JPS6211541A - Oil-in-water type emulsion - Google Patents

Oil-in-water type emulsion

Info

Publication number
JPS6211541A
JPS6211541A JP60148397A JP14839785A JPS6211541A JP S6211541 A JPS6211541 A JP S6211541A JP 60148397 A JP60148397 A JP 60148397A JP 14839785 A JP14839785 A JP 14839785A JP S6211541 A JPS6211541 A JP S6211541A
Authority
JP
Japan
Prior art keywords
saponin
oil
water
organic solvent
hydrophilic organic
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
JP60148397A
Other languages
Japanese (ja)
Inventor
Susumu Ogawa
進 小川
Fumikazu Murakami
村上 文和
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.)
Maruzen Kasei Co Ltd
Original Assignee
Maruzen Kasei 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 Maruzen Kasei Co Ltd filed Critical Maruzen Kasei Co Ltd
Priority to JP60148397A priority Critical patent/JPS6211541A/en
Publication of JPS6211541A publication Critical patent/JPS6211541A/en
Pending legal-status Critical Current

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  • Colloid Chemistry (AREA)
  • Edible Oils And Fats (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Abstract

PURPOSE:To increase the emulsion stability by emulsifying an oil phase component with the purified saponin obtained by on a synthetic high molecular adsorbent and deadsorbing this saponin with a hydrated hydrophilic organic solvent. CONSTITUTION:An extract contg. saponin is obtained by extracting a bark of Quillaja.saponalia or a pericarp of Sapindus mukurossi with water or a hydrated hydrophilic organic solvent. After treating this extract with a synthetic high molecular adsorbent, purified saponin is obtained by deadsorbing this saponin adsorbed on the high molecular adsorbent with the hydrated hydrophilic organic solvent. While stirring strongly the aq. soln. of the purified saponin, fat and oil are slowly added therein to emulsify the mixture and this is treated with a homogenizer or the like to prepare an oil-in-water type emulsion. As the above-mentioned hydrated hydrophilic organic solvent, ethanol and acetone, etc. are used and polyacrylic acid ester series are used as the synthetic high molecular adsorbent.

Description

【発明の詳細な説明】 本発明は、安定性のよい水中油型乳化物に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a highly stable oil-in-water emulsion.

鵞迷り共宛 キラヤ・サポナリア(Quillaia 5apona
ria MoLバラ科)の樹皮やムクロジ(Sapin
dus mukurossi GAERTNER+ムク
ロジ科)の果皮に含まれているサポニンは、その起泡力
を利用して、早くから洗剤、洗髪剤、セッケン代用品と
して用いられており、また、その乳化作用を利用して、
写真感光材料の乳液やシアシフピー用紙用の感剤乳液を
作るのに用いられてきた。そして近年、天然の界面活性
物質が安全性の点で合成物質よりも有利なことが認識さ
れるにつれて、サポニンも食品、化粧品、医薬品等のた
めの乳化剤として広く利用されるようになった。
Quillaia saponaria (to the strays)
ria MoL (Rosaceae) and the bark of Sapin (Sapin).
saponin contained in the pericarp of dus mukurossi GAERTNER + Sapindaceae) has been used as detergents, hair washes, and soap substitutes since early on by taking advantage of its foaming power.
It has been used to make emulsions for photographic materials and emulsions for sheet paper. In recent years, saponins have also come to be widely used as emulsifiers for foods, cosmetics, pharmaceuticals, etc., as it has been recognized that natural surfactants are more advantageous than synthetic substances in terms of safety.

