TWI244376B - Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product - Google Patents

Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product Download PDF

Info

Publication number
TWI244376B
TWI244376B TW93105614A TW93105614A TWI244376B TW I244376 B TWI244376 B TW I244376B TW 93105614 A TW93105614 A TW 93105614A TW 93105614 A TW93105614 A TW 93105614A TW I244376 B TWI244376 B TW I244376B
Authority
TW
Taiwan
Prior art keywords
phytosterol
saponin
patent application
oil phase
plant
Prior art date
Application number
TW93105614A
Other languages
Chinese (zh)
Other versions
TW200529762A (en
Inventor
Wen-Teng Wu
Jech-Wei Chen
Hsin-Ju Hsieh
Original Assignee
Wen-Teng Wu
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 Wen-Teng Wu filed Critical Wen-Teng Wu
Priority to TW93105614A priority Critical patent/TWI244376B/en
Publication of TW200529762A publication Critical patent/TW200529762A/en
Application granted granted Critical
Publication of TWI244376B publication Critical patent/TWI244376B/en

Links

Landscapes

  • Steroid Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Method of emulsifying phytosterol by natural saponins is disclosed including mixing an oil phase having phytosterol dissolved therein and an aqueous phase having a natural hydrophilic surfactant (saponins) therein to obtain an emulsion of phytosterol. A water dispersible phytosterol powder product can be formed by drying the emulsion, which is able to be dispersed in an aqueous solution or beverage. The phytosterol emulsion, the phytosterol powder product and the aqueous dispersion thereof may be used in the cosmetic products and food stuffs, thereby enhancing the value of the phytosterol.

