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Chronic subdural hematoma: concepts of physiopathogenesis. A review.

From the present review it seems clear that the physiopathogenesis of the chronic subdural hematoma is far from being completely understood. However, an analysis of the known data can be summarized as follows: The development of subdural hematomas most likely occurs following minimal trauma in those patients with predisposing factors. Experimental data substantiates the fact that an accumulation of clotted blood in the subdural or subcutaneous space induced the formation of the fibroplastic neomembrane. The hypothesis that blood must come in contact with cerebrospinal fluid in order for the growth to occur, is still controversial. It has been virtually disproven that osmosis, referring to the electrolyte gradient as measured by freezing point depression, has any significance as a growth inducing factor. The protein oncotic gradient theory, having been the most widely accepted explanation as to the progressive enlargement of the subdural hematoma sac, has little experimental data supporting it. A larger body of clinical evidence exists supporting the concept that plasma and/or erythrocytes continuously penetrate into the subdural cavity, where enhanced fibrinolytic activity is present. However, this chronic rebleeding cannot fully explain the observed growth, because the composition of the hematoma fluid is smoewhat different from serum or plasma, and the protein content is also progressively diluted by fluid arising from an unknown source. There is some clinical and experimental evidence to suggest that a production-reabsorption balance may be a significant growth variable. No work has been done to define the role, if any, of local inflammatory mechanisms in the chronic subdural hematoma. Sound clinical evidence has shown that after the initial formation of the subdural clot, growth follows, than a slow, complete reabsorption usually occurs. Aside from the plausible production-reabsorption balance concept, it is not known why the evolution proceeds in this manner.

Animals↗

Control of molecular weight selectivity in electrode modifications based on phase-inversion cellulose acetate membranes.

Modified electrodes with size selectivity are required for electrochemical blosensors and for analysis of biological samples. The phase-inversion process for making reverse osmosis membranes is used to make modified electrodes with the goals of decreasing thickness, improving response time, and understanding the influence of both casting solution composition and casting conditions on the resultant membrane's porosity. Poly(ethylene glycol) esters of ferrocene-carboxylic acid are used for the determination of the membrane's response time, selectivity, and structure. It is shown that there is an optimum composition range of greater than 95% acetone, less than 2% cellulose acetate, and less than 5% aqueous Mg(CIO4)2. This composition range gives the minimum response time (greater than 90% of maximum signal is obtained in less than 7 min), maximum reproducibility (less than 20% relative error), and best size selectivity in the few thousand daltons range.

Cellulose↗

Use of attenuated total reflection infrared spectroscopy for analysis of partitioning of solutes between thin films and solution.

The paper examines attenuated total reflection (ATR) spectroscopy as a tool for quantifying the partitioning of small molecular species between a solution and a thin film, while the film is directly exposed to the solution for equilibration. For the case of a thin film having a thickness substantially smaller than the decay length of the evanescent wave, we developed suitable linear relationships that relate the measured absorption of the characteristic band to the concentration of the species under study in the film and in solution. In the application of ATR-Fourier transform infrared spectroscopy, the method is particularly suitable for films a few tens to hundreds of nanometers thick and for solutes that preferentially partition into the film. As an example, the partitioning isotherm of 1-pentanol between water and a thin polyamide film separated from a reverse osmosis membrane was determined experimentally, and the limitations of the method are discussed.

Journal Article↗

Fractionation of natural organic matter in drinking water and characterization by 13C cross-polarization magic-angle spinning NMR spectroscopy and size exclusion chromatography.

Natural organic matter from drinking water sources was fractionated, and the fractions were characterized by NMR and SEC with the aim of relating NOM structure to treatability. Organic matter was isolated from two Australian surface waters (Horsham, Moorabool) by reverse osmosis and from a groundwater (Wanneroo) by anion exchange. The isolates were fractionated according to polarity and charge by resin adsorption. 13C NMR spectra of the freeze-dried fractions showed the most hydrophobic fraction to be high in aliphatic and aromatic carbon while slightly hydrophobic organics have more carbonyl and alkoxyl carbon. The Horsham and Wanneroo hydrophilic fractions show strong alkoxyl signals attributed to carbohydrate. Moorabool hydrophilics contain aromatic (phenolic) carbon; the apparent absence of carbohydrate appears to be an artifact. Size-exclusion chromatograms were recorded on the original and fractionated organics with both UV and dissolved organic carbon detection. The Horsham and Moorabool organics have similar molecular size distributions while Wanneroo is dominated by strongly absorbing species having large hydrodynamic radii. The hydrophobic and charged hydrophilic fractions also have high apparent MW, while the neutral fraction is higher in low-MW compounds of relatively low specific absorbance, suggestive of carbohydrates.

