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PubMed1992

Silver enhancement of gold antibody probes in pre-embedding electron microscopic immunocytochemistry.

In pre-embedding EM immunocytochemistry with gold probes, the gold must be small enough to penetrate through cell membranes treated with mild detergents. Antibodies labeled with small gold probes (1-1.4 nm) are too small to be resolved in thin sections but can be seen if they are silver-enhanced after the gold has bound to the antigens in the cells. We investigated several aspects of gum arabic-silver lactate-hydroquinone enhancement solution (Danscher solution) by examining gold-conjugated antibodies embedded in agar, sectioned on a vibrotome, and enhanced with different solutions. The rate of silver enhancement was optimized in 50% gum arabic and 200 mM HEPES buffer, pH 5.8. We also examined chemicals used as developers and found that N-propyl gallate (NPG) gave a more uniform development than the routinely used hydroquinone (HQ). The diameter of the silver-enhanced particles after incubation in osmium tetratoxide (OSO4) decreased somewhat with longer incubation time and higher percentages, but the density (number per unit area) of silver-enhanced particles was little changed. The loss of silver-enhanced particle diameter was reduced by lowering the concentration of OSO4 to 0.1%. Comparison of commercial small gold probes showed that NPG enhancement of Nanogold gave more uniform particle size and a better correlation between enhancement time and particle density. When this procedure was applied to cell cultures with monoclonal antibodies, the silver-enhanced particles were similar to those in the agar sections. When free-floating tissue sections were used, longer silver enhancement times were needed to obtain similarly sized particles. This new NPG-silver-enhancement procedure offers a reliable and easy method to localize proteins in cultured cells and tissue sections by pre-embedding electron microscopic immunocytochemistry.

Animals↗
PubMed1995

Comparison of silver nitrate and tetracycline as pleural sclerosing agents in rabbits.

The ideal agent to produce pleurodesis has not been identified. Tetracycline, the drug used most commonly in the 1980s, is no longer available. Talc either aerosolized or in a slurry is the agent used just most commonly at the present time, but there are concerns about its safety. Another possibility is silver nitrate, which was widely used in the past, but was abandoned on account of side effects. We hypothesized that lower concentrations of silver nitrate than had been used in the past would be effective in creating a pleurodesis in rabbits. The following medications in a total volume of 2 mL were instilled intrapleurally in three groups of ten anesthetized rabbits: 0.25% or 0.50% silver nitrate and 35 mg/kg tetracycline. Twenty-eight days after the injection, the animals were sacrificed and the pleural spaces were assessed grossly for evidence of pleurodesis and microscopically for evidence of fibrosis and inflammation. The intrapleural injection of 0.50% silver nitrate produced an effective pleurodesis. The mean degree of gross pleurodesis in the rabbits that received 0.50% silver nitrate (3.4 +/- 1.2) did not differ significantly from that of the rabbits that received tetracycline (3.5 +/- 0.7) (scale 0 to 4). The mean degree of microscopic pleural fibrosis in the rabbits that received 0.50% silver nitrate (3.4 +/- 0.7) did not differ significantly from that of the rabbits that received tetracycline (3.9 +/- 0.3). However, 0.25% silver nitrate was ineffective in creating pleural fibrosis, either grossly or microscopically. No rabbits died after the intrapleural injection of the drugs. There were no observed side effects after the injection of silver nitrate. The present study demonstrates that 0.50% silver nitrate instilled into the pleural space is an effective agent for producing pleurodesis in the rabbit; its effect is comparable to tetracycline 35 mg/kg. This agent should be compared with tetracycline derivatives and talc in studies in humans.

Analysis of Variance↗
PubMed2001

Experimental pleurodesis in rabbits induced by silver nitrate or talc: 1-year follow-up.

