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PubMedDate not supplied

Effect of viscosity upon hydrodynamically controlled natural aggregates of animal cells grown in stirred vessels.

The effect of medium viscosity upon cell growth and aggregate characteristics of baby hamster kidney (BHK) cells cultivated in stirred tanks was evaluated. Two thickening agents were tested, 9300 MW dextran and a low-viscosity sodium (carboxymethyl)-cellulose; both were used in two different sets of experiments: (i) 250 cm3 Wheaton spinner flasks with a ball impeller operated at 45 rpm; (ii) 500 cm3 Corning spinner flasks with a paddle impeller, operated at constant power dissipation (88 cm2 s-3). Aggregate diameter and the fraction of cells in aggregates increased with the increase in viscosity. Power laws were applied to the experimental results. A dependence of aggregate size upon power dissipation of the order of -0.19 and kinematic viscosity of 0.34 and 0.49 for the constant agitation and constant power dissipation tests were obtained, respectively. A model based upon the entire universal-equilibrium range (i.e., the entire spectrum of isotropic eddies) was used to predict theoretical relationships between the variables studied. The model leads to a power dependence of -0.25 for the energy dissipated in the entire universal-equilibrium range and between 0.25 and 0.5 for the kinematic viscosity in the viscous dissipation subrange, depending on the energy correlation used; it also gives a good explanation for the dependence of aggregate size on the hydrodynamics of the vessel.

Animals↗
PubMedDate not supplied

Hydrodynamic alterations during cyanobacteria (Arthrospira platensis) growth from low to high biomass concentration inside tubular photobioreactors.

The rheological behavior of an Arthrospira culture was studied from low to high biomass concentration. Two tubular undulating row photobioreactors (TURP-5r and TURP-10r), with a very short light path of 1.0 cm, were used during batch growth. In TURP-5r, the biomass concentration increased to 14.5 g(dw) L(-1), and alterations of the physical properties and hydrodynamic behavior occurred as a result. In the past, the rheological characteristics of photosynthetic-microbe cultures were rarely investigated because of the low biomass concentration attained in the systems. Developing closed photobioreactor technologies, the optimum biomass concentration rises and the viscosity, the generalized Reynolds number (N'(Re)), and the power required for culture recycling are also subject to alteration. Starting from a biomass concentration of 4.1 g(dw) L(-1), the Arthrospira culture already exhibits the characteristics of a non-Newtonian fluid. As a result of culture recycling from 2.0 to 20.5 g(dw) L(-1) and an available power of 1.67 W row(-1), we demonstrated that N'(Re) is reduced from 6265 to 1148. Our experimental results showed that N'(Re) of 2345 can be reached only at a cell concentration below 11.1 g(dw) L(-1), while at a cell concentration below 4.1 g(dw) L(-1) N'(Re) = 4080 was reached. The power consumption (P(c)) for culture recycling increased noticeably when the cell concentration rose; the highest P(c) increase attained was from 2.0 to 4.1 g(dw) L(-1). This is the range within which the Arthrospira culture changes from a Newtonian to a non-Newtonian fluid.

Bioreactors↗
PubMed2001

Determination of electrophoretic mobilities and hydrodynamic radii of three humic substances as a function of pH and ionic strength.

Capillary electrophoresis (CE) and fluorescence correlation spectroscopy (FCS) were employed to determine electrophoretic mobilities and hydrodynamic sizes of three humic substances (IHSS aquatic fulvic acid (FA), IHSS aquatic humic acid (HA), and IHSS peat humic acid (PHA)) as a function of pH and ionic strength. A slight aggregation corresponding to the formation of dimers and trimers was observed at low pH using fluorescence correlation spectroscopy (FCS). For example, for the peat humic acid, diffusion coefficients decreased from 2.1 x 10(-10) m2 s(-1) at pH 4 to 2.4 x 10(-10) m2 s(-1) at pH 11. For all three humic substances, electrophoretic mobilities were also shown to decrease significantly below pH 6. Calculated zeta potentials observed at high pH of -69 mV (FA), -62 mV (HA), and -63 mV (PHA) decreased to -39, -50, and -47 mV, respectively, under slightly acidic pH (4.5-4.8) conditions. No evidence of ionic strength induced aggregation was found using fluorescence correlation spectroscopy (FCS); diffusion coefficients increased slightly (<25%) with increasing ionic strength (up to 1 M). Negative electrophoretic mobilities decreased to a maximum measured ionic strength of 0.18 M. Above this ionic strength, no peaks were observed due to an increased HS adsorption to the capillary wall and an important decrease in electroosmotic flow. Interpretation of electrophoretic mobilities determined by CE is complicated by the fact that under certain conditions, HS appeared to be complexed by CE buffer systems, including MES, BES, and AMPSO.

