JPS60102169A - Carotenoid-containing composition and its production - Google Patents

Carotenoid-containing composition and its production

Info

Publication number
JPS60102169A
JPS60102169A JP58210420A JP21042083A JPS60102169A JP S60102169 A JPS60102169 A JP S60102169A JP 58210420 A JP58210420 A JP 58210420A JP 21042083 A JP21042083 A JP 21042083A JP S60102169 A JPS60102169 A JP S60102169A
Authority
JP
Japan
Prior art keywords
vitamin
carotenoid
carotenoids
carotene
composition
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
JP58210420A
Other languages
Japanese (ja)
Inventor
Akira Kamimura
明 上村
Nobuo Uchiyama
内山 信夫
Takayoshi Mitsunaga
光長 孝義
Hisao Tohiki
戸引 久雄
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP58210420A priority Critical patent/JPS60102169A/en
Publication of JPS60102169A publication Critical patent/JPS60102169A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To produce the titled composition having excellent discoloration stability, and useful as a colorant or a vitamin A source in the form of vitamin A precursor, by dissolving a carotenoid in vitamin E under heating. CONSTITUTION:A carotenoid (e.g. alpha-carotene) is dissolved in vitamin E (e.g. alpha- tocopherol) under heating. If necessary, a solution or dispersion of an antioxidant, a surface active agent, a density modifier, etc. is added to the above mixture, and the product is emulsified or pulverized with an emulsifier such as a homomixer. The produced oil phase of vitamin E containing the carotenoid can be supplied as it is according to the use such as a source of vitamin A or vitamin E, etc., or can be encapsulated to microcapsules.

Description

【発明の詳細な説明】 本発明は、カロチノイド類を含有するヒ゛タミンE組成
物およびその製法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vitamin E composition containing carotenoids and a method for producing the same.

カロチノイド類は、飲食品、医薬品等の着色剤あるいは
ビタミンAr’1illK体としてのビタミンA源とし
て繁用されでいる。しかし、カロチノイド類は水、アル
コ−1し等0)一般的な溶媒【こ1よほとんど溶解せず
、このため使用できろ溶媒#よ限定されざるを得ないの
が現状であった、そのため、従来のカロチノイド類含有
組成物としでは、カロチノイド類を動植物油類(例えば
大豆油、とうもろこし油、なたね油、スクワレン、スク
ワラン、レモン油、オレンジ油等)あるいはハロゲン系
有機溶媒(例えばり[10小ルム、四塩化炭素)等に溶
解し、さらに界面活性剤、高分子物質等を含む水溶液で
乳化するか、または粉末化するなどした組成物が用いら
れていたう このような従来技術においては、例えば動41F(物油
を用いる場合には、そのfI′9Aにもよるが、溶解し
たカロチノイド類の脱色安定性が悪い、特異なにおいが
ある、あるいはカロチノイド類を溶解するに十分な溶解
度がない等の問題があった。また精油類を用いる場合に
は溶)0r時に引火の危険性がある等の安全上の問題が
、F)す、ハロゲン系有機溶媒を用いる場合には溶媒の
残1胃性、製造の際の安全衛生等の問題があり、いずれ
にしてもカロチノイド類を有効に利月4するためには必
ずしも十分満足し得るものでIJなかった。
Carotenoids are frequently used as coloring agents for foods and drinks, medicines, etc., and as a source of vitamin A in the form of vitamin Ar'illK. However, carotenoids are hardly soluble in common solvents such as water and alcohol, and for this reason, the solvents that can be used are limited. In conventional carotenoid-containing compositions, carotenoids are extracted from animal and vegetable oils (e.g., soybean oil, corn oil, rapeseed oil, squalene, squalane, lemon oil, orange oil, etc.) or halogenated organic solvents (e.g., In these conventional techniques, a composition was used, which was dissolved in carbon tetrachloride, etc., and further emulsified or powdered with an aqueous solution containing a surfactant, a polymeric substance, etc. 41F (When using commercial oil, it depends on its fI'9A, but the decolorization stability of the dissolved carotenoids is poor, there is a peculiar odor, or the solubility is not sufficient to dissolve the carotenoids. In addition, when essential oils are used, there are safety issues such as the risk of ignition at zero temperature. However, there were problems with safety and health during production, and in any case, IJ was not always fully satisfactory for effectively converting carotenoids.

