INMdok (Leibniz Institute for New Materials)
Not a member yet
931 research outputs found
Sort by
Glycerylphytate as ionic crosslinker for 3D printing of multi-layered scaffolds with improved shape fidelity and biological features
Get PDFFabrication of intricate and long-term stable 3D polymeric scaffolds by 3D printing technique is still a challenge. The currently used polymeric materials need long post-printing processes and washing steps. In addition, highly concentrated solutions are necessary for maintaining shape fidelity after 3D deposition. This paper reports the fabrication of dual crosslinked 3D scaffolds using a low concentrated (<10 wt-%) ink of Gelatin Methacryloyl (GelMA)/Chitosan and a novel crosslinking agent, a glycerylphytate (G1Phy) to overcome the current limitations in the 3D printing field using hydrogels. The applied methodology consisted of a first ultraviolet light (UV) photopolymerization followed by a post-printing ionic crosslinking treatment with G1Phy. This crosslinker provides a robust framework and avoids the necessity of neutralization with strong bases. The blend ink showed shear-thinning behavior and excellent printability in the form of straight and homogeneous filament. UV curing was undertaken simultaneously to 3D deposition, which enhanced precision, shape fidelity (resolution ≈ 150 µm), and prevented from collapse of the subsequent printed layers (up to 28 layers). In the second step, the novel G1Phy ionic crosslinker agent provided swelling and long term stability properties to the 3D scaffolds. The multi-layered printed scaffolds were mechanically stable at physiological conditions for at least one month. Preliminary in vitro assays using L929 Fibroblasts showed very promising results in terms of adhesion, spreading, and proliferation in comparison to other phosphate-based traditional crosslinkers (i.e. TPP). We envision that the proposed combination of the blend ink and 3D printing approach can have widespread applications in the regeneration of soft tissues
3D Printing of a Reactive Hydrogel Bio-Ink Using a Static Mixing Tool
Get PDFHydrogel-based bio-inks have recently attracted more attention for 3D printing applications in tissue engineering due to their remarkable intrinsic properties, such as a cell supporting environment. However, their usually weak mechanical properties lead to poor printability and low stability of the obtained structures. To obtain good shape fidelity, current approaches based on extrusion printing use high viscosity solutions, which can compromise cell viability. This paper presents a novel bio-printing methodology based on a dual-syringe system with a static mixing tool that allows in situ crosslinking of a two-component hydrogel-based ink in the presence of living cells. The reactive hydrogel system consists of carboxymethyl chitosan (CMCh) and partially oxidized hyaluronic acid (HAox) that undergo fast self-covalent crosslinking via Schiff base formation. This new approach allows us to use low viscosity solutions since in situ gelation provides the appropriate structural integrity to maintain the printed shape. The proposed bio-ink formulation was optimized to match crosslinking kinetics with the printing process and multi-layered 3D bio-printed scaffolds were successfully obtained. Printed scaffolds showed moderate swelling, good biocompatibility with embedded cells, and were mechanically stable after 14 days of the cell culture. We envision that this straightforward, powerful, and generalizable printing approach can be used for a wide range of materials, growth factors, or cell types, to be employed for soft tissue regeneration
Liquid-phase electron microscopy : toward direct imaging of self-assembly processes in low-atomic number colloidal suspensions
Get PDFIt is of great technological interest to control the organization of nanoparticles (NPs) into functional devices that can make use of NP’s properties not found in the bulk form of the solid material. To this end, a major scientific challenge is to further elucidate inter-particle forces that govern spontaneous self-assembly processes in liquid suspensions. Liquid-phase electron microscopy (LPEM) can resolve morphological details of small objects in μm-thick liquid layers with nanometer resolution. The goal of this doctoral thesis has been to develop LPEM towards directly visualizing colloidal self-assembly processes in aqueous suspensions. As a model system, we used a colloidal binary system in which positively charged 30 nm nanoparticles (SiONP) form a shell around 100 nm, negatively charged polystyrene microspheres (PMS). Analytical calculations and Monte-Carlo simulations were performed to optimize experimental parameters and to validate contrast in data obtained with a scanning transmission electron microscope (STEM). The extent of radiolytic damage due to the electron beam (PMS) was directly analyzed from the image data and an acceptable dose range was defined. Within this range, the core-shell structure of the pre-assembled binary system was directly visualized. Finally, a novel liquid cell design was tested which enabled us to initiate colloidal assembly reactions in the confinement of the nanofluidic device.Es ist von großem technologischem Interesse, die Organisation von Nanopartikeln (NPs) in funktionellen Anlagen zu steuern. In diesem Kontext besteht eine große wissenschaftliche Herausforderung