Surface Patterning of Carbon Nanotubes Can Enhance Their Penetration through a Phospholipid Bilayer
Source abstract
Abstract
Nanotube patterning may occur naturally upon the spontaneous self-assembly of biomolecules onto the surface of single-walled carbon nanotubes (SWNTs). It results in periodically alternating bands of surface properties, ranging from relatively hydrophilic to hydrophobic, along the axis of the nanotube. Single-chain mean field (SCMF) theory has been used to estimate the free energy of systems in which a surface patterned nanotube penetrates a phospholipid bilayer. In contrast to unpatterned nanotubes with uniform surface properties, certain patterned nanotubes have been identified that display a relatively low and approximately constant system free energy (<±10 kT) as the nanotube traverses through the bilayer. These observations support the hypothesis that the spontaneous self-assembly of biomolecules on the surface of SWNTs may facilitate nanotube transduction through cell membranes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanopore and Nanochannel Transport Studies · Carbon Nanotubes in Composites · Lipid Membrane Structure and Behavior
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Departament d’Enginyeria Quimica, Universitat Rovira i Virgili, 26 Av. dels Paisos Catalans, 43007 Tarragona, Spain
Department of Chemical Engineering and Biotechnology, University of Cambridge, Pembroke Street, Cambridge CB2 3RA, United Kingdom
ICREA, 23 Passeig Lluis Companys, 08010 Barcelona, Spain
References (31)
Show source-provided references
1. Cheng C. · Biomaterials · 2009 · 30 · 415210.1016/j.biomaterials.2009.04.019 ↗
2. Davoren M. · Toxicol. in Vitro · 2007 · 21 · 43810.1016/j.tiv.2006.10.007 ↗
3. Liu J. · Chem. Res. Toxicol. · 2008 · 21 · 45910.1021/tx700392b ↗
4. Smart S. · Carbon · 2006 · 44 · 103410.1016/j.carbon.2005.10.011 ↗
5. Kam N. W. S. · J. Am. Chem. Soc. · 2005 · 127 · 602110.1021/ja050062v ↗
6. Kam N. W. S. · Angew. Chem., Int. Ed. · 2006 · 45 · 57710.1002/anie.200503389 ↗
7. Pantarotto D. · Chem. Commun. · 2004 · 1 · 1610.1039/b311254c ↗
8. Pantarotto D. · Angew. Chem., Int. Ed. · 2004 · 43 · 524210.1002/anie.200460437 ↗
9. Klumpp C. · Biochim. Biophys. Acta · 2006 · 1758 · 40410.1016/j.bbamem.2005.10.008 ↗
10. Liu Q. · Nano Lett. · 2009 · 9 · 100710.1021/nl803083u ↗
11. Balasubramanian K. · Anal. Bioanal. Chem. · 2006 · 385 · 45210.1007/s00216-006-0314-8 ↗
12. Kouklin N. A. · Appl. Phys. Lett. · 2005 · 87 · 17390110.1063/1.2112183 ↗
13. Pogodin S. · ACS Nano · 2010 · 4 · 529310.1021/nn1016549 ↗
14. Pogodin S. · Soft Matter · 2010 · 6 · 221610.1039/b927437e ↗
15. Chattopadhyay J. · Chem. Mater. · 2006 · 18 · 586410.1021/cm0611082 ↗
16. Porter A. E. · Nat. Nanotechnol. · 2007 · 2 · 71310.1038/nnano.2007.347 ↗
17. Porter A. E. · ACS Nano · 2009 · 3 · 148510.1021/nn900416z ↗
18. Richard C. · Science · 2003 · 300 · 77510.1126/science.1080848 ↗
19. Thauvin C. · Nat. Nanotechnol. · 2008 · 3 · 74310.1038/nnano.2008.318 ↗
20. Gigliotti B. · Nano Lett. · 2006 · 6 · 15910.1021/nl0518775 ↗
21. Tu X. · Nature · 2009 · 460 · 25010.1038/nature08116 ↗
22. Campbell J. F. · J. Am. Chem. Soc. · 2008 · 130 · 1064810.1021/ja801720c ↗
23. Zhang X. · ACS Nano · 2009 · 3 · 320010.1021/nn9006362 ↗
24. Numata M. · J. Am. Chem. Soc. · 2005 · 127 · 587510.1021/ja044168m ↗
25. Dieckmann G. R. · J. Am. Chem. Soc. · 2003 · 125 · 177010.1021/ja029084x ↗
26. Dalton A. B. · Adv. Funct. Mater. · 2004 · 14 · 114710.1002/adfm.200400190 ↗
27. Zorbas V. · J. Am. Chem. Soc. · 2004 · 126 · 722210.1021/ja049202b ↗
28. Ju S.-Y. · Nat. Nanotechnol. · 2008 · 3 · 35610.1038/nnano.2008.148 ↗
29. Vernizzi G. · Soft Matter · 2009 · 5 · 73610.1039/b814583k ↗
30. Verma A. · Nat. Mater. · 2008 · 7 · 58810.1038/nmat2202 ↗
31. Yang K. · Nat. Nanotechnol. · 2010 · 5 · 57910.1038/nnano.2010.141 ↗