JPH0451522B2 - - Google Patents
Info
- Publication number
- JPH0451522B2 JPH0451522B2 JP55172580A JP17258080A JPH0451522B2 JP H0451522 B2 JPH0451522 B2 JP H0451522B2 JP 55172580 A JP55172580 A JP 55172580A JP 17258080 A JP17258080 A JP 17258080A JP H0451522 B2 JPH0451522 B2 JP H0451522B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- present
- powder
- spherical porous
- water
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/12—Face or body powders for grooming, adorning or absorbing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
- A61K8/0279—Porous; Hollow
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/65—Characterized by the composition of the particulate/core
- A61K2800/654—The particulate/core comprising macromolecular material
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)
- Cosmetics (AREA)
Description
本発明は、化粧持続性の良い新規な化粧料に関
する。
本発明は、ソフトな使用感を与え、透明感に優
れ、皮脂との親和性が良く、白さの浮き防止効果
に優れ、さらにプレス充填性に優れた化粧持続性
の良い化粧料を開発すべく鋭意研究した結果、化
粧料において、特定の球状多孔性樹脂粉体を配合
したものが上記の優れた効果をすべて持合せてお
り、特にメークアツプ化粧料に好適であることを
見出し、ここに本発明を完成するに至つた。
従来、化粧料に汎用されている粉体としては各
種のものが挙げられるが、特にその使用性の点か
らタルク、絹雲母、白雲母等のように限られてい
る。これら天然鉱物は、粒子の厚さが不揃いで、
しかも粒子の結びつきが弱いため空気が残留しや
すく、プレス製品の割れかけや各種の問題の原因
となつている。
粉体化粧料において、化粧料を皮膚に塗布した
際に望まれる化粧持続性の良さは、粉体製品中に
含有される水分、油分の各々の吸収量と吸収速度
に依存する。すなわち、理想的な製品は吸油量と
吸水量がいずれも適度に高く、吸油速度が速くて
吸水速度が遅いという特性を持つ粉体を見出すこ
とにより達成される。しかしながら、現下の製品
においては、これらの条件を満足するのに決定的
なフアクターとなる粉体は殆んど皆無と云つてよ
い。一般の粉体製品のうち、適用される粉体は吸
油量、吸水量が高いものは少なく、しかもこれら
が高い場合であつても、吸油・吸水速度がいずれ
も早いか、いずれも遅いかの偏つた傾向をなすに
止つている。吸油・吸水速度がいずれも早い場
合、肌へ化粧料を塗布した際、肌が乾燥しやす
く、塗布時又は塗布後がムラつきの状態を呈す
る。また吸油・吸水速度がいずれも遅い場合、皮
膚から分泌される皮脂により、化粧くずれを生
じ、これを防ぐことは極めて困難が伴なう。この
ような傾向は近時提供されている無機の中空粉体
や多孔性粉体等の合成粉体についても例外でな
く、いずれにしても望ましい化粧持続性の良い化
粧料を得るための抜本的な解決が必要とされてい
た。
本発明の目的は、上記従来技術の問題点を解決
する化粧持続性の良い化粧料を提供することであ
り、本発明によれば次のメークアツプ化粧料によ
り上記目的を達成することができる。
ポリ酢酸ビニル、ポリN−ビニルピロリドン、
ポリ−2,4−ジアミノ−6−フエニル−1,
3,5−トリアジン、ポリメタクリル酸エステ
ル、ポリアクリル酸エステル、エチレン酢酸ビニ
ル共重合体から選択され、球体表面に最多孔径5
〜160Åの大小の空孔を有し、また粒子径が1〜
40μでかつ平均粒子径が2〜20μである球状多孔
性樹脂粉体を配合するメークアツプ化粧料。
本発明に適用される球状多孔性樹脂粉体は、粒
子径が1〜40μでかつ平均粒子径が2〜20μであ
り、その球体表面に最多孔径5〜160Åの大小の
空孔を有するものである。最多孔径5〜160Åと
は、最も多くを占める孔径(即ち、分布のピーク
値をなす孔径)が5〜160Åの範囲内に存在する
ことをいう。(本発明に於ける球状は当然のこと
ながら真球状のものの他に、だ円その他の類似形
状も包含する。)
本発明の球状多孔性樹脂粉体は、それ自体、透
明性(光透過性)があり、油剤に対して親和性が
あるもので、ポリ酢酸ビニル、ポリN−ビニルピ
ロリドン、ポリ2,4−ジアミノ−6−フエニル
−1,3,5−トリアジン、ポリメタクリル酸エ
ステル(メチルエステル、エチルエステル等)、
ポリアクリル酸エステル(メチルエステル、エチ
ルエステル等)、エチレン酢酸ビニル共重合体、
が挙げられる。
本発明に適用される球状多孔性樹脂粉体の特徴
について、次に詳細に述べるならば、まず第一に
従来各種粉体が化粧料に使用されて来たが、これ
らは殆んどが吸油量、吸水量が高くなく、又油に
対するなじみのよいものがなく、油に対する吸油
速度が遅いものが大半である。そのために、皮脂
の分泌と共に短時間で化粧くずれをするものが多
かつた。又、合成無機粉体では吸油量、吸水量の
高いものも中にはあるが、これらは吸油、吸水速
度が非常に速く、肌がつつぱつたり、肌が乾燥し
たりし、皿にはメークアツプがムラつきしやすい
ものでメークアツプ効果を損うものであつた。本
発明の球状多孔性樹脂粉体は吸油量、吸水量も大
きく、油に対してなじみやすく吸油速度がかなり
速く吸水速度は比較的遅い性質を持ち、水を蒸発
させる性質を有し、メークアツプ効果を長時間に
亘り持続させると共に肌に均一に塗布出来、肌に
異和感を感じさせないものである。
第二に、本発明に用いられる球状多孔性樹脂粉
体は粒子表面の光散乱が小さく、透過性が大きい
ために、肌上に塗布した場合、粒子が細かくなつ
ても通常の粉体よりもはるかに透明性があり、白
浮きがしない。
第三に、従来の無機粉体と異なり、粒子に弾力
性があり、使用感面でソフトで軟らか味のある感
触が得られる。更に従来の各種粉体の様に不定形
で厚みが不揃いという事がなく、ローリング効果
により延展性が良く、肌上の抵抗が小さく、伸び
の軽い感触が得られる。
第四に、従来の無機粉体は粒子径が不揃いで不
定形を有し、またその厚みが不揃いである事から
粉体のプレス製品に於いて、プレス製品内に空気
が残留しやすく、割れ、かけの原因になつていた
が、本発明微小球体を用いることにより、最密充
填構造をとりやすくなるため、それらの欠点を防
止できる。
第五に、最近、球状多孔性無機粉体や球状多孔
性樹脂粉体の合成が試みられているが、本発明の
球状多孔性粉体と比較して、肌上での透明感、密
着性、白さの浮き、弾性、肌へののりの均一性面
