Investigation of catalytic methane oxidation over Ag/Co2MOx (M = Co, Ni, Cu) catalysts with varying interfacial electron transfer.

Atom-doped Co3O4 catalysts loaded with Ag were examined as cost-effective catalysts for methane oxidation. The synthesized Ag/Co2NiOx catalysts exhibited distinctive surface characteristics in contrast with Ag/Co3O4 and Ag/Co2CuOx catalysts prepared using a similar method. Characterization results unveiled that Ag/Co2NiOx featured a higher presence of active surface oxygen species, lattice defects, a larger surface area, and enhanced reducibility. A methane oxidation catalytic performance followed the sequence: Ag/Co2NiOx > Ag/Co3O4 > Ag/Co2CuOx. The investigation delved into methane degradation pathways on the surfaces of three catalysts, examining their behavior under both aerobic and anaerobic atmospheres through in-situ DRIFTS analysis. Furthermore, introducing Ag showed a marked positive effect on Co-Ni mixed oxide, inducing electron transfer and a more active electron system, whereas it exhibited an inverse impact within the surface of Co-Cu mixed oxide. This work provides innovative perspectives on the development of forthcoming environmental catalysts.

Identification of NOx emissions and source characteristics by TROPOMI observations - A case study in north-central Henan, China.

With the development of industries, air pollution in north-central Henan is becoming increasingly severe. The TROPOspheric Monitoring Instrument (TROPOMI) provides nitrogen dioxide (NO2) column densities with high spatial resolution. Based on TROPOMI, in this study, the nitrogen oxides (NOx) emissions in north-central Henan are derived and the emission hotspots are identified with the flux divergence method (FDM) from May to September 2021. The results indicate that Zhengzhou has the highest NOx emissions in north-central Henan. The most prominent hotspots are in Guancheng Huizu District (Zhengzhou) and Yindu District (Anyang), with emissions of 448.4 g/s and 300.3 g/s, respectively. The Gaussian Mixture Model (GMM) is applied to quantify the characteristics of emission hotspots, including the diameter, eccentricity, and tilt angle, among which the tilt angle provides a novel metric for identifying the spatial distribution of pollution sources. Furthermore, the results are compared with the CAMS global anthropogenic emissions (CAMS-GLOB-ANT) and Multi-resolution Emission Inventory model for Climate and air pollution research (MEIC), and they are generally in good agreement. However, some point sources, such as power plants, may be missed by both inventories. It is also found that for emission hotspots near transportation hubs, CAMS-GLOB-ANT may not have fully considered the actual traffic flow, leading to an underestimation of transportation emissions. These findings provide key information for the accurate implementation of pollution prevention and control measures, as well as references for future optimization of emission inventories. Consequently, deriving NOx emissions from space, quantifying the characteristics of emission hotspots, and combining them with bottom-up inventories can provide valuable insights for targeted emission control.

One-pot synthesis of N-doped petroleum coke-based microporous carbon for high-performance CO2 adsorption and supercapacitors.

Waste resource utilization of petroleum coke is crucial for achieving global carbon emission reduction. Herein, a series of N-doped microporous carbons were fabricated from petroleum coke using a one-pot synthesis method. The as-prepared samples had a large specific surface area (up to 2512 m2/g), a moderate-high N content (up to 4.82 at.%), and high population (55%) of ultra-micropores (<0.7 nm). Regulating the N content and ultra-microporosity led to efficient CO2 adsorption and separation. At ambient pressure, the optimal N-doped petroleum coke-based microporous carbon exhibited the highest CO2 uptake of 4.25 mmol/g at 25°C and 6.57 mmol/g at 0°C. These values are comparable or even better than those of numerous previously reported adsorbents prepared by multistep synthesis, primarily due to the existence of ultra-micropores. The sample exhibited excellent CO2/N2 selectivity at 25°C owing to the abundant basic pyridinic and pyrrolic N species; and showed superior CO2 adsorption-desorption cycling performance, which was maintained at 97% after 10 cycles at 25°C. Moreover, petroleum coke-based microporous carbon, with a considerably high specific surface area and hierarchical pore structure, exhibited excellent electrochemical performance over the N-doped sample, maintaining a favorable specific capacitance of 233.25 F/g at 0.5 A/g in 6 mol/L KOH aqueous electrolyte. This study provides insight into the influence of N-doping on the porous properties of petroleum coke-based carbon. Furthermore, the as-prepared carbons were found to be promising adsorbents for CO2 adsorption, CO2/N2 separation and electrochemical application.

