JPH0625156A - Achromatic color product of beta-carotene and its production - Google Patents

Achromatic color product of beta-carotene and its production

Info

Publication number
JPH0625156A
JPH0625156A JP3078235A JP7823591A JPH0625156A JP H0625156 A JPH0625156 A JP H0625156A JP 3078235 A JP3078235 A JP 3078235A JP 7823591 A JP7823591 A JP 7823591A JP H0625156 A JPH0625156 A JP H0625156A
Authority
JP
Japan
Prior art keywords
carotene
beta
achromatic
clathrate
foods
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
JP3078235A
Other languages
Japanese (ja)
Inventor
Tadahisa Murao
尾 周 久 村
Tetsuhiko Maruyama
山 哲 彦 丸
Yasuyuki Takahashi
橋 康 之 高
Yoshinori Komatsu
松 恵 徳 小
Yoshiro Yamamoto
本 良 郎 山
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.)
Meiji Dairies Corp
Original Assignee
Meiji Milk Products Co Ltd
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 Meiji Milk Products Co Ltd filed Critical Meiji Milk Products Co Ltd
Priority to JP3078235A priority Critical patent/JPH0625156A/en
Publication of JPH0625156A publication Critical patent/JPH0625156A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the subject compound excellent in water dispersibility and useful in a wide use range such as foods. medicines and cosmetics by adding a complementary color pigment to the cyclodextrin clathrate of beta-carotene. CONSTITUTION:A cyclodextrin solution is mixed with an oily beta-carotene, and subsequently stirred by the use of a homomixer, etc., at a high rate under the control of the stirring condition to obtain a clathrate reduced in its chroma. In order to further reduce the chroma, the complementary color pigment of the clathrate is added to obtain the achromatic product of the beta-carotene. Even when the achromatic beta-carotene is added to foods, medicines, etc., the original colors of foods, etc., are not deteriorated, and medicines, etc., are excessively not colored. Thereby, the utilization range of the achromatic beta-carotene can be expanded, and the achromatic beta-carotene deteriorates the flavors of the foods, etc., because the characteristic flavor of the beta-carotene is masked.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、無彩色のβ−カロチン
及びその製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an achromatic β-carotene and a method for producing the same.

【0002】β−カロチンは、従来より黄色色素として
食品等に広く利用されているが、従来からのβ−カロチ
ン製剤はそれ自体が黄色であるがゆえに、添加する食品
の範囲、添加量がおのずと制限を受けるのに対し、本発
明に係るβ−カロチン無彩色物は添加する食品を黄色に
着色しないことから利用範囲が拡大できる。また本発明
に係るβ−カロチン無彩色物は、水系での分散性が良好
でβ−カロチン独特の風味がマスキングされているとい
う特徴もあわせ有するものである。
[0002] β-carotene has been widely used as a yellow pigment in foods and the like, but since the conventional β-carotene preparation is yellow in itself, the range and amount of food to be added are naturally limited. In contrast to the limitation, the β-carotene achromatic substance according to the present invention does not color the food to be added yellow, so that the range of application can be expanded. Further, the β-carotene achromatic product according to the present invention also has the characteristics that the dispersibility in an aqueous system is good and the flavor peculiar to β-carotene is masked.

【0003】また、β−カロチンはプロビタミンA剤や
抗酸化剤としての用途も有するが、本発明に係る無彩色
物のβ−カロチンによれば、無彩色のプロビタミンA剤
や抗酸化剤の調製も可能となる。更にまたβ−カロチン
は、抗癌作用を有し、特に肺癌の予防に有効であるし免
疫賦活作用も併有するものであるが、本発明によれば無
彩色の抗癌剤、免疫賦活剤も調製することができ、本発
明は、飲食品、医薬品、化粧品等各種の産業分野におい
て重要な役割を果すものである。
Further, β-carotene has applications as a provitamin A agent and an antioxidant, but according to the achromatic product β-carotene of the present invention, an achromatic provitamin A agent and an antioxidant are used. Can also be prepared. Furthermore, β-carotene has an anti-cancer effect, and is particularly effective in preventing lung cancer and also has an immunostimulatory effect, but according to the present invention, an achromatic anticancer agent and an immunostimulant are also prepared. Therefore, the present invention plays an important role in various industrial fields such as food and drink, pharmaceuticals, and cosmetics.