で劣り今迄の無機の球状多孔性粉体、球状中空多
孔性質粉体よりも本発明微小球体は優れている。
第六に、これまで一部において、色素類を混入
した球状粉体が見受けられるが、これらは、本発
明の球状樹脂粉体とは化学的組成・構造が異なる
だけでなく、吸水・吸油性や透明性がなく、色素
類本来の隠蔽力、着色効果を損なう他、多くの点
(例、使用感、充填性、コスト面など)で本発明
と相違し、何ら本発明とは関係のないものであ
る。
また、有機の球状多孔性粉体として特開昭52−
145527号においてポリアミノ酸類を用いた化粧料
が開示されているが、これにおいても上記と同じ
く本発明の球状多孔性樹脂粉体と化学的組成や物
理的特性が異なるだけでなく、実用上のコスト面
で難があり、本来の目的とすべき化粧料は得られ
ない。
次に、本発明に適用される球状多孔性粉体が化
粧持続性の良い化粧料を得る上で、如何に従来の
粉体類に比較して理想的なものであるかを立証す
るため、後記実施1〜実施例4の本発明微小球体
と従来粉体とを試料として用いて、吸油・吸水量
と吸油・吸水速度を測定した結果を下記第1表を
以つて示す。
TECHNICAL FIELD The present invention relates to a novel cosmetic with good makeup persistence. The present invention aims to develop cosmetics that give a soft feeling of use, have excellent transparency, have good affinity with sebum, have an excellent effect on preventing whitening, and have excellent press filling properties and long-lasting makeup. As a result of intensive research, we found that cosmetics containing a specific spherical porous resin powder have all of the above excellent effects and are particularly suitable for make-up cosmetics, and hereby we have published this book. The invention was completed. Conventionally, there are various powders commonly used in cosmetics, but they are limited to talc, sericite, muscovite, etc. from the viewpoint of usability. These natural minerals have irregular grain thickness,
Moreover, because the particles are tightly bound together, air tends to remain in the press, causing cracks in pressed products and various other problems. When powder cosmetics are applied to the skin, the desired cosmetic longevity depends on the amount and rate of absorption of water and oil contained in the powder product. That is, an ideal product can be achieved by finding a powder that has moderately high oil absorption and water absorption, and has the characteristics of fast oil absorption and slow water absorption. However, in current products, it can be said that there is almost no powder that is a decisive factor in satisfying these conditions. Among general powder products, there are few applicable powders with high oil absorption and water absorption, and even when these are high, the speed of oil and water absorption is either fast or slow. The trend remains lopsided. If both the oil absorption and water absorption speeds are high, when a cosmetic is applied to the skin, the skin tends to dry out, and the skin becomes uneven during or after application. Furthermore, if both the oil and water absorption speeds are slow, the sebum secreted from the skin will cause makeup to fade, making it extremely difficult to prevent this. This trend is no exception to the synthetic powders such as inorganic hollow powders and porous powders that have been provided recently. A solution was needed. An object of the present invention is to provide a cosmetic with good makeup persistence that solves the problems of the prior art, and according to the present invention, the above object can be achieved with the following make-up cosmetic. polyvinyl acetate, poly N-vinylpyrrolidone,
poly-2,4-diamino-6-phenyl-1,
Selected from 3,5-triazine, polymethacrylate, polyacrylate, and ethylene-vinyl acetate copolymer, the spherical surface has a maximum pore diameter of 5.
