Location: Svobody 8, 771 46 Olomouc
Phone: (+420) 58 563 4427
Fax: (+420) 58 563 4425
Oblast výzkumu:
Catalytic properties of Fe2O3 nanoparticles
Catalytic properties of Ag nanoparticles
Kvalifikace:
Mgr.: Inorganic chemistry, Palacký University
Ph.D.: Physical chemistry, Palacký University
Publications
2011
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J. Cuda, T. Kohout, J. Tucek, J. Haloda, J. Filip, R. Prucek, and R. Zboril, “Low-temperature magnetic transition in troilite: A simple marker for
highly stoichiometric FeS systems,” JOURNAL OF GEOPHYSICAL RESEARCH-SOLID EARTH, vol. 116, 2011.
[Bibtex]@article ISI:000297257000001, Author = Cuda, J. and Kohout, T. and Tucek, J. and Haloda, J. and Filip, J. and Prucek, R. and Zboril, R., Title = Low-temperature magnetic transition in troilite: A simple marker for highly stoichiometric FeS systems, Journal = JOURNAL OF GEOPHYSICAL RESEARCH-SOLID EARTH, Year = 2011, Volume = 116, Month = NOV 15, Abstract = Low-temperature magnetic evolution of troilite sample, extracted from the Cape York IIIA octahedrite meteorite, was investigated by employing macroscopic magnetic measurement, Mssbauer spectroscopy, scanning electron microscopy (SEM) and backscattered electrons (BSE) microscopy, X-ray diffraction (XRD), electron microprobe analysis (EMA), and atomic absorption spectrometry (AAS). The study identified a magnetic transition at approximate to 70 K manifested itself in a similar manner as previously reported for troilite from the Bruderheim L6 chondrite meteorite. The data show that this transition is unlikely driven by impurity such as chromite and seems to be rather an intrinsic property of troilite. In this study, we unambiguously exclude the relation of this transition to the structural rearrangement like the Morin transition in hematite. Similarly, in-field Mssbauer data do not support the change of the canting angle in the spin structure of FeS above and below the transition. Mssbauer, XRD, and magnetic data, newly measured also for troilite from the Bruderheim L6 chondrite, demonstrate that both studied troilite samples exhibit nearly the same magnetic and structural characteristics. Thus, the nature of the transition occurring at approximate to 70 K in both samples has identical characteristics and its detection can be used as a simple general marker for highly stoichiometric FeS systems., DOI = 10.1029/2011JB008232, Article-Number = B11205, ISSN = 0148-0227, Unique-ID = ISI:000297257000001, -
R. Prucek, J. Tucek, M. Kilianova, A. Panacek, L. Kvitek, J. Filip, M. Kolar, K. Tomankova, and R. Zboril, “The targeted antibacterial and antifungal properties of magnetic
nanocomposite of iron oxide and silver nanoparticles,” BIOMATERIALS, vol. 32, iss. 21, pp. 4704-4713, 2011.
