CN111700927A - A kind of medicine and food homologous composition with hypoglycemic effect and its preparation method and application - Google Patents
A kind of medicine and food homologous composition with hypoglycemic effect and its preparation method and application Download PDFInfo
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- CN111700927A CN111700927A CN202010799647.0A CN202010799647A CN111700927A CN 111700927 A CN111700927 A CN 111700927A CN 202010799647 A CN202010799647 A CN 202010799647A CN 111700927 A CN111700927 A CN 111700927A
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- extract
- medicine
- eucommia ulmoides
- acid
- extraction
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Abstract
本发明公开一种具有降血糖作用的药食同源组合物及其制备方法和应用,所述组合物由杜仲、木姜叶柯与平卧菊三七的提取物混合而成,其包括以下步骤:(1)将杜仲、木姜叶柯与平卧菊三七原料,经烘干、粉碎、过筛等步骤得到杜仲、木姜叶柯与平卧菊三七粉末;(2)杜仲、木姜叶柯与平卧菊三七粉末分别经溶剂提取、醇沉、萃取以及结晶得到杜仲、木姜叶柯与平卧菊三七提取物;(3)将杜仲、木姜叶柯与平卧菊三七提取物按照1:1:1‑1:1:3的方式混合、摇匀制备组合提取物。本发明产出来的药食同源组合物能够显著降低糖尿病患者血糖指数以及餐后血糖含量,对于糖尿病引起的并发症具有良好的预防和治疗作用,具有显著的社会和经济效益。
The invention discloses a medicine and food homologous composition with hypoglycemic effect and a preparation method and application thereof. The composition is prepared by mixing the extracts of Eucommia ulmoides, Alpinia officinalis and Panax notoginseng. The composition comprises the following steps: (1) by the raw materials of Eucommia ulmoides, Cordyceps sinensis and Panax notoginseng, through steps such as drying, pulverizing, sieving to obtain Eucommia, Cordyceps sinensis and Panax notoginseng powder; (2) Eucommia ulmoides, Cordyceps sinensis and Panax notoginseng The Panax notoginseng powder was extracted by solvent, alcohol precipitation, extraction and crystallization to obtain the extracts of Eucommia ulmoides, Cordyceps sinensis and Panax notoginseng. ‑1:1:3 method to mix and shake to prepare the combined extract. The medicine and food homologous composition produced by the invention can significantly reduce the blood sugar index and postprandial blood sugar content of diabetic patients, has good preventive and therapeutic effects on complications caused by diabetes, and has significant social and economic benefits.
Description
技术领域technical field
本发明属于植物有效活性成分提取与应用技术领域,尤其是涉及一种具有降血糖作用的药食同源组合物及其制备方法和应用。The invention belongs to the technical field of extraction and application of plant effective active ingredients, and in particular relates to a medicine-food homologous composition with hypoglycemic effect and a preparation method and application thereof.
背景技术Background technique
糖尿病是指由于胰岛素分泌不足、胰岛素作用障碍、葡萄糖代谢紊乱,是由于三者或三者组合引起的葡萄糖代谢紊乱的一种疾病,其症状特征是烦渴、多食、多尿和体重减轻。糖尿病是21世纪全球最大的突发卫生事件之一,全球患病率不断上升,目前影响8.8%的成人。糖尿病可诱发多种急性或慢性并发症,如心脑血管和糖尿病肾病等。持续的糖脂代谢紊乱可以导致大小血管、微血管、神经等系统出现很多疾病,导致组织结构和功能发生异常。糖尿病在医学界被称为“所有疾病的来源”,并危及世界人民的健康。市面上降糖类药物种类纷杂,大多数的此类药物因药物都是通过化学或者是生物合成,尽管降糖效果明显却同时带来了很多副作用,同时昂贵的价格也让人望而却步。近几年从天然产物中提取有效成分用来预防及治疗糖尿病的相关研究成为一大热点。因此,从资源丰富的中药中寻找高效,低毒,廉价的天然药物和保健食品是一个很大的发展趋势。Diabetes mellitus refers to a disease of glucose metabolism disorder caused by insufficient insulin secretion, insulin action disorder, glucose metabolism disorder, or a combination of the three. Its symptoms are polydipsia, polyphagia, polyuria and weight loss. Diabetes is one of the largest global health emergencies of the 21st century with a rising global prevalence and currently affects 8.8% of adults. Diabetes can induce a variety of acute or chronic complications, such as cardiovascular and cerebrovascular and diabetic nephropathy. Persistent glucose and lipid metabolism disorders can lead to many diseases in large and small blood vessels, microvessels, nervous systems, etc., resulting in abnormal tissue structure and function. Diabetes is known in the medical community as "the source of all diseases" and endangers the health of people around the world. There are various types of hypoglycemic drugs on the market. Most of these drugs are chemically or biologically synthesized. Although the hypoglycemic effect is obvious, they also bring many side effects. At the same time, the expensive price is also prohibitive. In recent years, researches on extracting active ingredients from natural products to prevent and treat diabetes have become a hot topic. Therefore, it is a great development trend to find high-efficiency, low-toxicity, and cheap natural medicines and health foods from the resource-rich traditional Chinese medicines.