It has large and small pores of ~160 Å, and the particle size is 1~160 Å.
A makeup cosmetic containing spherical porous resin powder having a particle diameter of 40μ and an average particle diameter of 2 to 20μ. The spherical porous resin powder applied to the present invention has a particle size of 1 to 40μ, an average particle size of 2 to 20μ, and has large and small pores with a maximum pore size of 5 to 160Å on the spherical surface. be. The maximum pore diameter of 5 to 160 Å means that the pore diameter that occupies the largest proportion (that is, the pore diameter that forms the peak value of the distribution) is within the range of 5 to 160 Å. (The spherical shape in the present invention naturally includes not only a true spherical shape but also an ellipse and other similar shapes.) The spherical porous resin powder of the present invention itself has transparency (light transmittance). ) and have an affinity for oils, including polyvinyl acetate, poly N-vinylpyrrolidone, poly2,4-diamino-6-phenyl-1,3,5-triazine, and polymethacrylic acid ester (methyl ester, ethyl ester, etc.),
Polyacrylic ester (methyl ester, ethyl ester, etc.), ethylene vinyl acetate copolymer,
can be mentioned. To describe in detail the characteristics of the spherical porous resin powder applied to the present invention, first of all, various powders have been conventionally used in cosmetics, but most of these powders are oil-absorbing. Most of them do not have a high amount of water absorption, are not compatible with oil, and have a slow oil absorption rate. As a result, makeup often comes off in a short period of time due to sebum secretion. Also, some synthetic inorganic powders have a high oil and water absorption rate, but these absorb oil and water at a very high rate, causing skin irritation and dryness, and make-up on dishes. It tends to cause unevenness and impairs the makeup effect. The spherical porous resin powder of the present invention has a large oil absorption amount and water absorption amount, is easily compatible with oil, has a fairly fast oil absorption rate, and has a relatively slow water absorption rate, and has the property of evaporating water, which has a makeup effect. It lasts for a long time, can be applied evenly to the skin, and does not make the skin feel uncomfortable. Second, the spherical porous resin powder used in the present invention has low light scattering on the particle surface and high transparency, so when applied to the skin, even if the particles are fine, it is better than normal powder. Much more transparent and no white cast. Thirdly, unlike conventional inorganic powders, the particles have elasticity, giving them a soft and mellow feel when used. Furthermore, unlike conventional powders, it does not have an irregular shape or uneven thickness, has good spreadability due to the rolling effect, has low resistance on the skin, and has a light feeling of elongation. Fourth, conventional inorganic powders have irregular particle sizes and irregular shapes, and their thickness is uneven, so air tends to remain in pressed products and cracks occur. However, by using the microspheres of the present invention, it becomes easier to form a close-packed structure, so these drawbacks can be prevented. Fifth, attempts have recently been made to synthesize spherical porous inorganic powders and spherical porous resin powders, but compared to the spherical porous powder of the present invention, they have poor transparency and adhesion on the skin. The microspheres of the present invention are superior to conventional inorganic spherical porous powders and spherical hollow porous powders, which are inferior in terms of floating whiteness, elasticity, and uniformity of application to the skin. Sixth, some spherical powders mixed with pigments have been seen up to now, but these not only have a different chemical composition and structure from the spherical resin powder of the present invention, but also have water and oil absorption properties. It is different from the present invention in many respects (e.g., usability, fillability, cost, etc.) and is not related to the present invention. It is something. In addition, as an organic spherical porous powder,
Cosmetics using polyamino acids are disclosed in No. 145527, but as with the above, this product not only differs in chemical composition and physical properties from the spherical porous resin powder of the present invention, but also has practical problems. Due to cost issues, the intended cosmetics cannot be obtained. Next, in order to prove how the spherical porous powder applied to the present invention is ideal compared to conventional powders in obtaining cosmetics with good makeup persistence, Table 1 below shows the results of measuring the amount of oil and water absorption and the rate of oil and water absorption using the microspheres of the present invention and the conventional powder of Examples 1 to 4 described below as samples.
