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Enzyme integrated silicate-Pt nanoparticle architecture: A versatile biosensing platform
被引:29
作者:
Jena, Bikash Kumar
[1
]
Raj, C. Retna
[1
]
机构:
[1] Indian Inst Technol, Dept Chem, Kharagpur 721302, W Bengal, India
关键词:
Nanoarchitecture;
Biosensor;
Pt nanoparticles;
Hydrogen peroxide;
Uric acid;
Cholesterol;
GLASSY-CARBON ELECTRODE;
HYDROGEN-PEROXIDE;
GOLD NANOPARTICLES;
ELECTROCHEMICAL OXIDATION;
PLATINUM NANOPARTICLES;
VOLTAMMETRIC DETECTION;
GLUCOSE-OXIDASE;
COMPOSITE FILM;
H2O2;
ARRAYS;
D O I:
10.1016/j.bios.2010.11.046
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
A novel 3-D nanoarchitectured platform based on Pt nanoparticles (nPts) is developed for the sensing of sub-nanomolar levels of hydrogen peroxide and for the fabrication of amperometric biosensor for uric acid, cholesterol and glucose. The nPts have been immobilized on the thiol functional group containing sol-gel silicate 3-0 network derived from 3-mercaptopropyltrimethoxysilane (MPTS). The nanoparticles on the 3-0 architecture have size distribution between 7 and 10 nm. The nPts on the platform efficiently catalyze the oxidation of H2O2 at the potential of +0.45 V in the absence of enzymes and redox mediators. This nanoarchitectured platform is highly sensitive and can detect H2O2 at sub-nanomolar levels (0.1 nM) in neutral solution. The nanoarchitectured platform does not suffer from interference due to other common easily oxidizable interfering agents. Excellent reproducibility, long-term storage and operational stability are observed. This platform is used to determine H2O2 concentration in rainwater and for the fabrication of biosensors. Amperometric oxidase-based biosensing platforms are developed by integrating the enzymes and nPts with the silicate network for the sensing of uric acid cholesterol and glucose. The enzyme encapsulated 3-D architecture retains the enzymatic activity and efficiently detects enzymatically generated H2O2 without any interference. These biosensors are stable and show excellent sensitivity and fast response time. A linear response was obtained for a wide concentration range of all analytes. The practical utilization of the biosensor for the measurement of uric acid, cholesterol and glucose in serum sample is demonstrated. The biological sample analysis was validated with clinical laboratory measurements. (C) 2010 Elsevier B.V. All rights reserved.
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页码:2960 / 2966
页数:7
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