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PubMed1998

Evaluation of erythrocyte morphology as deformability index in patients suffering from vascular diseases, with or without diabetes mellitus: correlation with blood viscosity and intra-erythrocytic calcium.

The aim of our study was to evaluate the erythrocytic morphology in vascular patients, with or without diabetes, showing cell alterations correlated to blood viscosity and intra-erythrocytic calcium. We studied 108 subjects: 20 normal subjects, 58 vascular patients (25 suffering from CHD, 19 from CVD, 14 from POAD) and 30 non-insulin-dependent diabetes patients with vascular disease in metabolic compensation (13 CHD, 9 CVD, 8 POAD). Erythrocytic morphology, blood viscosity and intra-erythrocytic calcium were evaluated. Our results show that bowls, the most deformable red cells, decreased significantly in vascular patients and in POAD diabetics, while the discocytes, having a stiffer form, greatly increased in subjects suffering from ischemic disease and in POAD diabetics. The altered red cells (echinocytes and knizocytes) reached a statistical significance in CVD and POAD diabetics. Comparing the percentage of discocytes to intraerythrocytic calcium content in vasculopathic subjects, we obtained a significant correlation. No evidence of a relationship between discocytes and blood viscosity was found, even if blood viscosity significantly increased in patients affected by ischemic disease. These results suggest that ischemia decreases the deformability of red cells which is supported by the study of red cells morphology, by the erythrocytic morphology index (EMI), which becomes < 1, and by the evaluation of cytosolic calcium content.

Adult↗
PubMed1998

Increased blood viscosity in iron-depleted elite athletes.

Since iron deficiency is associated with abnormal erythrocyte rheology, we investigated relationships between plasma ferritin and blood rheology in 36 male elite sportsmen (age: 22.38+/-0.9 years). On the whole, ferritin was negatively correlated with blood viscosity (r = -0.36, p < 0.05). When 23 subjects with low ferritin levels suggesting mild iron deficiency were compared with 13 matched sportsmen with normal ferritin levels, iron-deficient sportsmen were shown to have a higher blood viscosity at 1000 s(-l) (3.17+/-0.09 vs. 2.85+/-0.06 mPas, p < 0.05), explained by a higher plasma viscosity (1.38+/-0.02 vs. 1.31+/-0.02 mPa s, p < 0.05), while hematocrit and RBC rigidity index Tk were similar in the two groups. RBC aggregability index M (4.59+/-0.58 vs. 2.95+/-0.43 mPas, p < 0.05) and M1 (8.46+/-0.58 vs. 6.07+/-0.55, p < 0.01) were higher in iron-deficient subjects. Serum zinc was lower in iron-deficient sportsmen (0.73+/-0.02 vs. 0.83+/-0.02 mg/l, p < 0.01), but the score of early signs of overtraining was higher in this group (10.84+/-1.61 vs. 4.08+/-1.11, p < 0.01). These data suggest that mild iron deficiency as commonly seen in athletes, before anemia occurs, is associated with an increase in plasma viscosity and RBC aggregation, together with an increased subjective feeling of exercise overload.

Adult↗
PubMed1989

Changes in the viscosity of hyaluronic acid after exposure to a myeloperoxidase-derived oxidant.

Both purified hyaluronic acid (HA) and bovine synovial fluid react with OCI-, the major oxidant produced by the myeloperoxidase (MPO)/H2O2/CI- system, resulting in a decrease in their specific viscosity. This reaction is inhibited in the presence of excess methionine. H2O2 alone decreases the viscosity of HA, presumably by the Fenton reaction, in the absence (but not in the presence) of the iron chelator, diethyltriaminepentacetic acid (DETAPAC). In the presence of DETAPAC, incubation of HA with the complete MPO/H2O2/CI- system lowered the viscosity of HA. Analysis of 3H-HA exposed to OCI- by gel filtration chromatography indicated that cleavage of HA occurred only at higher OCI- concentrations. We suggest that the reduction in viscosity of HA by the MPO/H2O2/CI- system may be due to a combination of oxidative cleavage and changes in the conformation of the molecule. We speculate that the changes in the molecular size of rheumatoid synovial fluid HA may be due to the action of the neutrophil MPO/H2O2/CI- system.

Chemical Phenomena↗
PubMed2000

Viscosity of Nonionic Polymer/Anionic Surfactant Complexes in Water.

