JPS6397668A - Sunproof carotene - Google Patents

Sunproof carotene

Info

Publication number
JPS6397668A
JPS6397668A JP61242834A JP24283486A JPS6397668A JP S6397668 A JPS6397668 A JP S6397668A JP 61242834 A JP61242834 A JP 61242834A JP 24283486 A JP24283486 A JP 24283486A JP S6397668 A JPS6397668 A JP S6397668A
Authority
JP
Japan
Prior art keywords
carotene
oil
particle size
water
diluted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP61242834A
Other languages
Japanese (ja)
Inventor
Norio Odera
大寺 規夫
Masahiro Takizawa
滝沢 正博
Takeshi Kanamori
武 金森
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lion Corp
Original Assignee
Lion Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lion Corp filed Critical Lion Corp
Priority to JP61242834A priority Critical patent/JPS6397668A/en
Publication of JPS6397668A publication Critical patent/JPS6397668A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/31Hydrocarbons
    • 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
    • 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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • 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
    • 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
    • A61K2800/52Stabilizers

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To provide the title carotene which retains stably its color tone even when stored in the presence of oxygen, water, air, etc., under the irradiation with sunlight over a long period of time and is suitable for use as a food additive, by microencapsulating (oil-diluted) carotene with a specified shell-forming material. CONSTITUTION:Carotene (a) (e.g., one which is extracted from palm oil, concentrated and refined) is optionally diluted with food oil (b) (e.g., colza oil) to obtain (oil-diluted) carotene (A). Separately, 1-300wt% sunproofing agent (c) having a particle size of 0.01-50mum (e.g., TiO2) or 0.5-20wt% ultraviolet absorber (d) (e.g., alpha-bisabolol) is dispersed in a shell-forming material (e) (e.g., gelatin) to obtain a shell-forming material (B) contg. the component (c) or (d). The component A is microencapsulated by using the component B to obtain the title carotene having a particle size of 10-3,000mum, pref. 50-2,000mum.

Description

【発明の詳細な説明】 gMJJ■U租た訪 本発明は、一般食品等に配合して長期間保存しても、脱
色や退色のほとんどない安定性に優れた耐光性カロチン
に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a light-resistant carotene that exhibits excellent stability with almost no decolorization or fading even when added to general foods and stored for a long period of time.

一来の 1 び Iが ゛ しようとする司弘近年、黄
色又は赤色の天然着色剤として、カロチノイドが、食品
分野、医薬品分野、化粧品分野等に広く利用されている
。特に、各種カロチノイドのうちカロチンは、人間の体
内で代謝されてビ゛タミンAに変化することから、健康
上も欠くことのできない物質であり、その有用性は高い
In recent years, carotenoids have been widely used as yellow or red natural coloring agents in the food, pharmaceutical, and cosmetic fields. In particular, among various carotenoids, carotene is metabolized in the human body and converted into vitamin A, so it is an indispensable substance for health and is highly useful.

しかしながら、カロチンは酸素、水、空気等に接触した
り、日光に照射されろと脱色や退色が生じ、その色調が
不安定であるという欠点を有している。そこで、この欠
点を改良するため、カロチンを乳化安定剤を用いて乳化
させ、乾燥して安定化したり(特公昭35−8095号
、特開昭49−126727号)、乳化前又は乳化後に
糖類を加えてカロチンを安定化する(特開昭54−13
5822号、特開昭59−137410号)等の方法が
提案されている。
However, carotene has the disadvantage that it bleaches or fades when it comes into contact with oxygen, water, air, etc. or is exposed to sunlight, and its color tone is unstable. Therefore, in order to improve this drawback, carotene is emulsified using an emulsion stabilizer and stabilized by drying (Japanese Patent Publication No. 35-8095, Japanese Patent Application Laid-open No. 49-126727), or sugars are added before or after emulsification. In addition, it stabilizes carotene (Japanese Patent Application Laid-open No. 54-13
Methods such as No. 5822 and Japanese Unexamined Patent Publication No. 137410/1982 have been proposed.

