Characterization and enhanced antioxidant activity of the inclusion complexes of baicalin with p-sulfonatocalix[n]arenes

被引:5
|
作者
Chao, Jianbin [1 ]
Wang, Xiaolu [1 ,2 ]
Xu, Miao [1 ,2 ]
Zuo, Ying [3 ]
机构
[1] Shanxi Univ, Res Inst Appl Chem, Taiyuan 030006, Shanxi, Peoples R China
[2] Shanxi Univ, Sch Chem & Chem Engn, Taiyuan 030006, Shanxi, Peoples R China
[3] Shanxi Univ, Sci Instrument Ctr, Taiyuan 030006, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Baicalin; p-Sulfonatocalix[n]arenes; Antioxidant activity; Stability; SCUTELLARIAE-RADIX; BINDING BEHAVIORS; CALIXARENES; SULFONATOCALIXARENES; CYCLODEXTRINS; COMPONENTS; MOLECULES; ACID;
D O I
10.1007/s10847-019-00887-w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Baicalin, one of the main active constituents of the isolated root of Scutellaria baicalensis. It has many health-promoting properties. However, it is easy to be oxidized that impedes its application in the practical life. In this study, the inclusion complexes of baicalin with p-sulfonatocalix[n]arenes were studied by fluorescence spectroscopy, ultraviolet-visible spectroscopy (UV-vis), fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy, and atomic force microscopy. The results showed that baicalin was able to form inclusion complexes with p-sulfonatocalix[n]arenes in a molar ratio of 1:1 and the association constants (K) were different at different pH. Meanwhile, the antioxidant ability and stability experiments of baicalin and the inclusion complexes were done. The experimental results indicated that both the stability and the antioxidant activity of baicalin significantly increased by the formation of inclusion complexes with p-sulfonatocalix[n]arenes.
引用
收藏
页码:361 / 370
页数:10
相关论文
共 50 条
  • [31] Encapsulation of rhodamine-6G within p-sulfonatocalix[n]arenes: NMR, photophysical behaviour and biological activities
    Patil, Sanhita V.
    Athare, Sulakshana V.
    Jagtap, Ashok
    Kodam, Kisan M.
    Gejji, Shridhar P.
    Malkhede, Dipalee D.
    RSC ADVANCES, 2016, 6 (111) : 110206 - 110220
  • [32] A route to virtually unlimited functionalization of water-soluble p-sulfonatocalix[4]arenes
    Gorbunov, Alexander
    Iskandarova, Anna
    Puchnin, Kirill
    Nenajdenko, Valentine
    Kovalev, Vladimir
    Vatsouro, Ivan
    CHEMICAL COMMUNICATIONS, 2020, 56 (29) : 4122 - 4125
  • [33] Scandium(III) coordination polymers containing capsules based on two p-sulfonatocalix[4]arenes
    Webb, HR
    Hardie, MJ
    Raston, CL
    CHEMISTRY-A EUROPEAN JOURNAL, 2001, 7 (16) : 3616 - 3620
  • [34] Hierarchical Assembly Involving Hydroxyethyl-substituted Imidazolium Cations and p-Sulfonatocalix[4]arenes
    Ling, Irene
    Alias, Yatimah
    Skelton, Brian W.
    Raston, Colin L.
    AUSTRALIAN JOURNAL OF CHEMISTRY, 2010, 63 (10) : 1492 - 1496
  • [36] Cellular Uptake of Cell-Penetrating Peptides Activated by Amphiphilic p-Sulfonatocalix[4]arenes
    Huang, Chusen
    Liu, Yan-Cen
    Oh, Hyeyoung
    Guo, Dong-Sheng
    Nau, Werner M.
    Hennig, Andreas
    CHEMISTRY-A EUROPEAN JOURNAL, 2024, 30 (28)
  • [37] Supra-amphiphilic aggregates formed by p-sulfonatocalix[4]arenes and the antipsychotic drug chlorpromazine
    Qin, Zhanbin
    Guo, Dong-Sheng
    Gao, Xiao-Ning
    Liu, Yu
    SOFT MATTER, 2014, 10 (13) : 2253 - 2263
  • [38] Synthesis, structures and cytotoxicity studies of p-sulfonatocalix[4]arene lanthanide complexes
    Miller-Shakesby, David M.
    Burke, Benjamin P.
    Nigam, Shubhanchi
    Stasiuk, Graeme J.
    Prior, Timothy J.
    Archibald, Stephen J.
    Redshaw, Carl
    CRYSTENGCOMM, 2016, 18 (26): : 4977 - 4987
  • [39] Uranyl and mixed uranyl-lanthanide complexes with p-sulfonatocalix[4]arene
    Thuery, Pierre
    CRYSTENGCOMM, 2012, 14 (20): : 6369 - 6373
  • [40] Inclusion complexation of diphenylamine-4-diazonium chloride and p-sulfonatocalix[4]arene
    Zhang, YJ
    Tu, GZ
    Cao, WX
    SUPRAMOLECULAR CHEMISTRY, 2002, 14 (06) : 473 - 475