JPH05194141A - Cosmetic - Google Patents
CosmeticInfo
- Publication number
- JPH05194141A JPH05194141A JP517592A JP517592A JPH05194141A JP H05194141 A JPH05194141 A JP H05194141A JP 517592 A JP517592 A JP 517592A JP 517592 A JP517592 A JP 517592A JP H05194141 A JPH05194141 A JP H05194141A
- Authority
- JP
- Japan
- Prior art keywords
- particles
- cosmetic
- polyester
- feeling
- produced
- 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
Links
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- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Biological Depolymerization Polymers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は粒子含有化粧料に関す
る。詳しくは生分解性ポリエステル粒子を含有すること
によりのび特性、かさつき感、保湿性等が改善された粒
子含有化粧料に関する。FIELD OF THE INVENTION The present invention relates to a particle-containing cosmetic composition. More specifically, the present invention relates to a particle-containing cosmetic composition containing biodegradable polyester particles, which has improved spreadability, bulkiness, moisturizing properties and the like.
【0002】[0002]
【従来の技術】従来より、化粧料には各種の無機、有機
顔料等の化粧用粒子が添加、配合されてきた。特にメー
キャップ化粧料においては化粧用粒子の果たす役割は大
きく、化粧目的に応じて、また機能性を得るために、多
くの種類の化粧用粒子が用いられている。更には製品特
徴を出すために個々の粉体の特性を活用し、配合を組み
合わせる等の検討がなされてきた。2. Description of the Related Art Conventionally, cosmetic particles such as various inorganic and organic pigments have been added and blended in cosmetics. Particularly in makeup cosmetics, the cosmetic particles play a large role, and many kinds of cosmetic particles are used in accordance with the purpose of makeup and to obtain functionality. Furthermore, in order to obtain product characteristics, it has been studied to utilize the characteristics of individual powders and combine the formulations.
【0003】特にのび特性を向上させるために、従来は
球状ナイロン、球状ポリエチレン、球状ポリスチレン等
の球状合成樹脂粒子が使用されていた。最近では、つき
を向上させるために球状セルロース粒子も使用され、更
にこれらの粒子の欠点を解消するために種々の改良が提
案されている。例えば、N−アシルアミノ酸アミドで処
理する方法(特開平1−172312)、球状セルロー
ス粒子を保湿性高分子で処理する方法(特開平1−31
3413)等が挙げられる。Conventionally, spherical synthetic resin particles such as spherical nylon, spherical polyethylene and spherical polystyrene have been used in order to improve the spreadability. Recently, spherical cellulose particles have also been used to improve the stickiness, and various improvements have been proposed to eliminate the drawbacks of these particles. For example, a method of treating with N-acyl amino acid amide (JP-A-1-172312) and a method of treating spherical cellulose particles with a moisturizing polymer (JP-A-1-3112).
3413) and the like.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、前記N
−アシルアミノ酸アミドで処理する方法では化粧持続性
は向上するが、保湿性が充分でなく、保湿性高分子で処
理する方法では特殊な保湿性高分子を利用しなければな
らないという問題点があった。However, the above-mentioned N
-The method of treating with an acylamino acid amide improves the makeup durability, but the moisturizing property is not sufficient, and the method of treating with a moisturizing polymer requires the use of a special moisturizing polymer. It was
【0005】[0005]
【課題を解決するための手段】本発明者らは、化粧料の
のび特性、かさつき感、保湿性等を改善する化粧用粒子
について鋭意検討の結果、特定の範囲の粒径を持つ生分
解性ポリエステル粒子を化粧用粒子に適用することによ
り前記のような問題点のない、極めて優れた性能を持つ
化粧料が得られることを発見し本発明に到達した。Means for Solving the Problems As a result of intensive investigations by the present inventors regarding cosmetic particles for improving spreadability, bulkiness, moisturizing properties, etc., of cosmetics, biodegradation having a particle size within a specific range was conducted. The present invention has been accomplished by discovering that a cosmetic material having extremely excellent performance without the above-mentioned problems can be obtained by applying the hydrophilic polyester particles to cosmetic particles.
