RESUMEN
We have employed ptychographic coherent diffractive imaging to completely characterize the focal spot wavefield and wavefront aberrations of a high-resolution diffractive X-ray lens. The ptychographic data from a strongly scattering object was acquired using the radiation cone emanating from a coherently illuminated Fresnel zone plate at a photon energy of 6.2 keV. Reconstructed images of the object were retrieved with a spatial resolution of 8 nm by combining the difference-map phase retrieval algorithm with a non-linear optimization refinement. By numerically propagating the reconstructed illumination function, we have obtained the X-ray wavefield profile of the 23 nm round focus of the Fresnel zone plate (outermost zone width, Δr = 20 nm) as well as the X-ray wavefront at the exit pupil of the lens. The measurements of the wavefront aberrations were repeatable to within a root mean square error of 0.006 waves, and we demonstrate that they can be related to manufacturing aspects of the diffractive optical element and to errors on the incident X-ray wavefront introduced by the upstream beamline optics.
RESUMEN
Dispersions of Fe(3)C nanoparticles in several ionic liquids (ILs) have been investigated. The ILs are based on 1-ethyl-3-methylimidazolium [Emim] and 1-butyl-3-methylimidazolium [Bmim] cations. Anions are ethylsulfate [ES], methanesulfonate [MS], trifluoromethylsulfonate (triflate) [TfO], tetrafluoroborate [BF(4)], dicyanamide [N(CN)(2)], and thiocyanate [SCN]. Among the ILs studied, [Emim][SCN] and [Emim][N(CN)(2)] stand out because only in these ILs have stable and transparent nanoparticle dispersions been obtained. All other ILs lead to blackish, slightly turbid dispersions or to completely nontransparent suspensions, which often contain undispersed sediment. UV/vis spectroscopy, transmission electron microscopy, and X-ray scattering suggest that the reason for the stabilization of the Fe(3)C nanoparticles in [Emim][SCN] is the leaching of traces of iron from the particles (without affecting the crystal structure of the Fe(3)C particles). The resulting particle surface is thus carbon-rich, which presumably favors the stabilization of the particles. A similar explanation can be postulated for [Emim][N(CN)(2)], with the dicyanamide anion also being a good ligand for iron.
RESUMEN
Simple tripeptides are scaffolds for the synthesis and further assembly of peptide/silver nanoparticle composites. Herein, we further explore peptide-controlled silver nanoparticle assembly processes. Silver nanoparticles with a pH-responsive peptide coating have been synthesized by using a one-step precipitation/coating route. The nature of the peptide/silver interaction and the effect of the peptide on the formation of the silver particles have been studied via UV/Vis, X-ray photoelectron, and surface-enhanced Raman spectroscopies as well as through electron microscopy, small angle X-ray scattering and powder X-ray diffraction with Rietveld refinement. The particles reversibly form aggregates of different sizes in aqueous solution. The state of aggregation can be controlled by the solution pH value. At low pH values, individual particles are present. At neutral pH values, small clusters form and at high pH values, large precipitates are observed.
Asunto(s)
Nanopartículas del Metal/química , Oligopéptidos/química , Plata/química , Secuencia de Aminoácidos , Concentración de Iones de Hidrógeno , Análisis Espectral , Propiedades de Superficie , Difracción de Rayos XRESUMEN
Direct dissolution of glycosylated polybutadiene-poly(ethylene oxide) block copolymers can lead to the spontaneous formation of vesicles or membranes, which on the outside are coated with glucose and on the inside with poly(ethylene oxide).