The polymer-micelle model, formerly established by Cabane, is revised to develop a new viscosity equation to describe the dependence of dilute solution viscosity on polymer concentration in PEG/SDS aqueous solutions. Two parameters inthe new equation were proposed to characterize the influence of the polymer solution viscosity on the added surfactant. The viscosity data of polyethylene glycol (PEG) solutions containing sodium dodecyl sulfate (SDS) were measured by the Ubbelohde dilution viscometer and the new equation proved to be in good agreement with the experimental data. Copyright 2000 Academic Press.

Journal Article↗
PubMed2000

Surfactant-Influenced Gas-Liquid Interfaces: Nonlinear Equation of State and Finite Surface Viscosities.

A canonical flow geometry was utilized for a fundamental study of the coupling between bulk flow and a Newtonian gas-liquid interface in the presence of an insoluble surfactant. We develop a Navier-Stokes numerical model of the flow in the deep-channel surface viscometer geometry, which consists of stationary inner and outer cylinders, a floor rotating at a constant angular velocity, and an interface covered initially by a uniformly distributed surfactant. Here, the floor of the annular channel is rotated fast enough so the flow is nonlinear and drives the film toward the inner cylinder. The boundary conditions at the interface are functions of the surface tension, surface shear viscosity, and surface dilatational viscosity, as described by the Boussinesq-Scriven surface model. A physical surfactant system, namely hemicyanine, an insoluble monolayer on an air-water interface, with measured values of surface tension and surface shear viscosity versus concentration, was used in this study. We find that a surfactant front can form, depending on the Reynolds number and the initial surfactant concentration. The stress balance in the radial direction was found to be dominated by the Marangoni stress, but the azimuthal stress was only due to the surface shear viscosity. Numerical studies are presented comparing results of surfactant-influenced interface cases implementing the derived viscoelastic interfacial stress balance with those using a number of idealized stress balances, as well as a rigid no-slip surface, providing added insight into the altered dynamics that result from the presence of a surfactant monolayer. Copyright 2000 Academic Press.

Journal Article↗
PubMed2000

Viscosity-Concentration Equation for Emulsions of Nearly Spherical Droplets.

A new modified form of the equation of N. Phan-Thien and D. C. Pham (J. Non-Newtonian Fluid Mech. 72, 305 (1997)) is proposed to describe the viscosity-concentration behavior of emulsions of nearly spherical droplets. The proposed equation, as well as other existing theoretical equations, is evaluated in light of a large body of experimental data on concentrated emulsions, covering a broad range of dispersed-phase to continuous-phase viscosity ratios (4.15x10(-3) to 1.17x10(3)). In general, the experimental data exhibit large deviations from the existing theoretical equations; for example, the theoretical equation of Phan-Thien and Pham underpredicts the relative viscosity of concentrated emulsions by a large amount. The equation proposed in this work describes the experimental viscosity data of different emulsion systems remarkably well. Copyright 2000 Academic Press.

Journal Article↗
PubMed2001

On the Viscosity of Dilute Emulsions.

The slow motion of a liquid droplet in a shear flow in the presence of surfactants is studied. The effects of the interfacial viscosity, Gibbs elasticity, surface diffusion and bulk diffusion of surfactants in both phases are taken into account. The analytical solution of the problem for small Reynolds and Peclet numbers gives a simple criterion for estimation of the tangential mobility of the droplet interface. By applying the standard procedure for averaging of the stress tensor flux at an arbitrary surface of the dilute emulsion, an analytical formula for the viscosity of emulsions in the presence of surfactants is derived. The result is a natural generalization of the well-known formula of Einstein for the viscosity of monodisperse dilute suspensions and of the expressions derived by Taylor and Oldroyd for the viscosity of monodisperse dilute emulsions taking into account the Marangoni effect. Copyright 2001 Academic Press.

Journal Article↗
PubMed2002

Viscosity of colloidal suspensions in aqueous gelatin.

The low-shear viscosity eta(0) of colloidal suspensions of acrylic latex or silica in aqueous gelatin has been measured at a temperature above the sol-gel transition. Measurements were made on dilution of a concentrated suspension with water or a gelatin solution. Thus, either the gelatin : colloid ratio was maintained or it was varied at constant aqueous gelatin concentration. Systems were studied with four lime-processed gelatins of different molecular weights at two concentrations of added salt. In addition, the latex particle size and the thickness of the adsorbed gelatin layer were measured by photon correlation spectroscopy (PCS) under dilute conditions. The dependence of the low-shear viscosity eta(0) on particle concentration was exponential and did not follow the well-established Krieger-Dougherty model for simple hard-sphere suspensions over the concentration range studied. A simple phenomenological model, eta(0)=eta(o)10(phi(e)/phi(s)), was found to predict the behavior well. Here, eta(o) is the viscosity of a gelatin solution of the corresponding solution concentration, phi(e) is proportional to the volume fraction of the particles, and phi(s) is a scaling factor, which was determined to have a value of 0.85. With this value of phi(s), the dimensions determined from PCS could be used to predict the viscosity values.