【0006】すなわち、本発明の要旨は、平均粒径3〜
50μmの生分解性ポリエステル粒子を含有することを
特徴とする化粧料に存する。本発明における生分解性ポ
リエステルとは、微生物産生ポリエステルであり、例え
ばポリ(3−ヒドロキシブチレート)、ポリ(3−ヒド
ロキシブチレート)−ポリ(4−ヒドロキシブチレー
ト)共重合体、ポリ(3−ヒドロキシブチレート)−ポ
リ(3−ヒドロキシバレレート)共重合体等が挙げられ
る。That is, the gist of the present invention is that the average particle size is 3 to
A cosmetic composition is characterized by containing biodegradable polyester particles of 50 μm. The biodegradable polyester in the present invention is a polyester produced by a microorganism, for example, poly (3-hydroxybutyrate), poly (3-hydroxybutyrate) -poly (4-hydroxybutyrate) copolymer, poly (3 -Hydroxybutyrate) -poly (3-hydroxyvalerate) copolymer and the like.
【0007】これら微生物産生ポリエステルは、エネル
ギー貯蔵物質として数多くの微生物の菌体内に蓄積さ
れ、優れた生物分解性と生体適合性を示す熱可塑性高分
子であることから、環境を保全するクリーンプラスチッ
クとして注目され、医用材料や徐放性システム等多方面
への応用が期待されている。上記ポリエステル生産能を
有する微生物としては、例えば、アルカリゲネスフェカ
リス(Alcaligenes faecalis)、
アルカリゲネスルーランディィ(Alcaligene
s ruhlandii)、アルカリゲネス ユウトロ
フス(Alcaligenes eutrophs)等
のアルカリゲネス属等がある。Since these polyesters produced by microorganisms are thermoplastic polymers that accumulate in the cells of many microorganisms as energy storage substances and exhibit excellent biodegradability and biocompatibility, they are used as clean plastics that preserve the environment. It is attracting attention and is expected to be applied to various fields such as medical materials and sustained release systems. Examples of the microorganisms having the above-mentioned polyester-producing ability include, for example, Alcaligenes faecalis,
Alkaline Gene
s ruhlandii), Alcaligenes eutrophus and the like.
【0008】これらの菌種に属する菌株の代表例とし
て、アルカリゲネス ルーランディィATCC1574
9、アルカリゲネス ユウトロフスH−16ATCC1
7699およびこのH−16株の突然変異株であるアル
カリゲネス ユウトロフスNCIB11597、同NC
IB11598、同NCIB11599、同NCIB1
1600等を挙げることができる。アルカリゲネス属に
属するこれらの微生物の菌学的性質は、BERGEY’
MANUAL OF DETERMINATIVE B
ACTERIOLOGYに、また、アルカリゲネス ユ
ウトロフスH−16の菌学的性質は、例えばJ.GE
N.MICROBIOL.,115,185〜192
(1979)にそれぞれ記載されている。As a representative example of strains belonging to these bacterial species, Alcaligenes rulandi ATCC 1574
9, Alcaligenes Yutrofus H-16ATCC1
7699 and the mutant strain of this H-16 strain, Alcaligenes eutrophus NCIB11597, NC
IB11598, NCIB11599, NCIB1
1600 etc. can be mentioned. The mycological properties of these microorganisms belonging to the genus Alcaligenes are BERGEY '
MANUAL OF DETERMINATIVE B
ACTERIOLOGY, and the mycological properties of Alcaligenes yutrofus H-16 are described in, for example, J. GE
N. MICROBIOL. , 115, 185-192
(1979).
【0009】またポリ(3−ヒドロキシブチレート)−
ポリ(4−ヒドロキシブチレート)共重合体(以下P
(3HB−co−4HB)と略称する)は、例えば特開
昭64−48821等に記載の方法により、任意の組成
比の共重合体として製造することができる。ポリエステ
ル粒子の製造方法については特に限定されないが、例え
ばポリエステル可溶性の溶媒中に溶解させて溶液とし、
次に該溶液を攪拌されている貧溶媒中に滴下し、溶媒を
蒸発させながらポリエステル粒子を析出させ、その後、
通常のろ過、水洗、乾燥によって得られる。該ポリエス
テル粒子の粒径は溶液中のポリエステル溶解濃度、貧溶
媒の選定、あるいは貧溶媒の攪拌速度等により制御でき
る。これらについては、J.Controlled R
elease 4 1986 25−32やChem.
Pharm.Bull.29 113363−3368
等にも記載されている。Further, poly (3-hydroxybutyrate)-
Poly (4-hydroxybutyrate) copolymer (hereinafter P
(Abbreviated as 3HB-co-4HB) can be produced as a copolymer having an arbitrary composition ratio, for example, by the method described in JP-A-64-48821. The method for producing polyester particles is not particularly limited, for example, by dissolving in a polyester-soluble solvent to form a solution,
Next, the solution is dropped into a poor solvent that is being stirred, and polyester particles are deposited while evaporating the solvent, and then,
Obtained by ordinary filtration, washing with water and drying. The particle size of the polyester particles can be controlled by the concentration of polyester dissolved in the solution, selection of the poor solvent, stirring speed of the poor solvent, and the like. Regarding these, J. Controlled R
Release 4 1986 25-32 and Chem.
