فروغ گیلانی, زینب رفتنی امیری, رضا اسماعیل زاده کناری
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In this study, the effect of extraction methods (immersion and ultrasound) and different solvents (ethanol 100%, ethanol – water (50:50 V/V) and water) on amount of phenolic compounds and antioxidant properties of cornelian cherry fruit extract were investigated. \n \nMaterials and Methods: Qazvin cornelian cherry was purchased from the local market of Amol city, Mazandaran province, Iran. All solvents and chemicals used in this study were of analytical reagent grade and were prepared from Merck (Darmstadt, Germany) and Sigma–Aldrich (St. Louis, MO). Cornelian cherry was washed, core separated, dried in front of the sun for 5 days and then powdered with kitchen miller. Powdered cornelian cherry fruit was extracted using immersion extraction techniques, ultrasound and different solvents (ethanol 100%, ethanol –water (50:50 V/V) and water). In the immersion method, powdered cornelian cherry fruit were mixed with each solvent in the ratio of 1:10, individually. Then, the mixtures were shaken overnight at room temperature. After 24 hrs, the extracts were filtered through Whatman No. 42 filter paper and the solvents were evaporated in an oven at 55°C. In the ultrasound technique, the mixture of powdered samples with any solvent (1:10) was sonicated in an ultrasonic bath for 45 min at 35°C. The extracts were then filtered and the solvents were evaporated using an oven at 55°C. Finally, the extracts obtained from extraction methods were kept in a freezer for furthere experiments. The total phenolic content of the extracts was determined with the Folin-ciocalteau method, briefly, 0.5 mL of cornelian cherry fruit extracts with concentration of 1mg/mL were mixed with 2.5 mL of Folin–Ciocalteu reagent (previously diluted 10-fold with distilled water) and 2 mL of 7.5% sodium carbonate solution, then the samples were kept for 30 min at room temperature in the dark and at the end the absorbance of the solutions was read at 760 nm. The ability of the extracts to scavenge 2, 2-diphenyl-1-picrylhydrazyl radical (DPPH) was determined. 0.3 mL of each extract with a different concentration (500-3000μg/mL) was mixed with 2.7 mL of methanolic solution of DPPH (6 × 10 -5 mole/L), then the mixture was shaken vigorously and was placed in the dark for 60 min. Absorbance was recorded at 517 nm. The percentage of the DPPH radical scavenging was calculated according to the following equation: \n \n% inhibition of DPPH radical= [(ADPPH – AS) / ADPPH] ×100 \n \nAS and ADPPH are the absorbance of the solution the absorbance of the DPPH solution, respectively. Reducing power of extracts on iron ion was measured. 1mL of each extract with a different concentration (500-3000μg/mL) was mixed with 2.5 ml of phosphate buffer (0.2 M, pH= 6.6) and 2.5 ml potassium ferricyanide [K3Fe(CN)6] (1%), then the mixture was incubated at 50° C for 30 min. After that, 2.5 ml of 10% trichloroacetic acid were added to the mixture, then, was centrifuged at 1000g for 10 min. Subsequently, 2.5 ml of the upper layer solution was mixed with 2.5 ml of distilled water and 0.5 ml of 0.1% FeCl3. Finally, the absorbance values of the solutions were read at 700 nm. \n \nResults and discussion: The result of this study showed that the type of solvent and extraction method has been effective on amount of phenolic compounds of extracts, and also concentration dependent of phenolic compounds with antioxidant activity was observed in all extracts. The highest amount of phenolic compounds