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Surface Charge (surface + charge)
Kinds of Surface Charge Terms modified by Surface Charge Selected AbstractsIon and pH Sensing with Colloidal Nanoparticles: Influence of Surface Charge on Sensing and Colloidal PropertiesCHEMPHYSCHEM, Issue 3 2010Feng Zhang Dr. Abstract Ion sensors based on colloidal nanoparticles (NPs), either as actively ion-sensing NPs or as nanoscale carrier systems for organic ion-sensing fluorescent chelators typically require a charged surface in order to be colloidally stable. We demonstrate that this surface charge significantly impacts the ion binding and affects the read-out. Sensor read-out should be thus not determined by the bulk ion concentration, but by the local ion concentration in the nano-environment of the NP surface. We present a conclusive model corroborated by experimental data that reproduces the strong distance-dependence of the effect. The experimental data are based on the capability of tuning the distance of a pH-sensitive fluorophore to the surface of NPs in the nanometer (nm) range. This in turn allows for modification of the effective acid dissociation constant value (its logarithmic form, pKa) of analyte-sensitive fluorophores by tuning their distance to the underlying colloidal NPs. [source] Tailoring orthogonal proteomic routines to understand protein separation during ion exchange chromatographyJOURNAL OF SEPARATION SCIENCE, JSS, Issue 13 2008Rosa Cabrera Abstract Surface charge, molecular weight, and folding state are known to influence protein chromatographic behaviour onto ion exchangers. Experimentally, information related to such factors can be gathered via 2-DE methods. The application of 2-D PAGE under denaturing/reducing conditions was already shown to reveal separation trends within a large protein population from cell extracts. However, ion-exchange chromatography normally runs under native conditions. A tailored protocol consisting in a first separation based on IEF on ImmobilineTM strips under native conditions followed by a second dimension SDS-PAGE run was adopted. The chromatographic versus electrophoretic separation behaviours of two model proteins, thaumatin (TAU) and BSA, were compared to better understand which proteomic routine would be better suited to anticipate IEX chromatographic separations. It was observed that the information contained in the pI value obtained with the adapted 2-DE protocol showed better correlation with the IEX chromatographic behaviour. On the other hand, chromatographic separations performed in the presence of urea as a denaturant have demonstrated the potential influence of hydrodynamic radius/conformation on protein separation. Moreover, the information provided by such 2-D system correlated well with the chromatographic behaviour of an additional set of pure proteins. An initial prediction of protein ion-exchange chromatographic behaviour could be possible utilizing an experimental approach based on 2-DE running under milder chemical conditions. This technique provides information that more closely resembles the separation behaviour observed with a complex biotechnological feedstock. [source] Cover Picture: Electrophoresis 3'2010ELECTROPHORESIS, Issue 3 2010Article first published online: 29 JAN 2010 Issue no. 3 is a regular issue with Emphasis on "Proteins and Proteomics". The first part has 8 articles on proteins and proteomics covering various topics, e.g. preparative divergent flow IEF, multichannel gel electrophoresis, capillary gel electrophoresis, nanoparticle-based CE of proteins, 2-DE in a radial gel format, depletion of high abundance proteins, and proteomic investigation of fetal brain and lentil seed. The remaining 10 articles are concerned with nucleic acids, gene expression, methodologies and application. Featured articles include: Preparative divergent flow IEF without carrier ampholytes for separation of complex biological samples ((10.1002/elps.200900484)) SDS-PAGE and two-dimensional maps in a radial gel format ((10.1002/elps.200900526)) Analysis of Effect of Electrolyte Types on Electrokinetic Energy Conversion in Nanoscale Capillaries ((10.1002/elps.200900409)) A simple method to determine the surface charge in microfluidic channels ((10.1002/elps.200900603)) [source] Analysis of effect of electrolyte types on electrokinetic energy conversion in nanoscale capillariesELECTROPHORESIS, Issue 3 2010Reiyu Chein Abstract An analytical study on the effect of electrolyte types on the electrokinetic energy conversion is presented using nanoscale cylindrical capillary, which is either positively or negatively charged. The sign of surface charge determines the role and concentration magnitude of ions in the capillary and the energy conversion performance. Our study shows that the electrokinetic energy conversion performance (maximum efficiency, pressure rise and streaming potential) are approximately identical for 1:1 (KCl), 2:1 (CaCl2) and 3:1 (LaCl3) electrolytes when capillary is positively charged. For negatively charged capillary, energy conversion performance degrades significantly with the increase of counter-ion valence. For both positively and negatively charged capillaries, higher maximum efficiency can be resulted in low bulk concentration and surface charge density regimes. However, high maximum pressure rise generation for the pumping is found in the low bulk concentration and high surface charge density regimes. For the electric power generation, higher maximum streaming potential is found when both bulk concentration and surface charge density are low. [source] Capillary electrophoresis of liposomes functionalized for protein bindingELECTROPHORESIS, Issue 20 2006Gerhard Bilek Abstract CE enabled assessing the attachment of hexa-histidine-tagged proteins to functionalized