Nanoscale Polystyrene Research Articles

3D imaging photocatalytically degraded micro- and nanoplastics

Microplastics (MPs) and nanoplastics have been an emerging global concern, with hazardous effects on plant, animal, and human health. Their small size makes it easier for them to spread to various ecosystems and enter the food chain; they are already widely found in aqueous environments and within aquatic life, and have even been found within humans. Much research has gone into understanding micro-/nanoplastic sources and environmental fate, but less work has been done to understand their degradation. Photocatalytic degradation is a promising green technique that uses visible or ultraviolet light in combination with photocatalyst to degrade plastic particles. While complete degradation, reducing plastics to small molecules, is often the goal, partial degradation is more common. We examined microscale polyethylene (PE) (125–150 µm in diameter) and nanoscale polystyrene (PS) (∼300 nm in diameter) spheres both before and after degradation using multiple imaging techniques, especially electron tomography in addition to conventional electron microscopy. Electron tomography is able to image the 3D exterior and interior of the nanoplastics, enabling us to observe within aggregates and inside degraded spheres, where we found potentially open interior structures after degradation. These structures may result from differences in degradation and aggregation behavior between the different plastic types, with our work finding that PE MPs typically cracked into sharp fragments, while PS nanoplastics often fragmented into smoother, more curved shapes. These and other differences, along with interior and 3D surface images, provide new details on how the structure and aggregation of PE MPs and PS nanoplastics changes when degraded, which could influence how the resulting worn particles are collected or treated further.

Polystyrene size-dependent impacts on microbial decomposers and nutrient cycling in streams

The particle size of plastic is one of the most important factors influencing its ecotoxicity, but we are unclear about the effect of polystyrene (PS) particle size on microbial decomposers and consequent nutrient cycling in streams. Here, using microcosm experiments, we assessed how three PS sizes (50 nm, 1 μm, and 20 μm) influenced the process and consequences of leaf litter decomposition. Under acute exposure to 1 μm and 20 μm PS, fungal biomass significantly decreased, but microbial biomass significantly increased, indicating compensations may work between fungi and other microbial decomposers. After chronic exposure to 50 nm and 1 μm PS, the leaf decomposition rate decreased by 19.27 % and 15.22 %, respectively, due to the reduced microbial enzyme activity, fungal diversity, and dominance of Anguillospora. As a result, the regeneration of nutrients, especially phosphorus, was significantly depressed, which might influence the primary productivity of streams. Therefore, our results suggest that nanoscale PS has a greater impact on microbial activity, thus affecting their functioning in leaf litter decomposition and consequent nutrient cycling. The findings provide a data support for the risk assessment of plastic pollution in freshwater systems.

Size-dominated biotoxicity of microplastics laden with benzophenone-3 and ciprofloxacin: Enhanced integrated biomarker evaluation on mussels

Microplastics (MPs) are emerging pollutants with diverse sizes in aquatic environments. This paper investigates the toxicity of micron- and nano-scale polystyrene (50 μm, 5 μm, 0.5 μm) loaded with 2-hydroxy-4-methoxy-benzophenone (BP-3) and ciprofloxacin (CIP) by eight biomarker responses in mussels, perna viridis. The mussels were exposed to MPs and chemicals for 7 days before 7 days of depuration. Eight biomarkers were measured to determine biotoxicity over time by using the weighted integrated biomarkers index evaluation (EIBR). Mussels exposed to MPs on a daily basis demonstrated a cumulative toxic effect. The toxicity of MPs for mussels was inversely related to the size at which they can be ingested. Then toxicity was reversed when exposure was halted. EIBR mold has shown a significant difference in the biotoxicity of each biological level under different exposure scenarios. In general, the mussel toxicity influenced by BP-3 and CIP exposure without an adsorbent was insignificant. MPs laden with them increased the toxicity of mussels. Under condition of lower concentration of ECs (Emerging contaminants), the presence of MPs as a component of a combined pollutant in water dominated the biotoxicity for mussels. The EIBR assessment further validated that the biotoxicity of mussels was size-dependent. Its application simplified the biomarkers’ response index and enhanced the accuracy of evaluation by weighing on molecular, cellular and physiological level. Specifically, mussels were physiologically sensitive to nano-scale plastics, with nano-scale plastics causing a higher level of cellular immunity destruction and genotoxicity than micron-scale plastics. Enzymatic antioxidant systemswere upregulated based on size-differential plastics; however, the total antioxidant effect of non-enzymatic defenses appeared to be least affected by the size effect.