with 142.72 mg/g (based on Galic acid) was observed in sample extract obtained from solvent of water- ethanol (50:50 V/V) employing ultrasound method. Also, this extract with the lowest IC50 value with the amount of 0.955 mg/ml in the DPPH free radical scavenging method and the highest absorption with the amount of 0.601 in the reducing power of Iron III test, the highest antioxidant performance is shown. A negative correlation was observed between the total phenolic content and the IC50 value in the methods of measuring the antioxidant activity (DPPH and reducing power), which revealed the higher total phenolic content will give the lower IC50, that means the higher antioxidant activity. 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引用次数: 0

摘要

简介:山茱萸(Cornus mas L.),属于山茱萸科,生长在伊朗,在地区,如Qazvin和Arasbaran。这种水果具有抗炎和抗氧化的特性,在医学上被用作草药。从植物源中分离天然抗氧化化合物需要合适的提取方法,这是实现这些有价值的化合物的高效提取的有效因素。以山茱萸果为研究对象,考察了不同提取方法(浸泡和超声)和不同溶剂(乙醇100%、乙醇-水(50:50 V/V)和水)对山茱萸果提取物中酚类化合物含量和抗氧化性能的影响。材料与方法:从伊朗马赞达兰省Amol市当地市场采购。本研究中使用的所有溶剂和化学品均为分析试剂级,由默克公司(德国达姆施塔特)和西格玛-奥尔德里奇公司(密苏里州圣路易斯)制备。山茱萸洗净,核分离,在阳光下晒干5天,然后用厨房粉碎机磨粉。采用浸提法、超声波和不同溶剂(乙醇100%、乙醇-水(50:50 V/V)和水)提取山茱萸粉。在浸渍法中,将山茱萸粉分别与每种溶剂按1:10的比例混合。然后,将混合物在室温下摇一整夜。24h后,提取液用Whatman 42号滤纸过滤,溶剂在55℃烤箱中蒸发。在超声技术中,粉末样品与任何溶剂(1:10)的混合物在35°C的超声浴中超声45分钟。然后将萃取物过滤,溶剂在55°C的烤箱中蒸发。最后,通过提取方法获得的提取物保存在冰箱中,以备进一步的实验。采用Folin-ciocalteau法测定提取物中总酚含量,简单地将0.5 mL浓度为1mg/mL的山茱萸樱桃提取物与2.5 mL Folin-Ciocalteu试剂(用蒸馏水稀释10倍)和2 mL 7.5%碳酸钠溶液混合,室温避光保存30 min,最后在760 nm处读吸光度。测定了其对2,2 -二苯基-1-苦味肼基自由基(DPPH)的清除能力。取不同浓度(500-3000μg/mL)的各提取液0.3 mL与DPPH甲醇溶液(6 × 10 -5 mol /L) 2.7 mL混合,用力摇匀后置于暗处60 min,在517 nm处记录吸光度。清除DPPH自由基的百分比按下式计算:抑制DPPH自由基的百分比= [(ADPPH - AS) / ADPPH] ×100 AS和ADPPH分别为溶液的吸光度和DPPH溶液的吸光度。测定了提取物对铁离子的还原能力。1毫升每个提取物不同浓度(500 - 3000μg / mL)和2.5毫升的磷酸盐缓冲剂(0.2米,pH = 6.6)和2.5毫升铁氰化钾(K3Fe (CN) 6](1%),然后混合是在50°C的环境中30分钟。之后,2.5毫升的10%三氯乙酸被添加到混合,然后,在1000 g离心10分钟。随后,2.5毫升的上层的解决方案是混合2.5毫升蒸馏水和0.5毫升的0.1% FeCl3。最后,在700 nm处读取溶液的吸光度值。结果与讨论:本研究结果表明,溶剂类型和提取方法对提取物中酚类化合物的含量有影响,并且所有提取物中具有抗氧化活性的酚类化合物均具有浓度依赖性。以水-乙醇(50:50 V/V)为溶剂,超声提取的样品中酚类化合物含量最高,为142.72 mg/g(以没食子酸为基础)。在DPPH自由基清除试验中,IC50值最低,用量为0.955 mg/ml;在铁III还原力试验中,吸收率最高,用量为0.601,抗氧化性能最好。在测定抗氧化活性(DPPH和还原力)的方法中,总酚含量与IC50值呈负相关,表明总酚含量越高,IC50值越低,抗氧化活性越强。目前的研究结果表明,山茱萸果实是酚类化合物的天然来源,具有相当的抗氧化活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
اثر حلالهای مختلف و امواج فراصوت بر خاصیت آنتیاکسیدانی عصاره میوه زغال اخته
Introduction: Cornelian cherry (Cornus mas L.), which belongs to the family Cornaceae, grows in Iran, in areas such as Qazvin and Arasbaran. The fruit possesses anti-inflammatory and antioxidant properties and it is used as an herbal remedy in medicine. Separation of natural antioxidant compounds from plant sources requires an appropriate method of extraction, which is effective factor to achieve the higher efficiency of these valuable compounds. In this study, the effect of extraction methods (immersion and ultrasound) and different solvents (ethanol 100%, ethanol – water (50:50 V/V) and water) on amount of phenolic compounds and antioxidant properties of cornelian cherry fruit extract were investigated. Materials and Methods: Qazvin cornelian cherry was purchased from the local market of Amol city, Mazandaran province, Iran. All solvents and chemicals used in this study were of analytical reagent grade and were prepared from Merck (Darmstadt, Germany) and Sigma–Aldrich (St. Louis, MO). Cornelian cherry was washed, core separated, dried in front of the sun for 5 days and then powdered with kitchen miller. Powdered cornelian cherry fruit was extracted using immersion extraction techniques, ultrasound and different