TWI670067B - Wild bitter gourd extract technology - Google Patents

Wild bitter gourd extract technology Download PDF

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TWI670067B
TWI670067B TW102140028A TW102140028A TWI670067B TW I670067 B TWI670067 B TW I670067B TW 102140028 A TW102140028 A TW 102140028A TW 102140028 A TW102140028 A TW 102140028A TW I670067 B TWI670067 B TW I670067B
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extraction
bitter gourd
extract
ultrasonic
concentrated
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TW201517809A (en
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高美雯
褚俊傑
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美梭生技股份有限公司
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Abstract

本發明係有關一種具治療糖尿病症的山苦瓜萃取物之萃取技術,萃取流程主要包含預處理與苦瓜萃取所構成,所述之苦瓜萃取,主要係由投入循環槽、超音波集中萃取與取出萃取物等步驟所組成,該投入循環槽係將經處理的苦瓜粉末投入一萃取機的循環槽之中,並進行超音波集中萃取,該超音波集中萃取係將超音波集中於循環槽的一預定位置,令苦瓜粉末能在該位置被集中的超音波震碎,而在萃取結束後便可取出萃取物者,該利用超音波集中萃取的方式,以有效提高萃取率,降低生產成本。 The invention relates to an extraction technology of an extract of Momordica charantia L. with treatment for diabetes. The extraction process mainly comprises pretreatment and extraction of bitter gourd, and the bitter melon extraction is mainly carried out by input circulation tank, ultrasonic extraction and extraction extraction. The composition comprises the steps of: inputting the treated bitter gourd powder into a circulation tank of an extracting machine, and performing ultrasonic concentrated extraction, wherein the ultrasonic concentrated extraction system concentrates the ultrasonic wave on a predetermined time of the circulation tank The position is such that the bitter gourd powder can be shattered by the concentrated ultrasonic waves at the position, and the extract can be taken out after the extraction is completed, and the ultrasonic concentrated extraction method is adopted to effectively increase the extraction rate and reduce the production cost.

Description

具治療糖尿病症的山苦瓜萃取物之萃取技術 Extraction technology of extract of Momordica charantia L. with diabetes

本發明係有關一種具治療糖尿病症的山苦瓜萃取物之萃取技術,係指一用於萃取苦瓜的技術、方法,其萃取物可有效作為治療糖尿病之保健食品或醫療藥品者。 The invention relates to an extraction technology of a mountain bitter gourd extract for treating diabetes, and refers to a technique and a method for extracting bitter gourd, and the extract thereof can be effectively used as a health food or medical drug for treating diabetes.

糖尿病是當今最常見的代謝疾病之一,根據世界衛生組織(World Health Organization)的認定,全世界的糖尿病患已超過一億五千萬人以上,其中,95%的病患是屬於第二型糖尿病,第二型糖尿病的發生是β細胞功能喪失與胰島素抗性,在病理上的現象包含葡萄糖耐受度上升、血中胰島素增加,胰臟與腎臟損傷。目前,糖尿病的藥物仍然不足,發展新型藥劑有其迫切性,由具降血糖活性之藥用植物發展經濟且有效率的先導藥物是重要的研究方向。植物合成多樣性的化合物遂行其構造與功能之目的,而在這些豐富的分子類型中,有許多具有生物活性成分常被用作為治療疾病和維持健康用途,許多臨床研究報告已報導葫蘆科植物具有降血糖活性,在台灣民間,苦瓜屬(Momordica)植物,例如:山苦瓜常被使用於治療糖尿病。 Diabetes is one of the most common metabolic diseases today. According to the World Health Organization, more than 150 million people have diabetes in the world, 95% of whom are of the second type. In diabetes, type 2 diabetes occurs as a loss of beta cell function and insulin resistance. Pathological phenomena include increased glucose tolerance, increased insulin in the blood, and pancreas and kidney damage. At present, the drugs for diabetes are still insufficient. It is urgent to develop new drugs. It is an important research direction to develop economical and efficient lead drugs from medicinal plants with hypoglycemic activity. Plants synthesize diverse compounds for their structural and functional purposes, and many of these abundant molecular types are often used as therapeutic agents for health and maintenance purposes. Many clinical studies have reported that Cucurbitaceae plants have Hypoglycemic activity, in Taiwan folk, Momordica plants, for example: mountain bitter gourd is often used to treat diabetes.