Carbohydrates↗

Temperature effects on the morphology of porous thin film composite nanofiltration membranes.

Even though polymeric nanofiltration (NF) and reverse osmosis (RO) membranes often operate on surface waters and surficial groundwaters whose temperature varies over time and with season, very little detailed mechanistic information on temperature effects on membrane selectivity is available to date. Hence, a study was undertaken to investigate the effects of operating temperature (5-41 degrees C) on the morphology and structure of two commercially available thin film composite NF membranes. Application of hydrodynamic models to experimental rejection of dilute solutions of hydrophilic neutral alcohols, sugars, and poly(ethylene glycol)s revealed changes in both the sieving coefficient and permeability of solutes below the membrane glass transition temperature. The vast majority of pores were smaller than 2 nm for both membranes (network pores) even though evidence for a small fraction of larger aggregate pores (approximately 30 nm) was also obtained for one membrane. Increasing temperature appears to cause structural changes in network pores by increasing its pore size while simultaneously decreasing pore density. These increases in pore sizes partially explain reported reductions in contaminant (e.g. arsenic, salts, natural organic matter, hardness, etc.) removal by NF and RO membranes with increasing temperature.

Materials Testing↗

Fate of steroid estrogens in Australian inland and coastal wastewater treatment plants.

A comparison of estrone (E1), 17beta-estradiol (E2), and 17alpha-ethinylestradiol (EE2) removal at a coastal enhanced primary and inland advanced sewage treatment plant (STP) is reported. The average concentration of estrogens in the raw sewage is similar to that reported in other studies. The sequential batch reactor at the advanced STP removed on average 85% of the incoming E1 and 96% of the E2. Further removal was observed during later microfiltration with the estrogen concentration below detection (<0.1 ng x L(-1)) after reverse osmosis. Some 6% of the influent E1+E2 was removed in the waste activated sludge. The detection of EE2 in the waste activated sludge (0.42 ng x g(-1) solids dry weight), undetectable in the raw sewage, suggests that EE2 is resistant to biological treatment in the sequential batch reactor and is primarily removed due to sorption. Little estrogen removal was observed at the enhanced primary with only 7% of E1 and 0% of E2 removed. Low removal is expected based on the degree of estrogens partitioning in the organic fraction given the relatively low solids concentration, but surprisingly, some 43% of E2, 24% of E1, and 100% of EE2 remains associated with the solids fraction in the treated effluent. Further research is necessary to determine whether the low level of estrogen removal for the coastal treatment plant will adversely affect the receiving marine environment.

Australia↗

Trace analysis of semivolatile organic compounds in large volume samples of snow, lake water, and groundwater.

An analytical method was developed for the trace analysis of a wide range of semivolatile organic compounds (SOCs) in 50-L high-elevation snow and lake water samples. The method was validated for 75 SOCs from seven different chemical classes (polycyclic aromatic hydrocarbons, organochlorine pesticides, amides, triazines, polychlorinated biphenyls, thiocarbamates, and phosphorothioates) that covered a wide range of physical-chemical properties including 7 orders of magnitude of octanol-water partition coefficient (log K(ow) = 1.4-8.3). The SOCs were extracted using a hydrophobically and hydrophilically modified divinylbenzene solid-phase extraction device (modified Speedisk). The average analyte recovery from 50 L of reverse osmosis water, using the modified Speedisk, was 99% with an average relative standard deviation of 4.8%. Snow samples were collected from the field, melted, and extracted using the modified Speedisk and a poly(tetrafluoroethylene) remote sample adapter in the laboratory. Lake water was sampled, filtered, and extracted in situ using an Infiltrex 100 fitted with a 1-microm glass fiber filter to trap particulate matter and the modified Speedisk to trap dissolved SOCs. The extracts were analyzed by gas chromatographic mass spectrometry with electron impact ionization and electron capture negative ionization using isotope dilution and selective ion monitoring. Estimated method detection limits for snow and lake water ranged from 0.2 to 125 pg/L and 0.5-400 pg/L, respectively. U.S. historic and current-use pesticides were identified and quantified in snow and lake water samples collected from Rocky Mountain National Park, CO. The application of the analytical method to the analysis of SOCs in large-volume groundwater samples is also shown.

