Nm In Diameter Research Articles

Towards fully electrically controlled domain-wall logic

Utilizing magnetic tunnel junctions (MTJs) for write/read and fast spin-orbit-torque (SOT)-driven domain-wall (DW) motion for propagation, enables non-volatile logic and majority operations, representing a breakthrough in the implementation of nanoscale DW logic devices. Recently, current-driven DW logic gates have been demonstrated via magnetic imaging, where the Dzyaloshinskii-Moriya interaction (DMI) induces chiral coupling between perpendicular magnetic anisotropy (PMA) regions via an in-plane (IP) oriented region. However, full electrical operation of nanoscale DW logic requires electrical write/read operations and a method to pattern PMA and IP regions compatible with the fabrication of PMA MTJs. Here, we study the use of a Hybrid Free Layer (HFL) concept to combine an MTJ stack with DW motion materials, and He+ ion irradiation to convert the stack from PMA to IP. First, we investigate the free layer thickness dependence of 100-nm diameter HFL-MTJ devices and find an optimal CoFeB thickness, from 7 to 10 Å, providing high tunneling magnetoresistance (TMR) readout and efficient spin-transfer torque (STT) writing. We then show that high DMI materials, like Pt/Co, can be integrated into an MTJ stack via interlayer exchange coupling with the CoFeB free layer. In this design, DMI values suitable for SOT-driven DW motion are measured by asymmetric bubble expansion. Finally, we demonstrate that He+ irradiation reliably converts the coupled free layers from PMA to IP. These findings offer a path toward the integration of fully electrically controlled DW logic circuits.

Synthesized uniform-different sizes silver nanoparticles using TSC and SBH simultaneously for antibacterial application

Silver nanoparticles (AgNPs) in the form of nanospheres from a few nm to 100 nm in diameter were synthesized in a controlled manner using a combination of two reducing agents: sodium borohydride (SBH) and trisodium citrate (TSC). The influence of the size of AgNPs on antibacterial activity was investigated with different concentrations of AgNPs on two types of bacteria: Pseudomonas aeruginosa (PA) and Staphylococcus aureus resistant (SA) while the positive control was Ampicillin (Amp) 50 μg/ml and the negative control was water. AgNPs were investigated for morphology, size and size distribution using transmission electron microscopy (TEM) and dynamic light scattering (DLS) measurements. The optical properties of the AgNPs were investigated by recording their UV–vis absorption spectra. The antimicrobial activity of AgNPs was determined using the disc diffusion method. The results showed that the antibacterial ability of AgNPs depends on both concentration and particle size. With a particle concentration of 50 μg ml−1, the antibacterial ability is the best. The smaller the particle size, the higher the antibacterial ability. The simultaneous use of two reducing agents TSC and SBH is the novelty of the article to synthesize AgNPs particles that are uniform in shape and size while controlling the particle size. On that basis, their antibacterial performance is increased.

The influence of electrodeposition potential on the chemical composition, structure and magnetic properties of FeCoNi nanowires

FeCoNi alloyed nanowires with diameters of 40 nm and 100 nm and a length of 6 µm were electrodeposited in the polycarbonate membranes at constant cathodic potentials ranging from −1.0 to −1.8 V. The increase in cathodic potential caused an increase in Ni content with a simultaneous decrease in Fe and Co concentrations. The samples showed an fcc structure (with a small hcp fraction observed in one sample) with a preferred growth along [111] direction, which changed to a [220] texture at higher deposition potentials. With the increase in Ni content, a shortening of the lattice parameters and an increase in the crystallite size were observed. Various chemical compositions resulted in the modification of the magnetic properties of nanowires. The magnetization saturation value increased with increasing cathodic potential for both types of nanowires. However, coercivity and squareness rose for samples with a diameter of 40 nm and fell down for 100 nm diameter nanowires. This specific behavior was explained based on dipolar interactions, which can be neglected in 40 nm diameter nanowires, due to the low membrane porosity.

Mechanism of Viral DNA Packaging in Phage T4 Using Single-Molecule Fluorescence Approaches.