Ingested Polystyrene Nanospheres Translocate to Placenta and Fetal Tissues in Pregnant Rats: Potential Health Implications.

Recent studies in experimental animals found that oral exposure to micro- and nano-plastics (MNPs) during pregnancy had multiple adverse effects on outcomes and progeny, although no study has yet identified the translocation of ingested MNPs to the placenta or fetal tissues, which might account for those effects. We therefore assessed the placental and fetal translocation of ingested nanoscale polystyrene MNPs in pregnant rats. Sprague Dawley rats (N = 5) were gavaged on gestational day 19 with 10 mL/kg of 250 µg/mL 25 nm carboxylated polystyrene spheres (PS25C) and sacrificed after 24 h. Hyperspectral imaging of harvested placental and fetal tissues identified abundant PS25C within the placenta and in all fetal tissues examined, including liver, kidney, heart, lung and brain, where they appeared in 10-25 µm clusters. These findings demonstrate that ingested nanoscale polystyrene MNPs can breach the intestinal barrier and subsequently the maternal-fetal barrier of the placenta to access the fetal circulation and all fetal tissues. Further studies are needed to assess the mechanisms of MNP translocation across the intestinal and placental barriers, the effects of MNP polymer, size and other physicochemical properties on translocation, as well as the potential adverse effects of MNP translocation on the developing fetus.

Nanoporous membrane filter cascade for size‐selective analysis of nano‐ and microplastic particles

AbstractAnalytical routes for sampling and analysis of microplastic particles in the range of several 10 µm to 1000 µm are well established in environmental research. However, the current scientific efforts are targeting human health impact with an enhanced focus on nanoparticle analysis in drinking water, the food chain, and its disposition in the human body. A major challenge lies in the availability of cascade filter setups spanning several orders of magnitude down to 10 nm dimensions in a single filtration workflow allowing fast and reliable routines for size‐selective nano‐ and microplastic (NMP) particle analysis. In this work, we present a novel cascade filter system containing filters made of microporous Si (pore size >10 µm) and nanoporous Al2O3 (pore size 100 nm), thus realizing the corresponding NMP size selectivity. Inorganic filter materials are chosen due to their beneficial properties as substrates for NMP particle analysis, which are nonpolymer materials with high planarity for micro‐spectroscopy investigations. In our first experiments, we demonstrate the successful NMP size separation on Si and Al2O3 filter substrates. For this purpose, we implement a well‐defined NMP test material composed of a mixture of polyethylene terephthalate microplastic reference material and monodisperse nanoscale polystyrene particles. The NMP test material is applied in a laboratory filtration workflow for samples in liquid solution. Both filter stages are subsequently investigated with optical microscopy, electron microscopy (scanning electron microscopy), Raman spectroscopy, and scanning force microscopy (atomic force microscopy) to demonstrate their applicability as combined NMP particle analytic substrates. Here, we characterize the fundamental NMP properties such as particle shape, size, and spectroscopic fingerprints—optical and chemical—both qualitatively and quantitatively. Finally, requirements and limitations for a standardized NMP filtration and analytic workflow will be discussed.

Tri-templating Synthesis of Multilevel Mesoporous Silica Microspheres with a Complex Interior Structure for Efficient CO2 Capture and Catalysis.