Tuning the Hierarchical Pore Structure and the Metal Site in a Metal-Organic Framework Derivative to Unravel the Mechanism for the Adsorption of Different Volatile Organic Compounds.

Volatile organic compounds (VOCs) are one of the main classes of air pollutants, and it is important to develop efficient adsorbents to remove them from the atmosphere. To do this most efficiently, we need to understand the mechanism of VOC adsorption. In this work, we described how the metal organic framework (MOF), ZIF-8, was used as a precursor to generate MOF derivatives (Zn-GC) through temperature-controlled calcination, which had adjustable metal sites and hierarchical pore structure. It was used as a model adsorbent to study the adsorption and desorption characteristics of different VOCs. Zn-GC-850 with developed pores exhibited higher adsorption performance for the benzene series, whereas Zn-GC-650 with more metal sites had a better adsorption capacity for oxygen-containing VOCs. By tuning the molecular structure of the VOCs, we revealed the adsorption mechanism of different VOCs at the molecular level. The more developed hierarchical pore structure obtained at the higher temperature facilitates the diffusion of the benzene series, and the noncovalent interaction between their methyl group(s) and the carbonized MOF derivatives improves the adsorption affinity; while the higher exposure of Zn sites obtained at lower temperature favors the adsorption of oxygen-containing VOCs by Zn-O bonds. The mass transfers of VOCs and the role of the adsorbent were simulated by multiple theoretical models. This study strengthens the basis for the design and optimization of the adsorbent and catalyst for VOCs treatment.

The mechanism of action and biodistribution of a novel EGFR/VEGF bispecific fusion protein that exhibited superior antitumor activities.

Despite the promising clinical benefits of therapies targeting epidermal growth factor receptor (EGFR) or vascular endothelial growth factor (VEGF) with antibodies in various cancers, resistance to these therapies will inevitably develop following treatment. Recent studies suggest that crosstalk between the EGFR and VEGF signaling pathways might be involved in the development of resistance. Therefore, simultaneous blockade of EGFR and VEGF signaling may be able to counteract this resistance and improve clinical outcomes. Here, we devised a fusion protein with two copies of VEGFR1 domain 2 connected to the C-terminus of cetuximab that can simultaneously bind to EGFR and VEGF and effectively inhibit target cell growth mediated by these two pathways. Furthermore, the fusion protein could bring soluble VEGF into target cells for degradation through internalization upon binding to EGFR. Tissue distribution in mice confirmed that the fusion protein effectively accumulated in tumors compared to its mAb counterpart cetuximab. These features resulted in stronger antitumor efficacies in vivo than the combination of bevacizumab and cetuximab. Thus, we provide a promising new strategy for the treatment of EGFR-overexpressing cancers.

Research on the diurnal variation characteristics of ozone formation sensitivity and the impact of ozone pollution control measures in "2 + 26" cities of Henan Province in summer.

Near-surface ozone pollution is becoming an increasingly serious air quality issue in China, especially in "2 + 26" cities (Beijing-Tianjin-Hebei and nearby cities). HN2 + 26 cities ("2 + 26" cities of Henan Province) are located in the south of "2 + 26" cities, with frequent and severe ozone pollution events in recent years. This study investigated the diurnal evolution characteristics of ozone formation sensitivity (OFS) of HN2 + 26 cities from May to September in 2021 by the innovative combination of Global Ozone Monitoring Experiment (GOME-2B) and Ozone Monitoring Instrument (OMI) satellite data, and assessed the impact of ozone pollution control measures (OPCMs) implemented from June 26 to July 1, 2021. The localized FNR (ratio of formaldehyde to nitrogen dioxide of satellite measurement) threshold (1.4-2.55) was established, and it was found that OFS in May-September 2021 was mainly in VOCs-limited regime in the morning (∼10:00), while transitional/NOx-limited regime in the afternoon (∼14:00). Three periods (before, during and after the OPCMs) were divided to evaluate the impact of OPCMs on OFS. It was indicated that OPCMs had no impact on the morning OFS, but had a significant impact on the afternoon OFS. Specifically, the OFS in two industrial cities Xinxiang (XX) and Zhengzhou (ZZ) shifted from transitional regime to NOx-limited regime after the OPCMs. We further investigated OFS differences between urban and suburban areas and found that OFS shift of XX only existed in urban areas, while that of ZZ existed in both urban and suburban areas. We compared their measures and found that it is effective to take hierarchical control measures on different levels of ozone pollution days to alleviate ozone pollution. This study provides an improved understanding of diurnal evolution characteristics of OFS and the impacts of OPCMs on it, which will provide a theoretical basis for formulating more scientific ozone pollution control policies.

