JP2006176449A - Composition for cosmetic against ultraviolet - Google Patents

Composition for cosmetic against ultraviolet Download PDF

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JP2006176449A
JP2006176449A JP2004372073A JP2004372073A JP2006176449A JP 2006176449 A JP2006176449 A JP 2006176449A JP 2004372073 A JP2004372073 A JP 2004372073A JP 2004372073 A JP2004372073 A JP 2004372073A JP 2006176449 A JP2006176449 A JP 2006176449A
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ultraviolet
cosmetic composition
water
weight
composition
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JP4035133B2 (en
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Masataka Kato
昌孝 加藤
Kazuko Kato
和子 加藤
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YAMACHU Inc
Yamachu Co Ltd
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YAMACHU Inc
Yamachu Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11Encapsulated compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/68Sphingolipids, e.g. ceramides, cerebrosides, gangliosides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/735Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/41Particular ingredients further characterized by their size
    • A61K2800/412Microsized, i.e. having sizes between 0.1 and 100 microns

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Cosmetics (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a composition for a cosmetic against ultraviolet rays, having excellent characteristics for protecting the skin from the ultraviolet rays, simultaneously usable even for a person having the sensitive skin or causing allergic symptoms, hardly damaging the defence functions inherent in the skin, and hardly causing side effects; and to provide a method for producing the composition. <P>SOLUTION: The composition for the aqueous cosmetic against the ultraviolet contains (a) 2.5-30 wt.% microcapsules of a polysilicone including an ultraviolet absorber and having 0.02-3.5 μm average particle diameter, (b) 0.0001-0.1 wt.% astaxanthin and/or cantaxanthin-containing material, and (c) 0.01-10 wt.% viscous material containing hyaluronic acid or a salt thereof and/or ceramide. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、近年のオゾン層の破壊などにより増加する紫外線障害から、肌を保護するための、紫外線防御特性に優れた、特に敏感肌用の紫外線対抗水系化粧用組成物に関するものである。   The present invention relates to a UV-resistant water-based cosmetic composition that is excellent in UV protection properties, particularly for sensitive skin, for protecting the skin from UV damage that increases due to destruction of the ozone layer in recent years.

日常生活における皮膚への悪影響は、そのほとんどが、紫外線により発生する活性酸素、過酸化脂質に起因する物である。紫外線は、可視光線に近い、波長の長いほうから、A、B、Cに分けられる。C波は波長が約250nmと短く、エネルギーが大きく、皮膚癌の原因になるといわれているが、幸いなことに地表に届く前にほとんど吸収されている。A波(波長が約350nm)、B波(波長が約300nm)は、地表に届き、肌に酸化力として悪影響を与える。A波は皮膚の内部まで届き、シワの原因になるが、B波は皮膚の表面を焼き、一時的な軽いやけどをさせ、色黒を進行させる。   The adverse effects on the skin in daily life are mostly caused by active oxygen and lipid peroxide generated by ultraviolet rays. Ultraviolet light is divided into A, B, and C from the longer wavelength, which is close to visible light. The C-wave has a short wavelength of about 250 nm, has a large energy, and is said to cause skin cancer. Fortunately, it is almost absorbed before reaching the surface of the earth. A wave (wavelength is about 350 nm) and B wave (wavelength is about 300 nm) reach the earth's surface and adversely affect the skin as oxidizing power. The A wave reaches the inside of the skin and causes wrinkles, but the B wave burns the surface of the skin, causing a temporary light burn and a darkening of the color.

健康な肌は、外部の刺激から内部を守る自己防衛機能を持っている。しかし、近年の環境破壊から来る過度の刺激に対しては、自己防衛機能だけでは充分な防衛が出来ないのが現状である。外部刺激の主なものは紫外線による酸化反応である。紫外線による障害を防ぐためには、自己防衛機能を補足し、酸化チタン、酸化亜鉛等の紫外線反射(散乱)剤、ベンゾフェノン誘導体等の紫外線吸収剤などが有用である(特許文献1〜4参照)。しかし、これらの紫外線反射剤、紫外線吸収剤は、紫外線防御の持続性などの特性でなお不充分であり、また、いずれも敏感肌に悪影響を与える。特に、紫外線吸収剤は、紫外線を吸収する部分がベンゼン核であり、ベンゼン核は敏感肌の人にアレルギー症状を与える。   Healthy skin has a self-defense function that protects the inside from external stimuli. However, the current situation is that the self-defense function alone cannot provide sufficient defense against the excessive stimuli resulting from environmental destruction in recent years. The main external stimulus is an oxidation reaction by ultraviolet rays. In order to prevent damage due to ultraviolet rays, an ultraviolet reflecting (scattering) agent such as titanium oxide and zinc oxide, an ultraviolet absorber such as a benzophenone derivative, etc. are useful (see Patent Documents 1 to 4). However, these UV reflectors and UV absorbers are still insufficient in properties such as the durability of UV protection, and both have an adverse effect on sensitive skin. Particularly, in the ultraviolet absorber, the portion that absorbs ultraviolet rays is a benzene nucleus, and the benzene nucleus gives allergic symptoms to people with sensitive skin.

また、紫外線反射剤や紫外線吸収剤を配合した化粧品の場合には、その量にもよるが、安定性、におい、べたつきなどの問題が発生する。さらに、これらを多量に配合した場合には、塗布時に白浮きや、のびが悪くなるなどの使用感の問題が生じる。
特開平6−305949号公報 特開平7−145029号公報 特開平8−259419号公報 特開2002−128646号公報
In the case of cosmetics containing an ultraviolet reflector or ultraviolet absorber, problems such as stability, odor, and stickiness occur depending on the amount of cosmetics. Furthermore, when these are blended in a large amount, problems such as white floating at the time of application and a feeling of use such as poor spread occur.
JP-A-6-305949 Japanese Patent Laid-Open No. 7-145029 JP-A-8-259419 JP 2002-128646 A

本発明は、紫外線の肌に対する長時間にわたる防御特性に優れ、同時に敏感肌の人、アレルギー症状を起こす人でも使用でき、皮膚の本来持っている防御機能を損なうことのない、副作用の少ない紫外線対抗水系化粧用組成物、及びその製造方法を提供することを目的とする。   The present invention is excellent in the long-term protection property against ultraviolet skin, and can be used by people with sensitive skin and those who develop allergic symptoms at the same time, and does not impair the protective function of the skin and has less side effects. An object is to provide a water-based cosmetic composition and a method for producing the same.

本発明者、上記の目的を達成するために鋭意,研究を進めたところ、紫外線吸収剤を内包しかつ特定の平均粒径を有するポリシリコーンからなるマイクロカプセルを使用し、かつ該マイクロカプセルを、アスタキサンチン及び/又はカンタキサンチンの含有物質、及び、ヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質とともに含む水系の化粧用組成物は、紫外線防御の持続特性が著しく優れるだけでなく、該組成物は、アレルギー症状を起こす人や肌の敏感な人でも使用できる、副作用の少ない紫外線対抗化粧用組成物を形成することを見出した。   As a result of diligent and research in order to achieve the above object, the present inventor used a microcapsule containing a UV absorber and having a specific average particle diameter, and the microcapsule, An aqueous cosmetic composition containing an astaxanthin and / or canthaxanthin-containing substance and a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide not only has extremely excellent UV protection, but also the composition. Has found that it can form a UV-resistant cosmetic composition with few side effects that can be used by people with allergic symptoms or sensitive skin.

