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Results for “SILVER CITRATE”

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At least 55 records · Page 3Linked to original sources
PubMed1988

Ultrastructural heterogeneity in cerebral amyloid of Alzheimer's disease.

Cerebral amyloid deposits from five patients with presenile or senile cerebral disease of the Alzheimer type were stained with uranyl acetate and lead citrate or with periodic acid-thiocarbohydrazide-silver proteinate, and examined with traditional high-resolution electron microscopy and with a goniometer tilting stage. In addition to a carbohydrate-rich matrix, we also consistently found local cell-derived vesicles within plaque and dyshoric amyloid. The most likely source for these vesicles appeared to be degenerate neurites. Amyloid fibrils were intimately associated with plasmalemmata, particularly those of degenerate neurites, which supported a neuronal origin for the amyloid fibril of Alzheimer's disease.

Aged↗
PubMed2004

The mitochondrial tricarboxylate carrier of silver eel: chemical modification by sulfhydryl reagents.

The tricarboxylate (or citrate) carrier was purified from eel liver mitochondria and functionally reconstituted into liposomes. Incubation of the proteoliposomes with various sulfhydryl reagents led to inhibition of the reconstituted citrate transport activity. Preincubation of the proteoliposomes with reversible SH reagents, such as mercurials and methanethiosulfonates, protected the eel liver tricarboxylate carrier against inactivation by the irreversible reagent N-(1-pyrenyl)maleimide (PM). Citrate and L-malate, two substrates of the tricarboxylate carrier, protected the protein against inactivation by sulfhydryl reagents and decreased the fluorescent PM bound to the purified protein. These results suggest that the eel liver tricarboxylate carrier requires a single population of free cysteine(s) in order to manifest catalytic activity. The reactive cysteine(s) is most probably located at or near the substrate binding site of the carrier protein.

Anguilla↗
PubMed2005

Growth of silver nanowires from solutions: a cyclic penta-twinned-crystal growth mechanism.

Silver nanowires are synthesized by simple reduction of the silver ions with reductants such as glucose, sodium citrate, and sodium hypophosphite, etc., in the absence of the so-called surfactants or capping reagents at the temperature from 80 to 200 degrees C. Regardless of the reductants, the nanowires prepared at a given temperature are uniform in diameters, ranging from 30 to 50 nm at 100 degrees C. Nanoparticles coexist with nanowires in the products with larger diameters (usually larger than 50 nm). We find that all the silver nanowires in the as-prepared products are of cyclic penta-twinned structure, where five crystallites bond by the {111} facets. We propose that the intrinsic factor of the cyclic penta-twinned structure, i.e., the angular mismatch of the five crystallites in forming a gapless rod, controls the size of the nanowires and guides the directional growth of the nanowires with {110} as the active facets. The nanoparticles in the products are aggregates of imperfect penta-twinned crystals, which inhibits them from growing into nanowires and results in larger size. From the structural information of the nanoparticles synthesized at room temperature, we propose that the formation of the cyclic penta-twinned structure is due to the stacking fault and the intrinsic equilibrium structures of the lower energy.

Journal Article↗
PubMed2003

Preparation of silver nanocrystals in the presence of aniline.

The preparation and characterization of silver nanocrystals by chemical reduction of silver ions in the presence of aniline using hydrazine monohydrate (N(2)H(4).H(2)O) or sodium citrate as the reducing agent are described. A high yield of aniline-derivatized hexagonal silver nanoparticles is obtained by the reduction of Ag(2)SO(4) with N(2)H(4).H(2)O. An alternative strategy is the reduction of Ag(+) by citrate in the presence of aniline, by which the size and morphology of the Ag nanocrystals can be controlled to a certain degree by changing the concentration ratio of aniline to Ag(+). It is believed that the amount of aniline added in the starting solutions for the preparation influences the morphology of the Ag nanoparticles. In addition, the long Ag nanorods with a high mean aspect ratio are prepared in the presence of aniline at a low concentration or o-anisidine.

Journal Article↗
PubMed1999

Thrombogenicity testing of central venous catheters in vitro.

To date there have been no standard methods for assessing the thrombogenicity of central venous catheters. A procedure for testing the thrombogenicity of intravenous lines such as the silver-impregnated catheter by continuous blood flow in vitro was therefore developed. For this test, fresh blood was drawn from healthy human donors and anti-coagulated with sodium citrate (1:9). All material tested (catheter tubes with and without silver manufactured in the same way, polyethylene tubes and tubes with potentially thrombogenic material) were perfused through their lumen with anticoagulated blood for up to 31 hours. Blood samples were collected at different times from the test system at sites before and after the perfusion of the test catheters. The hemoglobin concentration, erythrocyte, leukocyte and thrombocyte counts and markers for thrombin activation (thrombin-antithrombin III-complex, F1 + 2)-prothrombin fragments) and for hyperfibrinolysis (d-dimers) were determined. No thrombin activation or signs of hyperfibrinolysis were detected in any material tested. Polyethylene tubes were found to cause hemolysis, as shown by a decrease in hemoglobin content from 15 g% to 4.5 g%. Tecothane tubes with and without silver did not induce hemolysis.

