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Biorheology is an international interdisciplinary journal that publishes research on the deformation and flow properties of biological systems or materials. It is the aim of the editors and publishers of
Biorheology to bring together contributions from those working in various fields of biorheological research from all over the world. A diverse editorial board with broad international representation provides guidance and expertise in wide-ranging applications of rheological methods to biological systems and materials.
The aim of biorheological research is to determine and characterize the dynamics of physiological processes at all levels of organization. Manuscripts should report original theoretical and/or experimental research promoting the scientific and technological advances in a broad field that ranges from the rheology of macromolecules and macromolecular arrays to cell, tissue and organ rheology. In all these areas, the interrelationships of rheological properties of the systems or materials investigated and their structural and functional aspects are stressed.
The scope of papers solicited by
Biorheology extends to systems at different levels of organization that have never been studied before, or, if studied previously, have either never been analyzed in terms of their rheological properties or have not been studied from the point of view of the rheological matching between their structural and functional properties. This biorheological approach applies in particular to molecular studies where changes of physical properties and conformation are investigated without reference to how the process actually takes place, how the forces generated are matched to the properties of the structures and environment concerned, proper time scales, or what structures or strength of structures are required.
Biorheology invites papers in which such 'molecular biorheological' aspects, whether in animal or plant systems, are examined and discussed. While we emphasize the biorheology of physiological function in organs and systems, the biorheology of disease is of equal interest. Biorheological analyses of pathological processes and their clinical implications are encouraged, including basic clinical research on hemodynamics and hemorheology.
In keeping with the rapidly developing fields of mechanobiology and regenerative medicine,
Biorheology aims to include studies of the rheological aspects of these fields by focusing on the dynamics of mechanical stress formation and the response of biological materials at the molecular and cellular level resulting from fluid-solid interactions. With increasing focus on new applications of nanotechnology to biological systems, rheological studies of the behavior of biological materials in therapeutic or diagnostic medical devices operating at the micro and nano scales are most welcome.
Abstract: Collagen fibrils in ligaments and tendons are highly organized into parallel arrays which influence interstitial fluid transport. Finite element (FE) models were developed analogous to the fibrillar arrays in ligaments and tendons to investigate interstitial fluid flow and tissue permeability as a function of interfibrillar spacing and fluid properties. Collagen fibrils were assumed to be a periodic square array of impermeable cylinders. A two‐dimensional FE model was used to study transverse fluid flow and a three‐dimensional model was used to study flow parallel to the collagen fibrils. Parametric FE analysis provided data to formulate empirical expressions for permeability (\kappa…) as a function of porosity (\phi ). Results show that longitudinal permeability (\kappa=1.1\cdot 10^{-15} \phi^{2.5}[1-\phi]^{-0.333} ) can be up to 50 times higher than transverse permeability (\kappa=1.2\cdot 10^{-15} \phi^{0.5}[\phi-\phi_{\min}]^{2.5} ) in a compact array. Maximum fluid shear stresses occur at the narrowest zones of adjacent fibrils (1.21 Pa or 12.1 dyn/cm^{2} at 10 \mu m/s of average transverse influx). If interstitial fluid is highly non‐Newtonian, the permeability should be considered as flow (shear)‐dependent. The computational results suggest that tissue permeability in ligaments and tendons is highly anisotropic, porosity‐dependent, and can be estimated by analytic expressions.
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Keywords: Finite element analysis, ligaments and tendons, interstitial fluid, tissue permeability, non‐Newtonian fluid
Citation: Biorheology,
vol. 35, no. 2, pp. 103-118, 1998
Abstract: A filtrometer is described for measuring the flow of fluids through microfilters. The flow of Newtonian fluids through the filters can be predicted from the diameter, length and number of pores. There are no physical artefacts such as turbulent flow or a significant lag period before steady‐state flow is achieved. The instrument has been used as a viscometer and has been used to record and analyse the flow of undiluted blood through 5 \mu m polycarbonate filters. The calculated viscosity of Newtonian fluids agrees well with those measured by a more conventional viscometer (Ostwald). Flow profiles of blood have…been analysed to give both the numbers and the flow properties of a small population of slow leukocytes which equate numerically with the monocytes. They are subdivided into three distinct sub‐populations, according to their rheological properties, and these are termed \mathit{SL}_{1} , \mathit{SL}_{2} and \mathit{PB} . The concentration of these cells, in blood, are 0.12\pm0.02 \times 10^{6} ml^{-1} , 0.11\pm0.02 \times 10^{6} ml^{-1} , 0.09\pm0.02 \times 10^{6} ml^{-1} in young females aged about 25 years. The transit time of these cells, through 5 \mu m pores, is 34.8\pm1.4 s, 147.5\pm2.5 s and > 300 s, respectively. Analysis of blood from older men (53–79 years) gives essentially the same results although the concentration of SL_{1} is slightly higher at 0.19\pm0.09 \times 10^{6} ml^{-1} .
