Silvia Irusta

Magnetically triggered nanocomposite membranes: a versatile platform for triggered drug release.

Drug delivery devices based on nanocomposite membranes containing thermoresponsive nanogels and superparamagnetic nanoparticles have been demonstrated to provide reversible, on-off drug release upon application (and removal) of an oscillating magnetic field. We show that the dose of drug delivered across the membrane can be tuned by engineering the phase transition temperature of the nanogel, the loading density of nanogels in the membrane, and the membrane thickness, allowing for on-state delivery of model drugs over at least 2 orders of magnitude (0.1-10 μg/h). The zero-order kinetics of drug release across the membranes permit drug doses from a specific device to be tuned according to the duration of the magnetic field. Drugs over a broad range of molecular weights (500-40000 Da) can be delivered by the same membrane device. Membrane-to-membrane and cycle-to-cycle reproducibility is demonstrated, suggesting the general utility of these membranes for drug delivery.

Mesoporous silica sphere-polysulfone mixed matrix membranes for gas separation.

A series of mixed matrix membranes were prepared comprising polysulfone Udel matrix and ordered mesoporous silica spheres as filler with loadings varying between 0 and 32 wt %. The interaction between the filler and the polymer was studied by scanning and transmission electron microscopy, thermogravimetry, differential scanning calorimetry and dynamic mechanical analyses, N2 porosity, X-ray photoelectron spectrometry, and attenuated total reflectance Fourier transform infrared spectroscopy. All these characterizations allowed us to infer an optimum interaction based on both the penetration of the polymer chains into the mesoporosity of the silica spheres and the establishment of hydrogen bondings between the hydroxyl-rich surface and the aryl ether groups of the polymer. An optimum loading of 8 wt % was found in terms of H2/CH4 separation performance. In addition, the optimum membrane was tested for CO2/N2 separation.

Development of Noncytotoxic Chitosan–Gold Nanocomposites as Efficient Antibacterial Materials

This work describes the synthesis and characterization of noncytotoxic nanocomposites either colloidal or as films exhibiting high antibacterial activity. The biocompatible and biodegradable polymer chitosan was used as reducing and stabilizing agent for the synthesis of gold nanoparticles embedded in it. Herein, for the first time, three different chitosan grades varying in the average molecular weight and deacetylation degree (DD) were used with an optimized gold precursor concentration. Several factors were analyzed in order to obtain antimicrobial but not cytotoxic nanocomposite materials. Films based on chitosan with medium molecular weight and the highest DD exhibited the highest antibacterial activity against biofilm forming strains of Staphylococcus aureus and Pseudomonas aeruginosa. The resulting nanocomposites did not show any cytotoxicity against mammalian somatic and tumoral cells. They produced a disruptive effect on the bacteria wall while their internalization was hindered on the eukaryotic cells. This selectivity and safety make them potentially applicable as antimicrobial coatings in the biomedical field.

Use of membranes in fischer-tropsch reactors

Water is one of the primary products in the Fischer-Tropsch (FT) process for the conversion of coal or natural gas derived synthesis gas to hydrocarbons. This reaction water oxidizes the FT active sites, thereby shortening, the catalyst life. For iron based catalysts it has the additional negative effect of inhibiting the reaction rate. A family of membranes has been developed for the highly selective in-situ removal of the FT reaction water. These membranes have proven to be effective at operating conditions typical of commercial fluidized and slurry bed FT reactors. The use of these membranes will not only result in longer FT catalyst life but also in a better reactor utilization.

Long-Lasting Antifouling Coating from Multi-Armed Polymer

We describe a new antifouling surface coating, based on aggregation of a short amphiphilic four-armed PEG-dopamine polymer into particles and on surface binding by catechol chemistry. An unbroken and smooth polymeric coating layer with an average thickness of approximately 4 μm was formed on top of titanium oxide surfaces by a single step reaction. Coatings conferred excellent resistance to protein adhesion. Cell attachment was completely prevented for at least eight weeks, although the membranes themselves did not appear to be intrinsically cytotoxic. When linear PEG or four-armed PEG of higher molecular weight were used, the resulting coatings were inferior in thickness and in preventing protein adhesion. This coating method has potential applicability for biomedical devices susceptible to fouling after implantation.

Smart Dressings Based on Nanostructured Fibers Containing Natural Origin Antimicrobial, Anti-Inflammatory, and Regenerative Compounds

