Carbon Nanotubes Decorated with Cationic Carbosilane Dendrons and Their Hybrids with Nucleic Acids
Source abstract
Abstract
Abstract The first example of non‐covalent functionalization of single‐ and multi‐walled carbon nanotubes (CNTs) with cationic carbosilane dendrons via pyrene anchor groups is reported herein. The non‐covalent functionalization of the CNT surface with dendrons is compatible with the covalent functionalization of CNT tips and defect sites with amino‐compounds. The modified CNTs have been shown to bind therapeutic oligonucleotides efficiently. The results obtained may provide useful insight for the design of multifunctional nanocarriers for nucleic acid delivery.
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Research context
OpenAlex topics: Carbon Nanotubes in Composites · Nanopore and Nanochannel Transport Studies · RNA Interference and Gene Delivery
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Departamento de Química Orgánica y Química Inorgánica Universidad de Alcalá, Campus Universitario, Edificio de Farmacia 28871 Alcalá de Henares Spain
Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) Madrid Spain
Institute of Chemical Biology and Fundamental Medicine SB RAS 8, Lavrentiev ave. 630090 Novosibirsk Russia
Funding
MINECO · 7th European Community Framework Program · Russian State · Scholarship of the President of the Russian Federation
References (47)
Show source-provided references
1. 10.1016/j.mattod.2014.07.00910.1016/j.mattod.2014.07.009 ↗
2. Vardharajula S. · Int. J. Nanomed. · 2012 · 2012 · 5361
3. Apartsin E. K. · 33
4. Apartsin E. K. · Genes and Cells · 2016 · 11 · 3210.23868/gc120566 ↗
5. 10.1093/nar/gkw23610.1093/nar/gkw236 ↗
6. 10.1039/c0py00356e10.1039/c0py00356e ↗
7. 10.1021/cr050569o10.1021/cr050569o ↗
8. 10.1016/j.nano.2009.07.00310.1016/j.nano.2009.07.003 ↗
9. 10.1016/j.tox.2010.01.00510.1016/j.tox.2010.01.005 ↗
10. 10.1016/j.colsurfb.2010.05.02310.1016/j.colsurfb.2010.05.023 ↗
11. 10.1016/j.nano.2016.02.01710.1016/j.nano.2016.02.017 ↗
12. 10.1002/smll.20130026410.1002/smll.201300264 ↗
13. 10.1088/1468-6996/16/2/02480210.1088/1468-6996/16/2/024802 ↗
14. 10.1021/bc900296z10.1021/bc900296z ↗
15. 10.1021/jp805424f10.1021/jp805424f ↗
16. Gavrel G. · 95
17. 10.1039/C7RA04933A10.1039/C7RA04933A ↗
18. 10.1021/ja062497410.1021/ja0624974 ↗
19. 10.1002/adfm.20120078410.1002/adfm.201200784 ↗
20. 10.1517/17425247.2015.100430910.1517/17425247.2015.1004309 ↗
21. 10.1016/j.jconrel.2014.02.02110.1016/j.jconrel.2014.02.021 ↗
22. 10.3390/ma502027810.3390/ma5020278 ↗
23. 10.1016/j.bbamem.2005.10.00810.1016/j.bbamem.2005.10.008 ↗
24. 10.1016/j.carbon.2010.12.06410.1016/j.carbon.2010.12.064 ↗
25. D. A. Tomalia J. B. Christensen U. Boas Dendrimers Dendrons and Dendritic Polymers 2012.10.1017/CBO9781139048859 ↗
26. 10.1039/C3RA45408H10.1039/C3RA45408H ↗
27. 10.1039/c4ob00162a10.1039/c4ob00162a ↗
28. 10.1016/j.jconrel.2014.12.04210.1016/j.jconrel.2014.12.042 ↗
29. 10.1016/j.jconrel.2008.07.03510.1016/j.jconrel.2008.07.035 ↗
30. 10.1016/j.ijpharm.2015.03.02410.1016/j.ijpharm.2015.03.024 ↗
31. 10.1016/j.ijpharm.2015.03.03410.1016/j.ijpharm.2015.03.034 ↗
32. 10.1021/om500464k10.1021/om500464k ↗
33. 10.1021/om301217g10.1021/om301217g ↗
34. 10.1016/j.tet.2010.09.06310.1016/j.tet.2010.09.063 ↗
35. Gutierrez-Ulloa C. E. · Org. Biomol. Chem. · 2017 · 10
36. 10.1016/j.jconrel.2015.06.00210.1016/j.jconrel.2015.06.002 ↗
37. 10.1002/chem.20150196610.1002/chem.201501966 ↗
38. 10.1002/chem.20150426210.1002/chem.201504262 ↗
39. 10.1021/am403472910.1021/am4034729 ↗
40. 10.1134/S199507801202002410.1134/S1995078012020024 ↗
41. 10.1039/c2nr30346a10.1039/c2nr30346a ↗
42. 10.1166/jnn.2007.41210.1166/jnn.2007.412 ↗
43. Wu W. · Water Res. · 2016 · 88 · 49210.1016/j.watres.2015.10.037 ↗
44. 10.1016/S0008-6223(00)00155-X10.1016/S0008-6223(00)00155-X ↗
45. 10.1021/ja903316z10.1021/ja903316z ↗
46. 10.1158/1541-7786.MCR-07-008010.1158/1541-7786.MCR-07-0080 ↗
47. 10.1016/0003-2697(81)90704-110.1016/0003-2697(81)90704-1 ↗