Tunable Multivalent Aptamer-Based DNA Nanostructures To Regulate Multiheteroreceptor-Mediated Tumor Recognition.

Precise mapping and regulation of cell surface receptors hold immense significance in disease treatment, such as cancer, infection, and neurodisorders, but also face enormous challenges. In this study, we designed a series of adjustable multivalent aptamer-based DNA nanostructures to precisely control their interaction with receptors in tumor cells. By profiling surface receptors on 12 cell lines using 10 different aptamers, we generated a heatmap that accurately distinguished between various tumor types based on multiple markers. We then incorporated these aptamers onto DNA origami structures to regulate receptor recognition, with patch-like structures demonstrating a tendency to be trapped on the cell surface and with tube-like structures showing a preference for internalization. Through precise control of aptamer species, valence, and geometric patterns, we found that multiheteroreceptor-mediated recognition not only favored the specific binding of nanostructures to tumor cells but also greatly enhanced intracellular uptake by promoting clathrin-dependent endocytosis. Specifically, we achieved over 5-fold uptake in different tumor cells versus normal cells using tube-like structures modified with different diheteroaptamer pairs, facilitating targeted drug delivery. Moreover, patch-like structures with triheteroaptamers guided specific interactions between macrophages and tumor cells, leading to effective immune clearance. This programmable multivalent system allows for the precise regulation of cell recognition using multiple parameters, demonstrating great potential for personalized tumor treatment.

Efficient treatment of surfactant containing wastewater by photocatalytic ozonation with BiPO4 nanorods.

In this study, monoclinic BiPO4 nanorods were fabricated by one-pot solvothermal method. Its catalytic capability in photocatalytic ozonation process was tested by degradation and mineralization of sodium dodecyl benzene sulfonate (SDBS) solution. The results demonstrated that the TOC removal rate was dramatically improved to 90.0% at 75 min for UV/O3/BiPO4 process, which was 4.9 and 3.8 times more than that of UV/BiPO4 and O3. Moreover, the pseudo-first-order kinetic constant (0.337 min-1) and mineralization rate (90.0%) for SDBS degradation using BiPO4 in UV/O3 process were 1.6 and 1.3 times as great as that of conventional TiO2 photocatalyst (0.206 min-1, 67.3%). The influence of BiPO4 dosage, O3 concentration initial pH and coexisted ions on SDBS degradation in UV/O3/BiPO4 process were also investigated. The outcome of quenching studies illustrated both ·OH and h+ contributed prominently to SDBS degradation in UV/O3/BiPO4 process, implying that high valence band position of BiPO4 could promote the synergism between photocatalysis and ozonation. The degradation pathway of SBDS was proposed by combination of intermediates analysis and DFT calculation. Real carwash wastewater was chosen as typical surfactant containing wastewater to explore the practical application of UV/O3/BiPO4 technology. During 30 min, COD and LAS removal efficiency reached 59.7% and 70.6%, respectively. The quality indices of effluent could meet the requirements for reuse of carwash water in Water Quality Standard for Urban Miscellaneous Use in China. Energy consumption in the process was calculated as 13.9 kW h m-3, which was about 3.6 and 2.2 times less than that of UV/BiPO4 and O3 process, respectively. The results suggest that UV/O3/BiPO4 system has an application potential for surfactant containing wastewater treatment or recycle.

The macro-economic and CO2 emissions impacts of COVID-19 and recovery policies in China.

The outbreak and ongoing evolution of the COVID-19 pandemic have dramatically impacted economic development and CO2 emissions. China is under simultaneous pressure to recover from the outbreak and meet its carbon reduction targets, and the government is endeavouring to stimulate economic recovery through fiscal and monetary policies. This paper uses a computable general equilibrium model to measure the impact on China's economic recovery and carbon emissions by incorporating the pandemic shock and related economic recovery policies of loan prime rate (LPR) and value-added tax (VAT) reduction. The study found that COVID-19 led to a simultaneous shock on China's supply and demand sides in which GDP dropped by 2.62% and carbon emissions fell by 2.53%, compared to the period prior to COVID-19. Although the LPR and VAT reduction effectively mitigated economic loss, the combined LPR and VAT reduction had a more substantial effect on boosting GDP than the single policies. The VAT cut expands production and was used to overcome supply-side shocks, while lowering LPR mitigates the damage of demand-side shocks. Compared to the VAT reduction policy, reduced LPR has smaller carbon emissions per unit of GDP output. Consequently, we recommend that the government concentrate on a combination of policies to navigate pandemic shocks, as the two economic stimulus policies are confirmed to complement one another in terms of strengths and shortcomings.