Journal Article↗
PubMed2004

Study on the viscosity of cationic gemini surfactant-nonionic polymer complex in water.

Interactions between a cationic gemini surfactant, 1,2-ethane bis(dimethyldodecylammonium bromide) (designated as 12-2-12), and a nonionic polymer polyvinyl alcohol (PVA) were investigated by means of viscosity and specific conductance. Results show that PVA displays special viscosity behavior in aqueous solutions containing the gemini surfactant 12-2-12, which is due to the molecular interaction of the polymer and the surfactant. It was found that the special viscosity depended on ionization of the surfactant, as well as polymer concentration and surfactant concentration in the nonionic polymer-surfactant system. A theoretical expression for the dependence of the solution viscosity on the ionization of the surfactant micelle was given, and the new equation proved to be in good agreement with the experimental data.

Journal Article↗
PubMed2007

A factorial, randomized trial of pentoxifylline or placebo, four-layer or single-layer compression, and knitted viscose or hydrocolloid dressings for venous ulcers.

OBJECTIVES: We evaluated the effectiveness of pentoxifylline, knitted viscose or hydrocolloid dressings, and single-layer or four-layer bandaging for venous ulceration. METHOD: A factorial randomized controlled trial with 24-week follow-up was conducted in leg ulcer clinics in Scotland with blinded allocation to pentoxifylline (1200 mg) or placebo, knitted viscose or hydrocolloid dressings, and single-layer or four-layer bandages. The study enrolled 245 adults with venous ulcers. The main outcome measure was time to complete healing. Secondary outcomes included proportions healed, withdrawals, and adverse events. Analysis was by intention to treat. RESULTS: There was no evidence of interaction between the drug, bandages, and dressings. Pentoxifylline was associated with nonsignificant increased ulcer healing (62% vs 53%; P = .21). Four-layer bandages were associated with significantly higher healing rates (67% vs 49%; P = .009). There was no difference in healing between knitted viscose and hydrocolloid dressings (58% and 57%; P = .88). Cox regression models increased the significance of the pentoxifylline effect (relative risk of healing, 1.4; 95% confidence interval, 1.0 to 2.0). CONCLUSIONS: Pentoxifylline increased the proportion healing compared with placebo to the same extent as shown in recent systematic reviews, although this finding was only statistically significant when a secondary adjusted analysis was conducted. Four-layer bandaging produced higher healing rates than single-layer bandaging. There was no difference in time to healing between knitted viscose and hydrocolloid dressings.

Administration, Oral↗
PubMed2002

Measurement of viscosity and shear wave velocity of a liquid or slurry for on-line process control.

An on-line sensor to measure the density of a liquid or slurry, based on longitudinal wave reflection at the solid-fluid interface, has been developed by the staff at Pacific Northwest National Laboratory. The objective of this research is to employ shear wave reflection at the solid-fluid interface to provide an on-line measurement of viscosity as well. Both measurements are of great interest for process control in many industries. Shear wave reflection measurements were conducted for a variety of liquids. By analyzing multiple reflections within the solid (only 0.63 cm thick-similar to pipe wall thickness) we increased the sensitivity of the measurement. At the sixth echo, sensitivity was increased sufficiently and this echo was used for fluid interrogation. Shear wave propagation of ultrasound in liquids is dependent upon the viscosity and the shear modulus. The data are analyzed using the theory for light liquids (such as water and sugar water solutions) and also using the theory for highly viscous liquids (such as silicone oils). The results show that, for light liquids, the shear wave reflection measurements interrogate the viscosity. However, for highly viscous liquids, it is the shear wave modulus that dominates the shear wave reflection. Since the density is known, the shear wave velocity in the liquid can be determined from the shear wave modulus. The results show that shear wave velocities in silicone oils are very small and range from 315 to 2389 cm/s. Shear wave reflection measurements are perhaps the only way that shear wave velocity in liquids can be determined, because the shear waves in liquids are highly attenuated. These results show that, depending on the fluid characteristics, either the viscosity or the shear wave velocity can be used for process control. There are several novel features of this sensor: (1) The sensor can be mounted as part of the wall of a pipeline or tank or submerged in a tank. (2) The sensor is very compact and can be located within the process stream. (3) The sensor can interrogate and characterize very attenuative liquids or slurries because the sensor operation depends upon reflection at the interface between the solid and the fluid, rather than on transmission through a liquid. (4) The sensor performance is not affected by fluid flow rate, entrained air, or vibration.