しかしなが呟上述のようなサポニン含有物質を水やアル
コールで抽出して得られた抽出物は、サポニンのほかに
タンパク質、糖類、アミノ酸、タンニン、黒磯塩類等、
多くの生体成分を含有するか呟抽出物を充分精製するこ
となく乳化剤として使用した場合は、反応性の強いタン
ニンや黒磯塩類等が乳化物の安定性を悪くする。このた
め、乳化剤に用いるサポニンとしては、なんらかの方法
で精製したものを用いるのが普通である。従来、キラヤ
樹皮やムクロジ果皮から得られたサポニン含有抽出液を
精製する方法としては、エーテル等を用いた溶媒沈殿を
繰返す方法、アルコール溶液から沈殿させる方法、活性
炭で処理する方法などがあるが、これらの精製法によっ
ては、乳化の安定性を損なう上記不純物を充分除去する
ことができなかった。したがって、精製サポニンを用い
た場合においても、サポニンを乳化剤とする乳化物の安
定性は多くの用途において不充分なものであった。
However, the extract obtained by extracting the saponin-containing substances mentioned above with water or alcohol contains, in addition to saponins, proteins, sugars, amino acids, tannins, Kuroiso salts, etc.
If the extract containing many biological components is used as an emulsifier without sufficient purification, highly reactive tannins and Kuroiso salts will deteriorate the stability of the emulsion. For this reason, saponins used in emulsifiers are usually purified by some method. Conventional methods for purifying saponin-containing extracts obtained from Quillaja bark and Sapindica peel include repeated solvent precipitation using ether, precipitation from an alcohol solution, and treatment with activated carbon. These purification methods have not been able to sufficiently remove the impurities that impair emulsion stability. Therefore, even when purified saponin is used, the stability of emulsions containing saponin as an emulsifier is insufficient for many applications.

発明が解決しようとする問題点 本発明の目的は、上述のような欠点のな51精製サポニ
ンによる水中油型乳化物を提供することにある。
Problems to be Solved by the Invention The object of the present invention is to provide an oil-in-water emulsion of purified saponin 51 that does not have the above-mentioned drawbacks.

問題点を解決するための手段 上記目的を達成することに成功した本発明の水中油型乳
化物は、キラヤ・サポナリアの樹皮またはムクロジの果
皮を水もしくは含水親水性有機溶媒で抽出して得られた
サポニン含有抽出物を合成高分子吸着体で処理し、該高
分子吸着体に吸着されたサポニンを含水親水性有機溶媒
で脱着させるという新規な精製法によって得られた精製
サポニンにより油相成分が乳化されてなるものである。
Means for Solving the Problems The oil-in-water emulsion of the present invention, which has succeeded in achieving the above objects, is obtained by extracting the bark of Quillaja saponaria or the pericarp of Sapindica with water or a hydrophilic organic solvent containing water. The purified saponin obtained by a new purification method involves treating a saponin-containing extract with a synthetic polymer adsorbent and desorbing the saponin adsorbed to the polymer adsorbent with a water-containing hydrophilic organic solvent. It is made by emulsification.

