Rheological assessment of the sol–gel transition for self-assembling low molecular weight gelators

2011 ◽  
Vol 44 (5) ◽  
pp. 1447-1451 ◽  
Author(s):  
Michael A. Rogers ◽  
Jae Hee Jennifer Kim
ChemistryOpen ◽  
2018 ◽  
Vol 7 (6) ◽  
pp. 457-462 ◽  
Author(s):  
Hao Wang ◽  
Qihong Liu ◽  
Yalong Hu ◽  
Miaochang Liu ◽  
Xiaobo Huang ◽  
...  

Gels ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 208
Author(s):  
Alexandra Croitoriu ◽  
Loredana E. Nita ◽  
Aurica P. Chiriac ◽  
Alina G. Rusu ◽  
Maria Bercea

In the last years, physical hydrogels have been widely studied due to the characteristics of these structures, respectively the non−covalent interactions and the absence of other necessary components for the cross−linking processes. Low molecular weight gelators are a class of small molecules which form higher ordered structures through hydrogen bonding and π−π interactions. In this context it is known that the formation of hydrogels based on FMOC−amino acids is determined by the primary structures of amino acids and the secondary structure arrangement (alpha−helix or beta−sheet motifs). The present study aimed to obtain supramolecular gels through co−assembly phenomenon using FMOC−amino acids as low molecular weight gelators. The stability of the new structures was evaluated by the vial inversion test, while FTIR spectra put into evidence the interaction between the compounds. The gel−like structure is evidenced by viscoelastic parameters in oscillatory shear conditions. SEM microscopy was used to obtain the visual insight into the morphology of the physical hydrogel network while DLS measurements highlighted the sol−gel transition. The molecular arrangement of gels was determined by circular dichroism, fluorescence and UV–Vis spectroscopy.


2014 ◽  
Vol 10 ◽  
pp. 3111-3121 ◽  
Author(s):  
Navneet Goyal ◽  
Hari P R Mangunuru ◽  
Bargav Parikh ◽  
Sonu Shrestha ◽  
Guijun Wang

Small molecular gelators are a class of compounds with potential applications for soft biomaterials. Low molecular weight hydrogelators are especially useful for exploring biomedical applications. Previously, we found that 4,6-O-benzylidene acetal protected D-glucose and D-glucosamine are well-suited as building blocks for the construction of low molecular weight gelators. To better understand the scope of D-glucosamine derivatives as gelators, we synthesized and screened a novel class of N-acetylglucosamine derivatives with a p-methoxybenzylidene acetal protective group. This modification did not exert a negative influence on the gelation. On the contrary, it actually enhanced the gelation tendency for many derivatives. The introduction of the additional methoxy group on the phenyl ring led to low molecular weight gelators with a higher pH responsiveness. The resulting gels were stable at neutral pH values but degraded in an acidic environment. The release profiles of naproxen from the pH responsive gels were also analyzed under acidic and neutral conditions. Our findings are useful for the design of novel triggered release self-assembling systems and can provide an insight into the influence of the the structure on gelation.


Polymer ◽  
2020 ◽  
Vol 190 ◽  
pp. 122250
Author(s):  
Hongxiang Chen ◽  
Wei Liu ◽  
Mei Hong ◽  
Ensong Zhang ◽  
Xuemin Dai ◽  
...  

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