The Impacts of COVID-19 Shock on Intergenerational Income Mobility: Evidence from China.

The COVID-19 crisis has caused a huge negative shock to economic activities worldwide, leading to a reduction in income and changes in income distribution. Intergenerational mobility is an important indicator of sustainable social development. This paper explores the short-term impacts of the sudden COVID-19 pandemic on intergenerational income mobility and personal income in China. Using the variation in the number of confirmed cases across provinces, we construct a province-level pandemic intensity index and combine it with individual data from the China Family Panel Studies (CFPS). We apply a general difference-in-difference strategy to identify the causal effect of the pandemic on intergenerational income mobility. We find that personal income is positively related to parental income, and that the COVID-19 crisis has caused a decline in individual income and exacerbated intergenerational income persistence. A more intense COVID-19 pandemic shock is associated with a larger increase in intergenerational income elasticity and intergenerational income rank-rank slope. We found that with one standard deviation increase in local pandemic intensity, the intergenerational income elasticity increases by 0.315 and the intergenerational income rank-rank slope increases by 0.198 on average. The mechanism testing suggests that heterogeneous effects among different groups are the force underlying the results. Low-income, low-skilled, and low-parental-income individuals have suffered a more severe impact from the pandemic shock.

Nanoparticle Tracking in Single-Antiresonant-Element Fiber for High-Precision Size Distribution Analysis of Mono- and Polydisperse Samples.

Accurate determination of the size distribution of nanoparticle ensembles remains a challenge in nanotechnology-related applications due to the limitations of established methods. Here, a microstructured fiber-assisted nanoparticle tracking analysis (FaNTA) realization is introduced that breaks existing limitations through the recording of exceptionally long trajectories of rapidly diffusing polydisperse nanoparticles, resulting in excellent sizing precision and unprecedented separation capabilities of bimodal nanoparticle mixtures. An effective-single-mode antiresonant-element fiber allows to efficiently confine nanoparticles in a light-guiding microchannel and individually track them over more than 1000 frames, while aberration-free imaging is experimentally confirmed by cross-correlation analysis. Unique features of the approach are (i) the highly precise determination of the size distribution of monodisperse nanoparticle ensembles (only 7% coefficient of variation) and (ii) the accurate characterization of individual components in a bimodal mixture with very close mean diameters, both experimentally demonstrated for polymer nanospheres. The outstanding performance of the FaNTA realization can be quantified by introducing a new model for the bimodal separation index. Since FaNTA is applicable to all types of nano-objects down to sub-20 nm diameters, the method will improve the precision standard of mono- and polydisperse nanoparticle samples such as nano-plastics or extracellular vesicles.

Three-dimensional tracking of nanoparticles by dual-color position retrieval in a double-core microstructured optical fiber.

Elastic light scattering-based three-dimensional (3D) tracking of objects at the nanoscale level is essential for unlocking the dynamics of individual species or interactions in fields such as biology or surface chemistry. In this work, we introduce the concept of dual-color 3D tracking in a double-core microstructured optical fiber that for the first time allows for full 3D reconstruction of the trajectory of a diffusing nanoparticle in a water-filled fiber-integrated microchannel. The use of two single-mode cores provides two opposite decaying evanescent fields of different wavelengths within the microchannel, bypassing spatial domains of ambiguous correlation between the scattered intensity and position. The novelty of the fiber design is the use of two slightly different single-mode cores, preventing modal crosstalk and thus allowing for longitudinally invariant dual-color illumination across the entire field of view. To demonstrate the capabilities of the scheme, a single gold nanosphere (80 nm) diffusing in the water-filled microchannel was tracked for a large number of images (about 32 000) at a high frame rate (1.389 kHz) over a long time (23 s), with the determined hydrodynamic diameters matching expectations. The presented 3D tracking approach yields unique opportunities to unlock processes at the nanoscale level and is highly relevant for a multitude of fields, particularly within the context of understanding sophisticated interaction of diffusing species with functionalized surfaces within the context of bioanalytics, nanoscale materials science, surface chemistry or life science.