Multilevel porous architectures with microscopic shape control and tailor-made complex structures offer great potential for various innovative applications, but their elaborate design and synthesis have remained a scientific and technological challenge. Herein, we report a simple and effective tri-templating method, in which microscale Pickering droplets, nanoscale polystyrene colloids (PS), and molecular cetyltrimethylammonium chloride micelles are synchronously employed, for the fabrication of such micro-nanohierarchical mesoporous silica microspheres. In this protocol, Pickering droplet-directed interfacial sol-gel growth and its spatially confined surfactant assembly-directed sol-gel coating on PS suspensions are coupled together, enabling the successful formation of structured mesoporous silica that consists of numerous nanocompartments enclosed by a permeable shell. By varying the quantity of PS colloidal templates, rational regulation of the complex interior structure is achieved. Also, ascribed to the multilevel arrangement, this peculiar architecture not only shows desirable fast mass transport of external molecules but also possesses easy handling ability. After loading with tetraethylenepentamine or enzyme species, the yielded microspherical CO2 sorbents or immobilized biocatalysts, respectively, exhibit enhanced CO2 capture capacity and enzymatic catalysis efficiency. Notably, taking advantage of their microscopic characteristics, the immobilized biocatalysts could be ideally packed in a fixed-bed reactor for long-term continuous-flow enzymatic reactions. This tri-templating strategy provides a new synthetic route to access other multilevel microscopic materials with fascinating complex structures and paves a way to promote their practical applications.

Nanoscale polystyrene intensified the microbiome perturbation and antibiotic resistance genes enrichment in soil and Enchytraeus crypticus caused by tetracycline

Defined as plastic debris with size of 1–1000 nm, nanoplastics might be potentially more hazardous than plastics with larger size. However, current studies of nanoplastics in terrestrial systems are still limited, especially for the understanding of the combined effects of nanoplastics and antibiotics on microbiome and antibiotic resistance genes (ARGs) in soil invertebrates under the agricultural soil ecosystem is largely unknown. Here, we used Enchytraeus crypticus as model species to study the effects of nanoscale polystyrene and tetracycline. We found that co-exposure to nanoscale polystyrene and tetracycline not only significantly lowered the reproduction rate and increased the body weight of E. crypticus, but also significantly decreased the microbial alpha diversity and disturbed the beta diversity of microbiome in agricultural soil and E. crypticus. Nanoscale polystyrene had limited impacts on soil microbiota either at phylum level or family level but significantly disturbed the microbiome of E. crypticus. More specifically, NPs mainly decreased the relative proportion of rare taxa rather than the dominant phyla, including Acidobacteria (from 2.66% to 0.57%), Chloroflexi (from 1.43% to 0.21%), and Gemmatinomades (from 0.69% to 0.07%) in E. crypticus. Furthermore, synergistic effects for microbiome in soil and E. crypticus were found with nanoscale polystyrene and tetracycline. Meanwhile, nanoscale polystyrene enhanced the toxicity of tetracycline and promoted the enrichment of ARGs, such as multidrug ARGs in soil, and Vancomycin ARGs, Tetracycline ARGs, MLSB ARGs and Chloramphenicol ARGs in E. crypticus. These results add to our understanding of the combined effects of nanoplastics and antibiotics on the microbiome and ARGs of soil invertebrates.

Modified Nanopolystyrene as a Plugging Agent for Oil-Based Drilling Fluids Applied in Shale Formation

Most nanoplugging agents have high surface free energy and tend to aggregate in oil-based drilling fluids (OBMs), failing to plug the nanopores in the formation. This paper introduces the synthesis and application of a surface-modified nanoscale polystyrene (NS) as a plugging agent for OBMs. With oleic acid acting as the surface modifier, the surface free energy of the NS can be effectively reduced, which is a crucial step in enhancing its dispersion stability in mineral oil. Besides, due to the nanoscale size and low surface free energy, NS adsorbing onto the rock surface could improve the contact angle of the mineral oil on the rock surface, reduce the imbibition amount of oil into the rock, and maintain the mechanical stability of the rock. The structure of NS was characterized by infrared spectroscopy and transmission electron microscopy. Thermal gravimetric analysis demonstrated that NS could resist up to 252 °C. The particle size distribution test showed that NS could maintain the nanoscale dispersion in mineral oil. NS could also increase the contact angle of mineral oil on the rock surface from 12 to 61° and reduce the oil spontaneous imbibition amount by 52.7%. After the addition of 2% NS to the base mud, the permeability plugging apparatus filtration loss was reduced by 67% compared with that of the base mud without NS, and in the pressure transmission test, the downstream pressure was still kept constant with no noticeable change after 60 h, showing an excellent plugging effect. Besides, after the rocks were immersed in the base mud and base mud containing 2% NS, the uniaxial compressive strength of the rock declined by 25.41 and 10.76%, respectively, indicating that NS could effectively alleviate the mechanical stability decrease of the rock.