Alkanesulfonic Acids↗
PubMed2002

Calibrating the uptake kinetics of semipermeable membrane devices in water: impact of hydrodynamics.

The use of lipid-containing semipermeable membrane devices (SPMDs) is becoming commonplace, but the potential effects of environmental variables affecting the accumulation of contaminants into SPMDs had not been characterized sufficiently, yet. To characterize the effect of hydrodynamic conditions on the contaminant uptake kinetics, accumulation of pentachlorobenzene, hexachlorobenzene, and hexachlorocyclohexane isomers from water into SPMD was studied at various water flow rates. The accumulation kinetics of hydrophobic compounds (log Kow > 4) are governed by the aqueous boundary layer in linear flow velocity range from 0.06 to 0.28 cm s(-1) and sensitive to slight changes in flow rate. The effect of flow velocity on the exchange kinetics increases with increasing hydrophobicity. Under faster, but still laminar flow conditions (0.28-1.14 cm s(-1)), the sensitivity to changes in flow decreases to a nonsignificant level for the substances under consideration. The results of this study confirm that the use of the laboratory-derived calibration data for estimation of analyte concentrations in the ambient environment is limited unless flow-sensitive performance reference compounds are used.

Calibration↗
PubMed2003

Hydrodynamics of biological aggregates of different sludge ages: an insight into the mass transport mechanisms of bioaggregates.

Internal permeation and its role in mass transport to biological aggregates are investigated through detailed settling experiments. Three groups of bacterial aggregates (0.8-3.2 mm), which were different in fractal dimension and porosity, were generated in batch activated sludge reactors with biomass residence times (BRTs) of 5, 10, and 20 days. An apparatus of vertically connected double settling columns, which were filled respectively with water and an EDTA solution of a higher density, was used to characterize the settling and permeability features of individual aggregates. The settling velocities observed in water were in good agreement with those predicted by Stokes' law for porous but impermeable aggregates. The BRT10 and BRT20 aggregates, with porosities that were generally less than 0.92, had fluid collection efficiencies ranging from 0 to 0.1, while the BRT5 aggregates with porosities that were generally higher than 0.97 were almost completely impermeable. It is suggested that bioaggregates with either a tightly or a loosely packed structure cannot be as highly permeable as characterized for nonbiological fractal aggregates. While falling from water into the denser EDTA liquid, many BRT10 and BRT20 aggregates stopped and stayed below the interface of the two liquids for a period that was more than an order of magnitude shorter than the prediction based on the assumption of molecular diffusion as the predominant mass transport mechanism to the aggregates. The results indicate that limited intra-aggregate convection, which may not be important to the hydrodynamic properties of bioaggregates, could significantly enhance mass transport to suspended aggregates in biological wastewater treatment reactors.

Biomass↗
PubMed2006

Hydrodynamic and microbial processes controlling nitrate in a fissured-porous karst aquifer of the Franconian Alb, southern Germany.

Concentrations and stable isotope compositions of nitrate from 11 karst springs in the Franconian Alb (southern Germany) were determined during low flow and high flow conditions to assess sources and processes affecting groundwater nitrate. During low flow, nitrate concentrations in groundwater were around 0.10 mM in springs draining forested catchments, whereas in agricultural areas nitrate concentrations were typically higher reaching up to 0.93 mM. The isotopic composition of groundwater nitrate during low flow (delta15N values of -3.1 to 6.7% per hundred, delta180 values of +2.1 to 4.0% per hundred) in concert with concentration data suggests that nitrate is formed by nitrification in forest and agricultural soils. In addition, synthetic fertilizer N that has undergone immobilization and subsequent remineralization likely constitutes an additional nitrate source in agriculturally used catchments. During recharge conditions, concentrations and delta15N values of groundwater nitrate changed little, but delta18O values were significantly elevated (up to 24.5%o per hundred suggesting that around 25% of the nitrate was directly derived from atmospheric deposition. Groundwater dating revealed that low nitrate concentrations in groundwater (_> or =0 years) are consistent with a mixture of old low nitrate-containing and young water, the latter being affected by anthropogenic N inputs predominantly in the agriculturally used catchment areas during the last few decades. Thermodynamic and hydrogeological evidence also suggests that denitrification may have occurred in the porous rock matrix of the karst aquifer. This study demonstrates that a combination of hydrodynamic, chemical, and isotopic approaches provides unique insights into the sources and the biogeochemical history of nitrate in karst aquifers, and therefore constitutes a valuable tool for assessing the vulnerability of karst aquifers to nitrate pollution in dependence on land use and assessing their self-purification capacity.