Description

I244376 玖、發明說明: 發明所屬之技術領域 本發明係關於一種植物固醇乳化方法,尤其有關一種 藉由天然界面活性劑的植物固醇乳化方法。 先前技術 植醇,全名為植物固醇(Phytosterol),包含C27 4-去甲 基(4_desmethyl)、C28 4-去甲基及C29 4_去曱基植物固醇三 大類。例如:先質(desmosterol),菜油固醇(campesterol), dihydrobrassicasterol,麥胚固醇(sitosterol),豆固烯醇 (stigmaster〇1)等。植醇和膽固醇的分子結構相近,所以會 在人體的腸道中干擾人體對膽固醇的吸收,藉此防止膽固 醇被攝取過高’以達到減低心血管疾病的發生率。除此之 外植醇在文獻中還有增強人體免疫力及降低癌症的發生率 的重要生理活性。 去年國人十大死因中就有許多與血膽固醇過高有關, 包括腦血管、心臟病、高血壓等,這些疾病和往年比較起 來’患病比例有年年增高的趨勢。如何降低血中膽固醇就 成了重要的醫療課題。 市面上現有的降膽固醇藥物以r Statins」為主,適用 於原發性高膽固醇血症患者,可以有效降低低密度脂蛋白 膽固醇’也可以稍微減少三酸甘油脂、增加高密度脂蛋白 膽固醇。Statins藥物可能會造成橫紋肌溶解這種嚴重的副 作用,如拜耳公司於1997年在美國核准上市之Bayc〇i 1244376 (cerivastatin)已造成全球100人以上因此藥的嚴重副作用 死亡,Bayer公司也面臨全球的鉅額賠償訴訟官司。 目萷銷售最好的降膽固醇Statins類處方藥,phizer藥 嚴的Lipitor ’依照處方的不同,降低總膽固醇的效果約在 29%〜45%之間。 植物固醇降低血中膽固醇的效果已經得到數十篇醫學 文獻的證實,一般來說每天攝取i.4克的植物固醇,持續 一個月,約可降低14〇/〇的總膽固醇濃度。雖然植物固醇的 效果比Statins類藥物稍差,但植物固醇具有天然、無副作 用,且生產成本較低的優點。因此美國食品藥物管理局 在2000年9月5日發表文件(T00-40),認可每天攝取i 3 克以上的植物固醇將可明顯降低LDL的膽固醇濃度,進而 有效降低心血管疾病(如冠狀動脈性心臟病)的發病率。 植物固醇在降低血中膽固醇的效果大約在5〇年前就 有人開始研究,但一直到1995年在芬蘭的以以〇公司才推 出全球第一個利用植物固醇做成的商品。其中最大的原因 在於純化的植物固#,在水或油及大部分的溶劑中都不易 溶解,造成植物固醇產品的設計困難。另一方面直接口服 純化植物固醇在人體的吸收率小於5%,而膽固醇在人體有 50/以上的吸收率。為了產品配方以及增加植物固醇的可 利用率,植物固醇必須在經過一些處理或配方轉換成適合 用於食品添加的形式。例如芬蘭的以如以及隨後推出產 口口的Umlever公司,都將植物固醇用不飽和脂肪酸酯化, 醋化後的植物固醇有良好的油溶性,再將其添加在奶油或 1244376 油製品中。酯化形式的植物固醇是第一種衍生物,也是目I244376 发明 Description of the invention: Technical field to which the invention belongs The present invention relates to a method for emulsifying plant sterols, and more particularly to a method for emulsifying plant sterols with natural surfactants. Prior technology Phytosterol, full name Phytosterol, contains three major classes of C27 4-desmethyl, C28 4-desmethyl and C29 4-demethyl phytosterol. For example: desmosterol, campesterol, dihydrobrassicasterol, sitosterol, stigmasterol1, etc. Phytol and cholesterol have similar molecular structures, so they interfere with the absorption of cholesterol in the human intestine, thereby preventing cholesterol from being taken too high 'to reduce the incidence of cardiovascular disease. In addition, exophytol has important physiological activities in the literature to enhance human immunity and reduce the incidence of cancer. Last year, many of the top ten causes of death among Chinese people were related to high blood cholesterol, including cerebrovascular disease, heart disease, high blood pressure, etc. These diseases have a tendency to increase year by year. How to lower blood cholesterol has become an important medical issue. The existing cholesterol-lowering drugs on the market are mainly "r Statins", which are suitable for patients with primary hypercholesterolemia and can effectively reduce low-density lipoprotein cholesterol ', can also slightly reduce triglycerides, and increase high-density lipoprotein cholesterol. Statins may cause serious side effects such as rhabdomyolysis. For example, Baycoi 1244376 (cerivastatin), which was approved for marketing in the United States in 1997, has caused more than 100 deaths worldwide due to severe side effects of the drug. Bayer also faces global Huge compensation lawsuit. The best-selling cholesterol-lowering Statins-type prescription drugs and phizers are strict Lipitor ’depending on the prescription, the total cholesterol lowering effect is about 29% to 45%. The effect of phytosterols on lowering blood cholesterol has been confirmed by dozens of medical literatures. Generally speaking, ingesting i.4 grams of phytosterols daily for one month can reduce the total cholesterol concentration by about 14/0. Although the effects of plant sterols are slightly worse than those of Statins, plant sterols have the advantages of natural, no side effects, and lower production costs. Therefore, the US Food and Drug Administration published a document (T00-40) on September 5, 2000, which acknowledged that daily intake of more than 3 grams of plant sterols can significantly reduce the cholesterol concentration of LDL, and thus effectively reduce cardiovascular disease (such as coronary Arterial heart disease). The effect of plant sterols on lowering cholesterol in blood was studied about 50 years ago, but it was not until 1995 that the company ○ in Finland introduced the world's first product made of plant sterols. The biggest reason is that the purified plant solids are difficult to dissolve in water or oil and most solvents, which makes the design of plant sterols difficult. On the other hand, the absorption rate of directly purified plant sterols in the human body is less than 5%, and the absorption rate of cholesterol in the human body is more than 50 /. In order to formulate products and increase the availability of phytosterols, phytosterols must be converted to a form suitable for food addition after some processing or formulation. For example, the Umlever company in Finland and later introduced the production of mouth, esterified plant sterols with unsaturated fatty acids. The vinegarized plant sterols have good oil solubility, and then add them to cream or 1244376 oil. Products. Phytosterols in esterified form are the first derivatives