In all tailed phages, the packaging of the double-stranded genome into the head by a terminase motor complex is an essential step in virion formation. Despite extensive research, there are still major gaps in the understanding of this highly dynamic process and the mechanisms responsible for DNA translocation. Over the last fifteen years, single-molecule fluorescence technologies have been applied to study viral nucleic acid packaging using the robust and flexible T4 in vitro packaging system in conjunction with genetic, biochemical, and structural analyses. In this review, we discuss the novel findings from these studies, including that the T4 genome was determined to be packaged as an elongated loop via the colocalization of dye-labeled DNA termini above the portal structure. Packaging efficiency of the TerL motor was shown to be inherently linked to substrate structure, with packaging stalling at DNA branches. The latter led to the design of multiple experiments whose results all support a proposed torsional compression translocation model to explain substrate packaging. Evidence of substrate compression was derived from FRET and/or smFRET measurements of stalled versus resolvase released dye-labeled Y-DNAs and other dye-labeled substrates relative to motor components. Additionally, active in vivo T4 TerS fluorescent fusion proteins facilitated the application of advanced super-resolution optical microscopy toward the visualization of the initiation of packaging. The formation of twin TerS ring complexes, each expected to be ~15 nm in diameter, supports a double protein ring-DNA synapsis model for the control of packaging initiation, a model that may help explain the variety of ring structures reported among pac site phages. The examination of the dynamics of the T4 packaging motor at the single-molecule level in these studies demonstrates the value of state-of-the-art fluorescent tools for future studies of complex viral replication mechanisms.

Enhancing the therapeutic potential of curcumin: a novel nanoformulation for targeted anticancer therapy to colorectal cancer with reduced miR20a and miR21 expression

Curcumin (Cur) possesses remarkable pharmacological properties, including cardioprotective, neuroprotective, antimicrobial, and anticancer activities. However, the utilization of Cur in pharmaceuticals faces constraints owing to its inadequate water solubility and limited bioavailability. To overcome these hurdles, there has been notable focus on exploring innovative formulations, with nanobiotechnology emerging as a promising avenue to enhance the therapeutic effectiveness of these complex compounds. We report a novel safe, effective method for improving the incorporation of anticancer curcumin to induce apoptosis by reducing the expression levels of miR20a and miR21. The established method features three aspects that, to our knowledge, have not been formally verified: (1) use of a novel formula to incorporate curcumin, (2) use of all biocompatible biodegradable materials to produce this formula without leaving harmful residues, and (3) an incorporation process at temperatures of approximately 50 °C. The formula was prepared from lecithin (LE), and chitosan (CH) with an eco-friendly emulsifying agent and olive oil as the curcumin solvent. The formula was converted to nanoscale through ultrasonication and probe sonication at a frequency of 20 kHz. Transmission electron microscopy showed that the nano formula was spherical in shape with sizes ranging between 49.7 nm in diameter and negative zeta potentials ranging from 28 to 34 mV. Primers miR20a and miR21 were designed for molecular studies. Nearly complete curcumin with an encapsulation efficiency of 91.1% was established using a straight-line equation. The nano formula incorporated with curcumin was used to prepare formulations that exhibited anticancer activities. The apoptosis pathway in cancer cells was activated by the minimum inhibitory concentration of the nano formula. These findings suggest the potential of this nanoformulation as an effective and selective cancer treatment that does not affect the normal cells.

Development of Hollow Gold Nanoparticles for Photothermal Therapy and Their Cytotoxic Effect on a Glioma Cell Line When Combined with Copper Diethyldithiocarbamate.

Gold-based nanoparticles hold promise as functional nanomedicines, including in combination with a photothermal effect for cancer therapy in conjunction with chemotherapy. Here, we synthesized hollow gold nanoparticles (HGNPs) exhibiting efficient light absorption in the near-IR (NIR) region. Several synthesis conditions were explored and provided monodisperse HGNPs approximately 95-135 nm in diameter with a light absorbance range of approximately 600-720 nm. The HGNPs were hollow and the surface had protruding structures when prepared using high concentrations of HAuCl4. The simultaneous nucleation of a sacrificial AgCl template and Au nanoparticles may affect the resulting HGNPs. Diethyldithiocarbamate (DDTC) is metabolized from disulfiram and is a repurposed drug currently attracting attention. The chelation of DDTC with copper ion (DDTC-Cu) has been investigated for treating glioma, and here we confirmed the cytotoxic effect of DDTC-Cu towards rat C6 glioma cells in vitro. HGNPs alone were biocompatible and showed little cytotoxicity, whereas a mixture of DDTC-Cu and HGNPs was cytotoxic in a dose dependent manner. The temperature of HGNPs was increased by NIR-laser irradiation. The photothermal effect on HGNPs under NIR-laser irradiation resulted in cytotoxicity towards C6 cells and was dependent on the irradiation time. Photothermal therapy by HGNPs combined and DDTC-Cu was highly effective, suggesting that this combination approach hold promise as a future glioma therapy.