[Ozone Pollution Characteristics and Sensitivity During the Ozone Pollution Days in Summer 2021 of Xinxiang City].

This study was based on the observation of volatile organic compounds (VOCs), conventional gaseous air pollutants, and meteorological parameters observed at the Xinxiang Municipal Party School site from June to August 2021. The ozone (O3) characteristics and sensitivity of O3 pollution days and the control strategy of its precursors were studied using an observation-based model (OBM). It was found that the meteorological conditions were characterized by high temperature, low humidity, and low pressure in O3-pollution days. The concentrations of O3 and its precursors all increased in the O3 pollution days. Oxygenated volatile organic compounds (OVOCs) and alkanes were the highest-concentration components of VOCs on O3 pollution days in Xinxiang, and OVOCs had the highest ozone formation potential (OFP) and hydroxyl (·OH) reactivity. According to the relative incremental reactivity (RIR) analysis, during the O3 pollution days in Xinxiang, O3sensitivity was in the VOCs-limited regime in June and in the transitional regime in July and August. Ozone production was more sensitive to alkenes and OVOCs. The RIR values of the precursors in June changed throughout the day, but O3 sensitivity remained the VOCs-limited regime. In July and August, O3 sensitivity was the VOCs-limited regime in the morning, transitional regime at noon, transitional and NOx-limited regime, respectively in the afternoon. By simulating different precursor-reduction scenarios, the results showed that the reduction of VOCs was always beneficial to the control of O3, whereas the reduction of NOx had little effect on the control of O3 and a risk of increasing O3.

Scalable Fabrication of Superhydrophobic Coating with Rough Coral Reef-Like Structures for Efficient Self-Cleaning and Oil-Water Separation: An Experimental and Molecular Dynamics Simulation Study.

Superhydrophobic coating has a great application prospect in self-cleaning and oil-water separation but remains challenging for large-scale preparation of robust and weather-resistant superhydrophobic coatings via facile approaches. Herein, this work reports a scalable fabrication of weather-resistant superhydrophobic coating with multiscale rough coral reef-like structures by spraying the suspension containing superhydrophobic silica nanoparticles and industrial coating varnish on various substrates. The coral reef-like structures effectively improves the surface roughness and abrasion resistance. Rapid aging experiments (3000 h) and the outdoor building project application (3000 m2 ) show that the sprayed superhydrophobic coating exhibits excellent self-cleaning properties, weather resistance, and environmental adaptability. Moreover, the combined silica-coating varnish-polyurethane (CSCP) superhydrophobic sponge exhibits exceptional oil-water separation capabilities, selectively absorbing the oils from water up to 39 times of its own weight. Furthermore, the molecular dynamics (MD) simulation reveals that the combined effect of higher surface roughness, smaller diffusion coefficient of water molecules, and weaker electrostatic interactions between water and the surface jointly determines the superhydrophobicity of the prepared coating. This work deepens the understanding of the anti-wetting mechanism of superhydrophobic surfaces from the perspective of energetic and kinetic properties, thereby paving the way for the rational design of superhydrophobic materials and their large-scale applications.

Insights into the Role of Nanorod-Shaped MnO2 and CeO2 in a Plasma Catalysis System for Methanol Oxidation.