[Bibtex]@article ISI:000291571400003, Author = Prucek, Robert and Tucek, Jiri and Kilianova, Martina and Panacek, Ales and Kvitek, Libor and Filip, Jan and Kolar, Milan and Tomankova, Katerina and Zboril, Radek, Title = The targeted antibacterial and antifungal properties of magnetic nanocomposite of iron oxide and silver nanoparticles, Journal = BIOMATERIALS, Year = 2011, Volume = 32, Number = 21, Pages = 4704-4713, Month = JUL, Abstract = Two types of magnetic binary nanocomposites, Ag@Fe(3)O(4) and gamma-Fe(2)O(3)@Ag, were synthesized and characterized and their antibacterial activities were tested. As a magnetic component, Fe(3)O(4) (magnetite) nanoparticles with an average size of about 70 nm and monodisperse gamma-Fe(2)O(3) (maghemite) nanoparticles with an average size of 5 nm were used. Nanocomposites were prepared via in situ chemical reduction of silver ions by maltose in the presence of particular magnetic phase and molecules of polyacrylate serving as a spacer among iron oxide and silver nanoparticles. In the case of the Ag@Fe(3)O(4) nanocomposite, silver nanoparticles, caught at the surfaces of Fe(3)O(4) nanocrystals, were around 5 nm in a size. On the contrary, in the case of the gamma-Fe(2)O(3)@Ag nanocomposite, ultrafine gamma-Fe(2)O(3) nanoparticles surrounded silver nanoparticles ranging in a size between 20 and 40 nm. In addition, the molecules of polyacrylate in this nanocomposite type suppress considerably interparticle magnetic interactions as proved by magnetization measurements. Both synthesized nanocomposites exhibited very significant antibacterial and antifungal activities against ten tested bacterial strains (minimum inhibition concentrations (MIC) from 15.6 mg/L to 125 mg/L) and four candida species (MIC from 1.9 mg/L to 31.3 mg/L). Moreover, acute nanocomposite cytotoxicity against mice embryonal fibroblasts was observed at concentrations of higher than 430 mg/L (Ag@Fe(3)O(4)) and 292 mg/L (gamma-Fe(2)O(3)@Ag). With respect to the non-cytotoxic nature of the polyacrylate linker, both kinds of silver nanocomposites are well applicable for a targeted magnetic delivery of silver nanoparticles in medicinal and disinfection applications. (C) 2011 Elsevier Ltd. All rights reserved., DOI = 10.1016/j.biomaterials.2011.03.039, ISSN = 0142-9612, Unique-ID = ISI:000291571400003, -
A. Panacek, R. Prucek, D. Safarova, M. Dittrich, J. Richtrova, K. Benickova, R. Zboril, and L. Kvitek, “Acute and Chronic Toxicity Effects of Silver Nanoparticles (NPs) on
Drosophila melanogaster,” ENVIRONMENTAL SCIENCE & TECHNOLOGY, vol. 45, iss. 11, pp. 4974-4979, 2011.
[Bibtex]@article ISI:000291128700045, Author = Panacek, Ales and Prucek, Robert and Safarova, Dana and Dittrich, Milan and Richtrova, Jana and Benickova, Katerina and Zboril, Radek and Kvitek, Libor, Title = Acute and Chronic Toxicity Effects of Silver Nanoparticles (NPs) on Drosophila melanogaster, Journal = ENVIRONMENTAL SCIENCE \& TECHNOLOGY, Year = 2011, Volume = 45, Number = 11, Pages = 4974-4979, Month = JUN 1, Abstract = The use of nanoscaled materials is rapidly increasing, however, their possible ecotoxicological effects are still not precisely known. This work constitutes the first complex study focused on in vivo evaluation of the acute and chronic toxic effects and toxic limits of silver nanoparticles (NPs) on the eukaryotic organism Drosophila melanogaster. For the purpose of this study, silver NPs were prepared in the form of solid dispersion using microencapsulation method, where mannitol was used as an encapsulation agent. This newly prepared solid dispersion with a high concentration of silver NPs was exploited to prepare the standard Drosophila culture medium at a silver concentration range from 10 mg . L(-1) to 100 mg . L(-1) of Ag in the case of the acute toxicity testing and at a concentration equal to S mg . L in the case of the chronic toxicity testing. The acute toxic effect of silver NPs on Drosophila melanogaster was observed for the silver concentration equal to 20 mg . L(-1). At this silver concentration, 50\% of the tested flies were unable to leave the pupae, and they did not finish their developmental cycle. Chronic toxicity of silver NPs was assessed by a long-term exposure of overall eight filial generations of Drosophila melanogaster to silver NPs. The long-term exposure to silver NPs influenced the fertility of Drosophila during the first three filial generations, nevertheless the fecundity of flies in subsequent generations consequently increased up to the level of the flies from the control sample due to the adaptability of flies to the silver NPs exposure., DOI = 10.1021/es104216b, ISSN = 0013-936X, Unique-ID = ISI:000291128700045, -
R. Prucek, A. Panacek, J. Soukupova, R. Novotny, and L. Kvitek, “Reproducible synthesis of silver colloidal particles tailored for
application in near-infrared surface-enhanced Raman spectroscopy,” JOURNAL OF MATERIALS CHEMISTRY, vol. 21, iss. 17, pp. 6416-6420, 2011.
