WO2010054520A1 - 净化血管的药物组合物及其制备方法 - Google Patents

净化血管的药物组合物及其制备方法 Download PDF

Info

Publication number
WO2010054520A1
WO2010054520A1 PCT/CN2008/073237 CN2008073237W WO2010054520A1 WO 2010054520 A1 WO2010054520 A1 WO 2010054520A1 CN 2008073237 W CN2008073237 W CN 2008073237W WO 2010054520 A1 WO2010054520 A1 WO 2010054520A1
Authority
WO
WIPO (PCT)
Prior art keywords
parts
weight
filtrate
plant extract
concentrate
Prior art date
Application number
PCT/CN2008/073237
Other languages
English (en)
French (fr)
Inventor
杜志政
唐见奎
Original Assignee
Du Zhizheng
Tang Jiankui
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 Du Zhizheng, Tang Jiankui filed Critical Du Zhizheng
Priority to EP08878080.4A priority Critical patent/EP2345416B1/en
Priority to CN200880130286.8A priority patent/CN102159227B/zh
Priority to US13/058,971 priority patent/US20110206722A1/en
Publication of WO2010054520A1 publication Critical patent/WO2010054520A1/zh

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/28Asteraceae or Compositae (Aster or Sunflower family), e.g. chamomile, feverfew, yarrow or echinacea
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/12Ketones
    • A61K31/122Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/24Apocynaceae (Dogbane family), e.g. plumeria or periwinkle
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/28Asteraceae or Compositae (Aster or Sunflower family), e.g. chamomile, feverfew, yarrow or echinacea
    • A61K36/286Carthamus (distaff thistle)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/31Brassicaceae or Cruciferae (Mustard family), e.g. broccoli, cabbage or kohlrabi
    • A61K36/315Isatis, e.g. Dyer's woad
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/48Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
    • A61K36/482Cassia, e.g. golden shower tree
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Definitions

