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Different pH Values (different + ph_value)
Selected AbstractsBrain temperature and pH measured by 1H chemical shift imaging of a thulium agentNMR IN BIOMEDICINE, Issue 2 2009Daniel Coman Abstract Temperature and pH are two of the most important physiological parameters and are believed to be tightly regulated because they are intricately related to energy metabolism in living organisms. Temperature and/or pH data in mammalian brain are scarce, however, mainly because of lack of precise and non-invasive methods. At 11.7,T, we demonstrate that a thulium-based macrocyclic complex infused through the bloodstream can be used to obtain temperature and pH maps of rat brain in vivo by 1H chemical shift imaging (CSI) of the sensor itself in conjunction with a multi-parametric model that depends on several proton resonances of the sensor. Accuracies of temperature and pH determination with the thulium sensor , which has a predominantly extracellular presence , depend on stable signals during the course of the CSI experiment as well as redundancy for temperature and pH sensitivities contained within the observed signals. The thulium-based method compared well with other methods for temperature (1H MRS of N -acetylaspartate and water; copper,constantan thermocouple wire) and pH (31P MRS of inorganic phosphate and phosphocreatine) assessment, as established by in vitro and in vivo studies. In vitro studies in phantoms with two compartments of different pH value observed under different ambient temperature conditions generated precise temperature and pH distribution maps. In vivo studies in , -chloralose-anesthetized and renal-ligated rats revealed temperature (33,34°C) and pH (7.3,7.4) distributions in the cerebral cortex that are in agreement with observations by other methods. These results show that the thulium sensor can be used to measure temperature and pH distributions in rat brain in vivo simultaneously and accurately with using biosensor imaging of redundant. Copyright © 2008 John Wiley & Sons, Ltd. [source] Influence of citric acid on calcium sulfate dihydrate crystallization in aqueous mediaCRYSTAL RESEARCH AND TECHNOLOGY, Issue 2 2007S. Titiz-Sargut Abstract The crystallization of Calcium sulfate dihydrate produced by the reaction between pure Ca(OH)2 suspension and H2SO4 solution was investigated at different pH values, temperatures and citric acid concentrations. Crystal size distributions, filtration rates and zeta potentials of gypsum were determined as a function of citric acid concentrations at pH 3.5 and 65°C. The influence of citric acid on the morphology of gypsum was also investigated and discussed. The average particle size of gypsum was reached to maximum in the presence of approximately 2500 ppm citric acid concentration, where the minimum cake resistance and maximum filtration rate were obtained. In the presence of citric acid, various crystal morphologies such as tabular, plate-like, double-taper leaf-like and flower-like, etc., were obtained. The change of morphology is related to the preferential adsorption of citric acid on different crystallographic faces. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] The Preliminary Studies of Electrochemical Behavior of Paracetamol and Its Metabolites on Glassy Carbon Electrode by Voltammetric MethodsELECTROANALYSIS, Issue 10 2009Irena Baranowska Abstract The new, rapid and sensitive method for the determination of paracetamol (PAR) and its glucuronide (PG) and sulfate (PS) metabolites is proposed. The electrochemical properties of the compounds were examined by cyclic voltammetry (CV) on glassy carbon electrode (GCE). All measurements were carried out in Britton,Robinson buffers (BR) with different pH values over the pH range 1.81,7.24. The preliminary research indicated that PAR could be determined simultaneously with one of its metabolites. The linearity of calibration curves was obtained for concentrations between 1.65×10,5 and 1.65×10,4 M for PAR, 1.53×10,5 and 1.53×10,4 M for PG and 2.17×10,5 and 1.52×10,4 M for PS. [source] Assignment of the [4Fe-4S] clusters of Ech hydrogenase from Methanosarcina barkeri to individual subunits via the characterization of site-directed mutantsFEBS JOURNAL, Issue 18 2005Lucia Forzi Ech hydrogenase from Methanosarcina barkeri is a member of a distinct group of membrane-bound [NiFe] hydrogenases with sequence similarity to energy-conserving NADH:quinone oxidoreductase (complex I). The sequence of the enzyme predicts the binding of three [4Fe-4S] clusters, one by subunit EchC and two by subunit EchF. Previous studies had shown that two of these clusters could be fully reduced under 105 Pa of H2 at pH 7 giving rise to two distinct S½ electron paramagnetic resonance (EPR) signals, designated as the g = 1.89 and the g = 1.92 signal. Redox titrations at different pH values demonstrated that these two clusters had a pH-dependent midpoint potential indicating a function in ion pumping. To assign these signals to the subunits of the enzyme a set of M. barkeri mutants was generated in which seven of eight conserved cysteine residues in EchF were individually replaced by serine. EPR spectra recorded from the isolated mutant enzymes revealed a strong reduction or