これらの方法によればカロチンの安定性が向上するが、
これらの方法を利用してカロチンを安定化しても、長期
間保存すると退色が生じる上、また、これらの方法では
カロチンの退色に最も影響を及ぼす日光の影響を防ぐこ
とができないため。
These methods improve the stability of carotene, but
Even if these methods are used to stabilize carotene, it will discolor when stored for a long period of time, and these methods cannot prevent the effects of sunlight, which has the greatest effect on carotene discoloration.

1」光を照射するとカロチンがわずか4〜5日で退色し
てしまうという問題点があった。
1" There was a problem in that carotene faded in just 4 to 5 days when irradiated with light.

このため、食品等各種製品に配合しても長期間安定な色
調を保持し得るカロチンの安定化方法のrA9!が要望
されていた。
For this reason, rA9!, a carotene stabilization method that can maintain a stable color tone for a long time even when incorporated into various products such as food! was requested.

本発明は上記事情に鑑みなされたもので、MJ、水、空
気等の存在下、更には日光の照射下においても長期間安
定な色調を保持することのできる耐光性カロチンを提供
することを目的とする。
The present invention was made in view of the above circumstances, and an object of the present invention is to provide a light-resistant carotene that can maintain a stable color tone for a long period of time even in the presence of MJ, water, air, etc., and even under sunlight irradiation. shall be.

肌孔化を  するための−  び作」一本発明者らは、
上記問題点を解決するため鋭意検討を重ねた結果、遮光
剤や紫外線吸収剤を分散含有する膜材にてカロチン又は
油脂希釈カロチンをマイクロカプセル化し、カロチンを
該膜材で封入することにより、酸素、水、空気等から完
全に遮断されるので、カロチンが保存時に酸素、水、空
気等との接触により分解されてその色調が脱色したり退
色することがほとんどなくなり、カロチンの色調が安定
に保持され、特に膜材中の遮光剤や紫外線吸収剤の遮光
効果により、カロチンがカロチンの退色に最も影響を及
ぼす日光からも遮断されるので、日光照射によるカロチ
ンの分解が確実に防止でき、従って、かかるカロチンの
カプセル化剤は、食品等各種製品に配合してもカロチン
の色調を長期間に互り極めて安定に保持し得ることを知
見し5本発明をなすに至った。
The inventors of the present invention
As a result of intensive studies to solve the above problems, we found that carotene or oil-diluted carotene was microencapsulated in a film material containing dispersed light shielding agents and ultraviolet absorbers, and by encapsulating carotene in the film material, oxygen Since it is completely shielded from water, air, etc., the color tone of carotene is almost never bleached or faded due to decomposition due to contact with oxygen, water, air, etc. during storage, and the color tone of carotene is maintained stably. In particular, due to the light-shielding effect of the light-shielding agent and ultraviolet absorber in the membrane material, carotene is shielded from sunlight, which has the greatest effect on carotene fading, so decomposition of carotene due to sunlight irradiation can be reliably prevented. The present inventors have discovered that such a carotene encapsulating agent can maintain the color tone of carotene extremely stably for a long period of time even when incorporated into various products such as foods, and have thus come up with the present invention.

従って、本発明は、遮光剤又は紫外線吸収剤を分散含有
した膜材にてカロチン又は油脂希釈カロチンをマイクロ
カプセル化してなることを特徴とする耐光性カロチンを
提供することを目的とする。
Therefore, an object of the present invention is to provide light-resistant carotene, which is characterized by microcapsulating carotene or oil-diluted carotene in a membrane material containing a light-shielding agent or an ultraviolet absorber dispersed therein.

以下、本発明について更に詳述する。The present invention will be described in further detail below.

