Search

Functional materials with high porosity and hierarchical structures are highly demanded for numerous material applications. In this study a magnetic hybrid material derived from wood and superparamagnetic iron oxide nanoparticles (SPIONs), was synthesized by microwave-assisted thermal decomposition. This novel in situ functionalization approach resulted in a homogeneous distribution of the integrated inorganic component within the entire complex wood cell wall structure, which was previously not achieved. In a detailed investigation based on confocal Raman microscopy imaging, transmission electron microscopy, and optical microscopy the precipitated phase and the resulting hybrid structure were characterized. Magnetic measurements revealed the impact of the anisotropic wood scaffold on the integrated magnetic functionality and confirmed the isotropic superparamagnetic characteristics of the in situ precipitated nanoparticles. Therewith, it is clearly demonstrated, that the anisotropic properties of the obtained hybrid material result from the particle organization in the given spruce wood structure and no alteration of particle properties is induced by the presence of the lignocellulosic material.

[ES] Método para la regeneración de tejidos vegetales dañados. La presente invención proporciona un método para regenerar tejidos vegetales dañados. Dicho método está basado en el uso de celulosa, preferiblemente celulosa bacteriana (CB), la cual se aplica directamente sobre la zona dañada permitiendo su rápida cicatrización. La presente invención demuestra así el potencial regenerador de la celulosa, preferiblemente celulosa bacteriana, sobre heridas en plantas. En una realización preferida del método de la invención, se emplea la celulosa en combinación con nanopartículas de plata para, además de regenerar el tejido, prevenir y/o tratar infecciones bacterianas en el mismo., [EN] The present invention relates to a method for regenerating damaged plant tissues. The method is based on the use of cellulose, preferably bacterial cellulose (CB), which is applied directly to the damaged area, allowing same to heal rapidly. In this way, the present invention demonstrates the regenerative potential of cellulose, preferably bacterial cellulose, on plant wounds. In a preferred embodiment of the method of the invention, cellulose is combined with silver nanoparticles in order to regenerate tissue, and also to prevent and/or treat bacterial infections in the tissue.

[EN] The present invention relates to a method for regenerating damaged plant tissues. The method is based on the use of cellulose, preferably bacterial cellulose (CB), which is applied directly to the damaged area, allowing same to heal rapidly. In this way, the present invention demonstrates the regenerative potential of cellulose, preferably bacterial cellulose, on plant wounds. In a preferred embodiment of the method of the invention, cellulose is combined with silver nanoparticles in order to regenerate tissue, and also to prevent and/or treat bacterial infections in the tissue., [ES] Método para la regeneración de tejidos vegetales dañados. La presente invención proporciona un método para regenerar tejidos vegetales dañados. Dicho método está basado en el uso de celulosa, preferiblemente celulosa bacteriana (CB), la cual se aplica directamente sobre la zona dañada permitiendo su rápida cicatrización. La presente invención demuestra así el potencial regenerador de la celulosa, preferiblemente celulosa bacteriana, sobre heridas en plantas. En una realización preferida del método de la invención, se emplea la celulosa en combinación con nanopartículas de plata para, además de regenerar el tejido, prevenir y/o tratar infecciones bacterianas en el mismo.

Understanding the in vivo fate and transport of nanoparticles (NPs) is challenging, but critical. We review recent studies of metal and metal oxide NPs using the model organism Caenorhabditis elegans, summarizing major findings to date. In a joint transdisciplinary effort, we highlight underutilized opportunities offered by powerful techniques lying at the intersection of mechanistic toxicology and materials science. To this end, we firstly summarize the influence of exposure conditions (media, duration, C. elegans lifestage) and NP physicochemical properties (size, coating, composition) on the response of the worm to NP treatment. Next, we focus on the techniques employed to study NP entrance route, uptake, biodistribution and fate, emphasizing the potential of extending the toolkit available with novel and powerful techniques. Next, we review findings on several NP-induced biological responses, namely transport routes and altered molecular pathways, and illustrate the molecular biology and genetic strategies applied, critically reviewing their strengths and weaknesses. Finally, we advocate the incorporation of a set of minimal materials and toxicological science experiments that will permit meta-analysis and synthesis of multiple studies in the future. We believe this review will facilitate coordinated integration of both well-established and underutilized approaches in mechanistic toxicology and materials science by the nanomaterials research community.

Gold nanoparticles (AuNPs) are present in many man-made products and cosmetics and are also used by the food and medical industries. Tight regulations regarding the use of mammalian animals for product testing can hamper the study of the specific interactions between engineered nanoparticles and biological systems. Invertebrate models, such as the nematode Caenorhabditis elegans (C. elegans), can offer alternative approaches during the early phases of nanoparticle discovery. Here, we thoroughly evaluated the biodistribution of 11-nm and 150-nm citrate-capped AuNPs in the model organism C. elegans at multiple scales, moving from micrometric to nanometric resolution and from the organismal to cellular level. We confirmed that the nanoparticles were not able to cross the intestinal and dermal barriers. We investigated the effect of AuNPs on the survival and reproductive performance of C. elegans, and correlated these effects with the uptake of AuNPs in terms of their number, surface area, and metal mass. In general, exposure to 11-nm AuNPs resulted in a higher toxicity than the larger 150-nm AuNPs. NP aggregation inside C. elegans was determined using absorbance microspectroscopy, which allowed the plasmonic properties of AuNPs to be correlated with their confinement inside the intestinal lumen, where anatomical traits, acidic pH and the presence of biomolecules play an essential role on NP aggregation. Finally, quantitative PCR of selected molecular markers indicated that exposure to AuNPs did not significantly affect endocytosis and intestinal barrier integrity.

