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  4. Selective Adsorption of Proteins on Single-Wall Carbon Nanotubes by Using a Protective Surfactant
 
research article

Selective Adsorption of Proteins on Single-Wall Carbon Nanotubes by Using a Protective Surfactant

Knyazev, Anton  
•
Louise, Loic
•
Veber, Michele
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2011
Chemistry - A European Journal

The dispersion of highly hydrophobic carbon materials such as carbon nanotubes in biological media is a challenging issue. Indeed, the nonspecific adsorption of proteins occurs readily when the nanotubes are introduced in biological media; therefore, a methodology to control adsorption is in high demand. To address this issue, we developed a bifunctional linker derived from pyrene that selectively ena-bles or prevents the adsorption of proteins on single-wall carbon nanotubes (SWNTs). We demonstrated that it is possible to decrease or completely suppress the adsorption of proteins on the nanotube sidewall by using proper functionalization (either covalent or noncovalent). By subsequently activating the functional groups on the nanotube derivatives, protein adsorption can be recovered and, therefore, controlled. Our approach is simple, straightforward, and potentially suitable for other biomolecules that contain thio or amino groups available for coupling.

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Type
research article
DOI
10.1002/chem.201101182
Web of Science ID

WOS:000298542300037

Author(s)
Knyazev, Anton  
Louise, Loic
Veber, Michele
Langevin, Dominique
Filoramo, Arianna
Prina-Mello, Adriele
Campidelli, Stephane
Date Issued

2011

Published in
Chemistry - A European Journal
Volume

17

Start page

14663

End page

14671

Subjects

adsorption

•

carbon nanotubes

•

proteins

•

scanning probe microscopy

•

Noncovalent Sidewall-Functionalization

•

Diimide-Activated Amidation

•

Human Macrophage Cells

•

In-Vitro

•

Water

•

Mice

•

Immobilization

•

Cytotoxicity

•

Toxicology

•

Biosensors

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LPMC  
Available on Infoscience
June 25, 2012
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/82196
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