  • the present invention relates to a plant extract composition and a method of producing the same, and, in particular, to a plant extract composition capable of cleaning blood vessels and a method of preparing the same.
  • BACKGROUND OF THE INVENTION With the development of social economy, people's diet structure has undergone many changes, eating more meat, milk, and egg foods, causing people to absorb more fat, protein, cholesterol, etc., and when human lipids When there are obstacles due to various reasons, excess blood clots such as cholesterol and triglycerides will accumulate in the body, causing atherosclerosis and clogging of the arteries.
  • HDL high-density lipoprotein
  • LDL Low-density lipoprotein
  • a Romanian professor has extracted from the drug anaesthetic procaine.
  • a substance called H3 can raise HDL by about 34%, but the toxic side effects of this substance are so large that it is difficult to use widely.
  • a plant extract composition having a blood vessel scavenger function is mainly composed of plant raw materials and extracts, wherein the plant raw materials include the following components by weight: 10-30 parts of Folium Isatidis, 15-35 parts of cassia seed, 10-20 parts of Cyclobalanopsis, 15-30 parts of safflower, Chrysanthemum 10-30 parts, 20-50 parts of Apocynum venetum; extracts include the following parts by weight: 20-40 parts of ginkgo flavonoids, 20-35 parts of emodin, 30-50 parts of hawthorn, 15-55 parts of Gynostemma , Panax notoginseng saponins 20-60 parts.
  • the plant material comprises the following components by weight: 15-25 parts of Folium, 20-30 parts of cassia, 12-18 parts of squid, 20-30 parts of safflower, 15-25 of chrysanthemum Amount, 30-40 parts of Apocynum venetum; extracts include the following parts by weight: 25-35 parts of ginkgo flavonoids, 25-35 parts of emodin, 30-40 parts of saponin, 20-40 parts of Gynostemma pentaphyllum, Sanqi Total saponin 30-50 parts.
  • the following two parts by weight may be added together with the following raw materials: lecithin 10-30 parts, black fungus 10-30 parts, solid acetic acid 20-80 weight Share.
  • lecithin is an extract
  • solid acetic acid is also extracted from plants, and therefore belongs to the extract in the present invention.
  • black fungus is a fungus, it is also classified as a plant raw material in the present invention.
  • Increased lecithin, black fungus and solid acetic acid can further soften the blood vessels, prevent hardening of the blood vessels, and speed up the repair of blood vessels.
  • the plant extract composition can be prepared into capsules, tablets, powders, granules with or without the addition of suitable adjuvants or carriers by the following preparation methods.
  • Another object of the present invention is to provide a process for the preparation of the above plant extract composition.
  • a preparation method comprising the above plant extract composition, comprising the steps of: a) pulverizing, respectively weighing the parts by weight of the plant material for pulverization; b) immersing, placing the pulverized plant material in the step a) In the container, press the weight ratio of solid to liquid 1: 4, and dip: 2:5 hours; c) ultrasonic extraction, extract the plant material and soaked liquid obtained in step b) in the ultrasonic tank, the temperature is from Normal temperature heating to a temperature not exceeding 40 °C, extraction time 50-60 minutes; d) filtration separation, the mixture obtained in step c) is filtered to obtain filtrate and filter residue, the filter residue is centrifuged to obtain secondary filtrate, two filtrates Combine the filtrate;
  • step g) adding the plant extract, weighing the extract into the concentrate in parts by weight, and mixing uniformly. h) drying, the mixture obtained in step g) is dried to obtain a dried product.
  • the stirring speed in the ultrasonic tank is 1500/min, ultrasonic power
  • ultrasonic intermittent time is 1.5 minutes.
  • vacuum drying or microwave drying may be used. Dry under negative pressure conditions. Negative pressure drying reduces the impact of air on the product.
  • the drying temperature is 4 ⁇ , the speed is fast, the chance of contact with the product is reduced, the pollution and oxidative deterioration are avoided, and the product is easy to be crushed.
  • the microwave drying is to irradiate the microwave generator with the material to be dried. When the microwave is injected into the material, the polar molecules such as water move synchronously with the frequency of the 4 wave, so that the material instantaneously generates frictional heat, which leads to the surface and interior of the material. At the same time, the temperature rises, a large amount of water molecules escape, and the material is dried.
  • the dried finished product of the plant extract composition made according to the present invention may be pulverized with or without the addition of a suitable adjuvant or carrier to prepare the desired dosage form.
  • a suitable adjuvant or carrier for example, capsules, tablets, powders, granules.
  • the above various dosage forms can be prepared according to a conventional method in the field of pharmacy.
  • the plant extract composition of the invention extracts plant material by ultrasonic wave, and the preparation process does not use chemical reagents, and retains the natural active active ingredient of the plant, and contains various natural flavonoids, soaps, phospholipids and various enzymes. class.
  • the plant extract composition of the present invention enters a blood vessel, it can increase the level of high-density lipoprotein (HDL) in the blood, efficiently and rapidly decompose the dissolved lipids and blood sediments in the blood; simultaneously dilate blood vessels, soften blood vessels, and restore blood vessels.
  • HDL high-density lipoprotein
  • Example 1 A plant extract composition having a vascular scavenger function, prepared as follows: a) crushing, weigh the plant raw materials by weight: 10 parts of Daqingye, 35 parts of cassia seed, 10 parts of spine flower, 15 parts of safflower, 10 parts of chrysanthemum, 50 parts of apocynum venetum; b) soaking, a) The pulverized plant material in the step is placed in a closed container, and then the solid-liquid weight ratio is 1:4 force p water, dip:; for 3 hours; c) ultrasonic extraction, the plant material obtained by step b) and soaking The liquid is extracted in an ultrasonic tank, the temperature is raised from
  • f) Concentrate and concentrate the filtrate to 75% concentrate. g) adding the plant extract, weighing the plant extract by weight: 40 parts of ginkgo flavonoids, 20 parts of emodin, 30 parts of hawthorn, 15 parts of Gynostemma pentaphyllum, 60 parts of panax notoginseng saponins added In the concentrate, mix well. h) Drying, the mixture obtained in step g) is dried under vacuum to obtain a dried product.
  • Example 2 A plant extract composition having a blood vessel scavenger function was prepared according to the following steps: a) pulverization, weighing plant materials by weight: 30 parts of Folium, 15 parts of cassia, and 20 30 parts of safflower, 30 parts of chrysanthemum, 20 parts of apocynum venetum; b) soaking, put the plant material crushed in step a) into a closed container, and then press the weight ratio of solid to liquid 1: 4 force p water, Dip:; package for 2 hours; c) ultrasonic extraction, the plant material and soaking liquid obtained by step b) are extracted in an ultrasonic tank, the temperature is raised from normal temperature to 35 ° C, and the extraction time is 50 minutes; d) filtration separation The filtrate obtained in step c) is filtered to obtain a filtrate and a filter residue, and the filter residue is subjected to centrifugal filtration to obtain a secondary filtrate, and the two filtrates are combined to obtain a filtrate;