如最普遍的衍生物形式(W0 9956558,1999年;US 2〇〇2/〇160990, 2〇〇2 年;US 6,492,538, 2〇〇2 年),但油溶性 的配方设汁乘大的問題在於攝取植醇的同時不可避免的會 同日守吃下大量的油脂,而油脂可能會造成肥胖等其他的問 題。 在植物固醇的乳化方面主要是利用乳化劑將植物固醇 包覆,在水性溶液中形成微脂粒,將可大幅提高植物固醇 的效果。在微細化方面是利用結晶或分散技術將植物固醇 的粒子盡可能縮小,以提高植物固醇的吸收率。最困難的 一種衍生物是將植物固醇做成水溶性的衍生物,可以直接 加入飲料或水中,達到最高的吸收率。這種方法需要較為 複雜的化學合成程序,改變了植物固醇的化學結構,在食 用女王性上也需要較多的考慮。美國的F〇ri)es Medi-Tech 公司將植物固醇接上維生素C,成功提高其水溶性。此水 溶性植物固醇被定位在新藥,美國正進行臨床實驗(phase II),並在2002年獲得專利(us 2002/0156021)。而將植物固 醇乳化形成微胞,讓植物固醇能夠分散懸浮於水中,這方 面的專利相當多(US 5,932,562,1999 年;US 6,063,776, 2000 年;WO 02/065859, 2002 年;W0 02/100412, 2002 年; JP 2002/29 1 442,2002年)。到目前為止乳化植物固醇的乳 化劑配方都疋使用卵碟脂或化學合成的介面活性劑,雖然 這些配方都能達到乳化的效果,但卵磷脂成本較高,而化 學合成的介面活性劑仍然含有大量的脂肪酸,所以我們想 1244376 開發一個更理想的植醇乳化的技術。 皂素(saponins)是萃取自植物的一種天然乳化劑,如: 茶皂素萃取自油茶(Camellia oleifera)屬的種子、無患子皂 素萃取自無患子(Sapindus)屬的種子,皂樹皮萃取物 (Quillaia)為磨碎内層樹皮或木材之水抽出物,絲蘭萃取物 (Yucca extract)為美國西南部沙漠植物中萃取而得。天然的 皂素可分解油脂及改變細胞滲透性來促進藥物吸收,並且 可改變水的表面張力。可為食品及調味飲料的添加劑及食 品天然泡沫形成之促成物。皂素在許多文獻中都提及具有 降膽固醇之效果,且也具有食用安全性,在人體測試的結 果顯示絲蘭皂素萃取物(Yucca sap〇nin extract)對人體有明 顯降膽固醇的功效。利用純化自然天然植物的皂素來形成 礼化的植物固醇混合物,對植物固醇的生理活性應有加成 的效果。此種乳化配方優於其他利用人工合成乳化劑來達 成乳化的配方。 發明内容 本案發明人進行了多次的實驗來測試不同的皂素對植 醇的乳化安定性,並將乳化後所獲得的植醇乳化液以冷凍 乾無或喷霧乾燥等方式乾燥,觀察乾燥後粉末再加入水溶 液中的分散性。結果發現茶皂素、無患子皂素、絲蘭萃取 广乂及皂树皮皂素萃取物eXtad)都能讓植物固 :形成穩定的乳化液及水分散液。在食用安全性及乳化乾 知粉末在水溶液再分散性的整體考量,以茶皂素和皂樹皮 1244376 皂素萃取物(Quillaia extract)的效果最好。 實施方式 本發明揭示一種植物固醇的乳化方法,包含下列步驟: a) 將植物固醇(Phy to sterol)溶解於一油相中; b) 將一皂素溶解於一水相中;及 c) 混合步驟a)和b)所獲得的油相溶液與水相溶液而形 成一乳化液。 較佳的,本發明方法進一步包含: d) 減壓蒸餾該乳化液,而移除大部份的油相;及 e) 乾燥步驟d)所獲得的油-於-水(〇ii_in_water)乳化 液’而得到一含有皂素和植物固醇的植物固醇粉末產品, 其可重新分散於水相中。 較佳的,步驟a)的油相包含一沸點低於水的有機溶 劑,及該步驟d)包含減壓蒸餾該乳化液,而獲得一水相分 散液。更佳的,步驟a)的油相包含異丙醇。 較佳的,步驟a)的油相包含植物油。 車父佳的’步驟a)的油相包含動物油。 較佳的,該皂素為萃取一植物的天然皂素(SaP〇nins), 又以萃取自油茶(Camellia oleifera)屬植物、無患子 (Sapindus)屬植物、息樹皮(QuiUaia)屬植物、及絲蘭(丫此⑶) 屬植物為更佳。 本發明亦提供一種植物固醇的乳化液,其係依前述本 發明方法所製備者。 1244376 本發明亦提供一種含有皂素和植物固醇的植物固醇粉 末產品,其係前述本發明方法所製備者。 本發明之其他特色及優點將於下列實施範例中被進一 步舉例與說明,而該實施範例僅作為輔助說明,而並非用 於限制本發明之範圍。 實施例1: 表1為製備植物固醇乳化液所使用的成份的重量%。 表1 成份 重量% 植醇 2.73 脂肪酸丙二醇酯 2.73 油菜籽油(Rapeseed oil) 29.11 皂素 13.09 果糖 26.17 h2〇 26.17 首先’先製備油相溶液:2·5克植物固醇(β-麥胚固醇 (sitosterol)又稱 24 β-乙基膽固醇(ethylcholesterol),純度 40/〇 包 δ 菜〆由固醇(campesterol)和 dihydrobrassicasterol, 由Sigma公司購得)和2·5克脂肪酸丙二醇酯(pr〇pyl⑶e glycol monostearate 90,簡稱 PGMS 90,其 HLB 值為 3.4), 溶解於26·7克油菜籽食用油(台糖芥花油)中;再進行製備 1244376 水相溶液⑴克茶皂素(Teasaponin,三水有機科技有限公 司)’以及24克果糖(台糖豐年果糖),添加μ克的去離子 水均勻令冑取後’將油相溶液與水相溶液在8〇。匚下利 用磁石擾拌器加以劇烈授拌’以達到均句且敎的混合效 果,經過七天的觀察期’發現乳化的植物固醇水溶液仍然 維持穩定。 重複水相溶液製備步驟,可,乂使用無患子息素 (Sapindaceae,三水有機科技有限公司)、絲蘭萃取物及息 樹皮皂素萃取物(GanidaInt.,USA)、來代替茶皂素,實驗 觀察發現所用的4種4素皆可讓植物固醇達到穩定的乳化 狀態。 實施例2: 在實施例1中,還是有用到人工合成的界面活性劑脂 肪酸丙二醇酯(propy丨ene glycol mon〇stearate 9〇)和油脂來 讓植物固醇溶解,在實施例2我們改用加熱的異丙醇 (Iso-propanol)來溶解植物固醇。 植物固醇5克溶於60°C的1〇〇 mL異丙醇中。再將5 克的各種皂素(茶皂素、無患子皂素、絲蘭萃取物以及皂 樹皮皂素萃取物)分別溶於1〇〇 mL的6〇°C水中,代替實 施例1中的水相溶液。同樣將油相溶液與水相溶液在6〇〇c 下’利用磁石攪拌器加以劇烈攪拌,以達到均勻且穩定的 混合效果。混合後的乳化液以減壓濃縮設備將異丙醇實質 上完全去除,觀察殘留的水相(植物固醇的油-於_水 1244376 (oil-in-water)乳化液)中植物固醇的分散安定性。 經過七天的觀察期,發現該植物固醇的乳化液仍然維 持穩定。將該植物固醇的水分散液冷凍乾燥後,即可得到 微細化的不同息素和植物固醇粉末產品。再將此乾燥後的 =產品重新加入水中,觀察乾燥後粉末產品再加入水溶 液中的分散性。