[Bibtex]@article ISI:000289524300045, Author = Prucek, Robert and Panacek, Ales and Soukupova, Jana and Novotny, Radko and Kvitek, Libor, Title = Reproducible synthesis of silver colloidal particles tailored for application in near-infrared surface-enhanced Raman spectroscopy, Journal = JOURNAL OF MATERIALS CHEMISTRY, Year = 2011, Volume = 21, Number = 17, Pages = 6416-6420, Abstract = Reproducible synthesis of silver colloidal particles, with diameters of hundreds of nanometres, represents an experimentally rather difficult task although they have revealed a great application potential in e. g. SERS. The newly developed method, based on the reduction of the complex anion [Ag(SO(3))(2)](3-), offers an approach enabling to manage the preparation of silver particles with adjustable average diameters in the interval from 200 nm up to 700 nm due to the choice of the reducing agent and the sulfite concentration. These particles proved their efficiency as substrates for surface enhanced Raman spectroscopy with the excitation in the near infrared region (lambda = 1064 nm) and therefore this newly developed method confirmed the expected application potential., DOI = 10.1039/c0jm03870a, ISSN = 0959-9428, Unique-ID = ISI:000289524300045, -
R. Prucek, A. Panacek, A. Fargasova, V. Ranc, V. Masek, L. Kvitek, and R. Zboril, “Re-crystallization of silver nanoparticles in a highly concentrated NaCl
environment-a new substrate for surface enhanced IR-visible Raman
spectroscopy,” CRYSTENGCOMM, vol. 13, iss. 7, pp. 2242-2248, 2011.
[Bibtex]@article ISI:000288562200014, Author = Prucek, Robert and Panacek, Ales and Fargasova, Ariana and Ranc, Vaclav and Masek, Vlastimil and Kvitek, Libor and Zboril, Radek, Title = Re-crystallization of silver nanoparticles in a highly concentrated NaCl environment-a new substrate for surface enhanced IR-visible Raman spectroscopy, Journal = CRYSTENGCOMM, Year = 2011, Volume = 13, Number = 7, Pages = 2242-2248, Abstract = The common approach of silver nanoparticles activation for surface enhanced Raman spectroscopy often exploits an addition of chloride ions, generally at low concentrations of about 0.1-10 mM in the final dispersion. For the first time, we report the applicability of a highly concentrated NaCl solution (final concentration of 400 mM) for the SERS activation of silver nanoparticles (similar to 30 nm). Microscopic, optical and particle size distribution measurements reveal the rapid and reproducible re-crystallization of the primary silver nanoparticles to one-order larger crystallites (similar to 400 nm) already after 15 min after NaCl addition. The crystal growth mechanism is discussed with respect to the proved essential role of oxygen in the reaction system. The specific action of chloride ions is demonstrated through a comparison with NaBr and NaI solutions of the identical concentrations, which do not induce the analogous crystallization process. The recrystallized silver particles are efficient in an enhancement of the Raman signal not only for visible (488 nm) but also for near infrared laser excitation (1064 nm) as illustrated with the representative spectra of adenine., DOI = 10.1039/c0ce00776e, ISSN = 1466-8033, Unique-ID = ISI:000288562200014,
2010
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J. Soukupova, L. Kvitek, M. Kratochvilova, A. Panacek, R. Prucek, and R. Zboril, “Silver Voyage from Macro- to Nanoworld,” JOURNAL OF CHEMICAL EDUCATION, vol. 87, iss. 10, pp. 1094-1097, 2010.