Agriculture↗
PubMed2003

Combined use of NMR relaxation measurements and hydrodynamic calculations to study protein association. Evidence for tetramers of low molecular weight protein tyrosine phosphatase in solution.

We describe a novel method for determining weak association constants of oligomeric protein complexes formed transiently under equilibrium conditions. This type of equilibrium process is recognized as being biologically important, but generally hard to study. Heteronuclear spin relaxation rates measured at multiple protein concentrations are analyzed using relaxation rates predicted from hydrodynamic calculations, yielding equilibrium constants and structural characterization of the protein complexes. The method was used to study the oligomerization equilibrium of bovine low molecular weight protein tyrosine phosphatase. X-ray structures of monomeric and dimeric forms of the protein have been reported previously. Using longitudinal and transverse (15)N relaxation rates measured at four different protein concentrations, we detected the monomer, dimer, and a previously unknown tetramer and measured the dissociation constants of the equilibria involving these species. A comparison of experimental and predicted relaxation rates for individual backbone amide (15)N spins enabled delineation of the tetramerization interface. The results suggest a novel concept for substrate modulation of enzymatic activity based on a "supramolecular proenzyme". The fast and reversible switching of the "supramolecular proenzyme" would have obvious advantages for the regulation of enzymes involved in cell signaling pathways.

Animals↗
PubMed2004

Marcus theory of outer-sphere heterogeneous electron transfer reactions: dependence of the standard electrochemical rate constant on the hydrodynamic radius from high precision measurements of the oxidation of anthracene and its derivatives in nonaqueous solvents using the high-speed channel electrode.

The validity of Marcus theory for outer-sphere heterogeneous electron transfer for the electro-oxidation of a range of anthracene derivatives in alkyl cyanide solvents is investigated. The precision measurement of these fast electron transfers (k(0) >or= 1 cm s(-1)) is achieved by use of the high-speed channel electrode and, where necessary, fast-scan cyclic voltammetry. First, the solvent effect on the rate of electron transfer is studied by considering the first oxidation wave of 9,10-diphenylanthracene in the alkyl cyanide solvents: acetonitrile, propionitrile, butyronitrile, and valeronitrile. Second, the variation of k(0) for a series of substituted anthracenes is investigated by analyzing the voltammetric response of the one-electron oxidations of 9-phenylanthracene, 9,10-dichloroanthracene, 9-chloroanthracene, 9,10-dicyanoanthracene, 9-cyanoanthracene, 9-nitroanthracene, 9,10-diphenylanthracene, and anthracene in acetonitrile. It is shown that the rate of electron transfer of a single compound in different alkyl cyanides is determined by the longitudinal dielectric relaxation properties of the solvent, while differences in rate between the substituted anthracenes in acetonitrile can be quantitatively rationalized by considering their relative hydrodynamic radii. This makes possible the accurate prediction of electron-transfer rates for a molecule by interpolation of rate constants known for related molecules.

Journal Article↗
PubMed2006

Diffusion-controlled reactions: hydrodynamic interaction between charged, uniformly reactive spherical reactants.

In this work, different models of hydrodynamic interaction (HI) are examined in the diffusion-controlled reaction between uniformly reactive charged spherical particles. In addition to Oseen "stick" and "slip" models of HI, one is considered that accounts for the disturbance of fluid flow by the ions around one reactive partner as they interact with a neighboring reactive species. This interaction is closely related to the "electrophoretic effect" in electrokinetics and can be described by a fairly simple electrophoretic, or E-tensor. These models are applied to the electron-transfer quenching reaction of Ru(bpy)3(2+) and methyl viologen (MV2+) over a wide range of NaCl concentrations (Chiorboli, C. et al., J. Phys. Chem. 1988, 92, 156). The back reaction is also considered. From a comparison of the salt dependence of the model and experimental rates, it is concluded that the "E-tensor" model works best and ignoring HI altogether works worst. The Oseen "stick" and "slip" models fall between these.

Journal Article↗
PubMed2005

Elastic-hydrodynamic transition of gel friction.

We report the surface sliding friction of a high strength gel against a glass substrate under a normal pressure range of 0.01-2.5 MPa. The friction of the gel swollen with different viscous solvents is investigated over a wide velocity range. A velocity-viscosity conversion relationship is established. From the velocity-viscosity conversion relationship, a master curve that is characteristic to the elastic-hydrodynamic transition is observed. The results indicate that the adsorption model proposed by our previous work is valid even under a pressure up to MPa orders, which is the order of pressure that a cartilage sustains in the articular joints.