蔓三七学名为“平卧菊三七(Gynura procumbens(Lour.)Merr.)”为菊科,三七属植物,又蛇接骨、续命草、神仙草,味辛、微苦、性凉,为多年生草本药食两用植物,广泛分布在中国、马来西亚、泰国、印度尼西亚、韩国和菲律宾等国家。平卧菊三七具有广泛的药理作用,2009年上半年,中国疾病预防控制中心、国家食品质量监督检验中心、中国食品发酵工业研究院等有关单位完成了平卧菊三七毒理学检验、卫生学检验和多种成分的检验,结论是:无毒、无致畸影响;其有效成份具有通经活络,消炎止咳,散淤消肿,活血生肌,治疗跌打损伤,支气管肺炎、肺结核等功效;能延缓衰老、激活免疫细胞、改善机体免疫功能、提高人体免疫力,增强人体的新陈代谢并对记忆障碍有一定改善作用;具有降血压、降血脂、降血糖、抗氧化、抗溃疡和预防慢性肾病、抑制乙型肝炎的显著效果;对预防和治疗心脑血管疾病、糖尿病等有一定的疗效;还具有抗病毒、抗菌活性、抑制骨髓癌和志贺样毒素细胞的活性。另一方面,平卧菊三七是一种药食兼可的独特植物,具有极好的营养价值,因此,广泛利用于食品医药工业、日用化工工业等领域,是一种极具潜力和高经济价值的药食两用植物。The scientific name of Mansanqi is "Gynura procumbens (Lour.) Merr.", which belongs to the Compositae family and belongs to the genus of Panax notoginseng. Cool, a perennial herbal medicinal and edible plant, widely distributed in China, Malaysia, Thailand, Indonesia, South Korea and the Philippines and other countries. Recumbent chrysanthemum Panax notoginseng has a wide range of pharmacological effects. In the first half of 2009, relevant units such as China Center for Disease Control and Prevention, National Center for Food Quality Supervision and Inspection, China Food and Fermentation Industry Research Institute and other relevant units completed the toxicology test, sanitation The results of scientific testing and testing of various components are as follows: non-toxic and non-teratogenic; its active ingredients have the functions of dredging meridians and activating collaterals, reducing inflammation and relieving cough, dispersing stasis and swelling, promoting blood circulation and promoting muscle growth, treating traumatic injuries, bronchial pneumonia, tuberculosis, etc. Efficacy; can delay aging, activate immune cells, improve immune function, enhance human immunity, enhance human metabolism and improve memory impairment; it has blood pressure, blood lipid, blood sugar, anti-oxidation, anti-ulcer and prevention. It has significant effects on chronic kidney disease and hepatitis B inhibition; it has certain curative effects on the prevention and treatment of cardiovascular and cerebrovascular diseases, diabetes, etc. On the other hand, Chrysanthemum Panax notoginseng is a unique plant that can be used for both medicine and food, and has excellent nutritional value. Therefore, it is widely used in the food and pharmaceutical industry, daily chemical industry and other fields. High economic value of medicinal and edible plants.
木姜叶柯(Lithocarpus polystachyus Rehd),又名多穗石柯、甜茶、多穗柯。多以野生状态分布于长江以南各省区,而以江西、湖南、福建、广西、安徽等省资源最为集中。根皮苷与三叶苷为其主要成分,含有量高达9.0%~14.60%。现代医学研究表明,木姜叶柯具有清热利尿、润肺镇咳、滋润肝肾等功效,可用于防治温热痢疾、痈疽恶疮、皮肤瘙痒等症,还有“三抗”、“三降”的作用。现代研究表明,木姜叶柯具有抗氧化、降血糖、降血脂、抗菌、抗炎、抗过敏等药理作用。Lithocarpus polystachyus Rehd, also known as Lithocarpus polystachyus Rehd. Most of them are distributed in the provinces south of the Yangtze River in the wild state, and the resources are most concentrated in Jiangxi, Hunan, Fujian, Guangxi, Anhui and other provinces. Phloridzin and trilobulin are the main components, and the content is as high as 9.0% to 14.60%. Modern medical research has shown that Cordyceps sinensis has the functions of clearing heat and diuresis, moistening the lungs and relieving cough, moisturizing the liver and kidney, etc. It can be used to prevent and treat warm dysentery, carbuncle malignant sores, skin itching, etc. effect. Modern research has shown that Cordyceps sinensis has antioxidant, hypoglycemic, hypolipidemic, antibacterial, anti-inflammatory, anti-allergic and other pharmacological effects.
杜仲(Eucommia ulmoides Oliver),又名胶木,是杜仲科杜仲属植物。为我国特有的名贵滋补中药材,药用价值高,现代药理学研究表明杜仲具有抗衰老、抗氧化、降血压、降血脂、降血糖、抗诱变抗癌、抗菌及抗病毒等作用。杜仲活性成分丰富,主要含有黄酮类、苯丙素类、环烯醚萜类、多糖类、多酚类、苯丙素类、木脂素类等,且杜仲药理作用突出,具有多种保健功效。杜仲全身都是宝,其籽、花、皮、叶均可食用。经毒理学鉴定,杜仲籽油和杜仲雄花都是安全无毒的,两者已被国家卫计委批准为新食品原料,杜仲叶也于2019年被国家卫健委批准列人药食同源试点名单中,在健康食品开发方面有很大的前景。Eucommia ulmoides Oliver, also known as bakelite, is a plant of the Eucommia family. It is a unique and precious nourishing Chinese medicinal material in my country with high medicinal value. Modern pharmacological studies have shown that Eucommia has anti-aging, anti-oxidation, lowering blood pressure, lowering blood lipids, lowering blood sugar, anti-mutagenic, anti-cancer, antibacterial and antiviral effects. Eucommia is rich in active ingredients, mainly including flavonoids, phenylpropanoids, iridoids, polysaccharides, polyphenols, phenylpropanoids, lignans, etc., and Eucommia has prominent pharmacological effects and has a variety of health care benefits. effect. The whole body of Eucommia is a treasure, and its seeds, flowers, skins, and leaves can be eaten. After toxicological identification, Eucommia seed oil and Eucommia male flower are safe and non-toxic. Both have been approved as new food raw materials by the National Health and Family Planning Commission. Eucommia ulmoides leaves were also approved by the National Health and Health Commission in 2019 to be listed as homologous to human medicine and food. In the pilot list, there are great prospects in the development of healthy food.
发明内容SUMMARY OF THE INVENTION
本发明的目的提供一种具有降血糖作用的药食同源组合物及其制备方法和应用,其利用不同的提取纯化方式,分别富集杜仲、木姜叶柯与平卧菊三七中的有效成分,并通过优化组合的方式将所得粉末进行组合,并对组合物进行降血糖活性测试,与单一的提取物相比,作用得以互补,降血糖效力得以协同提高。The object of the present invention is to provide a medicine and food homologous composition with hypoglycemic effect and its preparation method and application, which utilizes different extraction and purification methods to enrich the active ingredients in Eucommia ulmoides, Alpinia officinalis and Panax notoginseng respectively. , and the obtained powders are combined by optimizing the combination, and the composition is tested for hypoglycemic activity. Compared with a single extract, the effects are complemented, and the hypoglycemic effect can be synergistically improved.
