In situ photocrosslinkable hyaluronic acid-based surgical glue with tunable mechanical properties and high adhesive strength

2018 ◽  
Vol 57 (4) ◽  
pp. 522-530 ◽  
Author(s):  
Ajeesh Chandrasekharan ◽  
Keum-Yong Seong ◽  
Sang-Gu Yim ◽  
Sodam Kim ◽  
Sungbaek Seo ◽  
...  
2020 ◽  
Vol 12 (29) ◽  
pp. 33267-33275 ◽  
Author(s):  
Wangqu Liu ◽  
Ozan Erol ◽  
David H. Gracias

2012 ◽  
Vol 13 (6) ◽  
pp. 1818-1827 ◽  
Author(s):  
Emilie Hachet ◽  
Hélène Van Den Berghe ◽  
Eric Bayma ◽  
Marc R. Block ◽  
Rachel Auzély-Velty

2015 ◽  
Vol 132 (22) ◽  
pp. n/a-n/a ◽  
Author(s):  
Anahita Khanlari ◽  
Jason E. Schulteis ◽  
Tiffany C. Suekama ◽  
Michael S. Detamore ◽  
Stevin H. Gehrke

Materials ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 2919 ◽  
Author(s):  
Ma ◽  
He ◽  
Wan ◽  
Xiang ◽  
Fan ◽  
...  

In this study, benefiting from the sensitive molecular conformation transversion in azobenzene, a new strategy for fabricating alginate gels with the abilities of splicing and photo-responsive mechanical adjustment is reported. Firstly, a 4,4’-azobis(benzoylhydrazide) (Azo-hydrazide) linker was used to crosslink alginate physically via the electrostatic interaction between hydrazide groups and carboxyl groups. It was then shaped and transferred in situ to a chemically crosslinked gel via 450 nm light irradiation. Under the irradiation, the molecular conformation change of azobenzene in the linker was able to form covalent bonds at the crosslinking points of the gels. Furthermore, the reversible conformation transformation of azobenzene was able to induce the increase and decrease of the storage modulus under irradiation with 365 nm light and 450 nm light, respectively, while also providing gel-like mechanical properties, depending upon the irradiation time and given wavelength. Meanwhile, the results also indicated that active groups could contribute to the splicing ability of the gel and construct a hollow cavity structure. It is believed that this work could provide a versatile strategy for preparing photo-responsive gels with reversibly tunable mechanical properties.


2019 ◽  
Vol 7 (15) ◽  
pp. 2463-2473 ◽  
Author(s):  
Fenbo Ma ◽  
Yongmei Ge ◽  
Nian Liu ◽  
Xiangchao Pang ◽  
Xingyu Shen ◽  
...  

A composite hydrogel with tunable mechanical properties has been fabricated and characterized in this study.


Biomaterials ◽  
2010 ◽  
Vol 31 (14) ◽  
pp. 3930-3940 ◽  
Author(s):  
Stephanie K. Seidlits ◽  
Zin Z. Khaing ◽  
Rebecca R. Petersen ◽  
Jonathan D. Nickels ◽  
Jennifer E. Vanscoy ◽  
...  

2003 ◽  
Vol 778 ◽  
Author(s):  
Rajdip Bandyopadhyaya ◽  
Weizhi Rong ◽  
Yong J. Suh ◽  
Sheldon K. Friedlander

AbstractCarbon black in the form of nanoparticle chains is used as a reinforcing filler in elastomers. However, the dynamics of the filler particles under tension and their role in the improvement of the mechanical properties of rubber are not well understood. We have studied experimentally the dynamics of isolated nanoparticle chain aggregates (NCAs) of carbon made by laser ablation, and also that of carbon black embedded in a polymer film. In situ studies of stretching and contraction of such chains in the transmission electron microscope (TEM) were conducted under different maximum values of strain. Stretching causes initially folded NCA to reorganize into a straight, taut configuration. Further stretching leads to either plastic deformation and breakage (at 37.4% strain) or to a partial elastic behavior of the chain at small strains (e.g. 2.3% strain). For all cases the chains were very flexible under tension. Similar reorientation and stretching was observed for carbon black chains embedded in a polymer film. Such flexible and elastic nature of NCAs point towards a possible mechanism of reinforcement of rubber by carbon black fillers.


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