darin, die Kräfte zwischen den Partikeln, die die spontanen Selbstorganisationsprozesse (S-A) in flüssigen Suspensionen steuern, weiter aufzuklären. Die Flüssigphasen-Elektronenmikroskopie (LPEM) kann morphologische Details kleiner Objekte in μm-dicken Flüssigkeitsschichten im nm-Bereich auflösen. Ziel dieser Doktorarbeit war es, LPEM weiter zu entwickeln, um kolloidale S-A in wässrigen Suspensionen direkt sichtbar zu machen. Als Modellsystem verwendeten wir ein kolloidales Binärsystem, in dem positiv geladene 30-nm-Nanopartikel (SiONP) eine Hülle um negativ geladene 100-nm-Polystyrol-Mikrokugeln (PMS) bilden. Analytische Berechnungen und Monte-Carlo-Simulationen wurden durchgeführt, um experimentelle Parameter zu optimieren und die Kontrastbildung in rastertransmissionselektronenmikroskopischen Aufnahmen zu validieren. Das Ausmaß der radiolytischen Schädigung der PMS durch den Elektronenstrahl wurde anhand der Bilddaten analysiert, und ein akzeptabler Dosisbereich wurde definiert. Innerhalb dieses Bereichs wurde die Core-Shell-Struktur des vormontierten Binärsystems direkt visualisiert. Abschließend wurde ein neuartiges Flüssigkeitszelldesign getestet, das es uns ermöglichte, kolloidale S-A in der geschlossenen, nanofluidischen Vorrichtung zu initiieren und visualisieren
Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids
Get PDFNanoparticle superlattice films form at the solid-liquid interface and are important for mesoscale materials, but are notoriously difficult to analyze before they are fully dried. Here, the early stages of nanoparticle assembly were studied at solid-liquid interfaces using liquid-phase electron microscopy. Oleylamine-stabilized gold nanoparticles spontaneously formed thin layers on a silicon nitride (SiN) membrane window of the liquid enclosure. Dense packings of hexagonal symmetry were obtained for the first monolayer independent of the nonpolar solvent type. The second layer, however, exhibited geometries ranging from dense packing in a hexagonal honeycomb structure to quasi-crystalline particle arrangements depending on the dielectric constant of the liquid. The complex structures formed by the weaker interactions in the second particle layer were preserved, while the surface remained immersed in liquid. Fine-tuning the properties of the involved materials can thus be used to control the three-dimensional geometry of a superlattice including quasi-crystals
Silicon-Nanotube-Mediated Intracellular Delivery Enables Ex Vivo Gene Editing
Get PDFAbstract Engineered nano–bio cellular interfaces driven by vertical nanostructured materials are set to spur transformative progress in modulating cellular processes and interrogations. In particular, the intracellular delivery—a core concept in fundamental and translational biomedical research—holds great promise for developing novel cell therapies based on gene modification. This study demonstrates the development of a mechanotransfection platform comprising vertically aligned silicon nanotube (VA-SiNT) arrays for ex vivo gene editing. The internal hollow structure of SiNTs allows effective loading of various biomolecule cargoes; and SiNTs mediate delivery of those cargoes into GPE86 mouse embryonic fibroblasts without compromising their viability. Focused ion beam scanning electron microscopy (FIB-SEM) and confocal microscopy results demonstrate localized membrane invaginations and accumulation of caveolin-1 at the cell–NT interface, suggesting the presence of endocytic pits. Small-molecule inhibition of endocytosis suggests that active endocytic process plays a role in the intracellular delivery of cargo from SiNTs. SiNT-mediated siRNA intracellular delivery shows the capacity to reduce expression levels of F-actin binding protein (Triobp) and alter the cellular morphology of GPE86. Finally, the successful delivery of Cas9 ribonucleoprotein (RNP) to specifically target mouse Hprt gene is achieved. This NT-enhanced molecular delivery platform has strong potential to support gene editing technologies
Emerging Roles of 1D Vertical Nanostructures in Orchestrating Immune Cell Functions
Get PDFAbstract Engineered nano–bio cellular interfaces driven by 1D vertical nanostructures (1D-VNS) are set to prompt radical progress in modulating cellular processes at the nanoscale. Here, tuneable cell–VNS interfacial interactions are probed and assessed, highlighting the use of 1D-VNS in immunomodulation, and intracellular delivery into immune cells—both crucial in fundamental and translational biomedical research. With programmable topography and adaptable surface functionalization, 1D-VNS provide unique biophysical and biochemical cues to orchestrate innate and adaptive immunity, both ex vivo and in vivo. The intimate nanoscale cell–VNS interface leads to membrane penetration and cellular deformation, facilitating efficient intracellular delivery of diverse bioactive cargoes into hard-to-transfect immune cells. The unsettled interfacial mechanisms reported to be involved in VNS-mediated intracellular delivery are discussed. By identifying up-to-date progress and fundamental challenges of current 1D-VNS technology in immune-cell manipulation, it is hoped that this report gives timely insights for further advances in developing 1D-VNS as a safe, universal, and highly scalable platform for cell engineering and enrichment in advanced cancer immunotherapy such as chimeric antigen receptor-T therapy