かかる状況fに本発明者らは、上述の問題点を解決する
べくカロチノイド類を溶解する溶媒について種々検討を
重ねた結果、カロチノイド類がビタミンEに加熱溶解す
ることを見し)だし、さらに必要に応じて乳化または粉
末化して得られるカロチノイド類含有ビタミノE組成物
は着色剤あるいはビタミンA源としてずぐれt二組酸物
であることを見いだして本発明を完成するに至った、 すなわち、本発明は、カロチノイド類を溶解する溶媒と
しては全く知られていなかったビタミンEにカロチノイ
ド類を溶解させることによ−で得られ颯新規な組成物お
よびその製造方法を機供せんとするものであろう 本発明組成物を製造するには、カロチノイド類をビタミ
ンEに加熱溶解し、必要−こ応してさらに乳化まtごは
粉末化すればよL′″。
In order to solve the above-mentioned problem, the present inventors conducted various studies on solvents for dissolving carotenoids, and found that carotenoids dissolve in vitamin E by heating. The present invention was completed by discovering that the carotenoid-containing vitamin E composition obtained by emulsifying or powdering the carotenoid-containing vitamin E composition as a coloring agent or vitamin A source is a t-group acid. The present invention aims to provide a novel composition obtained by dissolving carotenoids in vitamin E, which has not been known as a solvent for dissolving carotenoids, and a method for producing the same. To produce the wax composition of the present invention, carotenoids are dissolved in vitamin E by heating, and if necessary, the emulsified eggs are further pulverized.

カロチノイド類としては、合成あるL)は天然のび一カ
ロチン、β−カロチン、r−カロチン、カンタキサンチ
ン、ビキシン、エチ」しもしくはメチルビキシン、クリ
プトキサンチン、キサントフィルなど、またはこれらの
ヒドロキシルもしくはカルボキシル誘導体のエステル類
を単独もしくは混合して使用することができる。
Carotenoids include synthetic carotene, β-carotene, r-carotene, canthaxanthin, bixin, methylbixin, cryptoxanthin, xanthophyll, etc., or esters of their hydroxyl or carboxyl derivatives. can be used alone or in combination.

ビタミンEとしては、合成あるいは天然のα−トコフェ
ロール、β−1・コフェロール、2゛−トコフェロール
、δ−トコフ毛ロール、ε−トコフェロール、タートコ
フLロール、q−トコフェロールなどの他、これらと酢
酸、ロハク酸またはニコチン酸等とのエステル類、さら
にはこれらのd 、 /−または(1/、異性体等を単
独もしくは混合して使用することができろ9 ビタミンBに力ローダ−ノイド類をJJll熱溶解する
には、目的とする制剤に合致する濃度になるように適宜
溶解条件を設定すればよい9ビタミンE中のカロチンイ
ド類含111が低ければ低温で、また逆にヒタミノE中
の力ロチノイド類含量が高ければ高温で溶解すればよく
、通常カロチノイド類をビタミンEに対し爪凪比で0.
1〜20%程度になるようにビタミンEを50゛C〜1
60゛′Cに加熱し溶解すればよい。
Examples of vitamin E include synthetic or natural α-tocopherol, β-1-copherol, 2-tocopherol, δ-tocopherol, ε-tocopherol, tartcopherol, q-tocopherol, and the like. Acids or esters with nicotinic acid, etc., and their d, /- or (1/, isomers, etc.) can be used alone or in mixtures. To dissolve, the dissolution conditions should be set appropriately so that the concentration matches the desired drug.9 If the carotenoids in vitamin E are low in 111, the lower the temperature, and vice versa, the lower the carotenoids in vitamin E. If the content of carotenoids is high, it is sufficient to dissolve them at high temperatures.Usually, carotenoids have a ratio of 0.0 to vitamin E.
Add vitamin E to 50°C to 1 to 20%.
It can be dissolved by heating to 60'C.

まtこカロチノイド類を溶解した該ビタミンE111に
はさらに必要に応じて他の成分、例えばBUT、B I
(A、没食子酸もしくはアスコルビン酸のエステル類、
エリソルビン酸、アスコルビン酸、没食子酸、フィチン
酸クリシン等の天然まtこは合成の抗酸化剤:ゼラチン
、ショ糖脂肪酸エステル、グリセリン脂肪酸エステル、
ソルビタン脂肪酸エステル、プロピレングリコール脂肪
酸エステル、アラビアガム、グアーガム、トラガントガ
ム等の界面活性剤;グリセリン、プロピレングリコール
、ソルビ・・lト等の比重調整剤;レシチン又は/及び
ポリグリセリン脂肪酸エステル等が適宜含有されていて
もよい。
The vitamin E111 in which carotenoids are dissolved may further contain other ingredients as necessary, such as BUT, B I
(A, esters of gallic acid or ascorbic acid,
Natural and synthetic antioxidants such as erythorbic acid, ascorbic acid, gallic acid, chrysin phytate, gelatin, sucrose fatty acid ester, glycerin fatty acid ester,
Surfactants such as sorbitan fatty acid ester, propylene glycol fatty acid ester, gum arabic, guar gum, and gum tragacanth; density regulators such as glycerin, propylene glycol, and sorbitan; lecithin and/or polyglycerin fatty acid ester, etc. may be appropriately contained. You can leave it there.