complete loss of the g = 1.92 signal whereas the g = 1.89 signal was still detectable as the major EPR signal in five mutant enzymes. It is concluded that the cluster giving rise to the g = 1.89 signal is the proximal cluster located in EchC and that the g = 1.92 signal results from one of the clusters of subunit EchF. The pH-dependence of these two [4Fe-4S] clusters suggests that they simultaneously mediate electron and proton transfer and thus could be an essential part of the proton-translocating machinery. [source] Escherichia coli thioredoxin inhibition by cadmiumFEBS JOURNAL, Issue 7 2004Asp2, Two mutually exclusive binding sites involving Cys3 Observations of thioredoxin inhibition by cadmium and of a positive role for thioredoxin in protection from Cd2+ led us to investigate the thioredoxin,cadmium interaction properties. We used calorimetric and spectroscopic methods at different pH values to explore the relative contribution of putative binding residues (Cys32, Cys35, Trp28, Trp31 and Asp26) within or near the active site. At pH 8 or 7.5 two binding sites were identified by isothermal titration calorimetry with affinity constants of 10 × 106 m,1 and 1 × 106 m,1. For both sites, a proton was released upon Cd2+ binding. One mole of Cd2+ per mole of reduced thioredoxin was measured by mass spectrometry at these pH values, demonstrating that the two binding sites were partially occupied and mutually exclusive. Cd2+ binding at either site totally inhibited the thiol,disulfide transferase activity of Trx. The absence of Cd2+ interaction detected for oxidized or alkylated Trx and the inhibition of the enzymatic activity of thioredoxin by Cd2+ supported the role of Cys32 at the first site. The fluorescence profile of Cd2+ -bound thioredoxin differed, however, from that of oxidized thioredoxin, indicating that Cd2+ was not coordinated with Cys32 and Cys35. From FTIR spectroscopy, we inferred that the second site might involve Asp26, a buried residue that deprotonates at a rather high and unusual pKa for a carboxylate (7.5/9.2). The pKa of the two residues Cys32 and Asp26 have been shown to be interdependent [Chivers, T. P. (1997) Biochemistry36, 14985,14991]. A mechanism is proposed in which Cd2+ binding at the solvent-accessible thiolate group of Cys32 induces a decrease of the pKa of Asp26 and its deprotonation. Conversely, interaction between the carboxylate group of Asp26 and Cd2+ at a second binding site induces Cys32 deprotonation and thioredoxin inhibition, so that Cd2+ inhibits thioredoxin activity not only by binding at the Cys32 but also by interacting with Asp26. [source] The effect of exogenous pectinase on DMHF and derivatives in clarified strawberry juice (Fragaria × ananassa, cv. Elsanta)FLAVOUR AND FRAGRANCE JOURNAL, Issue 5 2002Emanuela Mura Abstract The effect of exogenous pectinase on the levels of 2,5-dimethyl-4-hydroxy-2H -furan-one (DMHF) and DMHF-glucoside was studied in clarified strawberry juice (Fragaria × ananassa, cv. Elsanta). The extent of conversion of DMHF-malonyl glucoside to DMHF-glucoside and DMHF was monitored at three different temperatures (45 °C, 50 °C and 60 °C) and at three different pH values (pH 3.0, 4.0 and 5.4). The effect of using two different concentrations of pectinase was also studied. Based on these results, the endogenous levels of DMHF-malonyl glucoside were calculated for the first time in strawberries. Copyright © 2002 John Wiley & Sons, Ltd. [source] Solubility of root-canal sealers in water and artificial salivaINTERNATIONAL ENDODONTIC JOURNAL, Issue 10 2003E. Schäfer Abstract Aim, To compare the weight loss of eight different root-canal sealers in water and in artificial saliva with different pH values. Methodology, For standardized samples (n = 12 per group), ring moulds were filled with epoxy resin (AH 26, AH Plus)-, silicone (RSA RoekoSeal)-, calcium hydroxide (Apexit, Sealapex)-, zinc oxide,eugenol (Aptal-Harz)-, glass-ionomer (Ketac Endo)- and polyketone (Diaket)-based sealers. These samples were immersed in double-distilled water or artificial saliva with different pH values (7.0, 5.7 and 4.5) for 30 s, 1 min, 2 min, 5 min, 10 min, 20 min, 1 h, 2 h, 10 h, 24 h, 48 h, 72 h, 14 days and 28 days. Mean loss of weight was determined and analysed statistically using a one-way anova and Student,Newman,Keuls test for all pairwise comparisons. Results, Most sealers were of low solubility, although Sealapex, Aptal-Harz and Ketac Endo showed a marked weight loss in all liquids. Even after 28 days of storage in water, AH 26, AH Plus, RSA RoekoSeal, and Diaket showed less than 3% weight loss. At exposure times greater than 14 days, Sealapex showed the significantly greatest weight loss of all sealers tested (P < 0.05). Aptal-Harz and Ketac Endo were significantly more soluble in saliva (pH 4.5) than in water (P < 0.05). Conclusions, Under the conditions of the present study, AH Plus showed the least weight loss of all sealers tested, independent of the solubility medium used. Sealapex, Aptal-Harz and Ketac Endo had a marked weight loss in all liquids. [source] Colorimetric investigation of the reaction between p -phenylendiamine and meta -substituted derivatives of benzene on a model supportINTERNATIONAL JOURNAL OF COSMETIC SCIENCE, Issue 3 2010M. Scalzo