免柱基质固相分散萃取联用高效液相色谱测定喜树果中喜树碱的含量

喻琼林 梁坪 简伟 乔婷宜 董南

引用本文: 喻琼林, 梁坪, 简伟, 乔婷宜, 董南. 免柱基质固相分散萃取联用高效液相色谱测定喜树果中喜树碱的含量[J]. 分析化学, 2022, 50(8): 1217-1223. doi: 10.19756/j.issn.0253-3820.221066 shu
Citation:  YU Qiong-Lin,  LIANG Ping,  JIAN Wei,  QIAO Ting-Yi,  DONG Nan. Column-free Matrix Solid Phase Dispersion Extraction Based on Cucurbit[7]uril Coupled with High Performance Liquid Chromatography for Determination of Camptothecin Content in Camptotheca acuminate Decne[J]. Chinese Journal of Analytical Chemistry, 2022, 50(8): 1217-1223. doi: 10.19756/j.issn.0253-3820.221066 shu

免柱基质固相分散萃取联用高效液相色谱测定喜树果中喜树碱的含量

    通讯作者: 董南,E-mail:ndong@gzu.edu.cn
  • 基金项目:

    贵州省科学技术基金项目(No.ZK[2021]一般054)和国家自然科学基金项目(No.22164006)资助。

摘要: 建立了一种简单、快速、环保的免柱基质固相分散萃取(FMSPD)方法用于喜树果中喜树碱的萃取。基于七元瓜环(Q[7])对喜树碱的识别作用,将Q[7]作为FMSPD的固相分散剂,选择性地从喜树果中萃取出喜树碱,并将其转移到水相,采用高效液相色谱-紫外检测器(HPLC-UV)直接测定其含量。对各种影响萃取效率的因素,包括Q[7]的用量、研磨时间、加入水的量以及溶液的pH值进行了考察。在优化的实验条件下,建立的FMSPD-HPLC-UV分析方法的线性范围为1.0~100 μg/mL,检出限(S/N=3)为0.15 μg/mL,日内和日间精密度分别为4.5%和5.2%。4个浓度水平的加标回收率在97.1%~119.3%范围内。对3个不同产地喜树果中喜树碱的含量进行了测定,F检验法和t检验法表明,本方法与传统超声提取法之间无显著性差异,本方法具有更简单、快速和不使用有机溶剂的优点。

English


    1. [1]

      LIU Bo, LIU Xi-Zi, SU Lu-Hui, ZHU Li-Hong, YANG Yi. Forest. Sci. Tech., 2018, 43(1):13-16.刘波,刘曦子,苏禄晖,朱丽红,杨意.林业科技, 2018, 43(1):13-16.

    2. [2]

      SHEN Shao-Hua, LIU Ji-Yan, HU Jiang-Qin, CHEN Bo, WANG Li-Lin. Hubei Agr. Sci., 2011, 50(21):4459-4462.沈少华,刘姬艳,胡江琴,陈博,王利琳.湖北农业科学, 2011, 50(21):4459-4462.

    3. [3]

      YANG Kui-Hua, NIE Cong-Ling. J. Mianyang Teachers'College, 2018, 37(11):69-72.杨葵华,聂从玲.绵阳师范学院学报, 2018, 37(11):69-72.

    4. [4]

      HOFF R B, PIZZOLATO T M. TrAC, Trend. Anal. Chem., 2018, 109:83-96.HOFF R B, PIZZOLATO T M. TrAC, Trend. Anal. Chem., 2018, 109:83-96.

    5. [5]

      RAMOS L. TrAC, Trend. Anal. Chem., 2019, 118:751-758.RAMOS L. TrAC, Trend. Anal. Chem., 2019, 118:751-758.

    6. [6]

      PENG L Q, LI Q, CHANG Y X, AN M, YANG R, TAN Z J, HAO J, CAO J, XU J J, HU S S. J. Chromatogr. A, 2016, 1456:68-76.PENG L Q, LI Q, CHANG Y X, AN M, YANG R, TAN Z J, HAO J, CAO J, XU J J, HU S S. J. Chromatogr. A, 2016, 1456:68-76.

    7. [7]

      HU Y H, WANG Q Y, YE L H, YANG J, DONG X, ZHENG H, ZHOU J. Ind. Crop. Prod, 2019, 141:111752.HU Y H, WANG Q Y, YE L H, YANG J, DONG X, ZHENG H, ZHOU J. Ind. Crop. Prod, 2019, 141:111752.

    8. [8]

      LEON-GONZALEZ M E, ROSALES-CONRADA N. J. Chromatogr. A, 2017, 1514:88-94.LEON-GONZALEZ M E, ROSALES-CONRADA N. J. Chromatogr. A, 2017, 1514:88-94.

    9. [9]

      LOZOWICKA B, ILYASOVA G, KACZYNSKI P, JANKOWSKA M, RUTKOWSKA E, HRYNKO I, MOJSAK P, SZABUNKO J. Talanta, 2016, 151:51-61.LOZOWICKA B, ILYASOVA G, KACZYNSKI P, JANKOWSKA M, RUTKOWSKA E, HRYNKO I, MOJSAK P, SZABUNKO J. Talanta, 2016, 151:51-61.