【0004】[0004]

【従来の技術】β−カロチンは、カロチノイドの一つで
あって黄色を呈することが知られており(「化学大辞典
2」共立出版、昭42−9−10、p.606)、した
がって、界面活性剤を用いたβ−カロチン製剤も市販さ
れているが(特開昭62−267261号公報)、この
市販のβ−カロチンは、水系において強い黄色を呈する
ものである。もちろん、β−カロチン独特の風味のマス
キングもなされていない。
BACKGROUND ART β-Carotene is one of carotenoids and is known to have a yellow color ("Kagaku Daijiten 2" Kyoritsu Shuppan, Sho 42-9-10, p.606). A β-carotene preparation using a surfactant is also commercially available (JP-A-62-267261), but this commercially available β-carotene exhibits a strong yellow color in an aqueous system. Of course, the flavor peculiar to β-carotene is not masked.

【0005】[0005]

【発明が解決しようとする課題】上記したこれら既知の
β−カロチン製品は、水系で分散させた際に黄色を呈
し、しかも着色の度合いが強いし、β−カロチン独特の
風味のマスキングが充分ではないので、利用範囲及び添
加量に制限を受けるものである。
These known β-carotene products described above exhibit a yellow color when dispersed in an aqueous system, and have a high degree of coloring, and the masking of the flavor peculiar to β-carotene is not sufficient. Since it is not available, the range of use and the amount added are limited.

【0006】このように、水系で分散させた際に添加す
る対象食品が本来有する色をそこねることがないように
彩度が小さく、且つβ−カロチン独特の風味が充分にマ
スキングされたβ−カロチン製品は、従来全く知られて
おらず、本発明はこのような無彩色のβ−カロチン製品
を開発することを目的とするものである。
[0006] As described above, β-carotene having a small saturation and sufficiently masking the peculiar taste of β-carotene so as not to disturb the original color of the food to be added when dispersed in an aqueous system The product has never been known so far, and the present invention aims to develop such an achromatic β-carotene product.

【0007】[0007]

【課題を解決するための手段】本発明は、上記目的を達
成するためになされたものであって、各方面から検討の
結果、サイクロデキストリン(以下、CDということも
ある)による包接処理に着目する至り、更に研究した結
果、本発明の完成に到達したものである。したがって本
発明に係るβ−カロチンの無彩色物は、食品や医薬品等
に添加しても、食品等本来の色調をそこねることがない
し医薬品等を過度に着色することもないため、利用範囲
が拡大して各種の製品に広く利用することができ、ま
た、添加量を大幅に増加することが可能であるので、大
幅にβ−カロチンの強化量をふやしたりその含有量をふ
やしたりすることも可能である。以下、本発明について
詳しく説明する。
The present invention has been made in order to achieve the above-mentioned object, and as a result of examinations from various fields, it was found that the inclusion treatment with cyclodextrin (hereinafter sometimes referred to as CD) was performed. As a result of paying attention and further research, the present invention has been completed. Therefore, the achromatic product of β-carotene according to the present invention, even when added to foods and pharmaceuticals, does not spoil the original color tone of foods and does not excessively color pharmaceuticals, etc. Since it can be widely used in various products, and the addition amount can be significantly increased, it is possible to significantly increase the amount of β-carotene fortified or its content. Is. Hereinafter, the present invention will be described in detail.

【0008】本発明を実施するにおいては、β−カロチ
ンをサイクロデキストリンで包接するが、本発明ではα
−サイクロデキストリン(枝分かれα−サイクロデキス
トリンも含む)を使用する。このように、本発明に用い
るサイクロデキストリンにはα−サイクロデキストリン
が最も適しているが、α−サイクロデキストリンを含む
ものであればどのようなものでもよく、例えばCD粉飴
等をそのまま使用することも可能である。
In the practice of the present invention, β-carotene is clathrated with cyclodextrin.
Use cyclodextrin (including branched α-cyclodextrin). Thus, α-cyclodextrin is most suitable for the cyclodextrin used in the present invention, but any substance containing α-cyclodextrin may be used, for example, CD starch syrup or the like may be used as it is. Is also possible.

