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Self-assembled monolayers (SAMs) have recently emerged as excellent hole transport materials in inverted perovskite solar cells (PSCs) owing to their ability to minimize parasitic absorption, regulate energy level alignment, and passivate perovskite defects. Herein, we design and synthesize a novel dimethyl acridine-based SAM, [2-(9,10-dihydro-9,9-dimethylacridine-10-yl)ethyl]phosphonic acid (2PADmA), and employ it as a hole-transporting layer in inverted PSCs. Experimental results show that the 2PADmA SAM can modulate perovskite crystallization, facilitate carrier transport, passivate perovskite defects, and reduce nonradiative recombination. Consequently, the 2PADmA-based device achieves an enhanced power conversion efficiency (PCE) of 24.01% and an improved fill factor (FF) of 83.92% compared to the commonly reported [2-(9H-carbazol-9-yl)ethyl] phosphonic acid (2PACz)-based control device with a PCE of 22.32% and FF of 78.42%, while both devices exhibit comparable open-circuit voltage and short-circuit current density. In addition, 2PADmA-based devices exhibit outstanding dark storage and thermal stabilities, retaining approximately ~98% and 87% of their initial PCEs after 1080 h of dark storage and 400 h of heating at 85 °C, respectively, both considerably superior to the control device.

The use of a Controller Area Network (CAN) bus in the automotive industry for connecting electronic control units (ECUs) poses security vulnerabilities due to the lack of built-in security features. Intrusion Detection Systems (IDSs) have emerged as a practical solution for safeguarding the CAN bus. However, developing an effective IDS for in-vehicle CAN buses encounters challenges in achieving high precision for detecting attacks and meeting real-time requirements with limited computational resources. To address these challenges, we propose a novel method for anomaly detection on CAN data using windowed Hamming distance. Our approach utilizes sliding windows and Hamming distance to extract features from time series data. By creating benchmark windows that span at least one cycle of data, we compare newly generated windows with recorded benchmarks using the Hamming distance to identify abnormal CAN messages. During the experimental phase, we conduct extensive testing on both the public car-hack dataset and a proprietary dataset. The experimental results indicate that our method achieves an impressive accuracy of up to 99.67% in detecting Denial of Service (DoS) attacks and an accuracy of 98.66% for fuzzing attacks. In terms of two types of spoofing attacks, our method achieves detection accuracies of 99.48% and 99.61%, respectively, significantly outperforming the methods relying solely on the Hamming distance. Furthermore, in terms of detection time, our method significantly reduces the time consumption by nearly 20-fold compared to the approach using deep convolutional neural networks (DCNN), decreasing it from 6.7 ms to 0.37 ms.

Objective: Intervertebral disk degeneration (IDD) is a major cause of pain in the back, neck, and radiculus. Mesenchymal stem cells (MSCs)-derived extracellular vesicles (EVs) are therapeutic in musculoskeletal degenerative diseases such as IDD. This study explored the effect and functional mechanism of human bone MSCs (hBMSCs)-derived EVs in proliferation and apoptosis of degenerated nucleus pulposus cells (DNPCs) and extracellular matrix (ECM) synthesis.Methods: Extracellular vesicles were isolated from hBMSCs and identified. DNPCs were induced by TNF-α. EVs were incubated with DNPCs for 24h. Internalization of EVs by DNPCs, DNPCs proliferation, apoptosis, and expressions of ECM synthetic genes, degrading genes and miR-129-5p were assessed. Downstream target genes of miR-129-5p were predicted. Target relation between miR-129-5p and SRY-box transcription factor 4 (SOX4) was verified. DNPCs proliferation, apoptosis, and ECM synthesis were measured after treatment with EVs and miR-129-5p inhibitor or SOX4 overexpression. Expressions of SOX4 and Wnt/β-catenin pathway-related proteins were determined.Results: hBMSC-EVs promoted DNPCs proliferation, inhibited apoptosis, increased expressions of ECM synthetic genes, and reduced expressions of ECM degrading genes. hBMSC-EVs carried miR-129-5p into DNPCs. Silencing miR-129-5p in EVs partially inverted the effect of EVs on DNPCs proliferation and ECM synthesis. miR-129-5p targeted SOX4. SOX4 overexpression annulled the effect of EVs on DNPCs proliferation and ECM synthesis. Expressions of Wnt1 and β-catenin were decreased in EVs-treated DNPCs, while silencing miR-129-5p in EVs promoted expressions of Wnt1 and β-catenin.Conclusion: hBMSC-EVs promoted DNPCs proliferation and ECM synthesis by carrying miR-129-5p into DNPCs to target SOX4 and deactivating the Wnt/β-catenin axis.

Anterior cervical discectomy and fusion (ACDF) is a commonly used surgical method for the treatment of cervical spondylosis. As ACDF surgery is widely used in clinics, identifying suitable materials to design and prepare cervical interbody fusion cages is a hot research topic. Here, we describe a new three-dimensional (3D) printing approach to create stretchable and tough silk fibroin/nano-hydroxyapatite (SF/nHAp) composites with tunable mechanical properties. The compressive strength of the novel composites with biomimetic structure could reach more than 128 MPa. More importantly, the composites were prepared using 30% silk fibroin and 70% hydroxyapatite, a composition similar to the human bone tissue. Finite element analysis results indicate that the stress distribution of SF/nHAp composite cervical interbody fusion cages in vivo is more uniform than that of commercial Ti alloy cages. This study evaluates the effectiveness of SF/nHAp composites for application in cervical interbody fusion cages and in the field of bone tissue engineering.

Abstract Background Spinal cord injury (SCI) remains a huge medical problem nowadays as there is no hospital providing the versatile strategies for repairing central nervous system and restoring function. Herein, we focused on PC-12 cells as an important research tool and studied the potential role of resveratrol (RSV) in inflammation induced by LPS. Results RSV improved inflammatory injury and functional recovery in rat model of SCI. RSV inhibited LPS-induced inflammatory injury in PC-12 cells via increasing viability, decreasing apoptosis, and suppressing IL-1β, IL-6, and TNF-α expression. miR-132 was down-regulated after LPS treatment but up-regulated after RSV administration. miR-132 silence curbed the protective effect of RSV. The results including increase of cell growth, suppression of inflammatory response, and blocking of NF-κB and p38MAPK pathways produced by RSV were all reversed by miR-132 silence. Conclusion RSV could up-regulate miR-132 and further ameliorate inflammatory response in PC-12 cells by inhibiting NF-κB and p38MAPK pathways.