Journal
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 146, Issue -, Pages 907-915Publisher
ELSEVIER
DOI: 10.1016/j.ijbiomac.2019.09.213
Keywords
Lysine; Lysine oxidase nanoparticles (LOxNPs); Lysine biosensor; Gold electrode (AuE); Serum
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The fabrication of an amperometric lysine biosensor is described in this study, wherein nanoparticles (NPs) of lysine oxidase (LOx) are covalently immobilized onto gold electrode (AuE). The LOxNPs were prepared by desolvation method and characterized by UV Vis spectroscopy, Fourier transform infra red (FTIR) spectroscopy and transmission electron microscopy (TEM). The LOxNPs/AuE modified working electrode was studied by scanning electron microscope (SEM) and cyclic voltammetric (CV) techniques. The electrode exhibited optimum current within 3.5 s at applied potential, 0.8 V, pH 6.5 and temperature, 35 degrees C. The sensor displayed a linear relationship between lysine concentration and current in the range 10-800 mu M with a limit of detection of 10 mu M. Within assay and between batch coefficients of variation were 0.0751% and 0.0637% respectively. The analytical recoveries of added lysine at 10 mu M and 20 mu M in sera were 98.39% and 98.23% respectively. There was a good correlation between level of lysine in sera and milk samples (R-2 = 0.999 and R-2 = 0.98 respectively) as determined by the standard spectrophotometric method and the present method. The biosensor measured lysine levels in milk, pharmaceutical tablet and sera of healthy individuals and cancer patients. The biosensor showed slight interference by common interferents found in serum. (C) 2019 Elsevier B.V. All rights reserved.
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