【0009】包接物の製造方法としては、本発明におい
ては周知の従来法である飽和水溶液法ないし混練法を使
用するのでなく、サイクロデキストリン溶液と油状のβ
−カロチンとをホモミキサー等の高速攪拌機で比較的短
時間高速攪拌するものである。
In the present invention, the method for producing the clathrate does not use the saturated aqueous solution method or the kneading method, which is a well-known conventional method, but uses a cyclodextrin solution and an oily β.
-Carotene is rapidly stirred with a high-speed stirrer such as a homomixer for a relatively short time.

【0010】更に具体的には、本発明に係る包接物の製
造方法は任意の濃度のサイクロデキストリン溶液、望ま
しくはできるだけ高濃度の溶液(飽和濃度以上の濃度で
もよい)に油状のβ−カロチンを適当量添加し、ホモミ
キサー等で高速攪拌するというものである。CD溶液と
しては、水溶液を使用するが、メタノール、エタノー
ル、プロパノール等のアルコール類や、アセトンやケト
ン等のβ−カロチンを溶解しない有機溶媒を更に添加し
た水溶液を使用してもよい。また本発明において、β−
カロチンの適当量とはサイクロデキストリンが包接可能
な量に限界があることから、その限度内にすることが必
要である(α−CD1kgに対して、β−カロチン0.
5〜15g、更に好ましくは6〜10gが適当量であ
る)。
More specifically, the method for producing an inclusion complex according to the present invention is characterized in that an oily β-carotene is added to a cyclodextrin solution having an arbitrary concentration, preferably a solution having a concentration as high as possible (the concentration may be higher than the saturation concentration). Is added in an appropriate amount and stirred at high speed with a homomixer or the like. As the CD solution, an aqueous solution is used, but an aqueous solution further added with an alcohol such as methanol, ethanol, propanol or the like, or an organic solvent which does not dissolve β-carotene such as acetone or ketone may be used. In the present invention, β-
Since there is a limit to the amount of cyclodextrin that can be included in the appropriate amount of carotene, it is necessary to keep it within that limit (for 1 kg of α-CD, β-carotene 0.
A suitable amount is 5 to 15 g, more preferably 6 to 10 g).

【0011】本発明において更に特記すべき特徴のひと
つは、この際、攪拌条件を制御することにより彩度が制
御できる点である。攪拌速度が比較的速い条件と遅い条
件とを比較すると、包接物を水系に分散させた際、一般
的には彩度は後者の方が前者よりも小さくなる。したが
って本発明においては、β−カロチンをCDで包接する
ことによって彩度を低下させるのであるが、その際、攪
拌速度を比較的遅くすることによって更に彩度を小さく
するものである。
One of the more remarkable features of the present invention is that the saturation can be controlled by controlling the stirring conditions. Comparing the conditions in which the stirring speed is relatively high and the conditions in which the stirring speed is slow, when the clathrate is dispersed in the water system, the saturation is generally smaller in the latter than in the former. Therefore, in the present invention, the saturation is reduced by encapsulating β-carotene with CD, but at that time, the saturation is further reduced by relatively slowing the stirring speed.

【0012】しかしながら、このようにして調製したβ
−カロチンのCD包接物は、従来からのβ−カロチン製
剤と比較すればたしかに彩度が小さくなってはいるが、
無彩色というわけではない。
However, the β thus prepared
The CD inclusion of carotene is certainly less saturated than the conventional β-carotene preparation,
Not achromatic.

【0013】そこでこの点を限定するために鋭意研究の
結果、補色に着目し、β−カロチンのCD包接物の色調
に対して補色の関係にある色素を添加混合したところ、
更に彩度が小さくなり、ほとんど無彩色となることを確
認した。すなわち本発明は、β−カロチンをCDで包接
して彩度を小さくするだけでなく、これを更に彩度を低
下させるためにβ−カロチンのCD包接物の色調に対し
て補色に相当する色素を添加することにより無彩色のも
のまでも製造できる点を大きな特徴とするものである。
In order to limit this point, as a result of earnest research, as a result of paying attention to the complementary color, and adding and mixing a pigment having a complementary color to the color tone of the CD inclusion of β-carotene,
Furthermore, it was confirmed that the saturation became smaller and the color became almost achromatic. That is, the present invention not only reduces the color saturation by encapsulating β-carotene with CD but also corresponds to a color complementary to the color tone of the CD inclusion of β-carotene in order to further reduce the color saturation. A major feature is that even an achromatic color can be manufactured by adding a dye.