本発明に用いるカロチンは、天然のカロチンが好ましく
、特に、パーム油より抽出、濃縮、精製したカロチンが
好適である。このパーム油より得たカロチンは、α、β
等のカロチンの混和物であり、全トランス型β−カロチ
ン換算では6o〜70%存在している赤色不透明な油状
物である。
The carotene used in the present invention is preferably a natural carotene, and particularly preferably a carotene extracted, concentrated, and purified from palm oil. The carotene obtained from this palm oil is α, β
It is a red, opaque oil containing 60 to 70% of all-trans β-carotene.

なお、カロチンとして、種々カロチンを単独で用いても
2種以上を併用しても良く、また、クリプトキサンチン
、カンタキサンチン等のカロチノイドを用いても差支え
ない。
As the carotene, various carotenes may be used alone or in combination of two or more, and carotenoids such as cryptoxanthin and canthaxanthin may be used.

更に、本発明においては、上述のカロチンを油脂、特に
食用油脂と混和希釈して用いることが好ましい。この場
合、カロチンを食用油脂に溶解して食用油脂溶液として
も、また、カロチンを食用油脂中に分散させても良く、
このように、カロチンを食用油脂と混和して用いること
により、均一な溶液になると共に、希釈率に応じた任意
の色を確保することが可能となる。
Furthermore, in the present invention, it is preferable to use the above-mentioned carotene after diluting it with an oil or fat, particularly an edible oil or fat. In this case, carotene may be dissolved in edible oil or fat to form an edible oil or fat solution, or carotene may be dispersed in edible oil or fat.
In this way, by mixing carotene with edible fats and oils, it becomes possible to obtain a uniform solution and to ensure any color depending on the dilution rate.

ここで、食用油脂としては、動植物油が好適に使用し得
、具体的には、植物油として大豆油、落花生油、ひまわ
り油、菜種油、とうもろこし油、綿実油、ヤシ油、パー
ム油等が、動物油として牛脂、豚脂、魚油、スクワレン
等が例示される。これらは、単独で使用しても2種以上
を併用しても良い。
Here, animal and vegetable oils can be suitably used as the edible fats, and specifically, soybean oil, peanut oil, sunflower oil, rapeseed oil, corn oil, cottonseed oil, coconut oil, palm oil, etc. are used as the vegetable oil, and animal oils include soybean oil, peanut oil, sunflower oil, rapeseed oil, etc. Examples include beef tallow, lard, fish oil, and squalene. These may be used alone or in combination of two or more.

また、カロチンと油脂との配合割合は、特に制限されな
いが、油脂に対しカロチンの配合址を0.01〜30重
量%とすることが好ましい。
Further, the blending ratio of carotene and fat and oil is not particularly limited, but it is preferable that the blending ratio of carotene to fat and oil is 0.01 to 30% by weight.

本発明においては、カロチン又は前記油脂で希釈された
カロチンを膜材で被膜してカプセル化剤とする。この場
合、膜材は種々選択されるが、カロチンの被膜が可能で
あり、水又は熱水に溶解すると共に、人体の生理作用に
害のない物質が好適に採用し得ろ。このような膜材とし
て、具体的にはゼラチン、タンパク質、アラビアゴム、
カルボジキシメチルセルロース、アルギン酸塩等が例示
され、特にゼラチン、アラビアゴム、カルボジキシメチ
ルセルロース、アルギン酸塩が好適に用いられる。
In the present invention, carotene or carotene diluted with the oil or fat described above is coated with a membrane material to form an encapsulating agent. In this case, various membrane materials can be selected, but a carotene coating is possible, and a substance that dissolves in water or hot water and is not harmful to the physiological effects of the human body can be suitably used. Specific examples of such membrane materials include gelatin, protein, gum arabic,
Examples include carboxymethylcellulose and alginates, with gelatin, gum arabic, carboxymethylcellulose and alginates being particularly preferred.

