4.6 Review

Molecularly imprinted polymer-based electrochemical sensors for biopolymers

Journal

CURRENT OPINION IN ELECTROCHEMISTRY
Volume 14, Issue -, Pages 53-59

Publisher

ELSEVIER
DOI: 10.1016/j.coelec.2018.12.005

Keywords

Electropolymerization; Direct electron transfer; Redox marker; Epitope imprinting; Biomarker

Funding

  1. Deutsche Forschungsgemeinschaft (DFG, Germany) [EXC 314]
  2. ERA-Chemistry 2014 [61133]
  3. NKFIH OTKA (Hungary) [NN117637]
  4. BME-Nanotechnology (Hungary) FIKP grant of EMMI (BME FIKP-NAT)

Ask authors/readers for more resources

Electrochemical synthesis and signal generation dominate among the almost 1200 articles published annually on protein-imprinted polymers. Such polymers can be easily prepared directly on the electrode surface, and the polymer thickness can be precisely adjusted to the size of the target to enable its free exchange. In this architecture, the molecularly imprinted polymer (MIP) layer represents only one 'separation plate'; thus, the selectivity does not reach the values of 'bulk' measurements. The binding of target proteins can be detected straightforwardly by their modulating effect on the diffusional permeability of a redox marker through the thin MIP films. However, this generates an 'overall apparent' signal, which may include nonspecific interactions in the polymer layer and at the electrode surface. Certain targets, such as enzymes or redox active proteins, enables a more specific direct quantification of their binding to MIPs by in situ determination of the enzyme activity or direct electron transfer, respectively.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available