Interfacial interaction between micro/nanoplastics and typical PPCPs and nanoplastics removal via electrosorption from an aqueous solution

Micro/nanoplastics have raised worldwide concern with extensive research on its transfer, toxicity and removal. However, the primary environmental process-adsorption of nanoplastics has not been uncovered since the discovery of nanosized plastics. Here, we synthesized nanoscale polystyrene (PS) particles with mean diameter of ∼40 nm to avoid unknown properties from purchased ones, and thoroughly investigated its adsorption towards two typical pharmaceuticals and personal care products (PPCPs) with distinct characteristics, which are antibiotic (ciprofloxacin) and endocrine disruptor (bisphenol-A). Moreover, UV radiation is applied to simulate aging process in natural cases, and the carbonyl index derived from FTIR spectra increased clearly from 0.183 to 0.387. The adsorption capacity at equilibrium of CIP and BPA increased from 0.15 to 4.07 to 4.92 and 8.71 mg/g after weathering, respectively. Besides, the effect of environmental factors (pH, humic acid, salinity and cations) was also studied. Furthermore, electrosorption technology is applied to remove nanoplastics in solution for the first time, with the capacity of 0.707 g nano-polystyrene/g AC and 0.322 g aged-nano-polystyrene/g AC, suggesting that adsorption under electric field is presumably a feasible tertiary treatment method targeted at nanoplastics in wastewater treatment plants (WWTPs).

Continuous Enrichment and Separation of Nanoparticles via Acoustic Streaming.

Enrichment and separation of Micro/Nano-scale specimens are fundamental requirements in biomedical researches. In this paper, we demonstrated a simple and efficient microfluidic chip for the continuous enrichment and separation of nanoscale polystyrene particles using the acoustic streaming induced by gigahertz(GHz) bulk acoustic waves(BAW). The bulk acoustic resonator released ultrahigh frequency (2GHz) acoustic waves into the fluid and triggered the acoustic streaming. The nanoparticles were continuous concentrated and segregated by the combination action of the viscosity force and the acoustic radiation force. The separation of 300 and 100 nm particles was achieved with the high purity (92.4%). These data contribute proof-in-principle that acoustic streaming is a label-free strategy that can be used to enrich and separate nanoscale specimens with high efficiency.

Enhanced Electrical Properties of Polyethylene-Graft-Polystyrene/LDPE Composites.

Nanocomposite dielectrics show a great potential application in high voltage direct current cables for their obvious improvements in electrical properties. In the present manuscript, nanocomposite composed of low-density polyethylene and nanoscale polystyrene particles is studied by using low-density polyethylene grafted with polystyrene molecule. Fourier-transform infrared spectra reveal successful grafting of the polystyrene molecule onto the low-density polyethylene chain and the scanning electron microscope image shows the homogeneously dispersed nanoscale polystyrene particles. The presence of the polystyrene nanoparticles obviously improves the dielectric properties, such as the direct current breakdown strength and space charge inhibition. The conductivity and thermally stimulated current characteristics imply the deep traps in the composite increase obviously. Density functional theory calculation reveals that the grafted polystyrene can accommodate both shallow and deep electron carriers, and the depth of the hole traps are as deep as 2.07 eV.

Do combined nanoscale polystyrene and tetracycline impact on the incidence of resistance genes and microbial community disturbance in Enchytraeus crypticus?