Published papers highlight the roles of the catalysts in plasma catalysis systems, and it is essential to provide deep insight into the mechanism of the reaction. In this work, a coaxial dielectric barrier discharge (DBD) reactor packed with γ-MnO2 and CeO2 with similar nanorod morphologies and particle sizes was used for methanol oxidation at atmospheric pressure and room temperature. The experimental results showed that both γ-MnO2 and CeO2 exhibited good performance in methanol conversion (up to 100%), but the CO2 selectivity of CeO2 (up to 59.3%) was much higher than that of γ-MnO2 (up to 28.6%). Catalyst characterization results indicated that CeO2 contained more surface-active oxygen species, adsorbed more methanol and utilized more plasma-induced active species than γ-MnO2. In addition, in situ Raman spectroscopy and Fourier transform infrared spectroscopy (FT-IR) were applied with a novel in situ cell to reveal the major factors affecting the catalytic performance in methanol oxidation. More reactive oxygen species (O22-, O2-) from ozone decomposition were produced on CeO2 compared with γ-MnO2, and less of the intermediate product formate accumulated on the CeO2. The combined results showed that CeO2 was a more effective catalyst than γ-MnO2 for methanol oxidation in the plasma catalysis system.

Discovery of novel anti-cyanobacterial allelochemicals by multi-conformational QSAR approach.

Microcystis aeruginosa causes cyanobacterial harmful algal blooms (cHABs) in various freshwater environments. Due to global climate change, the cHABs have even spread to estuaries and coasts. Plant-derived flavones have been reported as allelochemicals that efficiently inhibit the growth of M. aeruginosa. Quantitative structure-activity relationship (QSAR) was applied to investigate the factors affecting the M. aeruginosa inhibitory activity of flavones, and to discover novel allelochemicals against M. aeruginosa. We constructed 2D and 3D-QSAR models based on the half maximum inhibitory concentration (IC50) of 22 flavones against M. aeruginosa, using molecular descriptors from multiple stable conformations. Both models showed satisfactory performances (2D-QSAR: r2=0.899, q2=0.596, rtest2=0.801; 3D-QSAR: r2=0.810, q2=0.516, rtest2=0.897). The 2D-QSAR model indicates that the anti-cyanobacterial activity is positively correlated with minimum and maximum surface electrostatic potential, and negatively correlated with polarity index and polar surface area. Through the 3D-QSAR approach, electronegative hydroxyl groups in 5- and 4'-position were favorable for the anti-cyanobacterial activity. In addition, we selected six untested flavones that fit the "activity-favorable" pattern of the visualized 3D-QSAR model. Five of the external flavones exhibited significant cyanobacterial inhibitory ability at their predicted IC50 by the 3D-QSAR model. In particular, diosmetin achieved an inhibition rate of 70.50±4.74%, which was much higher than expected. The flavones screened by the 3D-QSAR model are novel cyanobacterial inhibitors and should be fully exploited to mitigate cHABs.

Construction of a novel TROP2/CD3 bispecific antibody with potent antitumor activity and reduced induction of Th1 cytokines.

Many cancers, including triple-negative breast cancer, overexpress TROP2 on the surface of tumor cells. TROP2 has become a promising tumor associated antigen for the development of novel antibody-based targeted therapy. Herein, we constructed a novel bispecific antibody with the ability to simultaneously target TROP2 on the tumor surface and bind to CD3 to activate T cells. Given that the excessive production of Th1 cytokines induced by CD3-mediated T-cell overactivation may lead to toxicity in the clinic, we devised a strategy to modify this CD3-induced T cell activation by a two-step reduction in the bispecific antibody binding affinity for CD3 to a level that retained the ability of the bispecific antibody to effectively inhibit tumor growth while greatly reducing the amount of Th1 cytokines secreted by T cells. Thus, we provide insight into the design of T cell engagers that exhibit a promising toxicity profile while retaining inhibitory effects on tumor growth.

Systemic investigation of inetetamab in combination with small molecules to treat HER2-overexpressing breast and gastric cancers.