目前的萃取技術中,在天然物萃取方面,有多種操作方式,常見的有分餾法、沉澱法、昇華法、雜質脫去法與層析法等,而以使用溶劑分類較使用的有酒萃與水萃兩種,此兩種方式可視為 極性與非極性物質萃取的基本方法,步驟簡單,成本較為低廉,其缺點在於所萃得物質之純度甚低,不易針對將有效成分進行萃取;二氧化碳超臨界萃取技術是利用超臨界流體的溶解能力與密度的關係,利用壓力和溫度對超臨界流體溶解能力的影響而進行萃取,亦利用加入乙醇等輔助溶劑,在超臨界狀態下,將超臨界流體與待分離的物質接觸,使其選擇性的將極性大小與沸點高低的成分依次萃取出,對應各壓力範圍所得到的萃取物不可能是單一成分,可以控制條件得到最佳比例的混合成分,然後藉助減壓、升溫的方式使超臨界流體變成普通氣體,使萃取物質析出,從而達到分離純化的目的,具有能同時萃取極性與非極性物質的能力,二氧化碳為溶劑不致使有機溶劑殘留,當為一有效且良好的萃取方式,但因其產量較低且生產成本昂貴,在業界較難進行量產規模。 In the current extraction technology, there are various operation modes in the extraction of natural substances, such as fractionation, precipitation, sublimation, impurity removal and chromatography, etc., and the use of solvent classification is more And water extraction, these two ways can be regarded as The basic method for the extraction of polar and non-polar substances is simple in steps and relatively low in cost. The disadvantage is that the purity of the extracted material is very low, and it is not easy to extract the active ingredient; the supercritical carbon dioxide extraction technology utilizes the solubility of the supercritical fluid. The relationship between density and pressure, the extraction of the supercritical fluid by the influence of pressure and temperature, and the use of an auxiliary solvent such as ethanol to contact the supercritical fluid with the substance to be separated under supercritical conditions to make it selective. The components with the same polarity and boiling point are sequentially extracted, and the extract obtained corresponding to each pressure range cannot be a single component, and the mixed components can be controlled under the optimal conditions, and then the supercritical pressure is obtained by means of decompression and temperature rise. The fluid becomes an ordinary gas, and the extracted material is precipitated, thereby achieving the purpose of separation and purification, and has the ability to simultaneously extract polar and non-polar substances. Carbon dioxide is a solvent that does not cause residual organic solvents, and is an effective and good extraction method, but Its low output and high production cost are difficult in the industry Line mass production scale.

有鑑於上述缺失弊端,本發明人認為其有急待改正之必要,遂以其從事相關產品設計製造之多年經驗,及其一貫秉持具有之優良設計理念,針對以上不良處加以研究創作,在經過不斷的努力後,終乃推出本發明具治療糖尿病症的山苦瓜萃取物之萃取技術,其以更正優良之產品結構提升產品之功效。 In view of the above-mentioned shortcomings, the inventor believes that it has the urgent need to make corrections, and that it has been engaged in the design and manufacture of related products for many years, and has always adhered to the excellent design concept, and researched and created the above disadvantages. After continuous efforts, the extraction technology of the extract of Momordica charantia L. with the treatment of diabetes is finally introduced, which improves the efficacy of the product by correcting the excellent product structure.

本發明具治療糖尿病症的山苦瓜萃取物之萃取技術之主要目的係提供一可有效降低成本,並能提高其萃取率的苦瓜萃取技術者。 The main purpose of the extraction technique of the extract of Momordica charantia L. with the treatment of diabetes in the present invention is to provide a bitter melon extraction technique which can effectively reduce the cost and improve the extraction rate.

為達到前揭之目的,本發明具治療糖尿病症的山苦瓜萃取物之萃取技術,萃取流程主要包含預處理與苦瓜萃取所構成,該預 處理,主要係將苦瓜果實處理成粉末狀,而苦瓜萃取,主要係由投入循環槽、超音波集中萃取與取出萃取物等步驟所組成,該投入循環槽係將經處理的苦瓜粉末投入一萃取機的循環槽之中,並進行超音波集中萃取,該超音波集中萃取係將超音波集中於循環槽的一預定位置,令苦瓜粉末能在該位置被集中的超音波震碎,而在萃取結束後便可取出萃取物者,該使用超音波,將其聚焦集中振盪所產生的高能量氣泡,瞬間將苦瓜細胞壁震破,以使苦瓜養份完全釋出完全萃取,且全製程控制於低溫條件下,克服了傳統萃取方法對於養份破壞性高的缺點,並取代超臨界萃取於芳香成分萃取,解決超臨界萃取所面臨的非極性異臭味釋出問題瓶頸,而且以水為介質,不會有溶劑殘留的問題,還可降低生產成本,也降低廢棄成本,以有效提高萃取率,在通過動物模式評估,結果亦顯示具有明顯提升葡萄糖耐受性、提升胰島素敏感度等,實能成為一在保健食品開發的價值者。 In order to achieve the purpose of the foregoing disclosure, the present invention has an extraction technique of an extract of Momordica charantia L. for treating diabetes, and the extraction process mainly comprises pretreatment and extraction of bitter gourd, which is The treatment mainly consists of treating the bitter gourd fruit into a powder form, and the bitter gourd extract is mainly composed of a step of putting into a circulation tank, supersonic concentrated extraction and extracting the extract, and the input circulation tank is used to put the treated bitter gourd powder into an extraction. In the circulation tank of the machine, and performing ultrasonic concentrated extraction, the ultrasonic concentrated extraction system concentrates the ultrasonic waves on a predetermined position of the circulation groove, so that the bitter gourd powder can be shattered by the concentrated ultrasonic waves at the position, and the extraction is performed. After the end, the extract can be taken out. The ultrasonic wave is used to focus and illuminate the high-energy bubbles, and the cell wall of the bitter gourd is shaken in an instant, so that the bitter gourd nutrient is completely released and completely extracted, and the whole process is controlled at a low temperature. Under the condition, it overcomes the shortcomings of traditional extraction methods for high nutrient destructiveness, and replaces supercritical extraction in aromatic component extraction to solve the bottleneck of non-polar odor release problem faced by supercritical extraction, and uses water as medium, not There will be problems with solvent residue, which can also reduce production costs and reduce waste costs, so as to effectively increase the extraction rate in animal mode. Assessment, the results are also shown to have significantly improved glucose tolerance, improve insulin sensitivity, etc., can become a real person in the value of health food development.

