Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Colloids”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,063 records · Page 59Linked to original sources
PubMed2002

Colloid milium of the upper eyelid margins: a rare presentation.

AIM: To report a rare presentation of colloid milium occurring only on the upper eyelid margins. DESIGN: Interventional case report. METHODS: (1) Slit-lamp examination of eyelids and eyes and clinical examination including the face and a general physical examination; (2) photography of the lesions on the lids; and (3) excision biopsy and histopathologic examination. MAIN OUTCOME MEASURES: Histologic examination confirmed the clinical diagnosis. RESULTS: Clinical examination and histopathologic findings revealed the cysts to be colloid milium. CONCLUSIONS: Colloid milium can involve upper eyelids in isolation, sparing the lower eyelids and facial skin. Such rare presentations should be kept in mind while examining similar lesions.

Colloids↗
PubMed1982

The kinetics of phagocytosis of colloidal substances in experimental insulinopenic diabetes.

Because of a reduction in the rate of phagocytosis by the reticuloendothelial system, the removal of large doses of colloids from the blood is much slower in rats with experimentally induced insulinopenic diabetes than in controls having a normal metabolism. This kinetics corresponds to the exponential response reported in the literature for an injected dose exceeding the "critical dose", with phagocytosis being a crucial parameter. In the case of smaller doses of colloids, however, clearance follows a different kinetic pattern which is here formulated mathematically. It is determined largely by the rate of liver blood flow. In this case, it is not possible to obtain statistical evidence of differences between diabetic and normal rats on administration of gold. Colloidal gold and so-called biological ink proved themselves extremely useful for quantitative studies of phagocytosis, whereas indium proved to be unsuitable under the experimental conditions used in these studies.

Animals↗
PubMed1999

No beneficial effects of isocolloidoosmotic synthetic colloid addition to St. Thomas Hospital cardioplegic solution in ischemia-reperfusion injury in isolated perfused rat hearts.

1. Cardioplegic solutions provide the opportunity to operate on a nonbeating heart and to protect the heart against ischemic injury during cardiac surgery. The components of these solutions are constantly being modified in an effort to find the optimal solution. We studied the effects of colloidal volume replacers such as dextran, HES and gelatin as an isocolloidoosmotic addition to St. Thomas Hospital cardioplegic solution in ischemia-reperfusion injury of isolated rat hearts. 2. In the control group, after a stabilization period of 20 min, the hearts were arrested with St. Thomas Hospital cardioplegic solution for 3 min, then subjected to 30 min of global ischemia. Hearts then were reperfused for 10 min. In the experimental groups, the protocol was the same, but either HES 200/0.5 (50 g/L), modified fluid gelatin (30 g/l) or dextran 70 (25 g/L) were added to the St. Thomas Hospital solution. 3. All hearts were compared for their preischemic and postischemic contractility, heart rate, contractility rate product, coronary flow, lactate dehydrogenase, creatine phosphokinase enzyme leakage and wet/dry weight ratio. 4. All groups had similar contractility (for control, HES, gelatin and dextran groups the values at minute 10 of reperfusion were 59+/-9, 56+/-11%, 61+/-14%, 49+/-14% of initial values [P>0.05, respectively]) and enzyme leakage (lactate dehydrogenase 4.1+/-1.0, 8.1+/-1.5, 5.8+/-1.4, 3.7+/-1.2 [P>0.05] and for creatine phosphokinase 3.9+/-2.5, 6.4+/-3.7, 5.5+/-1.3, 5.5+/-0.8, P>0.05] IU xmin(-1) x g dry tissue(-1) in the reperfusion period, respectively) results as compared with the control group. 5. The addition of isocolloidoosmotic colloids to the cardioplegic solution did not appear to enhance the effectiveness of the crystalloid St. Thomas Hospital cardioplegic solution. If a colloid is to be chosen as a plasma replacer or an additive to priming solution in the preoperative period, or during open-heart surgery, it should be modified fluid gelatin-for no sign of cardiodepression was determined with the use of this agent.

Animals↗
PubMedDate not supplied

Slow dynamics in colloidal glasses and porous media as probed by NMR relaxometry: assessment of solvent levy statistics in the strong adsorption regime.