Fabrication of gelatin coated polycaprolactone nanofiber scaffolds co-loaded with luliconazole and naringenin for treatment of Candida infected diabetic wounds

The current study focuses on the development of gelatin-coated polycaprolactone (PCL) nanofibers co-loaded with luliconazole and naringenin for accelerated healing of infected diabetic wounds. Inherently, PCL nanofibers have excellent biocompatibility and biodegradation profiles but lack bioadhesion characteristics, which limits their use as dressing materials. So, coating them with a biocompatible and hydrophilic material like gelatin can improve bioadhesion. The preparation of nanofibers was done with the electrospinning technique. The solid state characterization and in-vitro performance assessment of nanofibers indicate the formation of uniformly interconnected nanofibers of 200–400 nm in diameter with smooth surface topography, excellent drug entrapment, and a surface pH of 5.6–6.8. The antifungal study showed that the nanofiber matrix exhibits excellent biofilm inhibition activity against several strains of Candida. Further, in-vivo assessment of nanofiber performance on C. albicans infected wounds in diabetic rats indicated accelerated wound healing efficacy in comparison to gauge-treated groups. Additionally, a higher blood flow and rapid re-epithelialization of wound tissue in the treatment group corroborated with the results obtained in the wound closure study. Overall, the developed dual-drug-loaded electrospun nanofiber mats have good compatibility, surface properties, and excellent wound healing potential, which can provide an extra edge in the management of complex diabetic wounds.

Efficient CO2 photoreduction enabled by the one-dimensional (1D) porous structured NiTiO3 nanorods

In this study, porous, and hollow nanorods of NiTiO3 (NiTiO3 NRs-p: 2–3 μm in length and 400 nm in diameter) are successfully prepared using an ethylene glycol-mediated approach at room temperature (25 °C), followed by calcination at 700 °C in air environment. Their rough surfaces and accumulated holes are advantageous for adsorption and subsequent photoreduction of carbon dioxide (CO2) under UV–vis irradiation. The NiTiO3 NRs-p exhibit superior performance in terms of photoconversion of CO2 (purity 99.999 %, 100 mL/min) into gaseous CO (57.833 μmolg−1 h−1) and CH4 (24.33 μmolg−1 h−1) with an overall CO2 selectivity (SCO2) of 89 %. In contrast, the solid NiTiO3 nanorods (NiTiO3 NRs) exhibit moderate performance in CO2 reduction, producing CO (30.33 μmolg−1 h−1) and CH4 (11.50 μmolg−1 h−1) with a CO2 selectivity of SCO2 = 60 %. NiTiO3 NRs-p exhibits superior photocatalytic activity against CO2 over other NiTiO3 morphologies with similar physical and chemical properties (such as nanoparticles (NPs) and nanofibers (NFs). This enhancement in photocatalytic activity can be attributed to the porous texture and hollow rod-like structure of NiTiO3 NRs-p, which provides a larger number of active sites to promote rapid mass transport. This unique one-dimensional (1D) structure also facilitates the separation of photogenerated electron-hole pairs, as demonstrated experimentally. This study opens a new room for a simple and facile routes for the photocatalytic conversion of CO2 into solar fuels.