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Abstract: We tested a new routine to eliminate leukocytes for blood rheology measurements using commercial leukocyte absorbing filters (here PALL RC400). These filters were punched out and fitted in smaller chambers through which blood was filtered under controlled suction pressure (<30 mm Hg). This technique resulted in a very effective leukocyte elimination to 0.0022% but also a platelet reduction to 0.2%. The process causes a small but significant hemolysis with free hemoglobin, of the order of 0.06% of the filtered erythrocytes. A small fraction of the erythrocytes were retained in the filter, versus plasma, to reduce the hematocrit on…the order of 1.4%. The leukocyte filtration did not cause any detectable functional trauma to the erythrocytes, measured as micro‐pore filterability of normal and glutaraldehyde (GA) hardened erythrocytes. However, when 10% of the erythrocytes were hardened with GA, which caused an increase in pore clogging slope (p<0.05 ), the additional passage through the leukocyte elimination filter removed this measured change in clogging. This observation suggests that the leukocyte elimination filter may selectively remove, not only leukocytes and platelets, but also hardened erythrocytes. Reticulocyte counting did not reveal any selective removal of young erythrocytes. In general, we find the presented method reproducible, efficient and easy for eliminating leukocytes for blood rheology research although the risk of removing undeformable erythrocytes must be considered.
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Keywords: RBC, filtration, WBC removal, rheology
Citation: Biorheology,
vol. 35, no. 2, pp. 131-140, 1998
Abstract: The results of most filtration assays for deformability of erythrocytes do not distinguish whether the entire population or only its small fraction exhibits abnormal rheological properties. We developed a simple filtration method for determination of the percentage of nonfilterable cells in erythrocyte suspension using membrane filters with mean pore diameter of 3.1 \mu m. This method makes it possible to detect even minor abnormal subpopulations in erythrocyte suspensions. The flow rate of buffer depends on the number of free pores of a filter. The plot of the number of pores clogged by nonfilterable cells vs the total number of…erythrocytes that were allowed to pass through the filter had a linear portion, with a slope representing the relative content, Z %, of nonfilterable cells in the suspension. We determined Z % for various medium osmolalities u and used the data to derive the distribution of erythrocytes in u_{\mathrm{cr}} (u_{\mathrm{cr}} is the maximum value of u at which an erythrocyte cannot pass through a pore of a given filter because of geometric limitations). The distribution of u_{\mathrm{cr}} in suspension of normal erythrocytes has a maximum of about 200 mOsm/kg and a half‐width of about 20 mOsm/kg. The distributions of u_{\mathrm{cr}} are altered in normal erythrocyte suspensions at decreased pH values, in cryopreserved and ATP‐depleted erythrocyte suspensions and in erythrocytes from a xerocytosis patient.
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Abstract: Electrostatic repulsion among erythrocytes in flow was evaluated through measurement of the thickness of the marginal cell‐free layer in narrow glass tubes of 20–50 \mu m in inner diameter. To reduce the electrostatic repulsive force, due mainly to sialic acid of the membrane glycoproteins, human erythrocytes were treated with neuraminidase. The surface negative charge of the erythrocytes, as determined from the electrophoretic mobility using free‐flow electrophoresis, was found to be proportional to the sialic acid content. When erythrocytes with decreased sialic acid content flowed through narrow tubes, the thickness of cell‐free layer determined using an image processor increased even…in the absence of erythrocyte aggregation in the suspension. The effect was more pronounced at acidic pH. The addition of Dextran T‐70 (70,400 Mol. Wt.) further increased the cell‐free layer thickness due to erythrocyte aggregation. Thus, reducing the negative charge density on the erythrocyte surface by itself accelerates the axial accumulation of erythrocytes in flow due to the decreased electrostatic repulsive force between the cells, even in the absence of erythrocyte aggregation.
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