【0014】図1に市販β−カロチン製剤、CD包接物
及び本発明に係る補色色素を添加したCD包接物(β−
カロチン濃度2mg/100ml、4mg/100m
l)をそれぞれ水に分散させ、色差計(東京電色
(株):MODEL TC−1500MC−88)を用
いて彩度を測定した結果を示した(UCS色度図)。図
1に示す通り、市販β−カロチン製剤と比較してβ−カ
ロチンのCD包接物は彩度が約40%程度であり、さら
にβ−カロチンのCD包接物に補色に相当する色素を添
加することによりさらに彩度は低下し、約17%程度と
なり、彩度が大幅に低下し、無彩色に近いものとなって
いることが確認される。
FIG. 1 shows a commercially available β-carotene preparation, a CD clathrate and a CD clathrate (β-
Carotene concentration 2mg / 100ml, 4mg / 100m
1) was dispersed in water and the chroma was measured using a color difference meter (Tokyo Denshoku Co., Ltd .: MODEL TC-1500MC-88). The results are shown (UCS chromaticity diagram). As shown in FIG. 1, compared to the commercially available β-carotene preparation, the CD inclusion of β-carotene had a saturation of about 40%, and the CD inclusion of β-carotene was supplemented with a dye corresponding to a complementary color. It is confirmed that the addition further reduces the saturation to about 17%, which greatly reduces the saturation and makes it close to an achromatic color.

【0015】上記したように本発明によれば、油状のβ
−カロチンをCDで包接することと、補色色素を添加す
ることの2段階の処理によってほとんど無彩色のβ−カ
ロチンが得られる。また、このようにして得られたもの
は粉末、液状、ペースト状のいずれの状態にも調製する
ことが可能で、添加する食品の形態に合わせて選択する
ことができ、水系での分散性が良好でβ−カロチン特有
の風味がマスキングされているという特徴をあわせもつ
ものである。
As described above, according to the present invention, oily β
-Almost achromatic β-carotene is obtained by the two-step treatment of inclusion of carotene with CD and addition of a complementary color dye. Further, the product thus obtained can be prepared in any state of powder, liquid and paste, and can be selected according to the form of the food to be added, and the dispersibility in the water system is It also has the characteristics that it is good and the flavor peculiar to β-carotene is masked.

【0016】β−カロチンのCD包接物は、一般に黄〜
赤色を呈するものであるから、本発明においては、これ
らの色の補色に相当するよう色素の種類及び配合量を適
宜定めればよく、青緑色系の色素を必要量使用すればよ
い。色素としては、合成系及び/又は天然系のものが適
宜使用可能である。
The CD inclusion of β-carotene is generally yellow to
Since it exhibits a red color, in the present invention, the type and blending amount of the dye may be appropriately determined so as to correspond to the complementary color of these colors, and the required amount of the blue-green dye may be used. As the dye, synthetic and / or natural dyes can be appropriately used.

【0017】以下、本発明の実施例について述べる。Examples of the present invention will be described below.

【0018】[0018]

【実施例1】α−サイクロデキストリンを約30%含む
サイクロデキストリン粉末400gと水600gを良く
混合し、β−カロチンを800mg添加しホモミキサー
にて約10分高速攪拌する。このとき、3000rpm
程度の条件で攪拌すれば包接物は水系に分散させたとき
赤色を呈する。この時の彩度については、従来からある
β−カロチン製剤と比較すると、3000rpm程度の
条件で攪拌して得た包接物は約3分の1である。このよ
うにして得られたβ−カロチンのCD包接物に、補色に
相当する青緑色の食用色素を補色の関係になるまで添加
混合する。得られたペースト状のβ−カロチンの無彩色
物は、同じくペースト状を呈し、市販のβ−カロチン製
剤の彩度の約5分の1以下の彩度しか示さず、また、乾
燥して粉末状にすることも可能であって、各種の用途に
しかも大量に使用することができる。
Example 1 400 g of cyclodextrin powder containing about 30% of α-cyclodextrin and 600 g of water were mixed well, 800 mg of β-carotene was added, and the mixture was stirred at high speed for about 10 minutes with a homomixer. At this time, 3000 rpm
When stirred under moderate conditions, the clathrate exhibits a red color when dispersed in an aqueous system. Regarding the color saturation at this time, the clathrate obtained by stirring under the condition of about 3000 rpm is about one-third as compared with the conventional β-carotene preparation. A β-carotene CD inclusion thus obtained is added and mixed with a blue-green edible dye corresponding to a complementary color until a complementary color relationship is established. The obtained paste-colored β-carotene achromatic substance also had a paste-like form and exhibited a saturation of about 1/5 or less of that of a commercially available β-carotene preparation, and it was dried and powdered. It can be formed into a shape, and can be used for various purposes and in a large amount.