STUDY OBJECTIVE: To compare the pleurodesis results from the intrapleural injection of silver nitrate and talc slurry over an observation period of 12 months in rabbits. DESIGN: Rabbits were randomized to receive 2 mL of 0.5% silver nitrate or 400 mg/kg of talc slurry in 2 mL intrapleurally. Ten rabbits in each group were killed at 1 month, 2 months, 4 months, 6 months, 8 months, 10 months, and 12 months after intrapleural injection. The degree of gross pleurodesis and the amount of microscopic pleural fibrosis and inflammation were graded on a scale of 0 to 4. RESULTS: The mean +/- SEM gross pleurodesis score in the 70 rabbits that received silver nitrate was 3.34 +/- 0.08, which was significantly higher than the score of 2.32 +/- 0.09 in the 70 rabbits that received talc. The mean gross pleurodesis score was significantly higher at each of the observation times (p < 0.05), except at 2 months, in the rabbits that received silver nitrate. The pleurodesis was distributed throughout the thorax in the rabbits that received silver nitrate, while it was only in the ventral thorax in the rabbits that received talc slurry. The gross pleurodesis scores showed no tendency to decrease during the 12-month observation period in either treatment group. The persistence of talc in the pleural space did not lead to chronic inflammatory changes because the inflammation scores were similar in both groups at all observation times. The microscopic pleural fibrosis score tended to decrease with time in the silver nitrate group but not in the talc slurry group. CONCLUSIONS: The intrapleural injection of 2 mL of 0.5% silver nitrate produces a better pleurodesis than does the intrapleural injection of 400 mg/kg of talc slurry in rabbits. The pleurodesis induced by silver nitrate persists for at least 1 year. The efficacy of silver nitrate as a sclerosing agent in humans should be evaluated.

Animals↗
PubMed1999

Two-body sliding wear of a direct-filling silver alternative to amalgam.

OBJECTIVE: This study investigated the wear resistance of a mercury-free silver direct-filling material and a dental amalgam. METHOD AND MATERIALS: A precipitated silver powder was rinsed with dilute fluoboric acid and consolidated into a cohesive solid. For tooth cavity restoration and flexural testing, the silver was consolidated with a dental amalgam plugger at a load of 15 N. For wear testing, because of the relatively large specimen size, the silver was pressed at a pressure of 150 MPa, yielding a density similar to that obtained by hand consolidation. RESULTS: The silver had a flexural strength twice that of amalgam. Pin-on-disk wear resulted in a smooth surface and hardening in silver, as measured by indentation inside the wear tracks, in contrast to the damage that was found in amalgam. The wear track cross-sectional area (n = 12) at 10(6) revolutions was not statistically significantly different among amalgam, polished silver, and burnished silver. CONCLUSION: The consolidated silver exhibited work hardening and surface densification during wear and, as a result, was more resistant to wear-induced damage than amalgam.

Analysis of Variance↗
PubMed1976

[Studies on the cytotoxicity of silver alloys be means of cell culture (author's transl)].

In order to investigate biocompatibility of silver alloys, which is widely used in Japan, L strain cells were brough contact with the alloys. Results were assessed by cell multiplication rate calculated from counting cell nuclei number per milliter of medium and morphological observation. The materials used were two from of silver-tin-zinc alloys, one form of silver-tin-zinc-cadmiumalloy and two forms of silver-copper alloys. Copper-zine alloy, which is reported to be highly cytotoxic, was alsoutilized as a positive control. Following results were obtained: 1) Ingot specimen of these alloys showed cytotoxicity, Silver-tin-zinc alloy, silver-tin-zinc-cadmium alloy and silver-copper alloy containing 10% or less of copper showed intense cytotoxicity initially, with diminishing cytotoxic action with time. On the otherhand, silver-copper alloy containing 20% or more of copper showed persistent cytotoxicity. Copper-zinc alloy showed intense cytotoxicity. 2) Cast specimen of these alloys showed increasing cytotoxicity with time campared to their ingot specimen. The results are seemed to owe much to inclusion of toxic substances from the alloy and investment material or alteration of surface characteristics of the alloys due to casting procedure. 3) Morphological observation did not differ from the results of cell nuclei counting. It is expected that the present results could give a clue on animal experiments or clinical use from the view point of biocompatibility of silver alloys.

