PVDF film tethered with RGD-click-poly(glycidyl methacrylate) brushes by combination of direct surface-initiated ATRP and click chemistry for improved cytocompatibility

RSC Advances ◽  
2014 ◽  
Vol 4 (1) ◽  
pp. 105-117 ◽  
Author(s):  
Fei He ◽  
Baiwen Luo ◽  
Shaojun Yuan ◽  
Bin Liang ◽  
Cleo Choong ◽  
...  
Polymer ◽  
2017 ◽  
Vol 111 ◽  
pp. 27-35 ◽  
Author(s):  
Massimiliano Mauri ◽  
Nina Tran ◽  
Oscar Prieto ◽  
Thomas Hjertberg ◽  
Christian Müller

2020 ◽  
Vol 11 (2) ◽  
pp. 298-303 ◽  
Author(s):  
David H. Howe ◽  
Ken J. Jenewein ◽  
James L. Hart ◽  
Mitra L. Taheri ◽  
Andrew J. D. Magenau

Polymer micelles were formed using thiol-epoxide “click” chemistry to trigger functionalization-induced self-assembly (FISA) of block copolymers by modifying a reactive glycidyl methacrylate block with solvophobes.


2016 ◽  
Vol 635 (1) ◽  
pp. 107-113 ◽  
Author(s):  
Yong Han Kim ◽  
Xuan Thang Cao ◽  
Seong-Soo Hong ◽  
Yeong Soon Gal ◽  
Kwon Taek Lim

Author(s):  
Yating Wang ◽  
Wenxiang Wang ◽  
Hou Chen ◽  
Liangjiu Bai ◽  
Hui Xu

A new approach for the preparation of polymer brush was developed via the union of controlled/“living” radical polymerization and click chemistry. The application of the approach realized the more quickly and accurate design and synthesis of the polymer brushes. A novel functional polymer brush of poly(acrylonitrile-g-glycidyl methacrylate) with tremendous application potential in the field of biology has been successfully synthesized via the new approach. The reaction conditions of click chemistry were optimized with the reaction time and the reactant ratio and judged from UV-vis spectra. Under the optimum of click chemistry, the novel functional polymer brushes were prepared. The GPC, FTIR analyses, 1H NMR spectrum and TGA were employed to ensure the successful synthesis of poly(acrylonitrile-g-glycidyl methacrylate) polymer brushes.


Author(s):  
Qinheng Zheng ◽  
Hongtao Xu ◽  
Hua Wang ◽  
Wen-Ge Han Du ◽  
Nan Wang ◽  
...  

The lack of simple, efficient [<sup>18</sup>F]fluorination processes and new target-specific organofluorine probes remains the major challenge of fluorine-18-based positron emission tomography (PET). We report here a fast isotopic exchange method for the radiosynthesis of aryl [<sup>18</sup>F]fluorosulfate based PET agents enabled by the emerging sulfur fluoride exchange (SuFEx) click chemistry. The method has been applied to the fully-automated <sup>18</sup>F-radiolabeling of twenty-five structurally diverse aryl fluorosulfates with excellent radiochemical yield (83–100%) and high molar activity (up to 281 GBq µmol<sup>–1</sup>) at room temperature in 30 seconds. The purification of radiotracers requires no time-consuming high-performance liquid chromatography (HPLC), but rather a simple cartridge filtration. The utility of aryl [<sup>18</sup>F]fluorosulfate is demonstrated by the <i>in vivo</i> tumor imaging by targeting poly(ADP-ribose) polymerase 1 (PARP1).


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