【表】
◎ 非常に速い ○ 速い △ かなり遅い × 非
常に遅い
(測定方法)
試料1〜5gを精秤しガラス板に取り、オレイ
ン酸(イオン交換水)をビユレツトから3〜7秒
に1滴づつ試料の中央に滴下し、その都度、全体
をヘラで充分に練り合せる。滴下及び練り合わせ
の操作を繰り返し、全体が初めて硬いパテ状の一
つのかたまりとなり鋼ベラでラセン形に巻き起こ
される程度になつた時を終点とし、それまでに使
用したオレイン酸(イオン交換水)の量を求め、
次式により吸油量、吸水量を求めた。但し、パテ
状のかたまりが巻き起らないものはオレイン酸
(イオン交換水)の1滴で急に軟らかくなりガラ
ス板に粘りつく直前に終点とした。
尚、球状多孔性ジビニルベンゼンピンホールポ
リマー、及び球状ナイロンについては水に濡れな
いため、イオン交換水の替わりに活性剤水溶液を
使用した。
H;オレイン酸の量(ml)又はイオン交換水の量
(ml)
S;採取した試料の重量
G;吸油量又は吸水量
G=H/S×100
吸油速度、吸水速度の測定は一定量をセルの中
でプレス充填し、その表面に一定量の水滴又は油
滴を滴下し、その吸収する速度を測定し、それを
類分けして表示した。
上記第1表より明らかな通り、従来から汎用さ
れているタルク類、セリサイト、カオリンのグル
ープは吸油量、吸水量いずれも低く、タルク類は
吸水速度が非常に遅いとされているが、同時に吸
油速度もかなり遅いので化粧くずれしやすい傾向
があり、セリサイトとカオリンは吸油速度が非常
に遅く、かつ吸水速度が非常に早いので、化粧持
続性の点からは最も難がある。またこれらを除い
た従来の無機粉体の場合、吸油量、給水量が格段
に高いと共に、吸油、吸水速度はいずれも速いの
で化粧塗布後に乾燥感が伴ない、しかも塗布時や
塗布直後のムラつきが著しく露呈される。更に、
従来より知られている有機粉体や有機多孔性粉体
は吸油量、吸水量がいずれも低く、吸油速度が非
常に早く、かつ吸水速度が非常に遅いので、皮脂
もしくは水、汗等により化粧くずれはより短時間
で進行して化粧持続性が悪い。これらに対し、本
発明の微小球体は実用的な粉体であるタルク類よ
りも吸油・吸水量が高く、望むべき吸油速度が速
くかつ吸水速度が遅いという特性を充足してお
り、まさに理想的な粉体と云える。
ここで、本発明に係る球状多孔性樹脂粉体(ポ
リメタクリル酸メチル)の粒子構造を示す電子顕
微鏡写真(3000倍:粒子径約22μm)を第1図に
示す。第1図により前記球状多孔性樹脂粉体が多
孔性構造を有していることがわかる。また、表面
張力による凝集を利用した溶融法により製造され
た市販のナイロンSPMの粒子構造を示す電子顕
微鏡写真(30000倍:粒子径約7μm)を比較例と
して第2図に示す。第2図に示された粒子は、本
願発明の球状多孔性樹脂粉体が有する多孔性構造
を有していないことがわかる。
前記球状多孔性樹脂粉体の細孔分布図を第3図
に示す。第3図は、前記球状多孔性樹脂粉体の20
℃における水蒸気吸着等温線からケルビンの式を
用い、アンデルソン(Anderson)の方法に従つ
て算出図示されたものである。
水蒸気吸着等温線の測定は、重量法(木下式水
分吸着測定装置KR−380)によつて行なつた。
第3図中、横軸は細孔径をÅ単位で、また縦軸
は、横軸の細孔径の範囲にある細孔の容量を%で
示す。
第3図の細孔分布図からは、70〜110Åの範囲
にある細孔が中心を占めていることが明らかであ
る。
さらに、本発明者は、本発明球状多孔性樹脂粉
体の化粧料としての使用性を確認すべく、後記実
施例1〜4に用いられる微小球体と従来粉体とを
用いて、原料(実施例1,2)そのものと化粧料
中(実施例1〜4)における使用テストを行なつ
た結果を比較品を対照として第2表、第3表に示
す。使用テストの項目は、A;ソフトで滑らかな
使用感、B;肌へのつきの均一性、C;透明感、
D;白さの浮き、E;密着性、F;化粧持ち、
G;総合評価(化粧料中のみ)である。
[Table] ◎ Very fast ○ Fast △ Fairly slow × Very slow (Measurement method) Precisely weigh 1 to 5 g of the sample, place it on a glass plate, and add 1 drop of oleic acid (ion-exchanged water) from a bottle every 3 to 7 seconds. Add a drop at a time to the center of the sample, and mix thoroughly with a spatula each time. The dropping and kneading operations are repeated, and the end point is when the whole becomes a hard putty-like lump that can be rolled up into a spiral shape with a steel spatula. Find the amount,
The oil absorption amount and water absorption amount were determined using the following formula. However, if a putty-like lump did not roll up, it suddenly became soft with one drop of oleic acid (ion-exchanged water), and the end point was taken as the end point was just before it became sticky to the glass plate. Note that since the spherical porous divinylbenzene pinhole polymer and the spherical nylon do not get wet with water, an aqueous activator solution was used instead of ion-exchanged water. H: Amount of oleic acid (ml) or amount of ion-exchanged water (ml) S: Weight of collected sample G: Oil absorption amount or water absorption amount G = H/S x 100 To measure oil absorption rate and water absorption rate, use a fixed amount. The material was press-filled into a cell, a certain amount of water or oil droplets were dropped on the surface of the cell, the rate of absorption was measured, and the results were categorized and displayed. As is clear from Table 1 above, the conventionally widely used groups of talc, sericite, and kaolin have low oil absorption and water absorption, and talc is said to have a very slow water absorption rate. Since the oil absorption rate is also quite slow, makeup tends to come off easily, and sericite and kaolin have a very slow oil absorption rate and a very fast water absorption rate, so they are the most difficult to make makeup last. In addition, in the case of conventional inorganic powders other than these, the amount of oil absorption and water supply are extremely high, and both the oil absorption and water absorption speed are fast, so there is a feeling of dryness after applying makeup, and there is no unevenness during or immediately after application. Tsuki is noticeably exposed. Furthermore,
