Amino‐Montmorillonite Crystalline Clay as Electrode Modifier for Electrochemical Detection of Ciprofloxacin in Presence of Cetyltrimethylammonium Bromide

Author:

Dongmo Liliane Medonbou1,Pecheu Chancellin Nkepdep1,Jiokeng Sherman Lesly Zambou123,Dzuibo Simonne Rose Ngoutane14,Djuffo Lottie Astree Yemene1,Tajeu Kevin Yemele1,Ngantchouko Claude Beranger Ngalemo4,François Kanmangne4,Tonle Ignas Kenfack1

Affiliation:

1. Electrochemistry and Chemistry of Materials Department of Chemistry University of Dschang P.O. Box 67 Dschang Cameroon.

2. Institut für Anorganische Chemie und Strukturchemie Heinrich-Heine-Universität Düsseldorf 40204 Düsseldorf Germany

3. Institute of Analytical and Bioanalytical Chemistry University of Ulm 89081 Ulm Germany

4. Department of Pharmacy Higher Institute of Health Sciences Université des Montagnes P.O. Box 208 Bangangte Cameroon

Abstract

AbstractThis research focused on harnessing amino‐functionalized montmorillonite (Mt) clay, achieved through the grafting of [3(2‐aminoethyl)amino]propyltrimethoxysilane (AEP‐TMS), as carbon paste electrode (CPE) modifier for the electroanalysis of ciprofloxacin (CF). The characterization of both Mt and the amino‐functionalized (Mt‐NH2) materials was carried out using various techniques including Fourier‐transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X‐ray diffraction (XRD). Afterwards, various CPEs modified using Mt and Mt‐NH2 were prepared and characterized employing SEM‐energy dispersive X‐ray (EDX), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). By EIS, Mt‐NH2‐CPE exhibited significantly faster electron transfer with lower charge‐transfer resistance (438.5 Ω) compared to Mt‐CPE (3572.1 Ω) and to the bare CPE (2066.1 Ω). Additionally, CV experiments performed by using redox probes demonstrated the excellent accumulation capability of [Fe(CN)6]3− ions on Mt‐NH2‐CPE surface. The Mt‐NH2‐CPE was subsequently applied using square wave voltammetry to determine CF in the presence of cetyltrimethylammonium bromide (CTAB), yielding an impressive linear range from 30 to 240 μM (R=0.999) and a low detection limit of 0.07 μM (23.2 μg L−1). The method exhibited stable and reproducible responses (RSD=3.25 %; n= 6) under optimized conditions. Following interference studies, the optimized method was effectively applied to quantify CF concentrations in pharmaceutical and water samples.

Publisher

Wiley

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