为实现上述发明目的,本发明采用如下技术方案:For realizing the above-mentioned purpose of the invention, the present invention adopts following technical scheme:
一种具有降血糖作用的药食同源组合物,分别以杜仲、木姜叶柯与平卧菊三七为原材料,分别提取杜仲提取物、木姜叶柯提取物、平卧菊三七提取物,然后将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按质量比1:1:1-1:1:3的比例混合得到组合提取物。A medicinal and food homologous composition with hypoglycemic effect, respectively using Eucommia, Alpinia officinalis and Panax notoginseng as raw materials, extracting Eucommia ulmoides extract, Alpinia officinalis extract, Panax notoginseng extract, and then The Eucommia ulmoides extract, the Cordyceps sinensis extract and the Panax notoginseng extract are mixed in a mass ratio of 1:1:1-1:1:3 to obtain a combined extract.
进一步优选,所述组合提取物中需包含绿原酸、隐绿原酸、咖啡酸、京尼平苷、车叶草苷、异绿原酸B、儿茶素、异槲皮苷、异绿原酸A、根皮苷、松脂醇二葡萄糖苷、异绿原酸C、三叶苷和芦丁等成分。Further preferably, the combined extract needs to contain chlorogenic acid, cryptochlorogenic acid, caffeic acid, geniposide, phytoside, isochlorogenic acid B, catechin, isoquercitrin, isogreen Orthoic acid A, phloridzin, pinoresinol diglucoside, isochlorogenic acid C, treloin and rutin.
一种具有降血糖作用的药食同源组合物制备方法,包括以下步骤:A preparation method of a medicine-food homologous composition with hypoglycemic effect, comprising the following steps:
步骤1):采集杜仲叶为原材料,干燥粉碎后采用水作为提取溶剂,提取温度为80℃,料液比为1:10-20,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入4倍量的无水乙醇,放入冰箱,过夜,离心收集上清液,浓缩至无醇味,加入等量蒸馏水超声波打散,加入等体积的溶剂萃取,萃取三次,合并萃取相,浓缩至干制备得杜仲叶提取物;Step 1): collecting Eucommia ulmoides leaves as raw materials, using water as extraction solvent after drying and pulverizing, the extraction temperature is 80 ° C, the material-liquid ratio is 1:10-20, stirring and extracting, filtering, and the combined filtrate is concentrated under reduced pressure to 1/1 of the original solution. 10. Add 4 times the amount of absolute ethanol, put it in the refrigerator, overnight, collect the supernatant by centrifugation, concentrate until there is no alcohol smell, add an equal volume of distilled water to ultrasonically disperse, add an equal volume of solvent for extraction, extract three times, and combine the extraction phases. , concentrated to dryness to prepare Eucommia ulmoides leaf extract;
步骤2):采集木姜叶柯叶为原材料,干燥粉碎后采用水作为提取溶剂,提取温度为70℃,料液比为1:10-20,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入10%的活性炭70℃搅拌脱色,滤液经喷雾干燥后得到木姜叶柯提取物;Step 2): collecting Cordyceps sinensis as raw material, using water as extraction solvent after drying and pulverizing, the extraction temperature is 70 ° C, the ratio of material to liquid is 1:10-20, stirring and extracting, filtering, and the combined filtrate is concentrated under reduced pressure to 1 of the original solution. /10, add 10% activated carbon at 70°C and stir to decolorize, and the filtrate is spray-dried to obtain the extract of Cordyceps sinensis;
步骤3):采集平卧菊三七叶为原材料,干燥粉碎后采用乙醇水溶液作为提取溶剂,离心收集上清液,浓缩至无醇味,浓缩至干制备得平卧菊三七叶提取物;Step 3): collecting the Panax notoginseng leaves as raw materials, using an aqueous ethanol solution as the extraction solvent after drying and pulverizing, collecting the supernatant by centrifugation, concentrating until there is no alcohol smell, and concentrating to dryness to prepare the Panax notoginseng leaf extract;
步骤4):将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按照比例混合、摇匀制备药食同源组合物。Step 4): Mix and shake the Eucommia ulmoides extract, the Cordyceps sinensis extract, and the Panax notoginseng extract according to the proportions to prepare a medicine and food homologous composition.
进一步地,步骤4)中,将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按质量比1:1:1-1:1:3的比例混合得到组合提取物。Further, in step 4), the extract of Eucommia ulmoides, the extract of Cordyceps sinensis, and the extract of Panax notoginseng are mixed in a mass ratio of 1:1:1-1:1:3 to obtain a combined extract.
进一步地,所述组合提取物中需包含绿原酸、隐绿原酸、咖啡酸、京尼平苷、车叶草苷、异绿原酸B、儿茶素、异槲皮苷、异绿原酸A、根皮苷、松脂醇二葡萄糖苷、异绿原酸C、三叶苷和芦丁等成分。Further, the composition extract needs to contain chlorogenic acid, cryptochlorogenic acid, caffeic acid, geniposide, phytoside, isochlorogenic acid B, catechin, isoquercitrin, isogreen Orthoic acid A, phloridzin, pinoresinol diglucoside, isochlorogenic acid C, treloin and rutin.
进一步地,步骤3)中,提取溶剂为PH=2-7的50-90%乙醇水溶液,液料比为1:10-20,提取温度为常温,超声提取2小时,滤液经减压浓缩至无醇味。Further, in step 3), the extraction solvent is 50-90% ethanol aqueous solution with PH=2-7, the liquid-material ratio is 1:10-20, the extraction temperature is normal temperature, the ultrasonic extraction is performed for 2 hours, and the filtrate is concentrated under reduced pressure to No alcohol smell.
进一步地,步骤1)中所用有机溶剂为石油醚、正己烷、二氯甲烷、乙酸乙酯、正丁醇、二氯甲烷/甲醇和石油醚/乙酸乙酯的任意一种。Further, the organic solvent used in step 1) is any one of petroleum ether, n-hexane, dichloromethane, ethyl acetate, n-butanol, dichloromethane/methanol and petroleum ether/ethyl acetate.
进一步地,优选地,步骤1)中所用萃取溶剂,所选萃取溶剂用乙酸乙酯/甲醇,乙酸乙酯/甲醇体积比4:1最佳。Further, preferably, the extraction solvent used in step 1), the selected extraction solvent is ethyl acetate/methanol, and the ethyl acetate/methanol volume ratio of 4:1 is the best.
本发明还提供了制备的药食同源组合物在制备糖尿病药物中的应用。The invention also provides the application of the prepared medicine and food homologous composition in the preparation of diabetes medicine.