Conventionally known organic powders and organic porous powders have low oil absorption and water absorption, and their oil absorption speed is very fast and water absorption speed is very slow. The deterioration progresses in a shorter period of time, and the longevity of the makeup is poor. On the other hand, the microspheres of the present invention have higher oil and water absorption than talc, which is a practical powder, and satisfy the desired characteristics of high oil absorption speed and slow water absorption speed, making them truly ideal. It can be said to be a fine powder. Here, FIG. 1 shows an electron micrograph (3000 times: particle diameter approximately 22 μm) showing the particle structure of the spherical porous resin powder (polymethyl methacrylate) according to the present invention. It can be seen from FIG. 1 that the spherical porous resin powder has a porous structure. Furthermore, as a comparative example, an electron micrograph (30,000 times: particle diameter approximately 7 μm) showing the particle structure of a commercially available nylon SPM manufactured by a melting method utilizing agglomeration due to surface tension is shown in FIG. It can be seen that the particles shown in FIG. 2 do not have the porous structure that the spherical porous resin powder of the present invention has. A pore distribution diagram of the spherical porous resin powder is shown in FIG. Figure 3 shows the spherical porous resin powder.
It was calculated and illustrated using the Kelvin equation from the water vapor adsorption isotherm at °C according to Anderson's method. The water vapor adsorption isotherm was measured by a gravimetric method (Kinoshita water adsorption measuring device KR-380).
In FIG. 3, the horizontal axis shows the pore diameter in angstroms, and the vertical axis shows the capacity of pores in the range of the pore diameter on the horizontal axis in %. From the pore distribution diagram in FIG. 3, it is clear that pores in the 70-110 Å range predominate. Furthermore, in order to confirm the usability of the spherical porous resin powder of the present invention as a cosmetic, the present inventor used the microspheres used in Examples 1 to 4 described later and a conventional powder to Tables 2 and 3 show the results of use tests for Examples 1 and 2) as such and in cosmetics (Examples 1 to 4) using comparative products as a control. The usage test items were: A: Soft and smooth feel, B: Uniformity of application to the skin, C: Transparency,
D: Whiteness floating, E: Adhesion, F: Makeup lasting,
G: Overall evaluation (only in cosmetics).
【表】【table】
【表】
次に本発明化粧持続性の良い化粧料の実施例を
述べる。使用割合は重量部である。
実施例1 フエースパウダー
球状多孔性ポリ酢酸ビニル(粒子径約13μ、平
均粒子径約6μ、最多孔径120Å)80.0部、シリカ
パウダー5.0部、セリサイト5.0部、微結晶性セル
ロース2.0部、タルク4.2部および弁柄0.3部をヘン
シエルミキサーで混合した後粉砕機で粉砕した。
これを再度ヘンシエルミキサーで攪拌しながら、
これに流動パラフイン1.5部とイソプロピルミリ
ステート2.5部を加えて10分間攪拌混合した。香
料0.5部を加えて3分間攪拌混合した。ブロワー
シフターで均質化し、容器に充填し、本発明フエ
ースパウダーを得た。
実施例2 プレストパウダー
球状多孔性エチレン酢酸ビニル共重合体とポリ
N−ビニルピロリドンの混合物(粒子径約13μ、
平均粒子径約6μ、最多孔径120Å)5.0部、タルク
49.3部、セリサイト10.0部、アルミニウムステア
レート3.0部、カオリン2.0部および弁柄0.2部をリ
ボンブレンダーで30分間攪拌混合した後、粉砕機
で粉砕した。その粉砕物をヘンシエルミキサーで
攪拌しつつ、これにスクワラン2.0部および2−
オクチルドデシルミリステート3.0部を加え12分
間攪拌混合した。更に、香料0.5部を加えて4分
間攪拌、混合した。ブロワーシフターで均質化
し、充填機で中皿に充填し、本発明プレストパウ
ダーを得た。
実施例3 乳化フアンデーシヨン
球状多孔性ポリ2,4−ジアミノ−6−フエニ
ル−1,3,5−トリアジン(粒子径20μ、平均
粒子径5μ、最多孔径60Å)4.4部、ステアリン酸
1.8部、スクワラン1.0部、2−オクチルドデシル
ミリステート2.0部、非イオン活性剤5.0部、色素
ペースト21.0部、ブチルパラベン0.1部およびB.