Pharm. Bull. 29 113363-3368
Etc.
【0010】上記溶媒としてはポリエステルを溶解でき
るものなら特に制限はないが、例えばクロロホルム、塩
化メチレン等の有機ハロゲン溶媒や酢酸メチルが好まし
い。貧溶媒としては水等でも利用可能であるが、ポリビ
ニルアルコール、ゼラチン、アルギン酸ナトリウム等の
0.1〜5重量%水溶液の方が狭い粒径分布のものが得
られるので好ましい。また粒径分布が広範囲の場合には
公知の方法により特定の粒径範囲のものだけにすること
も有効である。The solvent is not particularly limited as long as it can dissolve the polyester, but organic halogen solvents such as chloroform and methylene chloride and methyl acetate are preferable. Although water or the like can be used as the poor solvent, an aqueous solution of 0.1 to 5% by weight of polyvinyl alcohol, gelatin, sodium alginate or the like is preferable because a narrow particle size distribution can be obtained. When the particle size distribution is wide, it is effective to limit the particle size to a specific particle size range by a known method.
【0011】本発明の化粧料は、粉体を構成成分とする
ものであれば特に制限はなく、例えば白粉、ファウンデ
ーション、口紅、頬紅、アイライナー、マスカラ、アイ
シャドウ、下地クリーム、乳液、化粧水、クリーム等が
あげられる。本発明の化粧料は、微生物産生ポリエステ
ル粒子を含有するために保湿性があるが、用途に応じて
他の保湿剤を粒子に被覆、含浸させても良い。他の保湿
剤としては例えば、プロピレングリコール、グリセリン
等の多価アルコールやヒアルロン酸等の天然高分子等が
挙げられる。The cosmetic of the present invention is not particularly limited as long as it has powder as a constituent component, and for example, white powder, foundation, lipstick, blusher, eyeliner, mascara, eye shadow, base cream, emulsion, lotion. , Cream, etc. The cosmetic of the present invention has a moisturizing property because it contains the polyester particles produced by a microorganism, but other moisturizing agents may be coated or impregnated into the particles depending on the application. Examples of other moisturizers include polyhydric alcohols such as propylene glycol and glycerin, and natural polymers such as hyaluronic acid.
【0012】本発明に用いる微生物産生ポリエステル粒
子は平均粒径3〜50μm、好ましくは5〜35μmの
球状粒子である。下限以下の場合には、のびの効果が少
なく、上限以上の場合にはザラザラ感が生じやすく好ま
しくない。また、その効果をなくさない範囲において,
各種の目的に応じて,該粒子に公知の表面処理を行うこ
と、あるいは他の顔料類を併用すること等各種の添加剤
の利用ができる。The microorganism-produced polyester particles used in the present invention are spherical particles having an average particle size of 3 to 50 μm, preferably 5 to 35 μm. When the amount is less than the lower limit, the effect of spreading is small, and when the amount is more than the upper limit, a rough feeling tends to occur, which is not preferable. Also, within the range that does not lose its effect,
Depending on various purposes, various additives such as known surface treatment of the particles or combined use of other pigments can be used.
【0013】本発明の化粧料におけるポリエステル粒子
の含有量はその化粧料に応じて変化させるべきである
が、最も含有量の多い粉末化粧料の場合で0.1〜60
重量%の範囲である。本発明におけるポリエステル粒子
はその優れた生体適合性の為大量に含有させても、他の
合成樹脂粒子の様な肌あれ等の問題がない。The content of polyester particles in the cosmetic composition of the present invention should be changed according to the cosmetic composition, but 0.1-60 in the case of the powder cosmetic composition having the highest content.
It is in the range of% by weight. Due to its excellent biocompatibility, the polyester particles of the present invention do not have the problem of rough skin like other synthetic resin particles even when contained in a large amount.