本発明の乳化物のためのサポニンの精製法の詳細は次の
とおりである。まず常法によりサポニン含有樹皮もしく
は果皮の破砕物を水または含水親水性有機溶媒(たとえ
ばエタノール、アセトン、プロピルアルコール等)で抽
出処理し、サポニンを含有する抽出液を得る。得られた
抽出液は、有機溶媒を含む場合は溶媒を留去したのち、
合成高分子吸着体(たとえばスチレン・ジビニルベンゼ
ン共重合体系のもの、ポリアクリル酸エステル系のもの
など)に接触させてサポニンを吸着させる。抽出液と吸
着体とを接触させる方法は、バッチ法とカラム法のいず
れでも差支えない。抽出液中のサポニンのすべてを吸着
させるのに必要な吸着体量は吸着体の種類によって異な
るが、通常、原料のキラヤ樹皮またはムクロジ果皮の重
量の0.5〜10倍量である6サボニンを吸着した吸着
体をよく水洗したのち、含水親水性有機溶媒(たとえば
30〜80重景%の重量エタノール)と接触させると、
サポニンが脱着されてくるので、脱着液を集めて溶媒を
除いたのち乾燥すれば、淡褐色の精製サポニンが得られ
る。なお、吸着体にはサポニン以外の生体成分が一部吸
着され、それが上記肌着処理により肌着される。脱着処
理前に吸着体をアルカリ水溶液と接触させると、サポニ
ンは脱着されずにサポニン以外の上記生体成分が肌着さ
れるので、このアルカリ水溶液処理を施したのちサポニ
ンの肌着を行えば、より高純度で着色も少ないサポニン
を得ることができる。
Details of the saponin purification method for the emulsion of the present invention are as follows. First, crushed saponin-containing bark or pericarp is extracted with water or a water-containing hydrophilic organic solvent (eg, ethanol, acetone, propyl alcohol, etc.) by a conventional method to obtain a saponin-containing extract. If the obtained extract contains an organic solvent, the solvent is distilled off, and then
Saponin is adsorbed by contacting with a synthetic polymer adsorbent (eg, styrene/divinylbenzene copolymer type, polyacrylic acid ester type, etc.). The method for bringing the extract into contact with the adsorbent may be either a batch method or a column method. The amount of adsorbent required to adsorb all of the saponins in the extract varies depending on the type of adsorbent, but usually 6-saponin is used in an amount of 0.5 to 10 times the weight of Quillaja bark or Sapindica peel as the raw material. After thoroughly washing the adsorbed adsorbent with water, when it is brought into contact with a water-containing hydrophilic organic solvent (for example, 30-80% weight ethanol),
As the saponin is desorbed, by collecting the desorption liquid, removing the solvent, and drying it, a light brown purified saponin can be obtained. In addition, some biological components other than saponin are adsorbed to the adsorbent, which is then worn on the skin through the above-mentioned underwear treatment. If the adsorbent is brought into contact with an alkaline aqueous solution before the desorption treatment, the saponin will not be desorbed and the above biological components other than saponin will be attached to the skin, so if saponin is attached after the alkaline aqueous solution treatment, higher purity can be obtained. You can obtain saponin with less coloring.

上述のようにして得られる精製サポニンを乳化剤に用い
て本発明の水中油型乳化物を製造する方法は任意である
が、通常は、上記精製サポニンの水溶液を強攪拌しなが
らその中に油脂を徐々に加えて乳化し、更にホモジナイ
ザー等で処理して油滴の微細化と均一化を行うことが望
ましい。
The method for producing the oil-in-water emulsion of the present invention using the purified saponin obtained as described above as an emulsifier is arbitrary, but usually, fats and oils are added to the aqueous solution of the purified saponin with strong stirring. It is desirable to gradually add the oil to emulsify it, and then further treat it with a homogenizer or the like to make the oil droplets fine and uniform.

本発明の水中油型乳化物における乳化剤は、キラヤサポ
ニンおよびムクロジサポニンの単独ま、たは混合物のほ
か、これらと他の乳化剤(たとえばレシチン、シシ糖脂
肪酸エステル、グリセリン脂肪酸エステル、タウロコー
ル酸、タン汁酸等)との併用であってもよい。また本発
明の乳化物には、アラビアガム、キサンタンガム、プル
ラン等の多糖類やタンパク質などを安定剤として含有さ
せることができる。
The emulsifier in the oil-in-water emulsion of the present invention includes Quillajasaponin and Muclodisaponin alone or in a mixture, as well as other emulsifiers (for example, lecithin, sucrose fatty acid ester, glycerin fatty acid ester, taurocholic acid, tongue juice). (acids, etc.) may be used in combination. The emulsion of the present invention can also contain polysaccharides such as gum arabic, xanthan gum, pullulan, and proteins as stabilizers.

本発明の水中油型乳化物に含有させる油脂の種類に特に
制限はなく、豚脂、牛脂、大豆油、オリーブ油、コーン
油、ミツロウ、米ヌカ油、スクワランなどの動植物性油
脂のほか、脂溶性ビタミン、各種鉱物油などであり得る
There is no particular restriction on the type of fats and oils contained in the oil-in-water emulsion of the present invention, including animal and vegetable oils such as pork tallow, beef tallow, soybean oil, olive oil, corn oil, beeswax, rice bran oil, and squalane, as well as fat-soluble fats and oils. It can be vitamins, various mineral oils, etc.