J. Cosmet. Sci., 60, 429,436 (July/August 2009) Synopsis The aim of this work was the employment of colorimetric techniques in the analysis of the color formed, on a proteic substrate, by the reaction between p -phenylendiamine and some meta -substituted benzene derivatives in the presence of hydrogen peroxide and in media at different pH values. In particular we investigated the chromatic variations that take place on the substrate in dependence on different reaction conditions. The obtained results show that for each couple of reagents the colorimetric data, namely the reflectance of the formed color, change considerably with the pH of the reaction medium and demonstrate how this parameter can be considered a good descriptor of the composition of the formed pigment. [source] Assemblies of Metal Nanoparticles and Self-Assembled Peptide Fibrils,Formation of Double Helical and Single-Chain Arrays of Metal Nanoparticles,ADVANCED MATERIALS, Issue 11 2003X. Fu Double helical and single-chain arrays of Au and Pd metal nanoclusters have been achieved by assembling the corresponding metal nanoparticles on peptide nanofibril templates at different pH values. The assembled metal nanoparticles are useful for studying the superstructures of the peptide nanofibrils. Pd nanowires of different shapes have also been prepared by varying the amount of metal deposition. [source] Hollow, pH-sensitive calcium,alginate/poly(acrylic acid) hydrogel beads as drug carriers for vancomycin releaseJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2010Hong-Ru Lin Abstract In this study, hollow calcium,alginate/poly(acrylic acid) (PAA) hydrogel beads were prepared by UV polymerization for use as drug carriers. The hollow structure of the beads was fortified by the incorporation of PAA. The beads exhibited different swelling ratios when immersed in media at different pH values; this demonstrated that the prepared hydrogel beads were pH sensitive. A small amount (<9%) of vancomycin that had been incorporated into the beads was released in simulated gastric fluid, whereas a large amount (,67%) was released in a sustained manner in simulated intestinal fluid. The observed drug-release profiles demonstrated that the prepared hydrogel beads are ideal candidate carriers for vancomycin delivery into the gastrointestinal tract. Furthermore, the biological response of cells to these hydrogel beads indicated that they exhibited good biological safety and may have additional applications in tissue engineering. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Mercury removal: a physicochemical study of metal interaction with natural materialsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 11 2009Leticia Carro Abstract BACKGROUND: Mercury is considered one of the most harmful heavy metals to the environment and human health, so recently remediation processes have been developed to eliminate this metal from wastewaters. Metal retention by natural polymers is a good alternative technique to remove heavy metals from solution. RESULTS: A screening of 25 potential mercury sorbents was carried out at three different pH values in order to find appropriate biomass to remove this metal from polluted waters. High sorption capacities were found for many of the materials studied. Four of these materials were selected for further detailed study. Kinetic studies showed short times to reach equilibrium. For S. muticum, sorption isotherms were obtained at several temperatures and a sorption enthalpy value was obtained. Desorption experiments were performed to determine the possibility for recycling of this brown alga. CONCLUSIONS: Different materials have been found to be potentially good adsorbents of mercury. A detailed study showed that S. muticum is an excellent material with a mercury uptake about 200 mg g,1. This brown alga has a fast kinetic process (80% of metal is removed from solution in 30 min), and very high metal uptake over a wide pH range, up to 92% elimination for pH values above 3,4. Copyright © 2009 Society of Chemical Industry [source] Optimization of extraction of bulk enzymes from spent mushroom compostJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 7 2003Avneesh D Singh Abstract The profiling of ligninase, hemicellulase and cellulase of Pleurotus sajor-caju after inoculation of spawn in bags containing sawdust was done at monthly intervals for a period of 6 months. Xylanase (EC 3.2.1.8) was produced throughout the 6 months studied with the productivity range from 5.60 to 7.51 U g,1. Cellulase (EC 3.2.1.4) and ,-glucosidase (EC 3.2.1.21) productivities were highest at 4 months, producing 3.31 U g,1 and 121.13 U g,1 respectively. Laccase (EC 1.10.3.2) productivity was highest at 2 months with a value of 7.59 U g,1. Lignin peroxidase (EC 1.11.1.14) productivity was highest at 5 months with a value of 206.20 U g,1. Total soluble proteins were highest at 4 months with a value of 0.139 mg cm,3. The profiling of lignin peroxidase in 5-month-old spent mushroom compost was monitored over a period of 10 months. It was observed that lignin peroxidase was produced throughout the period but productivity was variable. The average lignin peroxidase productivity ranged from 30 to 110 U g,1. The activities of the enzymes extracted in