1‧‧‧預處理 1‧‧‧Pretreatment

2‧‧‧苦瓜萃取 2‧‧‧Bitter gourd extraction

21‧‧‧投入循環槽 21‧‧‧Into the circulation slot

22‧‧‧超音波集中萃取 22‧‧‧Ultrasonic concentrated extraction

23‧‧‧取出萃取物 23‧‧‧Remove the extract

3‧‧‧萃取機 3‧‧‧ extraction machine

31‧‧‧循環槽 31‧‧‧Circular trough

311‧‧‧幫浦 311‧‧‧

32‧‧‧集中槽 32‧‧‧concentration slot

33‧‧‧超音波器 33‧‧‧Supersonic

34‧‧‧冷卻機 34‧‧‧cooler

第一圖:本發明苦瓜萃取之流程示意圖 First: Schematic diagram of the process of extracting bitter gourd of the present invention

第二圖:本發明萃取機之結構示意圖 Second: Schematic diagram of the extraction machine of the present invention

第三圖:本發明進行動物模式試驗之小鼠在高脂質飼料誘導及給藥期間體重變化圖 Fig. 3 is a graph showing changes in body weight during induction and administration of high lipid feed in mice subjected to animal model tests of the present invention

第四圖:本發明進行動物模式試驗之小鼠在糖尿病動物模式給藥第四週之口服葡萄糖耐受性試驗圖 Figure 4: Oral glucose tolerance test for the fourth week of administration of the animal model in the animal model of the present invention

第五圖:本發明進行動物模式試驗之小鼠在糖尿病動物模式給藥第八週之口服葡萄糖耐受性試驗圖 Figure 5: Oral glucose tolerance test of the eighth week of administration of the animal model in the animal model of the present invention

第六圖:本發明進行動物模式試驗之小鼠在糖尿病動物模式給藥 第四週之胰島素耐受性試驗圖 Figure 6: The mice in the animal model test of the present invention are administered in a diabetic animal model. The fourth week of insulin tolerance test

第七圖:本發明進行動物模式試驗之小鼠在糖尿病動物模式給藥第八週之胰島素耐受性試驗圖 Figure 7: Insulin tolerance test of the eighth week of administration of the animal model in the animal model of the present invention

第八圖:本發明進行動物模式試驗之小鼠在血清生化值檢測,血清中總膽固醇含量(TC)於第四週之含量數據圖 Figure 8: Data of serum biochemical values in the animal model test of the present invention, and the total cholesterol content (TC) in the serum in the fourth week

第九圖:本發明進行動物模式試驗之小鼠在血清生化值檢測,血清中總膽固醇含量(TC)於第八週之含量數據圖 Ninth figure: The data of the serum biochemical value of the mice in the animal model test of the present invention, and the total cholesterol content (TC) in the serum in the eighth week

第十圖:本發明進行動物模式試驗之小鼠在血清生化值檢測,血清中三酸甘油脂含量(TG)於第四週之含量數據圖 The tenth figure: the data of the biochemical value of the mice in the animal model test of the present invention, and the content of the triglyceride content (TG) in the serum in the fourth week

第十一圖:本發明進行動物模式試驗之小鼠在血清生化值檢測,血清中三酸甘油脂含量(TG)於第八週之含量數據圖 Figure 11: The data of the biochemical value of the animal in the animal model test of the present invention, and the content of the triglyceride content (TG) in the serum in the eighth week

第十二圖:本發明進行動物模式試驗之小鼠在血清生化值檢測,血清中LDL/HEL比值於第四週之含量數據圖 Twelfth figure: The data of the biochemical value of the mouse in the animal model test of the present invention, and the LDL/HEL ratio in the serum in the fourth week

第十三圖:本發明進行動物模式試驗之小鼠在血清生化值檢測,血清中LDL/HDL比值於第八週之含量數據圖 Thirteenth figure: The data of the biochemical value of the mouse in the animal model test of the present invention, and the LDL/HDL ratio in the serum in the eighth week

本發明係有關一種具治療糖尿病症的山苦瓜萃取物之萃取技術,〔請參閱第一圖〕其流程主要包含預處理(1)與苦瓜萃取(2):預處理(1),主要係將選購來的苦瓜果實處理成粉末狀,成為苦瓜粉末,經此,便可進入萃取之程序,該所述之苦瓜果實係為苦瓜屬(Momordica)植物,例如:山苦瓜(Momordica charantia var.abbreviata.)或苦瓜(Momordica charantia Linn.)等; 苦瓜萃取(2),主要係由投入循環槽(21)、超音波集中萃取(22)與取出萃取物(23)等步驟所組成,該投入循環槽(21)係將經處理的苦瓜粉末投入一循環槽之中,並進行超音波集中萃取(22),該超音波集中萃取(22)係將超音波集中於循環槽的一預定位置,令苦瓜粉末能在該位置被集中的超音波震碎,而在萃取結束後便可取出萃取物(23),以完成其萃取程序者。 The invention relates to an extraction technique of an extract of Momordica charantia L. with diabetes treatment, [see the first figure]. The process mainly comprises pretreatment (1) and bitter gourd extraction (2): pretreatment (1), mainly The purchased bitter gourd fruit is processed into a powder form and becomes a bitter gourd powder, thereby entering the extraction process, and the bitter gourd fruit is a Momordica plant, for example, Momordica charantia var. abbreviata. .) or Momordica charantia Linn. The bitter gourd extract (2) is mainly composed of a step of introducing a circulation tank (21), ultrasonically extracting (22) and extracting an extract (23), and the input circulation tank (21) is used to input the treated bitter gourd powder. In a circulating tank, and performing ultrasonic concentrated extraction (22), the ultrasonic concentrated extraction (22) concentrates the ultrasonic waves on a predetermined position of the circulation groove, so that the bitter melon powder can be concentrated in the ultrasonic vibration at the position. Broken, and after the extraction is completed, the extract (23) can be taken out to complete the extraction procedure.

