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Novel I–V Disposable Urea Biosensor Based on a Dip‐coated Hierarchical Magnetic Nanocomposite (Fe 3 O 4 @SiO 2 @NH 2 ) on SnO 2 :F Layer
Author(s) -
Mikani Mohaddeseh,
Rahmanian Reza,
Karimnia Matin,
Sadeghi Ali
Publication year - 2017
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.201700256
Subject(s) - nanocomposite , biosensor , chemistry , glutaraldehyde , urea , substrate (aquarium) , urease , fourier transform infrared spectroscopy , nuclear chemistry , covalent bond , silicon dioxide , nanotechnology , inorganic chemistry , magnetic nanoparticles , chemical engineering , analytical chemistry (journal) , nanoparticle , organic chemistry , materials science , biochemistry , oceanography , geology , engineering
Silicon oxide was initially loaded on a Fe 3 O 4 magnetic nanoparticle substrate (Fe 3 O 4 @SiO 2 ) and then functionalized with ─NH 2 group (Fe 3 O 4 @SiO 2 @NH 2 ) to construct a novel hierarchical magnetic nanocomposite. A sensitive urea biosensor medium involving a dip‐coated hierarchical magnetic nanocomposite on F‐doped SnO 2 conducting glass was designed (Fe 3 O 4 @SiO 2 @NH 2 /SnO 2 :F) to achieve an excellent platform for urease (Urs) enzyme immobilization via covalent linking to the exposed NH 2 groups through glutaraldehyde (Urs/Fe 3 O 4 @SiO 2 @NH 2 /SnO 2 :F). The hierarchical magnetic nanocomposite selection criteria were based on enhancement of urea biosensing by Urs immobilization via covalent linking to the exposed NH 2 groups, while the SnO 2 :F selection as substrate was based on its ability to afford high electronic density to the biosensor surface as an electrostatic repulsion layer for the anionic interferents in the biological environment. FE‐SEM, TEM, FTIR, CV, EIS, and I–V techniques established the morphology of the modified electrode's surface and electrochemical behavior of urea on the fabricated Urs/Fe 3 O 4 @SiO 2 @NH 2 /SnO 2 :F biosensor. The sensing mechanism can be clarified on the basis of the two reactions, namely (1) catalytic reaction and (2) oxidation or reduction of metal oxides, same as in the case of solid‐state gas sensors. The I–V results display high sensitivity for urea detection of within 5–210 mg/dL and a limit of detection of 3 mg/dL.

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