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Sensitive fluorescent probes for determination of hydrogen peroxide and glucose based on enzyme-immobilized magnetite/silica nanoparticles.

Authors :
Qing Chang
Lihua Zhu
Guodong Jiang
Heqing Tang
Source :
Analytical & Bioanalytical Chemistry; Dec2009, Vol. 395 Issue 7, p2377-2385, 9p, 4 Charts, 7 Graphs
Publication Year :
2009

Abstract

Sensitive fluorescent probes for the determination of hydrogen peroxide and glucose were developed by immobilizing enzyme horseradish peroxidase (HRP) on Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> magnetic core–shell nanoparticles in the presence of glutaraldehyde. Besides its excellent catalytic activity, the immobilized enzyme could be easily and completely recovered by a magnetic separation, and the recovered HRP-immobilized Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> nanoparticles were able to be used repeatedly as catalysts without deactivation. The HRP-immobilized nanoparticles were able to activate hydrogen peroxide (H<subscript>2</subscript>O<subscript>2</subscript>), which oxidized non-fluorescent 3-(4-hydroxyphenyl)propionic acid to a fluorescent product with an emission maximum at 409 nm. Under optimized conditions, a linear calibration curve was obtained over the H<subscript>2</subscript>O<subscript>2</subscript> concentrations ranging from 5.0 × 10<superscript>−9</superscript> to 1.0 × 10<superscript>−5</superscript> mol L<superscript>−1</superscript>, with a detection limit of 2.1 × 10<superscript>−9</superscript> mol L<superscript>−1</superscript>. By simultaneously using glucose oxidase and HRP-immobilized Fe<subscript>3</subscript>O<subscript>4</subscript>/SiO<subscript>2</subscript> nanoparticles, a sensitive and selective analytical method for the glucose detection was established. The fluorescence intensity of the product responded well linearly to glucose concentration in the range from 5.0 × 10<superscript>−8</superscript> to 5.0 × 10<superscript>−5</superscript> mol L<superscript>−1</superscript> with a detection limit of 1.8 × 10<superscript>−8</superscript> mol L<superscript>−1</superscript>. The proposed method was successfully applied for the determination of glucose in human serum sample. [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16182642
Volume :
395
Issue :
7
Database :
Complementary Index
Journal :
Analytical & Bioanalytical Chemistry
Publication Type :
Academic Journal
Accession number :
45362960
Full Text :
https://doi.org/10.1007/s00216-009-3118-9