更に、本発明においては、上述した膜材中に遮光剤又は
紫外線吸収剤を分散、含有したものを使用するもので、
このようにカロチンを遮光剤や紫外線吸収剤を分散含有
する膜材で被覆することにより、カロチンを耐光化し得
、かつカロチンを酸素、水、空気等から完全に遮断する
ことができるので、本発明品を食品等に配合して保存す
る際の日光、酸素、水、空気等によるカロチンの分解を
勿果的に防止し、カロチンの色調を安定に保持し得る。
Furthermore, in the present invention, the above-mentioned film material containing a light shielding agent or an ultraviolet absorber dispersed therein is used.
In this way, by coating carotene with a film material containing dispersed light-shielding agents and ultraviolet absorbers, carotene can be made light-resistant, and carotene can be completely blocked from oxygen, water, air, etc., so the present invention The decomposition of carotene by sunlight, oxygen, water, air, etc. when the product is blended into food and stored is effectively prevented, and the color tone of carotene can be stably maintained.

この場合、遮光剤や紫外線吸収剤は適宜選択されるが、
遮光剤としては、二酸化チタン、炭酸カルシウム、リン
酸カルシウム、カオリン、タルク、麦飯石等の水不溶性
無機化合物の微粒子、でんぶん(コーンスターチ、ばれ
いしょでんぷん等)、カゼイン、魚鱗バク等の水不溶性
有機物の微粒子、三二酸化鉄1食用色素のアルミニウム
レーキ、銅クロロフィル等の水不溶性着色料、金、銀等
の金属箔又は微粉等が例示される。これら遮光剤の中で
は二酸化チタン、三二酸化鉄、金、鉄の微粒子が好適に
使用し得、特にその粒径が好ましくは0.01〜50μ
s、より好ましくは0.01〜207Jのものが用いら
れる。また、添加量は膜材に対して1〜300重量%、
特に10〜250重量%とすることが好ましい、添加量
が1%より少ないと遮光性に劣り、300%より多いと
均一な分散が困難となる。なお、遮光剤として二酸化チ
タンを使用する場合、二酸化チタンを膜材に150〜2
00重量%添加すると、日光をほぼ100%遮光するこ
とができる。また、二酸化チタンを使用する場合、二酸
化チタンを0.5〜3倍量の水に分散させて添加するこ
とが望ましく。
In this case, the light shielding agent and ultraviolet absorber are selected appropriately, but
As light shielding agents, fine particles of water-insoluble inorganic compounds such as titanium dioxide, calcium carbonate, calcium phosphate, kaolin, talc, and maifan stone, fine particles of water-insoluble organic compounds such as starch (cornstarch, potato starch, etc.), casein, and fish scale bacterium; Examples include aluminum lake of iron sesquioxide 1 food coloring, water-insoluble colorants such as copper chlorophyll, metal foils or fine powders of gold, silver, etc. Among these light-shielding agents, fine particles of titanium dioxide, iron sesquioxide, gold, and iron can be suitably used, and in particular, the particle size is preferably 0.01 to 50μ.
s, more preferably 0.01 to 207 J. In addition, the amount added is 1 to 300% by weight based on the membrane material.
In particular, it is preferably 10 to 250% by weight. If the amount added is less than 1%, the light shielding properties will be poor, and if it is more than 300%, uniform dispersion will be difficult. In addition, when using titanium dioxide as a light shielding agent, titanium dioxide is used as a film material at a concentration of 150 to 2
When added in an amount of 0.00% by weight, almost 100% of sunlight can be blocked. Moreover, when using titanium dioxide, it is desirable to disperse titanium dioxide in 0.5 to 3 times the amount of water and add it.

これにより二酸化チタンの凝集を防止して膜材に良好に
分散含有させることができる。
This prevents agglomeration of titanium dioxide and allows it to be well dispersed and contained in the membrane material.

また、紫外線吸収剤としては、γ−オリザノール、α−
ビサブロール(かみつれ油に50%含有)。
In addition, as ultraviolet absorbers, γ-oryzanol, α-
Bisabrol (contains 50% in mustard oil).