【0019】[0019]

【発明の効果】本発明のβ−カロチンのサイクロデキス
トリン包接物は、液状、ペースト状、粉末のいずれの最
終形態にでも調製可能で、添加する食品や医薬品等の形
態にあわせて選択することができる。本発明の包接物
は、水系での分散性にすぐれ、且つ彩度がゼロないし非
常に小さくなるので、各種用途に広範に使用することが
できる。
Industrial Applicability The cyclodextrin inclusion complex of β-carotene of the present invention can be prepared in any final form of liquid, paste and powder, and should be selected according to the form of the food or drug to be added. You can The clathrate of the present invention is excellent in dispersibility in an aqueous system and has a saturation of zero or very small, and thus can be widely used for various applications.

【0020】例えば、本発明に係るβ−カロチンの無彩
色物は、β−カロチンが本来有している黄色を呈さない
ので、食品、医薬品その他を着色することなく大量のβ
−カロチンで強化することができるのみでなく、無彩色
のプロビタミンA剤、抗酸化剤、抗癌剤等としての利用
も可能である。さらには強化剤、プロビタミンA剤、あ
るいは抗酸化剤等として使用する際のいずれの場合にお
いても、β−カロチン特有の風味がマスキングされてい
るので添加する対象の食品の風味をそこねることがな
い。
For example, since the achromatic product of β-carotene according to the present invention does not exhibit the yellow color which β-carotene originally has, a large amount of β-carotene can be obtained without coloring foods, pharmaceuticals and the like.
Not only can it be fortified with carotene, but it can also be used as an achromatic provitamin A agent, antioxidant, anticancer agent and the like. Furthermore, in any case when it is used as a fortifier, a provitamin A agent, an antioxidant, etc., the flavor peculiar to β-carotene is masked, so that the flavor of the food to be added is not damaged. .

【図面の簡単な説明】[Brief description of drawings]

【図1】市販β−カロチン製剤と本発明に係るβ−カロ
チンの無彩色化物との彩度の比較図である。
FIG. 1 is a comparison chart of chroma between a commercially available β-carotene preparation and an achromatic product of β-carotene according to the present invention.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 小 松 恵 徳 東京都東村山市栄町1の21の3 明治乳業 株式会社中央研究所内 (72)発明者 山 本 良 郎 東京都東村山市栄町1の21の3 明治乳業 株式会社中央研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Megumi Komatsu 1-21-3, Sakaemachi, Higashimurayama, Tokyo Meiji Dairy Co., Ltd. Central Research Laboratory (72) Ryoro Yamamoto 1-21, Sakaemachi, Higashimurayama, Tokyo No. 3 Meiji Dairy Co., Ltd. Central Research Institute

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 β−カロチンのサイクロデキストリン包
接物にその補色色素を添加してなることを特徴とする水
系での分散性が良好なβ−カロチンの無彩色物。
1. An achromatic product of β-carotene having good dispersibility in an aqueous system, which is obtained by adding a complementary colorant to a cyclodextrin inclusion product of β-carotene.
【請求項2】 α−サイクロデキストリンを含むサイク
ロデキストリン溶液に油状のβ−カロチンを添加し、攪
拌条件をコントロールすることによって彩度の小さい包
接物を調製し、更に彩度を小さくするために該包接物の
補色色素を添加することを特徴とするβ−カロチンの無
彩色物の製造方法。
2. A clathrate having low chroma is prepared by adding oily β-carotene to a cyclodextrin solution containing α-cyclodextrin and controlling stirring conditions to further reduce the chroma. A method for producing an achromatic product of β-carotene, which comprises adding a complementary color dye to the clathrate.
JP3078235A 1991-03-19 1991-03-19 Achromatic color product of beta-carotene and its production Pending JPH0625156A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3078235A JPH0625156A (en) 1991-03-19 1991-03-19 Achromatic color product of beta-carotene and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3078235A JPH0625156A (en) 1991-03-19 1991-03-19 Achromatic color product of beta-carotene and its production

