Linear coupling of spherical block copolymer micelles induced by gradually depositing an insoluble component onto the core–shell interface

Soft Matter ◽  
2012 ◽  
Vol 8 (33) ◽  
pp. 8636 ◽  
Author(s):  
Jing Ji ◽  
Yanbin Fan ◽  
Ming Jiang ◽  
Daoyong Chen
2021 ◽  
Author(s):  
Jiajia Xiang ◽  
Peiwen Xing ◽  
Liu Xin ◽  
Peihong Shen ◽  
Shiqun Shao ◽  
...  

Amphiphilic block copolymer prodrugs, which can self-assemble into stable core-shell micelles, have been widely used for anticancer drug delivery. However, a major challenge remains to design drug-conjugating linkers stable in...


2014 ◽  
Vol 5 (1) ◽  
pp. 234-240 ◽  
Author(s):  
Mingchang Lin ◽  
Guosong Chen ◽  
Ming Jiang

Nano Letters ◽  
2005 ◽  
Vol 5 (2) ◽  
pp. 315-319 ◽  
Author(s):  
Ning Kang ◽  
Marie-Ève Perron ◽  
Robert E. Prud'homme ◽  
Yubao Zhang ◽  
Geneviève Gaucher ◽  
...  

2001 ◽  
Vol 703 ◽  
Author(s):  
Hanying Zhao ◽  
Elliot P. Douglas

ABSTRACTA novel preparation method of CdS nanoparticles in the core or corona of micelles is presented. Poly(styrene-block-2-vinylpyridine) (PS-b-P2VP) and cadmium ions form aggregates of single micelles, called compound micelles, upon addition of the cadmium acetate salt into a solution of the block copolymer in tetrahydrofuran. The growth of CdS nanoparticles is confined to the core of single micelles after introduction of hydrogen sulfide gas into the solution. UV-visible spectroscopy, fluorescence spectroscopy, and transmission electron microscopy were employed to characterize the prepared core-embedded CdS nanoparticles. Corona-embedded CdS nanoparticles were prepared by dropping the core-embedded CdS nanoparticles into water with a low pH value. The location change of the CdS nanoparticles was accompanied by a structural change of the micelles, a change from compound micelles to single micelles. In a single micelle, CdS nanoparticles distribute randomly in the corona. The size of the nanoparticles increases slightly after the transition.


Nanoscale ◽  
2021 ◽  
Author(s):  
Chan-Jin Kim ◽  
Ga-Hyun Kim ◽  
Eun Hye Jeong ◽  
Hyukjin Lee ◽  
So-Jung Park

Here, we report how the nature of the hydrophobic core affects molecular interactions of DNA block copolymer assemblies. Three different amphiphilic DNA block copolymers, DNA-b-polystyrene (DNA-b-PS), DNA-b-poly(2-vinylpyridine) (DNA-b-P2VP), and DNA-b-poly(methyl...


2018 ◽  
Vol 9 (22) ◽  
pp. 3158-3168 ◽  
Author(s):  
Jianhua Lü ◽  
Bingxin Liu ◽  
Bingfeng Shi ◽  
Changli Lü

Thermo-responsive dual-emitting QD/BCP assemblies with QDs located in the core (CDMs), shell (SDMs) and the interface (IDMs) between the core and the shell of micelles were constructed via coordination-driven assemblies for the selective detection of TNP and Hg2+ ions.


2010 ◽  
Vol 6 (3) ◽  
pp. 277-284 ◽  
Author(s):  
Konstantinos Gardikis ◽  
Konstantinos Dimas ◽  
Aristidis Georgopoulos ◽  
Eleni Kaditi ◽  
Stergios Pispas ◽  
...  

1997 ◽  
Vol 62 (11) ◽  
pp. 1730-1736 ◽  
Author(s):  
Petr Munk ◽  
Zdeněk Tuzar ◽  
Karel Procházka

When two electrolyte solutions are separated and only some of the ions can cross the boundary, the concentrations of these ions are different on both sides of the boundary. This is the well-known Donnan effect. When weak electrolytes are involved, the imbalance includes also hydrogen ions: there is a difference of pH across the boundary and the dissociation of nondiffusible weak electrolytes is suppressed. The effect is very pronounced when the concentration of the weak electrolyte is high and ionic strength is low. The significance of this phenomenon is discussed for polyelectrolyte solutions, and particularly for block copolymer micelles with weak polyelectrolyte shells. The effect is quite dramatic in the latter case.


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