It has been proved that nanoplastics can effectively adsorb pollutants and thus influence their behavior and availability. The combined toxic effects of nanoplastic and its adsorbed pollutant on the soil fauna are still not well known. We used high-throughput quantitative PCR to explore the effects of oral nanoscale polystyrene and tetracycline exposure on antibiotic resistance genes in the soil invertebrate Enchytraeus crypticus, and used bacterial 16S rRNA gene amplification sequencing to examine the response of the microbiome of E. crypticus. After 14 days of tetracycline and nanoscale polystyrene exposure, we terminated exposure and monitored the restoration of ARGs and microbiome in the E. crypticus. Results showed that the number of ARGs, especially macrolide-lincosamide-streptogramin B (MLSB), tetracycline ARGs, as well as multidrug ARGs, increased with exposure to nanoscale polystyrene and tetracycline. The abundance of Aminoglycoside and Beta_Lactamase ARGs in E. crypticus also significantly increased. The exposure significantly perturbed the abundance of families Microbacteriaceae, Streptococcaceae, Enterobacteriaceae, Rhodocyclaceae and Sphinomonadaceae. After terminating exposure for 14 days, the diversity and abundance of ARGs were not completely restored, while the microbiome was not permanently changed but reversibly impacted.

Nanotopographical regulation of pancreatic islet-like cluster formation from human pluripotent stem cells using a gradient-pattern chip

Bioengineering approaches to regulate stem cell fates aim to recapitulate the in vivo microenvironment. In recent years, manipulating the micro- and nano-scale topography of the stem cell niche has gained considerable interest for the purposes of controlling extrinsic mechanical cues to regulate stem cell fate and behavior in vitro. Here, we established an optimal nanotopographical system to improve 3-dimensional (3D) differentiation of pancreatic cells from human pluripotent stem cells (hPSCs) by testing gradient-pattern chips of nano-scale polystyrene surface structures with varying sizes and shapes. The optimal conditions for 3D differentiation of pancreatic cells were identified by assessing the expression of developmental regulators that are required for pancreatic islet development and maturation. Our results showed that the gradient chip of pore-part 2 (Po-2, 200–300 nm diameter) pattern was the most efficient setting to generate clusters of pancreatic endocrine progenitors (PDX1+ and NGN3+) compared to those of other pore diameters (Po-1, 100–200 or Po-3, 300–400 nm) tested across a range of pillar patterns and flat surfaces. Furthermore, the Po-2 gradient pattern-derived clusters generated islet-like 3D spheroids and tested positive for the zinc-chelating dye dithizone. The spheroids consisted of more than 30% CD200 + endocrine cells and also expressed NKX6.1 and NKX2.2. In addition, pancreatic β- cells expressing insulin and polyhormonal cells expressing both insulin and glucagon were obtained at the final stage of pancreatic differentiation. In conclusion, our data suggest that an optimal topographical structure for differentiation to specific cell types from hPSCs can be tested efficiently by using gradient-pattern chips designed with varying sizes and surfaces. Statement of SignificanceOur study provides demonstrates of using gradient nanopatterned chips for differentiation of pancreatic islet-like clusters.Gradient nanopatterned chips are consisted of two different shapes (nanopillar and nanopore) in three different ranges of nano sizes (100–200, 200–300, 300–400 nm). We found that optimal nanostructures for differentiation of pancreatic islet-like clusters were 200–300 nm nano pores.Cell transplantation is one of the major therapeutic option for type 1 diabetes mellitus (DM) using stem cell-derived β-like cells. We generated 50 um pancreatic islet-like clusters in size, which would be an optimal size for cell transplantation. Futuremore, the small clusters provide a powerful source for cell therapy.Our findings suggest gradient nanopatterned chip provides a powerful tool to generate specific functional cell types of a high purity for potential uses in cell therapy development.

Effect of the Fabrication Parameters of the Nanosphere Lithography Method on the Properties of the Deposited Au-Ag Nanoparticle Arrays.