Adsorption↗
PubMed2005

The "Wimple": rippled deformation of a fluid drop caused by hydrodynamic and surface forces during thin film drainage.

It is well-known that hydrodynamic pressures in a thin draining liquid film can cause inversion of the curvature of a drop or bubble surface as it approaches another surface, creating a so-called "dimple". Here it is shown that a more complicated rippled shape, dubbed a "wimple", can be formed if a fluid drop that is already close to a solid wall is abruptly pushed further toward it. The wimple includes a central region in which the film remains thin, surrounded by a ring of greater film thickness that is bounded at the outer edge by a barrier rim where the film is thin. This shape later evolves into a conventional dimple bounded by the barrier rim, which then drains in the normal way. During the evolution from wimple to dimple, some of the fluid in the thicker part of the film ring flows toward the central region before eventually draining in the opposite direction. Although the drop is pressed toward the wall, the central part of the drop moves away from the wall before approaching it again. This is observed even when the inward push is too small to create a wimple.

Journal Article↗
PubMed2006

Stable jets of viscoelastic fluids and self-assembled cylindrical capsules by hydrodynamic focusing.

We demonstrate formation of long-lived cylindrical jets of a viscoelastic fluid using hydrodynamic focusing. A solution of polyacrylamide in water is driven coaxially with immiscible oil and subjected to strong extensional flow. At high flow rates, the aqueous phase forms jets that are 4-90 microm in diameter and several centimeters long. The liquid surfaces of these jets are then used as templates for assembly of microspheres into novel rigid and hollow cylinders.

Acrylic Resins↗
PubMedDate not supplied

Hydrodynamic properties and unperturbed dimensions of poly(gamma-hydroxy-L-proline) in aqueous solution.

Intrinsic viscosities and sedimentation coefficients have been measured as a function of molecular weight for poly(gamma-hydroxy-L-proline) in water. The molecular weight range covered is 9,000-35,000. High molecular weight poly(gamma-hydroxy-L-proline) in water has the hydrodynamic behavior of a random coil immersed in a good solvent, as judged by d ln [eta]/d ln M, d ln so/d ln M, dbeta/dM, and the size of beta[= nu rho (-1)]/1/3etaM-2/3(1 - nurho)-1]. The characteristic ratio, ((r2)o/nplp2) infinity, is found to be 15.9 +/- 1.6, which is not significantly different from the result of 13.7 +/- 0.9 obtained for poly(L-proline) by Mattice and Mandelkern under the same conditions. This observation casts doubt on the importance of intrachain hydrogen bonded bridges from the hydroxyl group to a carbonyl oxygen via a water molecule. The characteristic ratios and the effects of calcium chloride on the hydroynamic properties suggest that poly(L-proline) and poly(gamma-hydroxy-L-proline) possess a similar source of flexibility which is often overlooked. Two possibilities for this flexibility are a second energy minimum about the Calpha-C' bond and cis-trans isomerization about the peptide bond.

Hydrogen Bonding↗
PubMed1999

Hydrodynamic modelling of stress.

This work is a qualitative study of an organism's physiological adaptative response to stress. The experimental data were selected from a previous study leading to the conclusion that stress may be considered as a topological retraction within a vital space that must be more precisely defined. The experimental methodology uses rat poisoning by neurotoxins. The control parameter is the intensity of the toxic doses. Measured parameters are the animals' survival rate and the kinetics of cerebral acetylcholinesterase activity. The results, when expressed as a function of the inverted doses, show a characteristic evolution. The pattern of the curve closely resembles a vortex profile. This analogy is studied more extensively in both the physical and biological domains. These findings help to clarify the concept of biological stress which presents the same vectorial properties as hydrodynamic vorticity. In particular, the dissipation of stress and the dissipation of vorticity seem to obey the same laws. This observation is valid for both diffusion and convection processes. The decompensation phase of stress could be compared with the instability and turbulence in flows. Our approach in this paper is mainly to establish a general and phenomenological description of the stress response fitting experimental observations.

Acetylcholinesterase↗
PubMed1991

Experimental determinations of diffusion coefficients in dilute aqueous solution using the method of hydrodynamic stability.

