Dual mode gelation behavior of silk fibroin microgel embedded poly(ethylene glycol) hydrogels

2016 ◽  
Vol 4 (26) ◽  
pp. 4574-4584 ◽  
Author(s):  
S. Ryu ◽  
H. H. Kim ◽  
Y. H. Park ◽  
C.-C. Lin ◽  
I. C. Um ◽  
...  

Hydrogel formation by more than two cross-linking mechanisms is preferred for the sophisticated manipulation of hydrogel properties.

2015 ◽  
Vol 90 ◽  
pp. 21-24 ◽  
Author(s):  
Pamela de Cuadro ◽  
Tiina Belt ◽  
Katri S. Kontturi ◽  
Mehedi Reza ◽  
Eero Kontturi ◽  
...  

Synlett ◽  
2018 ◽  
Vol 29 (19) ◽  
pp. 2535-2541
Author(s):  
Alex Adronov ◽  
Kelvin Li ◽  
Stuart McNelles

A poly[(phenylene vinylene)-co-dibenzocyclooctyne] polymer prepared by Wittig polymerization chemistry between dibenzocyclooctyne bisaldehyde [DIBO-(CHO)2] and bis(triethyleneglycol)phenylbis(tributylphosphonium) dibromide is reported. The resulting polymer exhibits moderate molecular weight (Mn: 10.5 kDa, Mw: 21.3 kDa, Ð: 2.02) and is fluorescent. It could be readily functionalized by strain-promoted alkyne-azide cycloadditon with different azides, and fluorescence of the polymer was preserved after functionalization. Grafting azide-terminated 5 kDa poly(ethylene glycol) monomethyl ether chains drastically affected the solubility of the polymer. Cross-linking the polymer with poly(ethylene glycol) that was terminated at both ends with azide groups gave access to a fluorescent organogel that could be dried and reswollen with water to form a hydrogel.


2011 ◽  
Vol 60 (12) ◽  
pp. 1737-1744 ◽  
Author(s):  
Sandra Sampaio ◽  
Teresa M. R. Miranda ◽  
Jorge G. Santos ◽  
Graça M. B. Soares

2017 ◽  
Vol 12 (2) ◽  
pp. 02C414 ◽  
Author(s):  
Hanqi Wang ◽  
Fang Cheng ◽  
Wei He ◽  
Jiaohui Zhu ◽  
Gang Cheng ◽  
...  

2002 ◽  
Vol 13 (2) ◽  
pp. 232-239 ◽  
Author(s):  
Youmie Park ◽  
Kai Y. Kwok ◽  
Chawki Boukarim ◽  
Kevin G. Rice

2008 ◽  
Vol 1132 ◽  
Author(s):  
F. Bedoui ◽  
L. K. Widjaja ◽  
A. Luk ◽  
D. Bolikal ◽  
N. S. Murthy ◽  
...  

ABSTRACTIncrease in modulus upon hydration in copolymers of desaminotyrosyl-tyrosine ethyl ester (DTE) and poly(ethylene glycol) (PEG) with iodinated tyrosines, poly(I2DTE-co-PEG carbonate)s, was investigated by varying the fraction and the molecular weight of the hydrophilic PEG component. Water, as expected, acts as plasticizer in polymer with PEG content < 15 wt% and > 30 wt%. But, water has the opposite effect in iodinated polymers with moderate PEG contents, between 15 to 20 wt%: it enhances the Young's modulus. The strength and modulus of hydrated poly(I2DTE-co-15%PEG2K carbonate)s increased by as much as fifteen fold upon hydration. While the decrease in the mechanical properties in most polymeric materials with diluents such water is due to the solvent-induced swelling, the increase in strength and modulus that is observed is most likely due to the reinforcing effect of the increased cross-linking efficiency of the hydrated PEG domains in the iodinated polymer.


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