本発明の化粧用組成物が何故にこのような優れた特性を発揮するかについては必ずしも明らかではないが、おおよそ、次のように推定される。   The reason why the cosmetic composition of the present invention exhibits such excellent properties is not necessarily clear, but is roughly estimated as follows.

すなわち、本発明の水系化粧用組成物では、紫外線吸収剤は、ポリシリコーンからなるマイクロカプセルに内包され、肌に接触しないので、敏感肌の人にも悪影響を与えない。一方で、マイクロカプセルの材質のポリシリコーンは、紫外線に対して透明であるので、内包される紫外線吸収剤は、本来の紫外線防御特性を発揮する。しかし、該紫外線吸収剤を内包するマイクロカプセルは通常数μmの平均粒径を有するために粒子間に隙間を生じ、該隙間を通じて紫外線が通過するため紫外線防御は不充分である。本発明では、該マイクロカプセル粒子間の隙間を、抗酸化性をもつアスタキサンチン及び/又はカンタキサンチンの含有物質を含むヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質でジェリー状に均一に充填する。その結果、本発明の化粧用組成物によれば、薄くても緻密なバリアーフィルム(層)が形成され、紫外線を長時間にわたりほぼ完全にカットする防御特性が増大する。   That is, in the water-based cosmetic composition of the present invention, the ultraviolet absorber is contained in microcapsules made of polysilicon and does not come into contact with the skin, so that it does not adversely affect people with sensitive skin. On the other hand, since the polysilicon of the material of the microcapsule is transparent to ultraviolet rays, the encapsulated ultraviolet absorber exhibits the original ultraviolet protection properties. However, the microcapsules encapsulating the ultraviolet absorber usually have an average particle diameter of several μm, so that gaps are formed between the particles, and ultraviolet rays pass through the gaps, so that ultraviolet protection is insufficient. In the present invention, the gaps between the microcapsule particles are uniformly filled in a jelly-like manner with a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide containing an anti-oxidant astaxanthin and / or canthaxanthin-containing substance. . As a result, according to the cosmetic composition of the present invention, a thin and dense barrier film (layer) is formed, and the protective property of almost completely cutting off ultraviolet rays for a long time is increased.

一方で、本発明の化粧用組成物を形成するアスタキサンチン及び/又はカンタキサンチンの含有物質や、ヒアルロン酸若しくはその塩及び/又はセラミドは、いずれも、皮膚が本来持っている防御機能を損なうことのない、肌にやさしい物質である。従って、本発明の化粧用組成物は敏感肌の人、アレルギー症状を起こす人でも問題なく使用できるものである。   On the other hand, any of the substances containing astaxanthin and / or canthaxanthin, hyaluronic acid or a salt thereof, and / or ceramide forming the cosmetic composition of the present invention may impair the protective function inherent to the skin. No skin-friendly substance. Therefore, the cosmetic composition of the present invention can be used without problems even for people with sensitive skin and those who develop allergic symptoms.

かくして、本発明は下記の要旨を有するものである。
(1)紫外線吸収剤を内包し、平均粒径0.02〜3.5μmのポリシリコーンのマイクロカプセル:2.5〜30重量%と、(b)アスタキサンチン及び/又はカンタキサンチンの含有物質:0.0001〜0.1重量%と、(c)ヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質:0.01〜10重量%と、を含有することを特徴とする紫外線対抗水系化粧用組成物。
(2)更に、(d)抗菌剤0.01〜10重量%を含む上記(1)に記載の紫外線対抗水系化粧用組成物。
(3)(a)のポリシリコーンが、シリコーンレジン化ポリペプチドである上記(1)又は(2)に記載の紫外線対抗水系化粧用組成物。
(4)(a)の紫外線吸収剤が、アルコキシケイ皮酸2−エチルヘキシル及び/又は4−t-ブチル−4‘−メトキシジベンゾイルメタンである上記(1)〜(3)のいずれかに記載の敏感肌用紫外線対抗化粧用組成物。
(5)(c)の粘性物質が、ヒアルロン酸若しくはその塩及び/又はセラミドと、グリセリンとの混合物である上記(1)〜(4)のいずれかに記載の敏感肌用紫外線対抗化粧用組成物。
(6)(d)の抗菌剤が、直鎖状である、アルキレンジオール類、又はグリセロールエーテル類の上記(1)〜(5)のいずれかに記載の紫外線対抗化粧用組成物。
(7)(b)アスタキサンチン及び/又はカンタキサンチンの粉末と、(c)ヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質とを水の存在下に混合し、次いで、得られる混合物に、残余の水、及び(a)紫外線吸収剤を内包するポリシリコーンのマイクロカプセルを順次、又は同時に添加することを特徴とする紫外線対抗水系化粧用組成物の製造方法。
(8)(c)の粘性物質が、さらにグリセリンを含む上記(7)に記載の紫外線対抗水系化粧用組成物の製造方法。
(9)(d)抗菌剤を、いずれかの時点で添加する上記(7)又は(8)に記載の紫外線対抗水系化粧用組成物の製造方法。
Thus, the present invention has the following gist.
(1) Polysilicone microcapsules containing an ultraviolet absorber and having an average particle size of 0.02 to 3.5 μm: 2.5 to 30% by weight; (b) Substances containing astaxanthin and / or canthaxanthin: 0 And 0.1 to 0.1% by weight, and (c) a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide: 0.01 to 10% by weight object.
(2) The ultraviolet-resistant water-based cosmetic composition according to (1), further comprising (d) 0.01 to 10% by weight of an antibacterial agent.
(3) The ultraviolet-resistant anti-water cosmetic composition according to (1) or (2) above, wherein the poly-silicone of (a) is a silicone-resinized polypeptide.
(4) The ultraviolet absorber of (a) is any one of the above (1) to (3), which is 2-ethylhexyl alkoxycinnamate and / or 4-t-butyl-4′-methoxydibenzoylmethane. UV sensitive cosmetic composition for sensitive skin.
(5) UV sensitive cosmetic composition for sensitive skin according to any one of (1) to (4) above, wherein the viscous substance of (c) is a mixture of hyaluronic acid or a salt thereof and / or ceramide and glycerin object.
(6) The ultraviolet-resistant cosmetic composition according to any one of (1) to (5) above, wherein the antibacterial agent of (d) is a linear alkylene diol or glycerol ether.
(7) (b) Astaxanthin and / or canthaxanthin powder and (c) a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide are mixed in the presence of water, and then the remaining mixture is added to the remaining mixture. And (a) a microcapsule of a silicone encapsulating an ultraviolet absorber is added sequentially or simultaneously.
(8) The method for producing an ultraviolet-resistant cosmetic composition according to (7) above, wherein the viscous substance of (c) further contains glycerin.
(9) The method for producing an anti-water-based cosmetic composition for ultraviolet rays according to (7) or (8), wherein (d) the antibacterial agent is added at any time.

