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http://dx.doi.org/10.5012/bkcs.2011.32.8.2732

Graphite Furnace Atomic Absorption Spectrophotometric Determination of Trace Horseradish Peroxidase Using Nanosilver  

Jiang, Zhi-Liang (Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection, the Ministry of Education, School of Environment and Resource, Guangxi Normal University)
Tang, Ya-Fang (Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection, the Ministry of Education, School of Environment and Resource, Guangxi Normal University)
Wei, Lin (Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection, the Ministry of Education, School of Environment and Resource, Guangxi Normal University)
Liang, Ai-Hui (Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection, the Ministry of Education, School of Environment and Resource, Guangxi Normal University)
Publication Information
Abstract
In pH 4.2 HAc-NaAc buffer solution, horseradish peroxidase (HRP) catalyzed $H_2O_2$ oxidation of nanosilver to form $Ag^+$. After centrifugation, $Ag^+$ in the supernatant can be measured by graphite furnace atomic absorption spectrophotometry (GFAAS) at the silver absorption wavelength of 328.1 nm. When HRP concentration increased, the $Ag^+$ concentration in the supernatant increased, and the absorption value enhanced. The HRP concentration in the range of 0.84-50 $ng{\cdot}mL^{-1}$ was linear to the enhanced absorption value (${\Delta}A$), with a regression equation of ${\Delta}A$=0.012C+0.11, correlation coefficient of 0.9988, and detection limit of 0.41 $ng{\cdot}mL^{-1}$ HRP. The proposed GFAAS method was used to detect HRP in waste water samples, with satisfactory results.
Keywords
Horseradish peroxidase; Nanosilver; Graphite furnace atomic absorption spectrophotometry;
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