Asunto(s)
Glucosa/química , Polietilenglicoles/química , Polímeros/química , Vesículas Transportadoras/química , Estructura Molecular , Propiedades de SuperficieRESUMEN
Chiral metal-organic frameworks (MOFs) have attracted a growing interest for their potential use in energy technologies, asymmetric catalysis, chiral separation, and on a more basic level, the creation of new topologies in inorganic materials. The current paper is the first report on a peptide-based MOF, a metal peptide framework (MPF), constructed from an oligovaline peptide family developed earlier by our group (Mantion, A.; et al. Macromol. Biosci. 2007, 7, 208). We have used a simple oligopeptide, Z-(L-Val)2-L-Glu(OH)-OH, to grow porous copper and calcium MPFs. The MPFs form thanks to the self-assembling properties of the peptide and specific metal-peptide and metal-ammonia interactions. They are stable up to ca. 250 degrees C and have some internal porosity, which makes them a promising prototype for the further development of MPFs.
Asunto(s)
Materiales Biomiméticos/química , Calcio/química , Cobre/química , Compuestos Organometálicos/química , Péptidos/química , Materiales Biomiméticos/síntesis química , Cristalografía por Rayos X , Enlace de Hidrógeno , Ligandos , Modelos Moleculares , Conformación Molecular , Compuestos Organometálicos/síntesis química , Péptidos/síntesis química , Porosidad , Propiedades de Superficie , TemperaturaRESUMEN
l-Valine-based oligopeptides with the chemical structure Z-(l-Val)3-OMe and Z-(l-Val)2-l-Cys(S-Bzl)-OMe form stable organogels in butanol. Both peptides are efficient gelators, but Z-(l-Val)2-l-Cys(S-Bzl)-OMe crystallizes more readily than Z-(l-Val)3-OMe. The two peptides can form mixed fibers, which also gel butanol. The resulting organogels are very similar to oligovaline organogels reported earlier (Mantion and Taubert, Macromol. Biosci., 2007, 7, 208) as they also form highly ordered peptide fibers with a predominant ß-sheet structure and diameters of ca. 100 nm. The fibers can be mineralized with silver nanoparticles using DMF as a reducing agent. The fraction of the sulfur-containing peptide Z-(l-Val)2-l-Cys(S-Bzl)-OMe controls the shape and size of the resulting nanoparticles. At high Z-(l-Val)2-l-Cys(S-Bzl)-OMe content, small spherical particles are distributed all over the fiber. Lower contents of Z-(l-Val)2-l-Cys(S-Bzl)-OMe lead to a size increase of the particles and to more complex shapes like plate-like and raspberry-like silver particles. The interactions between peptide and silver ions or silver particles takes place via a complexation of the silver ions to the sulfur atom of the thioether moiety, and are shown to be the key interaction in controlling particle formation.
RESUMEN
L-Valine-based oligopeptides with the general structure Z-(L-Val)(n)-OMe or -OH (n = 1-4) form stable organogels in a variety of solvents, including the inorganic liquid tetraethylorthosilicate. The acid form Z-(L-Val)(n)-OH is a less efficient gelator than the methyl ester, but forms stable organogels in aromatic solvents and di- and trichloromethane. In all cases the peptides form micrometer long helical fibers with a beta-sheet structure. IR and X-ray diffraction show that the peptides have closely related structures in the crystalline state and the fibers in the organogels. The gels are efficient templates for the fabrication of complex titania architectures on a (sub)micron length scale: at low peptide concentrations titania spheres form and at higher concentrations one-dimensional shapes like hollow titania tubes or titania fibers are observed. The tubes are stable towards calcination whereas the fibers (partially) transform into spherical or even bulk particles.