Electrochemical nanosensor based on Ag-doped TiO2 nanotubes for detecting ascorbic acid

This work describes the development of an electrochemical nanosensor for the quantitative determination of ascorbic acid (AA). The transducer and receptor system of the nanosensor is based on a silver-doped titanium oxide nanotube (Ag-TiO2NTs) electrode synthesized by a one-step electrochemical anodization method followed by an annealing treatment. The synthesis was carried out at a constant potential of 30 V for 45 min in an organic electrolyte in the presence of F- ions and the dopant. The obtained structure was then subjected to morphological and compositional analysis. In addition, its analytical response to ascorbic acid was evaluated. The analytical techniques employed included scanning electron microscopy (SEM), X-ray diffraction (DRX), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). The results demonstrate the growth of a highly ordered nanotube array with average dimensions of 80 nm, 19 nm and 1660 nm for diameter, wall thickness and length, respectively, and suggest a major composition of silver-doped titanium oxide. The synthesized Ag-TiO2NTs successfully recorded electroanalytical activity for ascorbic acid, with a non-reversible, diffusion-controlled, and mostly capacitive electrochemical profile. It showed low resistance to change transfer and registered a sensitivity of 216.24μA/(mM∙cm2) and a detection limit of 11.1 μM in a linear range of 840–4000 μΜ. The sensor demonstrated repeatability and reproducibility with RSD values of 5.5% and 2.8%, respectively. In addition, it showed selectivity for AA in the presence of glucose at AA/GLU values (1:1, 1:10 and 1:100).

Piezoelectric reverse osmosis (RO) membrane: Fabrication and anti-fouling effect

In this study, a novel piezoelectric RO membrane with vibrating mechanism when exposed to an electric field was developed. The vibration due to the piezoelectric effect can disturb the concentration polarization layer on the membrane surface and minimize membrane fouling. Polyvinylidene fluoride (PVDF) which has piezoelectric properties was selected as the porous substrate for a thin film composite (TFC) polyamide RO membrane in this study. Electrical poling was performed to enhance the piezoelectric properties of the PVDF substrate. RO membranes fabricated via interfacial polymerization using different PVDF substrates (i.e., with and without pre-wetting the PVDF substrate, with and without polyethylene terephthalate (PET) non-woven fabric support (denoted as NWF and no-NWF, respectively), with and without electrical poling) were systematically investigated. The results indicated that RO membrane fabricated on poled PVDF-NWF substrate shows reasonable pure water permeability of ∼2 LMH/bar and sodium chloride (NaCl, 2000 ppm) rejection of ∼98.9 % when tested at 15 bar. In the accelerated fouling study using colloidal silica particles (∼20 nm in diameter, 200 ppm with background of 2000 mg/L NaCl), when the RO membrane fabricated using both unpoled and poled PVDF-NWF substrates were excited with AC signal, membrane fouling was significantly reduced. These findings suggested that electrical poling may not be necessary for such piezoelectric RO membrane.

Metagenomic of Liver Tissue Identified at Least Two Genera of Totivirus-like Viruses in Molossus molossus Bats.

The Totiviridae family of viruses has a unique genome consisting of double-stranded RNA with two open reading frames that encode the capsid protein (Cap) and the RNA-dependent RNA polymerase (RdRpol). Most virions in this family are isometric in shape, approximately 40 nm in diameter, and lack an envelope. There are five genera within this family, including Totivirus, Victorivirus, Giardiavirus, Leishmaniavirus, and Trichomonasvirus. While Totivirus and Victorivirus primarily infect fungi, Giardiavirus, Leishmaniavirus, and Trichomonasvirus infect diverse hosts, including protists, insects, and vertebrates. Recently, new totivirus-like species have been discovered in fish and plant hosts, and through metagenomic analysis, a novel totivirus-like virus (named Tianjin totivirus) has been isolated from bat guano. Interestingly, Tianjin totivirus causes cytopathic effects in insect cells but cannot grow in mammalian cells, suggesting that it infects insects consumed by insectivorous bats. In this study, we used next-generation sequencing and identified totivirus-like viruses in liver tissue from Molossus molossus bats in the Amazon region of Brazil. Comparative phylogenetic analysis based on the RNA-dependent RNA polymerase region revealed that the viruses identified in Molossus bats belong to two distinct phylogenetic clades, possibly comprising different genera within the Totiviridae family. Notably, the mean similarity between the Tianjin totivirus and the totiviruses identified in Molossus bats is less than 18%. These findings suggest that the diversity of totiviruses in bats is more extensive than previously recognized and highlight the potential for bats to serve as reservoirs for novel toti-like viruses.

