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Dive into the research topics where Ernest Mendoza is active.

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Featured researches published by Ernest Mendoza.


Nature Chemistry | 2013

Exceptional oxidation activity with size-controlled supported gold clusters of low atomicity

Avelino Corma; Patricia Concepción; Mercedes Boronat; María J. Sabater; Javier Navas; Miguel José Yacamán; Eduardo Larios; Alvaro Posadas; M. Arturo López-Quintela; David Buceta; Ernest Mendoza; Gemma Guilera; Alvaro Mayoral

The catalytic activity of gold depends on particle size, with the reactivity increasing as the particle diameter decreases. However, investigations into behaviour in the subnanometre regime (where gold exists as small clusters of a few atoms) began only recently with advances in synthesis and characterization techniques. Here we report an easy method to prepare isolated gold atoms supported on functionalized carbon nanotubes and their performance in the oxidation of thiophenol with O2. We show that single gold atoms are not active, but they aggregate under reaction conditions into gold clusters of low atomicity that exhibit a catalytic activity comparable to that of sulfhydryl oxidase enzymes. When clusters grow into larger nanoparticles, catalyst activity drops to zero. Theoretical calculations show that gold clusters are able to activate thiophenol and O2 simultaneously, and larger nanoparticles are passivated by strongly adsorbed thiolates. The combination of both reactants activation and facile product desorption makes gold clusters excellent catalysts.


ACS Applied Materials & Interfaces | 2014

Sonochemical Coating of Textiles with Hybrid ZnO/Chitosan Antimicrobial Nanoparticles

Petya Petkova; Antonio Francesko; Margarida M. Fernandes; Ernest Mendoza; Ilana Perelshtein; Aharon Gedanken; Tzanko Tzanov

Textiles are good substrates for growth of microorganisms especially under moisture and temperature conditions found in hospitals. Microbial shedding from the body occurs continuously at contact of the patient with textile materials used in medical practices, contributing to the occurrence of hospital acquired infections. Thus, the use of efficient antimicrobial textiles is necessary to prevent the transfer of pathogens and the infection incidence. In this work, hybrid antimicrobial coatings were generated on cotton fabrics by means of a one-step simultaneous sonochemical deposition of ZnO nanoparticles (NPs) and chitosan. The process was further optimized in terms of reagents concentration and processing time in order to improve the antibacterial properties of the fabric and ensure their biocompatibility. The highest antibacterial activity of the fabrics against two medically relevant bacterial species was achieved in a 30 min sonochemical coating process using 2 mM ZnO NPs suspension. When chitosan was simultaneously deposited with the same amount of ZnO, the obtained hybrid NPs coating displayed higher by 48 and 17% antibacterial activity against Staphylococcus aureus and Escherichia coli, respectively. The presence of biopolymer also improved the durability of the antimicrobial effect of the coatings by 21% for Staphylococcus aureus and 40% for Escherichia coli, evaluated after applying multiple washing cycles at hospital laundering regimes. Finally, 87% biocompatibility improvement supported by fibroblast viability was observed for the hybrid ZnO/chitosan coating compared to the steady decrease of cells viability over one week in contact with the fabrics coated with ZnO alone.


Journal of the American Chemical Society | 2011

Synthesis and Stabilization of Subnanometric Gold Oxide Nanoparticles on Multiwalled Carbon Nanotubes and Their Catalytic Activity

Leonor Alves; Belén Ballesteros; Mercedes Boronat; Jose R. Cabrero-Antonino; Patricia Concepción; Avelino Corma; Miguel A. Correa-Duarte; Ernest Mendoza

Small gold nanoclusters in a very narrow size distribution (1.1 ± 0.5 nm) have been stabilized onto multiwalled carbon nanotubes (MWCNT). Theoretical studies supported by XPS and (16)O(2)/(18)O(2) isotopic exchange experiments have shown that, on small gold nanoparticles (0.9-1.5 nm), dissociation of molecular O(2) and formation of a surface oxide-like layer is energetically favorable and occurs at room temperature, while O(2) recombination and desorption involves a larger activation barrier. CO titration experiments and theoretical studies demonstrate that the reactivity of the oxidized particles toward CO does not only depend on particle size but also on oxygen coverage. The oxidation-reduction process described is reversible, and the oxidized nanoparticles are active in the epoxidation of styrene with air.