phospholipid liposomes. The liposomes were made of 1-palmitoyl-2-oleoyl- sn -glycero-3-phosphocholine, phosphatidyl-ethanolamine, cholesterol and distearoyl-glycero-3-phosphoethanolamine- N -methoxy(polyethylene glycol) in a molar ratio of 29:26:40:5. The unilamellar vesicles, which had an average diameter of 170,nm, were labelled by inclusion of FITC-dextran for fluorescence detection. CE was carried out in poly(vinyl alcohol) (PVA)-coated capillaries at 25°C with a BGE consisting of Tris-HCl (50,mM, pH,8.0). For conjugation of the liposomes with the proteins (soluble synthetic receptor fragments with molecular mass of 60 and 70,kDa, respectively), Ni2+ was implanted into the vesicle surface by an anchor lipid containing a nitrilotriacetate acid (NTA) group as complexation agent for the metal ions. The difference in surface charge enabled the separation of the different species of interest by CE: plain vesicles, vesicles functionalised with Ni-NTA, vesicle,protein complexes and the species formed upon removal of the Ni-ions by complexation with EDTA. Loss of the Ni-ions resulted in the release of the proteins and the reappearance of the plain Ni-free NTA-liposome species in the electropherograms. [source] Evaluating the contribution of soil properties to modifying lead phytoavailability and phytotoxicity,ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 3 2006Elizabeth A. Dayton Abstract Soil properties affect Pb bioavailability to human and ecological receptors and should be considered during ecological risk assessment of contaminated soil. We used path analysis (PA) to determine the relative contribution of soil properties (pH, organic C [OC], amorphous Fe and Al oxides [FEAL], and cation-exchange capacity [CEC]) in modifying Pb bioavailability. The response of biological endpoints (bioaccumulation and dry matter growth [DMG]) of lettuce (Lactuca sativa) grown on 21 Pb-spiked (2,000 mg/kg) soils were determined. Lettuce tissue Pb ranged from 3.22 to 233 mg/kg, and relative DMG ranged from 2.5 to 88.5% of their respective controls. Simple correlation showed strong relationships between CEC and OC (p < 0.01) and weaker relationships between pH and FEAL (p < 0.05) and Pb bioaccumulation. Results of PA suggest that soil pH increased the negative surface charge of organic matter and clay, thereby increasing CEC and decreasing Pb bioaccumulation. Also, the direct effect of OC on tissue Pb can be attributed to formation of surface Pb complexes by organic matter functional group ligands. Increased OC and/or CEC reduced Pb solubility and bioavailability in the 21 soils in the present study. The relative importance of soil properties likely will vary between studies employing different soils. Soil properties should be considered during the ecological risk assessment of metal in contaminated soils. Path analysis is useful for ecological studies involving soils with a wide range of physicochemical properties and can assist in site risk assessment of metals and remediation decisions on contaminated sites. [source] Positively Charged Material Surfaces Generated by Plasma Polymerized Allylamine Enhance Vinculin Mobility in Vital Human Osteoblastss,ADVANCED ENGINEERING MATERIALS, Issue 8 2010Henrike Rebl Abstract Several studies suggest that the modification of an implant surface by chemical means plays an important role in bone tissue engineering. Previously we have shown that osteoblast cell adhesion and spreading can strongly be increased by a positively charged surface. Cell adhesion and migration are two vital processes that are completely dependent on coordinated formation of focal adhesions. Changes in the organization of the actin cytoskeleton and the focal adhesions are essential for numerous cellular processes including cell motility and tissue morphogenesis. We examined the mobility of the cytoskeletally associated protein vinculin on functionalized surfaces using plasma polymerized allylamine (PPAAm), a homogenous plasma polymer layer with randomly distributed amino groups. In living, GFP,vinculin transfected osteoblastic cells we determined a significant increase in vinculin mobility and vinculin contact length on PPAAm compared to collagen I coated surfaces during the initial adhesion phase. We suggest that positive charges control the cell physiology which seems to be dominant over the integrin receptor binding to collagen I. The results emphasize the role of the surface charge for the design of artificial scaffolds in bone repair. [source] Surface Physiochemistry Affects Protein Adsorption to Stoichiometric and Silicate-Substituted Microporous Hydroxyapatites,ADVANCED ENGINEERING MATERIALS, Issue 4 2010Katharina Guth An important factor in the bioactivity and success of a bone-graft substitute is the nature of the adsorbed protein layer, which plays a vital role in orchestrating cell attachment and development through the presence of adhesion proteins such as fibronectin (Fn) and vitronectin (Vn). In this study, microporous hydroxyapatite (HA) and silicate-substituted hydroxyapatite (SA) discs with matched porosity and surface morphology are developed to mimic the topography found in commercial bone-graft substitutes in order to identify whether the introduction of microporosity and associated surface roughness eliminates the beneficial effect that silicate substitution has on protein adsorption. The introduction of microporosity does not abolish the relative enrichment of the protein layer that is adsorbed to the microporous SA discs, as opposed to HA, but appears to accelerate it. Fibronectin and Vn adsorption in a range of competitive environments at physiological temperatures confirm that the microporous SA discs have a greater affinity for Fn and Vn compared with HA, suggesting differences in the mechanisms behind the surface affinity to