Green and efficient utilization of cellulose by in situ regenerating rod‐like cellulose crystals in dry blending rubber compounds

AbstractThe crystalline cellulose has captured much attention as reinforcement material in rubber composites, but no successful cases have been found till now. Here, a facile approach of cellulose utilization was proposed by in‐situ regenerating cellulose in dry rubber matrix. Cellulose was dissolved in ionic liquid (IL), and then directly mixed with dry rubber, silica, and other ingredients. Taking advantages of the strong interaction between IL and silica, the dissolution equilibrium of cellulose/IL was destroyed and resulted in the regeneration of cellulose crystals in rubber matrix. The regenerated cellulose appeared at dry blending stage, and showed an ideal rod‐like shape (10–100 nm in diameter and 200–500 nm in length). While it grew in size at curing stage, and finally reached 100–200 nm in diameter and 1–2 μm in length. The regenerated cellulose exhibited pronounced reinforcement efficiency. This methodology has no any waste liquid discharged, and has a promising use in the preparation of cellulose/rubber composites.Highlights Nanosized rod‐like cellulose was regenerated in dry rubber, instead of latex. Regeneration of cellulose was due to interaction between ionic liquid and silica. The in situ regenerated cellulose dispersed well in cured rubber compounds. The regenerated cellulose exhibited a good reinforcement efficiency in rubber. The whole machining process had no any waste liquid discharged.

Electrospun polyvinylidene fluoride with novel facile synthesized functionalized boron nitride quantum dots for neural applications

AbstractThe study aimed to develop a potential biomaterial for neuroregeneration by the electrospinning of the biocompatible polymer polyvinylidene fluoride (PVDF) with innovative functionalized boron nitride quantum dots (F‐BNQDs) synthesized via green chemistry using the amino acid taurine as a functionalization. The F‐BNQDs were characterized and were found to be 16–21 nm in diameter, showed good photoluminescent characteristics, and their elemental composition was confirmed by x‐ray photoelectron spectroscopy, Fourier‐transform infrared (FTIR), and ultraviolet spectroscopy. The PVDF with F‐BNQDs was prepared at three different concentrations, and the resulting electrospun fibers were characterized by scanning electron microscopy, FTIR, thermogravimetric analysis, contact angle, biodegradation, water uptake, Schwann cell cytotoxicity, and cell behavior studies. The results of the study showed that the addition of F‐BNQDs to PVDF resulted in enhanced mechanical properties, decreased contact angle, increased degradability, and water uptake. The lactate dehydrogenase assay revealed that 5% BN‐PVDF had the lowest cytotoxicity. Fluroscent 4',6‐diamidino‐2‐phenylindole (DAPI) staining showed that the increase in F‐BNQD concentration up to 5% BN‐PVDF enhanced cell behavior on the electrospun fibers. Therefore, the study concluded that 5% BN‐PVDF would be suitable for further testing as a potential biomaterial for neuroregeneration in vivo.Highlights Functionalized boron nitride quantum dots (F‐BNQDs) were prepared using amino acid taurine. The F‐BNQDs were characterized and electrospun with polyvinylidene fluoride (PVDF). The incorporation of F‐BNQDs to PVDF has enhanced its physicochemical properties. All samples showed a single βphase PVDF. Schwann cells showed excellent compatibility and cell adhesion on F‐BNQDs/PVDF.

Exploring the magnetic and magnetocaloric behavior of nanocrystalline melt-spun R2Fe17 (R = Pr, Nd) ribbons

Single-phase nanocrystalline R2Fe17 (R = Pr and Nd) ribbons with rhombohedral Th2Zn17-type crystalline structure (space group R3̅m) have been fabricated by melt-spinning technique. The microstructure of the polycrystalline ribbons is composed of quasi-spherical grains with an average size below 100 nm. Transmission electron microscopy reveals that these grains are formed by agglomeration of smaller nanocrystalline entities around 15 nm in diameter, separated by disordered boundaries where the long-range crystalline order is lost. Two different ferro-to-paramagnetic phase transitions are observed, one of them coincides with that of the parent bulk alloy (290 and 326 K for R = Pr and Nd, respectively), and the other one can be ascribed to the disordered boundaries (323 and 350 K for R = Pr and Nd, respectively). For R= Pr, this fact gives rise to a significant broadening (c.a. 120 K under a magnetic field change of 2 T) of the full-width at the half-maximum of the magnetic entropy change curve, |∆SM(T)| (that adopts a "table-like" shape), resulting in a considerable increase of the refrigerant capacity.