Mesoscopic media such as porous materials or colloidal pastes develop large specific surface area which strongly influence the dynamics of the embedded fluid. This fluid confinement can be used either to probe the interfacial geometry (frozen porous media) or the particle dynamics (paste and colloidal glass). In the strong adsorption regime, it was recently proposed that the effective surface diffusion on flat surface is anomalous and exhibits long time pathology (Lévy walks). This phenomena is directly related to the time and space properties of loop trajectories appearing in the bulk between a desorption and a readsorption step. The Lévy statistics extends the time domain of the embedded fluid dynamics toward the low frequency regime. An interesting way to probe such a slow interfacial process is to use field cycling NMR relaxometry. In the first part of this paper, we propose a simple theoretical model of NMR dispersion which only involves elementary time steps of the solvent dynamics near an interface (loops, trains, tails in relation with the confining geometry). In the second part, field cycling NMR relaxometry is used to probe the slow solvent dynamics in two type of interfacial systems: (i) a colloidal glass made of thin and flat particles (ii) two fully saturated porous media, the Vycor glass and MCM48 respectively. Experimental results are critically compared to closed-form analytical expressions and numerical simulations.

Adsorption↗
PubMed2004

Assignment of charge transfer absorption band in optical absorption spectra of the adsorbate-silver colloid system.

In this paper we reported the UV-visible-NIR optical absorption properties of silver colloid, employed as a high efficient substrate in surface-enhanced Raman spectra (SERS), under various conditions. Experimental results revealed that the new absorption band, usually appearing in the longer wavelength region due to the addition of molecules, was related to the direct adsorption of molecules on colloidal silver surface. When the adsorption occurred, this new band would appear. Once the molecules were desorbed from silver surface, the new band could not be observed. Some evidences inferred that the new absorption band was associated with the effect of charge-transfer transition between adsorbates and colloidal silver particles, while not with the effect of the surface plasma resonance due to the silver particles aggregation which was usually attributed to in previous research work.

Colloids↗
PubMed1979

Casein micelles: the colloid-chemical approach.

The colloidal properties of micellar casein are reviewed. It is shown that behaviour of intact micelles is much at variance with the predictions from the Schulze-Hardy rule, and that therefore their stability cannot be explained by the principles of the DLVO theory. Towards electrolyte, micelles behave as a protein rather than a lyophobic colloid. Casein is a strong protective colloid. In the micelle, however, it does not completely cover the inorganic constituent which remains sensitive to changes in the ionic environment. The rate theory of the enzyme-induced clotting of casein micelles is summarized. It is shown that the lag phase in the clotting is due to the second order of the co-agulation reaction. Flocculation rate constants of micelles have been deduced from clotting times. Their relatively low values can be attributed to an orientational constraint. Practical consequences of the theory with respect to clot structure, gelation of sterilized products and cheese manufacture are discussed.

Caseins↗
PubMed2005

Sub-part-per-billion analysis of aqueous lead colloids by ArF laser induced atomic fluorescence.

Highly sensitive analysis of aqueous lead carbonate colloids was demonstrated by two-pulse laser-induced atomic fluorescence. The first laser pulse at 1064 nm ablated the sample solution to create an expanding plume. The colloids, being heavier, trailed behind and became concentrated. They were then intercepted by an ArF laser pulse that induced prompt atomic fluorescence at 405.8 nm from the lead atoms. The detection limit for lead was 0.24 ppb. Tap water was analyzed, and lead emissions were clearly observed. Time-resolved spectroscopy revealed that the efficient 193-nm excitation of the analytes was more universal than expected. That was confirmed by the successful application of the technique to colloids and alloys other than lead.

Argon↗
PubMed2005

Magnetic bead-based chemiluminescent metal immunoassay with a colloidal gold label.

A novel, sensitive chemiluminescent (CL) immunoassay has been developed by taking advantage of a magnetic separation/mixing process and the amplification feature of colloidal gold label. First, the sandwich-type complex is formed in this protocol by the primary antibody immobilized on the surface of magnetic beads, the antigen in the sample, and the second antibody labeled with colloidal gold. Second, a large number of Au3+ ions from each gold particle anchored on the surface of magnetic beads are released after oxidative gold metal dissolution and then quantitatively determined by a simple and sensitive Au3+-catalyzed luminol CL reaction. Third, this protocol is evaluated for a noncompetitive immunoassay of a human immunoglobulin G, and a concentration as low as 3.1 x 10(-12) M is determined, which is competitive with colloidal gold-based anodic stripping voltammetry (ASV), colorimetric ELISA, or immunoassays based on fluorescent europium chelate labels. The high performance of this protocol is related to the sensitive CL determination of Au3+ ion (detection limit of 2 x 10(-10) M), which is 25 times higher than that by ASV at a single-use carbon-based screen-printed electrode. From the analytical chemistry point of view, this protocol will be quite promising for numerous applications in immunoassay and DNA hybridization.

