1999
DOI: 10.1016/s0927-7765(99)00004-1
|View full text |Cite
|
Sign up to set email alerts
|

The interaction of proteins and cells with self-assembled monolayers of alkanethiolates on gold and silver

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

7
365
1
1

Year Published

2000
2000
2013
2013

Publication Types

Select...
5
4
1

Relationship

0
10

Authors

Journals

citations
Cited by 447 publications
(374 citation statements)
references
References 167 publications
7
365
1
1
Order By: Relevance
“…Protein adsorption on a material is highly dependent upon the material's surface free energy and functionality (16,17,18). Numerous studies have been conducted to passivate material surfaces to cell and protein adhesion using simple hydrophobic and hydrophilic polymers and thin films.…”
Section: Introductionmentioning
confidence: 99%
“…Protein adsorption on a material is highly dependent upon the material's surface free energy and functionality (16,17,18). Numerous studies have been conducted to passivate material surfaces to cell and protein adhesion using simple hydrophobic and hydrophilic polymers and thin films.…”
Section: Introductionmentioning
confidence: 99%
“…A method often used to anchor macromolecular units, such as proteins or enzymes, onto a solid surface is the functionalization of a self-assembled monolayer (SAM) of alkanethiols [see, for example, refs [15][16][17][18][19][20][21][22][23][24][25][26][27]. The success of SAMs is due to the simplicity of the experimental procedure to prepare the films, their reproducibility, and the possibility of creating a wide range of surfaces via the incorporation of different groups at the end of the alkyl chains.…”
Section: Introductionmentioning
confidence: 99%
“…The ability to validate the exact spatial location of immobilised protein and the immobilised quantity thereof on a surface is important and techniques such as surface plasmon resonance [17,18], ellipsometry [19], optical waveguide lightmode spectroscopy [20], and quartz crystal microbalance [21] have been previously reported. These techniques quantitatively measure the amount of protein immobilised on flat, planar surfaces such as glass, gold, and plastic substrates, but these methods cannot easily be utilised for macroporous monolithic materials, because of the huge disparity between the surface area of a monolith compared with a flat surface.…”
Section: Introductionmentioning
confidence: 99%