結果以含茶息素和植物固醇 以及含皂樹皮萃取物和植物固 °口 好。 知的私末產品的水分散性最 12For example, the most common derivative form (W0 9956558, 1999; US 20002/0160990, 2002; US 6,492,538, 2002), but the problem of oil-soluble formulas is greatly increased. It is inevitable that while ingesting phytol, it will inevitably eat a lot of fat on the same day, and fat may cause other problems such as obesity. In terms of emulsifying plant sterols, it is mainly to use plant emulsifiers to coat plant sterols to form microlipids in aqueous solutions, which will greatly improve the effect of plant sterols. In the aspect of miniaturization, the particle size of plant sterols is reduced as much as possible by crystallization or dispersion technology to improve the absorption rate of plant sterols. One of the most difficult derivatives is to make plant sterols a water-soluble derivative that can be directly added to beverages or water to achieve the highest absorption rate. This method requires more complicated chemical synthesis procedures, changes the chemical structure of plant sterols, and requires more consideration in the queen of food. Fores es Medi-Tech Corporation of the United States successfully linked plant sterols to vitamin C and improved its water solubility. This water-soluble phytosterol is positioned as a new drug, and the United States is conducting clinical trials (phase II), and was patented in 2002 (us 2002/0156021). There are quite a few patents for emulsifying plant sterols to form microcells to allow them to be dispersed and suspended in water (US 5,932,562, 1999; US 6,063,776, 2000; WO 02/065859, 2002; WO 02 / 100412, 2002; JP 2002/29 1 442, 2002). So far, the emulsifier formulations for emulsifying plant sterols have not used egg disc lipids or chemically synthesized surfactants. Although these formulas can achieve the emulsification effect, the cost of lecithin is higher, and chemically synthesized surfactants are still Contains a large amount of fatty acids, so we want to develop a more ideal phytol emulsification technology in 1244376. Saponins are natural emulsifiers extracted from plants, such as: tea saponin is extracted from seeds of Camellia oleifera, saponin is extracted from seeds of Sapindus, and Quillaia ) Is the water extract of the ground bark or wood. Yucca extract is obtained from the desert plants in the southwestern United States. Natural saponins can break down oils and oils and alter cell permeability to promote drug absorption, and can change the surface tension of water. It can be the additive of food and flavoured beverage and the promoter of natural foam formation of food. Saponin has been mentioned in many literatures to have a cholesterol-lowering effect, and it is also edible safety. The results of human tests have shown that Yucca saponin extract has a significant cholesterol-lowering effect on the human body. The use of purified natural plant saponin to form a ceremonial plant sterol mixture