本発明によれば、後記する実施例に見られるように、紫外線の肌に対する長時間にわたる防御特性に優れ、同時に敏感肌の人、アレルギー症状を起こす人でも使用でき、皮膚の本来持っている防御機能を損なうことのない、副作用の少ない紫外線対抗化粧用組成物及びその製造方法が提供される。   According to the present invention, as will be seen in the examples described later, it has excellent protective properties against ultraviolet skin over a long period of time, and can be used even by people with sensitive skin and allergic symptoms at the same time. Provided are an anti-UV cosmetic composition with few side effects that does not impair the function and a method for producing the same.

本発明の紫外線対抗化粧用組成物に含有される(a)の紫外線吸収剤を内包するポリシリコーンのマイクロカプセルは、紫外線吸収性を有する物質を紫外線を通過させるポリシリコーン材料によりマイクロカプセル化させたものである。この場合の紫外線吸収剤としては、特に肌に対して大きい刺激性を有しない限り従来使用されている物質がいずれも使用できる。なかでも、本発明では、パラメトキシケイ皮酸−2−エチルヘキシル、メチレン(ビス−ベンゾトリアゾイルテトラメチルブチルフェノール)、4−tブチル−4’−メトキシジベンゾイルメタンなどの使用が好ましい。本発明では、紫外線のうち、B波の吸収に有効であるパラメトキシケイ皮酸−2−エチルヘキシル、及び/又はA波の吸収に有効である、4−tブチル−4’−メトキシジベンゾイルメタンとを使用するのが好ましい。特には、パラメトキシケイ皮酸−2−エチルヘキシルと、4−tブチル−4’−メトキシジベンゾイルメタンとを、前者/後者の重量比率が、6/1〜4/1にて使用が好ましい。   The polysilicon microcapsule encapsulating the ultraviolet absorber (a) contained in the ultraviolet anti-cosmetic composition of the present invention is obtained by microencapsulating a substance having ultraviolet absorptivity with a polysilicon material that transmits ultraviolet rays. Is. As the ultraviolet absorber in this case, any conventionally used substance can be used as long as it has no great irritation to the skin. Among them, in the present invention, it is preferable to use paramethoxycinnamic acid-2-ethylhexyl, methylene (bis-benzotriazoyltetramethylbutylphenol), 4-tbutyl-4'-methoxydibenzoylmethane, and the like. In the present invention, among the ultraviolet rays, 2-methoxyhexyl paramethoxycinnamate which is effective for absorption of B wave and / or 4-tbutyl-4′-methoxydibenzoylmethane which is effective for absorption of A wave. Are preferably used. In particular, it is preferable to use 2-methoxyhexyl paramethoxycinnamate and 4-tbutyl-4'-methoxydibenzoylmethane at a former / latter weight ratio of 6/1 to 4/1.

マイクロカプセルの材料であるポリシリコーンとしては、シリコーン部とコラーゲンやシルクタンパクなどを加水分解して得られるポリペプチド部とからなるシリコーンレジン化ポリペプチドが好ましく使用される。この材料は、ケイ素原子に直結する水酸基を2個以上有するシリル化ペプチドの1種以上と、加水分解によってケイ素原子に直結する水酸基が2個以上生じるシラン化合物の1種以上を組成比で5:1〜1:1の範囲で水溶系中にて縮重合させて得られる、シリル化ペプチド−シラン化合物共重合体が好ましい。該共重合体は、特開2002−121117号公報などに記載される。   As the polysilicon which is a material of the microcapsule, a silicone resinized polypeptide comprising a silicone part and a polypeptide part obtained by hydrolyzing collagen or silk protein is preferably used. This material is composed of one or more silylated peptides having two or more hydroxyl groups directly bonded to silicon atoms and one or more silane compounds in which two or more hydroxyl groups directly bonded to silicon atoms are formed by hydrolysis in a composition ratio of 5: A silylated peptide-silane compound copolymer obtained by condensation polymerization in an aqueous system in the range of 1: 1 to 1: 1 is preferable. The copolymer is described in JP-A No. 2002-121117.

かかるシリコーンレジン化ポリペプチド材料を使用し、上記の紫外線吸収剤を内包したマイクロカプセルを得る方法は、マイクロカプセル化する既知の方法が使用される。また、このような紫外線吸収剤を内包するマイクロカプセルは、「シラソーマ(成和化成社商品名)」として市販のものが使用できる。本発明では、かかる紫外線吸収剤を内包するポリシリコーンのマイクロカプセルとして、紫外線吸収剤が好ましくは70〜99重量%、特に好ましくは85〜95重量%内包されるマイクロカプセルの使用が好適である。紫外線吸収剤が70重量%より小さい場合には、紫外線防御特性が不充分なり、逆に大きい場合には、マイクロカプセルの強度が低下しいずれも好ましくはない。   A known method of microencapsulation is used as a method of obtaining a microcapsule encapsulating the above-mentioned ultraviolet absorber by using such a silicone-resinized polypeptide material. As the microcapsules enclosing such an ultraviolet absorber, those commercially available as "Shirasoma (trade name of Seiwa Kasei Co., Ltd.)" can be used. In the present invention, as the microcapsules of the polysilicon encapsulating such an ultraviolet absorber, it is preferable to use a microcapsule in which the ultraviolet absorber is preferably encapsulated in an amount of 70 to 99% by weight, particularly preferably 85 to 95% by weight. When the ultraviolet absorber is less than 70% by weight, the ultraviolet protection properties are insufficient, and when the ultraviolet absorber is large, the strength of the microcapsules is lowered, which is not preferable.

また、紫外線吸収剤を内包するポリシリコーンのマイクロカプセルの平均粒径は、本発明の組成物の紫外線防御特性にも関係し、本発明では、0.02〜3.5μm、好ましくは、0.5〜2.5μmであるのが好適である。マイクロカプセルの平均粒径が上記の範囲より小さい場合も、逆に大きい場合にも、紫外線防御特性が低下してしまう。   The average particle size of the microcapsules of the polysilicon encapsulating the ultraviolet absorber is also related to the ultraviolet protective properties of the composition of the present invention. In the present invention, the average particle diameter is 0.02 to 3.5 μm, preferably 0. The thickness is preferably 5 to 2.5 μm. Even when the average particle size of the microcapsules is smaller than the above range, or when the average particle size is larger, the ultraviolet protection properties are deteriorated.

