TY - JOUR
T1 - Competitive capacitive biosensing technique (CCBT)
T2 - A novel technique for monitoring low molecular mass analytes using glucose assay as a model study
AU - Labib, Mahmoud
AU - Hedström, Martin
AU - Amin, Magdy
AU - Mattiasson, Bo
N1 - Funding Information:
Acknowledgment Ministry of Higher Education, Egypt is gratefully acknowledged for financial support to Mahmoud Labib during his study at the Department of Biotechnology, Lund University.
PY - 2010/6
Y1 - 2010/6
N2 - A novel technique for monitoring of low molecular mass analytes using a flow-injection capacitive biosensor is presented. The method is based on the ability of a small molecular mass analyte to displace a large analyte-carrier conjugate from the binding sites of an immobilized biorecognition element with weak affinity to both compounds. A model study was performed on glucose as the small molecular mass analyte. In the absence of glucose, binding of a glucose polymer or a glycoconjugate to concanavalin A results in a capacitance decrease. Upon introduction of glucose, it displaces a part of the bound glucose polymer or glycoconjugate leading to a partial restoration of capacitance. Experimental results show that the change in capacitance depends linearly on glucose concentration within the range from 1.0×10-5 to 1.0×10-1 M, corresponding to 1.8 μg ml-1 to 18 mg ml-1 in a logarithmic plot, with a detection limit of 1.0×10-6 (0.18 μg ml-1) under optimized conditions. In addition, by modifying the molecular mass of the glucose polymer, amount of biorecognition element, and buffer composition, we were able to tune the analyte-sensing range. The developed technique has the benefits of expanded dynamic range, high sensitivity, and excellent reusability.
AB - A novel technique for monitoring of low molecular mass analytes using a flow-injection capacitive biosensor is presented. The method is based on the ability of a small molecular mass analyte to displace a large analyte-carrier conjugate from the binding sites of an immobilized biorecognition element with weak affinity to both compounds. A model study was performed on glucose as the small molecular mass analyte. In the absence of glucose, binding of a glucose polymer or a glycoconjugate to concanavalin A results in a capacitance decrease. Upon introduction of glucose, it displaces a part of the bound glucose polymer or glycoconjugate leading to a partial restoration of capacitance. Experimental results show that the change in capacitance depends linearly on glucose concentration within the range from 1.0×10-5 to 1.0×10-1 M, corresponding to 1.8 μg ml-1 to 18 mg ml-1 in a logarithmic plot, with a detection limit of 1.0×10-6 (0.18 μg ml-1) under optimized conditions. In addition, by modifying the molecular mass of the glucose polymer, amount of biorecognition element, and buffer composition, we were able to tune the analyte-sensing range. The developed technique has the benefits of expanded dynamic range, high sensitivity, and excellent reusability.
KW - Biosensor
KW - Competitive capacitive
KW - Concanavalin A
KW - Flow-injection
KW - Glucose
KW - Glycoconjugate
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U2 - 10.1007/s00216-010-3641-8
DO - 10.1007/s00216-010-3641-8
M3 - Article
C2 - 20401723
AN - SCOPUS:77953477424
SN - 0016-1152
VL - 397
SP - 1217
EP - 1224
JO - Fresenius Zeitschrift fur Analytische Chemie
JF - Fresenius Zeitschrift fur Analytische Chemie
IS - 3
ER -