Title of article :
Amperometric biosensors for NADH based on hyperbranched dendritic ferrocene polymers and Pt nanoparticles
Author/Authors :
Jiménez، نويسنده , , Almudena and Armada، نويسنده , , M. Pilar Garcيa and Losada، نويسنده , , José F. Villena، نويسنده , , Carlos and Alonso، نويسنده , , Beatriz and Casado، نويسنده , , Carmen M.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
9
From page :
111
To page :
119
Abstract :
The electrocatalytic performance of electrodes modified with Pt nanoparticles (PtNPs) and two dendritic hyperbranched carbosilane polymers, polydiallylmethylsilane (PDAMS) and polymethyldiundecenylsilane (PMDUS) with interacting ferrocenes, has been investigated for the NADH oxidation. The catalytic synergy of PtNPs with the interacting ferrocenes is discussed in relation with the polymer structure. This effect have allowed us to develop efficient biosensors capable of measuring NADH from +0.3 V (vs. SCE) providing a total protection vs. the poisoning of the electrodes. The polymer/PtNPs/Pt electrodes tolerate wide linear concentration ranges for NADH to 2.5 mM (R = 0.9979) and 2.1 mM (R = 0.99849), with detection limits of 4.78 μM and 6.18 μM and sensitivities of 68.24 and 40.21 μA mM−1 cm−2 for the PDAMS/PtNPs/Pt and PMDUS/PtNPs/Pt respectively. In the light of the good results obtained, novel amperometric alcohol biosensors were also successfully prepared with alcohol dehydrogenase (ADH). These devices showed more affinity for methanol than for ethanol, with a wide linear range to 30 mM and sensitivities of 0.957 and 0.756 μA mM−1 cm−2 for the ADH/PDAMS/PtNPs/Pt and ADH/PMDUS/PtNPs/Pt respectively. The oxidation potential of the NADH enzymatically produced was negatively shifted to +0.25 V.
Keywords :
Interacting ferrocenes , alcohol dehydrogenase , electrochemical biosensor , NADH , Pt nanoparticles , Bioelectrocatalysis
Journal title :
Sensors and Actuators B: Chemical
Serial Year :
2014
Journal title :
Sensors and Actuators B: Chemical
Record number :
1441764
Link To Document :
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