Pharmacokinetics, plasma protein binding, and metabolism of a potential natural chemosensitizer from Marsdenia tenacissima in rats.

ETHNOPHARMACOLOGICAL RELEVANCE: Marsdenia tenacissima (Roxb.) Wight et Arn is a medicinal plant mainly distributed in southwest China. It is used in folk medicine for the treatment of tumors and is synergistic with chemotherapies. In our previous study, 11α-O-2-methybutyryl-12ß-O-tigloyl-tenacigenin B (MT2), a main steroid aglycone isolated from the total aglycones of M. tenacissima, significantly enhanced the in vivo antitumor effect of paclitaxel in mice bearing human tumor xenografts, showing its potential as a chemosensitizer. However, the pharmacokinetic characteristics, plasma protein binding rate, and metabolic profile of MT2 remain unclear. AIM OF THE STUDY: To elucidate the pharmacokinetic characteristics, plasma protein binding rate, and metabolic profile of MT2 in rats. MATERIALS AND METHODS: MT2 in rat plasma and phosphate-buffered saline was quantified using ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method, while the MT2 metabolites in rat liver microsomes were analyzed using UPLC-triple time-of-flight MS/MS. RESULTS: For intravenously administered MT2, the maximum plasma concentration and the area under the plasma concentration-time curve indicated dose dependency, while the elimination half-life time, the mean residence time, apparent volume of distribution and total apparent clearance values remained relatively unchanged in both the 5 mg/kg and 10 mg/kg groups. For orally administered MT2, the bioavailability was 1.08-1.11%. In rat plasma, MT2 exhibited a protein binding rate of 93.84-94.96%. In rat liver microsomes, MT2 was metabolized by oxidation alone or in combination with demethylation, and five MT2 metabolites were identified. CONCLUSION: MT2 has low oral bioavailability and a high plasma protein binding rate in rats. After administration, MT2 is transformed into oxidative metabolites in the liver. To achieve a high blood concentration of MT2, it should be administered intravenously. These findings would serve as a reference for further MT2-based pharmacological study and drug development.

Role of the biochar modified with ZnCl2 and FeCl3 on the electrochemical degradation of nitrobenzene.

The Zn/Fe-modified biochar on nitrobenzene (NB) removal during the electrolysis was investigated in this study. Both the Fe and Zn-modified biochar enhanced the NB adsorption compared with the un-modified biochar due to their greater specific surface area and more abundant surface function groups, respectively. The electrolysis under 2-11 V with the assist of both Fe/Zn-modified biochar achieved effective NB removal (>93%). The removal rate under 2 V using Zn/Fe-modified biochar (∼94%) was higher than that of the un-modified biochar (∼80%), whereas the removal was similar for those under 5, 8 and 11 V. The NB removal under 2 and 5 V was attributed to both adsorption and electrochemical decomposition of NB molecules. Electrolysis under 5 V by Fe-modified biochar had a higher degree of NB mineralisation than that using un-modified and Zn-modified biochar. This was likely that the Fe-modified biochar exhibited higher electrocatalytic properties, facilitating the further NB mineralisation. The ∙OH played significant roles in the degradation of NB by Fe-modified and un-modified biochar but did not significantly participated for the test using Zn-modified biochar. This was possibly because the Zn-modified biochar could adsorb greater amounts of ∙OH into the inner pores of Zn-modified biochar via its greater porosity and specific surface area, which may prevent the contact between ∙OH and NB molecules.

Challenge for the detection of microplastics in the environment.

