Efficient cancer cell capturing SiNWAs prepared via surface-initiated SET-LRP and click chemistry

2015 ◽  
Vol 6 (19) ◽  
pp. 3708-3715 ◽  
Author(s):  
Lulu Xue ◽  
Zhonglin Lyu ◽  
Yafei Luan ◽  
Xinhong Xiong ◽  
Jingjing Pan ◽  
...  

Enhanced specific cancer cell capturing effect generated by combining a glycopolymer and aptamer through SI-SET-LRP and click chemistry.

2016 ◽  
Vol 8 (40) ◽  
pp. 27360-27367 ◽  
Author(s):  
Qing Bian ◽  
Wenshuo Wang ◽  
Shutao Wang ◽  
Guojie Wang

RSC Advances ◽  
2015 ◽  
Vol 5 (46) ◽  
pp. 36837-36844 ◽  
Author(s):  
Yan Zhang ◽  
Kaiwen Chang ◽  
Bin Xu ◽  
Jinlong Chen ◽  
Lulin Yan ◽  
...  

Near-infrared emissive organic dots with a high fluorescence quantum efficiency (AEE dots) are prepared by using an amphiphilic polymer PSMA and a novel small molecule fluorogen (DPPBPA).


2016 ◽  
Vol 11 (12) ◽  
pp. 1934578X1601101 ◽  
Author(s):  
Doan Duy Tien ◽  
Le Nhat Thuy Giang ◽  
Dang Thi Tuyet Anh ◽  
Nguyen Tien Dung ◽  
Thanh Nguyen Ha ◽  
...  

Dihydroartemisinin was converted to its corresponding alkyne-functionalized esters, which were subsequently deployed as substrates for a ‘click’ chemistry-mediated coupling with 3′-azido-3′-deoxythydimine (AZT) to furnish novel triazole–artesunate–AZT hybrid compounds. Moreover, various substituted triazole–artemisinin hybrids were synthesized based on ‘click’ chemistry between propargyl-substituted derivatives and artemisinin containing a 2-hydroxypropane unit. Fourteen new hybrids were thus successfully prepared and evaluated as cytotoxic agents, revealing an interesting anticancer activity of four triazole–artemisinin derivative hybrids in KB and HepG2 cancer cell lines.


2017 ◽  
Vol 41 (12) ◽  
pp. 696-698 ◽  
Author(s):  
Xiao-Hua Ma ◽  
Nan Liu ◽  
Jing-Li Lu ◽  
Jie Zhao ◽  
Xiao-Jian Zhang

A series of seven novel 1-aryl-1,2,3-triazole derivatives bearing a 4-(phenothiazin-10-ylmethyl) moiety were designed using a molecular hybridisation approach and synthesised by alkyne/azide click chemistry. Most of the synthesised compounds exhibited moderate to good antiproliferative activity (IC50 values: 0.5 to 6.7 μM) against stomach, oesophagus, prostate, breast and liver cancer cell lines, but a compound containing a 4-chlorophenyl moiety showed better activity against all cell lines than 5-fluorouracil.


2011 ◽  
Vol 226 (3) ◽  
pp. 482-494 ◽  
Author(s):  
Alvin J. X. Lee ◽  
Rebecca Roylance ◽  
Jil Sander ◽  
Patricia Gorman ◽  
David Endesfelder ◽  
...  

2021 ◽  
Author(s):  
Yuting Wen ◽  
Nana Nyarko Mensah ◽  
Xia Song ◽  
Jingling Zhu ◽  
Wui Siew Tan ◽  
...  

A hydrogel scaffold with non-fouling but specific cancer cell adhesive surface was fabricated through surface modification using β-cyclodextrin-based host-guest chemistry. Interestingly, the hydrogel surface not only selectively captured specific cancer...


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