本発明の水中油型乳化物は、乳化された油脂のほかにも
、その安定性を着しく損なわない限り、任意の物質を含
有させることができる。したがって本発明の水中油型乳
化物は、食品、化粧品、医薬品、その池各種の油脂製品
およびそれらの原料の形態をとることができる。
The oil-in-water emulsion of the present invention may contain any other substance in addition to the emulsified fat or oil, as long as the stability thereof is not seriously impaired. Therefore, the oil-in-water emulsion of the present invention can take the form of foods, cosmetics, pharmaceuticals, various oil and fat products, and raw materials thereof.

作用・効果 本発明の水中油型乳化物が乳化剤として含有する精製サ
ポニンは、従来この種の乳化物製造に使われてきたサポ
ニンに比べて、乳化安定性を悪くするタンニンおよび無
機塩類の含有率が低いという特長を持つ。したがって、
本発明による水中油型乳化物は長期間保存しても油層の
分離を示すことがなく、耐熱性、耐酸性にもすぐれてい
る。
Action/Effect The refined saponin that the oil-in-water emulsion of the present invention contains as an emulsifier has a lower content of tannins and inorganic salts that deteriorate emulsion stability than saponins conventionally used in the production of this type of emulsion. It has the feature of low therefore,
The oil-in-water emulsion according to the present invention does not show separation of the oil layer even when stored for a long period of time, and has excellent heat resistance and acid resistance.

医鳳倒 以下、実施例および比較例を示して本発明を説明する。medicine phoenix The present invention will be described below with reference to Examples and Comparative Examples.

実施例 1 キラヤ樹皮破砕物1kgに水10eを加え、70℃に加
温して2時間撹拌抽出した。抽出液をデカンテーシヨン
で採取し、更に水10eを用いて同じ抽出繰作を繰返し
て、抽出液合計16eを得た。ろ過して固形物を除いた
のち、この抽出液を合成高分子吸着体・ダイヤイオンH
P−20(三菱化成)2eを充填したカラムに空間速度
1e/Ltlrで供給した。この後、カラムを4Qの0
.03%アンモニア水で洗浄し、さらに水洗した。次い
で、60%エタノール10eを空間速度IQ/Q・Hr
で流してサポニンを肌着させ、脱着液を減圧下に濃縮乾
固して淡褐色の精製サポニン92gを得た。この精製サ
ポニンは、タンニン含有率6.4%、灰分2.8%、2
価金属(Mg+Ca)含有率1,960pp111のも
のであった。
Example 1 10 e of water was added to 1 kg of Quillaja bark crushed material, heated to 70° C., and extracted with stirring for 2 hours. The extract was collected by decantation, and the same extraction procedure was repeated using 10e of water to obtain a total of 16e of extract. After filtering to remove solid matter, this extract is treated with a synthetic polymer adsorbent, Diaion H.
It was supplied to a column packed with P-20 (Mitsubishi Kasei) 2e at a space velocity of 1e/Ltlr. After this, change the column to 4Q's 0
.. The sample was washed with 3% ammonia water and then with water. Next, 60% ethanol 10e was added to the space velocity IQ/Q・Hr
The desorbed solution was concentrated to dryness under reduced pressure to obtain 92 g of light brown purified saponin. This purified saponin has a tannin content of 6.4%, an ash content of 2.8%, and a
The valence metal (Mg+Ca) content was 1,960 pp111.