由于采用如上所述的技术方案,本发明具有如下优越性:Due to adopting the above-mentioned technical scheme, the present invention has the following advantages:
本发明通过不同的提取纯化方式,对杜仲、木姜叶柯与平卧菊三七有效成分进行富集,共获得14中有效成分,分别是绿原酸、隐绿原酸、咖啡酸、京尼平苷、车叶草苷、异绿原酸B、儿茶素、异槲皮苷、异绿原酸A、根皮苷、松脂醇二葡萄糖苷、异绿原酸C、三叶苷和芦丁,其含量占组合物粉末的90%,揭示了降血糖的物质基础,与传统中药相比,更有效的富集了有效成分,舍弃了一些无效成分。所制备的药食同源组合物对糖尿病患者具有特别好的效果,用过本提取物的患者痛风基本没有再复发过,效果明显好于单独的使用杜仲、木姜叶柯与平卧菊三七提取物。The present invention enriches the effective components of Eucommia ulmoides, Cordyceps sinensis and Panax notoginseng through different extraction and purification methods, and obtains a total of 14 effective components, which are chlorogenic acid, cryptochlorogenic acid, caffeic acid, and genipin. Glycosides, phytoside, isochlorogenic acid B, catechin, isoquercitrin, isochlorogenic acid A, phlorizin, pinoresinol diglucoside, isochlorogenic acid C, trilobin and rutin , and its content accounts for 90% of the composition powder, which reveals the material basis for lowering blood sugar. Compared with traditional Chinese medicine, it more effectively enriches the active ingredients and discards some ineffective ingredients. The prepared medicine and food homologous composition has a particularly good effect on diabetic patients, and the patients who have used the extract basically have no recurrence of gout, and the effect is obviously better than the single use of Eucommia ulmoides, Alpinia officinalis and Panax notoginseng extracts. thing.
附图说明Description of drawings
图1是本发明组合物的液相色谱图。Figure 1 is a liquid chromatogram of the composition of the present invention.
图2是本发明平卧菊三七提取物的液相色谱图。Fig. 2 is the liquid chromatogram of the Panax notoginseng extract of the present invention.
图3是本发明杜仲提取物的液相色谱图。Figure 3 is a liquid chromatogram of the Eucommia ulmoides extract of the present invention.
图4是本发明木姜叶柯提取物的液相色谱图。Fig. 4 is the liquid chromatogram of the Cordyceps sinensis extract of the present invention.
图5是本发明对比例提取物的液相色谱图。Fig. 5 is a liquid chromatogram of the extract of the comparative example of the present invention.
具体实施方式Detailed ways
参照以下实施例可以对本发明作进一步详细说明;但是,以下实施例仅仅是例证,本发明并不局限于这些实施例。The present invention can be further described in detail with reference to the following examples; however, the following examples are merely illustrative, and the present invention is not limited to these examples.
一种具有降血糖作用的药食同源组合物其制备方法,包括以下步骤:A preparation method of a medicine-food homologous composition with hypoglycemic effect, comprising the following steps:
步骤1):采集杜仲叶为原材料,干燥粉碎后采用水作为提取溶剂,提取温度为80℃,料液比为1:10-20,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入4倍量的无水乙醇,放入冰箱,过夜,离心收集上清液,浓缩至无醇味,加入等量蒸馏水超声波打散,加入等体积的溶剂萃取,萃取三次,合并萃取相,浓缩至干制备得杜仲叶提取物;Step 1): collecting Eucommia ulmoides leaves as raw materials, using water as extraction solvent after drying and pulverizing, the extraction temperature is 80 ° C, the material-liquid ratio is 1:10-20, stirring and extracting, filtering, and the combined filtrate is concentrated under reduced pressure to 1/1 of the original solution. 10. Add 4 times the amount of absolute ethanol, put it in the refrigerator, overnight, collect the supernatant by centrifugation, concentrate until there is no alcohol smell, add an equal volume of distilled water to ultrasonically disperse, add an equal volume of solvent for extraction, extract three times, and combine the extraction phases. , concentrated to dryness to prepare Eucommia ulmoides leaf extract;
步骤2):采集木姜叶柯叶为原材料,干燥粉碎后采用水作为提取溶剂,提取温度为70℃,料液比为1:10-20,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入10%的活性炭70℃搅拌脱色,滤液经喷雾干燥后得到木姜叶柯提取物;Step 2): collecting Cordyceps sinensis as raw material, using water as extraction solvent after drying and pulverizing, the extraction temperature is 70 ° C, the ratio of material to liquid is 1:10-20, stirring and extracting, filtering, and the combined filtrate is concentrated under reduced pressure to 1 of the original solution. /10, add 10% activated carbon at 70°C and stir to decolorize, and the filtrate is spray-dried to obtain the extract of Cordyceps sinensis;
步骤3):采集平卧菊三七叶为原材料,干燥粉碎后采用醇水作为提取溶剂,离心收集上清液,浓缩至无醇味,浓缩至干制备得平卧菊三七叶提取物;Step 3): collecting the Panax notoginseng leaves as raw materials, using alcohol water as the extraction solvent after drying and pulverizing, collecting the supernatant by centrifugation, concentrating until there is no alcohol smell, and concentrating to dryness to prepare the Panax notoginseng leaf extract;
步骤4):将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按照比例混合、摇匀制备药食同源组合物。组合提取物中经液相检测含有绿原酸、隐绿原酸、咖啡酸、京尼平苷、车叶草苷、异绿原酸B、儿茶素、异槲皮苷、异绿原酸A、根皮苷、松脂醇二葡萄糖苷、异绿原酸C、三叶苷和芦丁等成分。Step 4): Mix and shake the Eucommia ulmoides extract, the Cordyceps sinensis extract, and the Panax notoginseng extract according to the proportions to prepare a medicine and food homologous composition. The combined extract contains chlorogenic acid, cryptochlorogenic acid, caffeic acid, geniposide, phytoside, isochlorogenic acid B, catechin, isoquercitrin, isochlorogenic acid by liquid phase detection A. Phloridzin, Pinoresinol Diglucoside, Isochlorogenic Acid C, Trilobin and Rutin.
