A Journal of Environmental Sciences study reveals that metal-organic frameworks may be toxic
Peer-Reviewed Publication
Updates every hour. Last Updated: 17-Nov-2025 13:11 ET (17-Nov-2025 18:11 GMT/UTC)
Researchers at DTU have made a significant achievement by developing a new kind of electronic material that behaves almost exactly like human skin. That kind of substance could be useful in soft robotics, medicine, and healthcare.
A new study shows that giving households simple, low-cost information about their drinking water quality can greatly increase the use of safe water practices in communities at risk of contamination.
Influenza continues to pose a significant global health burden, with seasonal outbreaks causing substantial morbidity and mortality. Current antiviral therapies, such as neuraminidase inhibitors and M2 inhibitors, face challenges like drug resistance and variable efficacy. ADC189, a novel cap-dependent endonuclease (CEN) inhibitor structurally related to baloxavir marboxil, emerges as a potential therapeutic candidate. This study evaluates ADC189’s preclinical antiviral activity, pharmacokinetics, and safety in a first-in-human phase I trial. Preclinical results demonstrate potent inhibition of influenza polymerase activity across multiple strains, including oseltamivir-resistant variants, and robust efficacy in murine models. Phase I data reveal favorable pharmacokinetic profiles, prolonged half-life, and no food-related absorption interference, supporting its development as a single-dose oral therapy for influenza.
Diabetic cardiomyopathy (DCM), a major complication of diabetes mellitus, involves cardiac remodeling and dysfunction, often progressing to heart failure. Key pathological features include sarcoplasmic reticulum (SR) and mitochondrial calcium overload in cardiomyocytes, though the underlying mechanisms remain unclear. This study investigates the role of a cardiomyocyte-specific long noncoding RNA, Trdn-as, in DCM pathogenesis. Findings reveal that Trdn-as is significantly upregulated in cardiac tissues of diabetic mice and high glucose-treated cardiomyocytes. Experimental manipulation of Trdn-as in vivo and in vitro demonstrates its critical role in driving cardiac dysfunction and mitochondrial damage. Overexpression of Trdn-as in healthy mice induces DCM-like cardiac abnormalities, while silencing it in diabetic models alleviates structural and functional deficits, highlighting its potential as a therapeutic target.