Angewandte Chemie | 2008

Label-Free Pathogen Detection with Sensor Chips Assembled from Peptide Nanotubes

Roberto de la Rica; Ernest Mendoza; Laura M. Lechuga; Hiroshi Matsui

A robust viral sensor was developed by bridging a pair of gold electrodes with antibody-coated peptide nanotubes. The nanotubes concentrated the target virus on their surface by molecular recognition between the antibody and the virus (see picture). The nanotubes fit perfectly within the electric field line distribution to enable the extremely sensitive impedimetric detection of viral particles.


Small | 2008

Steam Purification for the Removal of Graphitic Shells Coating Catalytic Particles and the Shortening of Single‐Walled Carbon Nanotubes

Belén Ballesteros; Gerard Tobias; Lidong Shao; Eva Pellicer; J. Nogués; Ernest Mendoza; Malcolm L. H. Green

Purification and shortening of single-walled carbon nanotubes (SWNTs) is carried out by treatment with steam. During the steam purification the graphitic shells coating the catalytic metal particles are removed. Consequently, the exposed catalytic particles can be easily dissolved by treatment with hydrochloric acid. No damage to the carbon nanotube tubular structure is observed, even after prolonged treatment with steam. Samples are characterized by HRTEM, TGA, magnetic measurements, Raman spectroscopy, AFM, and XPS.


ACS Applied Materials & Interfaces | 2014

Building an Antifouling Zwitterionic Coating on Urinary Catheters Using an Enzymatically Triggered Bottom-Up Approach

Carlos Díaz Blanco; Andreas Ortner; Radostin Dimitrov; Antonio Navarro; Ernest Mendoza; Tzanko Tzanov

Catheter associated urinary tract infections are common during hospitalization due to the formation of bacterial biofilms on the indwelling device. In this study, we report an innovative biotechnology-based approach for the covalent functionalization of silicone catheters with antifouling zwitterionic moieties to prevent biofilm formation. Our approach combines the potential bioactivity of a natural phenolics layer biocatalytically conjugated to sulfobetaine-acrylic residues in an enzymatically initiated surface radical polymerization with laccase. To ensure sufficient coating stability in urine, the silicone catheter is plasma-activated. In contrast to industrial chemical methods, the methacrylate-containing zwitterionic monomers are polymerized at pH 5 and 50 °C using as an initiator the phenoxy radicals solely generated by laccase on the phenolics-coated catheter surface. The coated catheters are characterized by X-ray photoelectron spectroscopy (XPS), Fourier transformed infrared (FTIR) analysis, atomic force microscopy (AFM), and colorimetrically. Contact angle and protein adsorption measurements, coupled with in vitro tests with the Gram-negative Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus in static and dynamic conditions, mimicking the operational conditions to be faced by the catheters, demonstrate reduced biofilm formation by about 80% when compared to that of unmodified urinary catheters. The zwitterionic coating did not affect the viability of the human fibroblasts (BJ-5ta) over seven days, corresponding to the extended useful life of urinary catheters.


ACS Applied Materials & Interfaces | 2015

Quorum-Quenching and Matrix-Degrading Enzymes in Multilayer Coatings Synergistically Prevent Bacterial Biofilm Formation on Urinary Catheters

Kristina Ivanova; Margarida M. Fernandes; Antonio Francesko; Ernest Mendoza; Jamil Guezguez; Michael Burnet; Tzanko Tzanov

Bacteria often colonize in-dwelling medical devices and grow as complex biofilm communities of cells embedded in a self-produced extracellular polymeric matrix, which increases their resistance to antibiotics and the host immune system. During biofilm growth, bacterial cells cooperate through specific quorum-sensing (QS) signals. Taking advantage of this mechanism of biofilm formation, we hypothesized that interrupting the communication among bacteria and simultaneously degrading the extracellular matrix would inhibit biofilm growth. To this end, coatings composed of the enzymes acylase and α-amylase, able to degrade bacterial QS molecules and polysaccharides, respectively, were built on silicone urinary catheters using a layer-by-layer deposition technique. Multilayer coatings of either acylase or amylase alone suppressed the biofilm formation of corresponding Gram-negative Pseudomonas aeruginosa and Gram-positive Staphylococcus aureus. Further assembly of both enzymes in hybrid nanocoatings resulted in stronger biofilm inhibition as a function of acylase or amylase position in the layers. Hybrid coatings, with the QS-signal-degrading acylase as outermost layer, demonstrated 30% higher antibiofilm efficiency against medically relevant Gram-negative bacteria compared to that of the other assemblies. These nanocoatings significantly reduced the occurrence of single-species (P. aeruginosa) and mixed-species (P. aeruginosa and Escherichia coli) biofilms on silicone catheters under both static and dynamic conditions. Moreover, in an in vivo animal model, the quorum quenching and matrix degrading enzyme assemblies delayed the biofilm growth up to 7 days.