should have an additive effect on the physiological activity of plant sterols. This emulsification formula is superior to other formulas that use synthetic emulsifiers to achieve emulsification. SUMMARY OF THE INVENTION The inventors of the present case conducted multiple experiments to test the emulsification stability of phytol by different saponins, and dried the phytol emulsion obtained by emulsification by freeze-drying or spray-drying, and observed the drying. The powder is then added to the dispersibility in the aqueous solution. It was found that tea saponin, saponin saponin, yucca extract, patchouli and saponin bark saponin extract (eXtad) can make plants solid: form stable emulsions and water dispersions. In terms of edible safety and emulsification, the saponin and soap bark 1244376 Quillaia extract have the best effect on the overall consideration of powder redispersibility in aqueous solution. Embodiments The present invention discloses a method for emulsifying a phytosterol, comprising the following steps: a) dissolving phytosterol (Phy to sterol) in an oil phase; b) dissolving a saponin in an aqueous phase; and c ) Mixing the oil phase solution obtained in steps a) and b) with the aqueous phase solution to form an emulsion. Preferably, the method of the present invention further comprises: d) distilling the emulsion under reduced pressure to remove most of the oil phase; and e) drying the oil-in-water (〇ii_in_water) emulsion obtained in step d) 'And a plant sterol powder product containing saponin and phytosterol was obtained, which was re-dispersible in the aqueous phase. Preferably, the oil phase of step a) comprises an organic solvent having a boiling point lower than that of water, and the step d) comprises distilling the emulsion under reduced pressure to obtain a water phase dispersion. More preferably, the oil phase of step a) comprises isopropanol. Preferably, the oil phase of step a) comprises a vegetable oil. The oil phase of Chevrolet ' a) contains animal oil. Preferably, the saponin is a natural saponin (SaPonins) extracted from a plant, and is further extracted from a plant of Camellia oleifera, a plant of Sapindus, a plant of QuiUaia, and silk Orchid (Ya this ⑶) is better. The present invention also provides an emulsion of phytosterol, which is prepared according to the method of the present invention. 1244376 The present invention also provides a phytosterol powder product containing saponin and phytosterol, which is prepared by the method of the present invention. Other features and advantages of the present invention will be further exemplified and explained in the following implementation examples, and this implementation example is only used as an auxiliary description, and is not intended to limit the scope of the present invention. Example 1: Table 1 shows the weight percent of the ingredients used to prepare the phytosterol emulsion. Table 1 Ingredients by weight% Phytol 2.73 Fatty