Most patients with metastatic breast cancer or gastric cancer who are treated with trastuzumab, an anti-HER2 monoclonal antibody, become refractory to the drug within a year after the initiation of treatment. Although the combination of trastuzumab with pertuzumab produced synergetic effects in the treatment of HER2-overexpressing cancers, not all patients with HER2 overexpression benefited from the trastuzumab plus pertuzumab combination. To improve the clinical benefits of trastuzumab, we systemically investigated the combination of inetetamab (Cipterbin), an analog of trastuzumab, with a variety of small molecules, including tyrosine kinase inhibitors (TKIs) and chemotherapeutic agents in vivo. We showed that pan-TKIs-induced synergistic antitumor effects with inetetamab in the treatment of these two types of cancers and that adding chemotherapeutic agents to the existing TKI plus anti-HER2 monoclonal antibody combination strategies induced additional inhibitory effects, suggesting that such combination strategies may be choices for the treatment of these two tumors. Thus, combination therapies targeting distinct and broad pathways that are essential for tumor growth and survival can be effective for treating metastatic breast cancers and gastric cancers.

Precise preparation of biomass-based porous carbon with pore structure-dependent VOCs adsorption/desorption performance by bacterial pretreatment and its forming process.

Pore distribution characteristic is one of the most crucial factors for porous adsorption materials, and the variety of volatile organic compounds (VOCs) approaches about how to simply and accurately tailor practical porous carbons for VOCs adsorption has gradually attracted attention. Here, precursors with different lignocellulose mass ratios have been used to produce porous carbon for model experiments to investigate the influence of the precursor lignocellulose contents on the pore structure and distribution characteristics of porous carbon, and the applicability of these mechanisms to real biomass materials has been further verified through bacteria-targeted bagasse decomposition: the microvolumes of ultra-micropores have decreased with decrease in cellulose contents, while mesopores have followed the reverse trend. The dynamic toluene adsorption/desorption performances of the obtained samples have been tested. The BACs-36 exhibits high toluene adsorption performance in low concentration with 635 mg/g while the BACs-48 shows excellent reusability in 10 times cycles. Based on this the balance between the adsorptive and regenerative capacities has been observed which indicates that carbon materials with abundant micropores and narrow mesopores have much better adsorption performance than porous carbon with a hierarchical pore structure, while the latter show better regeneration abilities than the former, which resulting in less desorption as a counter-acting force at the pore wall. Furthermore, the porous carbon has been shaped by one-step co-pyrolysis method using phenolic resin, which can not only maintain the hardness but also can avoid pore plugging phenomenon.

Efficacy and Safety of Coronary Intervention via Distal Transradial Access (dTRA) in Patients with Low Body Mass Index.

The study aimed to investigate the efficacy and safety of coronary intervention via distal transradial access (dTRA) in patients with low body mass index (BMI). A total of 67 patients with low BMI who underwent coronary intervention, comprising 29 patients via dTRA and 38 patients via conventional transradial access (cTRA), were retrospectively included. There was no significant difference in the puncture success rate between the two groups (dTRA 96.6%, cTRA 97.4%, P=0.846). Compared with the cTRA group, the success rate of one-needle puncture in the dTRA group was lower (51.7% vs. 81.6%, P=0.020). The compression haemostasis time in the dTRA group was shorter than that in the cTRA group (P < 0.001). However, the incidence of radial artery occlusion was lower in the dTRA group than in the cTRA group (4.0% vs. 33.3%, P=0.007). In conclusion, coronary intervention via dTRA was safe and effective in patients with low BMI.

Characteristics and sources of volatile organic compounds (VOCs) in Xinxiang, China, during the 2021 summer ozone pollution control.

