ZHANG Pei, WU Nan, SONG Zhijun, et al. Purification of Calycosin from Astragalusme mbranceus with Macroporous Resins by Response Surface Analysis [J]. Science and Technology of Food Industry, 2021, 42(10): 209−214. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2020110048.
Citation: ZHANG Pei, WU Nan, SONG Zhijun, et al. Purification of Calycosin from Astragalusme mbranceus with Macroporous Resins by Response Surface Analysis [J]. Science and Technology of Food Industry, 2021, 42(10): 209−214. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2020110048.

Purification of Calycosin from Astragalusme mbranceus with Macroporous Resins by Response Surface Analysis

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  • Received Date: November 05, 2020
  • Available Online: March 21, 2021
  • To optimize the technical condition for purification of calycosin of Astragalus membranceus with macroporous resin, the static adsorption and desorption performance of macroporous resin of seventy types (H103, D101, AB-8, DM130, HPD-400, DM301, HPD-600) were compared for select the best type resin. The optimum process condition was obtained by single factor experiments and response surface experiment. The results showed that HPD-400 macroporous resin was the best macroporous resin for purification of calycosin of Astragalus membranceus, and the adsorption quantity of the resin was gradual decreasing with temperature increasing, and the adsorption process fitted characteristic of second-order kinetics model. The optimum process condition were as follows: The initial concentration of sample solution was 2.97 mg/mL, the volume was 60 mL with loading speed of 1.0 mL/min, the pH of sample solution was 4.9, and the volume fraction of ethanol was 79.8%, the eluent volume was 140 mL with flow rate of 1.0 mL/min. The contents of calycosin in product increased from 2.17% to 10.36%, which was about 4.8 times of that before purification. Therefore, the HPD-400 macroporous resin had good performance for separation and purification of calycosin from extracts, the purification process obtained in this study was suitable for the purification of Astragalus membranceus calycosin.
  • [1]
    Han J, Guo D, Sun X Y, et al. Comparison of the adhesion and endocytosis of calcium oxalate dihydrate to HK-2 cells before and after repair by Astragalus polysaccharide[J]. Int J Nanomed,2019,20(1):1164−1177.
    [2]
    张蔷, 高文远, 满淑丽, 黄芪中有效成分药理活性的研究进展[J]. 中国中药杂志, 2012, 37(21): 3203-3207.
    [3]
    Gai Q Y, Jiao J, Wang X, et al. Chitosan promoting formononetin and calycosin accumulation inAstragalus membranaceus hairy root cultures via mitogen-activated protein kinase signaling cascades[J]. Sci Rep,2019,9(1):1275−1283. doi: 10.1038/s41598-018-37987-5
    [4]
    Gao J Q, Liu Z J, Chen T, et al. Pharmaceutical properties of calycosin, the major bioactive isoflavonoid in the dry root extract of Radix astragali [J]. Pharm Biol,2014,52(9):1217−1222. doi: 10.3109/13880209.2013.879188
    [5]
    Li Y H, Wang C X, Li H Y, et al. Simultaneous determination of formononetin, calycosin and rhamnocitrin from Astragalus complanatus by UHPLC-MS-MS in rat plasma: application to a pharmacokinetic study[J]. J Chromatogr Sci,2016,40(3):702−708.
    [6]
    赵竞业, 容蓉, 巩丽丽, 等. 高速逆流色谱法分离纯化黄芪中毛蕊异黄酮苷和芒柄花苷[J]. 山东中医药大学学报,2017,41(2):178−181.
    [7]
    任汐月, 陈可妍, 戴京, 等. 花生芽中酚类物质的大孔树脂纯化工艺研究[J]. 食品研究与开发,2020,41(11):108−112.
    [8]
    葛水莲, 陈建中, 刘娜, 等. 响应面优化大孔树脂纯化太行菊总黄酮及其降糖活性[J]. 食品工业,2020,41(5):107−111.
    [9]
    段宙位, 陈婷, 何艾, 等. 大孔树脂纯化沉香叶黄酮工艺优化及纯化前后抗氧化性比较[J]. 食品工业科技,2020,41(17):161−166.
    [10]
    王秋阳, 赵欣锐, 王超, 等. 大孔树脂纯化红松松仁膜衣黄酮的抗氧化活性研究[J]. 食品科技,2019,44(9):223−227.
    [11]
    陈彩云. 黄芪中毛蕊异黄酮和芒柄花素的富集、分离纯化及抗氧化活性研究[D]. 哈尔滨: 东北林业大学, 2012.
    [12]
    马晓丰, 屠鹏飞, 陈英杰, 等. 高速逆流色谱法分离纯化黄芪中的芒柄花素和毛蕊异黄酮[J]. 色谱,2005,23(3):299−301.
    [13]
    张沛, 宋志军, 邰正福. 响应面法优化大孔树脂纯化黄精总皂苷提取物工艺[J]. 食品工业,2019,40(10):136−141.
    [14]
    栾朝霞. 肉苁蓉总多酚纯化工艺及其抗运动性疲劳作用研究[J]. 食品工业科技,2020,41(15):59−64.
    [15]
    Bai Y D, Ma J, Zhu W F, et al. Highly selective separation and purification of chicoric acid from Echinacea purpurea by quality control methods in macroporous adsorption resin column chromatography[J]. J Sep Sci,2019,42(5):1027−1036.
    [16]
    Zhang L, Zheng D, Zhang Q F. Purification of total flavonoids from Rhizoma smilacis Glabrae through cyclodextrin-assisted extraction and resin adsorption[J]. Food Sci Nutr,2019,7(2):449−456. doi: 10.1002/fsn3.809
    [17]
    刘琦. 大孔树脂对短梗五加多酚的纯化效果及多酚的抗疲劳作用研究[J]. 保鲜与加工,2020,20(4):171−177.
    [18]
    吴婕, 吴学慧, 徐高. 大孔树脂纯化甜茶叶总黄酮及其纯化前后的抗氧化性[J]. 江苏农业科学,2019,47(16):190−193.
    [19]
    Chen C Y, Zu Y G, Fu Y J, et al. Preparation and antioxidant activity of Radix Astragali residues extracts rich in calycosin and formononetin[J]. Biochem Eng J,2011,56(1-2):84−93. doi: 10.1016/j.bej.2011.04.015
    [20]
    朱晓亚. 天门冬总皂苷提取物的纯化及体内抗疲劳作用研究[J]. 食品科技,2019,44(9):263−269.
    [21]
    Kong Y, Yan M M, Liu W, et al. Preparative enrichment and separation of astragalosides from Radix Astragali extracts using macroporous resins[J]. J Sep Sci,2015,33(15):2278−2286.
    [22]
    王小明, 陈碧, 张鹏, 等. 甜茶叶中总黄酮大孔树脂纯化工艺及抗氧化活性研究[J]. 食品工业科技,2019,40(24):28−33.
    [23]
    李慧敏, 牛东攀, 陈丹阳, 等. 响应面法优化大孔树脂纯化杜仲绿原酸工艺研究[J]. 食品研究与开发,2018,39(13):40−46.
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