Biocompatible Materials↗
PubMedDate not supplied

Cytotoxicity of antimicrobial tissue conditioners containing silver-zeolite.

PURPOSE: The purpose of this study was to determine the effects of incorporating antimicrobial silver-zeolite on the in vitro cytotoxicities of five tissue conditioners against the living dermal model, which consisted of normal human dermal fibroblasts in a collagen lattice. MATERIALS AND METHODS: Samples of each tissue conditioner containing silver-zeolite (2 wt% and 5 wt%) were prepared; samples without silver-zeolite were used as a control. Cytotoxicity of each sample against the living dermal model was evaluated by cell viability with MTT assay. RESULTS: Cell viabilities for Visco-Gel, GC Soft-Liner, FITT, and SR-Ivoseal decreased with increasing silver-zeolite content. Cell viability for Shofu Tissue Conditioner showed no significant difference with degree of silver-zeolite incorporation and had higher values than other tissue conditioners. CONCLUSION: Individual compounds eluted from tissue conditioners and silver ions released from silver-zeolite might cause such cytotoxicity. The results suggest that Shofu Tissue Conditioner is a possible candidate for a novel antimicrobial tissue conditioner containing silver-zeolite because it showed the highest cell viability and the smallest influence of incorporating silver-zeolite.

Acrylic Resins↗
PubMed2004

The truth about silver.

Interest in silver as a topical agent in wound healing is undergoing a renaissance. Having basic information regarding silver's chemical properties and potential actions in the wound bed is important to its appropriate clinical use. Such information is also relevant to the interpretation of silver's in vitro antimicrobial (antiseptic) effects, which in turn relate to issues involved in the evaluation of the clinical effects of silver in vivo. Gaining an understanding of the basic science of silver products and the different challenges inherent to in vitro versus in vivo antimicrobial evaluations will allow clinicians to address several key questions inherent when considering the use of silver as a topical antimicrobial: 1) Are there different forms of silver? 2) How does the amount of silver released into the wound environment correlate with clinical benefit? 3) How does the rate of silver release correlate with clinical benefit?

Anti-Infective Agents, Local↗
PubMed1994

Silver peritoneal catheters reduce bacterial colonization.

Bacterial colonization potentials by Staphylococcus aureus (Staph. aureus) were determined in silver peritoneal dialysis (PD) catheter materials and were compared to colonization of the same bacteria in silastic catheter materials. The bacteria were colonized in two different experimental systems: In Vitro: In an in vitro biofilm bacterial culture system with a modified Robbins' device (MRD), seven different clinical strains of Staph. aureus were grown in PD effluents on silver or silastic catheter discs, each 0.5 cm in diameter. In identical experimental conditions, reduced bacterial growth was detected in silver catheter discs compared to growth on silastic discs, but the results were not statistically different (p = 0.12). In Vivo: In a rabbit model of PD the, in vivo colonization potential of Staph. aureus was examined in two groups of rabbits using silver (n = 3) and silastic (n = 3) PD catheters. The exit sites of the PD catheters were inoculated with a single strain of Staph. aureus for six days, followed by PD for six days. The rabbits were then sacrificed. After sacrifice, comparison between the bacterial counts of identical segments of silver and silastic catheters showed that there had been a reduction in the growth of Staph. aureus in vivo on silver PD catheters, contrary to the increased growth on the silastic catheters (p < 0.05). Reduced bacterial growth on the silver PD catheters in vivo indicates that the release of silver in tissues over time cause antibacterial effects in vivo. Further in vivo experiments are needed before future clinical use of silver catheters in PD patients.

Animals↗
PubMed1996

Evaluation of healing and external tunnel histology of silver-coated peritoneal catheters in rats.