Biosensing Techniques↗
PubMed2000

Polyampholyte gelatin adsorption to colloidal latex: pH and electrolyte effects on acrylic and polystyrene latices.

Polyampholytic gelatin adsorption onto two model, aqueous colloidal dispersions of like size and surface charge density, but varying hydrophobicity are reported. Adsorption isotherms and hydrodynamic layer thickness of the adsorbed gelatin layer are reported for variations of solution pH (above the gelatin IEP) and electrolyte concentration. A van't Hoff analysis of the temperature dependence of the dilute-limiting adsorption equilibrium constants provides evidence for adsorption driven by electrostatic polarization to like-charged surfaces, as well as additional hydrophobic interactions with polystyrene colloidal surfaces. It is demonstrated how these measurements can be used to predict the perikinetic stability of gelatin-coated colloidal latices and, hence, are useful for the rational formulation of dispersions containing polyampholytes.

Acrylates↗
PubMed2001

Modification of natural and artificial polymer colloids by "topology-controlled" emulsion polymerization.

A diffuse layer of water-soluble polymer chemically grafted to the surface of a hydrophobic polymer colloid has been created by the second-stage polymerization of dimethylaminoethyl methacrylate (DMAEMA) onto the biomacromolecule polyisoprene in natural rubber latex and also onto synthetic polybutadiene and polystyrene latexes. To control the locus of radical formation, the process was initiated by a redox couple wherein one component (e.g., cumene hydroperoxide) is hydrophobic and the other (e.g., tetraethylenepentamine) is hydrophilic. The modified latexes displayed a dramatic increase in colloidal stability at low pH which is attributed to grafted hydrophilic polymer acting as an electrosteric stabilizer; the effect is particularly remarkable in natural rubber latex, which usually has poor colloidal stability for pH less, similar 8. (13)C NMR was performed to verify the existence of the grafted copolymer and to quantify yield. The mechanism by which such a novel morphology can be generated is postulated to be via a process of radical formation at the particle surface followed by the subsequent grafting to the hydrophobic polymer backbone and polymerization of hydrophilic monomer in the aqueous phase. This technique is potentially useful for creating novel materials from natural rubber latex.

Butadienes↗
PubMedDate not supplied

Stimuli-responsive surfactant/phospholipid stabilized colloidal dispersions and their film formation.

Methyl methacrylate (MMA) and n-butyl acrylate (nBA) were copolymerized into stable colloidal particles in the presence of micelle forming sodium dioctyl sulfosuccinate (SDOSS) and liposome forming 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC) in aqueous media that serve as thermodynamically stable loci for lipophilic monomers and nanostructured templates. These studies show for the first time that hollow colloidal particles may coalesce to form polymeric films and the combination of SDOSS and DLPC dispersing agents provides a stimuli-responsive environment during film formation through which individual surface stabilizing components can be driven to the film-air (F-A) or film-substrate (F-S) interface. Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) of p-MMA/nBA colloidal dispersions revealed preferential and enhanced mobility of SDOSS and DLPC lipid rafts to the F-A and F-S interfaces in response to thermal, ionic, and enzymatic stimuli.

Colloids↗
PubMedDate not supplied

Film formation from colloidal dispersions stabilized by sugar derivatives and their controllable release for selective protein adsorption.

Although the use of sugar and sugar derivatives has been documented in polymer research for many years, there are no reports that would utilize these species as polymerization sites of colloidal polymeric particles that, later on, may be released during particle coalescence to form films with surfaces that differentiate protein adsorption. These studies show that, when n-dodecyl-beta-D-maltoside (DDM) is utilized for the synthesis and stabilization of poly[methyl methacrylate-co-(n-butyl acrylate)] (p-MMA/nBA) colloidal particles, upon particle coalescence DDM stratifies near the film-air (F-A) interface. By using attenuated total reflectance Fourier transform infrared (ATR FT-IR) spectroscopy and internal reflection infrared imaging (IRIRI), comparative adsorption studies on p-MMA/nBA surfaces exposed to globulin (Glo), fibrinogen (Fib), and bovine serum albumin (BSA) reveal that the presence of DDM selectively inhibits Glo and Fib adsorption, but does not affect BSA. The presence of DDM also enhances the rate of mobility of sodium dioctylsulfosuccinate (SDOSS) resulting from interactions between DDM and SDOSS moieties, and the surface morphologies change as a result of concentration variations of DDM in the colloidal dispersions.