[Bibtex]@article ISI:000281834400024, Author = Soukupova, Jana and Kvitek, Libor and Kratochvilova, Martina and Panacek, Ales and Prucek, Robert and Zboril, Radek, Title = Silver Voyage from Macro- to Nanoworld, Journal = JOURNAL OF CHEMICAL EDUCATION, Year = 2010, Volume = 87, Number = 10, Pages = 1094-1097, Month = OCT, DOI = 10.1021/ed1003405, ISSN = 0021-9584, Unique-ID = ISI:000281834400024,
2009
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A. Panacek, M. Kolar, R. Vecerova, R. Prucek, J. Soukupova, V. Krystof, P. Hamal, R. Zboril, and L. Kvitek, “Antifungal activity of silver nanoparticles against Candida spp.,” BIOMATERIALS, vol. 30, iss. 31, pp. 6333-6340, 2009.
[Bibtex]@article ISI:000270767300020, Author = Panacek, Ales and Kolar, Milan and Vecerova, Renata and Prucek, Robert and Soukupova, Jana and Krystof, Vladimir and Hamal, Petr and Zboril, Radek and Kvitek, Libor, Title = Antifungal activity of silver nanoparticles against Candida spp., Journal = BIOMATERIALS, Year = 2009, Volume = 30, Number = 31, Pages = 6333-6340, Month = NOV, Abstract = The antifungal activity of the silver nanoparticles (NPs) prepared by the modified Tollens process was evaluated for pathogenic Candida spp. by means of the determination of the minimum inhibitory concentration (MIC), minimum fungicidal concentration (MFC), and the time-dependency of yeasts growth inhibition. Simultaneously the cytotoxicity of the silver NPs to human fibroblasts was determined. The silver NPs exhibited inhibitory effect against the tested yeasts at the concentration as low as 0.21 mg/L of Ag. The inhibitory effect of silver NPs was enhanced through their stabilization and the lowest MIC equal to 0.05 mg/L was determined for silver NPs stabilized by sodium dodecyl sulfate against Candida albicans II. The obtained MICs of the silver NPs and especially of the stabilized silver NPs were comparable and in some cases even better than MICs of the conventional antifungal agents determined by E-test. The silver NPs effectively inhibited the growth of the tested yeasts at the concentrations below their cytotoxic limit against the tested human fibroblasts determined at a concentration equal to 30 mg/L of Ag. In contrast, ionic silver inhibited the growth of the tested yeasts at the concentrations comparable to the cytotoxic level (approx. 1 mg/L) of ionic silver against the tested human fibroblasts. (C) 2009 Elsevier Ltd. All rights reserved., DOI = 10.1016/j.biomaterials.2009.07.065, ISSN = 0142-9612, Unique-ID = ISI:000270767300020, -
R. Prucek, M. Hermanek, and R. Zboril, “An effect of iron(III) oxides crystallinity on their catalytic
efficiency and applicability in phenol degradation-A competition between
homogeneous and heterogeneous catalysis,” APPLIED CATALYSIS A-GENERAL, vol. 366, iss. 2, pp. 325-332, 2009.