H.T0.05部を混合し、85℃に加熱し、これに攪拌
下、1,3−ブチレングリコール8.0部、増粘剤
0.2部、メチルパラベン0.2部、トリエタノールア
ミン0.7部および精製水55.05部の混合物を90℃に
加熱したものを徐々に加えながら乳化した。攪拌
下冷却し45℃下で香料0.5部を加えた。35℃まで
攪拌を続け容器に充填し、本発明乳化フアンデー
シヨンを得た。
実施例4 コンパクトフアンデーシヨン
オゾケライト6.1部、セレシン7.1部、ラノリン
3.2部、マイクロクリスタリンワツクス1.6部、イ
ソプロピルミリステート15.0部、スクワラン3.0
部、非イオン活性剤0.3部および色素ペースト
53.2部の混合物を80℃に加温、攪拌しながら、こ
れに、球状多孔性ポリメタクリル酸メチル(粒子
径約13μ、平均粒子径約7μ、最多孔径80Å)10.0
部を少しづつ加え、よく分散した。更に攪拌しな
がら70℃まで放冷、冷却し容器に充填し、コンパ
クトフアンデーシヨンを得た。
参考例1 化粧クリーム
エチレン酢酸ビニル共重合体(粒子径約8μ、
平均粒子径約3μ、最多孔径20Å)3.0部、スクワ
ラン7.5部、イソプロピルミリステート5.0部、ト
リグリセリド2.5部、密ロウ2.0部、ラノリン1.0
部、非イオン活性剤4.5部、B.H.T0.02部、ブチル
パラペン0.1部および顔料ベース0.18部の混合物
を80℃に加熱溶解した。これに80℃に攪拌下、グ
リセリン5.1部、メチルパラベン0.1部、増粘剤1.0
部、中和剤0.3部および蒸溜水67.5部の混合物を
85℃に溶解したものを徐々に加えた。5分間80℃
に保持した後、40℃まで水冷した。これに香料
0.2部を加え30℃まで冷却した。容器に充填し本
発明のメークアツプ化粧料とは、別に参考例とし
てクリームを得た。
上記詳述した如く、本発明化粧持続性の良い化
粧料は、肌へ塗布した後における化粧くずれを防
止し、肌へのつきの均一性に優れ、透明感があ
り、白浮きを防ぎ、メークアツプ化粧料として著
しい多様性に富んだ効果を発揮するものであり、
ソフトで滑らかな使用感と充填性に優れたメーク
アツプ化粧料を提供するものである。[Table] Next, examples of the cosmetics of the present invention with good long-lasting makeup will be described. The proportions used are parts by weight. Example 1 Phase powder: 80.0 parts of spherical porous polyvinyl acetate (particle size: approx. 13μ, average particle size: approx. 6μ, maximum pore size: 120Å), 5.0 parts of silica powder, 5.0 parts of sericite, 2.0 parts of microcrystalline cellulose, 4.2 parts of talc. and 0.3 part of Bengara were mixed in a Henschel mixer and then ground in a grinder.
While stirring this again with the Henschel mixer,
1.5 parts of liquid paraffin and 2.5 parts of isopropyl myristate were added to this and mixed with stirring for 10 minutes. 0.5 part of fragrance was added and mixed with stirring for 3 minutes. The mixture was homogenized using a blower sifter and filled into a container to obtain a phase powder of the present invention. Example 2 Pressed powder A mixture of spherical porous ethylene vinyl acetate copolymer and polyN-vinylpyrrolidone (particle size approximately 13μ,
Average particle size approximately 6μ, maximum pore size 120Å) 5.0 parts, talc
After stirring and mixing 49.3 parts of sericite, 10.0 parts of sericite, 3.0 parts of aluminum stearate, 2.0 parts of kaolin, and 0.2 parts of Bengara in a ribbon blender for 30 minutes, the mixture was pulverized in a pulverizer. While stirring the pulverized product with a Henschel mixer, add 2.0 parts of squalane and 2-
3.0 parts of octyldodecyl myristate was added and mixed with stirring for 12 minutes. Further, 0.5 part of fragrance was added and stirred and mixed for 4 minutes. The mixture was homogenized using a blower sifter and filled into a medium tray using a filling machine to obtain a pressed powder of the present invention. Example 3 Emulsified foundation 4.4 parts of spherical porous poly-2,4-diamino-6-phenyl-1,3,5-triazine (particle size 20 μ, average particle size 5 μ, maximum pore size 60 Å), stearic acid
1.8 parts squalane, 1.0 parts 2-octyldodecyl myristate, 2.0 parts nonionic activator, 21.0 parts pigment paste, 0.1 part butylparaben, and B.
Mix 0.05 parts of H.T, heat to 85℃, add 8.0 parts of 1,3-butylene glycol and thickener to this with stirring.