Chemistry Techniques, Analytical↗

Electrodialysis for recovering salts from a urine solution containing micropollutants.

Electrodialysis was investigated for the separation of micropollutants from nutrients in anthropogenic urine. In a continuously operated process, the nutrients were concentrated up to a factor of 3.2. The concentration factor was limited by water transport across the membrane. Water transport was caused by osmosis and electroosmosis, and a model was developed to describe these phenomena. The removal of several spiked micropollutants was investigated in continuous electrodialysis experiments. Ethinylestradiol was removed completely during the whole operating period. Diclofenac and carbamazepine were initially retained, but limited permeation (5-10%) occurred after longer operating times (90 days). Retentions of propranolol and ibuprofen were also high initially, but substantial breakthroughs occurred during extended operation. Considerable adsorption on the membranes was observed for all compounds. The permeation mechanism of several compounds appears to depend on the adsorbed amount on the membrane, which indicates that partitioning and diffusion mechanisms play an important role in the permeation transport. Partial desorption occurred in leaching experiments with polarity reversal, and almost quantitative desorption was observed after incubation of the membranes with Filter Count Gel Solution. Because environmental concentrations are much lower than the concentrations spiked here, it can be anticipated that operation without significant permeation is possible in practice during extended periods of time.

Carbamazepine↗

Nature and abundance of organic radicals in natural organic matter: effect of pH and irradiation.

Dissolved natural organic matter (NOM) plays an essential role in freshwater geochemical and biochemical processes. A major property, its redox behavior, can be attributed to the chinone building blocks, which can form stable radicals. However, electron paramagnetic resonance (EPR) data indicating free radicals on solid NOM are sparse. Here we present EPR spectra of 23 NOM from European surface waters isolated by reverse osmosis. The organic radical concentrations of NOM ranged from 5 x 10(15) to 1.84 x 10(17) spins g(-1), and g values ranged from 2.0031 to 2.0045. Number and type of organic radicals in solid NOM are significantly influenced by the pH of raw water. EPR experiments indicate the presence of semiquinone-type radicals in coexistence with carbon-centered "aromatic" radicals, with the semiquinone-type radicals dominating at alkaline pH. Basically these processes are reversible. Organic radical concentrations in NOM adjusted to pH 6.5 before freeze-drying correlate with iron and aluminum contents. UV- and VIS-irradiation of solid NOM can lead to more than a 10-fold increase of the concentration of organic radicals. These radicals were long-lived and had the same g value as the original radical. Similar effects were not observed with isolated humic and fulvic acids, demonstrating the limited reflection of environmental properties of organic carbon by the classical isolation procedure.

Benzopyrans↗

Osmotic pressure control in response to a specific ion signal at physiological temperature using a molecular recognition ion gating membrane.

A molecular recognition gating ion membrane was prepared by graft copolymerization of N-isopropylacrylamide and benzo[18]crown-6-acrylamide onto the pore surface of porous polyethylene film. This membrane captured Ba2+ with its crown ether receptors and generated osmotic pressure in response to Ba2+ autonomously and reversibly. However, the membrane never generated osmotic pressure in response to Ca2+. In addition, the concentration gradient of both the ion and other solute such as dextran could be used as the driving force; using a dextran concentration gradient, we can control the critical concentration and the duration time of the osmosis response.

Barium↗

Model study on the effect of 15 phenolic olive mill wastewater constituents on seed germination and Vibrio fischeri metabolism.

Olive mill wastewaters (OMW) can be a severe problem when disposed of as untreated because of their high organic load, elevated concentration of polyphenols, and moderately low biodegradability. In the present study, the acute toxicity of 15 compounds with low molecular weight (<350 Da), catechol, four benzoic acids, three phenylacetic acids, three phenylethanols, and four cinnamic acids, already isolated from the reverse osmosis in the fractionation of OMW, was assessed on the marine bacterium Vibrio fischeri and on the seeds of two dicotyledonous species Cucumis sativus and Lepidium sativum, and on one monocotyledon Sorghum bicolor. Results of phytotoxicity showed that the most toxic compounds were catechol (EC50s ranging from 0.40 mmol/L for S. bicolor to 1.09 for C. sativus) and hydroxytyrosol, (EC50s ranging from 0.47 mmol/L for S. bicolor to 1.55 for C. sativus) while the toxic potential on bacteria was particularly elevated with EC50 values 1 or 2 orders less than phytotoxicity. These results suggested that the risk of OMW disposal may be more elevated for the water compartment than for the soil.