As an emerging contaminant in the environment, microplastics have attracted worldwide attention. Although research methods on microplastics in the environment have been reported extensively, the data on microplastics obtained cannot be comparable due to different methods. In this work, we critically reviewed the analytical methods of microplastics, including sample collection, separation, identification, and quantification. Manta trawl and tweezers or cassette corers are used to collect water samples and sediments, respectively. For biota sample, internal organs need to be dissected and separated to obtain microplastics. Density differences are often used to separate microplastics from the sample matrix. Visual classification is one of the most common methods for identifying microplastics, and it can be better detected by combining it with other instruments. However, they are not suitable for detection nanoplastics, which may lead to underestimation of risk. The abundance of microplastics varies with the detection method. Thus, the analytical methods for microplastics need to be standardized as soon as possible. Meanwhile, new methods for analyzing nanoplastics are urgently needed. PRACTITIONER POINTS: Sampling, separation, identification, and quantification are important procedures. The sampling and separation methods for microplastics need to be standardized. The organic matter can be removed by digestion to facilitate identification. Combine microscope with analytical instruments to better identify microplastics. There is still a challenge to quantification of smaller-sized plastic particles.

Hydrophobic Magnetic Porous Material of Eichhornia crassipes for Highly Efficient Oil Adsorption and Separation.

Many oil adsorption materials are composed of nonrenewable raw materials, and their disposal can increase resource consumption and cause new environmental pollution. In this paper, the carbonized Eichhornia crassipes (CEC) were immobilized with Fe3O4 magnetic nanoparticles and modified with 1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane (PFOS) to prepare an oil adsorption material, referred to here as CEC/Fe3O4/PFOS. The magnetic and mechanical strength of the CEC was enhanced by adding Fe3O4 magnetic particles, which enable it efficient to dispose the oil/water solution. CEC/Fe3O4/PFOS shows high porosity (83.53%), low skeletal density (0.487 g/cm3), excellent magnetism, ultrahigh oil absorption capacity (49.94-140.90 g/g), hydrophobic performances with a water contact angle of 150.1 ± 2.3°, and a sliding angle of 10.5°. It is worth noting that the material can be recycled, and the absorbed oil is obtained by distillation. Therefore, this work may provide a candidate for solving the problem of oil pollution using E. crassipes.

In situ surface-enhanced Raman spectroscopy for detecting microplastics and nanoplastics in aquatic environments.

The detection of microplastics and nanoplastics in the environment, especially plastic particles in aquatic environments in situ, still faces challenges due to the limitations of current methods, instruments and size of plastic particles. This paper evaluates the potential of surface-enhanced Raman spectroscopy for the analysis of microplastics and nanoplastics. The condition of different tests including the volume ratio of sample to silver colloid, the concentrations of NaCl, and the concentrations of the samples, are assessed for the study of microplastics and nanoplastics (polystyrene (PS), polyethylene (PE) and polypropylene (PP)) in pure water and seawater. A method based on SERS, that uses silver colloid as the active substrate, is developed for the qualitative analysis of microplastics and nanoplastics in aquatic environments. The particle sizes of microplastics and nanoplastics include 100 nm, 500 nm and 10 µm. The Raman signals of microplastics and nanoplastics in pure water and seawater both show good enhancement efficiency. The optimal enhancement factor is 4 × 104. The SERS-based detection method overcomes the limitations of microplastics and nanoplastics in liquids and can detect 100 nm plastics down to 40 µg/mL. It provides more possibility for the rapid detection of microplastics and nanoplastics in aquatic environments in the future.

Investigating the composition and distribution of microplastics surface biofilms in coral areas.