かかる(a)の紫外線吸収剤を内包するポリシリコーンのマイクロカプセルは、本発明の化粧用組成物中、好ましくは2.5〜30重量%、特に好ましくは5〜20重量%含有される。この(a)の含有量が2.5重量%より少ない場合には、紫外線防御特性が低下し、逆に、30重量%より大きいと、ある場合には臭いが発生し、また、化粧品としての特性である、肌触りやのびが悪くなり好ましくない。   Polysilicone microcapsules encapsulating the ultraviolet absorber (a) are preferably contained in the cosmetic composition of the present invention in an amount of 2.5 to 30% by weight, particularly preferably 5 to 20% by weight. When the content of (a) is less than 2.5% by weight, the UV protection property is lowered. Conversely, when the content is more than 30% by weight, an odor is generated in some cases, and as a cosmetic product. It is not preferable because the characteristics such as touch and spread are deteriorated.

本発明の化粧用組成物に含有される(b)のアスタキサンチン及び/又はカンタキサンチンの含有物質は、通常、天然のカロテノイドの一種で甲殻類や魚類、又はヘマスコッカス藻の培養物などから抽出される、ヘマトコッカス色素とも呼ばれる物質である。フリー体、モノエステル体、ジエステル体などの形態を有するが、いずれも抗酸化作用を有し、本発明ではそのいずれをも使用できる。これらの物質は、通常、粉末状、顆粒状、またはこれらを含む、オイル状、水溶液状などの形態で入手できる。本発明では、例えば、アスタキサンチンをデキストリンなどの糖類の水溶液に混合し、これを噴霧乾燥した粉末が、容易に水に溶解又は分散するので好ましく使用される。このような、噴霧乾燥粉末は、「アスタリーゼ(富士化学社商品名)」の名称で市販品として入手できる。   The astaxanthin and / or canthaxanthin-containing substance (b) contained in the cosmetic composition of the present invention is usually a kind of natural carotenoid and is extracted from crustaceans, fish, or a culture of Hemascoccus alga. It is a substance also called hematococcus pigment. Although it has a form such as a free form, a monoester form, a diester form, etc., all have an antioxidant action, and any of them can be used in the present invention. These substances are usually available in the form of powder, granules, or oils or aqueous solutions containing these substances. In the present invention, for example, a powder obtained by mixing astaxanthin with an aqueous solution of a saccharide such as dextrin and spray-drying it is preferably used because it is easily dissolved or dispersed in water. Such a spray-dried powder can be obtained as a commercial product under the name “Astarize (trade name of Fuji Chemical Co., Ltd.)”.

かかる(b)のアスタキサンチン及び/又はカンタキサンチンの含有物質は、本発明の化粧用組成物中、好ましくは0.0001〜0.1重量%(1〜1000ppm)、特に好ましくは0.0005〜0.01重量%(5〜100ppm)含有される。この(b)の含有量が0.0001重量%より少ない場合には、紫外線防御特性が低下し、逆に大きい場合には、紫外線防御特性が飽和に達し経済的でないばかりか、組成物の着色性が大きくなり、化粧品としての特性上好ましくない。   The (b) astaxanthin and / or canthaxanthin-containing substance is preferably 0.0001 to 0.1% by weight (1 to 1000 ppm), particularly preferably 0.0005 to 0 in the cosmetic composition of the present invention. 0.01% by weight (5 to 100 ppm) is contained. When the content of (b) is less than 0.0001% by weight, the ultraviolet protection property is lowered. On the contrary, when the content is large, the ultraviolet protection property reaches saturation and is not economical, and the composition is colored. This is not preferable in terms of cosmetic properties.

本発明の化粧用組成物において、(c)のヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質は、上記(b)成分を溶解又は分散する媒体して使用されるとともに、それ自体が保湿性を有し肌に対して潤いを与える機能を有する。ヒアルロン酸は、好ましくはナトリウム塩やカリウム塩が使用され、本発明の粘性物質としての効果が優れている。セラミドは、グリコシルセラミドとも称されるが、骨格構造であるセラミドに親水性の糖類が結合した複合糖脂質であるスフィンゴ糖脂質である。スフィンゴ糖脂質は、水に対して容易に均一に分散するもので、1糖結合型と4糖結合型を含む。発酵セラミドとして、微生物から製造される天然物として入手できる。   In the cosmetic composition of the present invention, the viscous substance containing hyaluronic acid or a salt thereof and / or ceramide (c) is used as a medium for dissolving or dispersing the component (b) and is itself moisturizing. Has a function to moisturize the skin. Hyaluronic acid is preferably a sodium salt or potassium salt, and is excellent in effect as a viscous substance of the present invention. Ceramide, which is also called glycosylceramide, is a glycosphingolipid that is a complex glycolipid in which a hydrophilic saccharide is bound to ceramide, which is a skeleton structure. Glycosphingolipids are easily and uniformly dispersed in water and include mono- and tetrasaccharide-linked types. Fermented ceramide can be obtained as a natural product produced from microorganisms.

かかるヒアルロン酸若しくはその塩及び/又はセラミドを含有する粘性物質は、本発明の化粧用組成物中、0.01〜10重量%、好ましくは0.1〜5重量%含有される。この(b)の含有量が0.01重量%より少ない場合には、充分な紫外線防御特性が得られず、逆に10重量%より大きい場合にも、組成物の粘性が強くなり、肌触りが悪くなるので好ましくない。   Such a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide is contained in the cosmetic composition of the present invention in an amount of 0.01 to 10% by weight, preferably 0.1 to 5% by weight. When the content of (b) is less than 0.01% by weight, sufficient UV protection properties cannot be obtained. Conversely, when the content is more than 10% by weight, the viscosity of the composition becomes strong and the touch is not good. Since it gets worse, it is not preferable.

さらに、本発明の(c)の粘性物質としては、ヒアルロン酸若しくはその塩及び/又はセラミドのほかに、グリセリン、コラーゲン、ポリアクリル酸ソーダ、アルギン酸ソーダ、カルボキシルビニルポリマを含有することができる。特に、グリセリンを好ましくは2〜5重量を併用する場合には、組成物の化粧品としての保湿性が増すとともに、各成分の混合状態がより均一な組成物が容易に得られるので特に好ましい。   Further, the viscous substance (c) of the present invention may contain glycerin, collagen, sodium polyacrylate, sodium alginate, and carboxyl vinyl polymer in addition to hyaluronic acid or a salt thereof and / or ceramide. In particular, when 2 to 5 weights of glycerin are used in combination, it is particularly preferable because the composition has a higher moisturizing property as a cosmetic and a composition in which the components are more uniformly mixed can be easily obtained.

本発明の化粧用組成物には、さらに、(d)成分として抗菌剤を含むことが好ましい。これらの抗菌剤は、上記(a)〜(c)を含む化粧用組成物において菌の発生を抑制する役割を果たし、本発明の化粧品組成物の耐久性を増大させる。かかる抗菌剤としては、直鎖状である、アルキレンジオール類及び/又はグリセロールエーテル類が好ましい。これらの好ましい具合例としては、1,3−ブチレングリコール、1,2−ペンチルグリコール、3−[(2−エチルヘキシル)オキシ]−1,2−プロパンジオールなどが挙げられる。なかでも、1,2−ペンチルグリコール、3−[(2−エチルヘキシル)オキシ]−1,2−プロパンジオールが特に好ましい。   The cosmetic composition of the present invention preferably further contains an antibacterial agent as the component (d). These antibacterial agents play a role of suppressing the generation of bacteria in the cosmetic composition containing the above (a) to (c), and increase the durability of the cosmetic composition of the present invention. As such an antibacterial agent, linear alkylene diols and / or glycerol ethers are preferable. Preferred examples of these include 1,3-butylene glycol, 1,2-pentyl glycol, 3-[(2-ethylhexyl) oxy] -1,2-propanediol, and the like. Of these, 1,2-pentyl glycol and 3-[(2-ethylhexyl) oxy] -1,2-propanediol are particularly preferable.