tap water at pH 8.4 were comparable to that extracted in 50 mmol sodium citrate buffer at pH 4.8 and distilled water at pH 5.2 at 4 °C using an incubator shaker at 200 rpm for 18 h. The optimum extraction time was 1 h using an incubator shaker at 4 °C. When an incubator shaker was used, there was no significant difference in the recovery of xylanase, cellulase and laccase at different pH values at 4 °C and 28 °C. No significant difference was observed in the recovery of ,-glucosidase using an incubator shaker at different pH values at 4 °C although the enzyme recovery was slightly higher at pH 8.12, with a value of 29.27 U g,1. The optimum extraction of ,-glucosidase was at pH 4 at room temperature using an incubator shaker. For the lignin peroxidase enzyme, the optimum pH for extraction was 6 at 4 °C and pH 7 at room temperature using an incubator shaker at 200 rpm for 1 h. Homogenization for 8 min at 8000 rpm using tap water at pH 4 had an advantage over the use of the incubator shaker for the extraction as high titers of enzymes were recovered. Copyright © 2003 Society of Chemical Industry [source] THE EFFECT OF REFRIGERATED STORAGE ON SENSORY PROFILE AND PHYSICAL-CHEMICAL CHARACTERISTICS OF MINIMALLY PASTEURIZED ORANGE JUICEJOURNAL OF FOOD PROCESSING AND PRESERVATION, Issue 2009TATIANA BEATRIS TRIBESS ABSTRACT Minimal pasteurization of orange juice (OJ) consists of using minimum holding time and temperature to ensure partial inactivation of pectin methylesterase (PME). This process produces juice with preserved sensory attributes and has a better acceptance by consumers when compared with commercially pasteurized OJ. Sensory profile and physical-chemical characteristics of minimally processed OJ was determined, during refrigerated storage, for two OJ blends with different pH values and the same level of PME thermal inactivation. A selected and trained sensorial panel (n = 16) performed sensory analysis, based on a quantitative descriptive analysis, twice a week for 30 days, evaluating the attributes of appearance (suspended particles and color intensity), odor (natural orange and fermented orange) and flavor (orange characteristic, fermented orange, acid and bitter taste). Storage presented great effect on OJ sensory profile; however, it was not noticeable on physical-chemical characteristics. PRACTICAL APPLICATIONS Minimal pasteurization of orange juice (OJ) consists of using minimum holding time and temperature to ensure partial inactivation of pectin methylesterase. This process produces juice with longer shelf life than fresh squeezed orange juice, preserved sensory attributes and better acceptance by consumers when compared with commercially pasteurized OJ. This study can contribute for quality evaluation of minimally pasteurized OJ under refrigeration. [source] Core-Shell Biopolymer Nanoparticles Produced by Electrostatic Deposition of Beet Pectin onto Heat-Denatured ,-Lactoglobulin AggregatesJOURNAL OF FOOD SCIENCE, Issue 6 2008R. Santipanichwong ABSTRACT:, The purpose of this study was to produce and characterize core-shell biopolymer particles based on electrostatic deposition of an anionic polysaccharide (beet pectin) onto amphoteric protein aggregates (heat-denatured ,-lactoglobulin [,-lg]). Initially, the optimum conditions for forming stable protein particles were established by thermal treatment (80 °C for 15 min) of 0.5 wt%,-lg solutions at different pH values (3 to 7). After heating, stable submicron-sized (d= 100 to 300 nm) protein aggregates could be formed in the pH range from 5.6 to 6. Core-shell biopolymer particles were formed by mixing a suspension of protein aggregates (formed by heating at pH 5.8) with a beet pectin solution at pH 7 and then adjusting the pH to values where the beet pectin is adsorbed (< pH 6). The impact of pH (3 to 7) and salt concentration (0 to 250 mM NaCl) on the properties of the core-shell biopolymer particles formed was then established. The biopolymer particles were stable to aggregation from pH 4 to 6, but aggregated at lower pH values because they had a relatively small ,-potential. The biopolymer particles remained intact and stable to aggregation up to 250 mM NaCl at pH 4, indicating that they had good salt stability. The core-shell biopolymer particles prepared in this study may be useful for encapsulation and delivery of bioactive food components or as substitutes for lipid droplets. [source] Solubilization of the lichen metabolite (+)-usnic acid for testing in tissue cultureJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 11 2002Thórdís Kristmundsdóttir The pharmacological testing of natural products can often be hampered by the poor solubility of such compounds in non-toxic solvents. There is thus a need for a suitable agent for solubilization of natural substances to allow testing on a variety of cell lines in-vitro. Such an agent should ideally have no direct effects on any of the commonly used cell lines from a variety of tissues and mammalian species to allow proper comparison. In this study, the lichen metabolite (+)-usnic acid, a dibenzofuran derivative, was used as a prototype for an insoluble natural product with the aim of finding a solvent that was both capable of solubilizing usnic acid and was free of direct activity against