SA. Thus, development of a surface protein layer on SA and HA is likely to be dependent on the nature of the local protein environment and a combination of factors that are associated with the addition of silicate: the surface charge, the nature of the ionic species at the interface and the resultant hydrophilicity of the surface. Total protein adsorption is not found to be a good indicator of potential implant performance, particularly at early time points. [source] The effect of surface,solute interactions on the transport of solutes through porous materialsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2009D. A. Rose Summary We have investigated the effect of differences in surface charge, valency of ion, solute concentration, solution flux and physical structure on the leaching and uptake of individual ions from simple solutions flowing through porous materials. We studied the miscible displacement of solutions of four salts (KBr, K2SO4, CaBr2 and CaSO4) having different cation : anion ratios separately through three inert materials (ballotini, pumice and ceramic) and two sizes of a reactive material (sepiolite) over several ranges of concentration (c) and at many pore-water velocities (v) under steady vertical saturated flow. Breakthrough curves of individual effluent ions (K+, Br,, Ca2+ and SO42,) were analysed by CXTFIT 2.0 to optimize transport parameters (retardation factor, R; dispersion coefficient, K) assuming that transport was governed by the convective,dispersion equation. In the inert materials, R did not differ significantly from 1 irrespective of c. In sepiolite, R was < 1 for anions and > 1 for cations, and became more extreme as c decreased. R varied with the valency of the anions, as predicted by diffuse double layer theory, and with that of the cations by a simple charge balance. Freundlich isotherms, reconstructed from R values, described the sorption of the cations and exclusion of the anions. For the inert materials, K did not depend on the ion or c and increased monotonically with v. For sepiolite, K also increased with v and with small but non-significant differences between ions and concentrations. The K(v) functions were consistent with Passioura's theory of dispersion in aggregated media, and the transport was reversible as R and K values did not depend on whether the media were being leached or resalinized. The effective dispersion coefficient of an ion is K* = K/R so, although K(v) appears to be unaffected by ion or concentration of solute in sepiolite, K*(v) will be affected. Thus, the controlling factor of these surface,solute interactions is R. [source] Analysis of the variable charge of two organic soils by means of the NICA-Donnan modelEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 6 2007B. Vasiliadis Summary We have tested to see if the generic set of NICA-Donnan model parameters, used to describe isolated humic substances, can also describe soil humic substances in situ. A potentiometric back-titration technique was used to determine the variable surface charge of two organic peat soils at three different ionic strengths. The non-ideal, competitive-adsorption NICA-Donnan model was used to simulate the surface charge, by assuming a bimodal distribution of H+ affinity on the soil solid phase. The model provided an excellent fit to the experimental data. The Donnan volume, VD, varied slightly with ionic strength, although the variation was less than for humic substances in solution. The values obtained for the parameters that define the affinity distributions, the intrinsic proton binding constant (log Kiint) and the heterogeneity of the site (mi), were similar to those observed for isolated soil humic acids. The abundance of carboxylic groups in the whole soil represented 30% of the typical value for isolated soil humic acids. The composition of the organic matter of the whole soils, obtained by 13C CPMAS NMR, was comparable to the characteristic composition of soil humic acids. [source] Delivery of Nucleic Acids through the Controlled Disassembly of Multifunctional NanocomplexesADVANCED FUNCTIONAL MATERIALS, Issue 24 2009Mahmoud Elsabahy Abstract In this study, novel pH-responsive polyion complex micelles (PICMs) were developed for the efficient delivery of nucleic acid drugs, such as antisense oligonucleotide (AON) and short interfering RNA (siRNA). The PICMs consisted of a poly(amidoamine) (PAMAM) dendrimer,nucleic acid core and a detachable poly(ethylene glycol)- block -poly(propyl methacrylate- co -methacrylic acid) (PEG- b -P(PrMA- co -MAA)) shell. The micelles displayed a mean hydrodynamic diameter ranging from 50 to 70,nm, a narrow size distribution, and a nearly neutral surface charge. They could be lyophilized without any additives and stored in dried form. Upon redispersion in water, no change in complexation efficiency or colloidal properties was observed. Entry of the micelles into cancers cells was mediated by a monoclonal antibody fragment positioned at the extremity of the PEG segment via a disulfide linkage. Upon cellular uptake and protonation of the MAA units in the acidic endosomal environment, the micelles lost their corona, thereby exposing their positively charged endosomolytic PAMAM/nucleic acid core. When these pH-responsive targeted PICMs were loaded with AON or siRNAs that targeted the oncoprotein Bcl-2, they exhibited a greater transfection activity than nontargeted PICMs or commercial PAMAM dendrimers. Moreover, their nonspecific cytotoxicity was lower than that of PAMAM. The pH-responsive PICMs reported here appear as promising carriers for the delivery of nucleic acids. [source] Chemical reactivity of microbe and mineral surfaces in hydrous ferric oxide depositing hydrothermal springsGEOBIOLOGY, Issue 3 2007S. V. LALONDE ABSTRACT The hot springs in Yellowstone National