かかる(d)の抗菌剤は、本発明の化粧用組成物中、好ましくは0.01〜10重量%、特に好ましくは1〜5重量%含有される。この(d)の含有量が0.01重量%より少ない場合には、抗菌性が充分ではなく、逆に10重量%より大きい場合には、化粧品としての肌触りなどが悪くなるので好ましくない。   The antibacterial agent (d) is preferably contained in the cosmetic composition of the present invention in an amount of 0.01 to 10% by weight, particularly preferably 1 to 5% by weight. When the content of (d) is less than 0.01% by weight, the antibacterial property is not sufficient. On the other hand, when the content is more than 10% by weight, the touch as a cosmetic is deteriorated.

本発明の化粧用組成物は、上記(a)〜(c)及び、必要に応じて(d)成分を使用して、好ましくは次のようにして調製される。すなわち、本発明では,まず、(b)のアスタキサンチン及び/又はカンタキサンチンの含有物質の平均粒径が好ましくは0.05〜1μmの粉末を用意し、これを(c)のヒアルロン酸若しくはその塩及び/又はセラミドを含有する粘性物質とを水の存在下に混合する。粘性物質としては、上記のように、グリセリンが併用されるのが好ましい。混合に際しては、必要に応じてホモジナイザーなどの混合機を使用することができる。   The cosmetic composition of the present invention is preferably prepared as follows using the components (a) to (c) and, if necessary, the component (d). That is, in the present invention, first, a powder having an average particle size of the astaxanthin and / or canthaxanthin-containing material (b) of preferably 0.05 to 1 μm is prepared, and this is prepared as hyaluronic acid or a salt thereof (c). And / or a ceramide-containing viscous material in the presence of water. As the viscous substance, glycerin is preferably used in combination as described above. In mixing, a mixer such as a homogenizer can be used as necessary.

得られる混合物は、(b)のアスタキサンチン及び/又はカンタキサンチンの含有物質が(c)のヒアルロン酸若しくはその塩及び/又はセラミドを含有する粘性物質中に均一に溶解又は分散した形態を有する。本発明では、このように、(b)と(c)とを先に混合することが必要であり、そうした場合には、優れた紫外線防御特性を有する組成物が容易に得ることができる。   The resulting mixture has a form in which the (b) astaxanthin and / or canthaxanthin-containing substance is uniformly dissolved or dispersed in the viscous substance containing (c) hyaluronic acid or a salt thereof and / or ceramide. In the present invention, it is necessary to first mix (b) and (c) as described above. In such a case, a composition having excellent UV protection properties can be easily obtained.

上記(b)と(c)との混合物に対して、残余の水、及び(a)の紫外線吸収剤を内包するポリシリコーンのマイクロカプセルを順次、又は同時に添加される。水、及び(a)の紫外線吸収剤を内包するポリシリコーンのマイクロカプセルを同時に添加する場合は、予め、(a)の紫外線吸収剤を内包するポリシリコーンのマイクロカプセルを水に分散させた分散液を使用してもよい。また、水分は、必要量を同時に添加してもよいし、また、分割して添加してもよい。これらの成分を添加し、混合するに際しては、必要に応じて、ホモジナイザーなどの混合機を使用することができる。   To the mixture of (b) and (c), the remaining water and the microcapsules of polysilicon encapsulating the ultraviolet absorber of (a) are added sequentially or simultaneously. In the case of simultaneously adding water and the polysilicon microcapsules encapsulating the ultraviolet absorber (a), a dispersion in which the microcapsules of the polysilicon encapsulating the ultraviolet absorber (a) are dispersed in water in advance. May be used. In addition, water may be added in a necessary amount at the same time, or may be added in divided portions. When these components are added and mixed, a mixer such as a homogenizer can be used as necessary.

本発明において、添加される水は、好ましくはカルシウムやマグネシウムを脱イオンした精製水が使用される。添加される水の量は、本発明の化粧用組成物を構成する上記(a)〜(c)の各成分がそれぞれ上記で規定する含有量になるようにせしめられる。   In the present invention, the water to be added is preferably purified water obtained by deionizing calcium or magnesium. The amount of water added is adjusted so that each of the components (a) to (c) constituting the cosmetic composition of the present invention has a content specified above.

本発明の化粧用組成物では、さらに、好ましくは(d)の抗菌剤が添加される。抗菌剤は、通常、水溶液の形態で使用されるので、組成物の添加時期は特に限定されず、上記(a)〜(c)の混合物を得る過程のいずれで行ってもよい。   In the cosmetic composition of the present invention, the antibacterial agent (d) is preferably further added. Since the antibacterial agent is usually used in the form of an aqueous solution, the addition timing of the composition is not particularly limited, and may be performed in any of the processes of obtaining the mixture of (a) to (c).

かくして本発明の紫外線対抗水系化粧用組成物は調製されるが、各成分の混合状態を更に均一にせしめるために、得られた組成物に対し、加熱処理や超音波処理を施すこともできる。また、本発明の化粧用組成物は、組成物中の水の含有量によって、種々の粘度を有するものが得られ、所謂乳液タイプ処方からクリームタイプ処方の形態をもつことができる。なかでも、本発明の紫外線対抗化粧用組成物の粘度は、好ましくは0.1〜100Pas、特には、5〜20Pasであるのが好ましい。   Thus, although the ultraviolet-resistant anti-water cosmetic composition of the present invention is prepared, in order to make the mixed state of each component more uniform, the obtained composition can be subjected to heat treatment or ultrasonic treatment. Further, the cosmetic composition of the present invention can be obtained in various viscosities depending on the water content in the composition, and can have a so-called emulsion type formulation to a cream type formulation. Among these, the viscosity of the ultraviolet light-resistant cosmetic composition of the present invention is preferably 0.1 to 100 Pas, and particularly preferably 5 to 20 Pas.

次に、実施例を挙げて本発明を更に具体的に説明するが、これは例示であって、本発明の解釈についてこれを制限するものではない。
実施例1
「サンプル液の調製」
本発明の紫外線対抗化粧用水系組成物として、以下のサンプル1〜3を調製した。
EXAMPLES Next, although an Example is given and this invention is demonstrated further more concretely, this is an illustration and does not restrict | limit this about the interpretation of this invention.
Example 1
"Preparation of sample solution"
The following samples 1 to 3 were prepared as the ultraviolet-resistant cosmetic water-based composition of the present invention.