a test cell line. Solubilization was measured at different pH values in various concentrations of co-solvents (glycofurol 75, propylene glycol, polyethylene glycol 400), surfactants (polysorbate 20 and Cremophor RH40), and the complexing agent 2-hydroxypropyl-,-cyclodextrin. The solubility achieved in a 20% aqueous solution was 0.11 mg mL,1 for propylene glycol, 0.19 for PEG 400, 0.27 for glycofurol 75, 0.57 for Cremophor RH40, 0.68 for 2-hydroxypropyl-,-cyclodextrin and 0.84 for polysorbate 20. The direct effects of the various solvent systems were tested on the human leukaemia cell line K-562 in a standard proliferation assay. Most of the solvents proved toxic with the exception of propylene glycol, PEG 400 and 2-hydroxypropyl-,-cyclodextrin. Anti-proliferative activity of usnic acid could be demonstrated with an ED50 (amount of substance required to reduce thymidine uptake to 50% of uptake by untreated control culture) of 4.7,g mL,1 using PEG 400 and 2-hydroxypropyl-,-cyclodextrin but only the latter gave satisfactory solubility. 2-Hydroxypropyl-,-cyclodextrin was thus identified as a solubilizing agent that fulfilled both set criteria of solubility and lack of toxicity against the test cells. [source] Raman spectroscopic analysis of azurite blackeningJOURNAL OF RAMAN SPECTROSCOPY, Issue 2 2008E. Mattei Abstract Azurite is a basic copper carbonate pigment largely employed in painting realization. The areas painted with azurite are easily alterable and are often less resistant than the other parts of artworks. The azurite alteration in a black pigment, the copper oxide (tenorite), has been studied by micro-Raman spectroscopy. The blackening can be due to thermal or chemical alterations: in the second case the alterations being due to the presence of alkaline conditions. Laser-induced degradation of azurite has been studied as a function of the grain size. The results show that the temperature of the grains decreases as the size increases, and azurite degrades into tenorite only below the critical value of 25 µm. To study the chemical alteration of azurite, the pigment has been applied on the plaster of terracotta samples and analyzed at different pH values by micro-Raman spectroscopy. As opposed to most part of the analytical techniques, it can detect the presence of both azurite and tenorite molecules in the same micro areas, and provides a valuable tool to determine azurite degradation. Copyright © 2008 John Wiley & Sons, Ltd. [source] Surface-enhanced Raman scattering study of the red dye laccaic acidJOURNAL OF RAMAN SPECTROSCOPY, Issue 10 2007M. V. Cañamares Abstract FT-Raman and surface-enhanced Raman scattering (SERS) spectroscopy were applied to the study of lac dye, a highly fluorescent anthraquinone red dye. The SERS spectra were obtained at different pH values, on Ag nanoparticles prepared by chemical reduction with citrate and hydroxylamine, and at several excitation wavelengths, in order to find the best experimental conditions for the detection of the lac dye. The lower detection limit was achieved using nanoparticles prepared by reduction with hydroxylamine, excitation at 514.5 nm, and slightly acidic pH conditions, thus exploiting a combination of factors including lower electrostatic repulsion between dye and nanoparticles and resonance Raman enhancement. A comparison between the adsorption of laccaic acid (LA) and carminic acid (CA), another anthraquinone red dye, was also done, based on the SERS spectra of both dyes. Copyright © 2007 John Wiley & Sons, Ltd. [source] Raman spectroscopy of hydrotalcites with phosphate in the interlayer: implications for the removal of phosphate from waterJOURNAL OF RAMAN SPECTROSCOPY, Issue 7 2006Ray L. Frost Abstract Hydrotalcites with phosphate in the interlayer were prepared at different pH values. At pH > 11.0 (PO4)3, was the intercalated ionic species, whereas at pH < 11.0 a mixture of (PO4)3, and (HPO4)2, ions was intercalated. Powder X-ray diffraction shows that the hydrotalcite formed at pH 9.5 is poorly diffracting with a d-spacing of 11.9 Å; whereas the d(003) spacing for the phosphate interlayered hydrotalcite formed at pH 11.9 and 12.5 was 8.0 and 7.9 Å respectively. The addition of a thermally activated ZnAl-HT to a phosphate solution resulted in the uptake of the phosphate and the reformation of the hydrotalcite. Raman spectroscopy of the phosphate interlayered hydrotalcites shows that the interlayered anion is pH dependent and only above pH 11.9 is the orthophosphate anion intercalated. At lower pH, the monohydrogen phosphate anion is intercalated. Raman spectroscopy shows that upon addition of the thermally activated hydrotalcite to an aqueous phosphate solution, results in the uptake of phosphate anion from the solution. Copyright © 2006 John Wiley & Sons, Ltd. [source] Purification of alkaloids from Corydalis yanhusuo W. T. Wang using preparative 2-D HPLCJOURNAL OF SEPARATION SCIENCE, JSS, Issue 9 2009Jing Zhang Abstract Two-dimensional preparative multi-channel parallel high performance liquid chromatography was successfully applied for the first time to isolate and purify alkaloids from Corydalis yanhusuo. The experiments were performed in off-line mode using the same preparative chromatographic column with pH 3.5 in the first and