Aliivibrio fischeri↗

Laser photophoretic migration with periodic expansion-contraction motion of photo-absorbing microemulsion droplets in water.

When the water-in-oil (w/o) microemulsion droplets including the Co(III)-pyridylazo complex as the photo-absorber were irradiated with a continuous-wave Ar(+) ion laser (514.5 nm), we have observed unexpected phenomenon that photo-absorbing microemulsion droplets in water repeated the expansion and the sudden contraction during the laser photophoretic migration. The period of the expansion-contraction cycle was inversely proportional to both the concentration of the complex and the irradiated laser power and was independent of the initial size of the droplet. The mechanism of the periodic motion of the droplet was investigated by local temperature measurement and Raman microscope spectroscopy. It was suggested that the first step was the phase separation of the bicontinuous microemulsion droplet into the normal w/o microemulsion outer phase and the aqueous inner phase in the droplet, which was caused by the laser-induced temperature gradient inside the droplet. Subsequently, an expansion of the inner aqueous phase was induced by the percolation of the external water by thermo-osmosis, which was caused by the laser-induced temperature gradient between the inside and the outside of the microemulsion liquid membrane of the droplet. When the liquid membrane became thinner to a critical thickness, the inner aqueous phase was released and the droplet shrank into the original size. The proposed mechanism can give an account of the unique cyclical motion.

Journal Article↗

The measurement of water activity in allogeneic skin grafts preserved using high concentration glycerol or propylene glycol.

In the presence of free water, many degradation reactions can occur within stored tissues including enzymatic digestion, oxidation (peroxidation) and hydrolytic reactions, as well as the detrimental effects of microbial growth, therefore most long-term banking techniques are designed to avoid free water. One method currently used for banking of skin grafts is the use of high concentration (85%) glycerol as a preservative. In this case, the glycerol was assumed to dehydrate the skin by osmosis and diffusion out of the cells and skin matrix respectively. We have recently shown that this assumption is incorrect and the converse occurs, i.e. glycerol enters the skin and sequesters the water. It was therefore essential to determine whether enough water had been immobilised to prevent degradation of the tissue. Using an instrument (Pawkit) designed to measure water activity (aw) it was shown that a stepwise reduction in aw was achieved when the skin was immersed in 50 and 85% glycerol or propylene glycol, respectively. At the end of the glycerolisation process, the final aw was shown to be circa 0.3. An aw of 0.3 is known to minimise lipid peroxidation and reduce other degradation reaction rates to very low levels. It was concluded that the current glycerolisation protocol results in effective sequestration of water avoiding degradation of the skin during storage. The method presented should be used as a quality control step to confirm adequacy of preservation for each batch of glycerolised skin.

Cadaver↗

Removal of bound calcium from nematocyst contents causes discharge.

Nematocysts are the stinging organelles of jellyfish, sea anemones and other cnidarians. Each one consists of a closed capsule filled with fluid. In the resting state, part of the surface of the capsule is inverted, forming a tubular thread, which is everted explosively on excitation. The mechanism of explosion is not yet understood, it may be relevant to exocytosis in general, as the nematocyst is a specialized type of exocytotic secretion originating in the Golgi apparatus. Picken and Skaer observed that the capsular fluid showed a large depression of freezing point, suggesting that the osmotic pressure might be as high as 140 bar. They tentatively ascribed the explosion to a sudden increase in permeability of the capsule wall, allowing a rapid osmotic influx of water. However, there is evidence that the material of the thread itself may be capable of some degree of extension and it has been suggested that osmosis plays no part in discharge. We present here a new theory: that the capsule wall is permeable to water even in the undischarged state; discharge is initiated by an increase in the osmotic pressure of the capsular fluid which is brought about by removal of bound calcium ions.

Animals↗

Electrokinetic shape changes of cochlear outer hair cells.

