scholarly journals Multi-orthogonal folding of single polymer chains into soft nanoparticles

Soft Matter ◽  
2014 ◽  
Vol 10 (27) ◽  
pp. 4813-4821 ◽  
Author(s):  
Federica Lo Verso ◽  
José A. Pomposo ◽  
J. Colmenero ◽  
Angel J. Moreno

Typical topologies of cross-linked nanoparticles are obtained by orthogonal folding of single chain polymer precursors. The number of different chemical species of the cross-linkers is 4 (top) and 6 (bottom). Dark blue beads correspond to inactive monomers. Beads of other colours correspond to the reactive linkers (a different colour for each chemical species, note the pairs of bonded linkers).

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 293
Author(s):  
Agustín Blazquez-Martín ◽  
Ester Verde-Sesto ◽  
Angel J. Moreno ◽  
Arantxa Arbe ◽  
Juan Colmenero ◽  
...  

The folding of certain proteins (e.g., enzymes) into perfectly defined 3D conformations via multi-orthogonal interactions is critical to their function. Concerning synthetic polymers chains, the “folding” of individual polymer chains at high dilution via intra-chain interactions leads to so-called single-chain nanoparticles (SCNPs). This review article describes the advances carried out in recent years in the folding of single polymer chains into discrete SCNPs via multi-orthogonal interactions using different reactive chemical species where intra-chain bonding only occurs between groups of the same species. First, we summarize results from computer simulations of multi-orthogonally folded SCNPs. Next, we comprehensively review multi-orthogonally folded SCNPs synthesized via either non-covalent bonds or covalent interactions. Finally, we conclude by summarizing recent research about multi-orthogonally folded SCNPs prepared through both reversible (dynamic) and permanent bonds.


Author(s):  
Agustín Blazquez-Martín ◽  
Ester Verde-Sesto ◽  
Angel J. Moreno ◽  
Arantxa Arbe ◽  
Juan Colmenero ◽  
...  

The folding of certain proteins (e.g., enzymes) into perfectly defined 3D conformations via multi-orthogonal interactions is critical to their function. Concerning synthetic polymers chains, the “folding” of individual polymer chains at high dilution via intra-chain interactions leads to so-called single-chain nanoparticles (SCNPs). This review article describes the advances carried out in recent years in the folding of single polymer chains into discrete SCNPs via multi-orthogonal interactions using different reactive chemical species where intra-chain bonding only occurs between groups of the same species. First, we summarize results from computer simulations of multi-orthogonally folded SCNPs. Next, we comprehensively review multi-orthogonally folded SCNPs synthesized via either non-covalent bonds or covalent interactions. Finally, we conclude by summarizing recent research about multi-orthogonally folded SCNPs prepared through both reversible (dynamic) and permanent bonds.


2014 ◽  
Vol 50 (15) ◽  
pp. 1871-1874 ◽  
Author(s):  
Ana Sanchez-Sanchez ◽  
David A. Fulton ◽  
José A. Pomposo

Dynamic covalent enamine cross-links facilitate the reversible structural interconversion of dynamic single-chain polymer nanoparticles into linear polymer chains using pH as a trigger.


2015 ◽  
Vol 6 (26) ◽  
pp. 4828-4834 ◽  
Author(s):  
Cunfeng Song ◽  
Longyu Li ◽  
Lizong Dai ◽  
S. Thayumanavan

We report a facile approach to form ultra-fine single-chain polymer nanoparticles (SCPNs)viadisulfide-based intrachain crosslinking of single polymer chains of a random copolymer poly(HEMA-co-PDSEMA).


2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Ana Sanchez-Sanchez ◽  
José A. Pomposo

Single-chain technology (SCT) allows the transformation of individual polymer chains to folded/collapsed unimolecular soft nanoparticles. In this work we contribute to the enlargement of the SCT toolbox by demonstrating the efficient synthesis of single-chain polymer nanoparticles (SCNPs)viaintrachain amide formation. In particular, we exploit cross-linking between active methylene groups and isocyanate moieties as powerful “click” chemistry driving force for SCNP construction. By employing poly(methyl methacrylate)- (PMMA-) based copolymers bearingβ-ketoester units distributed randomly along the copolymer chains and bifunctional isocyanate cross-linkers, SCNPs were successfully synthesized at r.t. under appropriate reaction conditions. Characterization of the resulting SCNPs was carried out by means of a combination of techniques including size exclusion chromatography (SEC), infrared (IR) spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, dynamic light scattering (DLS), and elemental analysis (EA).


2018 ◽  
Vol 54 (28) ◽  
pp. 3476-3479 ◽  
Author(s):  
Carolin Heiler ◽  
Simon Bastian ◽  
Paul Lederhose ◽  
James P. Blinco ◽  
Eva Blasco ◽  
...  

A simple and versatile tool for generating fluorescent single chain polymer nanoparticles with visible light.


2021 ◽  
Author(s):  
Fabian R. Bloesser ◽  
Sarah L. Walden ◽  
Ishrath M. Irshadeen ◽  
Lewis C. Chambers ◽  
Christopher Barner-Kowollik

We demonstrate the light-induced, crosslinker mediated collapse of linear polymer chains into single-chain nanoparticles (SCNPs) capable of self-reporting their unfolding.


2020 ◽  
Author(s):  
Dagmar D'hooge ◽  
Christopher Barner-Kowollik ◽  
Anastasia Kislyak ◽  
Francisco Arraez ◽  
Daniel Kodura ◽  
...  

Author(s):  
Ibon Odriozola ◽  
Miren Karmele Aiertza ◽  
Germán Cabañero ◽  
Hans-Jürgen Grande ◽  
Iraida Loinaz

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