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Electrochemical Investigation of Paracetamol at Poly(Glycine) Modified Carbon Paste Electrode: A Voltametric Study | OMICS International | Abstract
ISSN: 2155-9872

Journal of Analytical & Bioanalytical Techniques
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Research Article

Electrochemical Investigation of Paracetamol at Poly(Glycine) Modified Carbon Paste Electrode: A Voltametric Study

Chethan M kuskur1, Kumara Swamy BE1* and Jayadevappa H2

1Department of P.G. Studies and Research in Industrial Chemistry, Kuvempu University, Jnana Sahyadri, Shankaraghatta, Shimoga, Karnataka, India

2Department of Chemistry, Sahyadri Science College, Shimoga, Karnataka, India

*Corresponding Author:
Kumara Swamy BE
Department of P.G. Studies and Research in Industrial Chemistry
Kuvempu University, Jnana Sahyadri
Shankaraghatta, Shimoga
Karnataka 577451, India
Tel: +91-8282-256225
Fax: +91-8282-256255
E-mail: kumaraswamy21@yahoo.com

Received date: July 02, 2015; Accepted date: July 22, 2015; Published date: July 29, 2015

Citation: Kuskur CM, Kumara Swamy BE, Jayadevappa H (2015) Electrochemical Investigation of Paracetamol at Poly(Glycine) Modified Carbon Paste Electrode: A Voltametric Study. J Anal Bioanal Tech 6:260. doi: 10.4172/2155-9872.1000260

Copyright: © 2015 kuskur CM, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

The carbon paste electrode was modified by electropolymerisation of 1 mM Glycine in 0.2 M Acetate buffer solution (ABS) at pH-5. The voltammetric response of Paracetamol (PA) at Poly(Glycine) Modified carbon paste electrode (MCPE) shows excellent electrocatalytic activity when compared to bare carbon paste electrode (BCPE) at sweep rate of 100 mV/s-1. From the study of scan rate variation the electrode process was found to be diffusion controlled. The concentration effect of paracetamol was studied. The simulations determination of PA, DA and AA in their sample mixture was analyzed by using both cyclic voltammetric and differential pulse voltammetric techniques.

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