ラウソン、′ニゲロン等のベンゾキノン類、アンソロン
、アントラノール、アロイン等のアントラキノン類、ヘ
リクリジン−5−フラボノイド、アビゲニン、ケルセチ
ン、ケルシトリン、ヒペリン。
benzoquinones such as lauson, 'nigerone, anthraquinones such as antholone, anthranol, aloin, heliclidine-5-flavonoid, abigenin, quercetin, quercitrin, hyperin.

ルチン等のフラボノイド類、ベルガプテンウロカニン酸
、ウンベリフェロン、更にこれらを含む抽出物等の天然
系紫外線吸収剤が好ましく、その池水不溶性のものであ
ればカプセル膜中に選択的に入れて使用することができ
る。ここで、添加量は別に限定されないが、膜材に対し
て0.5〜20重量%が好ましい。
Natural ultraviolet absorbers such as flavonoids such as rutin, bergaptenurocanic acid, umbelliferone, and extracts containing these are preferred, and if they are insoluble in pond water, they can be selectively incorporated into the capsule membrane for use. be able to. Here, the amount added is not particularly limited, but is preferably 0.5 to 20% by weight based on the membrane material.

カプセルの製造方法は、使用目的や膜材等に応じ適宜選
択され、噴霧乾燥法、気中懸濁被覆法、粉床法、液中硬
化法、相分離法、融解分散冷却法、界面重合法、1ns
itu重合法、液中硬化法等、マイクロカプセルの製造
方法のいずれを利用しても差支えないが、特に相分離法
(コンプレックスコアセルベーション法、ソルトコアセ
ルベーション法)、液中硬化法等が好適に採用される。
Capsule manufacturing methods are appropriately selected depending on the purpose of use and membrane material, etc., and include spray drying, air suspension coating, powder bed method, liquid curing method, phase separation method, melt dispersion cooling method, and interfacial polymerization method. , 1ns
Any method for producing microcapsules, such as the in-tu polymerization method or the in-liquid curing method, may be used, but phase separation methods (complex coacervation method, salt coacervation method), in-liquid curing method, etc. Suitably adopted.

また、カプセルの粒径は10〜3000tsが好ましく
、特に50〜2000tunが好ましい。粒径が3o0
0pより大きいと、食品等にカプセル化剤を配合した場
合に口当たりが悪くなり、また、10声より小さいと粒
径に応じて膜厚が薄くなり、保存安定性に劣る。
Moreover, the particle size of the capsule is preferably 10 to 3,000 ts, particularly preferably 50 to 2,000 tun. Particle size is 3o0
If it is larger than 0p, the taste becomes poor when the encapsulating agent is blended into foods, etc., and if it is smaller than 10p, the film thickness becomes thinner depending on the particle size, resulting in poor storage stability.

本発明のカプセル化剤は、種々の製品に利用し得、特に
健康ドリンク、セパレートドレッシング。
The encapsulating agent of the present invention can be used in various products, especially health drinks and separate dressings.

ガム、ゼリー等、一般食品に有効に利用することができ
る。
It can be effectively used in general foods such as gum and jelly.

1皿り立米 以上説明したように、本発明のカロチンのカプセル化剤
は、カロチンを遮光剤又は紫外線を分散、含有した膜材
で被覆してカプセル化したことにより、Ni素、水、空
気等の存在下や日光の照射下においてもカロチンが分解
してその色調が脱色や退色することがほとんどない。従
って1本発明品を使用した食品は、従来の製品に比べて
保存期間を延ばすことができ、ビタミンAの前駆体を含
有する栄養強化食品として有効に利用することができる
As explained above, the carotene encapsulating agent of the present invention is obtained by coating carotene with a film material containing a light-shielding agent or a film material that disperses and contains ultraviolet rays and encapsulating the carotene. Even in the presence of water or sunlight, the carotene decomposes and the color tone rarely fades or fades. Therefore, foods using the product of the present invention can have a longer shelf life than conventional products, and can be effectively used as nutritionally fortified foods containing vitamin A precursors.