Antithrombin III↗
PubMed1993

A novel purification of ferric citrate receptor (FecA) from Escherichia coli UT5600 and further characterization of its binding activity.

In our earlier paper, it was demonstrated that the FecA receptor protein from Escherichia coli UT5600/pBB2 (leu-, proC-, trpE-, entA-, rpsl-, delta (ompT-fepA)-/Ampr, fepA) binds with ferric enterobactin. In order to explore this further the outer membrane receptor protein, FecA, has been isolated from UT5600 (fepA-) and purified to homogeneity by DE-52-cellulose anion exchange chromatography followed by MonoPFPLC chromatofocusing. Partially purified FecA and homogeneous FecA show binding activity to [55Fe]ferric enterobactin and the binding is specific. Binding activity of FecA can be enhanced by ferric citrate. Lipopolysaccharide-free FecA as ascertained by silver staining and the endotoxin test still retains the same activity. In vivo uptake studies using different strains of E. coli suggest that FecA in E. coli plays an important role in ferrienterobactin transport.

Bacterial Outer Membrane Proteins↗
PubMed1997

Structure-activity relation in camptothecin antitumor drugs: why a detailed molecular characterisation of their lactone and carboxylate forms by Raman and SERS spectroscopies?

Lactone and carboxylate forms of potent antitumor agents, camptothecins (CPTs) have been studied by Raman, Fourier-transform Raman (FT-Raman) and surface-enhanced Raman scattering (SERS) spectroscopy. Similarity of the Raman spectra of CPTs with corresponding FT-Raman spectra in the near-infrared allowed the latter to be compared with their SERS counterparts in order to analyse the interaction of the drugs with silver colloids. Different types of silver colloids (reduced with sodium borohydride or sodium citrate, with or without activation by anions) have been evaluated. Citrate-reduced colloid, activated with chloride anions (CAS) has been found to be the best compromise for SERS studies of both forms of CPTs. We suggest that in general CPTs are adsorbed on CAS via the nitrogen in ring B and are more inclined to a flat orientation than to a perpendicular one. However, probable interactions of substitution groups and/or of the COO- groups of hydrolysed CPTs with the CAS surface introduce some particularities in the adsorption patterns. As a result, SERS spectra are highly sensitive to hydrolysis and substitutions at distant rings of CPT and uniquely characteristic of each of the CPT derivatives. The pronounced hydrolysis-induced changes, similar in the Raman and SERS spectra of CPTs, involve similar vibrations in the spectra of different CPTs. Vibrational assignments, proposed for the main Raman and SERS bands of CPT and its derivatives (21-lactam-S-CPT, 10,11-(methylenedioxy)-CPT, CPT-11, SN-38 and topotecan) indicate that most of the bands which decreased upon lactone hydrolysis are those preferentially related to stretching modes of the quinoline rings A and B, and the bands which increased are those of the ring D stretching modes. Our data make the spectroscopic approach very promising for the further investigations of the molecular mechanisms of biological activity of CPTs.

Antineoplastic Agents↗
PubMed1980

Electron dense staining affinities of mouse oxytalan and elastic fibers.

The staining affinity of electron dense stains to mouse palatal elastic fibers and periodontal oxytalan fibers was assessed and compared. Tissues were stained routinely with uranyl acetate and lead citrate or with elastic tissue stains including: (1) silver tetraphenylporphine sulfonate, (2) tannic acid technique, and (3) a high iron diamine sequence. Staining results were assessed with an electron microscope. Palatal elastic fibers demonstrated staining affinity to all elastic stain techniques. Oxytalan fibers did not demonstrate affinity to elastic fiber stains used. Based on electron dense stains, elastic and oxytalan fibers were dissimilar, in contrast to results reported utilizing light microscopic stains.

Animals↗
PubMed1990

Tropical pyomyositis. Demonstration of extent and distribution of disease by gallium scintigraphy.

Pyomyositis is a Staphylococcus aureus infection of muscles reported primarily in tropical countries but seen with increasing frequency in temperate climates. Because of its rarity in the United States, the diagnosis may not be considered immediately, and involved muscles may break down and become abscessed. Diagnosis is most reliably made by the recovery of pus from a muscle aspirate. Ga-67 scan findings of an interesting case of pyomyositis involving many muscle groups in both upper and lower extremities is reported. Despite arthralgias and complicating adult respiratory distress syndrome, Ga-67 correctly localized the infection to muscles in the shoulders, upper thorax, buttocks, and thighs. A bone scan was negative, excluding the possibility of extension of the infection to bone.

