Yongqiang Ma, Jinhua Shao, Xianzhe Fan, Xingguang Zhuang, Fulin He
{"title":"大孔树脂优化分离纯化紫荆根总黄酮的工艺,并测定其抗氧化活性","authors":"Yongqiang Ma, Jinhua Shao, Xianzhe Fan, Xingguang Zhuang, Fulin He","doi":"10.4314/TJPR.V17I5.21","DOIUrl":null,"url":null,"abstract":"Purpose : To isolate, purify and determine the antioxidant property of total flavonoids from the roots of Ardisia mamillata, so as to provide a theoretical basis for development of natural antioxidants. Methods : Macroporous resin was used to optimize the isolation and purification of total flavonoids, taking adsorption rate and resolution rate as evaluation indices. The antioxidant property of the purified total flavonoids was determined using 1,1-diphenyl-2-picrylhydrazyl radical 2,2-diphenyl-1-(2,4,6- trinitrophenyl)hydrazyl (DPPH) radical scavenging activity. Results : The best conditions for separation and purification of total flavonoids from Ardisia mamillata roots were: use of ADS-7 resin, loading total flavonoid concentration of 0.8896 mg/mL, loading buffer flow rate of 1.5 mL/min, loading buffer pH of 4.48, elution ethanol concentration of 60 %, and flow rate of 2.5 mL/min. Under these conditions, the degree of purification of total flavonoids of Ardisia mamillata root was 76.43 ± 0.36 %, adsorption rate was 96.52 ± 0.19 %, while resolution rate was 99.31 ± 0.27 %. When the concentration of the purified total flavonoids was 4.0 mg/mL, its DPPH radical scavenging activity was stronger than that of the standard, butylated hydroxytoluene (BHT), but lower than that of vitamin C. Conclusion : ADS-7 resin is the best macroporous resin for the purification of total flavonoids from the radix of Ardisia mamillata Hance, under the optimized conditions. The purified total flavonoids of Ardisia mamillata root have stronger DPPH radical scavenging ability than the standard, BHT. Keywords : Szechwan raspberry root, Flavonoids, Macroporous adsorption resin, ADS-7 resin, Purification, Antioxidant","PeriodicalId":23347,"journal":{"name":"Tropical Journal of Pharmaceutical Research","volume":"99 1","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2018-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Optimization of isolation and purification of total flavonoids from Ardisia mamillata Hance roots using macroporous resins, and determination of their antioxidant activity\",\"authors\":\"Yongqiang Ma, Jinhua Shao, Xianzhe Fan, Xingguang Zhuang, Fulin He\",\"doi\":\"10.4314/TJPR.V17I5.21\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Purpose : To isolate, purify and determine the antioxidant property of total flavonoids from the roots of Ardisia mamillata, so as to provide a theoretical basis for development of natural antioxidants. Methods : Macroporous resin was used to optimize the isolation and purification of total flavonoids, taking adsorption rate and resolution rate as evaluation indices. The antioxidant property of the purified total flavonoids was determined using 1,1-diphenyl-2-picrylhydrazyl radical 2,2-diphenyl-1-(2,4,6- trinitrophenyl)hydrazyl (DPPH) radical scavenging activity. Results : The best conditions for separation and purification of total flavonoids from Ardisia mamillata roots were: use of ADS-7 resin, loading total flavonoid concentration of 0.8896 mg/mL, loading buffer flow rate of 1.5 mL/min, loading buffer pH of 4.48, elution ethanol concentration of 60 %, and flow rate of 2.5 mL/min. Under these conditions, the degree of purification of total flavonoids of Ardisia mamillata root was 76.43 ± 0.36 %, adsorption rate was 96.52 ± 0.19 %, while resolution rate was 99.31 ± 0.27 %. When the concentration of the purified total flavonoids was 4.0 mg/mL, its DPPH radical scavenging activity was stronger than that of the standard, butylated hydroxytoluene (BHT), but lower than that of vitamin C. Conclusion : ADS-7 resin is the best macroporous resin for the purification of total flavonoids from the radix of Ardisia mamillata Hance, under the optimized conditions. The purified total flavonoids of Ardisia mamillata root have stronger DPPH radical scavenging ability than the standard, BHT. 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Optimization of isolation and purification of total flavonoids from Ardisia mamillata Hance roots using macroporous resins, and determination of their antioxidant activity
Purpose : To isolate, purify and determine the antioxidant property of total flavonoids from the roots of Ardisia mamillata, so as to provide a theoretical basis for development of natural antioxidants. Methods : Macroporous resin was used to optimize the isolation and purification of total flavonoids, taking adsorption rate and resolution rate as evaluation indices. The antioxidant property of the purified total flavonoids was determined using 1,1-diphenyl-2-picrylhydrazyl radical 2,2-diphenyl-1-(2,4,6- trinitrophenyl)hydrazyl (DPPH) radical scavenging activity. Results : The best conditions for separation and purification of total flavonoids from Ardisia mamillata roots were: use of ADS-7 resin, loading total flavonoid concentration of 0.8896 mg/mL, loading buffer flow rate of 1.5 mL/min, loading buffer pH of 4.48, elution ethanol concentration of 60 %, and flow rate of 2.5 mL/min. Under these conditions, the degree of purification of total flavonoids of Ardisia mamillata root was 76.43 ± 0.36 %, adsorption rate was 96.52 ± 0.19 %, while resolution rate was 99.31 ± 0.27 %. When the concentration of the purified total flavonoids was 4.0 mg/mL, its DPPH radical scavenging activity was stronger than that of the standard, butylated hydroxytoluene (BHT), but lower than that of vitamin C. Conclusion : ADS-7 resin is the best macroporous resin for the purification of total flavonoids from the radix of Ardisia mamillata Hance, under the optimized conditions. The purified total flavonoids of Ardisia mamillata root have stronger DPPH radical scavenging ability than the standard, BHT. Keywords : Szechwan raspberry root, Flavonoids, Macroporous adsorption resin, ADS-7 resin, Purification, Antioxidant
期刊介绍:
We seek to encourage pharmaceutical and allied research of tropical and international relevance and to foster multidisciplinary research and collaboration among scientists, the pharmaceutical industry and the healthcare professionals.
We publish articles in pharmaceutical sciences and related disciplines (including biotechnology, cell and molecular biology, drug utilization including adverse drug events, medical and other life sciences, and related engineering fields). Although primarily devoted to original research papers, we welcome reviews on current topics of special interest and relevance.