[Bibtex]@article ISI:000270644800014, Author = Prucek, Robert and Hermanek, Martin and Zboril, Radek, Title = An effect of iron(III) oxides crystallinity on their catalytic efficiency and applicability in phenol degradation-A competition between homogeneous and heterogeneous catalysis, Journal = APPLIED CATALYSIS A-GENERAL, Year = 2009, Volume = 366, Number = 2, Pages = 325-332, Month = SEP 25, Abstract = Catalytic efficiency, stability and environmental applicability of five iron(III) oxide nanopowders differing in surface area and crystallinity were tested in degradation of concentrated phenolic aqueous solutions (100 g/L) at mild temperature (30 degrees C), initially almost neutral pH and equimolar ratio of hydrogen peroxide and phenol. The catalyst properties were easily controlled by varying in reaction time during isothermal treatment of ferrous oxalate dihydrate in air at 175 degrees C. Although the catalytic efficiency clearly increases with the surface area of the nanopowders, it is not due to the solely heterogeneous catalytic mechanism as would be expected. The amorphous Fe(2)O(3) nanopowders possessing the largest surface areas (401 m(2) g(-1), 386 m(2) g(-1)) are the most efficient catalysts evidently due to their highest susceptibility to leaching in acidic environment arising as a consequence of phenol degradation products. Thus, these amorphous samples act partially as homogeneous catalysts, which was confirmed by a high concentration of leached Fe(III) ions in the solution (similar to 19 ppm). The crystalline hematite (alpha-Fe(2)O(3)) samples, varying in surface area between 337 m(2) g(-1) and 245 m(2) g(-1), are generally less efficient when compared to the amorphous powders, however their catalytic action is almost exclusively heterogeneous as only 3 ppm of leached Fe(III) was found in the reaction systems catalyzed by nanohematite samples. A significant difference in relative contributions of heterogeneous and homogenous catalysis was definitely established in buffered reaction systems catalyzed by amorphous Fe(2)O(3) and nanocrystalline hematite. The nanohematite sample exhibiting the highest heterogeneous action was tested at decreased initial phenol concentration (10 g/L), which is closer to the real contents of phenol in waste waters, and at different hydrogen peroxide/phenol molar ratios to consider its environmental applicability. At the hydrogen peroxide/phenol ratio equal to 5, no traces of the leached iron were detected and the phenol conversion of 84\% was reached. Moreover, such a high degree of conversion is accompanied by a decrease of the chemical oxygen demand (COD) from the initial value of 11.23 g/L to 4.22 g/L after 125 min. This fact indicates that the considerable fraction of primary reaction products was totally degraded. (C) 2009 Elsevier B.V. All rights reserved., DOI = 10.1016/j.apcata.2009.07.019, ISSN = 0926-860X, Unique-ID = ISI:000270644800014, -
L. Kvitek, M. Vanickova, A. Panacek, J. Soukupova, M. Dittrich, E. Valentova, R. Prucek, M. Bancirova, D. Milde, and R. Zboril, “Initial Study on the Toxicity of Silver Nanoparticles (NPs) against
Paramecium caudatum,” JOURNAL OF PHYSICAL CHEMISTRY C, vol. 113, iss. 11, pp. 4296-4300, 2009.
[Bibtex]@article ISI:000264111300013, Author = Kvitek, Libor and Vanickova, Marketa and Panacek, Ales and Soukupova, Jana and Dittrich, Milan and Valentova, Eva and Prucek, Robert and Bancirova, Martina and Milde, David and Zboril, Radek, Title = Initial Study on the Toxicity of Silver Nanoparticles (NPs) against Paramecium caudatum, Journal = JOURNAL OF PHYSICAL CHEMISTRY C, Year = 2009, Volume = 113, Number = 11, Pages = 4296-4300, Month = MAR 19, Abstract = In this initial study, the toxicity effect of silver NPs against a model unicellular eukaryotic organism of Paramecium caudatum was studied. For the purpose of this study, a dialysis-based method was adapted, which allowed the preparation of stable aqueous dispersions of silver NPs in various silver concentrations that were necessary for the evaluation of toxicity limits of these particles. The obtained results demonstrate that the silver NPs do not exhibit any toxicity action against the tested unicellular eukaryotic organism below the concentration of 25 mg . L(-1) whereas ionic silver retains its toxicity even at a concentration of 0.4 mg . L(-1). Such a considerable difference in the toxicity effect of these two forms of silver has not been observed in the previously published study concerning bacteria (Panacek, A.; Kvitek, L.; Prucek, R.; Koldr, M.; Vecefova, R.; Pizurova, N.; Sharma, V. K.; Nevecna, T.; Zboril, R. J. Phys. Chem. B 2006, 110, 16248-16253). Additionally, it was proven that the surfactant/polymer modification can increase the toxicity of the silver NPs against the tested organism., DOI = 10.1021/jp808645e, ISSN = 1932-7447, Unique-ID = ISI:000264111300013, -
R. Prucek, L. Kvitek, A. Panacek, L. Vancurova, J. Soukupova, D. Jancik, and R. Zboril, “Polyacrylate-assisted synthesis of stable copper nanoparticles and
copper(I) oxide nanocubes with high catalytic efficiency,” JOURNAL OF MATERIALS CHEMISTRY, vol. 19, iss. 44, pp. 8463-8469, 2009.
