miRNA-142-3p aggravates hydrogen peroxide-induced human umbilical vein endothelial cell premature senescence by targeting SIRT1.

Vascular endothelial cell premature senescence plays an important part in stroke. Many microRNAs (miRNAs) are known to be involved in the pathological process of vascular endothelial cell premature senescence. The present study aimed to investigate the mechanism of hydrogen peroxide (H2O2)-induced premature senescence in human umbilical vein endothelial cells (HUVECs) and effect of miR-142-3p on hydrogen peroxide (H2O2)-induced premature senescence. HUVECs were exposed to H2O2 to establish a model premature senescence in endothelial cells. CCK-8 assay was performed to detect cell viability. Senescence-associated ß-galactosidase staining assay and senescence-related proteins p16 and p21 were used to detect changes in the degree of cell senescence. RT-qPCR and Western blot were conducted to measure mRNA and protein levels, respectively. The scratch wound-healing assay, transwell assay, and EdU assay were performed to evaluate the ability of migration and proliferation, respectively. miRNA-142-3p and silencing information regulator 2 related enzyme 1 (SIRT1) binding was verified using Targetscan software and a dual-luciferase assay. We found that miRNA-142-3p is abnormally up-regulated in HUVECs treated with H2O2. Functionally, miRNA-142-3p inhibition may mitigate the degree of HUVEC senescence and improve HUVEC migration and proliferation. Mechanistically, SIRT1 was validated to be targeted by miRNA-142-3p in HUVECs. Moreover, SIRT1 inhibition reversed the effects of miRNA-142-3p inhibition on senescent HUVECs exposed to H2O2. To our knowledge, this is the first study to show that miRNA-142-3p ameliorates H2O2-induced HUVECs premature senescence by targeting SIRT1 and may shed light on the role of the miR-142-3p/SIRT1 axis in stroke treatment.

Edge-exposed MoS2 nanospheres assembled with SnS2 nanosheet to boost NO2 gas sensing at room temperature.

SnS2 nanosheets (NSs) have become an ideal candidate for high performance gas sensors due to their unique sensing properties. However, the restacking and aggregation in the process of sensor manufacturing have great influence on the gas sensing performance. In this study, we synthesized a novel heterojunction of the flower-like porous SnS2 NSs with edge exposed MoS2 nanospheres via a facile hydrothermal method and sensitive response has achieved at room temperature (27℃). After functionalization, the SMS-Ⅱ showed excellent response (Ra/Rg = 25.9-100 ppm NO2), which is 22.3 times higher than that of the pristine SnS2 NSs. The sensor also has the characteristics of short response time of 2 s, excellent base line recovery (28.2 s), long-term stability and reliability within 16 weeks, good selectivity and low detection concentration of only 50 ppb. The p-n heterojunction formed between the edge-exposed spherical MoS2 and the 3D flower-like SnS2 NSs has a synergistic effect, providing a highly active sites for the adsorption of NO2 gas, which greatly enhance the sensitivity of the sensor. Simple fabrication and excellent gas sensing performance of the SnS2/MoS2 heterostructure nanomaterials (NMs) will highly effective for commercial gas sensing application.

Controllable synthesis of MoS2@MoO2 nanonetworks for enhanced NO2 room temperature sensing in air.

MoS2 nanosheets (NSs) are a promising gas sensing material at room temperature (RT) due to their unique properties and structures. Unfortunately, the activity of pure MoS2 NSs is highly affected by the adsorption of atmospheric oxygen, which strongly influences the stability of MoS2 sensing devices and significantly hinders the practical applications of these sensors in air. Heterostructure formation may be an effective approach to modulate the intrinsic electronic properties of MoS2 NSs. In this study, thin MoO2 nanoplates (NPs) were decorated with multilayer MoS2 NSs via one-step controllable sulfurization to fabricate MoS2@MoO2 nanonetworks, and remarkable gas sensing performance was achieved with high stability in air at RT. In particular, the MSO-2 (1 h sulfurization of the MoO2 NPs) nanonetworks with n-p heterojunctions demonstrated a high response of 19.4 to 100 ppm NO2 in a short period of time (1.06 s) with rapid recovery (22.9 s) to the baseline. The excellent gas sensing performance of the MSO-2 sensor is attributed to the synergistic effect of the MoS2 NSs and thin MoO2 NPs, which created heterojunctions/defects to easily transfer electrons and provide more active sites for NO2 gas. This simple synthetic method to design and fabricate n-p heterojunction sensors will be effective in commercial gas sensing applications.