Diffusion coefficients were experimentally determined in dilute aqueous solution at 25 +/- 0.1 degrees C, ionic strength 0.5 M, using Taylor's method of hydrodynamic stability. The methodology described is accurate enough to show significant differences in diffusion coefficients between the various ionic forms of the same species as a function of degree of ionization. In Taylor's method, diffusion coefficients were measured by allowing two solutions of differing solute concentration to contact in a capillary tube, forming a stable, measurable concentration gradient. The solute diffusion coefficient is a function of the gradient, the solution viscosity, the solution density, and some capillary dimensions. Viscosity was maintained constant across experiments and values of sufficient accuracy were available in the literature. Solution densities were measured with a tuning fork densimeter. Compounds studied were o-aminobenzoic acid, benzoate anion, the four forms of phosphate and citrate, and the zwitterionic forms of glycine, diglycine, and triglycine. Based on the results for the four forms of phosphate and citrate, experimental diffusivity values vary with the ionic state of the diffusant, presumably because of the altered state of hydration as charge varies. For the glycine series, the diffusivity showed an unexpected dependency on molecular weight (size).

Aminobenzoates↗
PubMed2002

Interpretation of 15N NMR relaxation data of globular proteins using hydrodynamic calculations with HYDRONMR.

HYDRONMR is an implementation of state of the art hydrodynamic modeling to calculate the spectral density functions for NH or C(alpha)-H vectors in a rigid protein structure starting from an atomic level representation. Thus HYDRONMR can be used to predict NMR relaxation times from a rigid model and to compare them with the experimental results. HYDRONMR contains a single adjustable parameter, the atomic element radius. A protocol to determine the value that gives the best agreement between calculated and experimental T1/T2 values is described. For most proteins, the value of the atomic element radius ranges between 2.8 A and 3.8 A with a distribution centered at 3.3 A. Deviations from the usual range towards larger values are associated to aggregation in several proteins. Deviations to lower values may be related to large-scale motions or inappropriate model structures. If the average structure is correct, deviations between experimental T1/T2 values and those calculated with HYDRONMR can be used to distinguish residues affected by anisotropic motion from those that are involved in chemical exchange.

Algorithms↗
PubMed1994

An application of the hydrodynamic pore theory to percutaneous absorption of drugs.

Skin permeability of drugs was evaluated based on the hydrodynamic pore theory. Four polar solutes were used, with differing molecular sizes--ethylene glycol, 1,3-butylene glycol, antipyrine and sucrose--and isosorbide dinitrate was also selected as a lipophilic drug. The skin permeations of solvent (D2O) and one of these drugs were measured simultaneously under various osmotic pressures to calculate the reflection coefficient. The clearance of isosorbide dinitrate was independent of the solvent flux, whereas a linear relationship was obtained between the solvent flux and the clearance of each hydrophilic drug except for sucrose. The reflection coefficient of the hydrophilic drugs increased with increasing molecular radius. These results suggest that the convective flow contributes significantly to the total skin permeability of hydrophilic drugs and that the extent of contribution decreases with increasing molecular size of the drugs. The pore radius of the skin barrier could be estimated from the reflection coefficient of the hydrophilic drugs and the resulting value was compared with that for the other absorption sites, jejunum, rectum, and nose. The apparent water influx was also compared to assess the volume occupied by the pores. The pore radius and apparent influx of skin were lower than those for the other absorption sites, which is apparently one reason for low skin permeability of drugs, especially hydrophilic drugs.

Animals↗
PubMed2004

Platelet receptor glycoprotein VI-mediated adhesion to type I collagen under hydrodynamic flow.

Glycoprotein VI (GPVI) is a platelet receptor that directly binds collagen. It has been shown by expressing GPVI in rat basophilic leukemia (RBL-2H3) cells that GPVI mediates adhesion to type I collagen under static conditions. However, the ability of GPVI to secure adhesion to collagen type I under flow has not been measured. We studied the interaction of GPVI and type I collagen under hydrodynamic flow using RBL-2H3 cells transfected with the GPVI receptor. We found that GPVI-expressing RBL-2H3 cells adhere to collagen under flow, significantly more so than non-GPVI-expressing RBL-2H3 cells. Inhibition of GPVI by the 11A12 anti-GPVI antibody significantly blocks adhesion to collagen, indicating that GPVI specifically interacts with collagen. Probing the role of signaling in GPVI binding to collagen, we used mutants of GPVI and observed that signal transduction did not inhibit adhesion. To test the correlation between receptor expression and adhesion, we tested three GPVI-expressing RBL-2H3 cell lines (A, B, and C) with different levels of receptor expression. At a single shear rate, the level of adhesion increases monotonically with surface expression. The results, using this model cell line, indicate that GPVI is capable of mediating adhesion to collagen under shear, in a density-dependent fashion that is independent of GPVI signaling.

Animals↗