Real-time monitoring of volatile organic compounds (VOCs) was conducted in Xinxiang, China, during the implementation of Xinxiang's ozone pollution control period (CP) in June 2021. To evaluate the effectiveness of the control measures, three study periods were determined by combining meteorological conditions and the implementation time of the control measures: before, during, and after the CP of ozone pollution (BCP, CP, and ACP, respectively). The average concentrations of VOCs during the three periods were 41.20 ± 4.99 ppbv, 33.64 ± 5.65 ppbv, and 37.42 ± 2.59 ppbv, respectively, with the same top three components, namely oxygenated VOCs (OVOCs), alkanes, and halogenated hydrocarbons (XVOCs). However, the concentrations of these three components decreased substantially during the CP (by 19 %, 18 %, and 11 %, respectively). The ozone formation potential (OFP) during the BCP was 144.47 ppbv, which was 1.2 times and 1.3 times higher than those during the ACP and CP periods, respectively. During the CP, the proportion of alkenes that contributed to the OFP decreased significantly by 24 %. Five types of VOCs sources were determined by positive matrix factorization (PMF): (1) solvent use, (2) biogenic, (3) secondary formation, (4) industrial process, and (5) vehicle exhaust and fuel evaporation sources. The VOCs emissions from industrial processes decreased by 54 % during the CP, whereas those from vehicle exhaust and fuel evaporation sources decreased by 36 %, indicating the effectiveness of emission control measures and the importance of these two sources for VOCs control in Xinxiang. In terms of regional transport, the results of the spatial analysis revealed that Hebi and Anyang in the northeast and Zhengzhou and Pingdingshan in the southwest, affected significantly the VOCs of Xinxiang. These results highlight the importance of controlling VOCs emissions in Xinxiang. Furthermore, attention should be paid to controlling the regional transport of surrounding cities.

Preparing hierarchical porous carbon with well-developed microporosity using alkali metal-catalyzed hydrothermal carbonization for VOCs adsorption.

Biomass-derived porous carbonaceous materials are efficient adsorbents for VOCs, but their traditional preparation method, pyrolysis combined with activation, suffers from high energy consumption, equipment corrosion, and low pore-making efficiency, which hinders their large-scale practical application. A novel method of alkali metal-catalyzed hydrothermal carbonization coupling with chemical activation for the preparation of microporous carbon is presented. Porous carbon with well-developed microporosity deriving from corn husk were prepared through the hydrothermal carbonization using potassium persulfate (K2S2O8) as a catalyst and programmed heating activation process. And the products were applied to removal of typical oxygen-containing VOCs, ethyl acetate. The addition of K2S2O8 in hydrothermal carbonization accelerated the biomass hydrolysis, decomposed the biopolymer, and formed functional hydrochars. Potassium salts introduced into the hydrochars, which acted as an activator in this programmed heating activation process, formed a great deal of micropores. The specific surface area of micropores increased by 81%, and the specific surface area of micropores less than 1 nm increased by 180%. The introduction of K2S2O8 in preparation improved the adsorption performance of CH-based porous carbons 16.46% and 60.00% respectively at different preparation temperatures (600 °C and 800 °C). Basing on these results, the improvement of micropores less than 1 nm is directly related to the adsorption performance. This indicates that pores (<1 nm) respond well to the adsorption of ethyl acetate.

A strategy for the efficient construction of anti-PD1-based bispecific antibodies with desired IgG-like properties.

Targeting PD1/PDL1 with blocking antibodies for cancer therapy has shown promising benefits in the clinic, but only approximately 20-30% of patients develop durable clinical responses to the treatment. Bispecific antibodies (BsAbs) that combine PD1/PDL1 blockade with the modulation of another immune checkpoint target may have greater potential to enhance immune checkpoint blockade therapy. In this study, we identified an anti-PD1 monoclonal antibody, 609A, whose heavy chain can pair with a variety of light chains from different antibodies while maintaining its PD1 binding/blocking activity. Taking advantage of this property and using a linear F(ab')2 format, we successfully produced a series of tetravalent IgG-like BsAbs that simultaneously target PD1 and other immune checkpoint targets, including PDL1 and CTLA4. The BsAbs exhibited superior bioactivities in vitro and in vivo compared to their respective parental mAbs. Importantly, the BsAbs demonstrated the desired IgG-like physicochemical properties in terms of high-level expression, ease of purification to homogeneity, good stability and in vivo pharmacokinetics. In summary, we describe a novel and flexible plug-and-play platform to engineer IgG-like BsAbs with excellent development potential for clinical applications.

Safety and efficacy of coronary angiography and percutaneous coronary intervention via distal transradial artery access in the anatomical snuffbox: a single-centre prospective cohort study using a propensity score method.