Nanotechnology | 2009

Plasma-activated multi-walled carbon nanotube-polystyrene composite substrates for biosensing.

César Fernández-Sánchez; Eva Pellicer; Jahir Orozco; Cecilia Jiménez-Jorquera; Laura M. Lechuga; Ernest Mendoza

Carbon nanotube-polymer composites have shown to be suitable materials for the fabrication of electrochemical transducers. The exposed surface of these materials is commonly passivated by a very thin layer of the polymer component that buries the conductive carbon particles. Working with multi-walled carbon nanotube-polystyrene (MWCNT-PS) composite structures, it was previously described how a simple low power oxygen plasma process produced an effective etching of the composite surface, thereby exposing the conductive surface of CNTs. This work shows how this plasma process not only gave rise to a suitable composite conductive surface for electrochemical sensing but simultaneously exposed and created a high density of oxygen-containing functional groups at both the CNT and the PS components, without affecting the materials mechanical stability. These chemical groups could be effectively modified for the stable immobilization of biological receptors. A detailed chemical characterization of the plasma-activated composite surface was possible using x-ray photoelectron spectroscopy. The material reactivity towards the tethering of a protein was studied and protein-protein interactions were then evaluated on the modified composite transducers by scanning electron microscopy. Finally, an amperometric immunosensor approach for the detection of rabbit Immunoglobulin G target analyte was described and a minimum concentration of 3 ng ml(-1) was easily measured.


Nanotechnology | 2008

Scalable fabrication of immunosensors based on carbon nanotube polymer composites

Ernest Mendoza; Jahir Orozco; Cecilia Jiménez-Jorquera; Ana Belén González-Guerrero; A. Calle; Laura M. Lechuga; César Fernández-Sánchez

In this work we present the fabrication and characterization of immunosensors based on polystyrene (PS)-multiwalled carbon nanotube (MWCNT) composites. The electrochemical properties of the sensors have been investigated and show that the surface area is increased upon addition of the MWCNT-PS layer. Furthermore, a plasma activation process is used to partially remove the PS and expose the MWCNTs. This results in a huge increase in the electrochemical area and opens up the possibility of binding biomolecules to the MWCNT wall. The MWCNTs have been functionalized covalently with a model antibody (rabbit IgG). The biosensors have been tested using amperometric techniques and show detection limits comparable to standard techniques such as ELISA.


Analytica Chimica Acta | 2008

Composite planar electrode for sensing electrochemical oxygen demand

Jahir Orozco; César Fernández-Sánchez; Ernest Mendoza; Mireia Baeza; Francisco Céspedes; Cecilia Jiménez-Jorquera

This work reports on the development of a graphite-polystyrene composite electrode of planar configuration, containing silver(II) oxide and copper(II) oxide catalysts (AgO-CuO), for the measurement of electrochemical oxygen demand (EOD). Optimisation studies of the composite composition as well as conditions for its processing on planar substrates and generation of an appropriate electrochemical active area resulted in the scalable fabrication of robust composite electrodes. These were evaluated with glucose as target analyte. They showed competitive low limits of detection in a linear concentration range from 5 mgL(-1) to 1400 mgL(-1) of O(2). Besides, they were stable for at least one year. The determination of EOD in wastewater samples coming from production lines of parenteral food and winemaking was successfully carried out.

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Tzanko Tzanov

Polytechnic University of Catalonia

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Antonio Francesko

Polytechnic University of Catalonia

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César Fernández-Sánchez

Spanish National Research Council

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Cecilia Jiménez-Jorquera

Spanish National Research Council

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Eva Pellicer

Spanish National Research Council

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Kristina Ivanova

Polytechnic University of Catalonia

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Margarida M. Fernandes

Polytechnic University of Catalonia

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Petya Petkova

Polytechnic University of Catalonia

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Jahir Orozco

University of California

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