    10. [10]

      CAPRIOTTI A L, CAVALIERE C, FOGLIA P, SAMPERI R, STAMPACHIACCHIERE S, VENTURA S, LAGANA A. TrAC, Trend. Anal. Chem., 2015, 71:186-193.CAPRIOTTI A L, CAVALIERE C, FOGLIA P, SAMPERI R, STAMPACHIACCHIERE S, VENTURA S, LAGANA A. TrAC, Trend. Anal. Chem., 2015, 71:186-193.

    11. [11]

      RAN J F, ZHANG L X, YAO J M, WANG S S, LIANG P, DONG N. Food Chem., 2021, 350:129236.RAN J F, ZHANG L X, YAO J M, WANG S S, LIANG P, DONG N. Food Chem., 2021, 350:129236.

    12. [12]

      GHOLAMI H, ARABI M, GHAEDI M, OSTOVAN A, BAGHERI A R. J. Chromatogr. A, 2019, 1594:13-22.GHOLAMI H, ARABI M, GHAEDI M, OSTOVAN A, BAGHERI A R. J. Chromatogr. A, 2019, 1594:13-22.

    13. [13]

      LEE J W, SAMAL S, SELVAPALAM N, KIM H J, KIM K. Acc. Chem. Res., 2003, 36(8):621-630.LEE J W, SAMAL S, SELVAPALAM N, KIM H J, KIM K. Acc. Chem. Res., 2003, 36(8):621-630.

    14. [14]

      ONG W, KAIFER A E. Organometallics, 2003, 22(21):4181-4183.ONG W, KAIFER A E. Organometallics, 2003, 22(21):4181-4183.

    15. [15]

      CHEN Shi-Yan, CUI Xiao-Wei, WANG Chuan-Zeng, NI Xin-Long, MA Pei-Hua, ZHANG Jian-Xin. Chem. J. Chin. Univ., 2015, 36(10):1919-1923.陈仕焰,崔晓伟,王传增,倪新龙,马培华,张建新.高等学校化学学报, 2015, 36(10):1919-1923.

    16. [16]

      LIANG F, YANG W S. Curr. Nanosci., 2019, 15:326-327.LIANG F, YANG W S. Curr. Nanosci., 2019, 15:326-327.

    17. [17]

      ELBASHIR A A, ABOUL-ENEIN H Y. Crit. Rev. Anal. Chem., 2015, 45:52-61.ELBASHIR A A, ABOUL-ENEIN H Y. Crit. Rev. Anal. Chem., 2015, 45:52-61.

    18. [18]

      MA D, HETTIARACHCHI G, NGUYEN D, ZHANG B, WITTENBERG J B, ZAVALIJ P Y, BRIKEN V, ISAACS L. Nat. Chem., 2012, 4(6):503-510.MA D, HETTIARACHCHI G, NGUYEN D, ZHANG B, WITTENBERG J B, ZAVALIJ P Y, BRIKEN V, ISAACS L. Nat. Chem., 2012, 4(6):503-510.

    19. [19]

      MACARTNEY D H. Isr. J. Chem., 2011, 51(5-6):600-615.MACARTNEY D H. Isr. J. Chem., 2011, 51(5-6):600-615.

    20. [20]

      CONG H, TAO Z, XUE S F, ZHU Q J. Curr. Org. Chem., 2011, 15(1):86-95.CONG H, TAO Z, XUE S F, ZHU Q J. Curr. Org. Chem., 2011, 15(1):86-95.

    21. [21]

      DONG N, XUE S F, ZHU Q J, TAO Z, ZHAO Y, ZHANG B, PENG Z B. Supramol. Chem., 2008, 20(7):659-665.DONG N, XUE S F, ZHU Q J, TAO Z, ZHAO Y, ZHANG B, PENG Z B. Supramol. Chem., 2008, 20(7):659-665.

    22. [22]

      DONG N, DONG M Y, ZHAO A T, ZHU Q J, TAO Z, ZHAO Y. Sci. China:Chem., 2010, 53(11):2304-2310.DONG N, DONG M Y, ZHAO A T, ZHU Q J, TAO Z, ZHAO Y. Sci. China:Chem., 2010, 53(11):2304-2310.

    23. [23]

      JIANG Bin. Inner Mongolia J. Tradit. Chin. Med., 2013, 22:120-123.江彬.内蒙古中医药, 2013, 22:120-123.

    24. [24]

      GEMPERLINE P J. Taylor&Francis Group, New York, 2006:18-25.GEMPERLINE P J. Taylor&Francis Group, New York, 2006:18-25.

  • 加载中
计量
  • PDF下载量:  9
  • 文章访问数:  576
  • HTML全文浏览量:  61
文章相关
  • 收稿日期:  2022-02-09
  • 修回日期:  2022-05-26
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章