  • step g) adding the plant extract, weighing the plant extract by weight: 20 parts of ginkgo flavonoids, 35 parts of emodin, 50 parts of hawthorn, 55 parts of Gynostemma pentaphyllum, 20 parts of panax notoginseng saponins added to the above In the concentrate, mix well. h) Drying, the mixture obtained in step g) is dried under vacuum to obtain a dried product.
  • Example 3 A plant extract composition having a blood vessel scavenger function was prepared according to the following steps: a) pulverization, weighing plant materials by weight: 15 parts of Folium, 30 parts of cassia, and 12 30 parts of safflower, 25 parts of chrysanthemum, 40 parts of apocynum smashed, and then weighed 10 parts of black fungus; b) soaked, put the crushed plant material and black fungus in step a) into a closed container, then According to the solid-liquid weight ratio 1: 4 force water, dip:; package for 4 hours; c) ultrasonic extraction, the plant material and soaking liquid obtained by step b) are extracted in the ultrasonic tank, the temperature is heated from normal temperature 40 °C , extraction time 50 minutes; d) filtration separation, the mixture obtained in step c) is filtered to obtain filtrate and filter residue, the filter residue is centrifuged to obtain secondary filtrate, and the two filtrates are combined to obtain a filtrate; e
  • f) Concentrate and concentrate the filtrate to 80% concentrate.
  • g) adding the plant extract, weighing 25 parts of the plant extract ginkgo flavonoids, 25 parts of emodin, 30 parts of saponin, 20 parts of Gynostemma pentaphyllum, 50 parts of Panax notoginseng saponins, and lecithin 30 A portion, solid acetic acid, 20 parts was added to the concentrate and mixed well.
  • Drying, the mixture obtained in step g) is subjected to microwave drying to obtain a dried product.
  • Example 4 A plant extract composition having a blood vessel scavenger function was prepared as follows: a) pulverized, and the plant materials were weighed by weight: 20 parts of Daqingye, 25 parts of cassia seed, 15 parts of spirulina, 25 parts of safflower, 20 parts of chrysanthemum, 30 parts of apocynum smashed, and then weighed 20 parts of black fungus; b) soaked, put the crushed plant material and black fungus into a closed step In the container, according to the weight ratio of solid to liquid 1: 4 force water, dip:; package for 3 hours; c) ultrasonic extraction, the plant material and soaking liquid obtained by step b) are extracted in the ultrasonic tank, the temperature is from normal temperature plus Temperature 30 ° C, extraction time 60 minutes; d) Filtration separation, the mixture obtained in step c) is filtered to obtain filtrate and filter residue, the filter residue is centrifuged to obtain secondary filtrate, and the two filtr
  • step g) adding the plant extract, weighing 30 parts of plant extract ginkgo flavonoids, 30 parts of emodin, 35 parts of saponin, 25 parts of Gynostemma pentaphyllum, 40 parts of Panax notoginseng saponins, and lecithin 20
  • a portion of solid acetic acid (80 parts) was added to the concentrate and mixed well.
  • step g) Drying, the mixture obtained in step g) is subjected to microwave drying to obtain a dried product.
  • Example 5 A plant extract composition having a blood vessel scavenger function was prepared according to the following steps: a) pulverization, weighing plant materials by weight: 25 parts of Folium, 20 parts of cassia, and 18 Serving, 20 parts of safflower, 15 parts of chrysanthemum, 30 parts of apocynum venetum; b) soaking, put the plant material crushed in step a) into a closed container, and then press the weight ratio of solid to liquid 1: 4 force p water, Dip:; package for 5 hours; c) ultrasonic extraction, the plant material and soaking liquid obtained by step b) are extracted in an ultrasonic tank, the temperature is heated from normal temperature to 40 ° C, and the extraction time is 50 minutes; d) filtration separation, The filtrate obtained in step c) is filtered to obtain a filtrate and a filter residue, and the filter residue is subjected to centrifugal filtration to obtain a secondary filtrate, and the two filtrates are combined to obtain a
  • step g) adding the plant extract, weighing the plant extract by weight: 35 parts of ginkgo flavonoids, 35 parts of emodin, 40 parts of kaempferol, 40 parts of Gynostemma pentaphyllum, 30 parts of Panax notoginseng saponins added to the above In the concentrate, mix well. h) Drying, the mixture obtained in step g) is dried under vacuum to obtain a dried product.
  • Example 6 A plant extract composition having a blood vessel scavenger function was prepared according to the following steps: a) pulverization, weighing the plant materials by weight: 20 parts of Folium, 25 parts of cassia, and 16 Serve, 25 parts of safflower, 20 parts of chrysanthemum, 35 parts of apocynum venetum, and then weigh 30 parts of black fungus; b) soak, put the plant material crushed in step a) into a closed container, and then press the weight of solid and liquid Ratio 1: 4 force p water, dip:; package for 3 hours; c) ultrasonic extraction, the plant material and soaking liquid obtained by step b) are extracted in an ultrasonic tank, the temperature is heated from normal temperature by 40 ° C, extraction time 50 minutes; d) filtration separation, the mixture obtained in step c) is filtered to obtain filtrate and filter residue, the filter residue is centrifuged to obtain secondary filtrate, and the two filtrates are combined to obtain a filtrate;
  • the conventional feed fed in Group A was added with the dried product of the composition prepared in Example 5 of the present invention, and the B group was fed with a conventional feed as a control group. Feeded every day, group B mice three times each. Observe for 30 days. Experimental results: During the 30-day feeding period, group A mice showed more active and higher sensitivity; group B mice did not like activities.
  • Example 8 Clinical practice 3 Methods: 5 patients with hypertension, 5 patients with stroke and 5 patients with angina pectoris. Each patient was given a dry powder of the composition prepared according to Example 4 of the present invention, three times a day, 3 g each time, boiled in warm boiled water, 30 days for one course of treatment, and eight courses of treatment. Results: Hypertensive patients
  • the symptoms of 5 patients were palpitation, shortness of breath, hernia, irregular pain in the chest, gasping, weakness in the legs and feet, and electrocardiogram showed severe blood supply.
  • One of the patients was 75 years old, so after 4 courses, they were taken 1.5 times a day, 3 times a day, and the remaining patients were taken 8 times.
  • 4 patients (including the above-mentioned 75-year-old patient) had basically disappeared.
  • the electrocardiogram showed normal blood supply.
  • One patient had hernia disappeared, and the time and frequency of chest pain decreased.
  • the electrocardiogram showed that the blood supply was basically normal.

