121 research outputs found

    Synthesis, Characterization and Properties Evaluation of Degradable Poly(vinyl-co-ester)s

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    The aim of my work is to provide basic understanding of polymerization behavior of cyclic ketene acetals with different vinyl monomers and their properties evaluation. First, functional degradable poly(ester-co-NIPAAm) is synthesized by free radical copolymerization. The copolymerization behavior is intensively analyzed. The resulting polymers are found to be hydrolytic degradable and thermal sensitive leading to a solution-suspension transition in water. Second, the strong reactivity of cyclic ketene acetals with Brönsted acids is intensively investigated, which provides important data for synthesis, cationic polymerization of cyclic ketene acetals and their copolymerization behavior with vinyl acids. Third, ion containing degradable polymers, including ionomers and polyelectrolytes, are synthesized by free radical polymerization and subsequent quaternization of amine in the chain. The resulting polymers obtain a variety of new properties, which can be easily tuned by changing the copolymer compositions and quaternization behaviors. Microstructures are intensively investigated by NMR, SAXA, TEM and DMA to establish the relationship between morphology and property

    SPHysics Simulation of Experimental Spillway Hydraulics

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    In this paper, we use the parallel open source code parallelSPHysics based on the weakly compressible Smoothed Particle Hydrodynamics (WCSPH) approach to study a spillway flow over stepped stairs. SPH is a robust mesh-free particle modelling technique and has great potential in treating the free surfaces in spillway hydraulics. A laboratory experiment is carried out for the different flow discharges and spillway step geometries. The physical model is constructed from a prototype reservoir dam in the practical field. During the experiment, flow discharge over the weir crest, free surface, velocity and pressure profiles along the spillway are measured. In the present SPH study, a straightforward push-paddle model is used to generate the steady inflow discharge in front of the weir. The parallelSPHysics model is first validated by a documented benchmark case of skimming flow over a stepped spillway. Subsequently, it is used to reproduce a laboratory experiment based on a prototype hydraulic dam project located in Qinghai Province, China. The detailed comparisons are made on the pressure profiles on the steps between the SPH results and experimental data. The energy dissipation features of the flows under different flow conditions are also discussed. It is shown that the pressure on the horizontal face of the steps demonstrates an S-shape, while on the vertical face it is negative on the upper part and positive on the lower part. The energy dissipation efficiency of the spillway could reach nearly 80%

    Vasculoprotective effects of rosiglitazone through modulating renin-angiotensin system in vivo and vitro

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    <p>Abstract</p> <p>Background</p> <p>The peroxisome proliferator-activated receptor-γ (PPARγ) agonist rosiglitazone has been suggested to exert cardiovascular protection through the improvement of lipid metabolism, anti-inflammation, anti-proliferation etc. However, whether renin-angiotensin system (RAS) is involved in the vascular protective effects of PPARγ agonists is not fully understood. The present study aimed to investigate the effects of the renin-angiotensin system in vascular protection mediated by PPARγ agonists.</p> <p>Objective</p> <p>To investigate the actions of the renin-angiotensin system in vascular protection mediated by activation of PPARγ in vivo and in vitro.</p> <p>Methods</p> <p>Rats were fed a regular diet (n = 8), a cholesterol-rich diet plus methylthiouracil (80 mg/Kg/day, n = 10), a cholesterol-rich diet plus methylthiouracil and rosiglitazone (4 mg/kg/day, n = 10). The rosiglitazone treatment was started from one month after the start of cholesterol-rich diet plus methylthiouracil, and lasted five months. Cultured vascular smooth muscle cells (VSMCs) were pretreated with 1 μmol/L angiotensin II (ANG II) for 6 h and randomly divided into the control group; the ANG II group (1 μmol/L ANG II); the groups respectively treated with different concentration rosiglitazone (20, 30, 50) μmol/L for 12 h; the groups treated with 30 μmol/L rosiglitazone for (6, 12, 24) h. Morphology changes of the aortic tissues were observed by hematoxylin and eosin stain. The VSMC growth was detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay. Angiotensin II and expression of angiotensin receptors were determined by radioimmunoassay, reverse transcription polymerase chain reaction (RT-PCR), western blot, and immunohistochemistry.</p> <p>Results</p> <p>After 6 months, lipid deposition, VSMC proliferation and migration toward intima were observed in aortic tissues in the rats on a cholesterol-rich diet plus methylthiouracil, while these pathological changes induced by the cholesterol-rich diet were significantly suppressed by rosiglitazone. In addition, VSMC proliferation induced by ANG II was markedly inhibited by rosiglitazone. Rosiglitazone markedly down-regulated expression of angiotensin type 1 receptor (AT<sub>1</sub>R) and up-regulated expression of angiotensin type 2 receptor (AT<sub>2</sub>R) in the aortic tissues and ANG II-treated VSMCs.</p> <p>Conclusions</p> <p>The present study demonstrated that PPARγ agonist rosiglitazone suppressed ANG II-induced VSMC proliferation in vitro and early atherosclerotic formation evoked by cholesterol-rich diet in vivo. These vasculoprotective effects of rosiglitazone were mediated at least partially by reduction in local tissue ANG II concentration, down-regulation of AT<sub>1</sub>R expression and up-regulation of AT<sub>2</sub>R expression both at the mRNA and protein levels.</p

