Construction and transformation of stimuli-responsive vesicles from the ferrocene derivative supramolecular amphiphiles

被引:17
作者
Li, Qiuhong [1 ,2 ]
Chen, Xiao [1 ]
Yue, Xiu [1 ]
Huang, Dandan [1 ]
Wang, Xudong [1 ]
机构
[1] Shandong Univ, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250100, Peoples R China
[2] Shandong Univ Technol, Sch Mat Sci & Engn, Zibo 255049, Peoples R China
基金
中国国家自然科学基金;
关键词
Ferrocene; Electrochemical oxidation; Vesicles; Cyclodextrins; Stimuli-responsive; CYCLODEXTRIN; ASSEMBLIES; SURFACTANT; NANOTUBES; ACID; AOT;
D O I
10.1016/j.colsurfa.2012.05.043
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The tough stimuli-responsive vesicles were prepared via electrochemical oxidation on the mixture solution of ferrocenylmerhyl-trimethylammonium iodide (FcMI) and sodium deoxycholate (NaDC). The vesicle structure and morphology are characterized respectively by transmission electron microscopy (TEM), dynamic light scattering (DLS) and atomic force microscopy (AFM). The vesicle shells can be clearly observed by TEM with the thickness ranging from several to several tens of nanometers and their outer diameters at the range of 50-200 nm. The formation of vesicular structures is also supported via AFM measurements. Such tough vesicles made up of ferrocene and deoxycholate blocks are redox-responsive, and their assembly or disassembly behaviors may be controlled by electrochemical methods through the change of ferrocene states between the neutral hydrophobic and the hydrophilic ferrocenium cation. In addition, the stimuli-responsive vesicles can also be formed from the supramolecular inclusion complex between the ferrocene blocks and the beta-cyclodextrin hosts, which can then be transformed into nanotubes with time. The obtained results are significant for the preparation of smart supramolecular aggregates. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 104
页数:7
相关论文
共 37 条
[1]   Enhanced emission and its switching in fluorescent organic nanoparticles [J].
An, BK ;
Kwon, SK ;
Jung, SD ;
Park, SY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (48) :14410-14415
[2]   IMPROVED ACYLATION RATES WITHIN CYCLODEXTRIN COMPLEXES FROM FLEXIBLE CAPPING OF THE CYCLODEXTRIN AND FROM ADJUSTMENT OF THE SUBSTRATE GEOMETRY [J].
BRESLOW, R ;
CZARNIECKI, MF ;
EMERT, J ;
HAMAGUCHI, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (02) :762-770
[3]  
Cramer F. D., 1965, REV PURE APPL CHEM, V5, P143
[4]   Photo-reversible supramolecular hyperbranched polymer based on host-guest interactions [J].
Dong, Ruijiao ;
Liu, Yong ;
Zhou, Yongfeng ;
Yan, Deyue ;
Zhu, Xinyuan .
POLYMER CHEMISTRY, 2011, 2 (12) :2771-2774
[5]   Tailor-Made Dual pH-Sensitive Polymer-Doxorubicin Nanoparticles for Efficient Anticancer Drug Delivery [J].
Du, Jin-Zhi ;
Du, Xiao-Jiao ;
Mao, Cheng-Qiong ;
Wang, Jun .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (44) :17560-17563
[6]   Strongly coupled excitonic states in H-aggregated single crystalline nanoparticles of 2,5-bis(4-methoxybenzylidene) cyclopentanone [J].
Fang, Qunling ;
Wang, Feng ;
Zhao, Hui ;
Liu, Xinran ;
Tu, Renyong ;
Wang, Dapeng ;
Zhang, Zhongping .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (10) :2837-2841
[7]   A review of stimuli-responsive nanocarriers for drug and gene delivery [J].
Ganta, Srinivas ;
Devalapally, Harikrishna ;
Shahiwala, Aliasgar ;
Amiji, Mansoor .
JOURNAL OF CONTROLLED RELEASE, 2008, 126 (03) :187-204
[8]   Stimuli-responsive supramolecular assemblies of linear-dendritic copolymers [J].
Gillies, ER ;
Jonsson, TB ;
Fréchet, JMJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (38) :11936-11943
[9]   Self-assembly vesicles made from a cyclodextrin supramolecular complex [J].
Jing, Bo ;
Chen, Xiao ;
Wang, Xudong ;
Yang, Chunjie ;
Xie, Yizhou ;
Qiu, Huayu .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (32) :9137-9142
[10]   Electrochemical control of vesicle formation with a double-tailed cationic surfactant bearing ferrocenyl moieties [J].
Kakizawa, Y ;
Sakai, H ;
Yamaguchi, A ;
Kondo, Y ;
Yoshino, N ;
Abe, M .
LANGMUIR, 2001, 17 (26) :8044-8048