サンプル1:
(b)成分としての、アスタリーズ粉末(アスタキサンチンを0.01重量%含有するデキストリン、富士化学社製)0.4gと、(c)成分としての、グリセリン10g及びヒアルロン酸ナトリウム0.08gとを密閉状態のホモジナーザーにて約1時間混合攪拌した。次いで、該混合物に対して、(a)成分としての、(2−メトキシケイ皮酸2−エチルヘキシルと4−t−ブチル−4’−メトキシジベンゾイルメタンとを4/1(重量比)で91重量%内包する、平均粒径2μmのマイクロカプセル(成和化成社商品名、シラソーマMEA)の55重量%水分散液7gを添加して攪拌した。得られた混合物に脱イオン水を添加して全体を200gの組成物(紫外線吸収剤:7重量%、アスタキサンチン:0.002重量%(20ppm)とした。
Sample 1:
(B) Asteries powder (dextrin containing 0.01% by weight of astaxanthin, manufactured by Fuji Chemical Co., Ltd.) 0.4 g as component, and 10 g of glycerin and sodium hyaluronate 0.08 g as component (c) are sealed. The mixture was stirred for about 1 hour with the homogenizer in the state. Next, (a) component (2-ethylhexyl 2-methoxycinnamate and 4-t-butyl-4′-methoxydibenzoylmethane) as the component (a) was added to the mixture in a ratio of 91 (weight ratio). 7 g of a 55% by weight aqueous dispersion of microcapsules (trade name of Seiwa Kasei Co., Ltd., Silosoma MEA) having an average particle diameter of 2 μm encapsulated in weight% was added and stirred, and deionized water was added to the resulting mixture. The whole was made into a composition of 200 g (ultraviolet absorber: 7% by weight, astaxanthin: 0.002% by weight (20 ppm)).

サンプル2:
(b)成分を使用しない他は、サンプル1と同様にして調製した。
サンプル3:
(a)成分を使用しない他は、サンプル1と同様にして調製した。
Sample 2:
(B) It was prepared in the same manner as Sample 1 except that the component was not used.
Sample 3:
(A) It was prepared in the same manner as Sample 1 except that the component was not used.

「評価方法」
上記各サンプル1〜3についての紫外線防御特性を、図1に示す紫外線照射測定装置により評価した。この測定装置は、ポリアクリル酸ソーダ液は紫外線により酸化され、定量的に粘度が低下するが、この粘度の低下の性質を利用するものである。
"Evaluation methods"
The ultraviolet protection characteristics of each of the samples 1 to 3 were evaluated using the ultraviolet irradiation measuring apparatus shown in FIG. In this measuring apparatus, the polyacrylic acid soda solution is oxidized by ultraviolet rays, and its viscosity is quantitatively lowered. However, this measuring device utilizes the property of lowering the viscosity.

なお、標準液として、ポリアクリル酸ソーダの0.1重量%水溶液を使用し、この標準液300mLを上記サンプル1〜4にも添加し、それぞれ各サンプル液1〜4とした。図1において、測定装置1では、150Lのステンレス製ドラム缶を測定容器にし、紫外線照射灯2を上部に設置した。標準液300mL及びサンプル液1〜5の500mLを、いずれも500mLのポリエチレン製容器に入れ、紫外線照射装置3(ソーラートーン ジャパン社製、波長280〜380nm)を使用した紫外線を照射し、照射時間における粘度を回転粘度計(回転数6rpm)で測定した。標準液はドラム缶の中心に配置し、周りにはサンプル液1〜3を配置した。   In addition, 0.1 wt% aqueous solution of sodium polyacrylate was used as a standard solution, and 300 mL of this standard solution was also added to the samples 1 to 4 to be sample solutions 1 to 4, respectively. In FIG. 1, in the measuring apparatus 1, a 150 L stainless steel drum was used as a measurement container, and the ultraviolet irradiation lamp 2 was installed at the top. 300 mL of the standard solution and 500 mL of the sample solutions 1 to 5 are all put in a 500 mL polyethylene container, irradiated with ultraviolet rays using an ultraviolet irradiation device 3 (manufactured by Solartone Japan, wavelength 280 to 380 nm), and irradiation time The viscosity was measured with a rotational viscometer (rotation speed: 6 rpm). The standard solution was arranged at the center of the drum, and sample solutions 1 to 3 were arranged around it.

「測定」
紫外線を照射し、24時間おきに標準液及びサンプル液1〜4を取り出し、粘度(Pas)を測定し、初期粘度を1とし、経時的な粘度の保持率を求めた。その結果を表1に示すともに、図1に示す。
"Measurement"
Ultraviolet rays were irradiated, the standard solution and sample solutions 1 to 4 were taken out every 24 hours, the viscosity (Pas) was measured, the initial viscosity was set to 1, and the viscosity retention over time was determined. The results are shown in Table 1 and shown in FIG.

Figure 2006176449
Figure 2006176449

表1及び図1から明らかなように、各サンプル液の粘度は時間とともに低下するが、本発明の実施例であるサンプル液1は、100時間経過後も、粘度はほとんど低下しない。これに比べて、比較例であるサンプル液2(b成分が含まれない)及びサンプル液3(a成分が含まれない)にける粘度の低下は極めて大きい。   As apparent from Table 1 and FIG. 1, the viscosity of each sample solution decreases with time, but the viscosity of the sample solution 1 which is an example of the present invention hardly decreases even after 100 hours. Compared to this, the decrease in viscosity in the sample liquid 2 (which does not include the component b) and the sample liquid 3 (which does not include the component a), which are comparative examples, is extremely large.

実施例2
実施例1と同様にして、紫外線対抗化粧用水系組成物として、以下のサンプル液11〜14を調製した。かかる組成物では、(b)成分の含有量を0.002重量%(20ppm)として一定に保持し、(a)成分の量を変化させて、その紫外線防御特性を調べた。
Example 2
In the same manner as in Example 1, the following sample liquids 11 to 14 were prepared as ultraviolet-resistant cosmetic water-based compositions. In such a composition, the content of the component (b) was kept constant at 0.002% by weight (20 ppm), and the amount of the component (a) was changed to examine the ultraviolet protection characteristics.

サンプル液11〜14:
(a)成分の含有量として、それぞれ、1重量%(サンプル液11)、2.5重量%(サンプル液12)、7重量%(サンプル液13)、及び25重量%(サンプル液14)である。
Sample solutions 11-14:
(A) As content of a component, 1 weight% (sample liquid 11), 2.5 weight% (sample liquid 12), 7 weight% (sample liquid 13), and 25 weight% (sample liquid 14), respectively is there.

「評価方法」及び「測定」
実施例1に準じて、標準液及びサンプル液11〜14を使用し、同じ紫外線照射測定装置を使用して、同様にして紫外線を照射して、24時間おきに標準液及びサンプル液11〜14を取り出し、粘度(Pas)を測定し、経時的な粘度の保持率を求めた。その結果を表2に示すともに、図2に示す。
"Evaluation method" and "Measurement"
According to Example 1, the standard solution and the sample solutions 11 to 14 were used, and the same ultraviolet irradiation measurement apparatus was used to irradiate the ultraviolet rays in the same manner. Was taken out, the viscosity (Pas) was measured, and the viscosity retention over time was determined. The results are shown in Table 2 and shown in FIG.