以下、実施例を挙げて本発明を具体的に説明するが、本
発明は下記の実施例に制限されるものではない。
EXAMPLES Hereinafter, the present invention will be specifically explained with reference to examples, but the present invention is not limited to the following examples.

〔実施例1〕 水950gに酸処理ゼラチン(ゼリー強度300ブルー
ム)25gとアラビアゴム25gを加え、40℃に加熱
して溶解した。
[Example 1] 25 g of acid-treated gelatin (jelly strength 300 bloom) and 25 g of gum arabic were added to 950 g of water and dissolved by heating to 40°C.

次いで、この水溶液に二酸化チタン40gを水40gの
割合で攪拌分散させたものを加え、攪拌して均一に分散
させた後、攪拌下で菜種油140gとカロチン60gと
の混合物を分散し、粒径を200−5004に調整した
Next, a mixture of 40 g of titanium dioxide and 40 g of water was added to this aqueous solution, and after stirring and dispersing it uniformly, a mixture of 140 g of rapeseed oil and 60 g of carotene was dispersed under stirring to reduce the particle size. Adjusted to 200-5004.

更に、40℃に加温し、20%酢酸水溶液を添加してp
 Hを4.2に調整した後、10℃まで冷却してほぼ球
状で粒径200〜500Amのマイクロカプセルを得た
。このカプセルをフルイで分離し、10℃の水で洗浄し
た後、20℃の乾燥空気(湿度40%)で乾燥した。
Furthermore, it was heated to 40°C, and a 20% acetic acid aqueous solution was added to p
After adjusting H to 4.2, the mixture was cooled to 10° C. to obtain microcapsules having a substantially spherical shape and a particle size of 200 to 500 Am. The capsules were separated using a sieve, washed with water at 10°C, and then dried with dry air at 20°C (40% humidity).

上記方法で得たカプセルを戸外の日光が良く島る場所に
放置し、カプセル中のカロチン残存量を経口的に定量し
た。なお、カロチンの定量は下記方法にて行い、対照と
して市販のカロチン色素をカプセルのカロチン濃度と同
一濃度に調整し、カプセルと同様に戸外に放置したもの
を用いた。
The capsules obtained by the above method were left outdoors in a place with good sunlight, and the amount of carotene remaining in the capsules was determined orally. The amount of carotene was determined by the following method. As a control, a commercially available carotene dye was adjusted to the same concentration as the capsule and left outdoors in the same way as the capsule.

友旦天λ立定盈 カプセル溶液を60℃に加温し、カプセルを破壊して試
料とした。この試料及び対照液を各々水で希釈し、その
一定量をシクロヘキサンで抽出した後、波長455nm
における吸光度[D]を測定し、次式によりカロチン含
量とカロチン残存率を算出した。
The Yudanten λ Lidingying capsule solution was heated to 60°C, and the capsules were broken and used as samples. The sample and control solution were each diluted with water, a certain amount of which was extracted with cyclohexane, and then extracted with a wavelength of 455 nm.
The absorbance [D] was measured, and the carotene content and carotene residual rate were calculated using the following formula.

結果を第1表に示す。The results are shown in Table 1.

残存率(%)=市×100 Co=日光照射前のカロチン量 C=一定期間経過後のカロチン量 第  1  表 〔実施例2〕 水965gに酸処理ゼラチン(ゼリー強度300ブルー
ム)25gとカルボジキシメチルセルロースナトリウム
(重合度100〜150)l Ogを40℃で溶解し、
これを500gづつ2分割した。この2分割した一方の
溶液にカミツレの精油3.5gをホモジナイザで粒径1
〜27mになるように分散して、カミツレ精油分散液を
調製した。
Residual rate (%) = city x 100 Co = amount of carotene before sunlight irradiation C = amount of carotene after a certain period of time Table 1 [Example 2] 25 g of acid-treated gelatin (jelly strength 300 bloom) and Carbodine were added to 965 g of water. Sodium oxymethylcellulose (degree of polymerization 100-150) 1 Og was dissolved at 40°C,
This was divided into two parts of 500 g each. Add 3.5 g of chamomile essential oil to one of the two divided solutions using a homogenizer to obtain a particle size of 1.
A chamomile essential oil dispersion was prepared by dispersing the oil to a length of ~27 m.