This work demonstrates the fabrication of partially mineralized scaffolds fabricated in 3D shapes using paper by folding, and by supporting deposition of calcium phosphate by osteoblasts cultured in these scaffolds. This process generates centimeter-scale free-standing structures composed of paper supporting regions of calcium phosphate deposited by osteoblasts. This work is the first demonstration that paper can be used as a scaffold to induce template-guided mineralization by osteoblasts. Because paper has a porous structure, it allows transport of O2 and nutrients across its entire thickness. Paper supports a uniform distribution of cells upon seeding in hydrogel matrices, and allows growth, remodelling, and proliferation of cells. Scaffolds made of paper make it possible to construct 3D tissue models easily by tuning material properties such as thickness, porosity, and density of chemical functional groups. Paper offers a new approach to study mechanisms of biomineralization, and perhaps ultimately new techniques to guide or accelerate the repair of bone.

A novel and convenient synthetic strategy for the preparation of magnetically responsive silica nanospheres decorated with mixed ligand protected gold nanoparticles is described. Gold nanoparticles are attached to the silica surface via stable amide bond formation. The hierarchical nanospheres show promising results as a reusable and efficient catalyst for esterification reactions and they can be recovered through a simple magnetic separation.

The variety of nanoparticles (NPs) used in biological applications is increasing and the study of their interaction with biological media is becoming more important. Proteins are commonly the first biomolecules that NPs encounter when they interact with biological systems either in vitro or in vivo. Among NPs, super-paramagnetic iron oxide nanoparticles (SPIONs) show great promise for medicine. In this work, we study in detail the formation, composition, and structure of a monolayer of bovine serum albumin (BSA) on SPIONs. We determine, both by molecular simulations and experimentally, that ten molecules of BSA form a monolayer around the outside of the SPIONs and their binding strength to the SPIONs is about 3.5 × 10−4 M, ten times higher than the adsorption of fetal bovine serum (FBS) on the same SPIONs. We elucidate a strong electrostatic interaction between BSA and the SPIONs, although the secondary structure of the protein is not affected. We present data that supports the strong binding of the BSA monolayer on SPIONs and the properties of the BSA layer as a protein-resistant coating. We believe that a complete understanding of the behavior and morphology of BSA-SPIONs and how the protein interacts with SPIONs is crucial for improving NP surface design and expanding the potential applications of SPIONs in nanomedicine.

The combination of iron oxide and gold in a single nanoparticle results in both magnetic and plasmonic properties that can stimulate novel applications in bio-sensing, medical imaging, or therapeutics. Microwave assisted heating allows the fabrication of multi-component, multi-functional nanostructures by promoting selective heating at desired sites. Recently, we reported a microwave-assisted polyol route yielding gold nanotriangles decorated with iron oxide nanoparticles. Here, we present an in-depth microstructural and compositional characterization of the system using scanning transmission electron microscopy (STEM) and electron energy loss spectroscopy (EELS). A method to remove the iron oxide nanoparticles from the gold nanocrystals and some insights on crystal nucleation and growth mechanisms are also provided.

Nanoparticles which surface adsorb proteins in an uncontrolled and non-reproducible manner will have limited uses as nanomedicinal products. A promising approach to avoid nanoparticle non-specific interactions with proteins is to design bio-hybrids by purposely pre-forming a protein corona around the inorganic cores. Here, we investigate, in vitro and in vivo, the newly acquired bio-identity of superparamagnetic iron oxide nanoparticles (SPIONs) upon their functionalization with a pre-formed and well-defined bovine serum albumin (BSA) corona. Cellular uptake, intracellular particle distribution and cytotoxicity were studied in two cell lines: adherent and non-adherent cells. BSA decreases nanoparticle internalization in both cell lines and protects the iron core once they have been internalized. The physiological response to the nanoparticles is then in vivo evaluated by oral administration to Caenorhabditis elegans, which was selected as a model of a functional intestinal barrier. Nanoparticle biodistribution, at single particle resolution, is studied by transmission electron microscopy. The analysis reveals that the acidic intestinal environment partially digests uncoated SPIONs but does not affect BSA-coated ones. It also discloses that some particles could enter the nematode's enterocytes, likely by endocytosis which is a different pathway than the one described for the worm nutrients. Statement of Significance Unravelling meaningful relationships between the physiological impact of engineered nanoparticles and their synthetic and biological identity is of vital importance when considering nanoparticles biomedical uses and when establishing their nanotoxicological profile. This study contributes to better comprehend the inorganic nanoparticles’ behavior in real biological milieus. We synthesized a controlled pre-formed BSA protein corona on SPIONs to lower unspecific cell uptake and decrease nanoparticle fouling with other proteins. Such findings may be of relev