Park, USA, provide concentrated microbial biomass and associated mineral crusts from which surface functional group (FG) concentrations and pKa distributions can be determined. To evaluate the importance of substratum surface reactivity for solute adsorption in a natural setting, samples of iron-rich sediment were collected from three different springs; two of the springs were acid-sulfate-chloride (ASC) in composition, while the third was neutral-chloride (NC). At one of the ASC springs, mats of Sº -rich Hydrogenobaculum -like streamers and green Cyanidia algae were also collected for comparison to the sediment. All samples were then titrated over a pH range of 3,11, and comparisons were made between the overall FG availability and the concentration of solutes bound to the samples under natural conditions. Sediments from ASC springs were composed of hydrous ferric oxides (HFO) that displayed surface FGs typical of synthetic HFO, while sediments from the NC spring were characterized by a lower functional group density, reflected by decreased excess charge over the titration range (i.e., lower surface reactivity). The latter also showed a lower apparent point of zero charge (PZC), likely due the presence of silica (up to 78 wt. %) in association with HFO. Variations in the overall HFO surface charge are manifest in the quantities and types of solutes complexed; the NC sediments bound more cations, while the ASC sediments retained significantly more arsenic, presumably in the form of arsenate (H2AsO4,). When the microbial biomass samples were analyzed, FG concentrations summed over the titratable range were found to be an order of magnitude lower for the Sº-rich mats, relative to the algal and HFO samples that displayed similar FG concentrations on a dry weight basis. A diffuse-layer surface complexation model was employed to further illustrate the importance of surface chemical parameters on adsorption reactions in complex natural systems. [source] Investigation of nanoscale electrohydrodynamic transport phenomena in charged porous materialsINTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN ENGINEERING, Issue 14 2005P. Pivonka Abstract Depending on the permeability of porous materials, different mass transport mechanisms have to be distinguished. Whereas mass transport through porous media characterized by low permeabilities is governed by diffusion, mass transport through highly permeable materials is governed by advection. Additionally a large number of porous materials are characterized by the presence of surface charge which affects the permeability of the porous medium. Depending on the ion transport mechanism various phenomena such as co-ion exclusion, development of diffusion,exclusion potentials, and streaming potentials may be encountered. Whereas these various phenomena are commonly described by means of different transport models, a unified description of these phenomena can be made within the framework of electrohydrodynamics. In this paper the fundamental equations describing nanoscale multi-ion transport are given. These equations comprise the generalized Nernst,Planck equation, Gauss' theorem of electrostatics, and the Navier,Stokes equation. Various phenomena such as the development of exclusion potentials, diffusion,exclusion potentials, and streaming potentials are investigated by means of finite element analyses. Furthermore, the influence of the surface charge on permeability and ion transport are studied in detail for transient and steady-state problems. The nanoscale findings provide insight into events observed at larger scales in charged porous materials. Copyright © 2005 John Wiley Sons, Ltd. [source] Adhesion of Listeria monocytogenes to materials commonly found in domestic kitchensINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 7 2008Pilar Teixeira Summary The aim of this work was to investigate the adhesion of Listeria monocytogenes ATCC 15313 to glass, granite, marble, polypropylene from a bowl (PPb), polypropylene from a cutting board (PPcb) and stainless steel (SS), which are materials commonly used in kitchens. Marble and granite were chosen because they are applied as kitchen bench covers and pavements in many countries and there are no literature reports on their behaviour in terms of microbial adhesion. The effect of surface hydrophobicity and roughness on the adhesion process was also analysed. The results showed that the highest extent of adhesion of L. monocytogenes occurred to stainless steel, followed by glass and in less extent to the other materials studied. However, it was not possible to establish a correlation between surface hydrophobicity or roughness and the extent of adhesion of L. monocytogenes. The adherence of L. monocytogenes should be dependent on other factors, like the presence of exopolymers and surface charge. [source] Isoelectric points of virusesJOURNAL OF APPLIED MICROBIOLOGY, Issue 2 2010B. Michen Summary Viruses as well as other (bio-)colloids possess a pH-dependent surface charge in polar media such as water. This electrostatic charge determines the mobility of the soft particle in an electric field and thus governs its colloidal behaviour which plays a major role in virus sorption processes. The pH value at which the net surface charge switches its sign is referred to as the isoelectric point (abbreviations: pI or IEP) and is a characteristic parameter of the virion in equilibrium with its environmental water chemistry. Here, we review the IEP measurements of viruses that replicate in hosts of kingdom plantae, bacteria and animalia. IEPs of viruses are found in pH range from 1·9 to 8·4; most frequently, they are measured in a band of 3·5 < IEP < 7. However, the data appear to be scattered widely within single virus species. This discrepancy is discussed and should be considered when