このように調製したカロチノイド類等を含むビタミンE
の油相は着色剤、ビタミンA源あるいはビタミンE源等
の使用目的に応じ、このままで供することもでき、また
マイクロカプセル化あるいはソフトカプセル化すること
もできる。
Vitamin E containing carotenoids etc. prepared in this way
The oil phase can be provided as it is or can be encapsulated into microcapsules or soft capsules depending on the intended use as a coloring agent, a source of vitamin A or a source of vitamin E, etc.

さらにはカロチノイド類等を含むビタミンEの油相は水
相成分、例えば水に前記の一般的な天然または合成の抗
酸化剤、界面活性剤または比重調製剤等を適宜必要に応
じて溶解もしくは分散したものと混合し、ホモミキサー
、ホモジナイザー等の乳化分散機を用いて公知の方法に
より乳化、分散させて0/W型エマルジヨンとすること
もできる。またこの0/W型エマルジヨンはさらに粉末
化が可能になるように設定した組成によりスプレードラ
イ、凍結乾繰等の従来技術により粉末化することもでき
る。
Furthermore, the oil phase of vitamin E, which contains carotenoids, etc., is prepared by dissolving or dispersing the above-mentioned general natural or synthetic antioxidants, surfactants, specific gravity adjusting agents, etc. in water phase components, for example, water as appropriate. It is also possible to prepare an 0/W type emulsion by mixing the mixture with the above-mentioned mixture and emulsifying and dispersing it by a known method using an emulsifying and dispersing machine such as a homomixer or a homogenizer. Further, this O/W type emulsion can be further pulverized by conventional techniques such as spray drying and freeze-drying, depending on the composition set to enable pulverization.

以上に説明したように、本発明組成物は従来技術による
組成物に比べてはるかに脱色安定性にすぐれており、着
色剤あるいはビタミンA nil枢体としてのビタミン
A源としてずぐれた組成物である。また溶媒であるビタ
ミンEの栄N源としての利用をはかれろ点でもa川な組
成物である。
As explained above, the composition of the present invention has far superior decolorization stability compared to compositions according to the prior art, and is an excellent composition as a coloring agent or a source of vitamin A as a vitamin A nil receptor. be. It is also an excellent composition in terms of the use of vitamin E, which is a solvent, as a source of energy and N.

次に本発明を実施例によりさらに詳細に説明する。Next, the present invention will be explained in more detail with reference to Examples.

実施例1 酢酸dt−α−トコフエU−ル40部にβ−カロチン結
晶1部を加え、かくは/シシながら約100°”Cに加
熱した。、1時間後、β−カロチンは完全に溶解し、こ
れを室温まで冷却しても結晶は析出せず、赤色油状のβ
−カロチン−ビタミンE製剤を得た。
Example 1 1 part of β-carotene crystals was added to 40 parts of dt-α-tocopheryl acetate and heated to about 100°C while stirring/swinging. After 1 hour, β-carotene was completely dissolved. However, even if this was cooled to room temperature, no crystals precipitated, and a red oily β
- A carotene-vitamin E preparation was obtained.

実施例2 酢酸dz−α−1・コフ工ロール9部にβ−カロチン結
晶1部を加え、かくはノししながら約120℃に加熱し
たう 1時間後、β−カロチンは完全に溶解しこれを室
温まで冷却しても結晶は析出せず、暗赤色油状のβ−カ
ロチン−ビタミンE組成物を得t:。
Example 2 1 part of β-carotene crystals was added to 9 parts of dz-α-1 acetate and cofferol, and the mixture was stirred and heated to about 120°C. After 1 hour, the β-carotene was completely dissolved. Even when this was cooled to room temperature, no crystals were precipitated, and a dark red oily β-carotene-vitamin E composition was obtained.

実施例8 実施例1のβ−カロチン−ビタミンE組成物4.10f
に大豆レシチン10fおよびソルビタン脂肪酸エステル
5gを加え120°Cで加熱溶解し、他方水455gに
ショ糖脂肪酸エステル20g、グリ−1!リンl 00
9を溶解し両液をホモジナイザーで乳化して橙色の乳剤
を得た、この乳剤を水に分11(シた液は分1敗性およ
び色調安定性にすぐれていた。
Example 8 β-carotene-vitamin E composition 4.10f of Example 1
10 f of soybean lecithin and 5 g of sorbitan fatty acid ester were added and dissolved by heating at 120°C, and on the other hand, 20 g of sucrose fatty acid ester was added to 455 g of water, and Gly-1! Lin 00
9 was dissolved and both liquids were emulsified with a homogenizer to obtain an orange emulsion. This emulsion was divided into water (11) (The resulting liquid had excellent stain resistance and color stability.