A previous study showed that silver-coating peritoneal catheters tended to decrease the incidence of early exit-site infections in rats. This study was designed to further evaluate the healing, biocompatability, and external tunnel morphology of standard and silver-coated catheters. Catheters were coated with silver by an ion beam-assisted process. Fourteen male Sprague-Dawley rats underwent implantation of either a standard or silver-coated double-cuff peritoneal catheter. Weekly observation and photographs documented exit-site characteristics. Erythema, exudate, loose fit, and poor hair growth were evidence of an inflamed exit. Overt infection was indicated by the presence of three or more of the following: erythema, purulent exudate, exuberant granulation tissue, loose fit, and poor hair growth. Animals were sacrificed at six weeks, and catheters were removed and processed for histology of the external tunnel. Multiple measurements were taken using a Filar eyepiece, and data were expressed as a mean of several readings. Inflammation, vascularity, and fibrosis were judged semiquantitatively. At the end of six weeks, six of the seven exits of the silver catheters showed excellent healing, while one exit site had signs of excessive inflammation. Four of the exit sites of the standard catheters healed well, two were inflamed, and one was overtly infected. The sinus tract of the standard and silver catheters had similar characteristics: keratinized and nonkeratinized epithelium lined the external part of the sinus tract and merged into granulation tissue. A fibrous sheath was noted in some sinus tracts between the granulation tissue and the cuff. The cuff evoked a foreign body reaction, with fibrosis, multiple giant cells, and vascularization. Poorly healing or infected sinus tracts had highly vascular granulation tissue with overlying exudate. The cuff of these catheters had marked inflammation and scanty giant cells, although collagen bundle thickness was similar to the well-healing catheters. In conclusion, silver-coating potentially enhances healing of the exit sites of peritoneal catheters. Additionally, the similarity of the tunnel histomorphology of standard and silver catheters confirms the favorable biocompatibility of silver.

Animals↗
PubMed1955

The demonstration of a blood-ocular barrier in the albino rat by means of the intravitam deposition of silver.

When silver nitrate is administered to rats in their drinking water for many months, they develop a generalized argyria. In the central nervous system, the deposition of silver follows the pattern of the so called hematoencephalic barrier (Wislocki and Leduc, (2); Dempsey and Wislocki, (3)). The present observations concern the deposition of silver in the rat's eye, investigated by both light microscopy and the electron microscope. In the eye, silver is not detected in the specific neural elements of the retina. Instead, it is heavily deposited in the basement membrane of the epithelium of the ciliary processes and in Bruch's basal membrane between the choriocapillary layer and the retinal epithelium. Traces of silver are visible in the basement membranes of the retinal capillaries with the electron microscope, but cannot be identified with the light microscope. In all of these respects, the pattern of the silver resembles the mode of its deposition in the brain. The heavy accumulation of metal in Bruch's membrane and the ciliary processes is analogous to that observed in the chorioid plexuses, and the traces encountered in the walls of the retinal capillaries correspond to traces observed in the basement membranes of the cerebral capillaries. Hence, with respect to silver, the eye possesses a blood-ocular barrier similar to the hematoencephalic barrier. Silver appears to be restrained from entering the aqueous humor by a barrier in the basement membrane of the ciliary processes, from reaching the photoreceptor elements of the retina by Bruch's basal membrane, and from penetrating the inner layers of the retina by a barrier in the basement membrane surrounding the retinal capillaries.

Animals↗
PubMed1998

Action of gold chloride ("gold toning") on silver-enhanced 1 nm gold markers.

In conventional immunoelectron microscopy (IEM), very small colloidal gold particles (0.8-3 nm), or the gold compound Nanogold (1.4 nm) are silver-enhanced for easy detection. However, silver enhancement has drawbacks. First, the silver layer is dissolved during fixation with osmium tetroxide, even if the concentration and incubation time are strongly reduced during pre-embedding labeling experiments in transmission electron microscopic (TEM) and scanning electron microscopic (SEM) studies. Second, after exposure to the electron beam the silver layer may migrate on the section or the whole particles may disappear. Sometimes silver migration can be observed even without irradiation. This effect strongly hampers reinvestigation of previously inspected areas, after some time of storage. In both cases, gold chloride treatment after silver enhancement is sufficient to completely protect the silver-enhanced 1 nm gold markers. Gold chloride treatment is part of the so-called "gold toning" procedure, which is a method used to substitute and/or cover the silver by a layer of gold. It can be applied in TEM and SEM experiments. As a serious drawback, gold chloride treatment slightly reduces the size of both unenhanced and silver-enhanced gold particles and can lead to disintegrated silver/gold particles. Therefore, this technique is useful for pre-embedding IEM, on-(resin)section, and ultrathin cryosection labeling experiments. However, it appears to be unsuitable for double-labeling studies using different gold sizes, for quantitation experiments, and in SEM.