Alteration of zeta potential and cell viability in rat-derived L6 skeletal muscle cells and H9c2 cardiomyocytes: A study with submicron polystyrene particles.

Microand nanoplastics pollution can cause substantial damage to ecosystems. Since scientists have focused mainly on their impact on aquatic environments, less attention has been paid to the accumulation of polymer particles in terrestrial organisms. We checked if submicron (<5 mm) polystyrene (PS) particles, which can accumulate in living organisms, lead to changes in the physicochemical properties of mammalian cell membranes. The influence of submicron PS particles on the properties of rat-derived L6 myocytes and H9c2 cardiomyocytes was analyzed. Non-functionalized and amine-functionalized PS particles of 100 nm and 200 nm in diameter were used. The MTT assay was performed to evaluate the viability of the polymers-treated cells. The effect of short (6 h) and prolonged (48 h) incubation with different concentrations of PS particles on the cell's zeta (ζ) potential was examined with the electrophoretic light scattering technique (ELS). Polystyrene particles' physicochemical characteristics (size and stability) were performed using dynamic light scattering (DLS) and electrophoretic light scattering methods. The results show that submicron PS particles affect cell viability and cause changes in the physiochemical parameters of rat cell membranes. Differences were observed depending on the origin of the cells. We observed doseand time-dependent alterations in the studied parameters after submicron PS particle incubation in L6 myotubes and H9c2 cardiomyocytes. The size and modification of PS particle surfaces determine the extent to which they affect the analyzed properties of rat cardiomyocytes and myocytes membranes.

Bio-based phenolic branched-chain fatty acid in wash water reduced populations of Listeria innocua on apple fruit

Phenolic branched-chain fatty acid (PBC-FA) emulsion was produced by dissolving it in ethanol and mixing with water (pH 7). The resulting monodispersed emulsion droplets were approximately 200 nm in diameter. The stability of the emulsion was evaluated by storing it at 4 and 20 °C for 30 days. The antimicrobial activity of the PBC-FA emulsion was tested against Escherichia coli and Listeria innocua (8 log CFU/mL) by determining the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) using a microdilution method. The PBC-FA was effective against L. innocua with MIC and MBC of 14.1 μg/mL and caused membrane permeation as determined with SEM and Live/Dead cell assay, but was not effective against E. coli O157:H7 at the tested concentrations (5–250 μg/mL). We also evaluated PBC-FA emulsion's potential to be used as a wash against L. innocua inoculated on apples. The results showed that the 500 μg/mL PBC-FA emulsion with 5 % ethanol had equivalent antimicrobial activity (2–3 logs reductions) against L. innocua as the 20 μg/mL chlorine solution, a commonly used sanitizer. 500 μg/mL PBC-FA emulsion had better antimicrobial efficacy when organic matter (chemical oxygen demand: 9.0 g/L) was present compared to 20 μg/mL of chlorine. The effect of PBC-FA on the quality of the apples, was determined by measuring changes in color, firmness, and soluble solids content over a 14-day storage period at 20 °C. The quality of the apples was not affected by PBC-FA over the 14-day storage period, suggesting that PBC-FA emulsion can be used as a wash for apples without affecting their quality.

Uptake of Cyclodextrin Nanoparticles by Macrophages is Dependent on Particle Size and Receptor-Mediated Interactions.

Physiochemical properties of nanoparticles, such as their size and chemical composition, dictate their interaction with professional phagocytes of the innate immune system. Macrophages, in particular, are key regulators of the immune microenvironment that heavily influence particle biodistribution as a result of their uptake. This attribute enables macrophage-targeted delivery, including for phenotypic modulation. Saccharide-based materials, including polyglucose polymers and nanoparticles, are efficient vehicles for macrophage-targeted delivery. Here, we investigate the influence of particle size on cyclodextrin nanoparticle (CDNP) uptake by macrophages and further examine the receptor-mediated interactions that drive macrophage-targeted delivery. We designed and synthesized CDNPs ranging in size from 25 nm to >100 nm in diameter. Increasing particle size was correlated with greater uptake by macrophages in vitro. Both scavenger receptor A1 and mannose receptor were critical mediators of macrophage-targeted delivery, inhibition of which reduced the extent of uptake. Finally, we investigated the cellular bioavailability of drug-loaded CDNPs using a model anti-inflammatory drug, celastrol, which demonstrated that drug bioactivity is improved by CDNP loading relative to free drug alone. This study thus elucidates the interactions between the polyglucose nanoparticles and macrophages, thereby facilitating their application in macrophage-targeted drug delivery that has applications in the context of tissue injury and repair.