上記精製サポニン1gを20%の液糖100gに溶解し
て60℃に加温し、4000rpmのホモミキサーで撹
拌しながら、ここに60℃の綿実サラダ油100gを滴
下し、さらに8000rpmで2分間攪拌して乳化させ
た。得られた乳化物は、30℃で放置した場合、1週間
以上安定な乳化状態を維持した。
Dissolve 1 g of the above purified saponin in 100 g of 20% liquid sugar, warm to 60°C, and while stirring with a homomixer at 4000 rpm, dropwise add 100 g of cottonseed salad oil at 60°C, and further stir for 2 minutes at 8000 rpm. and emulsified. The obtained emulsion maintained a stable emulsified state for more than one week when left at 30°C.

比較例 1 実施例1の場合と同様にして得られたキラヤ樹皮抽出液
3゜30を200m1に濃縮し、これにエタノール80
0輸1を加えてサポニンを沈殿させた。沈殿物をろ取し
、減圧下に乾燥し、13gの褐色粉末状精製サポニンを
得た。この精製サポニンは、タンニン含有率13.2%
、灰分10.8%、2価金属含有率19vllOppm
のものであった。
Comparative Example 1 3.30 ml of Quillaja bark extract obtained in the same manner as in Example 1 was concentrated to 200 ml, and 80 ml of ethanol was added to it.
0 and 1 were added to precipitate saponin. The precipitate was collected by filtration and dried under reduced pressure to obtain 13 g of brown powdered purified saponin. This purified saponin has a tannin content of 13.2%.
, ash content 10.8%, divalent metal content 19vllOppm
It belonged to

上記精製サポニン1gを用いて実施例1の場合と同様の
繰作により乳化物を作り、30℃で放置したところ、4
日目に乳化系が破壊した。
Using 1 g of the above purified saponin, an emulsion was prepared in the same manner as in Example 1 and left at 30°C.
The emulsification system was destroyed on the first day.

実施例 2 ムクロジ果皮1kgに80%エタノール10eを加え、
2時間還流抽出を行なった。抽出液をデカンテーション
で採取し、更に水10eを用いて同じ抽出操作を繰返し
て、抽出液合計18.5 gを得た。減圧下に加熱して
エタノールを留去し、残液260+nlに水5Cを加え
たものを合成高分子吸着体・アンバーライトXAD−7
(ロームアンドハース)3Cを充填したカラムに空間速
度1e/LHrで供給した。この後、カラムを109の
水で洗浄してから50%エタノール15Qを空間速度I
Q/Q−Hrで流してサポニンを肌着させ、脱着液を減
圧下に濃縮乾固して淡褐色の精製サポニン123gを得
た。
Example 2 Add 10e of 80% ethanol to 1kg of Sapindica peel,
Reflux extraction was performed for 2 hours. The extract was collected by decantation, and the same extraction operation was repeated using 10e of water to obtain a total of 18.5 g of extract. Ethanol was distilled off by heating under reduced pressure, and 5C of water was added to the residual liquid (260+nl) to prepare a synthetic polymer adsorbent, Amberlite XAD-7.
(Rohm and Haas) 3C was supplied to a column packed at a space velocity of 1e/LHr. After this, the column was washed with 109 water and then 50% ethanol 15Q was added at a space velocity I
The saponin was deposited on the skin by flowing with Q/Q-Hr, and the desorption solution was concentrated to dryness under reduced pressure to obtain 123 g of light brown purified saponin.

上記精製サポニン5gを50%液糖100gに溶解した
液に、ポリグリセリン脂肪酸エステル(サンプ7)Q−
17F;太陽化学株式会社製品)Igを加え、60℃に
加温してホモミキサーで撹拌した。次いでイーミックス
80(天然トコフェロール80%含有製剤;エーザイ株
式会社製品)Igを加え、ホモミキサー(8000rp
m)で2分間撹拌して乳化させた。
Polyglycerin fatty acid ester (Samp 7) Q-
17F; Taiyo Kagaku Co., Ltd. product) Ig was added, heated to 60°C, and stirred with a homomixer. Next, Emix 80 (preparation containing 80% natural tocopherol; manufactured by Eisai Co., Ltd.) Ig was added, and a homomixer (8000 rpm) was added.
m) for 2 minutes to emulsify.

