Real-time Assay of Toxic Lead in In Vivo Living Plant Tissue

A method of detecting lead was developed using square wave anodic stripping voltammetry (SWASV) with DNA-carbon nanotube paste electrode (CNTPE). The results indicated a sensitive oxidation peak current of lead on the DNA-CNTPE. The curves were obtained within a concentration range of 50 ngL−1- 20 m...

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Veröffentlicht in:Toxicological research (Seoul) 2013, 29(4), , pp.293-298
Hauptverfasser: Ly, S.W., Biosensor Research Institute in Seoul National University of Science and Technology, Seoul, Republic of Korea, Kim, N.J., Seoul National Univ. of Science and Technology, Seoul, Republic of Korea, Youn, M.S., Advanced Scientific Research Group in Shinil High School, Seoul, Republic of Korea, Kim, Y.W., 3Advanced Scientific Research Group in Shinil High School, Seoul, Republic of Korea, Sung, Y.M., Advanced Scientific Research Group in Shinil High School, Seoul, Republic of Korea, Kim, D.H., Advanced Scientific Research Group in Shinil High School, Seoul, Republic of Korea, Chung, T.H., Advanced Scientific Research Group in Shinil High School, Seoul, Republic of Korea
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Sprache:eng
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Zusammenfassung:A method of detecting lead was developed using square wave anodic stripping voltammetry (SWASV) with DNA-carbon nanotube paste electrode (CNTPE). The results indicated a sensitive oxidation peak current of lead on the DNA-CNTPE. The curves were obtained within a concentration range of 50 ngL−1- 20 mgL−1 with preconcentration time of 100, 200, and 400 sec at the concentration of mgL−1, μgL−1, and ngL−1, respectively. The observed relative standard deviation was 0.101% (n = 12) in the lead concentration of 30.0 μgL−1 under optimum conditions. The low detection limit (S/N) was pegged at 8 ngL−1 (2.6 × 10−8 M). Results showed that the developed method can be used in real-time assay in vivo without requiring any pretreatment and pharmaceutical samples, and food samples, as well as other materials requiring water source contamination analyses.
ISSN:1976-8257
2234-2753
DOI:10.5487/TR.2013.29.4.293