Dual Electrospun Supramolecular Polymer Systems for Selective Cell Migration

2018 ◽  
Vol 18 (7) ◽  
pp. 1800004
Author(s):  
Shraddha H. Thakkar ◽  
Andrea Di Luca ◽  
Sabrina Zaccaria ◽  
Frank P. T. Baaijens ◽  
Carlijn V. C. Bouten ◽  
...  
2019 ◽  
Vol 31 (37) ◽  
pp. 1970261
Author(s):  
Xing‐Huo Wang ◽  
Nan Song ◽  
Wei Hou ◽  
Chun‐Yu Wang ◽  
Yan Wang ◽  
...  

2019 ◽  
Vol 37 (12) ◽  
pp. 1183-1199 ◽  
Author(s):  
Hui-Tao Yu ◽  
Jun-Wen Tang ◽  
Yi-Yu Feng ◽  
Wei Feng

2016 ◽  
Vol 369 (1) ◽  
pp. 26-29
Author(s):  
Sudha J. Devaki ◽  
Neethu K. Sadanandhan ◽  
Rohini K. Narayanan

Polymer ◽  
2015 ◽  
Vol 69 ◽  
pp. 293-300 ◽  
Author(s):  
Lewis R. Hart ◽  
Ngoc A. Nguyen ◽  
Josephine L. Harries ◽  
Michael E. Mackay ◽  
Howard M. Colquhoun ◽  
...  

2021 ◽  
Author(s):  
Zaoming Wang ◽  
Christian Villa Santos ◽  
alexandre legrand ◽  
Frederik Haase ◽  
Yosuke Hara ◽  
...  

Assembly of permanently porous metal-organic cages with functional polymers forms soft supramolecular networks featuring both porosity and processability. However, the amorphous nature of such soft materials complicates their characterization and thus limits structural control. Here we demonstrated that aging is an effective strategy to control the hierarchical network of supramolecular gels, which are assembled from organic ligands as linkers and metal-organic polyhedra (MOP) as junctions. Normally, the initial gel formation by rapid gelation leads to a kinetically trapped structure with low controllability. Through a controlled post-synthetic aging process, we show that it is possible to tune the network of the linked MOP gel over multiple length scales. This process allows control on the molecular-scale rearrangement of interlinking MOPs, mesoscale fusion of colloidal particles and macroscale densification of the whole colloidal network. In this work we elucidate the relationships between the gel properties, such as porosity and rheology, and their hierarchical structures, which suggest that porosity measurement can be used as a powerful tool to characterize the microscale structural transition of the amorphous gels. This aging strategy can be applied in other supramolecular polymer systems particularly containing kinetically controlled structures and shows an opportunity to engineer the structure and porosity of amorphous porous soft materials for further applications.


2009 ◽  
Vol 42 (12) ◽  
pp. 3887-3891 ◽  
Author(s):  
Maricica Munteanu ◽  
SooWhan Choi ◽  
Helmut Ritter

Biomaterials ◽  
2006 ◽  
Vol 27 (32) ◽  
pp. 5490-5501 ◽  
Author(s):  
Patricia Y.W. Dankers ◽  
Ellen N.M. van Leeuwen ◽  
Gaby M.L. van Gemert ◽  
A.J.H. Spiering ◽  
Martin C. Harmsen ◽  
...  

2021 ◽  
Author(s):  
Zaoming Wang ◽  
Christian Villa Santos ◽  
alexandre legrand ◽  
Frederik Haase ◽  
Yosuke Hara ◽  
...  

Assembly of permanently porous metal-organic cages with functional polymers forms soft supramolecular networks featuring both porosity and processability. However, the amorphous nature of such soft materials complicates their characterization and thus limits structural control. Here we demonstrated that aging is an effective strategy to control the hierarchical network of supramolecular gels, which are assembled from organic ligands as linkers and metal-organic polyhedra (MOP) as junctions. Normally, the initial gel formation by rapid gelation leads to a kinetically trapped structure with low controllability. Through a controlled post-synthetic aging process, we show that it is possible to tune the network of the linked MOP gel over multiple length scales. This process allows control on the molecular-scale rearrangement of interlinking MOPs, mesoscale fusion of colloidal particles and macroscale densification of the whole colloidal network. In this work we elucidate the relationships between the gel properties, such as porosity and rheology, and their hierarchical structures, which suggest that porosity measurement can be used as a powerful tool to characterize the microscale structural transition of the amorphous gels. This aging strategy can be applied in other supramolecular polymer systems particularly containing kinetically controlled structures and shows an opportunity to engineer the structure and porosity of amorphous porous soft materials for further applications.


2021 ◽  
Author(s):  
Martina Crippa ◽  
Claudio Perego ◽  
Anna de Marco ◽  
Giovanni M. Pavan

Supramolecular polymers are composed of monomers that self-assemble non-covalently, generating distributions of monodimensional fibres in continuous communication with each other and with the surrounding solution. Fibres, exchanging molecular species, and external environment constitute a sole complex system, which intrinsic dynamics is hard to elucidate. Here we report coarse-grained molecular simulations that allow studying supramolecular polymers at the thermodynamic equilibrium, explicitly showing the complex nature of these systems, which are composed of exquisitely dynamic molecular entities. Detailed studies of molecular exchange provide insights into key factors controlling how assemblies communicate with each other, defining the equilibrium dynamics of the system. Using minimalistic and finer chemically relevant molecular models, we observe that a rich concerted complexity is intrinsic in such self-assembling systems. This offers a new dynamic and probabilistic (rather than structural) picture of supramolecular polymer systems, where the travelling molecular species continuously shape the assemblies that statistically emerge at the equilibrium.


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