Journal Article↗
PubMed2000

Blood viscosity and aging.

The objective of this study was to evaluate the relationship of whole blood viscosity and its major determinants (plasma fibrinogen level, hematocrit, hemoglobin and blood cell count) to advancing age. A total of 249 subjects (mean age 49.9+/-21.5; range 19-102 years) were included in the study. They were divided into three groups, (A) <30 years of age, n, 58; (B) 30-60 years, n, 107; (C) >60 years, n, 84. Whole blood viscosity at two different rates of shear (450 and 45 s(-1)) was evaluated using a cone-plate digital viscosimeter. The hematological parameters (hematocrit, hemoglobin and blood cell count) were evaluated using an automatic Coulter Counter. Plasma fibrinogen concentration was measured by a clotting method. When both sexes are considered together, whole blood viscosity shows no significant difference among age groups. Plasma fibrinogen concentration significantly increases with age (P<0.001); hemoglobin, red blood cell count and platelet count, on contrary, are significantly lower in aged group. In the male sex, blood viscosity at higher shear rate (450 s(-1)) negatively correlates with advancing age (P<0.005). The age-related decrease of hematocrit value in the male sex accounts for this occurrence.

Journal Article↗
PubMed2000

The effect of enzymes on semen viscosity in Llamas and Alpacas.

The effect of four enzymes: collagenase, fibrinolysin, hyalurodinase, and trypsin were recorded on the viscosity, motility, percent live spermatozoa and acrosome integrity of Llama and Alpaca semen. Semen samples were collected using a modified artificial vagina for each of the five llamas and five alpacas. A 25% solution of the of enzyme at a concentration of 1mg/ml was added to the ejaculate. Analysis of variance was used to determine differences in eliminating viscosity and alterations in motility, percent live spermatozoa and the acrosomal integrity at 0 (time of semen collection), 2 and 5min. In Llama and Alpaca semen, collagenase eliminated viscosity in 100 and 99% of the samples, respectively. Correspondingly, fibrinolysin in 89 and 59%; hyalurodinase in 88 and 36%; and trypsin in 55 and 68% of the samples (p<0.05). In the Llama sperm, motility decreased (p<0.05) with the addition of fibrinolysin (28%), trypsin (13%), hyalurodinase (12%), and collagenase (4%). In Alpaca semen, the enzymes used had no effect on sperm motility. Percent live spermatozoa variably decreased after the addition of fibrinolysin, hyalurodinase and trypsin. There was no significant difference in the acrosome integrity in Llama and Alpaca makes following the addition of the enzymes. Overall, collagenase had little or no influence in decreasing motility, percent live spermatozoa and acrosome integrity, whereas, it was effective in eliminating semen viscosity.

Journal Article↗
PubMedDate not supplied

Application of neural networks to modeling and estimating temperature-dependent liquid viscosity of organic compounds.

Back-propagation neural network models for correlating and predicting the viscosity-temperature behavior of a large variety of organic liquids were developed. Experimental values for the liquid viscosity for 1229 data points from 440 compounds containing C, H, N, O, S, and all halogens have been collected from the literature. The data ranges covered are from -120 to 160 degrees C for temperature and from 0.164 (trans-2-pentene at 20 degrees C) to 1.34 x 10(5) (glycerol at -20 degrees C) mPa.s for viscosity value. After dividing the total database of 440 compounds into training (237 with 673 data points), validation (124 with 423 data points), and test (79 with 133 data points) sets, the modeling performance of two separate neural network models with different architectures, one based on a compound-specific temperature dependence and the second based on a compound-independent one, has been examined. The resulting former model showed somewhat better modeling performance than latter, and the model gave squared correlation coefficients of 0.956, 0.932, and 0.884 and root mean-squares errors of 0.122, 0.134, and 0.148 log units for the training, validation, and test sets, respectively. The input descriptors include molar refraction, critical temperature, molar magnetic susceptibility, cohesive energy, temperatures, and five kinds of indicator variables for functionalities, alcohols/phenols, nitriles, amines, amides, and aliphatic ring. The reliability of the proposed model was assessed by comparing the results against calculated viscosities by two existing group-contribution approaches, the method of van Velzen et al. and the Joback and Reid method.

