Biology Reference
In-Depth Information
Table 4.5. Label-free electrochemical impedance and conductimetric
genosensors
Modified Electrode
Detection
Analyte
Substrate
Technique
Detection Limit Reference
×
10 11 M72
DNA PAT transgene
GCE
EIS
2.4
10 12 M
Synthetic DNA strains
GCE
EIS
73
Synthetic DNA strands
SNFETs
Conductance
100 fM
71
10 14 M
×
Synthetic DNA strands
SiO 2
Conductance
5
68
10 13 M21
PAT gene sequence
GCE
EIS
3.1
×
Thrombin
AuE
EIS
0.02 nM
70
Synthetic DNA strands
Quartzcrystal
Conductance
5.0 fmol
74
Synthetic DNA strands
Pt
Conductance
25 pmol
75
2.3 × 10 13 M76
CaMV35S gene fragment
CPE
EIS
6.7 × 10 13 M15
Synthetic DNA strands
AuE
EIS
5.6 × 10 13
PAT gene sequence
CPE
EIS
69
CaMV35S: 35S promoter from cauliflower mosaic virus; CPE: carbon paste electrode; EIS:
electrochemical impedance spectroscopy; GCE: glassy carbon electrode; PAT: phosphinothricin
acetyltransferase; SNFETs: field-effect transistors based on single-walled carbon nanotube
networks.
between the wanted signal augmentation and the reproducibility of
the assays [27]. Furthermore, strategies involving enlargement of
Au-NPshavebeenemployedaswelltoenhancetheelectroanalytical
signalmonitoringDNA hybridizationevents.
Silver enhancement is based on the reduction of silver ions from
one solution (usually the enhancer) by another (the initiator) in
the presence of Au-NPs [77]. The reduction reaction causes silver
to build up preferentially on the surface of the Au-NPs, giving rise
to a core-shell structure. An illustrative example is the work from
Bonanni et al. [78].Theyusedstreptavidin-coatedAu-NPsandsilver
enhancement kits to amplify the impedimetric signal generated in
a biosensor detecting the DNA hybridization event. The scheme
displaying the sensor preparation procedure is shown in Fig. 4.13.
A good reproducibility was achieved (RSD lower than 8.5%), the
detection limitbeing 11.8 pmol.
The same group discussed recently described impedimetric
detection methods for double-tagged DNA from PCR amplification
of Salmonella spp.[77].Oneofthesemethodsinvolvedamplification
of the impedimetric signal by using a monoclonal IgG1kappa anti-
 
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