Adult↗
PubMed1997

The effect of some metal ions on volatile sulfur-containing compounds originating from the oral cavity.

Halitosis originates mainly from the oral cavity, and the volatile sulfur-containing compounds (VSC) are the major contributors of the unpleasant odor. Anaerobic G- bacteria use sulfur-containing amino acids in their production of VSC. Zinc has been shown to inhibit production of odiferous VSC, and the mechanism proposed has been that zinc, with its affinity for sulfur, oxidizes thiol groups and thereby inhibits the precursors of VSC. The aim of the study was to investigate whether, and to what extent, other metal ions with affinity for sulfur exert the same effect and whether a correlation exists between the sulfur affinity and VSC-inhibiting activity of these metals. VSC levels were measured on the 'morning breath' of 10 test subjects, using a portable sulfide monitor. The mouthrinses tested were aqueous solutions of zinc chloride, zinc citrate, stannous fluoride, cuprous gluconate, ferrous gluconate, and silver acetate, and they contained equimolar amounts of metals (1.47 mmol/I). The results showed that the ranking of Zn++ and Sn++ differed in the clinical test compared with sulfur affinity, and likewise with Ag+ and Fe++. It may therefore be concluded that there is no positive correlation between the inhibiting effect of metal ions on VSC and their affinity for sulfur.

Acetates↗
PubMed2004

Phase transfer of Au-Ag alloy nanoparticles from aqueous medium to an organic solvent: effect of aging of surfactant on the formation of Ag-rich alloy compositions.

Mercaptopropionic acid (MPA) capped Au-Ag alloy nanoparticles consisting of various mole fractions of gold and silver have been synthesized in aqueous medium using a citrate reduction method. UV-visible spectra confirm the formation of alloy phases and transmission electron microscopy (TEM) reveals a rather uniform distribution of several nanometer-sized particles. The particles could easily be phase-transferred into organic solvents, isolated, and redispersed in a variety of solvents such as benzene, chloroform, and dichloromethane. The phase transfer from aqueous medium to an organic solvent does not alter the particle size and distribution. It is also recognized that the surfactant, alkaline MPA, should be aged for about 3 days in order to observe the formation of silver and silver-rich phases of alloy nanoparticles. The reason for this observation is discussed in terms of the competitive interaction between the Na+ and -COOH/-SH groups and subsequent reduction of metal ions.

Journal Article↗
PubMed2005

In vivo multitracer analysis technique: screening of radioactive probes for noninvasive measurement of physiological functions in experimental animals.

A novel screening experiment, to find radioactive probes for non-invasive measurements of physiological functions in experimental animals, was tested using the in vivo multitracer analysis technique. The details of the efficiency of the detector settings used in the in vivo multitracer analysis technique were examined by both computer simulations and practical measurements. Multiple radioactive isotopes, i.e. multitracer, were prepared by irradiating a silver foil target with a heavy ion beam at the RIKEN ring cyclotron. After chemical separation of the silver target, the multitracer was finally dissolved in isotonic citrate buffer. The multitracer solution was intravenously injected into rats. Using a gamma-ray detector equipped with a well-defined slit, the collimated gamma-rays from the upper abdomen of living rats were measured. After correction of detection efficiencies, it was possible to compare the distribution of radioactive elements between two groups of rats different in body weight. The in vivo measurement showed that the tissue substantial volume of the selenium-deficient (SeD) rat liver increased compared to normal rats. The possibility of a functional estimation of tissue/blood volume for living rats was proposed based on the characteristic in vivo distribution of 74As, 83Rb and 103Ru.

Abdomen↗
PubMed1978

[Maturation and aging of elastic fibers (authors transl)].

The non-sunexposed skin of 12 healthy individuals was investigated under the electron microscope and the fine structure of normal elastic fibers was compared by different methods in 3 groups of age: 1--10 years, 30--50 years, and 60 years. 1. The elastic fibers of human skin may be semiselectively stained with silver tetraphenylporphyrine sulfate (Ag-TPPS), uranyl acetate, lead citrate and tannic uranyl acetate. They are composed of an amorphous matrix which is interwoven and surrounded by microfilaments. Elastic fibers are fully developed in early periods of age, first showing numerous microfilaments as structural glycoproteins, and then the deposition of the amorphous proelastin to be transformed into elastin. 2. The period of maturation is followed continuously by processes of physiological aging: a) decreasing number of microfilaments, b) appearing of electron-dense inclusions into the elastin matrix and c) fragmentation and disintegration of the fiber. 3. These changes indicate that aging of the fiber includes diminished synthesis of structural glycoproteins (microfilaments) and increasing content of osmiophilic groups, such as polar aminoacids, fatty acids and calcium salts. The fiber becomes thus more susceptible to the activity of elastase, and may totally disintegrate in older age.