pH 10.0 in the second separation dimension. In the preparative process, UV-triggered fraction collection was used in the first dimension while UV and MS-triggered collection were used in the second dimension for reasons of sensitivity and complementarity. Two pure compounds and nine fractions were obtained in the first dimension. Then two representative fractions were further purified in the second dimension and six pure compounds were obtained. The results demonstrated that this procedure is an effective approach for the preparative isolation and purification of alkaloids from Corydalis yanhusuo. Based on the different pH values of the mobile phase in this method, it is also suitable for the preparative isolation and purification of other compounds from TCMs which are sensitive to the pH of the solutions. Moreover, this method will be a promising tool for the purification of low content compounds from natural products. [source] Controlled Delivery Achieved with Bi-Layer Matrix Devices Produced by Co-Injection MouldingMACROMOLECULAR BIOSCIENCE, Issue 8 2004Cláudia M. Vaz Abstract Summary: The aim of this study was to design new soy protein-based bi-layered co-injection moulded matrix systems aimed to achieve controlled drug delivery. The devices consisted of a drug-free outer layer (skin) and a drug-containing core. The systems overcame the inherent disadvantage of non-linear release associated with diffusion-controlled single-layer matrix devices by providing additional releasing area with time to compensate for the decreasing release rate. As expected, the bi-layer devices presented a significant decrease in drug release rate when compared with a correspondent single layer matrix system. The skin thickness and the degree of crosslinking of the core appeared to be very important tools to tailor the release patterns. Furthermore, due to the amphoteric nature of the soy protein, the developed devices evidenced a pH-dependent behaviour. The mechanisms of drug release were also elucidated at two different pH values: i) pH 5.0, near the isoelectric point of soy (low matrix solubility); and ii) pH 7.4, physiological pH (high matrix solubility). Consequently, changing the release medium from pH 5.0 to pH 7.4 after two hours, led to an abrupt increase in drug release and the devices presented a typical controlled drug delivery profile: slow release/fast release. These evidences may provide for the development of individual systems with different release onsets that in combination may exhibit drug releases at predetermined times in a pre-programmed way. Another possibility is the production of three-layer devices presenting bimodal release profiles (fast release/slow release/fast release) by similar technologies. Scanning electron micrograph of a developed bi-layer device. [source] Copolymerization of 2-Acrylamido-2-methyl-1-propanesulfonic Acid and 1-Vinylimidazole in Inverse MiniemulsionMACROMOLECULAR REACTION ENGINEERING, Issue 2 2008Susann Wiechers Abstract The copolymerization behavior of the acidic monomer 2-acrylamido-2-methyl-1-propanesulfonic acid (APSA) and 1-vinylimidazole in inverse miniemulsion was studied under various conditions. Initially, different surfactants and surfactant concentrations were investigated. After determining a suitable composition of the miniemulsion, changes in the reaction behavior under different pH values and monomer feed compositions were studied. The highest polymerization rates could be produced under neutral conditions over all monomer feed ratios. The addition of acid or base to change the pH value of the monomer mixture also has influence on the polymers obtained. The thermal stability, rheological stiffness and intrinsic viscosity increase when Na-APSA is incorporated. [source] Mechanical and corrosion behaviour of a Ti-Al-Nb alloy after deformation at elevated temperaturesMATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 12 2008M. V. Popa Abstract The mechanical properties of Ti6Al7Nb alloy deformed and heat treated at elevated temperatures were correlated with its microstructure and corrosion behaviour in Ringer (of different pH values: 2.49, 6.9 and 8.9) and Ringer,Brown solutions. Microstructural analysis revealed a Widmanstatten structure for the alloys deformed at 1100,°C (, field) and structure with , grains at 930,°C (,,+,, field). The thermo-mechanical processing improved the electrochemical behaviour of Ti6Al7Nb alloys, especially their passive state. Open circuit potential variations in time reflected more compact, stable, resistant passive films on the surface of the treated alloys. Open circuit potential gradients simulating the non-uniformities of pH along the implant surface have very low values that cannot generate galvanic corrosion. Corrosion rates and ion release are very much reduced. Impedance spectra were fitted with a two time-constants equivalent circuit for some alloys and with three time-constants equivalent circuit for other alloys. [source] Thermal kinetics of color degradation of mulberry fruit extractMOLECULAR NUTRITION & FOOD RESEARCH (FORMERLY NAHRUNG/FOOD), Issue 2 2003Hyung Joo Suh Abstract The effects of temperature and pH on color degradation kinetics of the mulberry fruit extract were investigated. The absorbance at 510 