得られた乳化物は、クエン酸でpHを4に調整し沸騰水
浴中で15分間加熱しても安定であった。
The resulting emulsion was stable even after adjusting the pH to 4 with citric acid and heating in a boiling water bath for 15 minutes.

比較例 2 実施例2の場合と同様にしてムクロジ果皮200gより
抽出液3.5eを得、エタノールを留去した。残液18
0m1に900IIllの7七トンを加え、生じた沈殿
物をろ取して減圧乾燥し、24gの黄褐色粉末状の精製
サポニンを得た。
Comparative Example 2 Extract 3.5e was obtained from 200 g of Sapindica pericarp in the same manner as in Example 2, and ethanol was distilled off. Residual liquid 18
77 tons of 900 IIll was added to 0 ml, and the resulting precipitate was collected by filtration and dried under reduced pressure to obtain 24 g of purified saponin in the form of a yellowish brown powder.

上記精製サポニン10gを用い、実施例2の場合と同様
の操作でイーミックス80の乳化を行なった。これによ
り乳白色の乳化物が得られたが、クエン酸でpHを4に
調整し沸騰水浴中で加熱したところ、5分間で乳化が破
壊した。
Emix 80 was emulsified in the same manner as in Example 2 using 10 g of the purified saponin. A milky white emulsion was obtained, but when the pH was adjusted to 4 with citric acid and heated in a boiling water bath, the emulsion was destroyed in 5 minutes.

実施例 3 実施例1および2で得られた精製サポニンを用いて、下
記!It成の水中油型乳化物を調製した。
Example 3 Using the purified saponins obtained in Examples 1 and 2, the following! An oil-in-water emulsion was prepared.

75%異性化液糖    35g 精製サポニン      15g 大豆レシチン      20g オリーブ油       30g 得られtこ乳化物はいずれも透明で、沸騰水浴中で30
分間加熱しても乳化の破壊は起こらなかった。また、こ
れを水で500倍に希釈したものは、透明感ある乳白色
の藁で、クエン酸でpHを4に調整し90℃に加熱して
も30分間安定であった。
75% high-fructose corn syrup 35g Refined saponin 15g Soybean lecithin 20g Olive oil 30g The resulting emulsions were all transparent and boiled in a boiling water bath for 30 g.
No breakage of the emulsion occurred even after heating for minutes. Further, when this was diluted 500 times with water, it was a transparent milky white straw that was stable for 30 minutes even after adjusting the pH to 4 with citric acid and heating to 90°C.

比較例 3 比較例1および2で得られた精製サポニンを用いて、実
施例3の場合と同じ組成の水中油型乳化物を調製した。
Comparative Example 3 Using the purified saponins obtained in Comparative Examples 1 and 2, an oil-in-water emulsion having the same composition as in Example 3 was prepared.

得られた乳化物はいずれも乳白色で、沸騰水浴中で30
分間加熱したところ油水分離が起こり、乳化は破壊した
All the emulsions obtained were milky white and heated in a boiling water bath for 30 minutes.
When heated for a minute, oil-water separation occurred and the emulsification was destroyed.

Claims (2)