Figure 2006176449
Figure 2006176449

表2及び図2に示されるように、各サンプル液の粘度は時間とともに低下し、比較例であるサンプル液11の紫外線の防御効果は経過時間につれて大きく低下する。一方、これに比べて、本発明の実施例のサンプル液12〜14の紫外線の防御特性はそれほど低下せず、特に、サンプル液13及び14は、100時間経過するもほとんど同じであることがわかる。   As shown in Table 2 and FIG. 2, the viscosity of each sample solution decreases with time, and the ultraviolet protective effect of the sample solution 11 as a comparative example greatly decreases with time. On the other hand, the ultraviolet protection properties of the sample liquids 12 to 14 of the examples of the present invention are not so much reduced, and in particular, the sample liquids 13 and 14 are almost the same even after 100 hours. .

実施例3
実施例1と同様にして、紫外線対抗化粧用水系組成物として、以下のサンプル液21〜24を調製した。かかる組成物では、(a)成分の含有量を7重量%として一定に保持し、(b)成分の量を変化させて、その紫外線防御特性を調べた。
Example 3
In the same manner as in Example 1, the following sample liquids 21 to 24 were prepared as ultraviolet-resistant cosmetic water-based compositions. In such a composition, the content of the component (a) was kept constant at 7% by weight, and the amount of the component (b) was changed, and the ultraviolet protection property was examined.

サンプル液21〜24:
(b)成分の含有量として、それぞれ、サンプル液21(0.00005重量%:0.5ppm)、サンプル液22(0.0005重量%:5ppm)、サンプル液23(0.002重量%:20ppm)、及び%サンプル液24(0.005重量%:50ppm)とした。
Sample solutions 21-24:
As the content of the component (b), sample liquid 21 (0.00005 wt%: 0.5 ppm), sample liquid 22 (0.0005 wt%: 5 ppm), sample liquid 23 (0.002 wt%: 20 ppm), respectively. ) And% sample solution 24 (0.005 wt%: 50 ppm).

「評価方法」及び「測定」
実施例1に準じて、標準液及びサンプル液21〜24を使用し、同じ紫外線照射測定装置を使用して、同様にして紫外線を照射して、24時間おきに標準液及びサンプル液21〜24を取り出し、粘度(Pas)を測定し、経時的な粘度の保持率を求めた。その結果を表3に示すともに、図3に示す。
"Evaluation method" and "Measurement"
In accordance with Example 1, the standard solution and the sample solutions 21 to 24 were used, and the same ultraviolet irradiation measurement apparatus was used to irradiate the ultraviolet rays in the same manner. Was taken out, the viscosity (Pas) was measured, and the viscosity retention over time was determined. The results are shown in Table 3 and shown in FIG.

Figure 2006176449
Figure 2006176449

表3及び図3に示されるように、各サンプル液の粘度は時間とともに低下し、比較例であるサンプル液21の紫外線の防御効果は経過時間につれて大きく低下する。一方、これに比べて、本発明の実施例のサンプル液22〜24の紫外線の防御特性はそれほど低下せず、特に、サンプル液23及び24は、100時間経過するもほぼ同じであることがわかる。   As shown in Table 3 and FIG. 3, the viscosity of each sample solution decreases with time, and the ultraviolet protective effect of the sample solution 21 as a comparative example greatly decreases with time. On the other hand, compared with this, the ultraviolet protection characteristics of the sample liquids 22 to 24 of the examples of the present invention do not deteriorate so much. In particular, it can be seen that the sample liquids 23 and 24 are substantially the same even after 100 hours. .

実施例4
実施例1において、ヒアルロン酸Na4gの代わりに、発酵セラミド(紀文フード社製)4gを使用したほかは実施例1と同様に実施して化粧品組成物としてのサンプル液を調製した。
Example 4
In Example 1, a sample solution as a cosmetic composition was prepared in the same manner as in Example 1 except that 4 g of fermented ceramide (manufactured by Kibun Food Co., Ltd.) was used instead of 4 g of hyaluronic acid Na.

このサンプル液を使用し、実施例1に準じて、標準液及び同じ紫外線照射測定装置を使用して、同様にして紫外線を照射して、24時間おきに標準液及びサンプル液を取り出して粘度(Pas)を測定し、経時的な粘度の保持率を求めた。その結果、初期のサンプル液の粘度を1とした場合、24時間経過後、48時間経過後、72時間経過後、96時間経過後及び120時間経過後は、それぞれ、0.98、0.97、0.95、0.94及び0.94であった。   Using this sample solution, in accordance with Example 1, using the standard solution and the same UV irradiation measuring device, irradiating with UV rays in the same manner, taking out the standard solution and sample solution every 24 hours, and using the viscosity ( Pas) was measured to determine the viscosity retention over time. As a result, when the viscosity of the initial sample solution is 1, after 24 hours, 48 hours, 72 hours, 96 hours and 120 hours, 0.98 and 0.97, respectively. 0.95, 0.94, and 0.94.

実施例5
実施例1のサンプル液1の紫外線対抗化粧組成物を、年齢が25〜40才の日本人女性のモニター10人を選び、紫外線防御例効果と肌への影響をテストした。
Example 5
Ten monitors of Japanese women aged 25 to 40 years were selected as the ultraviolet light-resistant cosmetic composition of Sample Solution 1 of Example 1, and the effects of UV protection examples and the effects on the skin were tested.

テストは、真夏の太陽が照りつける、本年8月、沖縄県那覇市にて実施した。実施例1のサンプル液1を各モニターの一方の腕に20cmの面積に塗布し、もう片方の腕には塗布せずに、4時間暴露した。その結果、いずれのモニターの場合も、サンプル液を塗布しない腕については、夜になって発熱感が生じるとともに、翌日には日焼け現象が見られた。一方、いずれのモニターの場合も、サンプル液を塗布した腕については、上記のごとき、発熱感も日焼け現象もほとんど見られなかった。 The test was conducted in Naha City, Okinawa Prefecture, in August this year, which is lit by the midsummer sun. Sample solution 1 of Example 1 was applied to one arm of each monitor in an area of 20 cm 2 and exposed to the other arm for 4 hours without being applied. As a result, in any of the monitors, the arm to which the sample solution was not applied had a feeling of exotherm at night and a sunburn phenomenon was observed on the next day. On the other hand, in any of the monitors, the heat-applied feeling and the sunburn phenomenon were hardly observed for the arm to which the sample solution was applied as described above.

また、サンプル液の肌に対する影響については、モニター10人中、9人は、肌への影響がほとんどないことが確認されたが、1人には肌にかゆみを伴った若干の赤みが見られた。   Regarding the influence of the sample liquid on the skin, it was confirmed that 9 out of 10 monitors had almost no effect on the skin, but one person showed some redness with itching on the skin. It was.