IEP values are used to account for virus sorption processes. [source] Factors affecting the attachment of micro-organisms isolated from ultrafiltration and reverse osmosis membranes in dairy processing plantsJOURNAL OF APPLIED MICROBIOLOGY, Issue 2 2009X. Tang Abstract Aims:, To identify the types of micro-organisms involved in the formation of biofilms on dairy ultrafiltration and reverse osmosis membranes and investigate factors affecting the attachment of those isolates. Methods and Results:, Micro-organisms isolated from industrial membranes following standard cleaning were identified using the API culture identification system. Thirteen different isolates representing eight genera were isolated and their ability to attach to surfaces was compared using a microtitre plate assay. Three Klebsiella strains attached best, while mixed strains of Pseudomonas and Klebsiella attached better than individual strains. Whey enhanced the attachment of the isolates. The micro-organisms were characterized according to cell surface hydrophobicity using the microbial adhesion to hydrocarbon (MATH) test, and cell surface charge by measuring the zeta potential. These cell surface characteristics did not show a clear relationship with the attachment of our strains. Conclusions:, A variety of different micro-organisms is associated with dairy ultrafiltration and reverse osmosis membranes after cleaning, suggesting several possible sources of contamination. The cleaning of these membranes may be inadequate. The attachment of the different isolates is highly variable and enhanced in the presence of whey. Significance and Impact of the Study:, Knowledge of persistent microflora colonizing dairy membrane systems will help develop strategies to mitigate biofilm development in this environment, improving hygiene in membrane processing plants. [source] Physicochemical properties of Shiga toxigenic Escherichia coliJOURNAL OF APPLIED MICROBIOLOGY, Issue 4 2005L. Rivas Abstract Aims:, To investigate the physicochemical surface properties, such as cellular surface charge, hydrophobicity and electron donor/acceptor potential of a selection of Shiga toxigenic Escherichia coli (STEC) isolates grown in broth and agar culture. Methods and Results:, Cellular surface charge was determined using zeta potential measurements. Hydrophobicity of the isolates was determined using bacterial adhesion to hydrocarbons assay, hydrophobic interaction chromatography and contact angle measurements. Microbial adhesion to solvents was used to determine the electron donor/acceptor characteristics. No differences of surface charge measurements were found between broth and agar grown cultures. Isolates belonging to serogroup O157 and serotypes O26:H11 and O111:H- were significantly (P < 0·05) less negatively charged than other STEC serotypes tested. All strains were hydrophilic with most methods and demonstrated a lower hydrophobicity in agar culture compared with broth culture. All strains demonstrated a strong microbial adhesion to chloroform indicating that STEC possess an electron donor and basic character. A relationship between serogroup O157 and other STEC serotypes was apparent using principal-component analysis (PCA). Conclusions:, Combining the results for physicochemical properties using PCA differentiated between strains belonging to the O157 serogroup and other STEC/non-STEC strains. PCA found similar results for broth and agar grown cultures. Significance and Impact of the Study:, Particular serotypes of STEC possess similar physicochemical properties which may play a role in their pathogenicity or potential attachment to various surfaces. [source] Preparation and adsorption properties of chitosan,poly(acrylic acid) nanoparticles for the removal of nickel ionsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Jian-Wen Wang Abstract Chitosan (CS) nanoparticles with different mean sizes ranging from 100 to 195 nm were prepared by ionic gelation of CS and poly(acrylic acid) (PAA). Variations in the final solution pH value and CS : PAA volume ratio were examined systematically for their effects on nanoparticle size, intensity of surface charge, and tendency toward particle aggregation. The sorption capacity and sorption isotherms of the CS,PAA nanoparticles for nickel ions were evaluated. The parameters for the adsorption of nickel ions by the CS,PAA nanoparticles were also investigated. The CS,PAA nanoparticles could sorb nickel ions effectively. The sorption rate for nickel ions was affected significantly by the initial concentration of the solution, sorbent amount, particle size, and pH value of the solution. The samples of nanoparticles were well correlated with Langmuir's isotherm model, and the adsorption kinetics of nickel correlated well with the pseudo-second-order model. The maximum capacity for nickel sorption deduced from the use of the Langmuir isotherm equation was 435 mg/g, which was significantly higher than that of the micrometer-sized CS. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008 [source] Comparison of ciprofloxacin hydrochloride-loaded protein, lipid, and chitosan nanoparticles for drug deliveryJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008Dharmendra Jain Abstract The aim of the present study was to develop single dose delivery systems based on nanotechnology for prolonged antibiotic release in a controlled manner. Five different drug,carrier ratios of ciprofloxacin hydrochloride-loaded nanoparticles of albumin, gelatin, chitosan (CS), and lipid [solid lipid nanoparticles (SLNs)] were prepared and characterized. Average particle size was found to be in the range of 73 ± 2 to 98 ± 44 nm for SLNs, 140 ± 7 to 175 ± 24 nm for albumin nanoparticles, 143 ± 18 to 184 ± 27 nm for gelatin nanoparticles, and 247 ± 48 to 322 ± 52 nm for CS nanoparticles. A drug-to-carrier ratio of 0.5:1 was preferred for CS nanoparticles having zeta potential of >20 mV and drug encapsulation of 35.01% ± 2.66%. Similarly, 0.6:1 ratio was preferred for albumin nanoparticles with zeta potential >16 mV and drug encapsulation 48.20% ± 3.01%. Zeta potentials of gelatin nanoparticles loaded with ciprofloxacin suggested that they were unstable and prone to flocculation. SLN with 0.25:1 drug carrier ratio showed 38.71% ± 2.38% drug entrapment and ,28 ± 1 mV surface charge. All the nanoparticles showed sustained drug release avoiding "burst effect" of the free drugs for up to 120 h for albumin nanoparticles, 96 h for CS and gelatin nanoparticles, and 80 h for SLNs. The drug release profiles followed Higuchi model. Results suggest that CS nanoparticles and SLNs can act as promising carriers for sustained ciprofloxacin release in infective conditions. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source] Assessment of a semi-quantitative method for estimation of the rejection of organic compounds in aqueous solution in nanofiltrationJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 7 2006Bart Van der Bruggen Abstract A large number of different mechanisms describing the retention of dissolved organic compounds in nanofiltration have been proposed. A recent review identified the parameters possibly involved in the separation performance and suggested a qualitative classification of dissolved compounds. Continuing this approach, a semi-quantitative assessment of the observed rejections in nanofiltration is given in this paper, based on threshold values of key parameters such as molecular weight and molecular weight cut-off (MWCO), molecular size, pH and pKa, hydrophobicity (logKow) and membrane charge. Experimental values and literature data were used to provide a broad basis for comparison. It was concluded that (a) all categories that contain hydrophobic components are badly defined, in particular for small components, with rejections varying from low to very high, (b) all components that contain hydrophilic components have relatively high rejections and (c) all categories that contain charged components have well-defined, high rejections (intermediate for membranes with low surface charge). In all cases, the average rejection is higher when the component's molecular weight is larger than the MWCO of the membrane and when the molecular size is larger than the pore size of the membrane. Copyright © 2006 Society of Chemical Industry [source] Nutshells as granular activated carbons: physical, chemical and adsorptive properties,JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2001H Wartelle Abstract Nutshells from seven different sources (pistachio, hazelnut, almond, black walnut, English walnut, macadamia nut, pecan) were converted to granular activated carbons (GACs) by carbon dioxide activation. A portion of the GACs were oxidized with compressed air and the physical (yield, surface area, attrition), chemical (pH, surface charge) and adsorptive (organics uptake, metal ion uptake) properties of both oxidized and non-oxidized carbons were determined. Differences in uptake of organics, especially of polar compounds, were found between GACs made from almond shells, the group consisting of black walnut shells, English walnut shells and pecan shells, and macadamia nutshells. Oxidation had its greatest effects on pH, surface charge and uptake of metal ions. The changes due to oxidation were found to be independent of carbon source material. GACs with specific properties can be produced with judicious selection of carbon precursor and oxidative treatment. © 2001 Society of Chemical Industry [source] Effect of K-Casein Deglycosylation on the Acid Coagulability of MilkJOURNAL OF FOOD SCIENCE, Issue 8 2003E. Cases ABSTRACT: The relationship between the content of N-acetylneuraminic acid residues of micellar K-casein and acid coagulability of milk was investigated. At 30 °C, partial deglycosylation of micellar K-casein does not significantly affect the content of micellar proteins, micellar surface charge, and micellar solvation. Casein micelles modified by the release of part of the N-acetylneuraminic acid residues showed a shorter acid gelation time, a higher rate of gel strengthening, and a higher final firmness. This enhancement in the gelation ability of the neuraminidase-treated casein micelles of milk should appear as the result of increase in number of hydrophobic sites on the surface of casein micelle due to enzymatic deglycosylation of micellar K-casein. [source] Fabrication, characterization and in vitro evaluation of poly(D,L -lactide- co -glycolide) microparticles loaded with polyamidoamine,plasmid DNA dendriplexes for applications in nonviral gene deliveryJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 1 2010Janjira Intra Abstract We report, for the first time, on the preparation, characterization and in vitro testing of poly(D,L -lactide- co -glycolide) (PLGA) microparticles loaded with polyamidoamine (PAMAM),plasmid DNA (pDNA) dendriplexes. Loading of pDNA into the PLGA microparticles increased by 150% when pDNA was first complexed with PAMAM dendrimers relative to loading of pDNA alone. Scanning electron microscopy (SEM) showed that the presence of PAMAM dendrimers in the PLGA microparticles created porous features and indentations on the surface of the microparticles. Loading PLGA microparticles with PAMAM,pDNA dendriplexes lowered the average PLGA microparticle size and changed the surface charge of the microparticles from negative to positive when compared to PLGA microparticles loaded with pDNA alone. The zetapotential and buffering capacity of the microparticles increased as the generation of the PAMAM dendrimer loaded in the PLGA microparticles increased. Gel electrophoresis assays showed that all the