実施例4 天然ビタミンE90yにグリセリン脂肪酸エステル2g
およびβ−カロヂン415−1.IIIえ、130°C
でβ−カロチンを加熱溶解しtこ溶液15部と他方水7
00gにアシド1ガム140f1デキストリン140f
、ショ糖11N l1lj 酸エステルlOfおよびポ
リグリ士リンnN肪酌j−ステル(IJLB 12)1
0fを溶解した溶液85部の両液をホモジナイザーで乳
化し、この0//Vv型エマルシヨンをスプレードライ
(7て橙色の粉末とした。この粉末は天然ビタミンE約
85 % (W / W ) I −力04− ン約1
.5%(W/W)を含み水に容易に分散、乳化させるこ
とができたう
Example 4 Natural vitamin E90y and glycerin fatty acid ester 2g
and β-carodin 415-1. III, 130°C
Heat and dissolve β-carotene in 15 parts of this solution and 7 parts of water on the other hand.
00g 1 acid 1 gum 140f 1 dextrin 140f
, sucrose 11N l1lj acid ester lOf and polyglycerin nN fatty acid ester (IJLB 12) 1
Both solutions (85 parts of the solution containing 0f) were emulsified using a homogenizer, and this 0//Vv type emulsion was spray-dried (7 steps) to form an orange powder. This powder contains about 85% (W/W) I of natural vitamin E. -Force 04- About 1
.. Contains 5% (W/W) and can be easily dispersed and emulsified in water.

Claims (2)

【特許請求の範囲】[Claims] (1) カロチノイド類を含有するビタミンE組成物う(1) Vitamin E composition containing carotenoids (2) カロチノイドをビタミンEに加熱溶解し、必要
に応じてさらに乳化または粉末化することを特徴とする
カロチノイド類含有ビタミンE組成物の製法。
(2) A method for producing a carotenoid-containing vitamin E composition, which comprises heating and dissolving carotenoids in vitamin E, and further emulsifying or powdering as necessary.
JP58210420A 1983-11-08 1983-11-08 Carotenoid-containing composition and its production Pending JPS60102169A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58210420A JPS60102169A (en) 1983-11-08 1983-11-08 Carotenoid-containing composition and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58210420A JPS60102169A (en) 1983-11-08 1983-11-08 Carotenoid-containing composition and its production

Publications (1)

Publication Number Publication Date
JPS60102169A true JPS60102169A (en) 1985-06-06

Family

ID=16589014

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58210420A Pending JPS60102169A (en) 1983-11-08 1983-11-08 Carotenoid-containing composition and its production

Country Status (1)

Country Link
JP (1) JPS60102169A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5234702A (en) * 1992-03-19 1993-08-10 Abbott Laboratories Antioxidant system for powdered nutritional products
JPH05505935A (en) * 1990-02-05 1993-09-02 ボード オブ リージェンツ,ザ ユニバーシティ オブ テキサス システム Extended release formulation of vitamins, minerals and other beneficial supplements
US5780056A (en) * 1996-05-10 1998-07-14 Lion Corporation Microcapsules of the multi-core structure containing natural carotenoid
JP2002171921A (en) * 2000-12-11 2002-06-18 T Hasegawa Co Ltd New powder material
WO2006030850A1 (en) * 2004-09-15 2006-03-23 San-Ei Gen F.F.I., Inc. Method of preparing solution of lipid-soluble ingredient
US8188406B2 (en) 2006-03-30 2012-05-29 Panasonic Corporation Steering wheel planar heat generating element

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05505935A (en) * 1990-02-05 1993-09-02 ボード オブ リージェンツ,ザ ユニバーシティ オブ テキサス システム Extended release formulation of vitamins, minerals and other beneficial supplements
US5234702A (en) * 1992-03-19 1993-08-10 Abbott Laboratories Antioxidant system for powdered nutritional products
US5780056A (en) * 1996-05-10 1998-07-14 Lion Corporation Microcapsules of the multi-core structure containing natural carotenoid
JP2002171921A (en) * 2000-12-11 2002-06-18 T Hasegawa Co Ltd New powder material
WO2006030850A1 (en) * 2004-09-15 2006-03-23 San-Ei Gen F.F.I., Inc. Method of preparing solution of lipid-soluble ingredient
JPWO2006030850A1 (en) * 2004-09-15 2008-05-15 三栄源エフ・エフ・アイ株式会社 Method for preparing solubilized product of fat-soluble component
US8188406B2 (en) 2006-03-30 2012-05-29 Panasonic Corporation Steering wheel planar heat generating element

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