Rapid mechanical changes have been associated with electrical activity in a variety of non-muscle excitable cells. Recently, mechanical changes have been reported in cochlear hair cells. Here we describe electrically evoked mechanical changes in isolated cochlear outer hair cells (OHCs) with characteristics which suggest that direct electrokinetic phenomena are implicated in the response. OHCs make up one of two mechanosensitive hair cell populations in the mammalian cochlea; their role may be to modulate the micromechanical properties of the hearing organ through mechanical feedback mechanisms. In the experiments described here, we applied sinusoidally modulated electrical potentials across isolated OHCs; this produced oscillatory elongation and shortening of the cells and oscillatory displacements of intracellular organelles. The movements were a function of the direction and strength of the electrical field, were inversely related to the ionic concentration of the medium, and occurred in the presence of metabolic uncouplers. The cylindrical shape of the OHCs and the presence of a system of membranes within the cytoplasm--laminated cisternae--may provide the anatomical substrate for electrokinetic phenomena such as electro-osmosis.

Animals↗

Influence of exchange volume and dialysate flow rate on solute clearance in peritoneal dialysis.

To find the ideal dialysate flow rate and exchange volume for use in long-term peritoneal dialysis, 10 patients were studied over a period of 1.5 yr. Exchange volumes of 1 or 2 liters and dialysate flow rates of 1, 2, 3, 4, and 6 liters/hr were tested. Dextrose concentration remained constant at 1.5 g/100 ml. Peritoneal clearances for BUN, creatinine, and uric acid were calculated at 2, 5, 10, 15, and 20 hr during dialysis making a total of 120 clearances for each patient. All patients used a reverse osmosis automatic machine. The clearance of all three solutes tended to be higher with exchange volumes of 2 liters than they did with 1 liter; this trend was significant for BUN (P less than 0.025) and uric acid (P less than 0.025) but not for creatinine. There was a significant rise in clearance with increasing flow rates per hour for all solutes as shown in the following table. (Formula: see text), Since patients could not tolerate a flow rate of 6 liters/hr, we conclude that flow rate of 4 liters/hr with a 2-liter exchange will give maximum efficiency.

Blood Glucose↗

Hemodialysis encephalopathy with osteomalacic fractures and muscle weakness.

The hemodialysis unit at Columbia, South Carolina, opened in April, 1974. By June of 1977, 7 patients had died from dialysis encephalopathy, and 16 of the 51 surviving patients showed speech disorders, fits, and myoclonic jerks. Pathologic fractures were seen in 22 patients. Bone histomorphometry showed severe osteomalacia with minimal, if any, osteitis fibrosa, and serum alkaline phosphatase activity was normal. The mean serum aluminum concentration in 33 random patients was elevated at 83.5 microgram/liter (control group, 13.9 microgram/liter, P less than 0.001). The mean bone aluminum concentration in 4 patients who died from this syndrome was 307 ppm of bone ash (normal, less than 10 ppm). Dialysis fluid aluminum was high at 140 microgram/liter. Purification of the dialysis fluid with a water softener, reverse osmosis and a deionizer and abandoning extra-strength Basaljel resulted in a notable clinical and EEG improvement. None of 81 new patients who started hemodialysis between July of 1977 and July of 1979 after the change in treatment have developed any such symptoms. A syndrome of hemodialysis encephalopathy accompanied by pathologic osteomalacic fractures is described. Recovery is possible. The syndrome was eradicated after purification of the dialysis fluid.

Aged↗

Mechanism of fluid secretion common to aglomerular and glomerular kidneys.

Isolated renal proximal tubules of sea water fish net secrete fluid in vitro. The principal electrolytes in secreted fluid are Na, Cl, Mg and S. Transepithelial voltages may be lumen-negative or -positive by a few millivolts, and transepithelial resistances are low partly due to high paracellular Na and Cl permeabilities. Transepithelial electrochemical potentials indicate secretion of Mg into the tubule lumen by active transport. As Mg concentration in secreted fluid rises, Na concentration falls. Surprisingly, these observations of fluid secretion are made in glomerular and aglomerular proximal tubules, suggesting a fundamental mechanism common to both. Central to this commonality appears to be their behavior as open Donnan systems. Mg actively secreted into the tubule lumen from which it cannot diffuse back into the peritubular medium causes the transepithelial secretion of diffusible Na and Cl. Water follows by osmosis. Since there is flow out of the distal end of the tubule Donnan equilibrium is not attained. Instead, a dynamic Donnan system is maintained, driven by active transport of Mg. A mathematical model of tubular electrolyte and fluid secretion confirms the operation of this open, dynamic Donnan system in aglomerular and glomerular proximal tubules.

Animals↗