (1) JP2001048743A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013082643A (en) * 2011-10-07 2013-05-09 Mikimoto Pharmaceut Co Ltd O/w type emulsion
US9345250B2 (en) 2006-09-20 2016-05-24 Tsuji Oil Mill Co., Ltd. Method for preparing solubilized composition containing oil-soluble substance

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9345250B2 (en) 2006-09-20 2016-05-24 Tsuji Oil Mill Co., Ltd. Method for preparing solubilized composition containing oil-soluble substance
JP2013082643A (en) * 2011-10-07 2013-05-09 Mikimoto Pharmaceut Co Ltd O/w type emulsion

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