nm was decreased with increase of heating time, but that at 420 nm was increased with the increase of heating time at 100°C. The change of the browning index (A510/A420) was increased with increase of pH and was lower at pH 2.0 than that at pH 5.0. The browning index variation was adequately described by both the first-order and the zero-order kinetic. However, the zero-order kinetic model was proposed because of the better fit. According to the Arrhenius model, the activation energies for the browning index in the range of 80,100°C for the four different pH values were 30.68 kJ/mol for pH 2.0, 35.87 kJ/mol for pH 3.0, 42.67 kJ/mol for pH 4.0, and 43.49 kJ/mol for pH 5.0. [source] Analysis of phenolic acids in honeys of different floral origin by solid-pase extraction and high-performance liquid chromatographyPHYTOCHEMICAL ANALYSIS, Issue 1 2007Burya Dimitrova Abstract The determination of 18 aromatic and arylaliphatic carboxylic acids in honey from different floral origin using solid-phase extraction (SPE) and reversed-phase high performance liquid chromatography (RP-HPLC) is reported. The behaviour of the solutes on SPE cartridges was predicted from preliminary calculations involving the pKa constants of the carboxylic groups, the n -octanol:water partition coefficients and the distribution coefficients at different pH values of the conditioning and washing solvents. The proposed SPE isolation and pre-concentration of the acids was achieved on reversed-phase Bond Elut C18 cartridges using an acetonitrile:tetrahydrofuran (1:1, v/v) elution system. RP-HPLC separations were performed on a Spherisorb ODS-2 column using linear gradient elution with a mobile phase composed of 20 mm phosphate buffer (pH 2.92) and methanol, and with UV detection. The reported SPE and RP-HPLC methods were applied to the analysis of 49 authentic honey samples from various floral sources and the results indicate that they may serve with respect to the quantitative control of a number of phenolic acids in plant-derived foods and medicinal plants. Copyright © 2006 John Wiley & Sons, Ltd. [source] Poly(4-hydroxyphenylacetic acid): A new material for immobilization of biomoleculesPOLYMER ENGINEERING & SCIENCE, Issue 10 2008Tatiana A.R. Silva The electrochemical modification, surface analysis, and electrochemical impedance spectroscopy of graphite electrodes modified with polymeric films derived from 4-hydroxyphenylacetic acid (4-HPA) were investigated. The electrooxidation and optimization of the immobilization of adenosine monophosphate (AMP) and guanosine monophosphate (GMP) onto poly(4-HPA) films at different pH values was carried out. Variation of the experimental conditions that influenced the electrode reaction, particularly the pH of the electrolytic solution, showed that the oxidation potentials of the immobilized AMP or GMP onto the modified electrodes decreased with increasing pH of the electrolyte. Higher oxidation current was obtained for AMP in phosphate buffer (pH 7.50) solution and GMP in acetate buffer (pH 4.50) solution. Film surface morphology and roughness in the absence or presence of AMP or GMP have been characterized by atomic force microscopy. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers [source] Synthesis, characterization and polychelatogenic properties of poly[(2-acrylamido-2-methyl-1-propane sulfonic acid)- co -(methacrylic acid)]POLYMER INTERNATIONAL, Issue 4 2001Bernabé L Rivas Abstract Poly(2-acrylamido-2-methyl-1-propanesulfonic acid), poly(methacrylic acid), and five copolymers of poly[(2-acrylamido-2-methyl-1-propanesulfonic acid)- co -(methacrylic acid)] were synthesized by radical polymerization and obtained in yields >97%. The polymers were characterized by FT-IR, [1H]NMR, and [13C]NMR and studied by means of the Liquid-phase Polymer-based Retention (LPR) technique. The metal ion retention ability of the copolymers for Cu(II), Cd(II), Co(II), Hg(II), Ni(II), Zn(II), Cr(III) and Ag(I) was investigated at different pH values because of their environmental and analytical interest. The retention profiles of the copolymers were compared with those of the corresponding homopolymers and retention of metal ions was found to increase with increasing pH. © 2001 Society of Chemical Industry [source] Modulation of gene expression by extracellular pH variations in human fibroblasts: A transcriptomic and proteomic studyPROTEINS: STRUCTURE, FUNCTION AND BIOINFORMATICS, Issue 5 2003Maja A. Bumke Abstract Homeostasis of the intracellular ionic concentration, in particular that of hydrogen ions, is pivotal to the maintenance of cell function and viability. Nonetheless, pH fluctuations in both the intracellular and the extracellular compartments can occurr during development, in physiological processes and in disease. The influence of pH variations on gene expression has been studied in different model systems, but only for a limited number of genes. We have performed a broad range analysis of the patterns of gene expression in normal human dermal fibroblasts at two different pH values (in the presence and in the absence of serum), with the aim of getting a deeper insight into the regulation of the transcriptional program as a response to a pH change. Using the Affymetrix gene chip system, we found that