Landscapes

  • Health & Medical Sciences (AREA)
  • Natural Medicines & Medicinal Plants (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Botany (AREA)
  • Mycology (AREA)
  • Microbiology (AREA)
  • Medical Informatics (AREA)
  • Biotechnology (AREA)
  • Alternative & Traditional Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Medicinal Preparation (AREA)

Description

净化血管的药物组合物及其制备方法
技术领域 本发明涉及植物提取物组合物及其制备方法,特别是涉及一种能清洁血 管的植物提取物组合物及其制备方法。 背景技术 随着社会经济的发展, 人们的饮食结构发生很多的改变, 食用更多的肉 类、 奶类、 蛋类食品, 导致人们吸收更多的脂肪、 蛋白质、 胆固醇等, 而当 人体脂质代谢由于种种原因出现障碍时,多余的胆固醇和甘油三酯等血管"垃 圾"就会在体内堆积起来, 使动脉血管发生粥样硬化和堵塞。 1985年, 美国学者 M.S.Brown和 J.L.Goldstein发现, 人体血液中有一 种高密度脂蛋白 (HDL ), 能促使肝脏分解血液中多余的胆固醇和甘油三酯, 逆转血管内皮功能不良, 抑制内皮细胞凋亡, 阻止低密度脂蛋白 (LDL ) 氧 化和血小板聚集, 但要将体内的 HDL提高到能够治疗高血脂症的水平, 目 前还很难做到,曾经有罗马尼亚的教授从麻醉品普鲁卡因里提取了一种叫 H3 的物质, 能把 HDL升高 34 %左右, 但这种物质的毒副作用 4艮大, 因而难以 广泛使用。 在血管堵塞还不严重, 没有出现症状前, 人们 艮难发现血管中已开始堆 积这些 "垃圾 ", 只有当出现心脑血管疾病的症状了, 人们才能意识到问题的 严重性, 而到这种时候, 清除血管堵塞就不是很容易的事情了, 一种方法是 进行手术, 搭桥或支架等, 手术的痛苦和风险众所周知; 另一种就是使用药 物, 对于高血脂疾病, 现在使用较多的是他汀类药物, 此类药物治疗效果较 好, 但还是有一定的肝脏和肌肉毒副作用, 而且使用药物也是人们不愿面对 的, 往往会导致依从性较差。 发明内容 本发明的目的是提供一种新的具有血管清道夫功能的植物提取物组合 物及其制备方法。 本发明的技术方案为: 一种具有血管清道夫功能的植物提取物组合物, 主要由植物原料、 提取物组成, 其中植物原料包括以下重量份的组分: 大青 叶 10-30份, 决明子 15-35份, 旋复花 10-20份, 红花 15-30份, 菊花 10-30 份, 罗布麻 20-50份; 提取物包括以下重量份的组分: 银杏黄酮 20-40份, 大黄素 20-35份, 山楂素 30-50份, 绞股蓝总甙 15-55份, 三七总皂甙 20-60 份。 本发明优选的方案是, 植物原料包括以下重量份的组分: 大青叶 15-25 份, 决明子 20-30份, 旋复花 12-18份, 红花 20-30份, 菊花 15-25份, 罗布 麻 30-40份;提取物包括以下重量份的组分:银杏黄酮 25-35份,大黄素 25-35 份, 山楂素 30-40份, 绞股蓝总甙 20-40份, 三七总皂甙 30-50份。 本发明优选的另一方案是, 还可以在以上两种技术方案的基础上, 再加 上下述重量份的原料: 卵磷脂 10-30份, 黑木耳 10-30份, 固体醋酸 20-80 重量份。 其中卵磷脂为提取物, 固体醋酸也是从植物中提取制备的, 因此在 本发明中也属于提取物, 黑木耳虽然为菌类,但在本发明中也归为植物原料。 增加卵磷脂、 黑木耳和固体醋酸可以更进一步软化血管, 防止血管硬化, 使 血管修复速度加快。 所述的植物提取物组合物经下述制备方法制备后的干燥品可以加入或 不加入适当的辅料或载体制成胶囊剂、 片剂、 粉剂、 颗粒剂。 本发明的另外一个目的是提供一种上述植物提取物组合物的制备方法。 一种含有上述植物提取物组合物的制备方法, 包括以下步骤: a )粉碎, 分别称取所述重量份的植物原料进行粉碎; b ) 浸泡, 将 a ) 步骤中粉碎的植物原料放入密闭容器中, 再按固液重 量比 1 : 4力口水, 浸:;包 2-5小时; c ) 超声波提取, 将经 b ) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温到温度不超过 40 °C , 提取时间 50-60分钟; d ) 过滤分离, 将 c ) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.5-7.7; f ) 浓缩, 将过滤液浓缩至 75-80 %的浓缩品。 g ) 加入所述的植物提取物, 按重量份称取所述的提取物加入所述的浓 缩品中, 混合均匀。 h ) 干燥, 将 g ) 步骤中获得混合物进行干燥得干燥成品。 所述的 c ) 步骤中, 超声波罐内的搅拌转速为 1500/分钟, 超声波功率