实施例1Example 1
取杜仲叶100g,干燥粉碎后采用水作为提取溶剂,提取温度为80℃,料液比为1:20,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入4倍量的无水乙醇,放入冰箱,过夜,离心收集上清液,浓缩至无醇味,加入等量蒸馏水超声波打散,加入等体积的正丁醇萃取,萃取三次,合并萃取相,浓缩至干制备得杜仲叶提取物2.35g,得率2.35%,杜仲提取物的液相色谱图如图3所示。Take 100 g of Eucommia ulmoides leaves, dry and pulverize, use water as the extraction solvent, the extraction temperature is 80 ° C, the material-liquid ratio is 1:20, stir and extract, filter, the combined filtrate is concentrated under reduced pressure to 1/10 of the original solution, and 4 times the amount of Absolute ethanol, put in the refrigerator, overnight, centrifuged to collect the supernatant, concentrated until there is no alcohol smell, add equal volume of distilled water to ultrasonically disperse, add equal volume of n-butanol for extraction, extract three times, combine the extract phases, and concentrate to dryness. 2.35 g of Eucommia ulmoides leaf extract was obtained, with a yield of 2.35%. The liquid chromatogram of the Eucommia ulmoides extract is shown in FIG. 3 .
取木姜叶柯100g,干燥粉碎后采用水作为提取溶剂,提取温度为70℃,料液比为1:20,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入10%的活性炭70℃搅拌脱色,滤液经喷雾干燥后得到木姜叶柯提取物6.42g,得率6.42%,木姜叶柯提取物的液相色谱图如图4所示。Take 100 g of Cordyceps sinensis, dry and pulverize, and use water as the extraction solvent, the extraction temperature is 70 ° C, and the ratio of material to liquid is 1:20, stirring and extracting, filtering, the combined filtrate is concentrated under reduced pressure to 1/10 of the original solution, and 10% of activated carbon is added. Stirring at 70° C. for decolorization, and the filtrate was spray-dried to obtain 6.42 g of the extract of Cordyceps sinensis, with a yield of 6.42%.
取平卧菊三七叶100g,干燥粉碎后采用PH=3的50%乙醇水溶液,料液比为1:10,提取温度为常温,超声提取2小时,滤液经减压浓缩至无醇味。浓缩至干制备得平卧菊三七叶提取物9.24g,得率9.24%,平卧菊三七提取物的液相色谱图如图2所示。Take 100 g of Panax notoginseng leaves, dry and pulverize, use 50% ethanol aqueous solution with pH=3, the material-liquid ratio is 1:10, the extraction temperature is normal temperature, ultrasonic extraction is carried out for 2 hours, and the filtrate is concentrated under reduced pressure until there is no alcohol smell. Concentrating to dryness to prepare 9.24 g of the Panax notoginseng leaf extract, the yield is 9.24%, and the liquid chromatogram of the Panax notoginseng extract is shown in Figure 2 .
将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按照质量比1:1:1的比例混合、摇匀制备药食同源组合物。组合提取物中经液相检测含有1绿原酸、2隐绿原酸、3咖啡酸、4京尼平苷、5车叶草苷、6异绿原酸B、7儿茶素、8异槲皮苷、9异绿原酸A、10根皮苷、11松脂醇二葡萄糖苷、12异绿原酸C、13三叶苷和14芦丁等成分,如图1所示。The eucommia ulmoides extract, the extract of Cordyceps sinensis, and the extract of Panax notoginseng are mixed and shaken in a mass ratio of 1:1:1 to prepare a medicine-food homologous composition. The liquid phase detection in the combined extract contains 1 chlorogenic acid, 2 cryptochlorogenic acid, 3 caffeic acid, 4 geniposide, 5 phytoside, 6 isochlorogenic acid B, 7 catechin, 8 isochlorogenic acid Quercitrin, 9 isochlorogenic acid A, 10 phloridzin, 11 pinoresinol diglucoside, 12 isochlorogenic acid C, 13 trilobulin and 14 rutin and other components, as shown in Figure 1.
实施例2Example 2
取杜仲叶100g,干燥粉碎后采用水作为提取溶剂,提取温度为80℃,料液比为1:10,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入4倍量的无水乙醇,放入冰箱,过夜,离心收集上清液,浓缩至无醇味,加入等量蒸馏水超声波打散,加入等体积的二氯甲烷/甲醇萃取,萃取三次,合并萃取相,浓缩至干制备得杜仲叶提取物4.18g,得率4.18%;Take 100 g of Eucommia ulmoides leaves, use water as the extraction solvent after drying and pulverizing, the extraction temperature is 80 ° C, the material-liquid ratio is 1:10, stir and extract, filter, combine the filtrate and concentrate under reduced pressure to 1/10 of the original solution, add 4 times the amount of Absolute ethanol, put in the refrigerator, overnight, centrifuged to collect the supernatant, concentrated until there is no alcohol smell, add equal volume of distilled water to ultrasonically disperse, add equal volume of dichloromethane/methanol for extraction, extract three times, combine the extract phases, and concentrate to Dry prepared Eucommia ulmoides leaf extract 4.18g, yield 4.18%;
取木姜叶柯100g,干燥粉碎后采用水作为提取溶剂,提取温度为70℃,料液比为1:10,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入10%的活性炭70℃搅拌脱色,滤液经喷雾干燥后得到木姜叶柯提取物4.25g,得率4.25%。Take 100 g of Cordyceps sinensis, dry and pulverize, use water as the extraction solvent, the extraction temperature is 70 ° C, the material-to-liquid ratio is 1:10, stir and extract, filter, the combined filtrate is concentrated under reduced pressure to 1/10 of the original solution, and 10% of activated carbon is added. Stirring at 70° C. for decolorization, the filtrate was spray-dried to obtain 4.25 g of the extract of Cordyceps sinensis, with a yield of 4.25%.
取平卧菊三七叶100g,干燥粉碎后采用PH=2的80%乙醇水溶液,料液比为1:20,提取温度为常温,超声提取2小时,滤液经减压浓缩至无醇味。浓缩至干制备得平卧菊三七叶提取物8.77g,得率8.77%。Take 100 g of Panax notoginseng leaves, dry and pulverize, use 80% ethanol aqueous solution with pH=2, the material-to-liquid ratio is 1:20, the extraction temperature is normal temperature, ultrasonic extraction is performed for 2 hours, and the filtrate is concentrated under reduced pressure until there is no alcohol smell. Concentrate to dryness to prepare 8.77 g of the extract of Panax notoginseng leaves, and the yield is 8.77%.