[Bibtex]@article ISI:000271744600027, Author = Prucek, Robert and Kvitek, Libor and Panacek, Ales and Vancurova, Lenka and Soukupova, Jana and Jancik, Dalibor and Zboril, Radek, Title = Polyacrylate-assisted synthesis of stable copper nanoparticles and copper(I) oxide nanocubes with high catalytic efficiency, Journal = JOURNAL OF MATERIALS CHEMISTRY, Year = 2009, Volume = 19, Number = 44, Pages = 8463-8469, Abstract = The synthesis of Cu nanoparticles (NPs) via the reduction of Cu ions with sodium borohydride in the presence of sodium polyacrylate is presented. The final Cu nanocrystals having a 14 nm diameter were generated via the aggregation and coalescence of the primarily formed ultrasmall particles (approx. 3 nm). Addition of sodium sulfite to the dispersions provided the protection of the Cu NPs against oxidation. On the other hand, the controlled aeration of the Cu NPs resulted in their transformation to Cu(2)O nanocubes with an average size of 18 nm. Both Cu NPs and Cu(2)O nanocubes can effectively catalyze reduction of 4-nitrophenol by sodium borohydride in aqueous solution., DOI = 10.1039/b913561h, ISSN = 0959-9428, Unique-ID = ISI:000271744600027,
2008
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L. Kvitek, A. Panacek, J. Soukupova, M. Kolar, R. Vecerova, R. Prucek, M. Holecova, and R. Zboril, “Effect of surfactants and polymers on stability and antibacterial
activity of silver nanoparticles (NPs),” JOURNAL OF PHYSICAL CHEMISTRY C, vol. 112, iss. 15, pp. 5825-5834, 2008.
[Bibtex]@article ISI:000254883100021, Author = Kvitek, Libor and Panacek, Ales and Soukupova, Jana and Kolar, Milan and Vecerova, Renata and Prucek, Robert and Holecova, Mirka and Zboril, Radek, Title = Effect of surfactants and polymers on stability and antibacterial activity of silver nanoparticles (NPs), Journal = JOURNAL OF PHYSICAL CHEMISTRY C, Year = 2008, Volume = 112, Number = 15, Pages = 5825-5834, Month = APR 17, Abstract = In this first systematic study, we describe the influence of various surfactants and polymers on aggregation stability and antibacterial activity of silver nanoparticles (NPs) prepared by a modified Tollens process. The surfactant/polymer stabilizing effect was monitored using the newly established method based on a titration of the aqueous dispersion of the silver NPs by aqueous solution of poly(diallyldimethylammonium) chloride (PDDA). The aggregation process was evaluated by the dynamic light scattering (DLS) and UV/vis spectra measurements and finally confirmed by TEM. Among all of the investigated modifiers, two surfactants (sodium dodecyl sulfate-SDS and polyoxyethylenesorbitane monooleate-Tween 80) and one polymer (polyvinylpyr-rolidone-PVP 360) exhibit superior stabilization of the silver NP dispersions against the process of aggregation. The differences in the stabilization ability of various tested substances are discussed with respect to their structure and possible mechanism of the surface interaction with the NPs. The antibacterial activity of the modified silver NPs was significantly enhanced especially when modified by SDS where the minimum inhibition concentration (MIC) decreased under the ``magical value'' of 1 mu g(.)mL(-1). A correlation was found between the aggregation stability and enhanced antibacterial activity in the system of the silver NPs modified by SDS, Tween 80, and high molecular polymer PVP 360., DOI = 10.1021/jp711616v, ISSN = 1932-7447, Unique-ID = ISI:000254883100021,
2006
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A. Panacek, L. Kvitek, R. Prucek, M. Kolar, R. Vecerova, N. Pizurova, V. K. Sharma, T. Nevecna, and R. Zboril, “Silver colloid nanoparticles: Synthesis, characterization, and their
antibacterial activity,” JOURNAL OF PHYSICAL CHEMISTRY B, vol. 110, iss. 33, pp. 16248-16253, 2006.