Acrylates↗
PubMed2004

Investigation of sorption behavior between pyrene and colloidal organic carbon from activated sludge processes.

The sorption behavior of pyrene for different size fractions of colloidal organic carbon (COC) originating from two biological wastewater treatment facilities (a full-scale activated sludge system (FSAS) and a membrane bioreactor (MBR)) was investigated by fluorescence quenching. Fluorescence lifetime measurements demonstrated a dynamic quenching component in all samples, including the colloidal-free filtrates. COC sorption coefficients (Kcoc) for pyrene ranged from <1 x 10(3) L/kgcoc to 80 x 10(3) L/kgcoc and were comparable to values obtained in the literature for natural organic matter. Both linear and nonlinear behaviors were observed in the Freundlich-described converted isotherms (n = 0.89-2.1). The aromatic content of COC was quantified by the molar extinction coefficient at 280 nm (e280). Good correlations were observed between COC-pyrene sorption coefficients and e280 coefficients, suggesting that e280 may be a useful tool for predicting colloidal transport of hydrophobic organic compounds (HOCs) from activated sludge systems. The removal of COC from treated effluents may appreciably reduce the concentrations of HOCs discharged to receiving streams.

Adsorption↗
PubMed2004

Sorption of 17beta-estradiol and 17alpha-ethinylestradiol by colloidal organic carbon derived from biological wastewater treatment systems.

Sorption coefficients (K(COC)) between 17beta-estradiol (E2), 17alpha-ethinylestradiol (EE2) and size-fractionated colloidal organic carbon (COC) derived from two biological wastewater treatment facilities were quantified by fluorescence quenching. The two wastewater treatment systems included a full-scale activated sludge system (FSAS) and a membrane bioreactor (MBR). The K(COC) coefficients were highly variable and ranged between (<1 to 179) x 10(3) L/kgCOC for E2 and (<1 to 430) x 10(3) L/kgCOC for EE2 and were higher than expected from the analytes octanol-water partition coefficient. Correlations between the molar extinction coefficients measured at 280 nm (e280) and K(COC) coefficients were weak but stronger for E2 compared to EE2. Attempts at correlating sorption behavior with colloidal protein and polysaccharide concentrations were only marginally successful (r2 approximately 0.4). These low correlations suggest that aromatic content, protein, or polysaccharide concentration can not adequately explain E2 and EE2 sorption behavior to COC and that other fractions of the organic matter pool play an important role in binding. A substantial portion of the aqueous E2 and EE2 concentrations (up to 60%) may be associated with colloidal material, suggesting that COC may play a role in the fate and transport of E2 and EE2 during the activated sludge process.

Adsorption↗
PubMed2005

Aggregation kinetics of kaolinite-fulvic acid colloids as affected by the sorption of Cu and Pb.

Aggregation kinetics of kaolinite-fulvic acid colloids, as influenced by two strongly sorbing trace metal cations, Cu(II) and Pb(II), was investigated by time-resolved dynamic laser light scattering experiments. The effects of Cu and Pb on the aggregation rate and electrophoretic mobilitywere compared with that of Ca, another major divalent metal cation which is less strongly adsorbed. Kaolinite-fulvic acid suspensions (in 0.01 M NaNO3 at pH 4 and pH 6) were spiked with solutions containing Cu, Pb, or Ca to give total divalent cation concentrations between 10(-5) and 8 x 10(-3) M. The concentration of kaolinite was varied between 25 and 200 mg L(-1), while the concentration of fulvic acid ranged from 0.15 to 1.2 mg L(-1). The mass ratio of kaolinite to fulvic acid was kept constant at 500:3 in all experiments. Relative aggregation rates, expressed as attachment efficiency alpha, were determined from linear increases in average hydrodynamic radius with time during the first 5-8 min of the aggregation experiments, always starting with a well-dispersed suspension at time zero. The corresponding slope for fast aggregation (alpha = 1) was measured for pure kaolinite suspended in 0.01 M NaNO3 at pH 4. Addition of fulvic acid to the suspensions completely inhibited kaolinite aggregation at pH 4 and pH 6. Additions of Cu, Pb, and Ca resulted in strongly increased aggregation rates of the kaolinite-fulvic acid particles. The potential of the three cations to enhance aggregation of the kaolinite-fulvic acid colloids increased in the order Ca < Cu < or = Pb. At pH 4, the relationship between particle electrophoretic mobility and aggregation rate was the same for all three divalent metal cations. In the presence of Ca, an increase in pH from 4 to 6 resulted in decreased aggregation rates. However, in the presence of Cu or Pb, the opposite trend was observed and the relationship between electrophoretic mobility and aggregation rate was different than at pH 4. The effects of Cu, Pb, and Ca on the aggregation rates of kaolinite-fulvic acid colloids are explained by the different sorption behavior of the three divalent metal cations.

