Hydrophobic Interface Cages in Microemulsions: Concept and Experiment Using Tetraphenylethylene-based Double-tailed Surfactant

Author(s):  
Weijiang Guan ◽  
Xiaofang Tang ◽  
Wei Wang ◽  
Yanjun Lin ◽  
Chao Lu
Virology ◽  
2006 ◽  
Vol 349 (2) ◽  
pp. 290-299 ◽  
Author(s):  
Zuoxiang Xiao ◽  
Elana Ehrlich ◽  
Yunkai Yu ◽  
Kun Luo ◽  
Tao Wang ◽  
...  

2020 ◽  
Vol 59 (24) ◽  
pp. 9498-9505 ◽  
Author(s):  
Mohammed Ahmed ◽  
Ken‐ichi Inoue ◽  
Satoshi Nihonyanagi ◽  
Tahei Tahara

2016 ◽  
Vol 138 (17) ◽  
pp. 5551-5560 ◽  
Author(s):  
Shunhao Xiao ◽  
Florian Figge ◽  
Guillaume Stirnemann ◽  
Damien Laage ◽  
John A. McGuire

2002 ◽  
Vol 321 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Jane A. Knappenberger ◽  
Jennifer E. Smith ◽  
Sarah H. Thorpe ◽  
Jill A. Zitzewitz ◽  
C.Robert Matthews

2008 ◽  
Vol 8 (7) ◽  
pp. 3386-3391
Author(s):  
ImShik Lee ◽  
Haiying Sun ◽  
Jingxia Song ◽  
Ying Zhang

Hydrophobitized polysaccharides were designed to form the self-assembled nanohydrogels (hydrogel nanoparticles) in the aqueous conditions. For improving their biocompatibilities, they were decorated with the biomembrane-mimetic 2-methacryloyloxyethy1 phosphory1choline (MPC) polymers. The interfacial roles of the decorated membrane-mimetic nanohydrogels were investigated by choosing MPC branched choresteryl-bearing pullulan (CHP). Tapping-mode atomic force microscopy was used to study its adsorption mechanism on the hydrophobic highly oriented pyrolytic graphite (HOPG) surface in aqueous conditions. Dynamic observation at the interfaces revealed two distinctive patterns: the immobilized nanohydrogel particles and the flatten layers. The flattening (unfolding) kinetics with and without MPC branched nanohydrogel revealed that the flattening energy was at ∼37 kBT. The flattening rate of the MPC decorated nanohydrogels was ∼1.7 times faster than that without MPC decoration, corresponding to minor reduction of the flattening activation energy.


2006 ◽  
Vol 103 (45) ◽  
pp. 16740-16745 ◽  
Author(s):  
C. Fang ◽  
A. Senes ◽  
L. Cristian ◽  
W. F. DeGrado ◽  
R. M. Hochstrasser

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