Cryoultramicrotomy↗
PubMed2002

Epithelia-mesenchyme interaction plays an essential role in transdifferentiation of retinal pigment epithelium of silver mutant quail: localization of FGF and related molecules and aberrant migration pattern of neural crest cells during eye rudiment formation.

Homozygotes of the quail silver mutation, which have plumage color changes, also display a unique phenotype in the eye: during early embryonic development, the retinal pigment epithelium (RPE) spontaneously transdifferentiates into neural retinal tissue. Mitf is considered to be the responsible gene and to function similarly to the mouse microphthalmia mutation, and tissue interaction between RPE and surrounding mesenchymal tissue in organ culture has been shown to be essential for the initiation of the transdifferentiation process in which fibroblast growth factor (FGF) signaling is involved. The immunohistochemical results of the present study show that laminin and heparan sulfate proteoglycan, both acting as cofactors for FGF binding, are localized in the area of transdifferentiation of silver embryos much more abundantly than in wild-type embryos. More intense immunohistochemical staining with FGF-1 antibody, but not with FGF-2 antibody, is also found in the neural retina, RPE, and choroidal tissue of silver embryos than in wild-type embryos. HNK-1 immunohistochemistry revealed that clusters of HNK-1-positive cells (presumptive migrating neural crest cells) are frequently located around the developing eyes and in the posterior region of the silver embryonic eye. Finally, chick-quail chimerical eyes were made by grafting silver quail optic vesicles to chicken host embryos: in most cases, no transdifferentiation occurs in the silver RPE, but in a few cases, transdifferentiation occurs where silver quail cells predominate in the choroid tissue. These observations together with our previous in vitro study indicate that the silver mutation affects not only RPE cells but also cephalic neural crest cells, which migrate to the eye rudiment, and that these crest cells play an essential role in the transdifferentiation of RPE, possibly by modifying the FGF signaling pathway. The precise molecular mechanism involved in RPE-neural crest cell interaction is still unknown, and the quail silver mutation is considered to be a good experimental model for studying the role of neural crest cells in vertebrate eye development.

Animals↗
PubMed2006

Investigation of silver binding to polyamidoamine (PAMAM) dendrimers by ESI tandem mass spectrometry.

Electrospray ionization tandem mass spectrometry (ESI-MS/MS) was used to probe the binding of silver ions and reduced silver species with polyamidoamine generation 1 amine-terminated (PAMAMG1NH2) and generation 2 hydroxyl-terminated (PAMAMG2OH) dendrimers. At Ag(+)/PAMAMG2OH molar ratios of </=1, 1:1 complexes are observed, while at ratios >1, 2:1 and low abundance 3:1 complexes emerge. Similar results were observed for PAMAMG1NH2. The collisional activated dissociation (CAD) patterns of the dendrimer ions are characterized by losses of amidoamine branches resulting largely from hydrogen migration and cleavage reactions. Ag+/dendrimer complexes are characterized by the loss of a dendrimer branch from the complex, with the silver ion remaining bound to a dendrimer fragment. When the Ag+-bound dendrimer complexes are reduced by hydrazine, low abundance complexes, whose m/z values are consistent with ones containing zerovalent silver species, are observed in the mass spectra. Complexes with three silver atoms are observed in the spectrum containing PAMAMG1NH2, and complexes with four and five silver atoms are observed with PAMAMG2OH. The CAD fragmentation patterns of the complexes formed after the silver reduction are different than those observed for complexes containing one silver ion and are characterized by the ejection of all silver species, possibly as a cluster, leaving the intact dendrimer ion. Experiments with Cu+, Cu2+, and Pt2+ binding to PAMAMG2OH were also done, but reduced metal clusters were not observed in the mass spectra after the addition of hydrazine.