本發明具治療糖尿病症的山苦瓜萃取物之萃取技術,〔請一併參閱第一圖與第二圖〕該苦瓜萃取(2)的流程可配合一萃取機(3)實施萃取,所述之萃取機(3)主要係具一循環槽(31),該循環槽(31)內盛裝有萃取溶液,並可藉一幫浦(311)使其萃取溶液於循環槽(31)內循環流動,在循環槽(31)一側銜接有一漏斗狀的集中槽(32),集中槽(32)中可填入純水作為傳遞超音波的介質,集中槽(32)的尖端與循環槽(31)銜接,並且對應於尖端的另一端則設置超音波器(33),藉之,投入苦瓜粉末至循環槽(31)內,可藉由幫浦(311)令苦瓜粉末於循環槽(31)內循環流動,而超音波器(33)可發出超音波至集中槽(32),超音波則能集中於集中槽(32)的尖端處,並使得對應於該處的循環槽(31)內的苦瓜粉末被超音波震碎,進以完成萃取並取得萃取物者。 The invention relates to an extraction technique of the extract of Momordica charantia L. for treating diabetes, [please refer to the first figure and the second figure together] The process of the bitter gourd extraction (2) can be carried out by an extraction machine (3), wherein The extracting machine (3) mainly has a circulation tank (31), and the circulation tank (31) contains an extraction solution, and a pump (311) can be used to circulate the extraction solution in the circulation tank (31). A funnel-shaped concentration groove (32) is connected to one side of the circulation groove (31), and the concentrated groove (32) can be filled with pure water as a medium for transmitting ultrasonic waves, and the tip end of the concentration groove (32) and the circulation groove (31) Connected, and corresponding to the other end of the tip, an ultrasonic device (33) is provided, by which the bitter gourd powder is introduced into the circulation tank (31), and the bitter melon powder can be placed in the circulation tank (31) by the pump (311). Circulating flow, and the ultrasonic (33) can emit ultrasonic waves to the concentrating groove (32), and the ultrasonic wave can be concentrated at the tip end of the concentrating groove (32), and corresponding to the inside of the circulating groove (31) The bitter gourd powder is shattered by ultrasonic waves, and the extract is obtained and the extract is obtained.

本發明具治療糖尿病症的山苦瓜萃取物之萃取技術,〔請一併參閱第一圖與第二圖〕本實施例以山苦瓜作為說明,該詳細的萃取流程為:首先將選購來的山苦瓜果實置於環境溫度於23±5℃下,噴製成粉,以成為山苦瓜粉末,經該預處理(1),將該山苦瓜粉末便可投入循環槽(31)之中,在本實施例中,該 循環槽(31)的容量為300L,投入的山苦瓜粉末為100kg,而在循環槽(31)中係以純水作為萃取介質,在維持環境溫度於23±5℃下,啟動幫浦(311)、超音波器(33)與冷卻機(34)並進行超音波集中萃取(22),該所述之超音波集中萃取(22)係以集中槽(32)將超音波的能量集中在循環槽(31)的一預定位置,山苦瓜粉末則能在該位置受超音波的能量而被震碎,而因為超音波振動會使溫度升高,冷卻機(34)則得以冷卻在該情況下的溫度,經2小時的萃取後,便完成萃取,經此,便能取出萃取物(23),以完成其萃取程序,而其萃取出的萃取物具有蛋白質、皂苷、多醣等成分。 The invention has the extraction technology of the extract of Momordica charantia L. for treating diabetes, [please refer to the first figure and the second figure together]. The present embodiment is described by the mountain bitter gourd. The detailed extraction process is: firstly, the selected one is selected. The fruit of Momordica charantia L. is placed at a temperature of 23±5°C, and is sprayed into powder to become a powder of Momordica charantia L.. After the pretreatment (1), the bitter gourd powder can be put into the circulation tank (31). In this embodiment, the The capacity of the circulation tank (31) is 300L, the input of the balsam pear powder is 100kg, and in the circulation tank (31), pure water is used as the extraction medium, and the pump is started at a temperature of 23±5°C. , the ultrasonic (33) and the chiller (34) are subjected to ultrasonic concentrated extraction (22), and the ultrasonic concentrated extraction (22) concentrates the ultrasonic energy in the circulation by the concentrating groove (32). At a predetermined position of the groove (31), the bitter gourd powder can be shattered by the ultrasonic energy at the position, and the ultrasonicizer (34) is cooled because the ultrasonic vibration causes the temperature to rise. The temperature is extracted after 2 hours of extraction, and the extract (23) can be taken out to complete the extraction process, and the extracted extract has the components of protein, saponin, polysaccharide and the like.