acid propylene glycol ester 2.73 Rapeseed oil 29.11 Saponin 13.09 Fructose 26.17 h2〇26.17 First, first prepare an oil phase solution: 2.5 grams of phytosterol (β-maiger sterol (sitosterol), also known as 24 β-ethylcholesterol, with a purity of 40/0 packs, δ cabbage is obtained from campesterol and dihydrobrassicasterol (available from Sigma) and 2.5 grams of fatty acid propylene glycol ester (propylCDe) Glycol monostearate 90 (referred to as PGMS 90, whose HLB value is 3.4) is dissolved in 26.7 grams of rapeseed edible oil (Taitang canola oil); and then a 1244376 aqueous phase solution of tea saponin (Teasaponin, Sanshui) is prepared. Organic Technology Co., Ltd.) 'and 24 grams of fructose (Tongsu Fengnian Fructose), add μg of deionized water evenly so that after the extraction, the oil phase solution and the water phase solution are at 80. His Majesty used a magnetic stirrer to vigorously mix it 'to achieve a homogeneous and effective mixing effect. After a seven-day observation period', it was found that the emulsified aqueous solution of phytosterols remained stable. Repeat the aqueous solution preparation step. Instead, saponin (Sapindaceae, Sanshui Organic Technology Co., Ltd.), Yucca extract, and bark saponin extract (GanidaInt., USA) can be used instead of tea saponin. Experiment It was found that the four kinds of four hormones used could make the plant sterols reach a stable emulsified state. Example 2: In Example 1, artificially synthesized surfactant fatty acid propylene glycol (propy ene glycol mon〇stearate 90) and fat were used to dissolve the phytosterols. In Example 2, we switched to heating Iso-propanol to dissolve phytosterols. 5 grams of plant sterols were dissolved in 100 mL of isopropanol at 60 ° C. Then 5 grams of various saponins (tea saponin, saponin saponin, yucca saponin, yucca extract and soap bark saponin extract) were separately dissolved in 100 mL of 60 ° C water instead of the water in Example 1. Phase solution. Similarly, the oil phase solution and the water phase solution are stirred vigorously at 600 ° C with a magnetic stirrer to achieve a uniform and stable mixing effect. The isopropyl alcohol was substantially completely removed from the mixed emulsion with a reduced pressure concentration device, and the residual water phase (oil-in-water emulsion of plant-sterol-oil-in-water emulsion) was observed for the Decentralized stability. After a seven-day observation period, it was found that the emulsion of the phytosterol remained stable. After freeze-drying the aqueous dispersion of phytosterol, micronized powders of different pheromones and phytosterols can be obtained. Then add this dried product back to water, and observe the dispersibility of the powder product after adding it to the water solution after drying. The results are good with tea-containing compounds and phytosterols and soap-containing bark extract and plant solids. Water Dispersibility of Known Private Products 12

