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These results may explain from a molecular perspective the beneficial effects of RT in the prevention of metabolic-associated disorders such as obesity, diabetes and related complications.Targeted delivery of anticancer drugs is one of the most promising methods for cancer therapy. However, barriers including complicated procedures, costly preparation, and toxic side effects have restricted the development of nuclear-targeted nanocarriers. Natural polysaccharides as extracellular matrix constituents or analogs play an important role in biomineralization. Herein, a simple, polysaccharide-intervened preparation of hydroxyapatite (HA) hybrid nanoparticles (NPs) with low crystallinity was used as a bio-safe carrier for targeting the delivery of doxorubicin (DOX) for efficient anticancer therapy. The poorly crystallized hybrid HA NPs were specifically taken up by cancer cells (HeLa cells), and subsequently, the abrupt degradation of HA nanoparticles would cause a change in the osmotic pressure, leading to the explosive death of cancer cells. Furthermore, the hybrid HA NPs were size changeable and capable of directly delivering the anti-cancer drug into the nucleus of cancer cells, thereby efficiently killing cancer cells. In addition, the HA/ALG NPs reduce the toxicity of DOX to L929 cells and cause little negative effect on normal tissue cells. The in vitro and in vivo experiments confirmed that the size-changeable HA-ALG/DOX could be a promising nuclear-targeted delivery nanocarrier for efficient cancer therapy.The transport of bio-particles in viscous flows exhibits a rich variety of dynamical behaviour, such as morphological transitions, complex orientation dynamics or deformations. Characterising such complex behaviour under well controlled flows is key to understanding the microscopic mechanical properties of biological particles as well as the rheological properties of their suspensions. While generating regions of simple shear flow in microfluidic devices is relatively straightforward, generating straining flows in which the strain rate is maintained constant for a sufficiently long time to observe the objects' morphologic evolution is far from trivial. In this work, we propose an innovative approach based on optimised design of microfluidic converging-diverging channels coupled with a microscope-based tracking method to characterise the dynamic behaviour of individual bio-particles under homogeneous straining flow. The tracking algorithm, combining a motorised stage and a microscopy imaging system controlled by external signals, allows us to follow individual bio-particles transported over long-distances with high-quality images. We demonstrate experimentally the ability of the numerically optimised microchannels to provide linear velocity streamwise gradients along the centreline of the device, allowing for extended consecutive regions of homogeneous elongation and compression. We selected three test cases (DNA, actin filaments and protein aggregates) to highlight the ability of our approach for investigating dynamics of objects with a wide range of sizes, characteristics and behaviours of relevance in the biological world.Incorporating molecular catalysts into metal-organic frameworks (MOFs) is a promising strategy for improving their catalytic longevity and recyclability. In this article, we investigate and compare synthetic routes for the incorporation of the potent water oxidation catalyst Ru(tda)(pyCO2H)2 (tda = 2,2'6',2''-terpyridine-6,6''-dicarboxylic acid, pyCO2H = iso-nicotinic acid) as a structural linker into a Zr-based UiO-type MOF. The task is challenging with this particular metallo-linker because of the equatorial dangling carboxylates that can potentially compete for Zr-coordination, as well as free rotation of the pyCO2H groups around the HO2CpyRupyCO2H axis. As a consequence, all attempts to synthesize a MOF with the metallo-linker directly under solvothermal conditions led to amorphous materials with the Ru(tda)(pyCO2H)2 linker coordinating to the Zr nodes in ill-defined ways, resulting in multiple waves in the cyclic voltammograms of the solvothermally obtained materials. On the other hand, an indirect post-synthetic approach in which the Ru(tda)(pyCO2H)2 linker is introduced into a preformed edba-MOF (edba = ethyne dibenzoic acid) of UiO topology results in the formation of the desired material. Interestingly, two distinctly different morphologies of the parent edba-MOF have been discovered, and the impact that the morphological difference has on linker incorporation is investigated.Hydrogen peroxide (H2O2) is an important mediator in biological medicine, disease diagnosis and environmental analyses and therefore it is essential to develop a detection approach for H2O2 in physical environments. Herein, we designed and prepared a series of AuNP-containing nanocomposites (AuNPs@NGO-PEG, AuNPs@G1-PAMAM-NGO-PEG and AuNPs@G3-PAMAM-NGO-PEG) for enhanced non-enzymatic H2O2 detection. We firstly demonstrated functionalized nanographene oxide (NGO) based materials, which combined advantages of biocompatible poly(ethylene glycol) (PEG), hyperbranched polyamidamine (PAMAM) dendrimer and thiol active site, as compatible platforms. Gold nanoparticles (AuNPs) were then aptly in situ grown on these functionalized NGO based materials via the reduction of HAuCl4 under mild conditions, i.e. AuNPs@NGO-PEG, AuNPs@G1-PAMAM-NGO-PEG and AuNPs@G3-PAMAM-NGO-PEG nanocomposites, which possess stable and uniform AuNPs standing on the functionalized NGO sheets. For H2O2 detection, these nanocomposites were cast on a glassy carbon electrode (GCE) conveniently, i.e. GCE/AuNPs@NGO-PEG, GCE/AuNPs@G1-PAMAM-NGO-PEG and GCE/AuNPs@G3-PAMAM-NGO-PEG. NSC-2260804 It is evident that these GCEs could be applied as efficient non-enzymatic H2O2 detectors resulting from the corresponding cyclic voltammetric curves and typical ready-state amperometric curves. GCE/AuNPs@G1-PAMAM-NGO-PEG exhibited the fastest electron transfer rate among these modified GCEs. We envisage that these GCEs could provide efficient sensors for H2O2 detection and a new strategy for sensor design.
Homepage: https://www.selleckchem.com/products/Rapamycin.html
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