上述之山苦瓜超音波萃取物,進一步與其他方法萃取出的萃取物做實驗比較,實驗之動物模式執行如下: The above-mentioned mountain bitter gourd ultrasonic extract is further compared with the extract extracted by other methods, and the experimental animal model is executed as follows:

(一)、體重監測:使用性別為雄性的小鼠(六週大),先給予脂肪含量40%之高脂質飼料八週之後,先以腹腔注射NA 200mg/Kg,15分鐘後再腹腔注射STZ 50mg/Kg連續七天,使其非禁食血糖值超過200mg/dl,之後分組實驗,一組各為6隻:各組分別為a未給藥(Normal)、b控制組(Control,為正常之小鼠)、c降血糖藥物(Rosiglitazone 10mg/kg)、d降血糖藥物+本發明苦瓜萃取物(Rosiglitazone 10mg/kg+BM RTSES 250mg/kg)、e山苦瓜乙酸乙脂層萃取物(BM EtOH 500mg/kg)、f山苦瓜正丁醇層萃取物(BM BuOH 500mg/kg)、g山苦瓜水層萃取物(BM Water 500mg/kg)、h本發明苦瓜萃取物濃縮(BM RTSES(condensed)500mg/kg)、i本發明苦瓜萃取物(BM RTSES 500mg/kg),各組皆以口服方式,每天餵食一次,連續八週。環境為12/12 光暗週期變換,溫度控制24±2℃,食物及水則無限量供應,並且每週測量一次體重,〔請參閱第三圖〕其實驗結果:實驗於一至三週時,各組體重都有些許的下降,推測應為初期餵藥動作適應期現象,於第三週後各組體重開始逐漸攀升,五至七週期間,山苦瓜各萃取物實驗組之體重介於26~29g之間,皆低於正負對照組。 (1) Weight monitoring: Male mice with sex (6-week-old) were given a high-fat diet with a fat content of 40% for eight weeks, followed by intraperitoneal injection of NA 200 mg/Kg, and 15 minutes later, intraperitoneal injection of STZ. 50mg/Kg for 7 consecutive days, so that the non-fasting blood glucose level exceeded 200mg/dl, then group experiments, each group of 6: each group is a not administered (Normal), b control group (Control, normal) Mouse), c hypoglycemic agent (Rosiglitazone 10mg/kg), d hypoglycemic agent + the bitter gourd extract of the invention (Rosiglitazone 10mg/kg + BM RTSES 250mg/kg), e mountain bitter gourd ethyl acetate extract (BM EtOH 500mg/kg), f. balsam pear n-butanol layer extract (BM BuOH 500mg/kg), g mountain bitter gourd aqueous layer extract (BM Water 500mg/kg), h the present invention bitter gourd extract concentrate (BM RTSES (condensed) 500 mg/kg), i the bitter melon extract (BM RTSES 500 mg/kg) of the present invention, each group was fed orally once a day for eight weeks. The environment is 12/12 Light and dark cycle change, temperature control 24±2°C, food and water are supplied in an unlimited amount, and body weight is measured once a week, [see the third figure]. Experimental results: During the first to third weeks of the experiment, each group has some weight The decline was presumed to be the initial adaptation period of the drug feeding action. After the third week, the weight of each group began to rise gradually. During the five to seven weeks, the weight of the experimental group of the mountain bitter gourd was between 26 and 29 g. Both were lower than the positive and negative control groups.