PLGA microparticle formulations were able to entrap the pDNA within the PLGA matrix. There was no significant difference in the cytotoxicity of PLGA microparticles loaded with PAMAM,pDNA dendriplexes when compared to PLGA microparticles loaded with pDNA alone. Furthermore, and in contrast to PAMAM dendrimers alone, the generation of the PAMAM dendrimer loaded in the PLGA microparticles had no significant impact on cytotoxicity or transfection efficiencies in human embryonic kidney (HEK293) or Monkey African green kidney fibroblast-like (COS7) cells. The transfection efficiency of PLGA microparticles loaded with generation 3 (G3) PAMAM,pDNA dendriplexes was significantly higher than PLGA microparticles loaded with pDNA alone in HEK293 and COS7 cells. PLGA microparticles loaded with G3 PAMAM,pDNA dendriplexes generated equivalent transfection efficiencies as (G3 to G6) PAMAM,pDNA dendriplexes alone in COS7 cells when the transfection was carried out in serum containing media. The delivery system developed in this report has low toxicity, high pDNA loading efficiencies and high transfection efficiencies that are not reduced in the presence of serum. A delivery system with these characteristics is expected to have significant potential for translational applications. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:368,384, 2010 [source] Cytotoxicity and apoptosis enhancement in brain tumor cells upon coadministration of paclitaxel and ceramide in nanoemulsion formulationsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 7 2008Ankita Desai Abstract The objective of this study was to examine augmentation of therapeutic activity in human glioblastoma cells with combination of paclitaxel (PTX) and the apoptotic signaling molecule, C6 -ceramide (CER), when administered in novel oil-in-water nanoemulsions. The nanoemulsions were formulated with pine-nut oil, which has high concentrations of essential polyunsaturated fatty acid (PUFA). Drug-containing nanoemulsions were characterized for particle size, surface charge, and the particle morphology was examined with transmission electron microscopy (TEM). Epi-fluorescent microscopy was used to analyze nanoemulsion-encapsulated rhodamine-labeled PTX and NBD-labeled CER uptake and distribution in U-118 human glioblastoma cells. Cell viability was assessed with the MTS (formazan) assay, while apoptotic activity of PTX and CER was evaluated with caspase-3/7 activation and flow cytometry. Nanoemulsion formulations with the oil droplet size of approximately 200 nm in diameter were prepared with PTX, CER, and combination of the two agents. When administered to U-118 cells, significant enhancement in cytotoxicity was observed with combination of PTX and CER as compared to administration of individual agents. The increase in cytotoxicity correlated with enhancement in apoptotic activity in cells treated with combination of PTX and CER. The results of these studies show that oil-in-water nanoemulsions can be designed with combination therapy for enhancement of cytotoxic effect in brain tumor cells. In addition, PTX and CER can be used together to augment therapeutic activity, especially in aggressive tumor models such as glioblastoma. © 2007 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 97:2745,2756, 2008 [source] Characterization of the interactions between polymethacrylate-based aqueous polymeric dispersions and aluminum lakesJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 12 2001Nasser Nyamweya Abstract Instability in film coating formulations can arise from interactions between aluminum lake pigments and aqueous polymeric dispersions. The purpose of this study was to characterize the interactions between three polymethacrylate-based aqueous polymeric dispersions (Eudragit® RS 30 D, Eudragit® L 30 D-55, and Eudragit® NE 30 D) and aluminum lakes. Particle size measurements, pH stability profiles, zeta potential measurements, and microscopy were used to study mixed dispersions of the polymeric latices and the lakes. Interactions leading to dispersion instability were related to the surface charge of the components in the formulation. Interactions between the ionic polymers and the lakes arose from instability of the lakes outside a certain pH range resulting in the release of electrolytes, which led to aggregation of the polymeric particles. Interactions between the nonionic polymer and the lakes were related to the polymer modifying the surface charge of the lakes, resulting in aggregation of the pigment particles. © 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:1937,1947, 2001 [source] ELECTROSTATIC EFFECTS ON PHYSICAL PROPERTIES OF PARTICULATE WHEY PROTEIN ISOLATE GELSJOURNAL OF TEXTURE STUDIES, Issue 4 2001MATTHEW K. McGUFFEY Physical properties of particulate whey protein isolate gels formed under varying electrostatic conditions were investigated using large strain rheological and microstructural techniques. The two treatment ranges evaluated were adjusting pH (5.2-5.8) with no added NaCl and adjusting the NaCl (0.2-0.6 M) at pH 7. Gels (10% protein w/v) were formed by heating at 80C for 30 min. The large strain properties of fracture strain (,f), fracture stress (,f), and a measure of strain hardening (R0.3) were determined using a torsion method. Gel microstructure was evaluated using scanning electron microscopy (SEM) and gel permeability (Bgel). Overlaying ,f and ,f curves for pH and NaCl treatments demonstrated an overlap where gels of equal ,f and ,f could be formed by adjusting pH or NaCl concentration. The high fracture stress (,f, 23 kPa and ,f, 1.86) pair conditions were pH 5.47 and 0.25 M NaCl, pH 7.0. The low fracture stress (,f, 13 kPa and ,f, 1.90) pair conditions were pH 5.68 and 0.6 M NaCl, pH 7.0. The 0.25 M NaCl, pH 7 treatment demonstrated higher R0.3 values than the pH 