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Functionalized Fe3o4/Graphene Oxide Nanocomposites With Hairpin Aptamers for the Separation and Preconcentration of Trace Pb2 + From Biological Samples Prior to Determination by Icp Ms Publisher Pubmed



Shamsipur M1 ; Farzin L2, 3 ; Amouzadeh Tabrizi M4 ; Sheibani S2
Authors
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Authors Affiliations
  1. 1. Department of Chemistry, Razi University, P. O. Box 67149-67346, Kermanshah, Iran
  2. 2. Radiation Application Research School, Nuclear Science and Technology Research Institute, P.O. Box 11365-3486, Tehran, Iran
  3. 3. Department of Analytical Chemistry, School of Chemistry, College of Science, University of Tehran, P. O. Box 14174-66191, Tehran, Iran
  4. 4. Research Center for Science and Technology in Medicine, Tehran University of Medical Sciences, P. O. Box 14197-33131, Tehran, Iran

Source: Materials Science and Engineering C Published:2017


Abstract

Lead (Pb) as a topically poisonous metal represents a serious threat to the ecological environment and especially to human beings. Therefore, it is urgent to develop a rapid and reliable monitoring technique for this heavy metal in the environmental samples. In the present study, we have designed a selective and sensitive method for the determination of ultratrace contents of Pb2 + in biological samples, based on the guanine (G)-quadruplex formed by the aptamer with hairpin structure and Pb2 +. For this purpose, Pb2 + specific aptamer serving as affinity probe to capture and separate trace amounts of the analyte, was covalently linked to Fe3O4/graphene oxide (GO) surface by using a suitable cross-linking agent. Then, the G-quadruplex complex was formed by the opening of the “neck- ring” of the hairpin structure of aptamer in the presence of Pb2 +. Inductively coupled plasma mass spectrometry (ICP-MS) was used for determination of Pb2 + in biological matrices. The analysis conditions were optimized and the performance of the proposed method was investigated. Under optimum conditions, the calibration curve was linear over the range of 0.3–867.5 μg L− 1 and an enrichment factor (EF) of 50 was obtained. The limit of detection (LOD) was 0.05 μg L− 1 and the relative standard deviation (RSD) for single-sorbent repeatability and sorbent-to-sorbent reproducibility were < 4.7% and 8.8% (n = 5), respectively. The accuracy of aptamer-based affinity purification method was confirmed by the analysis of quality control materials (QCMs, Seronorm™ Blood REF NO 201505 and Urine REF NO 2525). © 2017 Elsevier B.V.
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