(二)、口服葡萄糖耐受度測試(Oral Glucose Tolerance Test):小鼠在給藥前和給藥二週及四週時,測量葡萄糖耐受性異常程度。將小鼠禁食10小時後,先以尾部取血方式,使用血糖儀MAJOR II測定小鼠的空腹血糖,接著分組實驗,一組各為6隻:各組分別為a未給藥(Normal)、b以口服方式分別給予3mg/Kg葡萄糖至控制組(Control)、c降血糖藥物(Rosiglitazone 10mg/kg)、d降血糖藥物+本發明苦瓜萃取物(Rosiglitazone 10mg/kg+BM RTSES 250mg/kg)、e山苦瓜乙酸乙脂層萃取物(BM EtOH 500mg/kg)、f山苦瓜正丁醇層萃取物(BM BuOH 500mg/kg)、g山苦瓜水層萃取物(BM Water 500mg/kg)、h本發明苦瓜萃取物濃縮(BM RTSES(condensed)500mg/kg)、i本發明苦瓜萃取物(BM RTSES 500mg/kg),在給予葡萄糖後的15、45、95、135分鐘的時間點測量血糖值,觀察曲線變化,〔請參閱第四、五圖〕其實驗結果:(1)在第四週數據中,相較於正對照組比,萃取物實驗組中,葡萄糖耐受性恢復最多為e山苦瓜乙酸乙脂層萃取物,其次為i本發明苦瓜萃取物;(2)c降血糖藥物與d降血糖藥物+本發明苦瓜萃取物在 葡萄糖耐受性之表現上,添加本發明苦瓜萃取物並無明顯提升葡萄糖耐受性;(3)i本發明苦瓜萃取物在單位時間所承受之糖濃度面積,明顯低於正對照組,並且與其他各種萃取方式組別比較,只略高於e山苦瓜乙酸乙脂層萃取物,但與f山苦瓜正丁醇層萃取物、g山苦瓜水層萃取物兩組相比,具有明顯提升糖耐受度;(4)第八週數據中,c降血糖藥物與d降血糖藥物+本發明苦瓜萃取物在葡萄糖耐受性上,d降血糖藥物+本發明苦瓜萃取物並無明顯提升,與第四週結果相似。 (B) Oral Glucose Tolerance Test: The mice were measured for abnormal glucose tolerance before administration and two weeks and four weeks after administration. After the mice were fasted for 10 hours, the fasting blood glucose of the mice was measured by tail blood sampling using a blood glucose meter MAJOR II, followed by a group experiment, each of which was 6: each group was a not administered (Normal) , b orally administered 3mg/Kg glucose to the control group (Control), c hypoglycemic drug (Rosiglitazone 10mg/kg), d hypoglycemic agent + the bitter gourd extract of the invention (Rosiglitazone 10mg/kg + BM RTSES 250mg/kg ), e mountain bitter gourd ethyl acetate extract (BM EtOH 500mg/kg), f mountain bitter melon butanol layer extract (BM BuOH 500mg/kg), g mountain bitter gourd aqueous layer extract (BM Water 500mg/kg) , h BM RTSES (condensed 500mg / kg), i the bitter gourd extract (BM RTSES 500mg / kg), measured at 15, 45, 95, 135 minutes after glucose administration Blood glucose level, observation curve change, [see the fourth and fifth figures] The experimental results: (1) In the fourth week data, the glucose tolerance recovered most in the extract experimental group compared with the positive control group. It is an extract of e. sinensis acetate ethyl acetate layer, followed by i the bitter gourd extract of the present invention; (2) c hypoglycemic drug and d Bitter melon extract + glucose medicament of the present invention In the performance of glucose tolerance, the addition of the bitter gourd extract of the present invention does not significantly improve glucose tolerance; (3) i the sugar concentration area of the bitter gourd extract of the present invention per unit time is significantly lower than that of the positive control group, and Compared with other various extraction methods, it is only slightly higher than the extract of e. sinensis acetate ethyl sulphate, but it has a significant improvement compared with the two extracts of b. balsam, n-butanol layer extract and g. Sugar tolerance; (4) In the eighth week data, c hypoglycemic drugs and d hypoglycemic drugs + the bitter gourd extract of the present invention in glucose tolerance, d hypoglycemic drugs + the bitter gourd extract of the present invention is not significantly improved , similar to the results of the fourth week.

(三)、胰島素耐受性測試(Insulin Tolerance Test):小鼠在給藥前和給藥二週及四週時,測量胰島素耐受性。將小鼠禁食10小時後,先以尾部取血方式,使用血糖儀MAJORⅡ測定小鼠的空腹血糖,接著分組實驗,一組各為6隻:各組分別為a未給藥(Normal)、b腹腔注射胰島素0.5U/Kg至控制組(Control)、c降血糖藥物(Rosiglitazone10mg/kg)、d降血糖藥物+本發明苦瓜萃取物(Rosiglitazone10mg/kg+BM RTSES 250mg/kg)、e山苦瓜乙酸乙脂層萃取物(BM EtOH 500mg/kg)、f山苦瓜正丁醇層萃取物(BM BuOH 500mg/kg)、g山苦瓜水層萃取物(BM Water 500mg/kg)、h本發明苦瓜萃取物濃縮(BM RTSES(condensed)500mg/kg)、i本發明苦瓜萃取物(BM RTSES 500mg/kg),在注射胰島素後的15、45、95、135分鐘的時間點測量血糖值,觀察曲線變化,藉以得知每隻小鼠對胰島素的敏感度差異;若在注射完胰島素後,血糖濃度並未降低,即表示細胞無法接收到胰島素所攜帶的訊號,〔請參閱第六、七圖〕其實驗結果: (1)第四週之實驗組數據與正對照組比較,胰島素敏感度上升最明顯為h本發明苦瓜萃取物濃縮,其次d降血糖藥物+本發明苦瓜萃取物,其餘組別則無明顯提升胰島素敏感度效果;(2)比較c降血糖藥物與d降血糖藥物+本發明苦瓜萃取物,d降血糖藥物+本發明苦瓜萃取物具有明顯提升胰島素之敏感度現象;(3)第八週胰島素耐受性試驗中,e山苦瓜乙酸乙脂層萃取物有較提升胰島素敏感度的現象,其他各組之胰島素增敏現象較不明顯;(4)c降血糖藥物與d降血糖藥物+本發明苦瓜萃取物,在第八週之胰島素耐受性的數據中,較正對照組有明顯增加胰島素增敏度,但兩組之胰島素增敏程度並無明顯差距。 (C), Insulin Tolerance Test: The mice were measured for insulin resistance before administration and at two and four weeks after administration. After the mice were fasted for 10 hours, the fasting blood glucose of the mice was measured by tail blood sampling using a blood glucose meter MAJORII, followed by a group experiment, and each group consisted of 6: each group was a not administered (Normal), b intraperitoneal injection of insulin 0.5U / Kg to the control group (Control), c hypoglycemic drugs (Rosiglitazone 10mg / kg), d hypoglycemic drugs + the present bitter melon extract (Rosiglitazone 10mg / kg + BM RTSES 250mg / kg), e mountain bitter gourd Ethyl acetate layer extract (BM EtOH 500mg/kg), f. bitter gourd n-butanol layer extract (BM BuOH 500mg/kg), g. bitter gourd aqueous layer extract (BM Water 500mg/kg), h invented bitter gourd The extract was concentrated (BM RTSES (condensed) 500 mg/kg), i the bitter melon extract (BM RTSES 500 mg/kg), and the blood glucose level was measured at the time points of 15, 45, 95, and 135 minutes after the injection of insulin, and the curve was observed. Change, in order to know the difference in sensitivity of each mouse to insulin; if the blood glucose concentration does not decrease after the injection of insulin, it means that the cell can not receive the signal carried by insulin, [see Figure 6 and Figure 7] The experimental results: (1) Compared with the control group, the experimental data of the fourth week was the most obvious increase in insulin sensitivity. The extract of bitter gourd extract was concentrated in the present invention, followed by the hypoglycemic drug + the bitter gourd extract of the present invention, and the other groups showed no significant improvement. Insulin sensitivity effect; (2) comparing c hypoglycemic drugs and d hypoglycemic drugs + the bitter gourd extract of the invention, d hypoglycemic drugs + the bitter gourd extract of the invention has a significant increase in insulin sensitivity; (3) the eighth week In the insulin tolerance test, e-Moss bitter gourd ethyl acetate extract has a higher insulin sensitivity, and other groups of insulin sensitization are less obvious; (4) c hypoglycemic drugs and d hypoglycemic drugs + In the data of insulin tolerance of the eighth week of the bitter gourd extract of the present invention, the insulin sensitization degree was significantly increased in the control group, but there was no significant difference in the insulin sensitization degree between the two groups.