Adsorption↗
PubMed2004

Investigation of conventional membrane and tangential flow ultrafiltration artifacts and their application to the characterization of freshwater colloids.

Artifacts associated with the fractionation of colloids in a freshwater sample were investigated for conventional membrane filtration (0.45 microm cutoff), and two tangential flow ultrafiltration cartridges (0.1 microm cutoff and 3000 MW cutoff). Membrane clogging during conventional filtration removed some colloids smaller than 0.1 microm in diameter, much smaller than the nominal size of the filter. For certain constituents (e.g., Fe), filter clogging had a significant effect on filtrate concentrations, while artifacts associated with tangential flow ultrafiltration using a 0.1 microm cutoff were minimal. Artifacts occurred during tangential flow ultrafiltration with a 3000 MW cutoff, but did not deviate from predicted changes in concentration based on a standard permeation model. Comparison of filtrate concentrations for membrane filtration (at 1.0 and 0.45 microm) and tangential flow ultrafiltration (at 0.1 microm) for a large number of samples from Connecticut rivers shows that significant and consistent differences exist between their separation characteristics. Results for organic carbon, Fe, Mn, Al, Cu, and Pb demonstrate the magnitude of the effects of the fractionation technique on filtrate element concentration, show variability by element and flow condition, and highlight the importance of larger colloids to freshwater metal speciation. One implication of the research is that tangential flow ultrafiltration with large size cutoff membranes (e.g., approximately 0.1 microm) may be superior to conventional filtration with filters in the same size discrimination range, and potentially more appropriate for the fractionation of natural water samples.

Artifacts↗
PubMed2005

Coupled stream-subsurface exchange of colloidal hematite and dissolved zinc, copper, and phosphate.

Previous studies have shown that stream-subsurface exchange has important implications for both colloid and reactive solute transport in streams because it increases the opportunity for the interaction of stream-born substances with bed sediments. We executed a series of laboratory flume experiments to study the coupled stream-subsurface exchange of hematite and the sorbing solutes zinc, copper, and phosphate. A fundamental process-based transport model was applied to analyze the experimental results. We found that hematite had a significant effect on the transport of all ions tested. In addition, hematite mobility was substantially modified by the presence of these solutes. Batch and column experiments showed that the difference in hematite mobility was a direct effect of zinc, copper, and phosphate sorption to the hematite surface. Sorption substantially modified the hematite surface charge and subsequently hematite filtration behavior. These results suggest that the behavior of contaminants cannot be analyzed separately from colloids in surface and groundwater systems because surface-chemical processes can cause their behavior to be coupled. In particular, our results show that general and specific interactions between contaminants and iron oxide particles can alter colloid mobility, perturb natural fine particle dynamics, and either favor or disfavor contaminant mobility.

Adsorption↗
PubMed2005

Role of organic acids in promoting colloidal transport of mercury from mine tailings.

A number of factors affect the transport of dissolved and particulate mercury (Hg) from inoperative Hg mines, including the presence of organic acids in the rooting zone of vegetated mine waste. We examined the role of the two most common organic acids in soils (oxalic and citric acid) on Hg transport from such waste by pumping a mixed organic acid solution (pH 5.7) at 1 mL/min through Hg mine tailings columns. For the two total organic acid concentrations investigated (20 microM and 1 mM), particle-associated Hg was mobilized, with the onset of particulate Hg transport occurring later for the lower organic acid concentration. Chemical analyses of column effluent indicate that 98 wt % of Hg mobilized from the column was particulate. Hg speciation was determined using extended X-ray absorption fine structure spectroscopy and transmission electron microscopy, showing that HgS minerals are dominant in the mobilized particles. Hg adsorbed to colloids is another likely mode of transport due to the abundance of Fe-(oxyhydr)oxides, Fe-sulfides, alunite, and jarosite in the tailings to which Hg(II) adsorbs. Organic acids produced by plants are likely to enhance the transport of colloid-associated Hg from vegetated Hg mine tailings by dissolving cements to enable colloid release.

Chemical Fractionation↗