また、2分割した他方の溶液にカロチンを30%含有す
るサフラワー油140gを粒径300〜1000psに
なるように分散した。続いてこれに該カミツレ精油分散
液500gを加え、更に40℃で20%酢酸水溶液を添
加してpHを3.9に調整した。その後、10℃まで冷
却して、カプセル壁膜中にカミツレ精油の微細滴を含み
かつ30%カロチン含有サフサフラワー的包する粒径3
00〜1000uのほぼ球状のマイクロカプセルを得た
。このカプセルを20℃の15%硫酸すトリウム水溶液
で洗浄した後、フルイで分離して、20℃の乾燥空気に
より乾燥した。
In addition, 140 g of safflower oil containing 30% carotene was dispersed in the other divided solution so that the particle size was 300 to 1000 ps. Subsequently, 500 g of the chamomile essential oil dispersion was added thereto, and a 20% acetic acid aqueous solution was further added at 40°C to adjust the pH to 3.9. Thereafter, it is cooled to 10°C, and the particle size is 3, which contains fine droplets of chamomile essential oil in the capsule wall and encapsulates a safsa flower containing 30% carotene.
Almost spherical microcapsules of 00 to 1000 u were obtained. The capsules were washed with a 15% aqueous sodium sulfate solution at 20°C, separated using a sieve, and dried with dry air at 20°C.

このようにして得たマイクロカプセル中のカロチン含量
の安定性を実施例1と同様の方法で測定した。結果を第
2表に示す。
The stability of the carotene content in the microcapsules thus obtained was measured in the same manner as in Example 1. The results are shown in Table 2.

第  2  表 〔実施例3〕 水920gに酸処理ゼラチン(ゼリー強度250ブルー
ム)aogを加え、40℃で溶解した後。
Table 2 [Example 3] Acid-treated gelatin (jelly strength 250 bloom) aog was added to 920 g of water and dissolved at 40°C.

三二酸化鉄40gを加えて攪拌しながら均一に分散させ
た。次いで、この水溶液に攪拌下でカロチンを35%含
有する大豆油300gを分散し、続いて20%硫酸す1
ヘリウム水溶液670gを加えた後、20℃マチ冷却シ
テ粒径200〜5oO/jJI+のカプセルを得た。こ
のカプセルをろ過分離し、15%硫酸ナトリウム水溶液
で洗浄した後、20℃の乾燥空気中で乾燥した。
40 g of iron sesquioxide was added and uniformly dispersed with stirring. Next, 300 g of soybean oil containing 35% carotene was dispersed in this aqueous solution with stirring, followed by 20% sulfuric acid solution.
After adding 670 g of helium aqueous solution, capsules having a particle size of 200 to 5 oO/jJI+ were obtained by cooling at 20°C. The capsules were separated by filtration, washed with a 15% aqueous sodium sulfate solution, and then dried in dry air at 20°C.

上記カプセルのカロチン含量と残存率を実施例1と同様
の方法で測定し、算出した。
The carotene content and residual rate of the capsules were measured and calculated in the same manner as in Example 1.

結果を第3表に示す。The results are shown in Table 3.

第  3  表 第1表乃至第3表の結果より、従来の市販のカロチン色
素に比べて、本発明の天然カロチンを包含したマイクロ
カプセルは、カロチンを極めて長期間安定に保存できる
ことが確認された。
Table 3 From the results shown in Tables 1 to 3, it was confirmed that compared to conventional commercially available carotene pigments, the microcapsules containing natural carotene of the present invention can store carotene stably for an extremely long period of time.