1500W,超声波间歇时间为 1.5分钟。 所述的 h ) 步骤中, 可釆用负压干燥或微波干燥。 在负压条件下干燥。 负压干燥减轻了空气对产品的影响, 干燥温度 4氐, 速度快, 减少了产品与空 气接触机会, 避免了污染和氧化变质, 产品易于粉碎。 而微波干燥则是将微波发生器辐射需干燥的物料,当微波射入物料内部 时, 水等极性分子随 4啟波的频率故同步运动, 使物料瞬时产生摩擦热, 导致 物料表面和内部同时升温, 大量水分子逸出, 物料获得干燥。 微波干燥速度 快, 时间短, 加热均匀, 非常适合中药原材料的干燥灭菌, 由于干燥时间是 常规加热的十分之一或百分之一, 药材中的挥发性物质和芳香性物质损失较 少。 本发明制成的植物提取物组合物的干燥成品可以经粉碎加入或不加入 适当的辅料或载体制成需要的剂型。 比如胶囊剂、 片剂、 粉剂、 颗粒剂。 上 述各种剂型均可以按照药学领域的常规方法制备。 本发明的植物提取物组合物, 釆用超声波提取植物原料, 这个制备过程 不使用化学试剂, 保留了植物的天然活性有效成分, 使其中含有多种天然黄 酮、 皂类、 磷脂类和多种酶类。 本发明的植物提取物组合物进入血管后, 能 提高血液中高密度脂蛋白 (HDL ) 的水平, 高效快速分解溶化脂质及血液中 的血垢沉淀物; 同时扩张血管, 软化血管, 恢复血管的张力和弹性, 修复血 管减少血管阻力; 还能降氏血液粘度, 净化血液, 将血管内的有害物质、 垃 圾、 毒素清排到体外, 真正起到了血管清道夫的作用。 具体实施方式 实施例 1 : 一种具有血管清道夫功能的植物提取物组合物, 按以下步骤制备: a)粉碎, 分别按重量份称取植物原料: 大青叶 10份, 决明子 35份, 旋复花 10份, 红花 15份, 菊花 10份, 罗布麻 50份进行粉碎; b) 浸泡, 将 a) 步骤中粉碎的植物原料放入密闭容器中, 再按固液重 量比 1: 4力 p水, 浸:;包 3小时; c) 超声波提取, 将经 b) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温到 30 °C , 提取时间 60分钟; d) 过滤分离, 将 c) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.5;
f ) 浓缩, 将过滤液浓缩至 75%的浓缩品。 g) 加入所述的植物提取物, 按重量份称取植物提取物: 银杏黄酮 40 份, 大黄素 20份, 山楂素 30份, 绞股蓝总甙 15份, 三七总皂甙 60份加入 所述的浓缩品中, 混合均匀。 h) 干燥, 将 g) 步骤中获得混合物进行负压干燥得干燥成品。 实施例 2: 一种具有血管清道夫功能的植物提取物组合物, 按以下步骤制备: a)粉碎, 分别按重量份称取植物原料: 大青叶 30份, 决明子 15份, 旋复花 20份, 红花 30份, 菊花 30份, 罗布麻 20份进行粉碎; b) 浸泡, 将 a) 步骤中粉碎的植物原料放入密闭容器中, 再按固液重 量比 1: 4力 p水, 浸:;包 2小时; c) 超声波提取, 将经 b) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温到 35 °C, 提取时间 50分钟; d) 过滤分离, 将 c) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.6; f ) 浓缩, 将过滤液浓缩至 80 %的浓缩品。 g) 加入所述的植物提取物, 按重量份称取植物提取物: 银杏黄酮 20 份, 大黄素 35份, 山楂素 50份, 绞股蓝总甙 55份, 三七总皂甙 20份加入 所述的浓缩品中, 混合均匀。 h) 干燥, 将 g) 步骤中获得混合物进行负压干燥得干燥成品。 实施例 3: 一种具有血管清道夫功能的植物提取物组合物, 按以下步骤制备: a)粉碎, 分别按重量份称取植物原料: 大青叶 15份, 决明子 30份, 旋复花 12份, 红花 30份, 菊花 25份, 罗布麻 40份进行粉碎, 再称取黑木 耳 10份粉碎; b) 浸泡, 将 a) 步骤中粉碎的植物原料和黑木耳放入密闭容器中, 再 按固液重量比 1: 4力口水, 浸:;包 4小时; c) 超声波提取, 将经 b) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温 40 °C, 提取时间 50分钟; d) 过滤分离, 将 c) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.7;
f ) 浓缩, 将过滤液浓缩至 80 %的浓缩品。 g) 加入所述的植物提取物, 按重量份称取植物提取物银杏黄酮 25份, 大黄素 25份, 山楂素 30份, 绞股蓝总甙 20份, 三七总皂甙 50份, 以及卵 磷脂 30份、 固体醋酸 20份加入所述的浓缩品中, 混合均匀。 h) 干燥, 将 g) 步骤中获得混合物进行微波干燥得干燥成品。 实施例 4: 一种具有血管清道夫功能的植物提取物组合物, 按以下步骤制备: a)粉碎, 分别按重量份称取植物原料: 大青叶 20份, 决明子 25份, 旋复花 15份, 红花 25份, 菊花 20份, 罗布麻 30份进行粉碎, 再称取黑木 耳 20份粉碎; b) 浸泡, 将 a) 步骤中粉碎的植物原料和黑木耳放入密闭容器中, 再 按固液重量比 1: 4力口水, 浸:;包 3小时; c) 超声波提取, 将经 b) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温 30 °C, 提取时间 60分钟; d) 过滤分离, 将 c) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.5; f ) 浓缩, 将过滤液浓缩至 80 %的浓缩品。 