the expression of 2068 genes (out of 12,565) was modulated by more than two-fold at 24, 48 or 72 h after the shift of the culture medium pH to a more acidic value, stanniocalcin 1 being a remarkable example of a strongly up-regulated gene. Genes displaying a modulated pattern of expression included, among others, cell cycle regulators (consistent with the observation that acidic pH abolishes the growth of fibroblasts in culture) and relevant extracellular matrix (ECM) components. Extracellular matrix protein 2, a protein with a restricted pattern of expression in adult human tissues, was found to be remarkably overexpressed as a consequence of serum starvation. Since ECM components, whose expression is controlled by pH, have been used as targets for biomolecular intervention, we have complemented the Affymetrix analysis with a two-dimensional polyacrylamide gel electrophoresis analysis of proteins which are differentially secreted by fibroblasts at acidic or basic pH. Mass spectrometric analysis of more than 650 protein spots allowed the identification of 170 protein isoforms or fragments, belonging to 40 different proteins. Some proteins were only expressed at basic pH (including, for instance, tetranectin), while others (e.g., agrin) were only detectable at acidic pH. Some of the identified proteins may represent promising candidate targets for biomedical applications, e.g., for antibody-mediated vascular targeting strategies. [source] Interaction of methyltin(IV) compounds with carboxylate ligands.APPLIED ORGANOMETALLIC CHEMISTRY, Issue 1 2008Part 2: formation thermodynamic parameters, predictive relationships, sequestering ability Abstract Thermodynamic data of mono-, di- and tri-methyltin(IV)-carboxylate complexes (acetate, malonate, succinate, oxydiacetate, diethylenetrioxydiacetate, malate, citrate, 1,2,3-tricarballylate, 1,2,3,4-butanetetracarboxylate, 1,2,3,4,5,6-benzenehexacarboxylate) in aqueous solution are reported at t = 25 °C and I = 0 mol l,1. Thermodynamic parameters obtained were analysed to formulate empirical predictive relationships as a function of different parameters, such as the number of carboxylate groups of the ligand and the charge of the alkyltin(IV) cation. Sequestration diagrams of citrate and 1,2,3-tricarballylate towards alkyltin(IV) cations at different pH values are also reported and discussed. Copyright © 2007 John Wiley & Sons, Ltd. [source] Sperm motility in the steelhead Oncorhynchus mykiss (Walbaum): influence of the composition of the incubation and activation mediaAQUACULTURE RESEARCH, Issue 3 2006Joshua Woolsey Abstract This study examined the pH sensitivity of steelhead, Oncorhynchus mykiss (Walbaum), sperm motility relative to the composition of incubation and activation media. The percentage of sperm that initiated motility following incubation in a sperm immobilizing solution (SI) titrated to different pH values and subsequent activation by dilution in buffered swimming medium (SM) at pH 8.5 or 50% ovarian fluid (OF) showed little or no pH sensitivity; sperm diluted in de-ionized water (DI) showed no motility after incubation at any pH. In contrast, motility of sperm diluted in tap water (TAP) was highly sensitive to the pH of the incubation medium. Sperm incubated with buffered seminal plasma at high, but not low pH demonstrated high percent motility when diluted with DI. Sperm incubated in low-pH SI demonstrated high motility only when diluted into high-pH SM. The effects of the composition of incubation and activation media on sperm motility were generally reflected in comparable effects on fertility. Therefore, these data indicate that the pH sensitivity of sperm motility and fertility depends on the composition of commonly used incubation as well as activation media. [source] pH-dependent structural changes in haemoglobin component V from the midge larva Propsilocerus akamusi (Orthocladiinae, Diptera)ACTA CRYSTALLOGRAPHICA SECTION D, Issue 3 2010Takao Kuwada Haemoglobin component V (Hb,V) from the midge larva Propsilocerus akamusi exhibits oxygen affinity despite the replacement of HisE7 and a pH-dependence of its functional properties. In order to understand the contribution of the distal residue to the ligand-binding properties and the pH-dependent structural changes in this insect Hb, the crystal structure of Hb,V was determined under five different pH conditions. Structural comparisons of these Hb structures indicated that at neutral pH ArgE10 contributes to the stabilization of the haem-bound ligand molecule as a functional substitute for the nonpolar E7 residue. However, ArgE10 does not contribute to stabilization at acidic and alkaline pH because of the swinging movement of the Arg side chain under these conditions. This pH-dependent behaviour of Arg results in significant differences in the hydrogen-bond network on the distal side of the haem in the Hb,V structures at different pH values. Furthermore, the change in pH results in a partial movement of the F helix, considering that coupled movements of ArgE10 and the F helix determine the haem location at each pH. These results suggested that Hb,V retains its functional properties by adapting to the structural changes caused by amino-acid replacements. [source] | ||||||||||||||||||||||||||||||||||