接著,針對實驗鼠亦執行了血清生化值檢測,血清中總膽固醇含量(TC),〔請參閱第八圖〕其第四週的實驗結果:與b控制組相比,h本發明苦瓜萃取物濃縮其含量最低,證明能有效降低血中總膽固醇;〔請參閱第九圖〕其第八週的實驗結果:與b控制組相比,i本發明苦瓜萃取物其含量最低,證明能有效降低血中總膽固醇者。 Next, the serum biochemical value test was performed on the experimental rats, and the total cholesterol content (TC) in the serum, [see the eighth figure], the results of the fourth week of the experiment: compared with the b control group, the present invention bitter gourd extract Concentrated, the lowest content, proved to be effective in reducing total cholesterol in the blood; [Please refer to the ninth figure] The results of the eighth week of the experiment: Compared with the b control group, i the bitter gourd extract of the present invention has the lowest content, which proves to be effective in reducing The total cholesterol in the blood.

血清生化值檢測,血清中三酸甘油脂含量(TG),〔請參閱第十圖〕其第四週的實驗結果:與b控制組相比,c降血糖藥物、d降血糖藥物+本發明苦瓜萃取物、e山苦瓜乙酸乙脂層萃取物、f山苦瓜正丁醇層萃取物、i本發明苦瓜萃取物,皆能有效降低血中三酸甘油脂含量;〔請參閱第十一圖〕其第八週的實驗結果:與第四週相同,c降血糖藥物、d降血糖藥物+本發明苦瓜萃取物、e山苦瓜乙酸乙脂層萃取物、f山苦瓜正丁醇層萃取 物、i本發明苦瓜萃取物,皆能有效降低血中三酸甘油脂含量者。 Serum biochemical value test, serum triglyceride content (TG), [see the tenth figure] its fourth week of experimental results: compared with the b control group, c hypoglycemic drugs, d hypoglycemic drugs + the present invention The bitter gourd extract, the e-bitter melon ethyl acetate extract, the f-bitter melon butanol layer extract, and the begian melon extract of the present invention all effectively reduce the triglyceride content in the blood; [see the eleventh figure 〕 The results of the eighth week of the experiment: the same as the fourth week, c hypoglycemic drugs, d hypoglycemic drugs + the bitter gourd extract of the invention, e mountain bitter gourd ethyl acetate extract, f mountain bitter gourd n-butanol layer extraction The i., the bitter gourd extract of the present invention can effectively reduce the triglyceride content in the blood.

血清生化值檢測,血清中LDL/HDL比值,〔請參閱第十二圖〕其第四週的實驗結果:與b控制組相比,比值並無明顯降低之現象;〔請參閱第十三圖〕其第八週的實驗結果:與b控制組相比,e山苦瓜乙酸乙脂層萃取物、g山苦瓜水層萃取物、i本發明苦瓜萃取物比值皆具有降低的效果。 Serum biochemical value test, serum LDL/HDL ratio, [see Figure 12] The results of the fourth week of the experiment: compared with the b control group, the ratio did not significantly decrease; [see the thirteenth map 〕 The results of the eighth week of the experiment: compared with the b control group, e mountain bitter gourd ethyl acetate layer extract, g mountain bitter gourd aqueous layer extract, i the present bitter gourd extract ratio has a reduced effect.