BACKGROUND: This study investigated the safety and efficacy of coronary angiography (CAG) and percutaneous coronary intervention (PCI) via distal transradial artery access (d-TRA). METHODS: For this single-centre prospective cohort study, a total of 1066 patients who underwent CAG or PCI procedures from September 2019 to November 2020 were included. Patients were divided into two groups: the d-TRA group (346) and the conventional transradial artery access (c-TRA) group (720) based on access site. A total of 342 pairs of patients were successfully matched using propensity score matching (PSM) for subsequent analysis. RESULTS: No significant differences in puncture success rate, procedural method, procedural time, sheath size, contrast dosage or fluoroscopy time were noted between the two groups. The puncture time in the d-TRA group was longer than that in the c-TRA group (P < 0.01), and the procedure success rate was lower than that in the c-TRA group (90.94% vs. 96.49%, P = 0.01). The haemostasis time in the d-TRA group was shorter than that in the c-TRA group (P < 0.01), and the visual analogue scale (VAS) was lower than that in the c-TRA group (P < 0.01). In addition, the prevalence of bleeding and haematoma in the d-TRA group was lower than that in the c-TRA group (1.75% vs. 7.31%, P < 0.01; 0.58% vs. 3.22%, P = 0.01, respectively). No significant difference in the incidence of numbness was noted between the two groups. No other complications were found in two groups. CONCLUSION: d-TRA is as safe and effective as c-TRA for CAG and PCI. It has the advantages of improved comfort and fewer complications. Trail registration Chinese Clinical Trial Registry, ChiCTR1900026519.

Bispecific antibody simultaneously targeting PD1 and HER2 inhibits tumor growth via direct tumor cell killing in combination with PD1/PDL1 blockade and HER2 inhibition.

Immune checkpoint blockade has shown significant clinical benefit in multiple cancer indications, but many patients are either refractory or become resistant to the treatment over time. HER2/neu oncogene overexpressed in invasive breast cancer patients associates with more aggressive diseases and poor prognosis. Anti-HER2 mAbs, such as trastuzumab, are currently the standard of care for HER2-overexpressing cancers, but the response rates are below 30% and patients generally suffer relapse within a year. In this study we developed a bispecific antibody (BsAb) simultaneously targeting both PD1 and HER2 in an attempt to combine HER2-targeted therapy with immune checkpoint blockade for treating HER2-positive solid tumors. The BsAb was constructed by fusing scFvs (anti-PD1) with the effector-functional Fc of an IgG (trastuzumab) via a flexible peptide linker. We showed that the BsAb bound to human HER2 and PD1 with high affinities (EC50 values were 0.2 and 0.14 nM, respectively), and exhibited potent antitumor activities in vitro and in vivo. Furthermore, we demonstrated that the BsAb exhibited both HER2 and PD1 blockade activities and was effective in killing HER2-positive tumor cells via antibody-dependent cellular cytotoxicity. In addition, the BsAb could crosslink HER2-positive tumor cells with T cells to form PD1 immunological synapses that directed tumor cell killing without the need of antigen presentation. Thus, the BsAb is a new promising approach for treating late-stage metastatic HER2-positive cancers.

Key factors and primary modification methods of activated carbon and their application in adsorption of carbon-based gases: A review.

To achieve carbon neutrality, it is necessary to control carbon-based gas emissions to the atmosphere. Among the various carbon-based gas removal technologies reported to date, adsorption is considered one of the most promising because of its economic efficiency, reusability, and low energy consumption. Activated carbon is widely used to treat different types of carbon-based gases owing to its large specific surface area, abundant functional groups, and strong adsorption capacity. This paper reviews the recent research progress into activated carbon as an adsorbent for carbon-based gases. The key factors (i.e., specific surface area, pore structure, and surface functional groups) affecting the adsorption of carbon-based gases by activated carbon were analyzed. The main methods employed to modify activated carbon (i.e., surface oxidation, surface reduction, loading materials, and plasma modification methods) to improve its adsorption capacity are also discussed herein, along with the targeted applications of such material in the adsorption of different types of carbon-based gases (such as aldehydes, ketones, aromatic hydrocarbons, halogenated hydrocarbons, and carbon-based greenhouse gases). Finally, the future development directions and challenges of activated carbon are discussed. Our work will be expected to benefit the development of activated carbon exhibiting selective adsorption properties, and reduce the production costs of adsorbents.