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Multiplexing technology creates several orthogonal data channels and dimensions for high‐density information encoding and is irreplaceable in large‐capacity information storage, and communication, etc. The multiplexing dimensions are constructed by light attributes and spatial dimensions. However, limited by the degree of freedom of interaction between light and material structure parameters, the multiplexing dimension exploitation method is still confused. Herein, a 7D Spin‐multiplexing technique is proposed. Spin structures with four independent attributes (color center type, spin axis, spatial distribution, and dipole direction) are constructed as coding basic units. Based on the four independent spin physical effects, the corresponding photoluminescence wavelength, magnetic field, microwave, and polarization are created into four orthogonal multiplexing dimensions. Combined with the 3D of space, a 7D multiplexing method is established, which possesses the highest dimension number compared with 6 dimensions in the previous study. The basic spin unit is prepared by a self‐developed laser‐induced manufacturing process. The free state information of spin is read out by four physical quantities. Based on the multiple dimensions, the information is highly dynamically multiplexed to enhance information storage efficiency. Moreover, the high‐dynamic in situ image encryption/marking is demonstrated. It implies a new paradigm for ultra‐high‐capacity storage and real‐time encryption. [ABSTRACT FROM AUTHOR]

Research on active particles has primarily focused on transport in relatively weak flows, during which their active swimming plays a significant role. However, in natural or manmade waterways, the ambient flow velocity and water depth can be on the order of approximately 1 m/s and 1 m, respectively, generating turbulent diffusion that may be strong enough to potentially dominate the transport process, so that the active swimming might be negligible. In this paper, we propose a theoretical framework aiming at identifying the threshold at which the effects of active swimming become significant, under conditions of insufficient data for motion statistics of swimmers. While deriving the governing equation, we find that only the vertical component of the mean swimming has the potential to significantly influence the transport process. This manifests as the characteristic of inducing a non‐uniform vertical concentration distribution, in competition with the mechanism of turbulent diffusion, which leads to a uniform distribution. We obtain the analytical solution for the vertical concentration distribution, with the key dimensionless parameter α representing the interplay between the active swimming and turbulent diffusion. The threshold is found to be approximately at the order of magnitude of α ∼ 0.1, below which active swimming is considered negligible. The theoretical predictions are validated by numerical simulations employing Direct Numerical Simulation and particle tracking methods. Applying the theory to two types of microorganisms transported under different flow conditions suggests that there are typical scenarios where the active swimming is negligible, and the swimmers can be treated as passive particles. Key Points: Only the vertical component of the mean swimming velocity has the potential to significantly influence the transport of active swimmersThreshold for observable active behavior in transport reveals competition between active swimming and turbulent diffusionThere are typical scenarios where active swimming is negligible, and the swimmers can be treated as passive particles [ABSTRACT FROM AUTHOR]

Chalcone (1,3-diaryl-2-propen-1-one) is an α, β-unsaturated ketone that serves as an active constituent or precursor of numerous natural substances, exhibiting a broad spectrum of pharmacological effects. In this study, the classical Claisen–Schmidt condensation method was used to synthesize the chalcone derivative 2′,4′-dimethoxychalcone (DTC) and evaluate its pharmacological activity. By upregulating the expression of the epithelial cell marker E-cadherin and downregulating the expression of the mesenchymal cell marker vimentin, DTC was found to inhibit transforming growth factor-β1 (TGF-β1)-induced epithelial–mesenchymal transition (EMT) process in A549 cells, maintaining the cells' epithelial-like morphology and reducing the ability of the cells to migrate. Additionally, DTC demonstrated the ability to decrease the expression levels of nitric oxide (NO), tumor necrosis factor (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) in RAW264.7 cells, suggesting a possible anti-inflammatory effect. Furthermore, DTC was found to exhibit bacteriostatic activity against Staphylococcus aureus (S. aureus), Proteus vulgaris (P. vulgaris), methicillin-resistant Staphylococcus aureus (MRSA), and Candida albicans (C. albicans), indicating that this chemical may possess broad-spectrum antibacterial activity. [ABSTRACT FROM AUTHOR]

Pulmonary fibrosis (PF) is a disease characterised by diffuse nonspecific alveolar inflammation with interstitial fibrosis, which clinically manifests as dyspnoea and a significant decline in lung function. Many studies have shown that the epithelial–mesenchymal transition (EMT) plays a pivotal role in the pathogenesis of pulmonary fibrosis. Based on our previous findings, hypericin (Hyp) can effectively inhibit the process of the EMT to attenuate lung fibrosis. Therefore, a series of hyperoside derivatives were synthesised via modifying the structure of hyperoside, and subsequently evaluated for A549 cytotoxicity. Among these, the pre-screening of eight derivatives inhibits the EMT. In this study, we evaluated the efficacy of Z6, the most promising hyperoside derivative, in reversing TGF-β1-induced EMTs and inhibiting the EMT-associated migration of A549 cells. After the treatment of A549 cells with Z6 for 48 h, RT-qPCR and Western blot results showed that Z6 inhibited TGF-β1-induced EMTs in epithelial cells by supressing morphological changes in A549 cells, up-regulating E-cadherin (p < 0.01, p < 0.001), and down-regulating Vimentin (p < 0.01, p < 0.001). This treatment significantly reduced the mobility of transforming growth factor β1 (TGF-β1)-stimulated cells (p < 0.001) as assessed by wound closure, while increasing the adhesion rate of A549 cells (p < 0.001). In conclusion, our results suggest that hyperoside derivatives, especially compound Z6, are promising as potential lead compounds for treating pulmonary fibrosis, and therefore deserve further investigation. [ABSTRACT FROM AUTHOR]