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RETRACTED ARTICLE

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Anal Chim Acta. 2015 Jan 1;853:271-284. doi: 10.1016/j.aca.2014.10.030. Epub 2014 Oct 27.

Imprinted ZnO nanostructure-based electrochemical sensing of calcitonin: a clinical marker for medullary thyroid carcinoma.

Author information

1
Department of Applied Chemistry, Indian School of Mines, Dhanbad, Jharkhand 826 004, India.
2
Department of Applied Chemistry, Indian School of Mines, Dhanbad, Jharkhand 826 004, India. Electronic address: rshmmadhuri@gmail.com.
3
Functional Nanomaterials Research Laboratory, Department of Applied Physics, Indian School of Mines, Dhanbad, Jharkhand 826 004, India.

Abstract

The present work describes an exciting method for the selective and sensitive determination of calcitonin in human blood serum samples. Adopting the surface molecular imprinting technique, a calcitonin-imprinted polymer was prepared on the surface of the zinc oxide nanostructure. Firstly, a biocompatible tyrosine derivative as a monomer was grafted onto the surface of zinc oxide nanostructure followed by their polymerization on vinyl functionalized electrode surface by activator regenerated by electron transfer-atom transfer radical polymerization (ARGET-ATRP) technique. Such sensor can predict the small change in the concentration of calcitonin in the human body and it may also consider to be as cost-effective, renewable, disposable, and reliable for clinical studies having no such cross-reactivity and matrix effect from real samples. The morphologies and properties of the proposed sensor were characterized by scanning electron microscopy, cyclic voltammetry, difference pulse voltammetry and chronocoulometry. The linear working range was found to be 9.99 ng L(-1) to 7.919 mg L(-1) and the detection limit as low as 3.09±0.01 ng L(-1) (standard deviation for three replicate measurements) (S/N=3).

KEYWORDS:

Activator regenerated by electron transfer–atom transfer radical polymerization (ARGET–ATRP); Biomarker-sensor; Calcitonin; Surface imprinting; Zinc oxide nanostructure

PMID:
25467469
DOI:
10.1016/j.aca.2014.10.030
[Indexed for MEDLINE]

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