Phytochemical and antioxidant studies of methanol and chloroform extract from leaves of Azadirachta indica A. Juss. in Tropical region of Nepal

S. Dhakal, P. Aryal, S. Aryal, D. Bashyal, D. Khadka
{"title":"Phytochemical and antioxidant studies of methanol and chloroform extract from leaves of Azadirachta indica A. Juss. in Tropical region of Nepal","authors":"S. Dhakal, P. Aryal, S. Aryal, D. Bashyal, D. Khadka","doi":"10.5897/JPP2016.0425","DOIUrl":null,"url":null,"abstract":"This research was carried out with the aim of phytochemical analysis and determining antioxidant activity present in methanol and chloroform leaf extracts of Azadirachta indica. Due to its potential in curing various ailments as well as wide spread application of antioxidant activity such as in the field of cosmetology, the plant was selected for the study. The total phenolics contained in the plant extracts were also studied which are responsible for the antioxidant activity. Antioxidant activity of the extracts were evaluated by diphenyl-β-picrylhydrazyl (DPPH) free radical scavenging method using ascorbic acid as standard in the concentration of 100, 50, 25 and 12.5 µg/ml. Phytochemical analysis were done with the established procedure and total phenolic content (TPC) was determined by using Folin-Ciocalteu colorimetric method. Phytochemical screening revealed the presence of similar constituents in both methanol and chloroform extracts such as alkaloids, glycosides, carbohydrate, phenol, flavonoid, steroids, protein, and amino acids. Total phenolic content in methanol and chloroform extracts were 207.39 ± 8.77 and 58.08 ± 4.41 mg gallic acid equivalent (GAE)/g, respectively. The inhibitory concentration (IC50) value for methanol and chloroform extracts of A. indica were calculated and found to be 80.28 and 439.60 µg/ml, respectively. The finding suggests that methanol extract of the plant has significantly more antioxidant activity than the chloroform extract as clarified by total phenolics contained in the plant. \n \n Key words: Phytochemical screening, antioxidant activity, total phenolic content, Azadirachta indica.","PeriodicalId":16801,"journal":{"name":"Journal of Pharmacognosy and Phytotherapy","volume":"2016 1","pages":"203-208"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"16","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacognosy and Phytotherapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5897/JPP2016.0425","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16

Abstract

This research was carried out with the aim of phytochemical analysis and determining antioxidant activity present in methanol and chloroform leaf extracts of Azadirachta indica. Due to its potential in curing various ailments as well as wide spread application of antioxidant activity such as in the field of cosmetology, the plant was selected for the study. The total phenolics contained in the plant extracts were also studied which are responsible for the antioxidant activity. Antioxidant activity of the extracts were evaluated by diphenyl-β-picrylhydrazyl (DPPH) free radical scavenging method using ascorbic acid as standard in the concentration of 100, 50, 25 and 12.5 µg/ml. Phytochemical analysis were done with the established procedure and total phenolic content (TPC) was determined by using Folin-Ciocalteu colorimetric method. Phytochemical screening revealed the presence of similar constituents in both methanol and chloroform extracts such as alkaloids, glycosides, carbohydrate, phenol, flavonoid, steroids, protein, and amino acids. Total phenolic content in methanol and chloroform extracts were 207.39 ± 8.77 and 58.08 ± 4.41 mg gallic acid equivalent (GAE)/g, respectively. The inhibitory concentration (IC50) value for methanol and chloroform extracts of A. indica were calculated and found to be 80.28 and 439.60 µg/ml, respectively. The finding suggests that methanol extract of the plant has significantly more antioxidant activity than the chloroform extract as clarified by total phenolics contained in the plant. Key words: Phytochemical screening, antioxidant activity, total phenolic content, Azadirachta indica.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
印楝叶甲醇和氯仿提取物的植物化学和抗氧化研究。位于尼泊尔热带地区
本文对印楝叶甲醇提取物和氯仿提取物进行了植物化学分析和抗氧化活性测定。由于其治疗各种疾病的潜力以及抗氧化活性的广泛应用,例如在美容领域,因此选择该植物进行研究。研究了植物提取物中具有抗氧化活性的总酚类物质。以100、50、25、12.5µg/ml的抗坏血酸为标准,采用DPPH自由基清除法评价提取物的抗氧化活性。采用建立的方法进行植物化学分析,用Folin-Ciocalteu比色法测定总酚含量(TPC)。植物化学筛选显示,甲醇和氯仿提取物中存在类似的成分,如生物碱、糖苷、碳水化合物、酚、类黄酮、类固醇、蛋白质和氨基酸。甲醇和氯仿提取物中总酚含量分别为207.39±8.77和58.08±4.41 mg没食子酸当量(GAE)/g。计算甲醇和氯仿提取物的抑菌浓度(IC50)值,分别为80.28µg/ml和439.60µg/ml。研究结果表明,甲醇提取物的抗氧化活性明显高于氯仿提取物。关键词:植物化学筛选,抗氧化活性,总酚含量,印楝
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
0.10
自引率
0.00%
发文量
0
期刊最新文献
Effect of seasonal variations on the secondary metabolites and antioxidant activities of Bridelia ferruginea, Lippia multiflora, and Azadirachta indica leaves Determination of in vitro thrombolytic activity in isolated flavonoids of plant Madras Nelli In vitro anthelmintic activity against Haemonchus contortus of methanolic extracts of selected medicinal plants from Meru County, Kenya Physicochemical, phytochemical and pharmacognostical parameters of a herbal plant Dracaena steudneri Engl. Evaluation of the phenolic content and in vitro antioxidant potential of Bauhinia monandra Kurz (Fabaceae)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1