g) 加入所述的植物提取物, 按重量份称取植物提取物银杏黄酮 30份, 大黄素 30份, 山楂素 35份, 绞股蓝总甙 25份, 三七总皂甙 40份, 以及卵 磷脂 20份、 固体醋酸 80份加入所述的浓缩品中, 混合均匀。 h) 干燥, 将 g) 步骤中获得混合物进行微波干燥得干燥成品。 实施例 5: 一种具有血管清道夫功能的植物提取物组合物, 按以下步骤制备: a)粉碎, 分别按重量份称取植物原料: 大青叶 25份, 决明子 20份, 旋复花 18份, 红花 20份, 菊花 15份, 罗布麻 30份进行粉碎; b) 浸泡, 将 a) 步骤中粉碎的植物原料放入密闭容器中, 再按固液重 量比 1: 4力 p水, 浸:;包 5小时; c) 超声波提取, 将经 b) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温 40 °C, 提取时间 50分钟; d) 过滤分离, 将 c) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.6; f ) 浓缩, 将过滤液浓缩至 80 %的浓缩品。 g ) 加入所述的植物提取物, 按重量份称取植物提取物: 银杏黄酮 35 份, 大黄素 35份, 山楂素 40份, 绞股蓝总甙 40份, 三七总皂甙 30份加入 所述的浓缩品中, 混合均匀。 h ) 干燥, 将 g ) 步骤中获得混合物进行负压干燥得干燥成品。 实施例 6: 一种具有血管清道夫功能的植物提取物组合物, 按以下步骤制备: a )粉碎, 分别按重量份称取植物原料: 大青叶 20份, 决明子 25份, 旋复花 16份, 红花 25份, 菊花 20份, 罗布麻 35份进行粉碎, 再称取黑木 耳 30份; b ) 浸泡, 将 a ) 步骤中粉碎的植物原料放入密闭容器中, 再按固液重 量比 1 : 4力 p水, 浸:;包 3小时; c ) 超声波提取, 将经 b ) 步骤获得的植物原料及浸泡液在超声波罐内 进行提取, 温度从常温加温 40 °C , 提取时间 50分钟; d ) 过滤分离, 将 c ) 步骤获得的混合液过滤获得滤液和滤渣, 滤渣经 离心过滤获得二次滤液, 将两次滤液合并得过滤液; e ) 调节 PH值, 调节过滤液的 PH值到 7.7;
f ) 浓缩, 将过滤液浓缩至 80 %的浓缩品。 g ) 加入所述的植物提取物, 按重量份称取植物提取物银杏黄酮 30份, 大黄素 30份, 山楂素 35份, 绞股蓝总甙 30份, 三七总皂甙 40份, 以及, 以及卵磷脂 10份、 固体醋酸 60份加入所述的浓缩品中, 混合均匀。 h ) 干燥, 将 g ) 步骤中获得混合物进行微波干燥得干燥成品。 实施例 7: 动物实 3 实验方法: 将 10只小白鼠随机分为 A、 B两组, 每组 5只。 A组喂食 的常规饲料中加入了按本发明实施例 5制备的组合物干燥成品, B组喂食常 规饲料, 为对照组。 每天喂养 、 B组小白鼠各 3次。 观察 30天。 实验结果: 30天喂养期间, A组小白鼠表现得更加活跃, 灵敏度更高; B组小白鼠显得不爱活动。
30天后, 进行血脂分析发现: A组小白鼠血液中的高密度脂蛋白平均 高于 B组小白鼠高密度脂蛋白 32. 53% , A组小白鼠血液中的甘油三酯平均 低于 B组小白鼠的甘油三酯 27.16% , A组小白鼠的血液黏度低于 B组小白 鼠血液黏度 25%。 解剖发现, A组小白鼠的血管弹性正常, B组小白鼠的血 管硬化度增加了 15%以上, 血管内壁厚度增加了 13.2%。 A组 5只小白鼠解 剖后对肝肾未发现损害。 实施例 8: 临床实 3 实 方法: 高血压病人 5例, 中风瘫痪病人 5例, 心绞痛病人 5例。 分 别给予每位病人按本发明实施例 4制备的组合物干燥成品粉末, 每日三次, 每次 3g, 温开水冲服, 30天为 1个疗程, 服用 8个疗程。 实 结果: 高血压病人
5例病人舒张压超过 180, 收缩压超过 110, 主诉头昏、 耳鸣、 胸闷、 气短、 失眠, 头颅多普勒显示血管有部分堵塞。 使用本发明的组合物 8个疗程后, 有 3例病人舒张压降低到 140以下, 收缩压 100左右, 主诉症状消失, 头颅多普勒显示血管未发现异常, 心电图 显示心脑供血正常; 1例病人舒张压 150, 收缩压 100, 主诉症状基本消失, 头颅多普勒显示血管未发现异常, 心电图显示心脑供血正常; 1例病人无效。 中风病人
5例病人症状为神志不清, 眼斜口歪, 瘫痪卧床, 其中 1例病人卧床一 年。 使用本发明的组合物 8个疗程后,有 4例病人可以自己下床,扶杖慢行, 并自理一些简单家务; 1 例病人头脑开始清醒, 基本能说话, 手和腿可以自 己抬起。 心绞痛病人
5例病人的症状为心慌, 气短, 憋气, 胸口无规律疼痛发作, 走路喘气, 腿脚无力, 心电图显示供血严重不足。 其中 1例病人因 75岁, 因此在 4个疗程后, 按每次 1.5g, 每天 3次的 方法服用, 其余病人正常服用 8个疗程。 其中 4例病人 (包括上述 75岁的 病人) 症^ 基本消失, 心电图显示供血正常, 1 例病人憋气症 消失, 胸口 痛发作时间和次数减少, 心电图显示供血基本正常。