Nanomaterials give rise to unique biological reactivity that needs to be thoroughly investigated. The quest for enhanced magnetic nanomaterials of different shapes, magnetic properties, or surface coatings continues for applications in drug delivery, targeting therapies, biosensing, and magnetic separation. In this context, the use of simple in vivo models, such as Caenorhabditis elegans, to biologically evaluate nanoparticles is currently in increasing demand as it offers low-cost and information-rich experiments. In this work, we evaluated how surface modification (citrate- and protein-coated) of superparamagnetic iron oxide nanoparticles (C-SPIONs and BSA-SPIONs, respectively) induces changes in their toxicological profile and biodistribution using the animal model C. elegans and combining techniques from materials science and biochemistry. The acute toxicity and nanoparticle distribution were assessed in two populations of worms (adults and larvae) treated with both types of SPIONs. After 24 h treatment, nanoparticles were localized in the alimentary system of C. elegans; acute toxicity was stronger in adults and larvae exposed to C-SPIONs rather than BSA-SPIONs. Adult uptake was similar for both SPION types, whereas uptake in larvae was dependent on the surface coating, being higher for BSA-SPIONs. Nanoparticle size was evaluated upon excretion, and a slight size decrease was found. Interestingly, all results indicate the protective effects of the BSA to prevent degradation of the nanoparticles and decrease acute toxicity to the worms, especially at high concentrations. We argue that this relevant information on the chemistry and toxicity of SPIONs in vivo could not be gathered using more classical in vitro approaches such as cell culture assays, thus endorsing the potential of C. elegans to assess nanomaterials at early stages of their synthetic formulations.

We report a novel hybrid T1/T2 dual MRI contrast agent by the encapsulation of SPIONs (T2 contrast agent) into an iron-based coordination polymer with T1-weighted signal. This new hybrid material presents improved relaxometry and low cytotoxicity, which make it suitable for its use as contrast agent for MRI.

Superparamagnetic iron oxide nanoparticles (SPIONs) are widely used for biological applications due to their unique properties compared to their bulk counterparts, simplified SPIONs stabilization protocols applicable for a wide spectra of biological media remains a challenging issue. In this work, SPIONs with different surface coatings, tetramethylammonium hydroxide-coated SPIONs (T-SPIONs), and citrate-coated SPIONs (C-SPIONs) were synthesized by a facile, rapid and cost effective microwave-assisted method. C-SPIONs show robust stability in biological media of phosphate buffered saline and Roswell Park Memorial Institute Medium, while destabilize in DMEM. T-SPIONs were found to aggregate rapidly and significantly in all tested media. Then, a modified pH adjusted-BSA adsorption protocol and an addition of excess trisodium citrate dihydrate (Na3Cit) were used to enhance their stability in the media. The BSA adsorption protocol showed great efficiency in stabilizing the dispersed state of both SPIONs in the tested media, while the addition of excess Na3Cit showed limited effect, and it was only applicable for C-SPIONs. The formed BSA layer on SPIONs could be imaged by negative staining TEM, and revealed by Cryo-TEM, FTIR, DLS, and the zeta potential measurements. Results indicated that BSA forms a monolayer of a thickness of about 3 ± 1 nm and BSA interacts with C-SPIONs and T-SPIONs through their coating, rather than by replacing them. This synthetic method and stabilization protocol offer a general methodology to obtain SPIONs with a variety of surfactants, stable in different biological media in few minutes. © 2014 Springer Science+Business Media.

© 2014, Springer Science+Business Media Dordrecht. Structural properties of bacterial cellulose (BC) depend on the microstructure of the material, which in turn is influenced by the bacterial strain. This paper reports the production of BC thin films from two bacterial strains, gluconacetobacter xylinus (GX) and gluconacetobacter europaeus (GE), and three methods of drying the films; at room temperature, freeze drying and supercritical drying. The porosity, transparency, water absorption capacity (WAC) and mechanical properties of the obtained films are further investigated. We conclude that materials with different properties can be fabricated by selecting the bacterial strain or the drying method. Supercritical drying of films of GE achieved mechanically robust and extremely light films, 0.05 g/mL, with up to 96 % of porosity, and with a WAC up 110 times their dried weight. We determined that materials resulting from GE strain are not much affected by the drying method. On the other hand, GX produced BC films more sensitive to the drying method used. Films are denser, 0.6–0.2 g/mL, with tunable porosity from 60 to 90 % and their maximum WAC is 66 times their dried weight.

In the title compound, 1,2-(SCH3)2-1,2-closo-C2B10H10 or C4H16B10S2, the methylsulfanyl groups are bonded to the C atoms of the 1,2-dicarba-closo-dodecaborane cage. The Ccage-Ccage distance is 1.8033 (18) Å and the S-Ccage-Ccage-S torsion angle is 1.07 (13)°. The Ccage-Ccage distance is compared with those in other 1,2-dicarba-closo-dodecaborane derivatives.