Claims (1)

1244376 拾、申請專利範圍: 1 · 一種植物固醇的乳化方法,包含下列步驟: a)將植物固醇(Phy to sterol)溶解於一油相中; b )將一皂素溶解於一水相中;及 c) 混合步驟a)和b)所獲得的油相溶液與水相溶液而形 成一乳化液。 2·如申請專利範圍第1項的方法,其進一步包含·· d) 減壓蒸餾該乳化液,而移除大部份的油相·,及 馨 e) 乾煉步驟d)所獲得的油·於— 乳化 · 液而得到一含有皂素和才直物固_的植物固醇粉末產&," 其可重新分散於水相中。 3·如申請專利範圍第2項的方法,其中步驟a)的油相 包含一彿點低於水的有機溶劑’及該步驟❼包含減壓蒸餾 該乳化液,而獲得一水相分散液。 4·如申請專利範圍第3項的方法,其中步驟約的油相 包含異丙醇。 如申叫專利範圍第!項的方法,其中步驟約的油相 包含植物油。 如申叫專利圍帛i項的方法,其中步驟&)的油相 13 1244376 . I 包含動物油。 7 ·如申請專利範圍第1項至第6項中任一項所述的方 法’其中該皂素為萃取一植物的天然皂素(Saponins)。 8·如申請專利範圍第7項的方法,其中該植物是選自 油茶(Camellia〇leifera)屬植物、無患子(Sapindus)屬植物、 皂樹皮(Quillaia)屬植物、及絲蘭(Yucca)屬植物所組成的 族群。 9.-種植物固醇的乳化液’其係依申請專利範圍第i 項的方法所製備者。 W·—種含有皂素和植物固醇的植 係依申請糞刹梦网# U ^ ^末產品,其 月專利祀圍第2、3或4項的方法所製備者。1244376 Patent application scope: 1. A method for emulsifying phytosterols, including the following steps: a) dissolving phytosterols in an oil phase; b) dissolving a saponin in an aqueous phase And c) mixing the oil phase solution obtained in steps a) and b) and the aqueous phase solution to form an emulsion. 2. The method according to item 1 of the patent application scope, further comprising: d) distilling the emulsion under reduced pressure to remove most of the oil phase, and e) the oil obtained in the dry refining step d) • Yu-emulsify the liquid to obtain a plant sterol powder containing saponin and solids, which can be re-dispersed in the aqueous phase. 3. The method according to item 2 of the scope of patent application, wherein the oil phase of step a) comprises an organic solvent having a water point lower than that of water 'and the step ❼ comprises distilling the emulsion under reduced pressure to obtain a water phase dispersion. 4. The method according to item 3 of the patent application, wherein the oil phase of the step step comprises isopropanol. Such as applying for the scope of patents! The method of clause, wherein the oil phase of step about comprises a vegetable oil. As claimed, the method of patent enclave i, wherein the oil phase of step &) 13 1244376. I contains animal oil. 7. The method according to any one of claims 1 to 6 of the patent application scope, wherein the saponin is a natural saponin from which a plant is extracted. 8. The method according to item 7 of the patent application scope, wherein the plant is selected from the group consisting of Camellia oleifera, Sapindus, Quillaia, and Yucca Formed by the ethnic group. 9.-Emulsion of plant sterols, which is prepared according to the method of item i of the scope of patent application. W · —A plant containing saponin and phytosterols was prepared according to the method of applying for the fecal brake dream net #U ^ ^ final product, the monthly patent enumerating items 2, 3 or 4. 1414
TW93105614A 2004-03-03 2004-03-03 Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product TWI244376B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
TW93105614A TWI244376B (en) 2004-03-03 2004-03-03 Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TW93105614A TWI244376B (en) 2004-03-03 2004-03-03 Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product