A mixture of 0.2 parts of methylparaben, 0.7 parts of triethanolamine, and 55.05 parts of purified water was heated to 90° C. and emulsified while gradually adding the mixture. The mixture was cooled with stirring and 0.5 part of fragrance was added at 45°C. Stirring was continued up to 35°C and the mixture was filled into a container to obtain an emulsified foundation of the present invention. Example 4 Compact foundation 6.1 parts of ozokerite, 7.1 parts of ceresin, lanolin
3.2 parts, microcrystalline wax 1.6 parts, isopropyl myristate 15.0 parts, squalane 3.0 parts
1 part, 0.3 part nonionic activator and dye paste
While heating 53.2 parts of the mixture to 80°C and stirring, add 10.0 parts of spherical porous polymethyl methacrylate (particle size: approx. 13μ, average particle size: approx. 7μ, maximum pore size: 80Å).
portion was added little by little until well dispersed. Further, while stirring, the mixture was left to cool to 70°C, and the cooled mixture was filled into a container to obtain a compact foundation. Reference example 1 Cosmetic cream Ethylene vinyl acetate copolymer (particle size approximately 8μ,
Average particle diameter approximately 3 μ, maximum pore diameter 20 Å) 3.0 parts, squalane 7.5 parts, isopropyl myristate 5.0 parts, triglyceride 2.5 parts, wax wax 2.0 parts, lanolin 1.0
A mixture of 1 part, 4.5 parts of nonionic activator, 0.02 part of BHT, 0.1 part of butylparaben, and 0.18 part of pigment base was heated and dissolved at 80°C. Add this to 80℃ with stirring, 5.1 parts of glycerin, 0.1 part of methylparaben, and 1.0 part of thickener.
0.3 parts of neutralizing agent and 67.5 parts of distilled water.
The solution at 85°C was gradually added. 80℃ for 5 minutes
It was then cooled with water to 40°C. Add fragrance to this
0.2 part was added and cooled to 30°C. A cream was obtained as a reference example separately from the makeup cosmetic of the present invention by filling it into a container. As detailed above, the cosmetic with good long-lasting makeup of the present invention prevents makeup from fading after being applied to the skin, has excellent uniformity of application to the skin, is transparent, prevents white cast, and is suitable for makeup makeup. It exhibits a remarkable variety of effects as a food ingredient.
The present invention provides a make-up cosmetic that has a soft and smooth feel and excellent filling properties.
第1図は本発明の球状多孔性樹脂粉体の粒子構
造を示す電子顕微鏡写真、第2図は溶融法により
製造されたナイロンSPMの粒子構造を示す電子
顕微鏡写真(比較例)、第3図は本発明の球状多
孔性樹脂粉体の細孔分布図である。
Fig. 1 is an electron micrograph showing the particle structure of the spherical porous resin powder of the present invention, Fig. 2 is an electron micrograph showing the particle structure of nylon SPM produced by the melting method (comparative example), and Fig. 3 is a pore distribution diagram of the spherical porous resin powder of the present invention.
Claims (1)
ポリ−2,4−ジアミノ−6−フエニル−1,
3,5−トリアジン、ポリメタクリル酸エステ
ル、ポリアクリル酸エステル、エチレン酢酸ビニ
ル共重合体から選択され、球体表面に最多孔径5
〜160Åの大小の空孔を有し、また粒子径が1〜
40μでかつ平均粒子径が2〜20μである球状多孔
性樹脂粉体を配合することを特徴とするメークア
ツプ化粧料。 polyvinyl acetate, poly N-vinylpyrrolidone,
poly-2,4-diamino-6-phenyl-1,
Selected from 3,5-triazine, polymethacrylate, polyacrylate, and ethylene-vinyl acetate copolymer, the spherical surface has a maximum pore diameter of 5.
It has large and small pores of ~160 Å, and the particle size is 1~160 Å.