    SWE-SPHysics Simulation of Dam Break Flows at South-Gate Gorges Reservoir

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    This paper applied a Smoothed Particle Hydrodynamics (SPH) approach to solve Shallow Water Equations (SWEs) to study practical dam-break flows. The computational program is based on the open source code SWE-SPHysics, where a Monotone Upstream-centered Scheme for Conservation Laws (MUSCL) reconstruction method is used to improve the Riemann solution with Lax-Friedrichs flux. A virtual boundary particle method is applied to treat the solid boundary. The model is first tested on two benchmark collapses of water columns with the existence of downstream obstacle. Subsequently the model is applied to forecast a prototype dam-break flood, which might occur in South-Gate Gorges Reservoir area of Qinghai Province, China. It shows that the SWE-SPH modeling approach could provide a promising simulation tool for practical dam-break flows in engineering scale

    Rutin Protects against Pirarubicin-Induced Cardiotoxicity through TGF- β

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    We investigated the potential protective effect of rutinum (RUT) against pirarubicin- (THP-) induced cardiotoxicity. THP was used to induce toxicity in rat H9c2 cardiomyoblasts. Positive control cells were pretreated with a cardioprotective agent dexrazoxane (DZR) prior to treatment with THP. Some of the cells were preincubated with RUT and a p38 mitogen-activated protein kinase (MAPK) inhibitor, SB203580, both individually and in combination, prior to THP exposure. At a dose range of 30–70 μM, RUT significantly prevented THP-induced reduction in cell viability; the best cardioprotective effect was observed at a dose of 50 μM. Administration of RUT and SB203580, both individually as well as in combination, suppressed the elevation of intracellular ROS, inhibited cell apoptosis, and reversed the THP-induced upregulation of TGF-β1, p-p38 MAPK, cleaved Caspase-9, Caspase-7, and Caspase-3. A synergistic effect was observed on coadministration of RUT and SB203580. RUT protected against THP-induced cardiotoxicity by inhibition of ROS generation and suppression of cell apoptosis. The cardioprotective effect of RUT appears to be associated with the modulation of the TGF-β1-p38 MAPK signaling pathway

    Population genetics analysis of the black rockfish <em>Sebastes schlegelii</em> in Northern China based on 2b-RAD simplified genome sequencing

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    The black rockfish Sebastes schlegelii is an important fishery species in Japan, South Korea, and China. Overfishing has severely depleted the natural resources of S. schlegelii in recent years, leading to the initiation of programs aimed at enhancing fish stock. However, the genetic structure of northern populations remains elusive, posing challenges in collecting and preserving germplasm resources. In this study, a total of 191 S. schlegelii individuals from seven populations, including one cultured population (Changdao: CDYZ) and six wild populations (Lianyungang: LYG; Qingdao: QD; Weihai: WH; Changdao: CDYS; Beidaihe: BDH) sequenced by 2b-RAD method and their population genetics was analyzed using 27,064 SNPs obtained. The results indicated low genetic diversity in both wild and cultured populations (PIC Ho: 0.174-0.273, He: 0.173-0.234), with the cultured population exhibiting higher diversity than the wild ones. Moderate genetic differentiation existed between the cultured population and six wild populations (0.05 Fst Fst Nm > 1). This study provides a theoretical basis for conserving and rationalizing germplasm resources for S. schlegelii

    Angiopoietin-2 impairs collateral artery growth associated with the suppression of the infiltration of macrophages in mouse hindlimb ischaemia

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    Abstract Background Angiopoietin-2 (Ang-2), a ligand of the Tie-2 receptor, plays an important role in maintaining endothelial cells and in destabilizing blood vessels. Collateral artery growth (arteriogenesis) is a key adaptive response to arterial occlusion. It is unknown whether the destabilization of blood vessels by Ang-2 can affect arteriogenesis and modulate mononuclear cell function. This study aimed to investigate the effects of Ang-2 on collateral artery growth. Methods Hindlimb ischaemia model was produced in C57BL/6 mice by femoral artery ligation. Blood flow perfusion was measured using a laser Doppler perfusion imager quantitative RT-PCR analysis was applied to identify the level of angiogenic factors. Results After the induction of hindlimb ischaemia, blood flow recovery was impaired in mice treated with recombinant Ang-2 protein; this was accompanied by a reduction of peri-collateral macrophage infiltration. In addition, quantitative RT-PCR analysis revealed that Ang-2 treatment decreased monocyte chemotactic protein-1 (MCP-1), platelet-derived growth factor-BB (PDGF-BB) mRNA levels in ischaemic adductor muscles. Ang-2 can lead to macrophage M1/M2 polarization shift inhibition in the ischaemic muscles. Furthermore, Ang-2 reduced the in vitro inflammatory response in macrophages and vascular cells involved in arteriogenesis. Conclusions Our results demonstrate that Ang-2 is essential for efficient arteriogenesis, which controls macrophage infiltration

    Biodegradable polyester-based nano drug delivery system in cancer chemotherapy: a review of recent progress (2021–2023)

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    Cancer presents a formidable threat to human health, with the majority of cases currently lacking a complete cure. Frequently, chemotherapy drugs are required to impede its progression. However, these drugs frequently suffer from drawbacks such as poor selectivity, limited water solubility, low bioavailability, and a propensity for causing organ toxicity. Consequently, a concerted effort has been made to seek improved drug delivery systems. Nano-drug delivery systems based on biodegradable polyesters have emerged as a subject of widespread interest in this pursuit. Extensive research has demonstrated their potential for offering high bioavailability, effective encapsulation, controlled release, and minimal toxicity. Notably, poly (ε-caprolactone) (PCL), poly (lactic-co-glycolic acid) (PLGA), and polylactic acid (PLA) have gained prominence as the most widely utilized options as carriers of the nano drug delivery system. This paper comprehensively reviews recent research on these materials as nano-carriers for delivering chemotherapeutic drugs, summarizing their latest advancements, acknowledging their limitations, and forecasting future research directions
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