Claims

权 利 要 求 书
1. 一种具有血管清道夫功能的植物提取物组合物, 主要由植物原料、 提 取物组成, 其中植物原料包括以下重量份的组分: 大青叶 10-30份, 决明子 15-35份, 旋复花 10-20份, 红花 15-30份, 菊花 10-30份, 罗 布麻 20-50份; 提取物包括以下重量份的组分: 银杏黄酮 20-40份, 大 黄素 20-35份, 山楂素 30-50份, 绞股蓝总甙 15-55份, 三七总皂甙 20-60份。
2. 才艮据权利要求 1所述的植物提取物组合物, 其特征在于植物原料的重 量份为: 大青叶 15-25份, 决明子 20-30份, 旋复花 12-18份, 红花 20-30份, 菊花 15-25份, 罗布麻 30-40份; 提取物的重量份为: 银杏 黄酮 25-35份, 大黄素 25-35份, 山楂素 30-40份, 绞股蓝总甙 20-40 份, 三七总皂甙 30-50份。
3. 根据权利要求 1所述的植物提取物组合物, 其特征在于还包括下述重 量份的原料: 卵磷脂 10-30份, 黑木耳 10-30份, 固体醋酸 20-80份。
4. 才艮据权利要求 2所述的植物提取物组合物, 其特征在于还包括下述重 量份的原料: 卵磷脂 10-30份, 黑木耳 10-30份, 固体醋酸 20-80份。
5. 根据权利要求 1-4任一项所述的植物提取物组合物, 其特征在于组合 物的剂型可以是胶囊剂、 片剂、 粉剂、 颗粒剂。
6. 一种含有权利要求 1-4任一项所述的植物提取物组合物, 包括以下步 骤:
a ) 粉碎, 分别称取所述重量份的植物原料进行粉碎; b )浸泡, 将 a )步骤中粉碎的植物原料放入密闭容器中, 再按固 液重量比 1 : 4力口水, 浸:;包 2-5小时;
c )超声波提取, 将经 b )步骤获得的植物原料及浸泡液在超声波 罐内进行提取, 温度从常温加温到温度不超过 40 °C , 提取时间 50-60 分钟;
d )过滤分离, 将 c )步骤获得的混合液过滤获得滤液和滤渣, 滤 渣经离心过滤获得二次滤液, 将两次滤液合并得过滤液; e) 调节 PH值, 调节过滤液的 PH值到 7.5-7.7;
f ) 浓缩, 将过滤液浓缩至 75-80%的浓缩品。
g) 加入所述的植物提取物, 按重量份称取所述的提取物加入所 述的浓缩品中, '混合均匀。 h) 干燥, 将 g) 步骤中获得混合物进行干燥得干燥成品。 根据权利要求 6所述的制备方法, 其特征在于所述 c)步骤中, 超声波 罐内的搅拌转速为 1500/分钟, 超声波功率 1500W,超声波间歇时间为 1.5分钟。 根据权利要求 7所述的制备方法, 其特征在于所述 h) 步骤可以釆用 负压干燥或微波干燥。
PCT/CN2008/073237 2008-11-14 2008-11-28 净化血管的药物组合物及其制备方法 WO2010054520A1 (zh)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP08878080.4A EP2345416B1 (en) 2008-11-14 2008-11-28 Pharmaceutical composition for purifing vein and preparation method thereof
CN200880130286.8A CN102159227B (zh) 2008-11-14 2008-11-28 净化血管的药物组合物及其制备方法
US13/058,971 US20110206722A1 (en) 2008-11-14 2008-11-28 Pharmaceutical Composition For Purifying Blood Vessels And Preparation Method Thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN200810172194.8 2008-11-14
CNA2008101721948A CN101474243A (zh) 2008-11-14 2008-11-14 具有血管清道夫功能的植物提取物组合物及其制备方法

Publications (1)

Publication Number Publication Date
WO2010054520A1 true WO2010054520A1 (zh) 2010-05-20

Family

ID=40835082

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2008/073237 WO2010054520A1 (zh) 2008-11-14 2008-11-28 净化血管的药物组合物及其制备方法

Country Status (4)

Country Link
US (1) US20110206722A1 (zh)
EP (1) EP2345416B1 (zh)
CN (2) CN101474243A (zh)
WO (1) WO2010054520A1 (zh)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7590352B2 (en) 2001-03-15 2009-09-15 Vladimir Isfandeyarovich Adzhalov Access method for data packet networks
CN113694168A (zh) * 2021-10-14 2021-11-26 山东华威药业有限公司 一种降压降脂中药制剂及其制备方法