将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按照质量比1:1:2的比例混合、摇匀制备药食同源组合物。组合提取物中经液相检测含有绿原酸、隐绿原酸、咖啡酸、京尼平苷、车叶草苷、异绿原酸B、儿茶素、异槲皮苷、异绿原酸A、根皮苷、松脂醇二葡萄糖苷、异绿原酸C、三叶苷和芦丁等成分。The eucommia ulmoides extract, the extract of Cordyceps sinensis, and the extract of Panax notoginseng are mixed according to the mass ratio of 1:1:2, and shaken to prepare a medicine-food homologous composition. The combined extract contains chlorogenic acid, cryptochlorogenic acid, caffeic acid, geniposide, phytoside, isochlorogenic acid B, catechin, isoquercitrin, isochlorogenic acid by liquid phase detection A. Phloridzin, Pinoresinol Diglucoside, Isochlorogenic Acid C, Trilobin and Rutin.
实施例3Example 3
取杜仲叶100g,干燥粉碎后采用水作为提取溶剂,提取温度为80℃,料液比为1:15,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入4倍量的无水乙醇,放入冰箱,过夜,离心收集上清液,浓缩至无醇味,加入等量蒸馏水超声波打散,加入等体积的石油醚/乙酸乙酯萃取,萃取三次,合并萃取相,浓缩至干制备得杜仲叶提取物2.04g,得率2.04%。Take 100 g of Eucommia ulmoides leaves, dry and pulverize, use water as the extraction solvent, the extraction temperature is 80 ° C, the material-liquid ratio is 1:15, stir and extract, filter, the combined filtrate is concentrated under reduced pressure to 1/10 of the original solution, and 4 times the amount of Absolute ethanol, put in the refrigerator, overnight, centrifuged to collect the supernatant, concentrated until there is no alcohol smell, add equal volume of distilled water to ultrasonically disperse, add equal volume of petroleum ether/ethyl acetate for extraction, extract three times, combine the extract phases, and concentrate To dryness, 2.04 g of Eucommia ulmoides leaf extract was prepared, and the yield was 2.04%.
取木姜叶柯100g,干燥粉碎后采用水作为提取溶剂,提取温度为70℃,料液比为1:15,搅拌提取,过滤,合并滤液减压浓缩至原液的1/10,加入10%的活性炭70℃搅拌脱色,滤液经喷雾干燥后得到木姜叶柯提取物7.44g,得率7.44%。Take 100 g of Cordyceps sinensis, use water as extraction solvent after drying and pulverizing, the extraction temperature is 70 ° C, the ratio of material to liquid is 1:15, stirred and extracted, filtered, the combined filtrate was concentrated under reduced pressure to 1/10 of the original solution, and 10% of activated carbon was added. Stirring and decolorizing at 70° C., the filtrate was spray-dried to obtain 7.44 g of the extract of Cordyceps sinensis, with a yield of 7.44%.
取平卧菊三七叶100g,干燥粉碎后采用PH=7的60%乙醇水溶液,料液比为1:15,提取温度为常温以及超声提取2小时,滤液经减压浓缩至无醇味。浓缩至干制备得平卧菊三七叶提取物10.45g,得率10.45%。Take 100 g of Panax notoginseng leaves, dry and pulverize, use a 60% ethanol aqueous solution with pH=7, the material-to-liquid ratio is 1:15, the extraction temperature is normal temperature and ultrasonic extraction for 2 hours, and the filtrate is concentrated under reduced pressure until there is no alcohol smell. Concentrate to dryness to prepare 10.45 g of the extract of Panax notoginseng leaves, and the yield is 10.45%.
将杜仲提取物、木姜叶柯提取物、平卧菊三七提取物按照质量比1:1:3的比例混合、摇匀制备药食同源组合物。组合提取物中经液相检测含有绿原酸、隐绿原酸、咖啡酸、京尼平苷、车叶草苷、异绿原酸B、儿茶素、异槲皮苷、异绿原酸A、根皮苷、松脂醇二葡萄糖苷、异绿原酸C、三叶苷和芦丁等成分。The eucommia ulmoides extract, the extract of Cordyceps sinensis, and the extract of Panax notoginseng are mixed and shaken in a mass ratio of 1:1:3 to prepare a medicine-food homologous composition. The combined extract contains chlorogenic acid, cryptochlorogenic acid, caffeic acid, geniposide, phytoside, isochlorogenic acid B, catechin, isoquercitrin, isochlorogenic acid by liquid phase detection A. Phloridzin, Pinoresinol Diglucoside, Isochlorogenic Acid C, Trilobin and Rutin.
对比例Comparative ratio
取杜仲叶、木姜叶柯与平卧菊三七各100g,使用粉碎机一起粉碎后加入锥形瓶中,提取溶剂为PH=5的90%乙醇水溶液,料液比为1:15,提取温度为常温以及超声提取2小时,过滤,滤液经减压浓缩至无醇味。向所得溶液中加入4倍体积的100%的乙醇溶液,放入4℃冰箱过夜进行醇沉,离心收集上清液,减压浓缩至无醇味,得到混合提取液,混合提取液经溶剂萃取,所用萃取溶剂为正丁醇,合并萃取液、减压浓缩、以及干燥得到混合提取物4.52g,混合提取物中含有绿原酸、异绿原酸B、异绿原酸A、根皮苷、异绿原酸C和芦丁等成分。化合物隐绿原酸、咖啡酸、京尼平苷、车叶草苷、儿茶素、异槲皮苷、松脂醇二葡萄糖苷与三叶苷未检出。Take 100 g each of Eucommia ulmoides leaves, Cordyceps sinensis and Pseudomonas notoginseng, pulverize them together with a pulverizer, and add them to a conical flask. The extraction solvent is a 90% ethanol aqueous solution with pH=5, the material-to-liquid ratio is 1:15, and the extraction temperature is Extracted at room temperature and ultrasonic for 2 hours, filtered, and the filtrate was concentrated under reduced pressure until there was no alcohol smell. Add 4 times the volume of 100% ethanol solution to the obtained solution, put it in a 4°C refrigerator overnight for alcohol precipitation, collect the supernatant by centrifugation, and concentrate under reduced pressure until there is no alcohol odor to obtain a mixed extract, which is subjected to solvent extraction. , the extraction solvent used was n-butanol, the extracts were combined, concentrated under reduced pressure, and dried to obtain 4.52 g of a mixed extract containing chlorogenic acid, isochlorogenic acid B, isochlorogenic acid A, phloridzin , isochlorogenic acid C and rutin. Compounds cryptochlorogenic acid, caffeic acid, geniposide, phytoside, catechin, isoquercitrin, pinoresinol diglucoside and trefoil were not detected.