A fast and effective wound healing process would substantially decrease medical costs, wound care supplies, and hospitalization significantly improving the patients’ quality of life. The search for effective therapeutic approaches seems to be imperative in order to avoid the aggravation of chronic wounds. In spite of all the efforts that have been made during the recent years towards the development of artificial wound dressings, none of the currently available options combine all the requirements necessary for quick and optimal cutaneous regeneration. Therefore, technological advances in the area of temporary and permanent smart dressings for wound care are required. The development of nanoscience and nanotechnology can improve the materials and designs used in topical wound care in order to efficiently release antimicrobial, anti-inflammatory and regenerative compounds speeding up the endogenous healing process. Nanostructured dressings can overcome the limitations of the current coverings and, separately, natural origin components can also overcome the drawbacks of current antibiotics and antiseptics (mainly cytotoxicity, antibiotic resistance, and allergies). The combination of natural origin components with demonstrated antibiotic, regenerative, or anti-inflammatory properties together with nanostructured materials is a promising approach to fulfil all the requirements needed for the next generation of bioactive wound dressings. Microbially compromised wounds have been treated with different essential oils, honey, cationic peptides, aloe vera, plant extracts, and other natural origin occurring antimicrobial, anti-inflammatory, and regenerative components but the available evidence is limited and insufficient to be able to draw reliable conclusions and to extrapolate those findings to the clinical practice. The evidence and some promising preliminary results indicate that future comparative studies are justified but instead of talking about the beneficial or inert effects of those natural origin occurring materials, the scientific community leads towards the identification of the main active components involved and their mechanism of action during the corresponding healing, antimicrobial, or regenerative processes and in carrying out systematic and comparative controlled tests. Once those natural origin components have been identified and their efficacy validated through solid clinical trials, their combination within nanostructured dressings can open up new avenues in the fabrication of bioactive dressings with outstanding characteristics for wound care. The motivation of this work is to analyze the state of the art in the use of different essential oils, honey, cationic peptides, aloe vera, plant extracts, and other natural origin occurring materials as antimicrobial, anti-inflammatory and regenerative components with the aim of clarifying their potential clinical use in bioactive dressings. We conclude that, for those natural occurring materials, more clinical trials are needed to reach a sufficient level of evidence as therapeutic agents for wound healing management.

Au-PLA nanocomposites for photothermally controlled drug delivery

Stimuli-responsive drug delivery systems were obtained by encapsulating near-infrared (NIR) sensitive hollow gold nanoshells (HGNs) together with the molecule to be released into biodegradable poly-lactic acid (PLA) sub-micron particles. The rapid heating of the PLA particles caused by NIR radiation enabled use of the PLA-HGN composites as a photo-triggered drug release system. Rhodamine was used as a test molecule to obtain release profiles under different irradiation conditions. HGNs (32 nm diameter, 4.5 nm shell thickness) were synthesized via galvanic replacement of cobalt nanoparticles, using poly(vinylpyrrolidone) (PVP) as a stabilizer. PLA-HGN sub-micron particles (with mean diameters around 200 nm) encapsulating rhodamine were obtained using the supercritical emulsion extraction (SEE) technique. A good gold dispersion and a loading efficiency around 50% in the polymeric matrix were obtained for different HGN loadings. The release rate could be tuned by controlling the intensity of NIR exposition. Rhodamine release was completed in less than 10 hours when applying intense NIR irradiation for a few minutes, whereas 12 days of release was necessary in its absence. The system also allowed rhodamine release in a pulsed pattern.

Effects of NO and solids on the oxidation of methane to formaldehyde

The selective oxidation of methane has been studied both in the presence and absence of solids (inert or catalysts) with and without NO added, at 1 bar of total pressure. NO enhances the yield to formaldehyde, while the solids favor its decomposition. These results, together with abundant literature data, show a maximum for formaldehyde yield of about 4.0%.

Comparison of Dust Release from Epoxy and Paint Nanocomposites and Conventional Products during Sanding and Sawing

The release of dust generated during sanding or sawing of nanocomposites was compared with conventional products without nanomaterials. Epoxy-based polymers with and without carbon nanotubes, and paints with different amounts of nano-sized titanium dioxide, were machined in a closed aerosol chamber. The temporal evolution of the aerosol concentration and size distribution were measured simultaneously. The morphology of collected dust by scanning electron microscopy was different depending on the type of nanocomposites: particles from carbon nanotubes (CNTs) nanocomposites had protrusions on their surfaces and aggregates and agglomerates are attached to the paint matrix in particles emitted from alkyd paints. We observed no significant differences in the particle size distributions when comparing sanding dust from nanofiller containing products with dust from conventional products. Neither did we observe release of free nanomaterials. Instead, the nanomaterials were enclosed or partly enclosed in the matrix. A source strength term Si (cm(-3) s(-1)) that describes particle emission rates from continuous sources was introduced. Comparison between the Si parameters derived from sanding different materials allows identification of potential effects of addition of engineered nanoparticles to a composite.

Development and application of perovskite‐based catalytic membrane reactors

The preparation and characterization of catalytic membranes containing La‐based perovskites are reported. The membranes were prepared by in situ crystallization of different perovskites inside a porous α‐alumina matrix. Preponderance of the Knudsen‐diffusion regime during membrane operation was obtained with perovskite loads of 2 wt% and higher. The catalytic membranes obtained were used as combustors of VOCs (toluene and methyl ethyl ketone) contained in air streams, at concentrations between 875 and 3450 ppmV, and space velocities of up to 27200 h-1. The membranes were operated in the flow‐through mode, which resulted in total VOC combustion at moderate temperatures.