Adult↗
PubMed1988

Promoters and transcription of the plasmid-mediated citrate-utilization system in Escherichia coli.

The nucleotide sequence of an 878-bp BamHI-BglII restriction endonuclease fragment from citrate utilization transposon Tn3411 was determined, and was compared with that from plasmid pMS185 [Sasatsu et al., J. Bacteriol. 164 (1985) 983-993]. A long open reading frame for a 379-amino acid (aa) polypeptide (citB) was found 5' to the citA gene (431-aa membrane protein) in Tn3411 as well as in pMS185. Promoter regions were identified by RNA polymerase filter-binding assays, S1 nuclease mapping and cit-lac fusion experiments. The results indicated that two genes (citA and citB) have separate promoters, and the location of the promoter for the citB gene in the Tn3411 nucleotide sequence was different from that in pMS185. The regulation of transcription of the two genes (citA and citB) was characterized by the use of cit-lacZ fusions. The level of the citB promoter activity was about five-fold higher than that of the citA gene promoter, and transcription from both was not induced by citrate. Synthesis of the mRNA for the citB gene (especially with the wild-type Cit+ determinant) was suppressed by citrate, accompanying growth suppression of Escherichia coli. The citB gene expressed in E. coli minicells produced a membrane-associated 37.5-kDa polypeptide.

Amino Acid Sequence↗
PubMed1986

A method for visualizing the acrosome by light microscopy.

A silver staining technique applied to squash preparations of material previously fixed in 3:1 ethanol:acetic acid produces differential staining of the acrosomal region of spermatids during spermiogenesis in orthopteroid species. The method includes treatment with saline sodium citrate solution for 15 min at 60 C, and staining with 50% aqueous silver nitrate adjusted to pH 2.9 with formic acid.

Acrosome↗
PubMed1993

Use of tannic acid and silver enhancer to improve staining for electron microscopy and immunogold labeling.

Staining by uranyl acetate and lead citrate (UA-LC) of immunolabeled sections of unfixed glomerular basement membrane (GBM) digests embedded in low-acid glycol methacrylate (LA-GMA) is poor. The following were investigated for their ability to enhance contrast when applied to sections before UA-LC: potassium permanganate, phosphotungstic acid, gold chloride, osmium tetroxide, glutaraldehyde-osmium tetroxide, colloidal gold-silver enhancer, tannic acid, and glutaraldehyde-tannic acid. Silver enhancer (2 min incubation, no sodium thiosulfate step) gave dense GBM staining but not with immunogold labeling. Silver enhancer is recommended as a simple alternative to routine silver stains but not for contrast enhancement with immunogold labeling. Tannic acid (1% for 1 min or 0.005% for 10 sec) and glutaraldehyde (2.5% for 5 min) followed by tannic acid enhanced contrast and, when applied after immunolabeling, did not appear to affect probe levels. Tannic acid also enhanced the staining of fixed tissue in LR Gold acrylic resin and LA-GMA, but not of glutaraldehyde-osmium-fixed tissue in epoxy resin, even after sodium metaperiodate treatment. Treatment of sections with tannic acid is recommended for contrast enhancement in immunogold studies when osmium and tannic acid post-fixation must be avoided and the tissue is embedded in methacrylate or acrylic resin.

Basement Membrane↗
PubMed1991

Selective analysis of antitumor drug interaction with living cancer cells as probed by surface-enhanced Raman spectroscopy.

A new technique for the selective measurement of small amounts of antitumor drugs in the nucleus and cytoplasm of a living cancer cell, based on surface-enhanced Raman spectroscopy (SERS), is proposed. The ability to detect SERS signals from very dilute (up to 10(-10) M) solutions of doxorubicin or adriamycin (DOX), and 4'O-tetrahydropyranyl-adriamycin (THP-ADM), as well as from their complexes with targets in vitro and in vivo, has been demonstrated. SERS spectra were obtained from a population as well as from single living erythroleukaemic K562 cells treated with DOX. The results of the measurements on the population of cells containing DOX in nuclei or in the cytoplasm are well correlated with the microscopic SERS measurements on the single cells treated with DOX, obtained by selectively recording signals from the living cell nucleus or from the cytoplasm. Possibilities for the application of this new technique in different aspects of cancer research are discussed.

Antineoplastic Agents↗