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黄芪趁鲜切制饮片与传统饮片化学成分及体外抗氧化活性比较研究
引用本文:吴红伟,李东辉,宋沁洁,李国峰,李咸慰,杨新荣,李越峰.黄芪趁鲜切制饮片与传统饮片化学成分及体外抗氧化活性比较研究[J].中草药,2022,53(22):7039-7047.
作者姓名:吴红伟  李东辉  宋沁洁  李国峰  李咸慰  杨新荣  李越峰
作者单位:甘肃中医药大学, 甘肃 兰州 730000;甘肃省中药质量与标准研究重点实验室, 甘肃 兰州 730000;甘肃中医药大学, 甘肃 兰州 730000;甘肃省中药质量与标准研究重点实验室, 甘肃 兰州 730000;甘肃省中药制药工艺工程研究中心, 甘肃 兰州 730000
基金项目:国家自然科学基金资助项目(81960713);国家自然科学基金资助项目(82160750);基础研究创新群体项目(21JR7RA569);甘肃省教育厅产业支撑计划项目(2021CYZC-21);甘肃省中药制药工艺工程研究中心开放课题(ZYGY202003);国家药品监督管理局中药材及饮片质量控制重点实验室项目(2020GSMPA-KL15);甘肃省高等学校产业支撑计划项目——四种道地陇药绿色规范化产业发展示范推广(2020C-09);民生科技专项(科技特派员专题)——中药材引种驯化与道地药材产业化扶贫示范推广(20CX9NA070);甘肃省科学技术厅——科技计划(创新基地与人才计划)双一流科研重点项目(GSSYLXM-05);甘肃省中药炮制技术传承基地项目
摘    要:目的 采用HPLC、UV等方法测定并比较黄芪趁鲜切制饮片与黄芪传统饮片的指标性成分及体外抗氧化活性,为不同加工方式的黄芪饮片质量控制提供科学依据。方法 采用HPLC、UV等方法对黄芪趁鲜切制饮片与黄芪传统饮片的7种指标性成分(黄芪甲苷、毛蕊异黄酮葡萄糖苷、芒柄花苷、毛蕊异黄酮、总黄酮、总多糖、水溶性浸出物)进行含量测定,采用熵权法结合逼近理想解排序法(technique for order preference by similarity to ideal solution,TOPSIS)评价不同产地加工方式对黄芪药材质量的影响,并结合主成分分析(principal component analysis,PCA)和偏最小二乘判别分析(partial least squares discriminant analysis,PLS-DA)等化学计量学方法对黄芪趁鲜切制饮片与黄芪传统饮片进行区分和比较,同时以DPPH自由基、羟基自由基和ABTS自由基清除能力为评价指标对黄芪趁鲜切制饮片与黄芪传统饮片的体外抗氧化活性进行比较。结果 通过熵权综合评分法比较2种不同加工方式对黄芪饮片质量的影响,结果发现黄芪趁鲜切制饮片综合评分均高于黄芪传统饮片;同时,黄芪趁鲜切制饮片组与黄芪传统饮片组在体外抗氧化活性方面,DPPH自由基清除能力的半抑制浓度(half maximal inhibitory concentration,IC50)分别为5.560、8.168mg/mL,羟基自由基清除能力的IC50分别为10.994、15.045mg/mL,ABTS自由基清除能力的IC50分别为8.126、14.546mg/mL,表明黄芪趁鲜切制饮片体外抗氧化活性强于黄芪传统饮片。结论 通过熵权TOPSIS综合评分法结合化学计量学分析方法及体外抗氧化活性对黄芪趁鲜切制饮片与黄芪传统饮片进行分析,为不同加工方式的黄芪饮片质量控制提供参考。

关 键 词:黄芪  产地加工  体外抗氧化  化学模式识别分析  质量控制  黄芪甲苷  毛蕊异黄酮葡萄糖苷  芒柄花苷  毛蕊异黄酮  总黄酮  总多糖  水溶性浸出物
收稿时间:2022/5/23 0:00:00

Comparative study on chemical composition and in vitro anti-oxidant activity of Astragali Radix fresh-cut pieces and traditional pieces
WU Hong-wei,LI Dong-hui,SONG Qin-jie,LI Guo-feng,LI Xian-wei,YANG Xin-rong,LI Yue-feng.Comparative study on chemical composition and in vitro anti-oxidant activity of Astragali Radix fresh-cut pieces and traditional pieces[J].Chinese Traditional and Herbal Drugs,2022,53(22):7039-7047.
Authors:WU Hong-wei  LI Dong-hui  SONG Qin-jie  LI Guo-feng  LI Xian-wei  YANG Xin-rong  LI Yue-feng
Institution:Gansu University of Chinese Medicine, Lanzhou 730000, China;Key Laboratory of Standard and Quality of Chinese Medicine Research of Gansu, Lanzhou 730000, China; Gansu University of Chinese Medicine, Lanzhou 730000, China;Key Laboratory of Standard and Quality of Chinese Medicine Research of Gansu, Lanzhou 730000, China;Gansu Engineering Research Center for Chinese Medicine Pharmaceutical Technology, Lanzhou 730000, China
Abstract:Objective HPLC, UV and other methods were used to determine and compare the index components and in vitro antioxidant activities of fresh-cut pieces and traditional pieces of Huangqi (Astragali Radix), providing scientific basis for quality control of Astragali Radix pieces with different processing methods. Methods HPLC, UV and other methods were used to determine the contents of 7 index components (astragaloside IV, calycosin-7-glucoside, ononin, calycosin, total flavonoids, total polysaccharides, water-soluble extract) in fresh-cut and traditional pieces of Astragali Radix. The effect of different processing methods on the quality of Astragali Radix was evaluated by the entropy weight method combined with technique for order preference by similarity to an ideal solution (TOPSIS). In addition, chemometric methods such as principal component analysis (PCA) and partial least squares- discriminant analysis (PLS-DA) were used to differentiate and compare the fresh-cut pieces of Astragali Radix with the traditional pieces of Astragali Radix. At the same time, DPPH free radical, hydroxyl free radical and ABTS radical scavenging ability were used as evaluation indexes to compare the in vitro antioxidant activity of fresh-cut pieces of Astragali Radix and traditional pieces of Astragali Radix. Results The entropy weight comprehensive score method was used to compare the effects of two different processing methods on the quality of Astragali Radix decoction pieces. The results showed that the comprehensive score of fresh-cut Astragali Radix decoction pieces was higher than that of traditional Astragali Radix decoction pieces. In vitro antioxidant activities of Astragali Radix in the fresh-cut group and the traditional group were 5.560, 8.168 mg/mL for IC50 of DPPH radical scavenging capacity, the IC50 of hydroxyl radical scavenging capacity was 10.994, 15.045 mg/mL, and the IC50 of ABTS radical scavenging capacity was 8.126, 14.546 mg/mL, respectively. The above results showed that the in vitro antioxidant activity of fresh-cut pieces of Astragali Radix was stronger than that of traditional slices of Astragali Radix. Conclusion In this study, the entropy weight TOPSIS comprehensive scoring method combined with chemometrics analysis method and in vitro antioxidant activity were used to analyze the fresh-cut slices and traditional slices of Astragali Radix, so as to provide reference for the quality control of Astragali Radix slices with different processing methods.
Keywords:Astragali Radix  producing area processing  in vitro antioxidant  chemical pattern recognition analysis  quality control  astragaloside IV  calycosin-7-glucoside  ononin  calycosin  total flavonoids  total polysaccharides  water-soluble extract
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