TY - JOUR
T1 - Flow-injection electrochemical immunosensor for the detection of human IgG based on glucose oxidase-derivated biomimetic interface
AU - Tang, Dianping
AU - Niessner, Reinhard
AU - Knopp, Dietmar
N1 - Funding Information:
This project was supported by (i) the Alexander von Humboldt-Foundation, Germany, and (ii) the Postgraduate Science and Technology Innovation Program, and Foundation of Excellent Ph.D. Dissertation of SWU (grant no. 200602), China to Dr. Tang.
PY - 2009/3/15
Y1 - 2009/3/15
N2 - A newly flow-through electrochemical immunosensor for monitoring IgG in human serum has been developed by using core-shell SiO2/Au nanocomposites and poly(amidoamine) G4 dendrimer as matrices. The ferrocenecarboaldehyde-labeled anti-IgG biomolecules were initially chemisorbed onto the nanoparticle surface, and then glucose oxidase (GOx), as a blocking reagent instead of bovine serum albumin (BSA), was backfilled onto the modified surface. The formation of the antibody-antigen complex by a simple one-step immunoreaction between the immobilized anti-IgG and IgG in sample solution introduced a barrier of direct electrical communication between the immobilized GOx and the base surface, and decreased the immobilized GOx toward the catalytic oxidation of glucose. The performance and factors influencing the performance of the immunosensor were evaluated. Under optimal conditions, the linear range of the developed immunosensor by using GOx as enhancer was from 5.0 × 10-6 to 9.6 × 10-4 mol/L with a detection limit of 8.0 × 10-7 mol/L IgG (at 3δ), while the detection limit by using BSA was 1.5 × 10-5 mol/L IgG (at 3δ) with the linear range from 3.5 × 10-5 to 1.2 × 10-3 mol/L. The selectivity, reproducibility and stability of the proposed immunosensor were acceptable. The IgG contents in 37 human serum samples obtained by the proposed method are identical with the data of clinical laboratory.
AB - A newly flow-through electrochemical immunosensor for monitoring IgG in human serum has been developed by using core-shell SiO2/Au nanocomposites and poly(amidoamine) G4 dendrimer as matrices. The ferrocenecarboaldehyde-labeled anti-IgG biomolecules were initially chemisorbed onto the nanoparticle surface, and then glucose oxidase (GOx), as a blocking reagent instead of bovine serum albumin (BSA), was backfilled onto the modified surface. The formation of the antibody-antigen complex by a simple one-step immunoreaction between the immobilized anti-IgG and IgG in sample solution introduced a barrier of direct electrical communication between the immobilized GOx and the base surface, and decreased the immobilized GOx toward the catalytic oxidation of glucose. The performance and factors influencing the performance of the immunosensor were evaluated. Under optimal conditions, the linear range of the developed immunosensor by using GOx as enhancer was from 5.0 × 10-6 to 9.6 × 10-4 mol/L with a detection limit of 8.0 × 10-7 mol/L IgG (at 3δ), while the detection limit by using BSA was 1.5 × 10-5 mol/L IgG (at 3δ) with the linear range from 3.5 × 10-5 to 1.2 × 10-3 mol/L. The selectivity, reproducibility and stability of the proposed immunosensor were acceptable. The IgG contents in 37 human serum samples obtained by the proposed method are identical with the data of clinical laboratory.
KW - Biomimetic interface
KW - Bovine serum albumin
KW - Electrochemical immunosensor
KW - Glucose oxidase
KW - Human IgG
UR - http://www.scopus.com/inward/record.url?scp=60349113398&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2008.11.008
DO - 10.1016/j.bios.2008.11.008
M3 - Article
C2 - 19109003
AN - SCOPUS:60349113398
SN - 0956-5663
VL - 24
SP - 2125
EP - 2130
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
IS - 7
ER -