[Bibtex]@article ISI:000239818000019, Author = Panacek, Ales and Kvitek, Libor and Prucek, Robert and Kolar, Milan and Vecerova, Renata and Pizurova, Nadezda and Sharma, Virender K. and Nevecna, Tat'jana and Zboril, Radek, Title = Silver colloid nanoparticles: Synthesis, characterization, and their antibacterial activity, Journal = JOURNAL OF PHYSICAL CHEMISTRY B, Year = 2006, Volume = 110, Number = 33, Pages = 16248-16253, Month = AUG 24, Abstract = A one-step simple synthesis of silver colloid nanoparticles with controllable sizes is presented. In this synthesis, reduction of [Ag(NH3)(2)](+) complex cation by four saccharides was performed. Four saccharides were used: two monosaccharides (glucose and galactose) and two disaccharides (maltose and lactose). The syntheses performed at various ammonia concentrations (0.005-0.20 mol L-1) and pH conditions (11.5-13.0) produced a wide range of particle sizes (25-450 nm) with narrow size distributions, especially at the lowest ammonia concentrations. The average size, size distribution, morphology, and structure of particles were determined by dynamic light scattering (DLS), transmission electron microscopy (TEM), and UV/Visible absorption spectrophotometry. The influence of the saccharide structure (monosacharides versus disaccharides) on the size of silver particles is briefly discussed. The reduction of [Ag(NH3)(2)](+) by maltose produced silver particles with a narrow size distribution with an average size of 25 nm, which showed high antimicrobial and bactericidal activity against Gram-positive and Gram-negative bacteria, including highly multiresistant strains such as methicillin-resistant Staphylococcus aureus. Antibacterial activity of silver nanoparticles was found to be dependent on the size of silver particles. A very low concentration of silver (as low as 1.69 mu g/mL Ag) gave antibacterial performance., DOI = 10.1021/jp063826h, ISSN = 1520-6106, Unique-ID = ISI:000239818000019,
2005
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L. Kvitek, R. Prucek, A. Panacek, R. Novotny, J. Hrbac, and R. Zboril, “The influence of complexing agent concentration on particle size in the
process of SERS active silver colloid synthesis,” JOURNAL OF MATERIALS CHEMISTRY, vol. 15, iss. 10, pp. 1099-1105, 2005.
[Bibtex]@article ISI:000227320600013, Author = Kvitek, L and Prucek, R and Panacek, A and Novotny, R and Hrbac, J and Zboril, R, Title = The influence of complexing agent concentration on particle size in the process of SERS active silver colloid synthesis, Journal = JOURNAL OF MATERIALS CHEMISTRY, Year = 2005, Volume = 15, Number = 10, Pages = 1099-1105, Abstract = A one-step chemical reduction route towards silver colloid particles with controllable sizes ranging from 45 to 380 nm is reported in this article. Silver particles, prepared by the reduction of [Ag(NH3)(2)](+) complex with various reducing sugars, were characterised by means of transmission electron microscopy ( TEM), dynamic light scattering ( DLS) measurement of particle size distribution, and UV-VIS spectroscopy. The concentration of ammonia in the reaction mixture and the choice of the reducing sugar are the key parameters in the control of particle size. Synthesised silver colloid particles were successfully tested for use in surface-enhanced Raman spectroscopy (SERS) with 1-methyladenine as a testing substance., DOI = 10.1039/b417007e, ISSN = 0959-9428, Unique-ID = ISI:000227320600013,