Journal Article↗
PubMed2003

Silver(I) coordination chemistry of 2,6-diarylpyrazines. Pi-stacking, anion coordination, and steric control.

The silver(I) coordination chemistry of 2,6-diarylpyrazines is reported. Discrete coordination complexes and two-dimensional coordination networks were characterized. The substitution pattern on the pendant aryl groups controlled the type of coordination chemistry involved. Thus, o-methyl-substituted aryl groups held the aryl groups orthogonal to the central pyrazine ring, opening the "hindered" nitrogen atoms to complexation, and polymeric networks were characterized. In the absence of the o-methyl groups, discrete coordination complexes were characterized. Thus, a dimeric 2:1 ligand-silver(I) complex was isolated and characterized on reaction of 2,6-bis(3',5'-dimethylphenyl)pyrazine with silver(I) trifluoroacetate in acetonitrile solvent, while a 2:2 complex was isolated from dichloromethane solvent. Two trifluoroacetate ligands bridge two silver cations in both complexes. Reaction of the same pyrazine ligand with silver(I) tetrafluoroborate yielded a discrete 2:1 complex. A 2:1 complex was isolated on reaction of 2,6-diphenylpyrazine with silver(I) nitrate. These complexes were interlinked by weakly coordinating nitrate anions to form interwoven one-dimensional ribbons. Two-dimensional networks were obtained on reaction of silver(I) trifluoroacetate with either 2,6-bis(2',6'-dimethylphenyl)pyrazine or 2-(2',6'-dimethylphenyl)-6-(3',5'-dimethylphenyl)pyrazine. The networks comprised pyrazine-silver(I) strands cross-linked with complex bridged silver(I) trifluoroacetates.

Journal Article↗
PubMed2004

Silver(I) complexes of a sterically demanding fluorinated triazapentadienyl ligand [N((C3F7)C(Dipp)N)2]- (Dipp = 2,6-diisopropylphenyl).

Sterically demanding triazapentadiene [N((C3F7)C(Dipp)N)2]H affords the isolation of thermally stable, two- and three-coordinate silver complexes. The free ligand [N((C3F7)C(Dipp)N)2]H has a W-shaped ligand backbone in the solid state.[N((C3F7)C(Dipp)N)2]H reacts with silver(I) oxide in acetonitrile leading to CH(3)CNAg [N((C3F7)C(Dipp)N)2]HIt features a two-coordinate silver center and a kappa(1)-coordinated triazapentadienyl ligand. This silver acetonitrile complex serves as an excellent precursor to obtain thermally stable, silver isocyanide t-BuNCAg [N((C3F7)C(Dipp)N)2]Hand silver phosphine [[N((C3F7)C(Dipp)N)2]HAgPPh(3) adducts. IR spectroscopic data for the silver(I) isocyanide t-BuNCAg [N((C3F7)C(Dipp)N)2]Hshows nu(CN) at 2219 cm(-)(1). The silver ion coordinates to the triazapentadienyl ligand via the central nitrogen atom. The silver PPh(3) adduct,[N((C3F7)C(Dipp)N)2]HAgPPh(3), was synthesized by treating CH3CNAg [N((C3F7)C(Dipp)N)2]Hwith PPh(3). It displays relatively large Ag-P coupling in the (31)P NMR spectrum. The triazapentadienyl ligand in[N((C3F7)C(Dipp)N)2]HAgPPh(3) acts as a chelating kappa(2)-donor. The Ag-P bond is relatively short (2.3487(10) A).

