TY - JOUR
T1 - Development of a real-time capacitive biosensor for cyclic cyanotoxic peptides based on Adda-specific antibodies.
AU - Lebogang, Lesedi
AU - Hedström, Martin
AU - Mattiasson, Bo
PY - 2014
Y1 - 2014
N2 - The harmful effects of cyanotoxins in surface waters have led to increasing demands for accurate early warning methods. This study proposes a capacitive immunosensor for broad-spectrum detection of the group of toxic cyclic peptides called microcystins (∼80 congeners) at very low concentration levels. The novel analytical platform offers significant advances compared to the existing methods. Monoclonal antibodies (mAbs, clone AD4G2) that recognize a common element of microcystins were used to construct the biosensing layer. Initially, a stable insulating anchor layer for the mAbs was made by electropolymerization of tyramine onto a gold electrode surface, with subsequent incorporation of gold nanoparticles (AuNPs) on the glutaraldehyde (5%) activated polytyramine surface. The biosensor responded linearly to microcystin concentrations from 1×10(-13)M to 1×10(-10)M MC-LR standard with a limit of detection of 2.1×10(-14)M. The stability of the biosensor was evaluated by repeated measurements of the antigen and by determining the capacitance change relative to the original response, which decreased below 90% after the 30th cycle.
AB - The harmful effects of cyanotoxins in surface waters have led to increasing demands for accurate early warning methods. This study proposes a capacitive immunosensor for broad-spectrum detection of the group of toxic cyclic peptides called microcystins (∼80 congeners) at very low concentration levels. The novel analytical platform offers significant advances compared to the existing methods. Monoclonal antibodies (mAbs, clone AD4G2) that recognize a common element of microcystins were used to construct the biosensing layer. Initially, a stable insulating anchor layer for the mAbs was made by electropolymerization of tyramine onto a gold electrode surface, with subsequent incorporation of gold nanoparticles (AuNPs) on the glutaraldehyde (5%) activated polytyramine surface. The biosensor responded linearly to microcystin concentrations from 1×10(-13)M to 1×10(-10)M MC-LR standard with a limit of detection of 2.1×10(-14)M. The stability of the biosensor was evaluated by repeated measurements of the antigen and by determining the capacitance change relative to the original response, which decreased below 90% after the 30th cycle.
U2 - 10.1016/j.aca.2014.03.028
DO - 10.1016/j.aca.2014.03.028
M3 - Article
C2 - 24793855
SN - 1873-4324
VL - 826
SP - 69
EP - 76
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
ER -