药食同源组合物对链脲佐菌素致小鼠血糖的影响Effects of medicinal and food homologous compositions on blood glucose in mice induced by streptozotocin
选择130只健康雄性昆明小鼠(约20g)作为实验动物,随机分为13组:(空白对照组,模型对照组,阳性对照组(阿卡波糖),混合提取物=1:1:1高剂量组,混合提取物=1:1:1低剂量组,混合提取物=1:1:2高剂量组,混合提取物=1:1:2低剂量组,混合提取物=1:1:3高剂量组,混合提取物=1:1:3低剂量组,木姜叶柯提取物组,平卧菊三七提取物组,杜仲叶提取物组,对比例组)各组10只。第一周选用普通饲料提供充足食物与水分,以避免环境变化带来异常。一周后,所有小鼠开始快速喂水,12h后,在空白对照组外腹腔注射0.1mol/L STZ溶液。每只小鼠的注射剂量选择以60mg/kg以建立2型糖尿病的模型,并且空白对照组注射等体积的蒸馏水。注射后,给空白对照组小鼠喂食正常饲料,给剩下的小鼠喂食高糖和高脂肪饮食5天。建模5天后,测试小鼠的血糖,血糖范围为11-25mmol/L被认为是成功的。如果存在血糖值小于11mmol/L的小鼠,则需要继续补充注射STZ,将STZ溶解在pH4.2和4.5之间的柠檬酸盐缓冲液中。并将其储存在用箔纸包裹的试管中。并在30min中快速注射到小鼠的腹腔内。数据结果采用平均数±标准差(x±s)表示,各组之间的差异性采用单向方差分析通过统计软件包SPSS 19.0版,P<0.05认为有显著性差异,P>0.05则无显著性差异。130 healthy male Kunming mice (about 20g) were selected as experimental animals and randomly divided into 13 groups: (blank control group, model control group, positive control group (acarbose), mixed extract = 1:1:1 High-dose group, mixed extract=1:1:1 Low-dose group, mixed extract=1:1:2 High-dose group, mixed extract=1:1:2 Low-dose group, mixed extract=1:1 : 3 high-dose group, mixed extract = 1:1:3 low-dose group, Radix chinensis extract group, Panax notoginseng extract group, Eucommia ulmoides leaf extract group, control group) 10 in each group. In the first week, ordinary feed was used to provide sufficient food and water to avoid abnormalities caused by environmental changes. One week later, all mice were fed with water quickly, and 12 hours later, 0.1 mol/L STZ solution was injected into the abdomen outside the blank control group. The injection dose of each mouse was selected to be 60 mg/kg to establish a model of type 2 diabetes, and the blank control group was injected with an equal volume of distilled water. After injection, mice in the blank control group were fed a normal chow diet, and the remaining mice were fed a high-sugar and high-fat diet for 5 days. After 5 days of modeling, the blood glucose of the mice was tested, and a blood glucose range of 11-25 mmol/L was considered successful. If there are mice with blood glucose values less than 11 mmol/L, supplementary injection of STZ is required, and STZ is dissolved in citrate buffer between pH 4.2 and 4.5. And store it in a test tube wrapped in foil. And in 30min rapid injection into the abdominal cavity of mice. The data results are expressed as mean ± standard deviation (x ± s), and the differences between groups are expressed by one-way analysis of variance through the statistical software package SPSS version 19.0. sexual differences.
将造模后血糖浓度在11-25mmol/L内的小鼠分别按照体重及血糖浓度均匀分配成13组,按照表1进行灌胃。Mice with blood glucose concentration within 11-25 mmol/L after modeling were evenly divided into 13 groups according to body weight and blood glucose concentration, and were given intragastric administration according to Table 1.
表1动物实验分组Table 1 Animal experiment grouping
如表2所示,从表中可以看出,成功建模后糖尿病小鼠的空腹血糖水平显著增加。并保持高血糖水平,与空白对照组相比,存在非常显著的差异(p<0.01),STZ成功诱导并模拟了小鼠糖尿病的高血糖模型。在整个给药期间,空白对照组的平均血糖水平稳定在5mmol/L,而模型对照组的小鼠随给药周期逐渐增加。说明糖尿病病情逐渐严重,直到第四、五周保持在25mmol/L左右,并且与组合物低、高剂量组之间存在显著或极显著差异(P<0.01或P<0.05)。As shown in Table 2, it can be seen from the table that the fasting blood glucose levels of the diabetic mice were significantly increased after successful modeling. And maintain high blood sugar level, compared with blank control group, there is a very significant difference (p<0.01), STZ successfully induced and simulated the hyperglycemia model of mouse diabetes. During the entire administration period, the average blood glucose level of the blank control group was stable at 5 mmol/L, while the mice in the model control group gradually increased with the administration period. It indicated that the condition of diabetes was gradually serious until the fourth and fifth weeks, which remained at about 25mmol/L, and there was a significant or extremely significant difference with the low and high dose groups of the composition (P<0.01 or P<0.05).
在阳性对照组和混合提取物=1:1:1高剂量组,混合提取物=1:1:1低剂量组,混合提取物=1:1:2高剂量组,混合提取物=1:1:2低剂量组,混合提取物=1:1:3高剂量组,混合提取物=1:1:3低剂量组中,前三周小鼠的血糖水平随着治疗期的增加而增加。但是,它比模型对照组慢。自第4周起,阳性对照组显著降低糖尿病小鼠的空腹血糖水平;灌胃五周后,阳性对照组小鼠血糖较模型对照组小鼠血糖下降了45.54%,存在显著性差异。In positive control group and mixed extract=1:1:1 high dose group, mixed extract=1:1:1 low dose group, mixed extract=1:1:2 high dose group, mixed extract=1:1 1:2 low-dose group, mixed extract=1:1:3 high-dose group, mixed extract=1:1:3 low-dose group, the blood glucose level of mice in the first three weeks increased with the treatment period . However, it was slower than the model control group. From the 4th week, the positive control group significantly reduced the fasting blood glucose level of the diabetic mice; after five weeks of gavage, the blood glucose of the positive control group decreased by 45.54% compared with the model control group, a significant difference.