Publications (1)

Publication Number Publication Date
JPH0625156A true JPH0625156A (en) 1994-02-01

Family

ID=13656382

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3078235A Pending JPH0625156A (en) 1991-03-19 1991-03-19 Achromatic color product of beta-carotene and its production

Country Status (1)

Country Link
JP (1) JPH0625156A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5834445A (en) * 1989-08-11 1998-11-10 Sikorski; Christopher Process for preparing decolorized carotenoid-cyclodextrin complexes
JP2002348276A (en) * 2001-05-25 2002-12-04 Fuji Chem Ind Co Ltd Stable astaxanthin-cyclodextrin inclusion compound, production method for the same, and solutions, food and drink, feed, medicinal drugs and cosmetics containing the same
KR20100084970A (en) * 2009-01-19 2010-07-28 리나타에이지 Galvanic element for high stresses
US11419820B2 (en) 2016-03-30 2022-08-23 Riken Vitamin Co., Ltd. Carotenoid-containing particles

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5834445A (en) * 1989-08-11 1998-11-10 Sikorski; Christopher Process for preparing decolorized carotenoid-cyclodextrin complexes
JP2002348276A (en) * 2001-05-25 2002-12-04 Fuji Chem Ind Co Ltd Stable astaxanthin-cyclodextrin inclusion compound, production method for the same, and solutions, food and drink, feed, medicinal drugs and cosmetics containing the same
KR20100084970A (en) * 2009-01-19 2010-07-28 리나타에이지 Galvanic element for high stresses
US11419820B2 (en) 2016-03-30 2022-08-23 Riken Vitamin Co., Ltd. Carotenoid-containing particles

Similar Documents

Publication Publication Date Title
US4263333A (en) Curcumin-metal color complexes
JP3176934B2 (en) Water-dispersible formulations containing hydrophobic natural pigments, their production and use
JP3190465B2 (en) Stable liquid products containing fat-soluble substances
US6500473B1 (en) Coloring substance composition and a method of manufacturing same
EP2176357B1 (en) A colouring composition comprising starch derivatives as a hydrocolloid
JP4673273B2 (en) Water-dispersible oil-soluble dye crystal formulation
JPS62240364A (en) Production of fine granular carotinoid product dispersible in water
WO2009147158A2 (en) Compositions of fat-soluble active ingredients containing gum ghatti
JPH03160946A (en) Norbixin adduct, water-solublr or water-dispersible protein or branched-chain or cyclic polysaccharide
CN113645855A (en) Stabilization of phycocyanin
JPH0625156A (en) Achromatic color product of beta-carotene and its production
JP6078043B2 (en) Water dispersible composition of lycopene crystals
CN103188948A (en) Carotenoid compositions containing octenyl succinate anhydride-modified gum acacia
CN105419390A (en) Natural pigment composition and preparation method thereof
JP6100227B2 (en) Water-dispersible composition of β-carotene crystals
JPH04244059A (en) Cyclodextrin clathrate compound of beta-carotene and its production
US4139645A (en) Coloring agents for edible materials
JP2838051B2 (en) Water-soluble lycopene preparation
US3940504A (en) Oleomargarine with yellow food coloring
CA1054155A (en) Color composition
RU2139935C1 (en) Method of preparing water-soluble vitamin preparation and method of preparing vitamin preparation
Su et al. Microencapsulation to improve the stability of natural pigments and their applications for meat products
CN101616606B (en) Use of water-dispersible carotinoid nanoparticles as taste modulators, taste modulators containing water-dispersible carotinoid nanoparticles, and method for taste modulation
JP2506102B2 (en) Stabilization method of anthocyanin dye
JPH10110109A (en) Monascus color improved in light resistance and improvement of light resistance