An improved technique for solving two‐dimensional shallow water problems

A numerical model for solving the 2D shallow water equations is proposed herewith. This model is based on a finite volume technique in a generalized co‐ordinate system, coupled with a semi‐implicit splitting algorithm in which a Helmholtz equation is used for the surface elevation. Several benchmark problems have proven the good accuracy of this method in complex geometries. Nevertheless, several numerical perturbations were noted in the surface elevation. After finding the origin, a new numerical technique is suggested, to avoid these perturbations. Several severe tests are proposed to validate this technique. Copyright © 1999 John Wiley & Sons, Ltd.     

Paclitaxel‐Loaded Stabilizer‐Free Poly(D,L‐lactide‐co‐glycolide) Nanoparticles Conjugated with Quantum Dots for Reversion of Anti‐Cancer Drug Resistance and Cancer Cellular Imaging

We prepared the PLGA‐loaded anti‐cancer drug and coated it with quantum dots to make it a dual‐function nanoparticles, and analyzed its potential use in cellular imaging and curing cancers. Two cancer cell lines, paclitaxel‐sensitive KB and paclitaxel‐resistant KB paclitaxel‐50 cervical carcinoma cells, were the relativistic models for analysis of the cytotoxicity of free paclitaxel and paclitaxel‐loaded PLGA conjugated with quantum‐dot nanoparticles. The paclitaxel‐loaded PLGA conjugated with quantum dots nanoparticles were significantly more cytotoxic than the free paclitaxel drug in paclitaxel‐resistant KB paclitaxel‐50 cells. This might have been because the cancer cells developed multi‐drug resistance (MDR), which hampered the action of free paclitaxel by pumping its molecules to extracellular areas. Addition of verapamil, a P‐glycoprotein inhibitor, reversed the MDR mechanism and significantly reduced KB paclitaxel‐50 cell viability. As a result, KB paclitaxel‐50 was highly associated with MDR on the cell membrane. The cytotoxicity results indicated that PLGA nanoparticles served as drug carriers and protected the drugs from MDR‐accelerated efflux. Combined quantum dots with PLGA nanoparticles allowed additional functionality for cellular imaging.     

Schwarz domain decomposition for the incompressible Navier–Stokes equations in general co‐ordinates

This paper describes a domain decomposition method for the incompressible Navier–Stokes equations in general co‐ordinates. Domain decomposition techniques are needed for solving flow problems in complicated geometries while retaining structured grids on each of the subdomains. This is the so‐called block‐structured approach. It enables the use of fast vectorized iterative methods on the subdomains. The Navier–Stokes equations are discretized on a staggered grid using finite volumes. The pressure‐correction technique is used to solve the momentum equations together with incompressibility conditions. Schwarz domain decomposition is used to solve the momentum and pressure equations on the composite domain. Convergence of domain decomposition is accelerated by a GMRES Krylov subspace method. Computations are presented for a variety of flows. Copyright © 2000 John Wiley & Sons, Ltd.     

Homology and cohomology intersection numbers of GKZ systems

We describe the homology intersection form associated to regular holonomic GKZ systems in terms of the combinatorics of regular triangulations. Combining this result with the twisted period relation, we obtain a formula of cohomology intersection numbers in terms of a Laurent series. We show that the cohomology intersection number depends rationally on the parameters. We also prove a conjecture of F. Beukers and C. Verschoor on the signature of the monodromy invariant hermitian form.     

高效液相色谱法直接拆分非甾体解热镇痛药物对映体

使用Kromasil CHI-TBB手性固定相,分离了非甾体解热镇痛药卡洛芬,氟吡洛芬,非诺洛芬,酮洛芬,吡咯芬和萘普生等对映体。结果表明,这种以酒石酸二酰胺为手性中心的商业化手性固定相,适合于在正相条件下分离上述药物对映体,对映体分离因子和分析时间可以通过向流动相中添加极性物质如异丙醇,甲基叔丁醚等来进行调节。     

Blends of starch with ethylene vinyl alcohol copolymers: effect of water,glycerol, and amino acids as plasticizers

Blends of thermoplastic starch with poly(ethylene‐co‐vinyl alcohol) copolymer (EVOH) were melt extruded with water/glycerol as plasticizer and a series of amino acid additives. The biggest factor in end‐use mechanical properties proved to be the relative humidity (RH) during storage. Plasticized starch‐EVOH blends stored at 0 and 50% RH changed significantly over time, with, for example, the tensile strength (TS) of the glycerol‐plasticized blend increasing from 4.7 to 26.3 MPa over 8 weeks when maintained at 0% RH. In contrast, the TS of this same sample stored at 75% RH remained unchanged for 8 weeks. Amino acids provided relatively minor, but significant changes in mechanical properties with time. Based on TS, elongation‐to‐break, and modulus, it may be concluded that β‐alanine, sarcosine, and L ‐proline were more effective than glycerol at maintaining strong flexible blends. Increases in crystallinity and changes in morphology with time, as described by modulated DSC were correlated to these changes in mechanical properties. Published in 2007 by John Wiley & Sons, Ltd.     

超临界二氧化碳中药物控制释放体系的一步法制备研究

用一步法首次制备了以N-异丙基丙烯酰胺类共聚物为基料的药物释放体系。在此法中,超临界二氧化碳同时作为聚合介质和渗透试剂。制得的聚合物微球用扫描电镜、差示扫描量热仪、透射电镜、X射线衍射仪等进行了表征,并用体外释放模拟考察了原位法制备的微凝胶对渗入的目标药物布洛芬的释放效果。     

低热-高压法制备PLGA多孔支架及其体外降解研究

采用低热-高压法制备了聚(dl-丙交酯／乙交酯)75／25(PLGA75／25)组织工程多孔支架。该方法避免了使用有机溶剂，支架的孔隙率在90％以上，孔径大小分布均匀。多孔支架经过酒精处理后，支架表面产生许多微小的凹陷；用藻酸钙改性处理后，支架形态保持良好。两种处理都使支架的压缩强度有所增大，亲水性增强。虽然孔隙率高的支架降解速率稍慢，但其体外降解规律基本一致：特性粘数争力学强度衰减快，而质量损失较慢，降解6周后，支架的质量损失仅为3％左右；体外降解3周后，支架的形态保持良好，可望在细胞移植争组织修复的早期发挥支撑作用。     

粘塑性薄壁管中复合应力波的传播特性研究

以本构关系一般理论为基础,导出了计及材料功硬化效应和应变率硬化效应的粘塑性薄壁管的本构关系及管中复合应力波的控制方程,应用有限差分方法研究了在压扭复合冲击载荷作用下粘塑性薄壁管中复合应力波的传播特性与演化规律,分析了复合应力波的耦合效应以及薄壁管中粘塑性参数和功硬化效应对复合应力波传播与演化规律的影响,并对有关现象进行了分析和解释。