本發明具治療糖尿病症的山苦瓜萃取物之萃取技術,其優點在於,該苦瓜利用超音波集中萃取的方式,使用超音波,將其聚焦集中振盪所產生的高能量氣泡,瞬間將苦瓜細胞壁震破,以使苦瓜養份完全釋出完全萃取,且全製程控制於低溫條件下,克服了傳統萃取方法對於養份破壞性高的缺點,並取代超臨界萃取於芳香成分萃取,解決超臨界萃取所面臨的非極性異臭味釋出問題瓶頸,而且以水為介質,不會有溶劑殘留的問題,還可降低生產成本,也降低廢棄成本,以有效提高萃取率,另外,綜觀各實驗結果,乙酸乙酯萃取物具有優異的表現,而本發明苦瓜萃取物在各項動物實驗中,也有一定的顯著效果,甚至超越山苦瓜乙酸乙酯萃取組,乙酸乙酯終究為有機溶劑,對人體仍淺藏一定的危害性,而本發明苦瓜萃取物,是以水作為萃取介質,完全沒有有機溶劑殘留的疑慮,因此,於苦瓜萃取開發中具有相當大的優勢,是其他萃取方式無法比擬的,實能成為一在保健食品開發的價值。 The invention has the advantages that the extracting technology of the extract of Momordica charantia L. with the treatment of diabetes has the advantage that the bitter gourd uses the ultrasonic concentrated extraction method, uses the ultrasonic wave, focuses the high energy bubbles generated by the concentrated oscillation, and instantly shakes the bitter gourd cell wall. Broken, so that the bitter gourd nutrients are completely released for complete extraction, and the whole process is controlled under low temperature conditions, which overcomes the shortcomings of traditional extraction methods for high nutrient destructiveness, and replaces supercritical extraction in aromatic component extraction to solve supercritical extraction. The non-polar odor that is faced with the problem bottleneck is released, and water is used as the medium, there is no problem of solvent residue, the production cost can be reduced, the waste cost can be reduced, and the extraction rate can be effectively improved. In addition, the experimental results are comprehensively observed. The ethyl acetate extract has excellent performance, and the bitter gourd extract of the present invention has certain remarkable effects in various animal experiments, even surpassing the ethyl acetate extracting group of the mountain bitter gourd, and the ethyl acetate is finally an organic solvent, still on the human body. It has a certain hazard, but the bitter gourd extract of the present invention uses water as an extraction medium and has no Solvent residue doubts, therefore, have to develop in bitter melon extract considerable advantage, other extraction methods can not match, can become a real value in health food development.

綜上所述,當知本發明具有新穎性,且本發明未見之於任何刊物,當符合專利法第21、22條之規定。 In summary, it is understood that the present invention is novel, and the present invention is not found in any publication, and is in compliance with the provisions of Articles 21 and 22 of the Patent Law.

唯以上所述者,僅為本發明之一較佳實施例而已,當不能以 之限定本發明之範圍。即大凡依本發明申請專利範圍所作之均等變化與修飾,皆應仍屬本發明專利涵蓋之範圍內。 Only the above description is only a preferred embodiment of the present invention, when It is intended to limit the scope of the invention. That is, the equivalent changes and modifications made by the invention in accordance with the scope of the invention are still within the scope of the invention.

Claims (1)

一種具治療糖尿病症的山苦瓜萃取物之萃取技術,主要包含:預處理,主要係將選購來的苦瓜果實處理成粉末狀,成為苦瓜粉末,所述之苦瓜果實係使用山苦瓜,且環境溫度於23±5℃下,經此,便可進入萃取之程序;苦瓜萃取,主要係由投入循環槽、超音波集中萃取與取出萃取物等步驟所組成,該投入循環槽係將經處理的苦瓜粉末100kg投入一萃取機的容量為300L的循環槽之中,並於環境溫度於23±5℃下進行超音波集中萃取,而在循環槽中係以純水作為萃取介質,該超音波集中萃取係將超音波集中於循環槽的一預定位置,令苦瓜粉末能在該位置被集中的超音波震碎,而在萃取2小時結束後取出萃取物者。 The invention relates to an extraction technique of a mountain bitter gourd extract for treating diabetes, which mainly comprises: pretreatment, which mainly processes the purchased bitter gourd fruit into a powder form, and becomes a bitter gourd powder, wherein the bitter gourd fruit uses the mountain bitter gourd, and the environment The temperature is at 23±5°C, and then the extraction process can be entered; the bitter gourd extraction is mainly composed of steps of inputting a circulation tank, supersonic concentrated extraction and extracting the extract, and the input circulation tank system will be treated. 100kg of bitter gourd powder is put into a circulating tank with a capacity of 300L in an extractor, and ultrasonic concentrated extraction is performed at an ambient temperature of 23±5° C., and pure water is used as an extraction medium in the circulation tank, and the ultrasonic concentration is concentrated. The extraction system concentrates the ultrasonic waves at a predetermined position of the circulation tank, so that the bitter gourd powder can be shattered by the concentrated ultrasonic waves at the position, and the extract is taken out after the end of the extraction for 2 hours.
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TWI271220B (en) * 2004-06-30 2007-01-21 Mesophase Technologies Inc An ultrasonic disintegrator

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TWI271220B (en) * 2004-06-30 2007-01-21 Mesophase Technologies Inc An ultrasonic disintegrator

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