Journal Article↗
PubMed2001

Temperature and viscosity dependence in the stereoselective formation of the inverted housane for the photochemical nitrogen loss from the deuterium-stereolabeled parent diazabicyclo[2.2.1]hept-2-ene.

For the liquid-phase photolytic denitrogenation of the stereolabeled DBH derivative exo-d2-diazabicyclo[2.2.1]heptene (exo-d2-1), the k(inv)/k(ret) ratio of the inverted [2(inv)] and retained [2(ret)] housanes (bicyclo[2.1.0]pentanes) depends on the viscosity of the medium. For this purpose, the viscosity was varied by changing the solvent (various alcohols and diols, n-hexane, and acetonitrile) at constant temperature and by changing the temperature (-50 to +100 degrees C) in one single solvent, namely n-butanol. This viscosity effect is consistent with a stepwise denitrogenation mechanism in the liquid-phase photolysis of DBH, which proceeds through an unsymmetrical, nitrogen-containing transient, namely the singlet diazenyl diradical. The simple free-volume model adequately accounts for the observed viscosity behavior of the k(inv)/k(ret) ratio in terms of frictional effects. The temperature dependence discloses a small but measurable difference in the internal activation energies for the inversion and retention processes of the proposed diazenyl diradical.

Journal Article↗
PubMed2001

Viscosity effects on the thermal decomposition of bis(perfluoro-2-N-propoxypropionyl) peroxide in dense carbon dioxide and fluorinated solvents.

The thermal decomposition of the free-radical initiator bis(perfluoro-2-N-propoxyprionyl) peroxide (BPPP) was studied in dense carbon dioxide and a series of fluorinated solvents. For the fluorinated solvents, the observed first-order decomposition rate constants, k(obs), increased with decreasing solvent viscosity, suggesting a single-bond decomposition mechanism. The k(obs) values are comparatively larger in dense carbon dioxide and similar to the "zero-viscosity" rate constants extrapolated from the decomposition kinetics in the fluorinated solvents. The decomposition activation parameters demonstrate a compensation behavior of the activation enthalpy with the activation entropy upon change in solvent viscosity. Comparison of the change in activation parameter values upon change in solvent viscosity for BPPP with two additional initiators, acetyl peroxide (AP) and trifluoroacetyl peroxide (TFAP), further suggests that carbon dioxide exerts a very minimal influence on the decomposition mechanism of these initiators through solvent-cage effects.

Journal Article↗
PubMed2005

Photoinduced reversible change of fluid viscosity.

We report a reversible photoinduced fluid viscosity change. A small amount of a "photoswitchable" azobenzene-modified cationic surfactant (4-butylazobenzene-4'-(oxyethyl)trimethylammonium bromide, AZTMA) was added to a wormlike micellar solution of cetyltrimethylammonium bromide (CTAB) containing sodium salicylate (NaSal). The trans-AZTMA solution had a remarkably high viscosity as a result of the entangled network of wormlike micelles. UV light irradiation on the trans-AZTMA solution remarkably decreased the viscosity of the solution because the bulky structure of cis-AZTMA is likely to disrupt the network structure of wormlike micelles. This photoinduced viscosity change is perfectly reversible between the trans- and cis-AZTMA solutions.

Journal Article↗
PubMed2005

Generic van der Waals equation of state, modified free volume theory of diffusion, and viscosity of simple liquids.

The shear viscosity formula derived by the density fluctuation theory in previous papers is computed for argon, krypton, and methane by using the self-diffusion coefficients derived in the modified free volume theory with the help of the generic van der Waals equation of state. In the temperature regime near or above the critical temperature, the density dependence of the shear viscosity can be accounted for by ab initio calculations with the self-diffusion coefficients provided by the modified free volume theory if the minimum (critical) free volume is set equal to the molecular volume and the volume overlap parameter (alpha) is taken about unity in the expression for the self-diffusion coefficient. In the subcritical temperature regime, if the density fluctuation range parameter is chosen appropriately at a temperature, then the resulting expression for the shear viscosity can well account for its density and temperature dependence over the ranges of density and temperature experimentally studied. In the sense that once the density fluctuation range is fixed at a temperature, the theory can account for the experimental data at other subcritical temperatures on the basis of the intermolecular force only; the theory is predictive even in the subcritical regime of temperature. Theory is successfully tested in comparison with experimental data for self-diffusion coefficients and shear viscosity for argon, krypton, and methane.

Journal Article↗