〔実施例4〕 実施例1と同様の方法で調整したカプセルを5℃まで冷
却した後、0.05%タンニン酸水溶液500dを徐々
に加え、30分間攪拌して硬化処理した。このカプセル
を分離、洗浄し、乾燥してカロチン含有カプセルを得た
[Example 4] After cooling the capsules prepared in the same manner as in Example 1 to 5° C., 500 d of 0.05% tannic acid aqueous solution was gradually added, and the capsules were stirred for 30 minutes for hardening treatment. The capsules were separated, washed and dried to obtain carotene-containing capsules.

〔実施例5〕 カプセル粒径を100〜200pに調整する以外は実施
例3と同様の方法で調製し、5℃まで冷却した後、10
%ミョウバンカリウム水溶液2500d(pH4)を徐
々ニ加え、2時間攪拌して硬化処理した。このカプセル
を分離、洗浄し、乾燥してカロチン含有カプセルを得た
[Example 5] Capsules were prepared in the same manner as in Example 3 except that the particle size was adjusted to 100 to 200p, and after cooling to 5°C,
% alum potassium aqueous solution (pH 4) was gradually added and stirred for 2 hours for hardening treatment. The capsules were separated, washed and dried to obtain carotene-containing capsules.

以上の硬化処理したカプセルもカロチンの安定保存性に
優れていた。
The hardened capsules described above also had excellent carotene stability.

Claims (1)

【特許請求の範囲】[Claims] 1、遮光剤又は紫外線吸収剤を分散含有した膜材にてカ
ロチン又は油脂希釈カロチンをマイクロカプセル化して
なることを特徴とする耐光性カロチン。
1. A light-resistant carotene characterized by microcapsulating carotene or oil-diluted carotene in a membrane material containing a light-shielding agent or an ultraviolet absorber dispersed therein.
JP61242834A 1986-10-13 1986-10-13 Sunproof carotene Pending JPS6397668A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61242834A JPS6397668A (en) 1986-10-13 1986-10-13 Sunproof carotene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61242834A JPS6397668A (en) 1986-10-13 1986-10-13 Sunproof carotene

Publications (1)

Publication Number Publication Date
JPS6397668A true JPS6397668A (en) 1988-04-28

Family

ID=17094982

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61242834A Pending JPS6397668A (en) 1986-10-13 1986-10-13 Sunproof carotene

Country Status (1)

Country Link
JP (1) JPS6397668A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996033611A3 (en) * 1995-04-27 1996-11-28 Zeneca Ltd Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
WO2002041711A1 (en) * 2000-11-24 2002-05-30 Unilever N.V. Food product comprising carotenoids
WO2024003266A1 (en) * 2022-06-30 2024-01-04 Kapsera S.A.S. Microcapsules comprising a uv filter

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58121210A (en) * 1971-08-24 1983-07-19 バイエル・アクチエンゲゼルシヤフト Manufacture of instantaneous mouth discharging sublingual soft capsule medicine

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58121210A (en) * 1971-08-24 1983-07-19 バイエル・アクチエンゲゼルシヤフト Manufacture of instantaneous mouth discharging sublingual soft capsule medicine

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5846554A (en) * 1993-11-15 1998-12-08 Zeneca Limited Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
US6077522A (en) * 1993-11-15 2000-06-20 Zeneca Limited Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
US6149843A (en) * 1993-11-15 2000-11-21 Zeneca Limited Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
WO1996033611A3 (en) * 1995-04-27 1996-11-28 Zeneca Ltd Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
EA000219B1 (en) * 1995-04-27 1998-12-24 Зенека Лимитед Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
AU711892B2 (en) * 1995-04-27 1999-10-21 Syngenta Limited Microcapsules containing suspensions of biologically active compounds and ultraviolet protectant
WO2002041711A1 (en) * 2000-11-24 2002-05-30 Unilever N.V. Food product comprising carotenoids
WO2024003266A1 (en) * 2022-06-30 2024-01-04 Kapsera S.A.S. Microcapsules comprising a uv filter

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