solvents (ethanol 100%, ethanol –water (50:50 V/V) and water). In the immersion method, powdered cornelian cherry fruit were mixed with each solvent in the ratio of 1:10, individually. Then, the mixtures were shaken overnight at room temperature. After 24 hrs, the extracts were filtered through Whatman No. 42 filter paper and the solvents were evaporated in an oven at 55°C. In the ultrasound technique, the mixture of powdered samples with any solvent (1:10) was sonicated in an ultrasonic bath for 45 min at 35°C. The extracts were then filtered and the solvents were evaporated using an oven at 55°C. Finally, the extracts obtained from extraction methods were kept in a freezer for furthere experiments. The total phenolic content of the extracts was determined with the Folin-ciocalteau method, briefly, 0.5 mL of cornelian cherry fruit extracts with concentration of 1mg/mL were mixed with 2.5 mL of Folin–Ciocalteu reagent (previously diluted 10-fold with distilled water) and 2 mL of 7.5% sodium carbonate solution, then the samples were kept for 30 min at room temperature in the dark and at the end the absorbance of the solutions was read at 760 nm. The ability of the extracts to scavenge 2, 2-diphenyl-1-picrylhydrazyl radical (DPPH) was determined. 0.3 mL of each extract with a different concentration (500-3000μg/mL) was mixed with 2.7 mL of methanolic solution of DPPH (6 × 10 -5 mole/L), then the mixture was shaken vigorously and was placed in the dark for 60 min. Absorbance was recorded at 517 nm. The percentage of the DPPH radical scavenging was calculated according to the following equation: % inhibition of DPPH radical= [(ADPPH – AS) / ADPPH] ×100 AS and ADPPH are the absorbance of the solution the absorbance of the DPPH solution, respectively. Reducing power of extracts on iron ion was measured. 1mL of each extract with a different concentration (500-3000μg/mL) was mixed with 2.5 ml of phosphate buffer (0.2 M, pH= 6.6) and 2.5 ml potassium ferricyanide [K3Fe(CN)6] (1%), then the mixture was incubated at 50° C for 30 min. After that, 2.5 ml of 10% trichloroacetic acid were added to the mixture, then, was centrifuged at 1000g for 10 min. Subsequently, 2.5 ml of the upper layer solution was mixed with 2.5 ml of distilled water and 0.5 ml of 0.1% FeCl3. Finally, the absorbance values of the solutions were read at 700 nm. Results and discussion: The result of this study showed that the type of solvent and extraction method has been effective on amount of phenolic compounds of extracts, and also concentration dependent of phenolic compounds with antioxidant activity was observed in all extracts. The highest amount of phenolic compounds with 142.72 mg/g (based on Galic acid) was observed in sample extract obtained from solvent of water- ethanol (50:50 V/V) employing ultrasound method. Also, this extract with the lowest IC50 value with the amount of 0.955 mg/ml in the DPPH free radical scavenging method and the highest absorption with the amount of 0.601 in the reducing power of Iron III test, the highest antioxidant performance is shown. A negative correlation was observed between the total phenolic content and the IC50 value in the methods of measuring the antioxidant activity (DPPH and reducing power), which revealed the higher total phenolic content will give the lower IC50, that means the higher antioxidant activity. The results of present research showed that cornelian cherry fruit is a natural source of phenolic compounds and have considerable antioxidant activity.
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