Light-enhanced catalytic activity of stable and large gold nanoparticles in homocoupling reactions.

Validating the direct photocatalytic activity of colloidal plasmonic nanoparticles is challenging due to their limited stability and needed support materials that can often contribute to the chemical reactions. Stable gold nanoparticles (AuNPs) with tunable sizes are prepared across porous polymer particles without any chemical bonds where the resulting composite particles exhibit intense surface plasmon resonances (SPRs) in the visible region. These composite particles are then tested as photocatalysts under a broadband solar-simulated light source to examine the contribution degree of photothermal heating and SPR coming from the incorporated AuNPs in the C-C bond forming homocoupling reaction. Generally, the thermal and photothermal heating are the main driving force to increase the reactivity of relatively smaller AuNPs (~ 44 nm in diameter) with a narrower SPR band. However, the SPR-induced catalytic activity is much greater for the composite particles containing larger AuNPs (~ 87 nm in diameter) with a broader SPR. As the polymer particle matrix does not influence the catalytic activity (e.g., inducing charge delocalization and/or separation), the unique SPR role of the colloidal AuNPs in the catalytic reaction is assessable under light irradiation. This study experimentally demonstrates the possibility of evaluating the direct contribution of SPRs to photocatalytic chemical reactions.

A comprehensive review of the medical and cosmetic applications of exosomes in dermatology.

Exosomes are a subset of extracellular vesicles that are released by all cell types and are theorized to play a crucial role in intercellular communication. Ranging from 40 to 160 nm in diameter, exosomes contain a variety of genetic materials including DNA, RNA, mRNA, metabolites, proteins, and lipids depending on their cellular origin. Given that intercellular communication is abetted by the exchange of cellular components via exosomes, their applied use can have important implications for disease pathology and exosome-based therapeutics. We provide a comprehensive review of the current application of exosomes in medical (and skin) diseases and in cutaneous medical aesthetics. A literature search was conducted on PubMed reviewing exosomes and their application in medical and aesthetic fields. While the therapeutic use of exosomes in the treatment of medical and cosmetic dermatological procedures is promising, it is also important to note that most studies implementing exosomes as therapeutic agents have been conducted in preclinical models, thus highlighting the need for additional studies and clinical trials. One more important note in the aesthetic world associated with exosomes is that in the United States, at the time of this writing, exosomes may only be topically applied and not injected into the skin, as is done in many countries worldwide. There is a need for additional studies and clinical trials to evaluate the safety and therapeutic effect and safety of exosomes in medical and aesthetic fields.

Atomic-scale observation of nucleation- and growth-controlled deformation twinning in body-centered cubic nanocrystals

Twinning is an essential mode of plastic deformation for achieving superior strength and ductility in metallic nanostructures. It has been generally believed that twinning-induced plasticity in body-centered cubic (BCC) metals is controlled by twin nucleation, but facilitated by rapid twin growth once the nucleation energy barrier is overcome. By performing in situ atomic-scale transmission electron microscopy straining experiments and atomistic simulations, we find that deformation twinning in BCC Ta nanocrystals larger than 15 nm in diameter proceeds by reluctant twin growth, resulting from slow advancement of twinning partials along the boundaries of finite-sized twin structures. In contrast, reluctant twin growth can be obviated by reducing the nanocrystal diameter to below 15 nm. As a result, the nucleated twin structure penetrates quickly through the cross section of nanocrystals, enabling fast twin growth via facile migration of twin boundaries leading to large uniform plastic deformation. The present work reveals a size-dependent transition in the nucleation- and growth-controlled twinning mechanism in BCC metals, and provides insights for exploiting twinning-induced plasticity and breaking strength-ductility limits in nanostructured BCC metals.