Squalenyl Hydrogen Sulfate Nanoparticles for Simultaneous Delivery of Tobramycin and an Alkylquinolone Quorum Sensing Inhibitor Enable the Eradication of P. aeruginosa Biofilm Infections
Get PDFAbstract Elimination of pulmonary Pseudomonas aeruginosa (PA) infections is challenging to accomplish with antibiotic therapies, mainly due to resistance mechanisms. Quorum sensing inhibitors (QSIs) interfering with biofilm formation can thus complement antibiotics. For simultaneous and improved delivery of both active agents to the infection sites, self-assembling nanoparticles of a newly synthesized squalenyl hydrogen sulfate (SqNPs) were prepared. These nanocarriers allowed for remarkably high loading capacities of hydrophilic antibiotic tobramycin (Tob) and a novel lipophilic QSI at 30 % and circa 10 %, respectively. The drug-loaded SqNPs showed improved biofilm penetration and enhanced efficacy in relevant biological barriers (mucin/human tracheal mucus, biofilm), leading to complete eradication of PA biofilms at circa 16-fold lower Tob concentration than Tob alone. This study offers a viable therapy optimization and invigorates the research and development of QSIs for clinical use
High-performance aqueous rechargeable potassium batteries prepared via interfacial synthesis of a Prussian blue-carbon nanotube composite
Get PDFAqueous rechargeable batteries are sustainable energy storage devices with the potential to replace the current state-of-the-art organic phase secondary batteries. Electrode materials for secondary batteries are often based on composite structures, which combine an electronically conducting scaffold with an ionic conductor, whose properties define battery capacity. Optimal integration of these components can be challenging: here we describe a novel approach to prepare electrode materials based on growth at the liquid-liquid interface. This is illustrated with the synthesis of a carbon nanotube/Prussian blue nanocomposite as free-standing transparent thin films, which are applied as cathodes for aqueous rechargeable potassium batteries. Prussian blue is synthesized through an acid-induced decomposition of ferricyanide, promoted by an interfacial electron transfer from an organic phase donor (1,1′-dimethylferrocene) under ambient conditions. The interfacial synthesis yields selective growth of cubic Prussian blue crystals on the carbon nanotube walls, enhancing interaction between the ionic and electronically conducting components, and resulting in a self-assembled film at the liquid/liquid interface. The films are readily transferred to flexible membranes and applied as cathodes in an aqueous rechargeable K+ battery. Coin-cell devices with activated carbon anodes gave a capacity of 47.6 mAh g−1 at 0.25 A g−1 with an energy density of 33.75 Wh kg−
Double-Hydrophobic-Coating through Quenching for Hydrogels with Strong Resistance to Both Drying and Swelling
Get PDFAbstract In recent years, various hydrogels with a wide range of functionalities have been developed. However, owing to the two major drawbacks of hydrogels—air-drying and water-swelling—hydrogels developed thus far have yet to achieve most of their potential applications. Herein, a bioinspired, facile, and versatile method for fabricating hydrogels with high stability in both air and water is reported. This method includes the creation of a bioinspired homogeneous fusion layer of a hydrophobic polymer and oil in the outermost surface layer of the hydrogel via a double-hydrophobic-coating produced through quenching. As a proof-of-concept, this method is applied to a polyacrylamide hydrogel without compromising its mechanical properties. The coated hydrogel exhibits strong resistance to both drying in air and swelling in multiple aqueous environments. Furthermore, the versatility of this method is demonstrated using different types of hydrogels and oils. Because this method is easy to apply and is not dependent on hydrogel surface chemistry, it can significantly broaden the scope of next-generation hydrogels for real-world applications in both wet and dry environments
Hybrid Anodes of Lithium Titanium Oxide and Carbon Onions for Lithium-Ion and Sodium-Ion Energy Storage
Get PDFThis study demonstrates the hybridization of Li4Ti5O12 (LTO) with different types of carbon onions synthesized from nanodiamonds. The carbon onions mixed with a Li4Ti5Ox precursor for sol–gel synthesis. These hybrid materials are tested as anodes for both lithium-ion battery (LIB) and sodium-ion battery (SIB). Electrochemical characterization for LIB application is carried out using 1 m LiPF6 in a 1:1 (by volume) ethylene carbonate and dimethyl carbonate as the electrolyte. For lithium-ion intercalation, LTO hybridized with carbon onions from the inert-gas route achieves an excellent electrochemical performance of 188 mAh g−1 at 10 mA g−1, which maintains 100 mAh g−1 at 1 A g−1 and has a cycling stability of 96% of initial capacity after 400 cycles, thereby outperforming both neat LTO and LTO with onions obtained via vacuum treatment. The performance of the best-performing hybrid material (LTO with carbon onions from argon annealing) in an SIB is tested, using 1 m NaClO4 in ethylene/dimethyl/fluoroethylene carbonate (19:19:2 by mass) as the electrolyte. A maximum capacity of 102 mAh g−1 for the SIB system is obtained, with a capacity retention of 96% after 500 cycles