ABSTRACT
Activation of inflammasomes-immune system receptor sensor complexes that selectively activate inflammatory responses-has been associated with diverse human diseases, and many nanomedicine studies have reported that structurally and chemically diverse inorganic nanomaterials cause excessive inflammasome activation. Here, in stark contrast to reports of other inorganic nanomaterials, we find that nickel-cobalt alloy magnetic nanocrystals (NiCo NCs) actually inhibit activation of NLRP3, NLRC4 and AIM2 inflammasomes. We show that NiCo NCs disrupt the canonical inflammasome ASC speck formation process by downregulating the lncRNA Neat1, and experimentally confirm that the entry of NiCo NCs into cells is required for the observed inhibition of inflammasome activation. Furthermore, we find that NiCo NCs inhibit neutrophil recruitment in an acute peritonitis mouse model and relieve symptoms in a colitis mouse model, again by inhibiting inflammasome activation. Beyond demonstrating a highly surprising and apparently therapeutic impact for an inorganic nanomaterial on inflammatory responses, our work suggests that nickel- and cobalt-containing nanomaterials may offer an opportunity to design anti-inflammatory nanomedicines for the therapeutics of macrophage-mediated diseases.
ABSTRACT
Optical antireflection has been employed for a variety of applications in terahertz spectroscopy and detectors. However, current methods encounter challenges in terms of cost, bandwidth, structural complexity, and performance. In this study, a low-cost, broadband, and easily processed THz antireflection coating scheme based on the model of impedance-matching effect is proposed, using a 6 wt % d-sorbitol-doped poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (s-PEDOT:PSS) film. By adjusting the thickness of the s-PEDOT:PSS film, these biocompatible conductive polymers enable a significant reduction of Fresnel reflection and operate over a broad bandwidth between 0.2 and 2.2 THz. Applying the antireflective coating to the surface of the sample substrate and electro-optic probe crystal in THz spectroscopy and near-field imaging shows that the spectral resolution is significantly improved, and the devices exhibit more excellent intended performance. The findings of this study could aid in improving the measurement capability of various THz time-domain spectroscopy and imaging system.
ABSTRACT
Pancharatnam-Berry (PB) metasurfaces have demonstrated mighty capability to manipulate electromagnetic (EM) waves, and exhibited potential applications for devices with broadband and efficient functionality. However, it remains a challenge to simultaneously achieve broadband and efficient wavefront manipulation for terahertz (THz) components with simple profiles. Herein, we introduce a simple ultra-thin PB metasurface with superior properties in the THz region. The structure is composed of a simple metallic C-Shaped Split Ring Resonator (CSRR) patterned on a flexible polyimide support layer. It is verified that the circular transmission efficiency is close to the theoretical limit of the single-layer metasurface in the range of 0.6 - 1.2 THz. Furthermore, we design metasurfaces based on the PB meta-atoms with spatially rotated orientation to achieve beam steering and superposition of vortex waves. The results are basically in line with expectations, validating the good performances of our proposal. This simple and easily deployable metasurface will give rise to more possibilities for the design of THz functional devices.
ABSTRACT
Intracellular delivery of macromolecules is a critical procedure for biological research and drug discovery, including proteins, peptides, vaccines, antibodies and genes. The penetration of macromolecule therapeutics through the cell membrane to intracellular targets is a prerequisite for their biological activity, but most delivery systems rely on the endocytic pathway to enter the cell and confront an inability to escape from the lysosome. A profound understanding of the cellular internalization of transporting carriers can (i) optimize the design of drug delivery systems, (ii) maintain the biological activity of biomolecular drugs, (iii) improve the efficiency of intracellular macromolecule transport and release, (iv) bring new opportunities for the discovery of macromolecule therapeutics and treatment of refractory disease. This article summarizes the uptake pathway of intracellular delivery vehicles for macromolecule drugs, hoping to provide ideas and references for macromolecule therapeutics delivery systems.