【0014】[0014]
【実施例】以下に、本発明を実施例により具体的に説明
するが、本発明はその要旨を逸脱しない限りこれら実施
例に何ら制限されるものではない。参考例 [P(3HB−co−4HB)粒子の製造] P(3HB−co−4HB)1gを塩化メチレン150
mlに溶解させた。つぎに該溶液を攪拌速度1200r
pmで攪拌下の0.5重量%のポリビニルアルコール水
溶液中に滴下した。滴下によりP(3HB−co−4H
B)が乳化した。更に室温下で攪拌を続けることによ
り、塩化メチレンを蒸発させた。EXAMPLES The present invention will now be described in detail with reference to examples, but the present invention is not limited to these examples without departing from the gist thereof. Reference Example [Production of P (3HB-co-4HB) Particles] 1 g of P (3HB-co-4HB) was added to 150 g of methylene chloride.
It was dissolved in ml. Next, the solution is stirred at a stirring rate of 1200 r
It was added dropwise to a 0.5 wt% polyvinyl alcohol aqueous solution with stirring at pm. By dropping, P (3HB-co-4H
B) emulsified. The methylene chloride was evaporated by continuing stirring at room temperature.
【0015】完全に塩化メチレンを蒸発させた後、ろ
過、水洗、減圧下での乾燥を行い、平均粒径が29μm
のP(3HB−co−4HB)粒子を作成した。尚、こ
の平均粒径は光学顕微鏡(BH−2;オリンパス光学工
業(株)製)を用いて測定した。実施例1 [パウダーファウンデーション] 下記(1)〜(5)をヘンシェルミキサーで混合し,こ
れに(6)〜(11)を加熱溶解したものを添加し,混
合粉砕した。これを中皿に成型してパウダーファウンデ
ーションを得た。(数字は重量%、以下同じ) (1)セリサイト;47.28(重量%) (2)タルク;15.0 (3)参考例で作成したP(3HB−co−4HB)粒
子;15.0 (4)二酸化チタン;6.5 (5)酸化鉄;3.5 (6)トリメチロールプロパントリイソステアレート;
5.0 (7)スクワラン;6.0 (8)ソルビタンセスキオレート;1.0 (9)防腐剤;0.5 (10)酸化防止剤;0.02 (11)香料;0.2After evaporating methylene chloride completely, filtration, washing with water and drying under reduced pressure were carried out to obtain an average particle size of 29 μm.
P (3HB-co-4HB) particles were prepared. The average particle size was measured using an optical microscope (BH-2; manufactured by Olympus Optical Co., Ltd.). Example 1 [Powder foundation] The following (1) to (5) were mixed with a Henschel mixer, and the mixture of (6) to (11) heated and dissolved was added thereto, and mixed and pulverized. This was molded into a medium plate to obtain a powder foundation. (Numbers are% by weight, the same below) (1) Sericite; 47.28 (% by weight) (2) Talc; 15.0 (3) P (3HB-co-4HB) particles prepared in Reference Example; 0 (4) titanium dioxide; 6.5 (5) iron oxide; 3.5 (6) trimethylolpropane triisostearate;
5.0 (7) Squalane; 6.0 (8) Sorbitan sesquioleate; 1.0 (9) Preservative; 0.5 (10) Antioxidant; 0.02 (11) Perfume; 0.2
【0016】比較例1 [パウダーファウンデーショ
ン] 下記組成で実施例1と同様にしてパウダーファウンデー
ションを得た。 (1)セリサイト;47.28(重量%) (2)タルク;15.0 (3)球状ナイロン12;15.0 (4)二酸化チタン;6.5 (5)酸化鉄;3.5 (6)トリメチロールプロパントリイソステアレート;
5.0 (7)スクワラン;6.0 (8)ソルビタンセスキオレート;1.0 (9)防腐剤;0.5 (10)酸化防止剤;0.02 (11)香料;0.2評価 実施例1と比較例1のパウダーファウンデーションを実
使用テストにて20名の被験者で比較した。結果を以下
に示す。 Comparative Example 1 [Powder Foundation] A powder foundation having the following composition was obtained in the same manner as in Example 1. (1) Sericite; 47.28 (wt%) (2) Talc; 15.0 (3) Spherical nylon 12; 15.0 (4) Titanium dioxide; 6.5 (5) Iron oxide; 3.5 ( 6) trimethylolpropane triisostearate;
5.0 (7) Squalane; 6.0 (8) Sorbitan sesquioleate; 1.0 (9) Preservative; 0.5 (10) Antioxidant; 0.02 (11) Perfume; 0.2 Evaluation The powder foundations of Example 1 and Comparative Example 1 were compared in an actual use test with 20 test subjects. The results are shown below.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【発明の効果】本発明の化粧料は、のび、つき等が良好
であり、肌に塗布した後の粉浮きがなく、かさつき感や
ばさつき感がなく、総合的な仕上がりがよい。また、本
発明における微生物産生ポリエステル粒子は優れた生体
適合性の為、大量に含有させても肌あれ等の問題がな
い。EFFECTS OF THE INVENTION The cosmetic composition of the present invention has good spreadability, stickiness, etc., no powder floating after being applied to the skin, no feeling of bulkiness or roughness, and good overall finish. In addition, since the microorganism-produced polyester particles of the present invention have excellent biocompatibility, there is no problem such as rough skin even when contained in a large amount.
フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 67/04 KJT 8933−4J Continuation of front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area C08L 67/04 KJT 8933-4J
Claims (2)
ステル粒子を含有することを特徴とする化粧料。1. A cosmetic material comprising biodegradable polyester particles having an average particle diameter of 3 to 50 μm.
ヒドロキシブチレート)系重合体粒子であることを特徴
とする請求項第1項記載の化粧料。2. The biodegradable polyester particles are poly (3-
2. The cosmetic according to claim 1, wherein the cosmetic is particles of hydroxybutyrate).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP517592A JPH05194141A (en) | 1992-01-14 | 1992-01-14 | Cosmetic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP517592A JPH05194141A (en) | 1992-01-14 | 1992-01-14 | Cosmetic |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05194141A true JPH05194141A (en) | 1993-08-03 |
Family
ID=11603906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP517592A Pending JPH05194141A (en) | 1992-01-14 | 1992-01-14 | Cosmetic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05194141A (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002100357A1 (en) * | 2001-06-12 | 2002-12-19 | Trial Corporation | Cosmetic |
JP2004026788A (en) * | 2002-05-08 | 2004-01-29 | Asahi Kasei Chemicals Corp | Body cleaning cosmetic |
JP2005281295A (en) * | 2004-03-01 | 2005-10-13 | Kose Corp | Cosmetic |
WO2006081517A2 (en) * | 2005-01-28 | 2006-08-03 | Tepha, Inc. | Embolization using poly-4-hydroxybutyrate particles |
JP2016102152A (en) * | 2014-11-28 | 2016-06-02 | 東レ株式会社 | Polymer fine particles |
US9555155B2 (en) | 2014-12-11 | 2017-01-31 | Tepha, Inc. | Methods of orienting multifilament yarn and monofilaments of poly-4-hydroxybutyrate and copolymers thereof |
WO2017195642A1 (en) * | 2016-05-10 | 2017-11-16 | 住友精化株式会社 | Cosmetic |
US10111738B2 (en) | 2003-05-08 | 2018-10-30 | Tepha, Inc. | Polyhydroxyalkanoate medical textiles and fibers |
US10500303B2 (en) | 2014-08-15 | 2019-12-10 | Tepha, Inc. | Self-retaining sutures of poly-4-hydroxybutyrate and copolymers thereof |
CN110753569A (en) * | 2017-03-30 | 2020-02-04 | 博奥股份公司 | Cosmetic composition comprising biodegradable polyester and oil phase |
US10626521B2 (en) | 2014-12-11 | 2020-04-21 | Tepha, Inc. | Methods of manufacturing mesh sutures from poly-4-hydroxybutyrate and copolymers thereof |
WO2022081762A1 (en) * | 2020-10-14 | 2022-04-21 | Dermbiont, Inc. | Compositions and methods for improving skin health and for the treatment and prevention of diseases, disorders and conditions associated with fungi and other pathogenic microbes |
US12064459B2 (en) | 2019-04-09 | 2024-08-20 | Dermbiont, Inc. | Compositions and methods for improving skin health and for the treatment and prevention of diseases, disorders and conditions associated with pathogenic microbes |
US12065548B2 (en) | 2016-07-22 | 2024-08-20 | Sekisui Plastics Co., Ltd. | Generally spherical resin particles formed of thermoplastic resin, method for producing same and use of same |
-
1992
- 1992-01-14 JP JP517592A patent/JPH05194141A/en active Pending
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002100357A1 (en) * | 2001-06-12 | 2002-12-19 | Trial Corporation | Cosmetic |
JP2004026788A (en) * | 2002-05-08 | 2004-01-29 | Asahi Kasei Chemicals Corp | Body cleaning cosmetic |
US10314683B2 (en) | 2003-05-08 | 2019-06-11 | Tepha, Inc. | Polyhydroxyalkanoate medical textiles and fibers |
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