5.47 treatment. When the sulfhydryl blocker n-ethylmaleimide was added at 2 mM to the 0.25 M NaCl, pH 7 gel treatment, its rheological behavior was NSD (p>0.05) to the pH 5.47 gel treatment, indicating disulfide bond formation regulated strain hardening. Altering surface charge or counterions, and disulfide bonding, was required to produce gels with similar large strain rheological properties. An increase in gel permeability coincided with an increase in pore size as observed by SEM, independent of rheological properties. This demonstrated that at the length scales investigated, microstructure was not linked to changes in large strain rheological properties. [source] Ca2+ -Mediated Interaction Between Microsilica and Polycarboxylate Comb Polymers in a Model Cement Pore SolutionJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2010Matthias Lesti Interaction between polycarboxylate (PCE) comb polymers and microsilica suspended in a highly alkaline, Ca2+ -loaded model cement pore solution was studied via zeta potential, adsorption, and paste flow experiments. Zeta potential measurements reveal that in an alkaline suspension, microsilica possesses a negative surface charge stemming from deprotonated silanolate groups. Addition of soluble calcium salts (e.g., CaCl2) was found to cause a charge reversal to positive, owing to the adsorption of Ca2+ ions forming a monolayer on the microsilica surface. Further experiments demonstrate that through Ca2+ mediation, anionic PCE graft polymers adsorb in high amount on the microsilica surface. Polymers possessing a stronger anionic character exhibit a higher affinity to the positive microsilica surface, and consequently, exercise a more powerful dispersing effect than PCE showing less anionic character. A model summarizing the processes occurring at the surface of microsilica in this fluid system is proposed. The study suggests that the high fluidity of concrete containing microsilica depends on the effective dispersion of microsilica, and not of cement. [source] Influence of a Ceramic Substrate on Aqueous Precipitation and Structural Evolution of Alumina Nano-Crystalline CoatingsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2007Marie Mahé Either boehmite (,-AlOOH) or gibbsite (,-Al(OH)3) nanocrystalline thin films (h,100 nm) can be precipitated from AlCl3 solution at fixed pH and temperature onto different substrates. It depends on the nature of the substrate (mica flakes, SiO2 flakes, or ,-Al2O3 flakes), on their crystallographic properties (crystalline or amorphous), and on some experimental parameters (agitation rate, addition rate). According to the surface charge of the substrates, different alumina species are involved in the precipitation process. When negative charges are present on the substrate, the [Al3O(OH)3(OH2)9]4+ polycation is promoted, leading to the formation of the (Al4) tetramer ([Al4O(OH)10(OH2)5]o) and then to the precipitation of bohemite. When positive charges are present, a ligand bridge containing complex ([Al3O(OH)3(O2H3)3(OH2)9]+) is likely favored, giving rise to hexagonal ring structures or amorphous solids that lead to the formation of gibbsite. Besides the surface effects, crystalline substrates can act as a template during precipitation of aluminum species as shown for the formation of gibbsite on muscovite. Finally, calcination at 850°C of boehmite samples leads to porous ,-Al2O3 layers, while calcination of gibbsite leads to ,-Al2O3 layers. [source] Aqueous Processing and Stabilization of Manganese Zinc Ferrite Powders via a Passivation,Dispersion ApproachJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 9 2002Michael M. Mandanas A dispersion scheme for aqueous processing of manganese zinc ferrite suspensions is presented. The addition of oxalic acid leads to the formation of a uniform negative charge on the surface such that a cationic polyelectrolyte, polyethyleneimine (PEI), adsorbs and provides electrosteric dispersion. At 0.5 w/w (weight percent with respect to the dry powder) oxalic acid addition, there is a relatively uniform negative surface charge (approximately ,30 mV) within the suspension pH range investigated (3,10), eliminating the isoelectric point (pH ,7.6) present for the as-received metal oxide powder. At the addition of 0.5 w/w PEI on an oxalate-treated surface, the surface charge is constant and positive (,20 mV) through a wide pH range, ,5,10. The resulting rheological data for passivation,dispersion of relatively high-solids manganese zinc ferrite suspensions (,80 wt%) demonstrate improved colloid stability with improved rheological properties. The resulting apparent viscosity and Bingham yield point is 0.01 Pa·s (12.0 cP) and 0.24 Pa (2.4 dynes/cm2), respectively. A sulfonated napthalene-based dispersant, typically used in industry, gives an apparent viscosity and Bingham yield point of 0.03 Pa·s (32 cP) and 3.1 Pa (31 dynes/cm2), respectively. [source] In Situ Surface Modification of Silicon Carbide Particles Using Al3+ Complexes and Polyelectrolytes in Aqueous SuspensionsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 3 2002Yongheng Zhang Silicon carbide (SiC) particles were modified in situ, using Al3+ complexes in aqueous media, via control of Al(NO3)3concentration and pH. The Al3+ formed hydrolyzed complexes that adsorbed onto the charged sites on the SiC particle surfaces. As a result, the surface-modified SiC particles behaved in an alumina-like manner in the approximate pH range 5,8. The modified SiC particles were further treated with two types of polyelectrolytes that were sequentially adsorbed onto the particle surface, to give a maximum surface charge. As a result of this surface-modification process, the SiC could be dispersed with Al2O3in aqueous media without heteroaggregation. [source] | ||||||||||||||||||||||||||||||||||