In recent years, global climate change and pollution of the marine environment have caused large-scale coral deaths and severe damages to coral reef ecosystems. Numerous studies have shown that coral diseases are closely related to microorganisms. And microplastics (MPs) are a potential threat to corals. In marine ecosystems, MPs are an emerging contaminant. MPs have a strong adsorption effect on pollutants in the water environment, and they are very easily colonized by microorganisms to form biofilms. Biofilms may accumulate many pathogens, increasing the probability of coral disease. However, there is no report about the composition of biofilms on the surface of microplastics in coral growth areas. In this study, nine kinds of MPs were chosen in the experiments, which are commonly found in the ocean. Four stakeout points were selected in the coral area. Biofilms were cultivated in natural environment. The composition and distribution of biofilms on the surface of the MPs were analyzed by 16 S rRNA sequencing. The characteristics of biofilms were observed by scanning electron microscopy (SEM). The experimental results show that the species composition and abundance distribution of the biofilm on the MP surface are significantly different from the surrounding seawater. The type of MPs and the stake out point are important factors affecting the structure of the biofilm bacterial community. Compared to seawater samples, MPs are enriched with certain dominant bacteria such as Vibrionaceae, Rhodobacteraceae, Flavobacteraceae, Microtrichaceae and Sphingomonadaceae. Among them, Vibrionaceae, Rhodobacteraceae and Flavobacteraceae are closely related to the tissue damage of stony corals, and Vibrios are also the main pathogens of coral albinism. In addition, Pseudomonas and Bbellvibrio cholerae are also detected on the MPs biofilm. SEM graphs of the MPs after culture could clearly observe rod-shaped bacteria and Streptococci. This study can provide a new direction for the study of coral toxicology by MPs and provide basic data for the toxicology research of MPs.

Three dimensional spatiotemporal nano-scale position retrieval of the confined diffusion of nano-objects inside optofluidic microstructured fibers.

Understanding the dynamics of single nano-scale species at high spatiotemporal resolution is of utmost importance within fields such as bioanalytics or microrheology. Here we introduce the concept of axial position retrieval via scattered light at evanescent fields inside a corralled geometry using optofluidic microstructured optical fibers allowing to unlock information about diffusing nano-scale objects in all three spatial dimensions at kHz acquisition rate for several seconds. Our method yields the lateral positions by localizing the particle in a wide-field microscopy image. In addition, the axial position is retrieved via the scattered light intensity of the particle, as a result of the homogenized evanescent fields inside a microchannel running parallel to an optical core. This method yields spatial localization accuracies <3 nm along the transverse and <21 nm along the retrieved directions. Due to its unique properties such as three dimensional tracking, straightforward operation, mechanical flexibility, strong confinement, fast and efficient data recording, long observation times, low background scattering, and compatibility with microscopy and fiber circuitry, our concept represents a new paradigm in light-based nanoscale detection techniques, extending the capabilities of the field of nanoparticle tracking analysis and potentially allowing for the observation of so far inaccessible processes at the nanoscale level.

Potential Application of Nitrogen-Doped Carbon Quantum Dots Synthesized by a Solvothermal Method for Detecting Silver Ions in Food Packaging.

In this paper, nitrogen-doped carbon quantum dots (N-CQDs) were synthesized by a solvothermal method using 1,2,4-triaminobenzene as a carbon precursor. The surface of the synthesized N-CQDs was modified with amino functional groups. The results indicated that N-CQDs had various N-related functional groups and chemical bonds and were amorphous in structure. At the same time, the quantum yield of N-CQDs was 5.11%, and the average lifetime of fluorescence decay was 5.79 ns. The synthesized N-CQDs showed good selectivity for and sensitivity to Ag+. A linear relationship between N-CQDs detection efficiency and Ag+ concentration was observed for concentration ranges of Ag+ corresponding to 0-10 µM and 10-30 µM. In addition, N-CQDs were used for the detection of trace Ag+ in food packaging material. The silver ion content of the sample determined by the N-CQDs detection method was 1.442 mg/L, with a relative error of 6.24% with respect to flame atomic absorption spectrometry, according to which the Ag+ content was 1.352 mg/L. This indicates that the N-CQDs detection method is reliable. Therefore, the N-CQDs prepared in this paper can detect Ag+ rapidly, simply, and sensitively and are expected to be a promising tool for the detection of trace Ag+ in food packaging materials.

Tunable KTA Stokes laser based on stimulated polariton scattering and its intracavity frequency doubling.

