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Janus nanostructures that possess two or more distinct components and surface functions have attracted more and more attention. Here, we present a seed-shape defined growth mechanism for the preparation of anisotropic Janus nanostructures, in which the shape of periodic mesoporous organosilica (PMO) is determined by the shape of Au nanoparticles. Various shaped Au@PMO composite nanostructures, such as rods, spheres, and plates, are prepared based on this general growth mechanism. By adjusting the reaction parameters (temperature, surfactant), various shaped AuNR@PMO Janus nanostructures, including horsebean- and fingernail-like nanostructures, have been successfully prepared. We also demonstrate the potential applications of such composite nanostructures. As an example, the as-prepared rod-like Janus Au@PMO nanostructures show great performance in chemo-photothermal combination therapy because of the excellent photothermal effect of Au nanorods and the high surface area of PMO nanorods. This research may open a new direction to the controllable synthesis and practical application of dedicated nanostructures with desired properties.
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http://dx.doi.org/10.1039/c7nr01047h | DOI Listing |
Exp Appl Acarol
September 2025
School of Life Science, Nanchang University, Nanchang, 330031, China.
Lead (Pb) contamination, a kind of heavy metal pollution, severely impacts organism growth and reproduction. Although vitellogenin (Vg) has been studied in many species, its characteristics in the pest Aleuroglyphus ovatus (Troupeau) (Acari: Acaridae) remain unknown. In this study, the full-length Vg gene of A.
View Article and Find Full Text PDFCell Death Differ
September 2025
Graduate Institute of Physiology, College of Biomedical Sciences, National Defense Medical University, Taipei, Taiwan, Republic of China.
Peroxisome proliferator-activated receptor alpha (PPARα) is a crucial transcriptional factor that regulates fatty acid β-oxidation and ketogenesis in response to fasting. However, the mechanisms underlying PPARα function remain unclear. This study identified a novel PPARα-binding protein-RING finger protein 128 (RNF128)-that facilitates PPARα polyubiquitination, resulting in the degradation and suppression of PPARα function during fasting.
View Article and Find Full Text PDFNat Commun
September 2025
State Key Laboratory of Loess Science, Institute of Earth Environment, Chinese Academy of Sciences, Xi'an, China.
How terrestrial mean annual temperature (MAT) evolved throughout the past 2 million years (Myr) remains elusive, limiting our understanding of the patterns, mechanisms, and impacts of past temperature changes. Here we report a ~2-Myr terrestrial MAT record based on fossil microbial lipids preserved in the Heqing paleolake, East Asia. The increased amplitude and periodicity shift of glacial-interglacial changes in our record align with those in sea surface temperature (SST) records.
View Article and Find Full Text PDFNature
September 2025
Department of Neurology, Brigham and Women's Hospital, Boston, MA, USA.
Neural activity is increasingly recognized as a crucial regulator of cancer growth. In the brain, neuronal activity robustly influences glioma growth through paracrine mechanisms and by electrochemical integration of malignant cells into neural circuitry via neuron-to-glioma synapses. Outside of the central nervous system, innervation of tumours such as prostate, head and neck, breast, pancreatic, and gastrointestinal cancers by peripheral nerves similarly regulates cancer progression.
View Article and Find Full Text PDFNature
September 2025
Centre for Evolution and Cancer, Institute of Cancer Research, London, UK.
Cancer development and response to treatment are evolutionary processes, but characterizing evolutionary dynamics at a clinically meaningful scale has remained challenging. Here we develop a new methodology called EVOFLUx, based on natural DNA methylation barcodes fluctuating over time, that quantitatively infers evolutionary dynamics using only a bulk tumour methylation profile as input. We apply EVOFLUx to 1,976 well-characterized lymphoid cancer samples spanning a broad spectrum of diseases and show that initial tumour growth rate, malignancy age and epimutation rates vary by orders of magnitude across disease types.
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