A make-up cosmetic comprising spherical porous resin powder having a particle size of 40μ and an average particle diameter of 2 to 20μ.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17258080A JPS5798205A (en) | 1980-12-09 | 1980-12-09 | Cosmetic giving durable make-up |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17258080A JPS5798205A (en) | 1980-12-09 | 1980-12-09 | Cosmetic giving durable make-up |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5798205A JPS5798205A (en) | 1982-06-18 |
| JPH0451522B2 true JPH0451522B2 (en) | 1992-08-19 |
Family
ID=15944470
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17258080A Granted JPS5798205A (en) | 1980-12-09 | 1980-12-09 | Cosmetic giving durable make-up |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5798205A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013114653A1 (en) | 2012-01-31 | 2013-08-08 | 積水化成品工業株式会社 | Porous resin particle, method for producing same, dispersion liquid, and application thereof |
| WO2014156994A1 (en) | 2013-03-29 | 2014-10-02 | 積水化成品工業株式会社 | Porous resin particle, method for producing same, dispersion, and application thereof |
| WO2020149121A1 (en) | 2019-01-16 | 2020-07-23 | 株式会社トクヤマデンタル | Curable composition for denture base |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5993013A (en) * | 1982-11-16 | 1984-05-29 | Pola Chem Ind Inc | Pressed powdery cosmetic |
| JPS59172408A (en) * | 1983-03-22 | 1984-09-29 | Sumitomo Chem Co Ltd | Cosmetic component |
| JPH0611685B2 (en) * | 1984-03-02 | 1994-02-16 | ポーラ化成工業株式会社 | Cosmetics |
| JPS62221614A (en) * | 1986-03-24 | 1987-09-29 | Sekisui Plastics Co Ltd | Cosmetic |
| JPH0651614B2 (en) * | 1987-05-29 | 1994-07-06 | 東芝シリコ−ン株式会社 | Makeup cosmetics |
| EP0585239B1 (en) * | 1991-02-05 | 1998-09-23 | Sun Smart, Inc. | Visibly transparent uv sunblock agents and methods of making same |
| FR2673372B1 (en) * | 1991-02-28 | 1993-10-01 | Oreal | COSMETIC COMPOSITION CAPABLE OF REDUCING SKIN DEFECTS. |
| JP3488719B2 (en) * | 1992-01-30 | 2004-01-19 | 株式会社コーセー | Porous spherical powder and cosmetic containing the same |
| TW513309B (en) | 1998-07-01 | 2002-12-11 | Kao Corp | Powder-based solid cosmetic composition and preparation process thereof |
| JP3850612B2 (en) | 1999-12-28 | 2006-11-29 | 花王株式会社 | Solid powder cosmetic |
| JP4651883B2 (en) * | 2001-09-05 | 2011-03-16 | ガンツ化成株式会社 | Skin cosmetics containing spherical porous crosslinked polymer particles |
| JP3596534B2 (en) * | 2002-03-14 | 2004-12-02 | 富士ゼロックス株式会社 | Emulsified cosmetic |
| JP4170106B2 (en) | 2003-02-04 | 2008-10-22 | 花王株式会社 | Porous particles and cosmetics |
| JP2007518761A (en) * | 2004-01-23 | 2007-07-12 | ユニリーバー・ナームローゼ・ベンノートシヤープ | Taurate-containing pigmented cosmetic composition with soft focus and shine |
| FR2874321B1 (en) * | 2004-08-17 | 2010-11-26 | Oreal | TOPICAL COMPOSITION COMPRISING POROUS CHARGED PARTICLES AND A SEBUM ABSORBING COMPOUND |
| RU2011141343A (en) | 2009-04-03 | 2013-05-10 | Шисейдо Компани, Лтд. | COSMETIC PRODUCT IN THE FORM OF POWDER AND METHOD FOR PRODUCING IT |
| JP6029507B2 (en) | 2012-03-27 | 2016-11-24 | 積水化成品工業株式会社 | Porous resin particles, method for producing porous resin particles, and use thereof |
| US9814656B2 (en) | 2012-09-26 | 2017-11-14 | Sekisui Plastics Co., Ltd. | Porous resin particles, method of manufacturing porous resin particles, and use of porous resin particles |
| KR102116545B1 (en) * | 2015-06-30 | 2020-05-28 | (주)아모레퍼시픽 | Composite Powder of Porous Polymer Impregnated with Jade Powder Particle, Cosmetic Composition Comprising the Same and the Manufacturing Method Thereof |
| JP7607436B2 (en) * | 2020-11-11 | 2024-12-27 | 株式会社 資生堂 | Powder cosmetics |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5343577B2 (en) * | 1973-09-26 | 1978-11-21 | ||
| JPS52145527A (en) * | 1976-05-28 | 1977-12-03 | Kouichi Ogawa | Cosmetics |
| JPS5474886A (en) * | 1977-11-28 | 1979-06-15 | Asahi Chem Ind Co Ltd | Preparation of polymer micro-spheres |
| JPS6021567B2 (en) * | 1979-03-23 | 1985-05-28 | 株式会社肌粧品科学開放研究所 | Patch cosmetics |
-
1980
- 1980-12-09 JP JP17258080A patent/JPS5798205A/en active Granted
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013114653A1 (en) | 2012-01-31 | 2013-08-08 | 積水化成品工業株式会社 | Porous resin particle, method for producing same, dispersion liquid, and application thereof |
| US9532940B2 (en) | 2012-01-31 | 2017-01-03 | Sekisui Plastics Co., Ltd. | Porous resin particles, method for manufacturing the same, dispersion liquid, and use thereof |
| WO2014156994A1 (en) | 2013-03-29 | 2014-10-02 | 積水化成品工業株式会社 | Porous resin particle, method for producing same, dispersion, and application thereof |
| US9982106B2 (en) | 2013-03-29 | 2018-05-29 | Sekisui Plastics Co., Ltd. | Porous resin particles, method of manufacturing porous resin particles, dispersion liquid, and use of porous resin particles |
| WO2020149121A1 (en) | 2019-01-16 | 2020-07-23 | 株式会社トクヤマデンタル | Curable composition for denture base |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5798205A (en) | 1982-06-18 |
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