This paper presents the tunable Stokes laser characteristics of KTiOAsO4 (KTA) crystal based on stimulated polariton scattering (SPS). When the pumping laser wavelength is 1064.2 nm, the KTA Stokes wave can be discontinuously tuned from 1077.9 to 1088.4 nm with four gaps from 1079.0 to 1080.1 nm, from 1080.8 to 1082.8 nm, from 1083.6 to 1085.5 nm, and from 1085.8 to 1086.8 nm. When a frequency doubling crystal LiB3O5 (LBO) is inserted into the Stokes laser cavity, the frequency-doubled wave can be discontinuously tuned from 539.0 to 539.5 nm, from 540.1 to 540.4 nm, from 541.3 to 541.8 nm, from 542.7 to 542.9 nm and from 543.4 to 544.2 nm. With a pumping pulse energy of 130.0 mJ and an output coupler reflectivity of about 30%, the obtained maximum Stokes laser pulse energy at 1078.6 nm is 33.9 mJ and the obtained maximum frequency-doubled laser pulse energy at 543.8 nm is 15.7 mJ. By using the most probably coupled transverse optical modes obtained from the literature, the polariton refractive indexes, and the simplified polariton Sellmeier equations, the polariton dispersion curve is obtained. The formation of the Stokes frequency gaps is explained.

Tunable Stokes laser generation based on the stimulated polariton scattering in KTiOPO4 crystal.

The tunable Stokes laser characteristics based on the stimulated polariton scattering in KTiOPO4 (KTP) crystal and the intracavity frequency doubling properties for the Stokes laser are investigated for the first time. When the pumping laser wavelength is 1064.2 nm, and the angle between the pumping and Stokes beams outside the KTP crystal changes from 1.875° to 6.750°, the obtained tunable Stokes laser wavelength varies discontinuously from 1076.5 nm to 1091.4 nm with four gaps. When the pumping pulse energy is 120.0 mJ, the maximum Stokes pulse energy is 46.5 mJ obtained at the wavelength of 1086.6 nm. By inserting a LiB3O5 (LBO) crystal into the cavity, the obtained frequency-doubled laser wavelength is inconsecutive tunable from 538.5 nm to 543.8 nm. The maximum frequency-doubled laser pulse energy is 15.9 mJ at the wavelength of 543.5 nm.

A dye-sensitized visible light photocatalyst-Bi24O31Cl10.

The p-block semiconductors are regarded as a new family of visible-light photocatalysts because of their dispersive and anisotropic band structures as well as high chemical stability. The bismuth oxide halides belong to this family and have band structures and dispersion relations that can be engineered by modulating the stoichiometry of the halogen elements. Herein, we have developed a new visible-light photocatalyst Bi24O31Cl10 by band engineering, which shows high dye-sensitized photocatalytic activity. Density functional theory calculations reveal that the p-block elements determine the nature of the dispersive electronic structures and narrow band gap in Bi24O31Cl10. Bi24O31Cl10 exhibits excellent visible-light photocatalytic activity towards the degradation of Rhodamine B, which is promoted by dye sensitization due to compatible energy levels and high electronic mobility. In addition, Bi24O31Cl10 is also a suitable photoanode material for dye-sensitized solar cells and shows power conversion efficiency of 1.5%.

Research on real time detection of departure angle for the laser beam through atmospheric channels.

The precision of departure angle detection for the laser beam can be improved by optimizing algorithms by which the high precision and stability of the laser beam pointing and tracking would be obtained, namely, improving the performance and accommodation of the free space optical communications. Atmospheric turbulence-induced optical intensity scintillations have a strong impact on the location precision of the laser spot through the atmospheric channels. Consequently, new requests come into view for the optimization of the algorithms. In the paper, the advantages and disadvantages of the traditional centroid method are analyzed. In terms of variations of laser spot, combined with the requests for real-time detection of departure angle, we proposed a new detection method. The edge of the laser spot on the detection sensor was redefined, and then the redefined spot was used to calculate the departure angle of the laser beam. The results of the simulations and experiments show that the precision of departure angle detection has been improved by more than 16%, which could reduce the effect of detection errors on the tracking procedure.