Porous 3D flower-like CoAl-LDH nanocomposite with excellent performance for NO2 detection at room temperature.

The 3D flower-like CoAl-layered double hydroxide (CoAl-LDH) was successfully prepared using the functional template agent of fluoride ions via a facile one-step hydrothermal route. Various techniques proved that all the samples presented 3D flower-like microstructural morphology. Representatively, the CA-2 sample, which was synthesized with the molar ratio of Co : Al of 3.65 : 1, had considerably abundant pores in its thin nanosheets. The average pore size was 2-4 nm, the specific surface area was equal to 49.45 m2 g-1, and the thickness of nanosheets was approximately 3.068 nm. The CA-2 sample showed an excellent response to 0.01-100 ppm NO2 with ultrafast response/recovery time at room temperature (RT). The detection limit of the sensor even reached 10 ppb. The superior gas sensing performance could be attributed to the synergistic effects of the functional template agent of fluoride ions and specific porous 3D flower-like nanostructure. The current study showed that the 3D flower-like CoAl-LDHs might a promising material in practical detection of NO2 at RT.

One-step synthesis of palladium oxide-functionalized tin dioxide nanotubes: Characterization and high nitrogen dioxide gas sensing performance at room temperature.

Mesoporous palladium oxide (PdO)-functionalized tin dioxide (SnO2) composite nanotubes (SPCTs) were prepared via one-step synthesis by electrospinning technology using ethanol and N,N-dimethylformamide (DMF) as solvents. Compared with pure SnO2 nanotubes, there were abundant mesopores and multiheterojunctions in PdO-functionalized SnO2 nanotubes. The sample with the molar ratio of SnO2:PdO of 100:3 (3-SPCT) exhibited excellent response (∼20.30) as a sensor with fast gas response speed (∼1.33 s) to 100 ppm nitrogen dioxide (NO2) at room temperature (RT), and the detection limit reached to 10 ppb. The improved gas sensing performance of the 3-SPCT sensor was mainly attributed to the synergistic effect: the unique SnO2 tubular structure and well-dispersed mesopores provided the gas diffusion and adsorption channels, oxygen defects and chemisorbed oxygen were taken as the electron trap and charge transfer active sites, and a large number of heterojunctions acted as electron transport channels, thereby increasing the transfer rate.

Facile Synthesis of Highly Dispersed Co3O4 Nanoparticles on Expanded, Thin Black Phosphorus for a ppb-Level NO x Gas Sensor.

Expanded few-layer black phosphorus nanosheets (FL-BP NSs) were functionalized by branched polyethylenimine (PEI) using a simple noncovalent assembly to form air-stable overlayers (BP-PEI), and a Co3O4@BP-PEI composite was designed and synthesized using a hydrothermal method. The size of the highly dispersed Co3O4 nanoparticles (NPs) on the FL-BP NSs can be controlled. The BP-C5 (190 °C for 5 h) sensor, with 4-6 nm Co3O4 NPs on the FL-BP NSs, exhibited an ultrahigh sensitivity of 8.38 and a fast response of 0.67 s to 100 ppm of NO x at room temperature in air, which is 4 times faster than the response of the FL-BP NS sensor, and the lower detection limit reached 10 ppb. This study points to a promising method for tuning properties of BP-based composites by forming air-stable overlayers and highly dispersed metal oxide NPs for use in high-performance gas sensors.