【特許請求の範囲】[Claims] (1)キラヤ・サポナリアの樹皮またはムクロジの果皮
を水もしくは含水親水性有機溶媒で抽出して得られたサ
ポニン含有抽出物を合成高分子吸着体で処理し、該高分
子吸着体に吸着されたサポニンを含水親水性有機溶媒で
脱着させることにより得られた精製サポニンにより油相
成分が乳化されてなる水中油型乳化物。
(1) A saponin-containing extract obtained by extracting the bark of Quillaja saponaria or the pericarp of Sapindica with water or a hydrophilic organic solvent containing water is treated with a synthetic polymer adsorbent, and the saponin-containing extract is adsorbed on the polymer adsorbent. An oil-in-water emulsion in which an oil phase component is emulsified with purified saponin obtained by desorbing saponin with a water-containing hydrophilic organic solvent.
(2)精製サポニンが、脱着処理前にアルカリ水溶液で
洗浄した合成高分子吸着体より脱着されたものである特
許請求の範囲第1項記載の水中油型乳化物。
(2) The oil-in-water emulsion according to claim 1, wherein the purified saponin is desorbed from a synthetic polymer adsorbent that has been washed with an alkaline aqueous solution before desorption treatment.
JP60148397A 1985-07-08 1985-07-08 Oil-in-water type emulsion Pending JPS6211541A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60148397A JPS6211541A (en) 1985-07-08 1985-07-08 Oil-in-water type emulsion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60148397A JPS6211541A (en) 1985-07-08 1985-07-08 Oil-in-water type emulsion

Publications (1)

Publication Number Publication Date
JPS6211541A true JPS6211541A (en) 1987-01-20

Family

ID=15451866

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60148397A Pending JPS6211541A (en) 1985-07-08 1985-07-08 Oil-in-water type emulsion

Country Status (1)

Country Link
JP (1) JPS6211541A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63157934A (en) * 1986-12-20 1988-06-30 Nippon Oil & Fats Co Ltd O/w-type emulsion composition
ES2259935A1 (en) * 2005-04-15 2006-10-16 Alfonso Iglesias Garcia Cosmetic basal formula based on killay and jaboncillo along with romero, tomillo and salvia, obtaining procedure and uses of this formula in soap products, perfumery and cosmetics. (Machine-translation by Google Translate, not legally binding)
ES2259933A1 (en) * 2005-04-14 2006-10-16 Alfonso Iglesias Garcia Production of extract rich in quillaia and soapberry saponins combined with rosemary, sage and thyme
US8318233B2 (en) 2010-03-26 2012-11-27 Corn Products Development Inc Emulsions useful in beverages
JP2017048143A (en) * 2015-09-02 2017-03-09 株式会社 わかさ生活 Oil-in-water type emulsion composition blended with essential oil, and method of producing the same
JP2020022387A (en) * 2018-08-07 2020-02-13 国立大学法人 香川大学 Emulsified euphausiapacifica oil
CN114540045A (en) * 2022-01-26 2022-05-27 中国科学院兰州化学物理研究所 Soapberry modified attapulgite and preparation method of O/W type Pickering emulsion of plant essential oil of soapberry modified attapulgite

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63157934A (en) * 1986-12-20 1988-06-30 Nippon Oil & Fats Co Ltd O/w-type emulsion composition
ES2259933A1 (en) * 2005-04-14 2006-10-16 Alfonso Iglesias Garcia Production of extract rich in quillaia and soapberry saponins combined with rosemary, sage and thyme
ES2259935A1 (en) * 2005-04-15 2006-10-16 Alfonso Iglesias Garcia Cosmetic basal formula based on killay and jaboncillo along with romero, tomillo and salvia, obtaining procedure and uses of this formula in soap products, perfumery and cosmetics. (Machine-translation by Google Translate, not legally binding)
US8318233B2 (en) 2010-03-26 2012-11-27 Corn Products Development Inc Emulsions useful in beverages
JP2017048143A (en) * 2015-09-02 2017-03-09 株式会社 わかさ生活 Oil-in-water type emulsion composition blended with essential oil, and method of producing the same
JP2020022387A (en) * 2018-08-07 2020-02-13 国立大学法人 香川大学 Emulsified euphausiapacifica oil
CN114540045A (en) * 2022-01-26 2022-05-27 中国科学院兰州化学物理研究所 Soapberry modified attapulgite and preparation method of O/W type Pickering emulsion of plant essential oil of soapberry modified attapulgite
CN114540045B (en) * 2022-01-26 2022-10-28 中国科学院兰州化学物理研究所 Preparation method of plant essential oil O/W type Pickering emulsion

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