混合提取物=1:1:1高剂量组、混合提取物=1:1:2高剂量组、混合提取物=1:1:3高剂量组小鼠空腹血糖值自灌胃第四周开始均有不同程度的下降,并且与模型对照组相比表现出显著或极显著差异((P<0.01或P<0.05),灌胃5周后,混合提取物=1:1:1高剂量组、混合提取物=1:1:2高剂量组、混合提取物=1:1:3高剂量组小鼠血糖相对于模型组小鼠血糖平均下降了80%,可证明组合物对糖尿病可能有一定的控制作用。Mixed extract=1:1:1 high-dose group, mixed extract=1:1:2 high-dose group, mixed extract=1:1:3 high-dose group Fasting blood glucose values of mice started from the fourth week of gavage There were different degrees of decline, and compared with the model control group, there was a significant or extremely significant difference ((P<0.01 or P<0.05), after 5 weeks of gavage, mixed extract = 1:1:1 high-dose group , mixed extract = 1:1:2 high-dose group, mixed extract = 1:1:3 high-dose group, the blood sugar of mice in the high-dose group decreased by an average of 80% compared with the blood sugar of the model group mice, which can prove that the composition may have effects on diabetes. certain control.
木姜叶柯提取物组,平卧菊三七提取物组,杜仲叶提取物组,对比例组小鼠空腹血糖值与混合提取物高低剂量组呈现出相同的趋势,所不同的是,木姜叶柯提取物组,平卧菊三七提取物组,杜仲叶提取物组,在第四周与第五周所呈现的效果比混合提取物组要差,但是木姜叶柯提取物组,平卧菊三七提取物组,杜仲叶提取物组在第四周与第五周小鼠空腹血糖值比对比例组相比要小,表明同等剂量下,混合提取物效果优于单独的三个药食同源植物的提取物,对比例的效果最差。The fasting blood glucose values of the mice in the Mice extract group, the Periphora Radix Notoginseng extract group, the Eucommia ulmoides leaf extract group, and the control group showed the same trend as the high and low dose groups of the mixed extracts. In the fourth and fifth weeks, the effect of the extract group, the Radix Notoginseng extract group, and the Eucommia ulmoides leaf extract group was worse than that of the mixed extract group, but the Radix Radix et Rhizoma extract group, the Radix Radix Notoginseng In the extract group and the Eucommia ulmoides leaf extract group, the fasting blood glucose values of the mice in the fourth and fifth weeks were lower than those in the control group, indicating that at the same dose, the effect of the mixed extract was better than that of the three medicines and food homology alone. The plant extract, the comparative example had the worst effect.
表2混合提取物对糖尿病小鼠血糖值的影响Table 2 Effects of mixed extracts on blood glucose levels in diabetic mice
与正常对照组相比,##P<0.01;与模型组相比,*P<0.05,**P<0.01和***P<0.001。 ## P<0.01 compared with normal control group; * P<0.05, ** P<0.01 and *** P<0.001 compared with model group.
以上所述仅为本发明的较佳实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内所作的任何修改、等同替换和改进等,均应包含在本发明的保护范围之内。The above descriptions are only preferred embodiments of the present invention and are not intended to limit the present invention. Any modifications, equivalent replacements and improvements made within the spirit and principles of the present invention shall be included in the protection of the present invention. within the range.
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112843009A (en) * | 2021-03-26 | 2021-05-28 | 广西壮族自治区林业科学研究院 | Method for preparing phlorizin mixed hypoglycemic preparation |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101260131A (en) * | 2008-04-19 | 2008-09-10 | 吉首大学 | Method for extracting iridoid active site and monomer from Eucommia ulmoides |
CN101602668A (en) * | 2009-07-13 | 2009-12-16 | 江西省科学院应用化学研究所 | A method for extracting chlorogenic acid |
CN101904882A (en) * | 2010-07-28 | 2010-12-08 | 广西壮族自治区中医药研究院 | Preparation method of lithocarpus litseifolius total flavone |
CN102670696B (en) * | 2012-05-03 | 2014-04-16 | 中国药科大学 | Eucommia ulmoids leaf extracts and preparation method and application thereof |
CN108689852A (en) * | 2018-06-26 | 2018-10-23 | 江西省科学院应用化学研究所 | A method of chlorogenic acid extracting and isochlorogenic acid from Gynura procumbens (Lour.) Merr |
CN110893197A (en) * | 2019-12-05 | 2020-03-20 | 江西省科学院应用化学研究所 | Mangosteen extract for treating gout and preparation method thereof |
CN111281902A (en) * | 2018-12-06 | 2020-06-16 | 常州高新技术产业开发区三维工业技术研究所有限公司 | Application of lithocarpus litseifolius or active extract thereof |
-
2020
- 2020-08-11 CN CN202010799647.0A patent/CN111700927B/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101260131A (en) * | 2008-04-19 | 2008-09-10 | 吉首大学 | Method for extracting iridoid active site and monomer from Eucommia ulmoides |
CN101602668A (en) * | 2009-07-13 | 2009-12-16 | 江西省科学院应用化学研究所 | A method for extracting chlorogenic acid |
CN101904882A (en) * | 2010-07-28 | 2010-12-08 | 广西壮族自治区中医药研究院 | Preparation method of lithocarpus litseifolius total flavone |
CN102670696B (en) * | 2012-05-03 | 2014-04-16 | 中国药科大学 | Eucommia ulmoids leaf extracts and preparation method and application thereof |
CN108689852A (en) * | 2018-06-26 | 2018-10-23 | 江西省科学院应用化学研究所 | A method of chlorogenic acid extracting and isochlorogenic acid from Gynura procumbens (Lour.) Merr |
CN111281902A (en) * | 2018-12-06 | 2020-06-16 | 常州高新技术产业开发区三维工业技术研究所有限公司 | Application of lithocarpus litseifolius or active extract thereof |
CN110893197A (en) * | 2019-12-05 | 2020-03-20 | 江西省科学院应用化学研究所 | Mangosteen extract for treating gout and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
倪青主编: "《糖尿病中医循证治疗学》", 31 May 2015, 科学技术文献出版社 * |
王娟娟 等: "杜仲化学成分、药理活性和质量控制现状研究进展", 《中草药》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112843009A (en) * | 2021-03-26 | 2021-05-28 | 广西壮族自治区林业科学研究院 | Method for preparing phlorizin mixed hypoglycemic preparation |
CN112843009B (en) * | 2021-03-26 | 2022-08-05 | 广西壮族自治区林业科学研究院 | A kind of method for preparing phloridzin mixed hypoglycemic preparation |
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