Bacterial cultures exposed to iron-doped apatite nanoparticles (IDANPs) prior to the introduction of antagonistic viruses experience up to 2.3 times the bacterial destruction observed in control cultures. Maximum antibacterial activity of these bacteria-specific viruses, or phage, occurs after bacterial cultures have been exposed to IDANPs for 1 hr prior to phage introduction, demonstrating that IDANP-assisted phage therapy would not be straight forward, but would instead require controlled time release of IDANPs and phage. These findings motivated the design of an electrospun nanofiber mesh treatment delivery system that allows burst release of IDANPs, followed by slow, consistent release of phage for treatment of topical bacterial infections. IDANPs resemble hydroxyapatite, a biocompatible mineral analogous to the inorganic constituent of mammalian bone, which has been approved by the Food and Drug Administration for many biomedical purposes. The composite nanofiber mesh was designed for IDANP-assisted phage therapy treatment of topical wounds and consists of a superficial, rapid release layer of polyethylene oxide (PEO) fibers doped with IDANPs, followed by inner, coaxial polycaprolactone / polyethylene glycol (PCL/PEG) blended polymer fiber layer for slower phage delivery. Our investigations have established that IDANP-doped PEO fibers are effective vehicles for dissemination of IDANPs for bacterial exposure and resultant increased bacterial death by phage. In this work, slower delivery of the phage behind IDANPs was accomplished using coaxial, electrospun fibers composed of PCL/PEG polymer blend.
Abstract:The fabrication of photonic and electronic structures and devices has directed the manufacturing industry for the last 50 years. Currently, the majority of small-scale photonic devices are created by traditional microfabrication techniques that create features by processes such as lithography and electron or ion beam direct writing. Microfabrication techniques are often expensive and slow. In contrast, the use of electrospinning (ES) in the fabrication of microand nano-scale devices for the manipulation of photons and electrons provides a relatively simple and economic viable alternative. ES involves the delivery of a polymer solution to a capillary held at a high voltage relative to the fiber deposition surface. Electrostatic force developed between the collection plate and the polymer promotes fiber deposition onto the collection plate. Issues with ES fabrication exist primarily due to an instability region that exists between the capillary and collection plate and is characterized by chaotic motion of the depositing polymer fiber. Material limitations to ES also exist; not all polymers of interest are amenable to the ES process due to process dependencies on molecular weight and chain entanglement or incompatibility with other polymers and overall process compatibility. Passive and active electronic and photonic fibers fabricated through the ES have great potential for use in light generation and collection in optical and electronic structures/ devices. ES produces fiber devices that can be combined with inorganic, metallic, biological, or organic materials for novel device design. Synergistic material selection and postprocessing techniques are also utilized for broad-ranging applications of organic nanofibers that span from biological to electronic, photovoltaic, or photonic. As the ability to electrospin optically and/or electronically active materials in a controlled manner continues to improve, the complexity and diversity of devices fabricated from this process can be expected to grow rapidly and provide an alternative to traditional resource-intensive fabrication techniques.
A novel fabrication technique for producing hybrid organic–inorganic perovskite impregnated poly(styrene) microfibers in situ in a melt electrospinner is presented. The relationship between the hybrid perovskite precursors, electrospun fiber morphology, and chemical phase domains was investigated using light microscopy, scanning electron microscopy, x-ray diffraction spectroscopy, and energy dispersive spectroscopy. The method was successful in producing composite microfibers and revealed information regarding the nature of encapsulated hybrid perovskites under higher-than-normal temperature conditions during the synthesis and subsequent annealing process.
The concentration of nitrate in natural surface waters by agricultural runoff remains a challenging problem in environmental chemistry. One promising denitrification strategy is to utilize photocatalysts, whose light-driven excited states are capable of reducing nitrate to nitrogen gas. We have synthesized and characterized pristine and silver-loaded graphitic carbon nitrides and assessed their activity for photocatalytic nitrate reduction at neutral pH. While nitrate reduction does occur on the pristine material, the silver cocatalyst greatly enhances product yields. Kinetic studies performed in batch photoreactors under both UV and visible excitation suggest that nitrate reduction to produce aqueous nitrite, ammonium, and nitrogen gas proceeds via a cooperative water reduction on the silver metal domains to produce adsorbed H atoms. By varying the percentage of silver loading onto the g-C 3 N 4 , the density of metal domains can be adjusted, which in turn tunes the reduction selectivity toward various products.
In this study, a new method for producing fibers with hybrid organic–inorganic perovskite (HOIP) cores and hydrophobic polystyrene shells via coaxial electrospinning is introduced. The presence of the HOIP, CH3NH3PbI3, was verified through the use of ultraviolet to visible spectroscopy and x-ray diffractography to confirm successful synthesis in situ. Morphologies of the coaxial fibers were investigated using scanning electron microscopy to confirm the core/shell geometry and assess the fiber diameter. Finally, the interaction of liquid water and the fiber mats was studied to assess improvements to moisture resistance garnered from encapsulation in coaxial electrospun fibers.
Electrospinning (ES) can readily produce polymer fibers with cross-sectional dimensions ranging from tens of nanometers to tens of microns. Qualitative estimates of surface area coverage are rather intuitive. However, quantitative analytical and numerical methods for predicting surface coverage during ES have not been covered in sufficient depth to be applied in the design of novel materials, surfaces, and devices from ES fibers. This article presents a modeling approach to ES surface coverage where an analytical model is derived for use in quantitative prediction of surface coverage of ES fibers. The analytical model is used to predict the diameter of circular deposition areas of constant field strength and constant electrostatic force. Experimental results of polyvinyl alcohol fibers are reported and compared to numerical models to supplement the analytical model derived. The analytical model provides scientists and engineers a method for estimating surface area coverage. Both applied voltage and capillary-to-collection-plate separation are treated as independent variables for the analysis. The electric field produced by the ES process was modeled using comsol Multiphysics software to determine a correlation between the applied field strength and the size of the deposition area of the ES fibers. matlab scripts were utilized to combine the numerical comsol results with derived analytical equations. Experimental results reinforce the parametric trends produced via modeling and lend credibility to the use of modeling techniques for the qualitative prediction of surface area coverage from ES.
A new organometallic halide perovskite (OHP) synthesis method, whereby a polymer melt is used to thermodynamically drive the reaction that forms OHP crystallites, is demonstrated. The synthesis method allows for the facile encapsulation of moisture-sensitive OHP without the loss of simplicity during fabrication, which makes OHP materials so attractive for the photovoltaic industry. Degradation of OHP crystallites embedded in a polystyrene matrix was studied using UV-Vis absorbance over a period of several days. The OHP crystallites degrade as a result of the reversible nature of the reaction that forms the crystallites. After the reversion to precursors (PbI2 and CH3NH3I) the CH3NH3I irreversibly degrades [2] allowing the degradation to be tracked via optical interrogation. Additionally, surface morphology and elemental analysis of fabricated samples was carried out using SEM/EDS techniques.
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