The nanosphere lithography (NSL) method can be developed to deposit the Au-Ag triangle hexagonal nanoparticle arrays for the generation of localized surface plasmon resonance. Previously, we have found that the parameters used to form the NSL masks and the physical methods required to deposit the Au-Ag thin films had large effects on the geometry properties of the nanoparticle arrays. Considering this, the different parameters used to grow the Au-Ag triangle hexagonal nanoparticle arrays were investigated. A single-layer NSL mask was formed by using self-assembly nano-scale polystyrene (PS) nanospheres with an average radius of 265 nm. At first, the concentration of the nano-scale PS nanospheres in the solution was set at 6 wt %. Two coating methods, drop-coating and spin-coating, were used to coat the nano-scale PS nanospheres as a single-layer NSL mask. From the observations of scanning electronic microscopy (SEM), we found that the matrixes of the PS nanosphere masks fabricated by using the drop-coating method were more uniform and exhibited a smaller gap than those fabricated by the spin-coating method. Next, the drop-coating method was used to form the single-layer NSL mask and the concentration of nano-scale PS nanospheres in a solution that was changed from 4 to 10 wt %, for further study. The SEM images showed that when the concentrations of PS nanospheres in the solution were 6 and 8 wt %, the matrixes of the PS nanosphere masks were more uniform than those of 4 and 10 wt %. The effects of the one-side lifting angle of substrates and the vaporization temperature for the solvent of one-layer self-assembly PS nanosphere thin films, were also investigated. Finally, the concentration of the nano-scale PS nanospheres in the solution was set at 8 wt % to form the PS nanosphere masks by the drop-coating method. Three different physical deposition methods, including thermal evaporation, radio-frequency magnetron sputtering, and e-gun deposition, were used to deposit the Au-Ag triangle hexagonal periodic nanoparticle arrays. The SEM images showed that as the single-layer PS nanosphere mask was well controlled, the thermal evaporation could deposit the Au-Ag triangle hexagonal nanoparticle arrays with a higher quality than the other two methods.

Improvement of a block co-polymer (PS-b-PMMA)-masked silicon etch profile using a neutral beam

Bottom-up block copolymer (BCP) lithography mediated by self-assembly of polystyrene (PS)/poly-methyl methacrylate (PMMA) is widely used as an alternative patterning method for various deep nanoscale devices, such as optical devices and transistors, replacing conventional top-down photolithography. However, the nanoscale BCP mask features formed on the substrates after direct self-assembly of BCP tend to be easily damaged during exposure to the following plasma processing. In this study, silicon masked with a nanoscale BCP mask (PS) was etched by irradiating with a Cl2/Ar neutral beam in addition to a Cl2/Ar ion beam, and the effect of a Cl2/Ar neutral beam instead of a Cl2/Ar ion beam on damage to the PS mask and the silicon etch characteristics of nanodevices was investigated. The results show that the use of a neutral beam instead of an ion beam decreased degradation of the BCP mask during etching; therefore, a more anisotropic silicon etch profile in addition to improved etch selectivity of silicon compared to the BCP mask was observed. Moreover, by using the neutral beam, the sidewall roughness and sidewall angle also improved due to the decreased surface charge and reduced damage to the nanoscale PS mask resulting from use of a highly directional radical beam instead of a conventional ion-based beam.

Fabrication of a Au–polystyrene sphere substrate with three-dimensional nanofeatures for surface-enhanced Raman spectroscopy

Methods for fabricating three-dimensional nanofeature arrays for surface-enhanced Raman spectroscopy (SERS) substrates were explored by combining the self-assembly of nanoscale polystyrene (PS) spheres with subsequent Au film ion sputter coating modulation. The substrate's nanoscale hot-spot features were controlled using the Au coating film thickness regulation and focused ion beam (FIB) nano-patterning regulation methods. Scanning electron microscopy and Raman spectroscopy were employed to analyze the substrate morphology and the enhancement mechanism of the three-dimensional SERS substrate. PS microspheres with diameters of 151nm and 360nm were coated with Au layers of different thicknesses ranging from 10nm to 270nm. The configuration of the Au–PS spheres can be regulated to hexagonal close packing with nanoscale V-shaped slits with a 10–20nm gap pattern. Nanoscale Au particles and clusters with a clear outline covered the surface of the PS spheres, in which the multiple-scale structures increase the specific surface area of the SERS-active substrate. Nanoscale cracks formed on the smaller Au–PS spheres with a diameter of 151nm, which also exhibited strong SERS activity. The substrate surface temperature regularly increased after Au coating, and the thermal expansion coefficient difference and PS glass transition properties were studied to explain the Au–PS spheres nanofeature configuration development. The fabricated Au–PS spheres SERS feature is a type of three-dimensional and highly ordered array, which can show Raman scattering characteristics by providing a SERS enhancement factor of greater than 107.