Journal Article↗
PubMed1999

Synthesis and Characterization of Functionalized N,N'-Diphenylformamidinate Silver(I) Dimers: Solid-State Structures and Solution Properties.

Functionalized N,N'-diphenylformamidines and their deprotonated silver(I) complexes have been synthesized: silver(I) N,N'-di(4-alkyl)phenylformamidinate (alkyl = methyl, ethyl, n-butyl, and n-hexadecyl) 1-4; silver(I) N,N'-di(4-trifluoromethyl)phenylformamidinate 5, silver(I) N,N'-di(3-methoxy)phenylformamidinate 6, silver(I) N,N'-di(3-methylmercapto)phenylformamidinate 7, silver(I) N,N'-di(2-methoxy)phenylformamidinate 8, silver(I) N,N'-di(2-methylmercapto)phenylformamidinate 9. The effects of increasing the coordination number of the silver(I) centers by donor substituents on the phenyl groups have been investigated by solution and solid-state studies. Variable-temperature proton NMR (223-303 K) for 1-4 shows coupling between the proton attached to the amidinate carbon and the (107/109)Ag centers at room temperature which is unaffected by cooling (2). For the four-coordinate complexes, 8 and 9, such coupling is only observed on cooling. Molecular weight measurements recorded in solution by vapor pressure osmometry at 310 K show some aggregation to higher molecular weight species than simple dimers for 1-4 and 6, but 8 and 9 exist as discrete dimeric species. Measurement of thermal stability shows the expected increase in stability with increasing coordination number. Compounds 8 and 9 were structurally characterized by X-ray methods. Both show four-coordinate silver dimers bridged by two amidinate ligands with additional longer interactions with the ether oxygens or thioether sulfurs.

Journal Article↗
PubMed2005

Preparation, characterization, and surface modification of silver nanoparticles in formamide.

The reduction of silver ions in formamide is shown to take place spontaneously at room temperature without addition of any reductant. The growth of Ag particles was found to be dependent on Ag+ ion concentration. In the absence of any stabilizer, deposition of silver film on the glass walls of the container takes place. However, in the presence of poly(N-vinyl-2-pyrrolidone) (PVP) or colloidal silica (SiO2), which are capable of stabilizing silver nanoparticles by complexing and providing support, a clear dispersion was obtained. The formation of the silver nanoparticles under different conditions was investigated through UV-visible absorption spectrophotometry, gas chromatography, and also electron and atomic force microscopic techniques. Atomic force microscopy results for silver films prepared in the absence of any stabilizer showed the formation of polygonal particles with sizes around 100 nm. Transmission electron microscopy results showed that the prepared silver particles in the presence of PVP were around 20 nm. The Ag nanoparticles get oxidized in the presence of chloroform and toluene. Surface modification of silver film was done in the presence of the tetrasodium salt of ethylenediaminetetraaceticacid (Na4EDTA). It was shown that the reactivity of the silver film increased in its presence. The Fermi potential of silver particles in the presence of Na4EDTA seems to lie between -0.33 and -0.446 V vs NHE.

Journal Article↗
PubMed1981

Sulfadiazine silver-resistant Pseudomonas in Burns. New topical agents.

Sulfadiazine silver-resistant strains of Pseudomonas aeruginosa isolated from burned patients from several countries are sensitive to sulfadiazine silver in vitro, but in burned mice and rats resist topical therapy with sulfadiazine silver. In searching for an effective topical agent against these resistant organisms, we found that FPQC (1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7[1-piperazinyl]-quinoline-carboxylic acid) and its silver salt are effective both in vitro and in vivo. In vitro, their minimal inhibitory concentrations are ten to 20 times lower than that of sulfadiazine silver. In burned mice infected with resistant Pseudomonas strains, mortality in groups receiving topical therapy with FPQC or FPQC silver is 0%, but 80% to 100% with sulfadiazine silver and 100% without treatment. Similar results were obtained in burned rats. The efficacy of FPQC and FPQC silver in vivo may represent discovery of new agents of known low toxicity that are useful in topical burn therapy.

Administration, Topical↗