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High Shear (high + shear)
Terms modified by High Shear Selected AbstractsHaemorheology in Gaucher diseaseEUROPEAN JOURNAL OF HAEMATOLOGY, Issue 3 2005Bridget E. Bax Abstract:, In Gaucher disease, a deficiency of glucocerebrosidase results in the accumulation of glucocerebroside within the lysosomes of the monocyte,macrophage system. Prior to the availability of enzyme replacement therapy (ERT), splenectomy was often indicated for hypersplenism. Haemorheological abnormalities could be expected in view of the anaemia and abnormal lipid metabolism in these patients and the role of the spleen in controlling erythrocyte quality. Objectives: To investigate the effect of Gaucher disease on blood and plasma viscosity, erythrocyte aggregation and erythrocyte deformability, and to determine whether observed rheological differences could be attributed to splenectomy. Methods: Haematological and haemorheological measurements were made on blood collected from 26 spleen-intact patients with Gaucher disease, 16 splenectomised patients with Gaucher disease, 6 otherwise healthy asplenic non-Gaucher disease subjects and 15 healthy controls. Results: No haemorheological differences could be demonstrated between spleen-intact patients with Gaucher disease and the control group. Compared to controls, both asplenic Gaucher disease and asplenic non-Gaucher disease study groups had a reduced MCHC (P = 0.003 and 0.005, respectively) and increased whole blood viscosity at 45% haematocrit (Hct), relative viscosity and red cell aggregation index , all measured at low shear (P < 0.05 for all). Additionally, asplenic patients with Gaucher disease alone showed an increased MCV (P = 0.006), an increased whole blood viscosity at 45% Hct measured at high shear (P = 0.019), and a reduced relative filtration rate (P = 0.0001), compared to controls. Conclusion: These observations demonstrate a direct and measurable haemorheological abnormality in Gaucher disease only revealed when there is no functioning spleen to control erythrocyte quality. [source] A spectral projection method for the analysis of autocorrelation functions and projection errors in discrete particle simulationINTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN FLUIDS, Issue 7 2008André Kaufmann Abstract Discrete particle simulation is a well-established tool for the simulation of particles and droplets suspended in turbulent flows of academic and industrial applications. The study of some properties such as the preferential concentration of inertial particles in regions of high shear and low vorticity requires the computation of autocorrelation functions. This can be a tedious task as the discrete point particles need to be projected in some manner to obtain the continuous autocorrelation functions. Projection of particle properties on to a computational grid, for instance, the grid of the carrier phase, is furthermore an issue when quantities such as particle concentrations are to be computed or source terms between the carrier phase and the particles are exchanged. The errors committed by commonly used projection methods are often unknown and are difficult to analyse. Grid and sampling size limit the possibilities in terms of precision per computational cost. Here, we present a spectral projection method that is not affected by sampling issues and addresses all of the above issues. The technique is only limited by computational resources and is easy to parallelize. The only visible drawback is the limitation to simple geometries and therefore limited to academic applications. The spectral projection method consists of a discrete Fourier-transform of the particle locations. The Fourier-transformed particle number density and momentum fields can then be used to compute the autocorrelation functions and the continuous physical space fields for the evaluation of the projection methods error. The number of Fourier components used to discretize the projector kernel can be chosen such that the corresponding characteristic length scale is as small as needed. This allows to study the phenomena of particle motion, for example, in a region of preferential concentration that may be smaller than the cell size of the carrier phase grid. The precision of the spectral projection method depends, therefore, only on the number of Fourier modes considered. Copyright © 2008 John Wiley & Sons, Ltd. [source] Metal-exchanged clay and zeolite additives as smoke suppressants and fire retardants for poly(vinyl chloride)JOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 2 2009Alexander G. Zestos Cone calorimetry studies showed that various metal-exchanged clays and zeolites containing only 3,4% of Cu(II), Cu(I), Zn(II), or Al(III) were effective smoke suppressants and fire retardants for plasticized poly(vinyl chloride). Copper(II)-Zn(II) and Cu(II)-Al(III) synergism for smoke and heat reduction was observed with binary blends of the clays, and the effectiveness of the additives was usually improved considerably by heating plasticizer-additive mixtures under very high shear before combining them with the polymer. Possible mechanisms of action of the additives are described. J. VINYL ADDIT. TECHNOL., 2009. © 2009 Society of Plastics Engineers [source] Interactions of Platelets with Subendothelium and EndotheliumMICROCIRCULATION, Issue 3 2005JUNMEI CHEN PhD ABSTRACT In this review, the authors summarize how platelets interact with subendothelium when the vessel wall is damaged or with intact endothelium in the inflammatory state. When subendothelium is exposed to rapidly flowing blood upon vessel damage, platelets adhere rapidly to the exposed surface, decelerate, and aggregate to arrest bleeding. Under high shear stress, such as is found in the microcirculation, the interaction between subendothelial von Willebrand factor (VWF) and its platelet receptor, glycoprotein (GP) Ib-IX-V, is required to slow down platelets and allow the platelet collagen receptors ,2,1 and GP VI to bind to collagen. GP VI and ,2,1 play important roles to activate platelets in the early stage and work with GP Ib-IX-V to fully activate platelets to form thrombi. GP Ib-IX-V and GP VI employ similar signaling pathways for platelet activation and the signals from both receptors are down-modulated by PECAM-1 (platelet,endothelial,cell adhesion molecule 1) to prevent unnecessary platelet activation under high shear. During inflammatory states, intact endothelial cells release VWF and P-selectin from their Weibel-Palade bodies. Both molecules are ligands for GP Ib-IX-V. The newly released VWF is larger and stickier than the form normally found in plasma and binds platelets spontaneously. Normally, VWF is processed by proteolysis by the plasma metalloprotease ADAMTS-13. Failure of this processing results in the microvascular thrombotic disorder thrombotic thrombocytopenic purpura. In this review, the authors also use available crystal structures of platelet receptors and ligands to explain the details of their interactions. [source] Response of a concentrated monoclonal antibody formulation to high shearBIOTECHNOLOGY & BIOENGINEERING, Issue 5 2009Jared S. Bee Abstract There is concern that shear could cause protein unfolding or aggregation during commercial biopharmaceutical production. In this work we exposed two concentrated immunoglobulin-G1 (IgG1) monoclonal antibody (mAb, at >100 mg/mL) formulations to shear rates between 20,000 and 250,000 s,1 for between 5 min and 30 ms using a parallel-plate and capillary rheometer, respectively. The maximum shear and force exposures were far in excess of those expected during normal processing operations (20,000 s,1 and 0.06 pN, respectively). We used multiple characterization techniques to determine if there was any detectable aggregation. We found that shear alone did not cause aggregation, but that prolonged exposure to shear in the stainless steel parallel-plate rheometer caused a very minor reversible aggregation (<0.3%). Additionally, shear did not alter aggregate populations in formulations containing 17% preformed heat-induced aggregates of a mAb. We calculate that the forces applied to a protein by production shear exposures (<0.06 pN) are small when compared with the 140 pN force expected at the air,water interface or the 20,150 pN forces required to mechanically unfold proteins described in the atomic force microscope (AFM) literature. Therefore, we suggest that in many cases, air-bubble entrainment, adsorption to solid surfaces (with possible shear synergy), contamination by particulates, or pump cavitation stresses could be much more important causes of aggregation than shear exposure during production. Biotechnol. Bioeng. 2009;103: 936,943. © 2009 Wiley Periodicals, Inc. [source] |