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A novel ternary NiFe2O4/CuO/FeO-chitosan nanocomposite as a cholesterol biosensor
Authors:Jay Singh  Manish Srivastava  Prasanta Kalita  Bansi D Malhotra
Institution:1. Department of BIN Fusion Technology and Department of Polymer-Nano Science and Technology, Chonbuk National University, Jeonju, Jeonbuk 561-756, Republic of Korea;2. Department of Physics, Dehradun Institute of Technology (DIT), School of Engineering, Greater Noida 201308, India;3. Department of Science and Technology, Centre on Biomolecular Electronics Biomedical Instrumentation Section, National Physical Laboratory (CSIR), Dr. K.S. Krishnan Marg, New Delhi 110012, India;4. Department of Biotechnology, Delhi Technological University, Shahbad Daulatpur, Main Bawana Road, Delhi 110042, India;5. Centre for nanoBioiengineering & Spintronics, Chungnam National University, 220, Gung-Dong, Yuseong-gu, Daejeon, 305-704, Korea
Abstract:We report the results of studies relating to the in situ synthesis of a novel ternary NiFe2O4/CuO/FeO-chitosan nanocomposite, which could be utilized as a cholesterol biosensor. The phase identification, morphology and particle size of the NiFe2O4/CuO/FeO nanocomposite have been investigated via X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscope (HR-TEM) and Fourier transform infrared (FTIR) spectroscopy. The quantification of cholesterol was accomplished by immobilizing cholesterol oxidase (ChOx) onto a chitosan-NiFe2O4/CuO/FeO nanocomposite (NiFe2O4/CuO/FeO-CH NC) deposited onto an indium-tin-oxide (ITO) glass substrate via the sol–gel technique. The electrochemical study results of the biocompatible ChOx/NiFe2O4/CuO/FeO-CH/ITO electrode reveal good linearity (50–5000 mg/L), a low detection limit (313 mg/L), high sensitivity (0.043 μA/(mg/L cm?2)), a fast response time (10 s) and a shelf-life of 3 months. The low Michaelis–Menten constant (Km) of 80 mg/L (0.21 mM) indicates the high affinity of ChOx for the analytes. Further, this bioelectrode has been used in clinical applications to estimate cholesterol levels with negligible interference (2%) from analytes present in human serum samples.
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