Publications (2)

Publication Number Publication Date
TW200529762A TW200529762A (en) 2005-09-16
TWI244376B true TWI244376B (en) 2005-12-01

Family

ID=37154785

Family Applications (1)

Application Number Title Priority Date Filing Date
TW93105614A TWI244376B (en) 2004-03-03 2004-03-03 Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product

Country Status (1)

Country Link
TW (1) TWI244376B (en)

Also Published As

Publication number Publication date
TW200529762A (en) 2005-09-16

Similar Documents

Publication Publication Date Title
KR102569534B1 (en) Method for Selective Extraction of Cannabinoids from Plant Sources
US20220257510A1 (en) Compositions for Nanoemulsion Delivery Systems
US9775910B2 (en) Stable aqueous suspension
JP6534731B2 (en) Use for improving the menopausal phase of a composition containing a combined extract of red clover and pomegranate as an active ingredient
JP5128801B2 (en) High water dispersible powder and method for producing the same
JP2019532940A (en) Cannabinoid dilutable preparation and preparation method thereof
TWI243060B (en) Dispersion formulations containing lipase inhibitors
JP2019528297A (en) Subcutaneous injection preparation used for weight loss and use thereof
Sindi et al. Preparation and evaluation of protective effect of pumpkin seed oil based self nanoemulsifying oral delivery system against ibuprofen-induced peptic ulcer
US20070014819A1 (en) Method of emulsifying phytosterol by natural saponin,emulsion prepared thereby and water dispersible phytosterol powder product
CN101094596A (en) Edible compositions comprising a primary lipid, a co-lipid a lipophilic physiologically active ingredient and water, and their preparation
JP4630658B2 (en) Methods and formulations for improving hydrophobic drug absorption and gastrointestinal bioavailability
KR20190040305A (en) Subcutaneous injections for weight loss and uses thereof
JP5937816B2 (en) Formulation containing sterol glycoside
TWI244376B (en) Method of emulsifying phytosterol by natural saponins, emulsion prepared thereby and water dispersible phytosterol powder product
JP2004521941A (en) Method for producing free-flowing powder containing water-dispersible sterols
JP2007029048A (en) Method for emulsifying phytosterol, emulsion prepared thereby and phytosterol powder product
AU2004292418A1 (en) Methods and formulations for the treatment of medical conditions related to elevated dihydrotestosterone
JP6675413B2 (en) Formulations for effective delivery of tocotrienol
CN106456783B (en) Oral homogeneous preparation containing omega-3 polyunsaturated fatty acid and resveratrol
JP2022546815A (en) A Microemulsion Delivery System for Alcohol-Soluble Species Containing Underivatized Hormones
UA80633C2 (en) Semi-solid compound containing azetidine derivative and polimer e-vitamine (tpgs), method of its preparation and make-up
JP2004067526A (en) Composition effective for prevention/alleviation of symptom of atopic disease
EP2844265A1 (en) Pomegranate oil for preventing and treating neurodegenerative diseases
Garti et al. Improved solubilization and bioavailability of nutraceuticals in nanosized self‐assembled liquid vehicles

Legal Events

Date Code Title Description
MK4A Expiration of patent term of an invention patent