Publications by authors named "Ignas Tonle"

In this work, the electrochemical behavior of 4-phenylurazole (Ph-Ur) was studied and the latter was used as a molecular anchor for the electrochemical bioconjugation of tyrosine (Y). Cyclic voltammetry (CV) and controlled potential coulometry (CPC) allowed the in-situ generation of the PTAD (4-phenyl-3 H-1,2,4-triazole-3,5(4 H)-dione) species from phenylurazole on demand for tyrosine electrolabeling. The chemoselectivity of the reaction was studied with another amino acid (lysine, Lys) and no changes in Lys were observed.

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Epinephrine (EP, also called adrenaline) is a compound belonging to the catecholamine neurotransmitter family. It can cause neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, Huntington's disease and amyotrophic lateral sclerosis. This work describes an amperometric sensor for the electroanalytical detection of EP by using an inkjet-printed graphene electrode (IPGE) that has been chemically modified by a thin layer of a laponite (La) clay mineral.

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In this work, biomass lignocellulosic materials extracted via chemical and physical treatments from bean and pistachio pod waste were used for the optimized elimination of Indigo Carmine (IC) from aqueous medium, using a design of experiments methodology. The physicochemical properties of the studied materials (raw and treated counterparts) used for the sorption of IC were investigated by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with EDX, and thermal analysis. Key variables influencing the adsorption of IC, namely the initial IC concentration, the pH of the solution, the stirring time and the mass of adsorbents, were optimized by the central composite design (CCD) with three center points, the measured response being the amount of IC adsorbed.

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A talc-like magnesium phyllosilicate functionalized with amine groups (TalcNH), useful as sensor material in voltammetry stripping analysis, was synthesized by a sol-gel-based processing method. The characterizations of the resulting synthetic organoclay by scanning electron microscopy (SEM), X-ray diffraction, N sorption isotherms (BET method), Fourier transform infrared spectroscopy (FTIR), CHN elemental analysis and UV-Vis diffuse reflectance spectroscopy (UV-Vis-DRS) demonstrated the effectiveness of the process used for grafting of amine functionality in the interlamellar clay. The results indicate the presence of organic moieties covalently bonded to the inorganic lattice of talc-like magnesium phyllosilicate silicon sheet, with interlayer distances of 1568.

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Article Synopsis
  • This study focuses on using an amino-functionalized clay mineral (amino laponite) to enhance the electrochemical detection of quercetin (QCT) using a glassy carbon electrode (GCE).
  • The modified electrode was characterized using multiple techniques like X-ray diffraction and SEM, confirming the successful attachment of the organosilane and demonstrating enhanced performance in QCT detection through cyclic and differential pulse voltammetry.
  • The developed sensor showed a strong linear response to varying QCT concentrations, with a low detection limit, and was validated by comparing its results to UV-visible spectrometry in human urine samples.
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An amperometric sensor was developed by depositing a film coating of hydroxyapatite (HA)/L-lysine (Lys) composite material on a glassy carbon electrode (GCE). It was applied for the detection of Nile blue A (NBA). Hydroxyapatite was obtained from snail shells and its structural properties before and after its combination with Lys were characterized using X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) surface area analyses.

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The aminated metal-organic framework HN-MIL-101(Cr) was used as the carbon paste electrode (CPE) modifier for the determination of tartrazine (Tz) in soft drinks. The amino material was characterized by electrochemical impedance spectroscopy and showed significantly faster electron transfer with lower charge-transfer resistance (0.13 kΩ) compared to the electrode modified with the unfunctionalized MIL-101(Cr) material (1.

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and experimental models, mainly based on cell cultures, animals, healthy humans and clinical trials, are useful approaches for identifying the main metabolic pathways. However, time, cost, and matrix complexity often hinder the success of these methods. In this study, we propose an alternative non-enzymatic method, using electrochemistry (EC) coupled to liquid chromatography (LC) - high resolution mass spectrometry (HRMS) - DFT theoretical calculations (EC/LC-MS/DFT) for the mimicry/simulation of the environmental degradation of phenylurea herbicides, and for the mechanism elucidation of this class of herbicides.

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A composite material prepared by polymerization of β-cyclodextrin (β-CD) on the surface of natural hydroxyapatite using citric acid as cross linker, was employed as electrode material for the detection of Pb(II). Hydroxyapatite was obtained from bovine bones, following a three-step procedure including pre-calcination, chemical treatment with (NH)HPO and calcination. The structure and morphology of the pristine hydroxyapatite (NHAP) and its functionalized counterpart (NHAP-CA-β-CD) were examined using XRD, FTIR, and SEM.

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An amperometric sensor based on an inkjet-printed graphene electrode (IPGE) modified with amine-functionalized montmorillonite (Mt-NH) for the electroanalysis and quantification of gentisic acid (GA) has been developed. The organoclay used as IPGE modifier was prepared and characterized by infrared spectroscopy, X-ray diffraction, scanning electron microscopy, CHN elemental analysis, and thermogravimetry. The electrochemical features of the Mt-NH/IPGE sensor were investigated by cyclic voltammetry and electrochemical impedance spectroscopy.

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The present work reports the development of a low-cost and reliable differential pulse adsorptive stripping voltammetric procedure for the detection of diquat (DQ) in water, using a glassy carbon electrode (GCE) modified with β-cyclodextrin (β-CD)/Natural hydroxyapatite (NHAP) composite material. The structural characterization of the natural hydroxyapatite and its modified counterpart was achieved using several techniques including X-ray Diffraction, Fourier Transform Infrared Spectroscopy and Thermal Analysis. By comparing the physico-chemical characteristics of hydroxyapatite material before and after reaction with β-CD, all of these techniques have demonstrated the successful grafting process of β-CD on the surface hydroxyl groups of hydroxyapatite, using citric acid (CA) as cross linker.

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Currently, there is a growing interest in the study of environmental degradation pathways of organic contaminants such as pesticides, with the objective to better understand their potential risk for environmental systems and living organisms. In this context, DFT (conceptual density functional theory) and predictive methods may systematically be used to simplify and accelerate the elucidation of environmental degradation. We report herein the electrochemical behavior/degradation of the carbendazim (CBZ) fungicide widely used to treat cereal and fruit crops.

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In this work, a Layered Double Hydroxide (NiAl-LDH) was obtained by coprecipitation method and used to elaborate an electrochemical sensor for the determination of isoproturon, which is a hazardous pollutant, widely used in agriculture, and its residue is distributed into aqueous environment through run-off and leaching from the soil. Various physicochemical techniques such as FT-IR spectroscopy, X-ray diffraction, and thermal analysis were used to characterize this material. The anionic exchange capacity of NiAl-LDH on carbon paste modified electrode was investigated toward [Fe(CN)] using cyclic voltammetry.

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Article Synopsis
  • - The study examined the effectiveness of cetyltrimethylammonium bromide (CTAB)-modified palm oil fiber (POF) in removing indigo carmine (IC) and 2,6-dichlorophenolindophenol (2,6-DCPIP) from water, using various characterization techniques to analyze the modified fibers.
  • - Results indicated that optimal dye removal occurred at pH 2, with IC reaching equilibrium at 30 minutes and 2,6-DCPIP at 20 minutes, and adsorption capacity increased with higher initial dye concentrations and mass of the fibers.
  • - The adsorption data was best described by the Freundlich and Temkin isotherms for IC and 2,
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Background: A series of recently reported phenolic azo dyes 7a-e were prepared by coupling the thienyl diazonium sulfate of 3-Amino-4H-benzo[f]thieno[3,4-c](2H)chromen-4-one with selected diversely substituted phenolic and naphtholic derivatives. These compounds were evaluated for their antibacterial and antifungal activities. Furthermore their voltammetric behavior was compared at a glassy carbon electrode.

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This work describes the development of a low-cost and reliable adsorptive stripping voltammetric method for the detection of PNP in water. Organoclays were prepared by intercalation in various loading amounts of cetyltrimethylammonium ions (CTA(+)) in the interlayer space of a smectite-type clay mineral. Their structural characterization was achieved using several techniques including X-ray diffraction (XRD), N2 adsorption-desorption (BET method) and Fourier Transform Infrared spectroscopy (FTIR) that confirmed the intercalation process and the presence of the surfactant ions within the clay mineral layers.

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A natural Cameroonian smectite-type clay (SaNa) was exchanged with cationic surfactants, namely cetyltrimethylammonium (CTA) and didodecyldimethyl ammonium (DDA) modifying its physico-chemical properties. The resulting organoclays that have higher adsorption capacity for mesotrione than the pristine SaNa clay, have been used as modifiers of glassy carbon electrode for the electrochemical detection of this herbicide by square wave voltammetry. The stripping performances of SaNa, SaCTA and SaDDA modified electrodes were therefore evaluated and the experimental parameters were optimized.

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In this study, an hybrid material obtained by the intercalation of a gemini surfactant between the layers of smectite-type clay, was fully characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR) and N(2) adsorption-desorption experiments (BET method). To ascertain the intercalation process of the starting clay by the dimeric surfactant, the permselectivity and ion exchange properties of the organoclay were investigated by ion exchange voltammetry using [Fe(CN)(6)](3-) and [Ru(NH(3))(6)](3+) as redox probes, by the means of a clay film-modified electrode. Due to its organophilic character, the surfactant-intercalated complex was evaluated as electrode modifier for the accumulation of methylparathion (MP) pesticide.

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In this work, a thiol functionalized-clay was prepared by the covalent grafting of 3-mercaptopropyltrimethoxysilane (MPTMS) onto the surface of a natural smectite clay mineral originating from Cameroon. Effectiveness of the grafting process and properties of the resulting hybrid material were studied by various physico-chemical techniques, such as Fourier transform infrared (FTIR) spectroscopy, N(2) adsorption-desorption experiments (surface area measurements by the BET method) and thermal gravimetric analysis (TGA) coupled with mass spectrometry (MS). Sorption of methylene blue (MB), an electroactive cationic dye, was investigated for both the raw clay and its modified counterpart, as a function of shaking time, adsorbate concentration and pH, through batch experiments.

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