Impedimetric immunosensor for the specific label free detection of ciprofloxacin antibiotic

2007 ◽  
Vol 23 (4) ◽  
pp. 549-555 ◽  
Author(s):  
Rodica E. Ionescu ◽  
Nicole Jaffrezic-Renault ◽  
Laurent Bouffier ◽  
Chantal Gondran ◽  
Serge Cosnier ◽  
...  
2010 ◽  
Vol 25 (11) ◽  
pp. 2447-2453 ◽  
Author(s):  
Guo-Jun Zhang ◽  
Zhan Hong Henry Luo ◽  
Min Joon Huang ◽  
Guang Kai Ignatius Tay ◽  
Eu-Jin Andy Lim

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
JingJing Fu ◽  
ZhuanZhuan Shi ◽  
Man Li ◽  
Yangyang Wang ◽  
Ling Yu

The chondroitin sulphate proteoglycan 4 (CSPG4), also known as high molecular weight-melanoma associated antigen (HMW-MAA), is a tumor-associated antigen that is expressed in more than 85% of surgically removed melanoma lesions but has restricted distribution in normal tissues. The diagnostic and therapeutic value of CSPG4 drives a need for sensitive and low-cost detection approaches. To this end, we developed a polyaniline/graphene oxide nanocomposite (PANI@GO) that was electrochemically codeposited on indium tin oxide (ITO) electrode. Glutaraldehyde mediated the covalent immobilization of CSPG4 specific antibody mAbD2.8.5 to construct a CSPG4 immunosensor using cell culture media and cell lysate as samples. The fully assembled impedimetric immunosensor was used to detect CSPG4 in CSPG4-positive cell lines M14/CSPG4 and MV3. No impedance signal changes could be observed from CSPG4-negative cell lines M14 and mAbMk2-23 showing the specificity of the CSPG4-impedimetric immunosensor. This low-cost, simple, and label-free analytical method is an alternative to enzyme-linked immunosorbent assay and flow cytometry in screening of CSPG4 in complex biological samples.


2009 ◽  
Vol 2009 ◽  
pp. 1-12 ◽  
Author(s):  
Imen Hafaid ◽  
Asma Gallouz ◽  
Walid Mohamed Hassen ◽  
Adnane Abdelghani ◽  
Zina Sassi ◽  
...  

This work has explored the development of impedimetric immunosensors based on magnetic iron nanoparticles (IrNP) functionalized with streptavidin to which a biotinylated FAB part of the antibody has been bound using a biotin-streptavidin interaction. SPR analysis shows a deviation on the measured (angle) during antigen-antibody recognition whereas label free detection using by EIS allows us to monitor variation of polarization resistance. Before detection, layers were analyzed by FTIR and AFM. Compared to immobilization of antibody on bare gold surface using aminodecanethiol SAM, antibody immobilization on nanoparticles permitted to reach lower detection limit: 500 pg/ml instead of 1 ng/ml to in the case of EIS and 300 ng/ml instead of 4.5 μg/ml in the case of SPR. Thus, it permitted to improve the sensitivity: from 257.3 Ω⋅cm2⋅μg−1⋅mlto 1871 Ω⋅cm2⋅μg−1⋅mlin the case of EIS and from0.003°μg−1⋅mlto0.094°μg−1⋅mlin the case of SPR.


2007 ◽  
Vol 22 (11) ◽  
pp. 2464-2470 ◽  
Author(s):  
Md. Aminur Rahman ◽  
Muhammad J.A. Shiddiky ◽  
Jang-Su Park ◽  
Yoon-Bo Shim

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