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101474243A (zh) * 2008-11-14 2009-07-08 杜志政 具有血管清道夫功能的植物提取物组合物及其制备方法
CN102599484B (zh) * 2012-03-31 2013-12-18 王康 一种黑木耳含片的制备方法
CN102599485B (zh) * 2012-03-31 2014-06-18 嵊州市林美生物科技有限公司 一种黑木耳含片
CN109043098A (zh) * 2018-07-24 2018-12-21 天津民生生物工程股份有限公司 一种食用地龙蛋白压片糖果及其加工工艺
CN110856530A (zh) * 2018-08-24 2020-03-03 牡丹江友邦生物科技股份有限公司 一种桦树茸保健饮品
CN112220889A (zh) * 2019-06-26 2021-01-15 席圣林 一种防治心脑血管疾病的中药及其制备方法
CN111671078A (zh) * 2020-04-17 2020-09-18 山东哈维药业有限公司 含克弗尔发酵乳粉的血管养护组合物及其制备方法
CN114272223B (zh) * 2021-12-31 2023-07-07 江西樟树市正康医药生物科技有限公司 一种三七红曲银杏叶胶囊及其生产工艺

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1586598A (zh) * 2004-07-26 2005-03-02 黑龙江省完达山制药厂 乌杞调脂口服液
CN1623578A (zh) * 2003-12-03 2005-06-08 李树旺 一种降脂药物
CN101474243A (zh) * 2008-11-14 2009-07-08 杜志政 具有血管清道夫功能的植物提取物组合物及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7626017B2 (en) * 1997-10-31 2009-12-01 Pressure Biosciences, Inc. Pressure-enhanced extraction and purification
CN1119105C (zh) * 2000-01-26 2003-08-27 易四卷 娃娃护康枕及其制作方法
CN1364505A (zh) * 2001-01-12 2002-08-21 杨孟君 纳米七味铁屑制剂药物及其制备方法
CN1375295A (zh) * 2001-03-19 2002-10-23 雷学军 一种含抗氧自由基天然药物成份的功能水及其制作方法
JP2009512675A (ja) * 2005-10-21 2009-03-26 エフエックス ライフ サイエンス インターナショナル ジーエムビーエイチ ハーブ抽出物の抗酸化剤及びFe2+キレート形成剤としての特性

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1623578A (zh) * 2003-12-03 2005-06-08 李树旺 一种降脂药物
CN1586598A (zh) * 2004-07-26 2005-03-02 黑龙江省完达山制药厂 乌杞调脂口服液
CN101474243A (zh) * 2008-11-14 2009-07-08 杜志政 具有血管清道夫功能的植物提取物组合物及其制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2345416A4 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7590352B2 (en) 2001-03-15 2009-09-15 Vladimir Isfandeyarovich Adzhalov Access method for data packet networks
CN113694168A (zh) * 2021-10-14 2021-11-26 山东华威药业有限公司 一种降压降脂中药制剂及其制备方法

Also Published As

Publication number Publication date
EP2345416A4 (en) 2012-04-18
US20110206722A1 (en) 2011-08-25
CN102159227A (zh) 2011-08-17
CN102159227B (zh) 2014-11-19
EP2345416B1 (en) 2013-06-19
EP2345416A1 (en) 2011-07-20
CN101474243A (zh) 2009-07-08

Similar Documents

Publication Publication Date Title
WO2010054520A1 (zh) 净化血管的药物组合物及其制备方法
CN102872306B (zh) 治疗心脑血管疾病的复方富硒中药组合物及其制备方法
CN104208302A (zh) 一种降血脂的金樱子保健口服液及其制备方法
CN102113599B (zh) 一种杜仲金银花茶及其制作方法
CN101695539A (zh) 一种延缓衰老的药物及其制备方法
CN103735835A (zh) 一种治疗少白头的中药制剂及其制备方法
CN103749824B (zh) 一种绞股蓝降糖降压保健茶及其制备方法
CN104127813A (zh) 一种治疗气血两虚型褥疮的中药组合物及其制备方法
CN103877247A (zh) 用于治疗褥疮的药物及其制备方法
KR20160013227A (ko) 녹용차 제조방법
CN103933405A (zh) 用于治疗气血两虚型烧伤的药物组合物及其制备方法
CN104645077A (zh) 防治缺血性脑血管病的中药制剂及其制备方法
CN106334135A (zh) 一种养胃护胃中药饮片的制备方法
CN105943619A (zh) 全麻素在制备防治老年痴呆症药物中的应用
CN104324081A (zh) 一种延胡索超细粉体及其制备方法和应用
CN103845535A (zh) 一种清创消炎的药物组合物
JPH0773478B2 (ja) 保健食品組成物の製造方法
CN112057535B (zh) 一种预防或/和治疗血脂异常的中药组合物的制备方法
CN112057536B (zh) 一种预防或/和治疗血脂异常的中药组合物及其应用
CN106819252A (zh) 降血脂养颜美容茶及其制备方法
CN105919098A (zh) 一种用于治疗高血压和慢性便秘的保健品及其制备方法
CN105998190A (zh) 全麻素在制备治疗痛风性关节炎的药物中的应用
CN105106757A (zh) 用于治疗肥胖母牛综合征的药物及其制备方法
CN105169259A (zh) 治疗癫狂的方剂及制备方法
CN104147245B (zh) 一种猪毛菜组合物、其制备方法及其在制备减肥降脂药物中的应用

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880130286.8

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08878080

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2008878080

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 13058971

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE