ORCID Profile
0000-0003-1932-9300
Current Organisation
CNRS
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Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D1CE01281A
Abstract: The formation of caffeine and 1-hydroxy-2-naphtoic acid cocrystals at a water–oil interface was controlled by potential difference, Δwo ϕ , favouring one polymorphic form of the cocrystal.
Publisher: American Chemical Society (ACS)
Date: 25-06-2008
DOI: 10.1021/AC800089P
Abstract: The detection of peptides is an important bioanalytical challenge, as they are a generic class of potent molecules of biomedical and biopharmaceutical significance. In this work, the electrochemistry of seven oligopeptides at microscaled interfaces between two immiscible electrolyte solutions (microITIES) was investigated. Their transfer across the polarized interface was assisted by dibenzo-18-crown-6 (DB18C6). The ion transfer potentials of these oligopeptides were dependent on their hydrophobicities and their interaction with DB18C6. Micropore arrays, which were fabricated in silicon by a combination of wet and dry etch techniques, were used to enhance mass transfer and thus analytical sensitivities. The use of a gellified organic phase allowed the implementation of voltammetric stripping techniques at the liquid-organogel interface. The combination of interface miniaturization and stripping voltammetry provided limits of detection at submicromolar concentration levels. The sensitivities (calibration graph slopes) were -3205 nA microM(-1) cm(-2) for Phe-Phe, -1791 nA microM(-1) cm(-2) for Leu-Leu, -6014 nA microM(-1) cm(-2) for Lys-Lys, and -9611 nA microM(-1) cm(-2) for Lys-Lys-Lys. Mixtures of peptides were also investigated with this technique, illustrating the possibility to detect certain mixture combinations.
Publisher: American Chemical Society (ACS)
Date: 31-05-2008
DOI: 10.1021/JF7035966
Abstract: Electrochemistry at the liquid-liquid interface enables the detection of nonredoxactive species with electroanalytical techniques. In this work, the electrochemical behavior of two food additives, aspartame and acesulfame K, was investigated. Both ions were found to undergo ion-transfer voltammetry at the liquid-liquid interface. Differential pulse voltammetry was used for the preparation of calibration curves over the concentration range of 30-350 microM with a detection limit of 30 microM. The standard addition method was applied to the determination of their concentrations in food and beverage s les such as sweeteners and sugar-free beverages. Selective electrochemically modulated liquid-liquid extraction of these species in both laboratory solutions and in beverage s les was also demonstrated. These results indicate the suitability of liquid-liquid electrochemistry as an analytical approach in food analysis.
Publisher: American Scientific Publishers
Date: 08-2013
Abstract: The modification of stent surfaces with nano-structures has the potential for limiting late stent restenosis. We report here the patterning of 316L austentitic stainless steel with arrays of nano-pits of two nominal diameters: 120 and 180 nm. These nano-textured surfaces were prepared by focused ion beam milling. The influence of the ion beam current on the nano-features was investigated by scanning electron and atomic force microscopies. The optimum ion beam currents were 280 pA for 120 nm nano-pits and 920 pA for 180 nm nano-pits. The depths of the nano-pits formed were (65 +/- 24) nm (120 nm) and (84 +/- 36) nm (180 nm). This wide distribution of the depths is due to the polycrystalline nature of 316 L stainless steel, which has a strong influence on the milling rates. Endothelial cells were grown in vitro on these substrates for 1, 3 and 5 days. The cells were viable for the duration of the cell culture on the nano-textured substrates. There was no significant difference in the adhesion and the proliferation based on the nano-pit diameter.
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8FD00019K
Abstract: FIB/SEM tomography and energy dispersive X-ray (EDX) spectroscopy are employed to study the interface between two immiscible electrolyte solutions at nanopore arrays, which were electrochemically modified by silica.
Publisher: Elsevier BV
Date: 03-2010
Publisher: Wiley
Date: 11-11-2022
Abstract: Dissolution and hydrolysis processes are important in a variety of settings, including industrial and environmental applications. In this work, the hydrolysis of pyrosulfate (disulfate) was investigated by ion‐transfer electrochemistry at an array of microinterfaces between two immiscible electrolyte solutions (μITIES). Current associated with pyrosulfate transfer was observed, but it decreased with time. This is due to the hydrolysis of pyrosulfate to hydrogen sulfate and sulfate. Corroborating data for the hydrolysis was obtained from pH measurements (acidification of the aqueous solution) and Raman spectroscopy (formation of sulfate and hydrogen sulfate). Measurement of the ion‐transfer potential from the voltammograms enabled estimation of pyrosulfate's Gibbs energy of transfer between the phases. Quantum mechanical calculations were employed to estimate the thermodynamics for the reactions of pyrosulfate, hydrogen sulfate and sulfate, which supported the experimentally observed trends. Altogether, these results illustrate the use of electrochemistry at the μITIES to characterise dissolution and hydrolysis processes.
Publisher: Elsevier BV
Date: 2003
Publisher: Elsevier BV
Date: 10-2008
Publisher: Wiley
Date: 10-2005
Publisher: American Chemical Society (ACS)
Date: 17-12-2003
DOI: 10.1021/AC026093F
Abstract: Development of an approach to prevention of electrode surface fouling by surfactants in s les is demonstrated. Spontaneously adsorbed monolayer systems employing short alkyl chains and bulky end groups are used to form porous disorganized monolayers on gold electrodes. Detection of copper by stripping of underpotential deposits formed at electrodes modified with disorganized films of mercaptoethanesulfonate (MES), mercaptopropanesulfonate, mercaptoacetic acid, and mercaptopropanoic acid was possible, and to a much lesser extent at aminoethanethiol and L-cysteine films. Use of short deposition times in conjunction with linear sweep anodic stripping voltammetry allowed detection of Cu2+ ions down to 1 x 10(-6) M in sulfuric acid solution, using underpotential deposition as the deposition step of the procedure. Calibration graphs were linear in the concentration range (1-80) x 10(-6) M Cu2+ using 15-s deposition at 0.00 V versus Ag/AgCl. The surfactants Tween 20, Tween 80, and Triton X-100 were found to have no affect on detection of Cu2+ ions in the calibration curve concentration range using MES-modified gold electrodes, whereas at unmodified gold electrodes very severe attenuation of the detection capability was manifested. The average slope for all calibration curves at the MES-modified electrode in the absence and presence of the surfactants at two different concentration levels was 0.0710 +/- 0.0024 microA microM(-1) in contrast, the slope of the calibration line at uncoated gold electrodes in the presence of surfactant was 0.0268 microA microM(-1). These results indicate the excellent ability of a disorganized, porous monolayer for prevention of fouling of the electrode surface by the surfactants.
Publisher: Elsevier BV
Date: 07-2011
Publisher: Elsevier BV
Date: 04-2009
DOI: 10.1016/J.BIOS.2009.01.026
Abstract: In this work, the surface functionalisation of the commercially available cyclic olefin copolymer (COC) materials, Zeonor and Zeonex, has been studied. The methodology employed involved oxidation in oxygen plasma, functionalisation of the oxidized surface with aminopropyl triethoxy silane and, finally, attachment of antibody using covalent linker molecules. 1,4-Phenylene diisothiocyanate was selected as the most suitable cross-linker for the attachment of protein, as assessed by fluorescent intensity measurements on immobilised FITC-labelled IgG antibody. The modification method was characterised by contact angle measurements, ellipsometry, X-ray photoelectron spectroscopy (XPS) and fluorescence microscopy. The data are consistent with the deposition of a polymeric film of the silane chemisorbed to the oxidised plastic surface. The functionalised surfaces were employed in a sandwich immunoassay format using the reagents goat anti-human IgG (G alphaHIgG) and fluorescently labelled G alphaHIgG (Cy5-G alphaHIgG) as capture and detection antibodies, respectively, and with human IgG (HIgG) as the model analyte. The lowest concentration of HIgG detected was 0.1 ng ml(-1), with a relative standard deviation of 15%. Non-specific binding effects were also assessed. The method and supporting data demonstrate that simple approaches to surface functionalisation can be adapted to plastic-based devices.
Publisher: Wiley
Date: 11-11-2022
Abstract: The simultaneous measurement of potential and current variations at the interface between two immiscible electrolyte solutions, which was polarised using tetraalkylammonium cations as a common ion, is reported here. Various concentration ratios of tetramethyl‐, tetraethyl‐, or tetrapropylammonium were dissolved in each phase. Such biphasic systems were then used to verify that the measured interfacial potential difference agreed with theory. This experimental set‐up was then used to probe the interfacial cocrystallisation process of hydrophilic, cationic caffeine with lipophilic 1‐hydroxy‐2‐naphtoic acid (1H2N). The presence of caffeine in the aqueous phase led to higher current values, caused by interfacial charge transfer. Electrochemical noise analysis suggested that a two‐step process was occurring at the ITIES (i) a potential‐driven nucleation with the transfer of caffeine from the aqueous to the organic phase (ii) a growth stage where the interfacial potential no longer plays a role.
Publisher: American Chemical Society (ACS)
Date: 10-12-2010
DOI: 10.1021/AC901909J
Abstract: The development of new methods for the detection of proteins and peptides is of widespread importance. In this work, the electrochemical behavior of peptide mixtures resulting from proteolytic digestion of proteins was investigated at the polarized liquid|liquid interface (or the interface between two immiscible electrolyte solutions, ITIES). The influence of pepsin digestion on three proteins (hemoglobin, lysozyme, and cytochrome c) was studied, and it was revealed that resulting cyclic voltammograms of the three protein digests were different due to the unique peptide mixtures for a given protein. Differential pulse stripping voltammetry of protein digests enabled the detection of digested proteins at concentrations ranging between 0.55 and 4.22 microM. A limit of detection of 0.55 microM of the initial concentration of protein was achieved, demonstrating the analytical possibilities of such an electrochemical method. These results show that ion-transfer voltammetry offers the opportunity to study and develop label-free detection of peptides resulting from enzymatic digestions of proteins and may thus have a role in development of new proteomic technologies.
Publisher: Elsevier BV
Date: 08-2010
DOI: 10.1016/J.BIOELECHEM.2009.09.012
Abstract: The behaviour of proteins on surfaces and at interfaces is an important field with applications in drug development, clinical diagnostics and studies of device biocompatibility. A key factor is the conformation of surface-bound proteins, which can affect chemical signalling and drug binding. A recent study of the interactions of haemoglobin with hydrophobic anions at a liquid-liquid interface has shown that a pH- and orientation-dependent conformational change occurs in the haemoglobin molecule upon interaction with these anions. To corroborate these results, we use an acoustic wave detector to study binding of solution-phase hydrophobic anions to surface-adhered haemoglobin. The orientation of protein is controlled by thiol chemistry, which generates hydrophilic and hydrophobic surfaces. Tetraphenylborate-based anions are introduced to the haemoglobin coated surface via an on-line flow-injection system to monitor the signal in real-time. Changes in the acoustic properties of the surface, measured piezoelectrically, are related to interactions between the protein and the anions. Signal strength is proportional to the degree of interaction between the salts and the haemoglobin, which in turn, is influenced by its conformation.
Publisher: Wiley
Date: 10-2009
Abstract: In this research, ion transfer across the interface between two immiscible electrolyte solutions (ITIES) was used as a method of detection in a CE separation system. This method allows for the electrochemical detection of ionic analytes that cannot be easily oxidized or reduced. Method development revealed that the optimal separation conditions for three model ions (tetraethylammonium, tetrabutylammonium, and benzensulfonate) were found to be 5 mM sodium tetraborate buffer pH 9.2 with a separation voltage of 20 kV using a 40 cm, 50 microm id fused silica capillary. Constant potential erometry and pulsed erometric detection were applied at the ITIES in which the organic phase was gelled. A miniaturized ITIES within a pipette tip was investigated, which resulted in improved separation efficiency and LOD. To demonstrate the ability of the system to detect substances of bioanalytical interest, the beta-adrenergic receptor blockers timolol and propranolol were detected. The simplicity of the detection platform means that it may be useful for analytical situations not requiring trace or ultratrace detection capabilities.
Publisher: Wiley
Date: 03-2005
Abstract: Platinum and gold microelectrode arrays (MEAs), fabricated on silicon substrates with different geometric characteristics, were surface‐modified by the potentiostatic electropolymerization of the pyrrole‐ferrocene derivative Py(CH 2 ) 3 NHCOFc, in the case of the platinum MEAs, and chemisorption of the thiol‐functionalized ferrocene HS(CH 2 ) 6 N + (CH 3 ) 2 Fc, in the case of the gold MEAs. Cyclic voltammetry of these MEAs was typical of thin film behavior. The modified MEAs were investigated for the detection of the dihydrogen phosphate mono‐anion in non‐aqueous media via differential pulse voltammetry. This was based on electrostatic interaction and/or hydrogen‐bonding between the target anion and the amide‐ferrocene or ammonium‐ferrocene functionalized electrode surfaces. A decrease in the ferrocene (Fc) oxidation peak current with a concomitant increase in the peak current of a new peak at lower potentials was observed when the concentration of the dihydrogen phosphate was increased.
Publisher: Wiley
Date: 07-12-2011
Publisher: Springer Science and Business Media LLC
Date: 06-09-2012
Publisher: Elsevier BV
Date: 10-2008
Publisher: Wiley
Date: 30-07-2012
DOI: 10.1002/JBM.B.32772
Abstract: Coronary artery disease (CAD) kills millions of people every year. It results from a narrowing of the arteries (stenosis) supplying blood to the heart. This review discusses the merits and limitations of balloon angioplasty and stent implantation, the most common treatment options for CAD, and the pathophysiology associated with these treatments. The focus of the review is heavily placed on research efforts geared toward the modification of stent surfaces for the improvement of stent-vascular compatibility and the reduction in the occurrence of related pathophysiologies. Such modifications may be chemical or physical, both of which are surveyed here. Chemical modifications may be passive or active, while physical modification of stent surfaces can also provide suitable substrates to manipulate the responses of vascular cells (endothelial, smooth muscle, and fibroblast). The influence of micro- and nanostructured surfaces on the in vitro cell response is discussed. Finally, future perspectives on the combination of chemical and physical modifications of stent surfaces are also presented.
Publisher: American Scientific Publishers
Date: 04-2011
DOI: 10.1166/SL.2011.1601
Publisher: Elsevier BV
Date: 28-02-2007
DOI: 10.1016/J.TALANTA.2006.05.090
Abstract: This paper describes the electrochemical characterisation of a range of gold and platinum microelectrode arrays (MEAs) fabricated by standard photolithographic methods. The inter-electrode spacing, geometry, numbers and dimensions of the electrodes in the arrays were found to influence the voltammetric behaviours obtained. Excellent correlation was found between experimental data and theoretical predictions employing published models of microelectrode behaviour. Gold MEAs were evaluated for their applicability to copper determination in a soil extract s le, where agreement was found between the standard analytical method and a method based on underpotential deposition-anodic stripping voltammetry (UPD-ASV) at the MEAs, offering a mercury-free alternative for copper sensing.
Publisher: Springer Science and Business Media LLC
Date: 21-05-2014
Publisher: The Electrochemical Society
Date: 25-04-2011
DOI: 10.1149/1.3571974
Abstract: We report on the electrochemical characterization of regularly-aligned cylindrical nanopore arrays supported in silicon nitride membranes and preliminary results for the detection of nucleic acid hybridization on the nanopore walls. A range of nanopore arrays with diameters between 30 and 150 nm were examined. We tested the effect of pore diameter, number of pores, electrolyte concentration and surface chemistry on the conductance of the nanopore membranes. The pores were functionalized with single-stranded DNA and conductance measurements were performed before and after hybridization. In many cases, changes in current rectification were observed following hybridization, which is discussed as a strategy for nucleic acid hybridization and interactions.
Publisher: Elsevier BV
Date: 03-2010
Publisher: Elsevier BV
Date: 02-2017
Publisher: Springer Science and Business Media LLC
Date: 19-08-2009
Publisher: Elsevier BV
Date: 03-2005
Publisher: American Chemical Society (ACS)
Date: 17-06-2016
DOI: 10.1021/ACS.ANALCHEM.6B00513
Abstract: The direct experimental characterization of diffusion processes at nanoscale remains a challenge that could help elucidate processes in biology, medicine and technology. In this report, two experimental approaches were employed to visualize ion diffusion profiles at the orifices of nanopores (radius (ra) of 86 ± 6 nm) in array format: (1) electrochemically assisted formation of silica deposits based on surfactant ion transfer across nanointerfaces between two immiscible electrolyte solutions (nanoITIES) (2) combined atomic force - scanning electrochemical microscopy (AFM-SECM) imaging of topography and redox species diffusion through the nanopores. The nature of the diffusion zones formed around the pores is directly related to the interpore distance within the array. Nanopore arrays with different ratios of pore center-to-center separation (rc) to pore radius (ra) were fabricated by focused ion beam (FIB) milling of silicon nitride (SiN) membranes, with 100 pores in a hexagonal arrangement. The ion diffusion profiles determined by the two visualization methods indicated the formation of overlapped or independent diffusion profiles at nanopore arrays with rc/ra ratios of 21 ± 2 and 91 ± 7, respectively. In particular, the silica deposition method resulted in formation of a single deposit encompassing the complete array with closer nanopore arrangement, whereas in idual silica deposits were formed around each nanopore within the more widely spaced array. The methods reveal direct experimental evidence of diffusion zones at nanopore arrays and provide practical illustration that the pore-pore separation within such arrays has a significant impact on diffusional transport as the pore size is reduced to the nanoscale. These approaches to nanoscale diffusion zone visualization open up possibilities for better understanding of molecular transport processes within miniaturized systems.
Publisher: Informa UK Limited
Date: 2004
DOI: 10.1081/AL-120029738
Publisher: Royal Society of Chemistry (RSC)
Date: 2009
DOI: 10.1039/B905441N
Abstract: The interaction of proteins with interfaces and surfaces provides a basis for studying their behaviour and methods to detect them. This paper is concerned with elucidation of the mechanism of electrochemical detection of haemoglobin (Hb) at the interface between aqueous and organic electrolyte solutions. The adsorption of Hb at the interface was investigated by alternating current (AC) voltammetry. It was found that addition of Hb to the aqueous phase induced a shift of the potential of zero charge at the liquid/liquid interface, due to interfacial adsorption of Hb. The influence of the nature and the concentration of the organic phase electrolyte on the electrochemical signal was investigated by cyclic voltammetry (CV). It was found that the electrochemical signal, in the presence of aqueous phase Hb, was due to the facilitated transfer of the anion of the organic phase electrolyte to the aqueous phase. The transfer current was dependent on both the nature and concentration of the organic phase electrolyte anion. These results confirm that adsorbed Hb molecules at the liquid/liquid interface interact with small ionised molecules and facilitate their transfer across the interface. The results will provide a basis for both biomolecular detection methods and for the study of protein-small ionised molecule interactions.
Publisher: Royal Society of Chemistry (RSC)
Date: 2007
DOI: 10.1039/B701472D
Abstract: Electrochemical methods for the detection of amino acids, peptides, and proteins in a variety of media are reviewed. Label-free strategies in which the detection is based on the inherent electrochemical properties of the analyte are discussed. Various processes such as direct or mediated (in solution or immobilised) redox processes and interfacial ion transfers have been employed for the electrochemical detection and determination of the target analytes. The various methods covered encompass voltammetry at uncoated and modified electrodes and at immiscible liquid-liquid interfaces, potentiometry at polymer membrane electrodes and electrochemical impedance spectroscopy. The determination of the target analytes in complex biological matrices is discussed. The various approaches highlighted here illustrate the rich capabilities of electrochemical methods as simple, low-cost, sensitive tools for the determination of these important biological analytes at trace and ultra-trace levels.
Publisher: American Chemical Society (ACS)
Date: 12-06-2012
DOI: 10.1021/AC300856W
Abstract: In this work, the electrochemical behavior of nonredox-active poly-L-lysine dendrigraft molecules of four different generations was investigated at the interface between two immiscible electrolyte solutions (ITIES). The influence of the dendrigraft generation on the electrochemical response, sensitivity of the calibration curves, and limit of detection was studied. Cyclic voltammetry at the ITIES revealed that the sensitivity increased (1840 to 25 800 nA μM(-1)) and the limit of detection decreased (11.10 to 0.65 μM) as the dendrigraft generation increased from generation G2 through to generation G5, respectively. The results are compared to those for protein voltammetry at the ITIES. Our studies suggest that the sensitivity expected for a synthetic ionized macromolecule can be predicted on the basis of its net charge and its diffusion coefficient. However, electrochemistry at the ITIES demonstrates a greater sensitivity toward proteins, which is attributed to their tertiary structure.
Publisher: Springer Science and Business Media LLC
Date: 20-06-2009
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D2CE01102F
Abstract: Interfacial ion transfer from organic phase to aqueous phase is employed as the basis for formation of barium sulfate crystals close to the interface.
Publisher: IOP Publishing
Date: 17-08-2011
Publisher: IOP Publishing
Date: 17-08-2011
Publisher: Elsevier BV
Date: 05-2004
No related grants have been discovered for Gregoire Herzog.