Subwavelength imaging of self-assembled triangular array through a silver superlens

Superlens nanolithography is a promising technique for patterning nanoscale structures because of its ability to overcome the diffraction limit. In this paper, subwavelength imaging of triangular particle array through a silver superlens is investigated. The superlens structure was optimized by means of the transfer transmission matrix method. The triangular array was obtained by self-assembly of nanoscale polystyrene spheres (PSS) and was successfully replicated into the photoresist. Experimental results show that the superlens structure provides at least 50nm resolution, about 1/7 of the incidence wavelength.

Étude des allergènes impliqués dans deux cas d’allergie à la pomme de terre fraîche

Superlens nanolithography is a promising technique for patterning nanoscale structures because of its ability to overcome the diffraction limit. In this paper, subwavelength imaging of triangular particle array through a silver superlens is investigated. The superlens structure was optimized by means of the transfer transmission matrix method. The triangular array was obtained by self-assembly of nanoscale polystyrene spheres (PSS) and was successfully replicated into the photoresist. Experimental results show that the superlens structure provides at least 50 nm resolution, about 1/7 of the incidence wavelength.

Large-scale SiO2 photonic crystal for high efficiency GaN LEDs by nanospherical-lens lithography

Wafer-scale SiO2 photonic crystal (PhC) patterns (SiO2 air-hole PhC, SiO2-pillar PhC) on indium tin oxide (ITO) layer of GaN-based light-emitting diode (LED) are fabricated via novel nanospherical-lens lithography. Nanoscale polystyrene spheres are self-assembled into a hexagonal closed-packed monolayer array acting as convex lens for exposure using conventional lithography instrument. The light output power is enhanced by as great as 40.5% and 61% over those of as-grown LEDs, for SiO2-hole PhC and SiO2-pillar PhC LEDs, respectively. No degradation to LED electrical properties is found due to the fact that SiO2 PhC structures are fabricated on ITO current spreading electrode. For SiO2-pillar PhC LEDs, which have the largest light output power in all LEDs, no dry etching, which would introduce etching damage, was involved. Our method is demonstrated to be a simple, low cost, and high-yield technique for fabricating the PhC LEDs. Furthermore, the finite difference time domain simulation is also performed to further reveal the emission characteristics of LEDs with PhC structures.

A novel assay for the quantification of internalized nanoparticles in macrophages

One of the most urgent requirements in nanotoxicology is a quantitative assessment of internalized nanomaterials in cells. We present an in vitro assay called ‘max-flat’ for the measurement of internalized particles in macrophages. Fluorescent polystyrene (PS) beads of diameters 1 µm, 500 nm, 200 nm, 100 nm and 20 nm were employed. Different concentrations of fibronectin (FN) coated substrates were tested to achieve a maximal cell spreading area and minimal nucleus height, hence ‘max-flat’. We found this cell spreading area depends on FN concentration, and it is independent of particle concentration. An optimal condition of FN was found at 2.5×10−3 mg/ml, and it was selected for the max-flat assay to assess the internalization of PS beads. Cells under these conditions neither generate reactive oxygen species nor show noticeable differences in pro-survival/pro-apoptotic signals. Confocal images were employed for the max-flat assay and we set the interval scanning for a Z-stack as nucleus height divided by particle diameter. The max-flat assay provided a significantly higher number of internalized particles and the saturation is reached faster for nano-scale PS beads. We show how the proposed max-flat assay clearly outperform existing techniques by providing easier, more precise and far more reliable access to the number of internalized nanoparticles in macrophages.