本発明で使用した紫外線照射測定装置の概略図である。It is the schematic of the ultraviolet irradiation measuring apparatus used by this invention. 実施例1における各サンプルの紫外線防御効果の経時変化を示す。The time-dependent change of the ultraviolet-ray protective effect of each sample in Example 1 is shown. 実施例2における各サンプルの紫外線防御効果の経時変化を示す。The time-dependent change of the ultraviolet-ray protective effect of each sample in Example 2 is shown. 実施例3における各サンプルの紫外線防御効果の経時変化を示す。The time-dependent change of the ultraviolet-ray protective effect of each sample in Example 3 is shown.

符号の説明Explanation of symbols

1.紫外線測定装置
2.紫外線照射灯
3.紫外線
4.標準液
5.サンプル液
1. 1. Ultraviolet measuring device 2. UV irradiation lamp UV4. Standard solution5. Sample solution

Claims (9)

(a)紫外線吸収剤を内包し、平均粒径0.02〜3.5μmのポリシリコーンのマイクロカプセル:2.5〜30重量%と、(b)アスタキサンチン及び/又はカンタキサンチンの含有物質:0.0001〜0.1重量%と、(c)ヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質:0.01〜10重量%と、を含有することを特徴とする紫外線対抗水系化粧用組成物。   (A) Polysilicone microcapsules containing an ultraviolet absorber and having an average particle size of 0.02 to 3.5 μm: 2.5 to 30% by weight; (b) Substances containing astaxanthin and / or canthaxanthin: 0 And 0.1 to 0.1% by weight, and (c) a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide: 0.01 to 10% by weight object. 更に、(d)抗菌剤0.01〜10重量%を含む請求項1に記載の紫外線対抗水系化粧用組成物。   Furthermore, (d) UV-anti-water type cosmetic composition of Claim 1 containing 0.01 to 10 weight% of antibacterial agents. (a)のポリシリコーンが、シリコーンレジン化ポリペプチドである請求項1又は2に記載の紫外線対抗水系化粧用組成物。   The ultraviolet-resistant water-based cosmetic composition according to claim 1 or 2, wherein the (a) polysilicone is a silicone-resinized polypeptide. (a)の紫外線吸収剤が、2−メトキシケイ皮酸2−エチルヘキシル及び/又は4−t−ブチル−4’−メトキシジベンゾイルメタンである請求項1〜3のいずれかに記載の紫外線対抗水系化粧用組成物。   The ultraviolet light-resistant system according to any one of claims 1 to 3, wherein the ultraviolet absorber of (a) is 2-ethylhexyl 2-methoxycinnamate and / or 4-t-butyl-4'-methoxydibenzoylmethane. Cosmetic composition. (c)の粘性物質が、ヒアルロン酸若しくはその塩及び/又はセラミドと、グリセリンとの混合物である請求項1〜4のいずれかに記載の紫外線対抗水系化粧用組成物。   The UV-resistant water-based cosmetic composition according to any one of claims 1 to 4, wherein the viscous substance (c) is a mixture of hyaluronic acid or a salt thereof and / or ceramide and glycerin. (d)の抗菌剤が、直鎖状である、アルキレンジオール類又はグリセロールエーテル類である請求項1〜5のいずれかに記載の紫外線対抗水系化粧用組成物。   The antimicrobial agent for ultraviolet rays according to any one of claims 1 to 5, wherein the antibacterial agent (d) is a linear alkylene diol or glycerol ether. (b)アスタキサンチン及び/又はカンタキサンチンの粉末と、(c)ヒアルロン酸若しくはその塩及び/又はセラミドを含む粘性物質とを水の存在下に混合し、次いで、得られる混合物に、残余の水、及び(a)紫外線吸収剤を内包するポリシリコーンのマイクロカプセルを順次、又は同時に添加することを特徴とする紫外線対抗水系化粧用組成物の製造方法。   (B) a powder of astaxanthin and / or canthaxanthin and (c) a viscous substance containing hyaluronic acid or a salt thereof and / or ceramide in the presence of water, and then the remaining water, And (a) A method for producing an ultraviolet-resistant water-based cosmetic composition, comprising sequentially or simultaneously adding polysilicon microcapsules encapsulating an ultraviolet absorber. (c)の粘性物質が、さらにグリセリンを含む請求項7に記載の紫外線対抗水系化粧用組成物の製造方法。   The method for producing an ultraviolet-resistant anti-water cosmetic composition according to claim 7, wherein the viscous substance of (c) further contains glycerin. (d)の抗菌剤を、いずれかの時点で添加する請求項7又は8に記載の紫外線対抗水系化粧用組成物の製造方法。   The method for producing an ultraviolet-resistant water-based cosmetic composition according to claim 7 or 8, wherein the antibacterial agent (d) is added at any time.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008273874A (en) * 2007-04-27 2008-11-13 Fuji Chem Ind Co Ltd External preparation for scalp
JP2014129290A (en) * 2012-12-28 2014-07-10 Kirin Holdings Co Ltd Dermopathy protective and therapeutic agent
CN113081869A (en) * 2021-04-16 2021-07-09 云南爱尔康生物技术有限公司 Haematococcus pluvialis astaxanthin microcapsule and preparation method thereof

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6383017A (en) * 1986-09-25 1988-04-13 Ichimaru Pharcos Co Ltd Anti-suntan cosmetic
JP2619491B2 (en) * 1988-08-11 1997-06-11 サントリー株式会社 Astaxanthin-containing composition
JPH07330505A (en) * 1994-06-08 1995-12-19 Masato Suzuki Antimicrobial composition
JPH09255519A (en) * 1996-03-19 1997-09-30 Noevir Co Ltd Antibacterial low irritating cosmetic material
JPH11302155A (en) * 1998-04-24 1999-11-02 La Shinshia Kk Skin external preparation for atopic dermatitis
JP2000319171A (en) * 1999-03-03 2000-11-21 Nof Corp Bactricidal skin lotion composition
JP2001049233A (en) * 1999-08-05 2001-02-20 Seiwa Kasei:Kk Ultraviolet-absorbing composition
JP2002053428A (en) * 2000-08-12 2002-02-19 Tadashi Fukiya Skin care preparation
JP2003212715A (en) * 2002-01-11 2003-07-30 Tokyo Kasei Kogyo Kk Sheet for cosmetic use
JP2003335621A (en) * 2002-05-16 2003-11-25 Noevir Co Ltd Antifungal low irritative cosmetic

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008273874A (en) * 2007-04-27 2008-11-13 Fuji Chem Ind Co Ltd External preparation for scalp
JP2014129290A (en) * 2012-12-28 2014-07-10 Kirin Holdings Co Ltd Dermopathy protective and therapeutic agent
CN113081869A (en) * 2021-04-16 2021-07-09 云南爱尔康生物技术有限公司 Haematococcus pluvialis astaxanthin microcapsule and preparation method thereof
CN113081869B (en) * 2021-04-16 2022-06-03 云南爱尔康生物技术有限公司 Haematococcus pluvialis astaxanthin microcapsule and preparation method thereof

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