Asunto(s)
Geles/síntesis química , Oligopéptidos/química , Oligopéptidos/síntesis química , Titanio/química , Valina/química , Geles/química , Espectroscopía de Resonancia Magnética , Microscopía Electrónica de Rastreo , Estructura Molecular , Difracción de Rayos XRESUMEN
We have recently reported (Angew. Chem. Int. Ed. 2004, 43 (40), 5380) the formation of CuCl nanoplatelets from an ionic liquid crystal precursor (ILCP) consisting of a 50/50 (wt/wt) mixture of bis(dodecylpyridinium) tetrachlorocuprate 1 and 6-O-palmitoyl ascorbic acid 2. Here we present the full ILCP phase diagram and the thermal behavior from a mixing ratio of 1/0 (i.e., pure 1) to 0/1 (i.e., pure 2). The ILCP exhibits a crystalline-smectic-isotropic phase transition at all mixing ratios, and the liquid crystal region is up to 90 degrees C wide. DSC shows a broad exothermic peak between ca. 70 and 170 degrees C, which is associated with the thermally induced CuCl formation. The reaction enthalpies reach -150 kJ/mol at around 50/50 (wt/wt) mixtures of the two components, and the activation energy for CuCl formation is ca. 190 kJ/mol. Thermogravimetric analysis shows that the samples degrade above ca. 200 degrees C.
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The synthesis, characterization, self-assembly, and gel formation of poly(γ-benzyl-l-glutamate) (PBLG) in a molecular weight range from ca. 7,000-100,000 g/mol and with narrow molecular weight distribution are described. The PBLG is synthesized by the nickel-mediated ring-opening polymerization and is characterized by size-exclusion chromatography coupled with multiple-angle laser light scattering, NMR, and Fourier transform infrared spectroscopy. The self-assembly and thermoreversible gel formation in the helicogenic solvent toluene is investigated by transmission electron microscopy, atomic force microscopy, small-angle X-ray scattering, and synchrotron powder X-ray diffraction. At concentrations significantly below the minimum gelation concentration, spherical aggregates are observed. At higher concentrations, gels are formed, which show a 3D network structure composed of nanofibers. The proposed self-assembly mechanism is based on a distorted hexagonal packing of PBLG helices parallel to the axis of the nanofiber. The gel network forms due to branching and rejoining of bundles of PBLG nanofibers. The network exhibits uniform domains with a length of 200 ± 42 nm composed of densely packed PBLG helices.
RESUMEN
In the body, nanoparticles can be systemically distributed and then may affect secondary target organs, such as the central nervous system (CNS). Putative adverse effects on the CNS are rarely investigated to date. Here, we used a mixed primary cell model consisting mainly of neurons and astrocytes and a minor proportion of oligodendrocytes to analyze the effects of well-characterized 20 and 40 nm silver nanoparticles (SNP). Similar gold nanoparticles served as control and proved inert for all endpoints tested. SNP induced a strong size-dependent cytotoxicity. Additionally, in the low concentration range (up to 10 µg/ml of SNP), the further differentiated cultures were more sensitive to SNP treatment. For detailed studies, we used low/medium dose concentrations (up to 20 µg/ml) and found strong oxidative stress responses. Reactive oxygen species (ROS) were detected along with the formation of protein carbonyls and the induction of heme oxygenase-1. We observed an acute calcium response, which clearly preceded oxidative stress responses. ROS formation was reduced by antioxidants, whereas the calcium response could not be alleviated by antioxidants. Finally, we looked into the responses of neurons and astrocytes separately. Astrocytes were much more vulnerable to SNP treatment compared with neurons. Consistently, SNP were mainly taken up by astrocytes and not by neurons. Immunofluorescence studies of mixed cell cultures indicated stronger effects on astrocyte morphology. Altogether, we can demonstrate strong effects of SNP associated with calcium dysregulation and ROS formation in primary neural cells, which were detectable already at moderate dosages.
Asunto(s)
Calcio/metabolismo , Nanopartículas del Metal , Neuronas/efectos de los fármacos , Estrés Oxidativo , Plata/química , Animales , Células Cultivadas , Microscopía Electrónica de Transmisión , Neuronas/citología , Neuronas/metabolismo , Ratas , Especies Reactivas de Oxígeno/metabolismoRESUMEN
Silica and silver nanoparticles are relevant materials for new applications in optics, medicine, and analytical chemistry. We have previously reported the synthesis of pH responsive, peptide-templated, chiral silver nanoparticles. The current report shows that peptide-stabilized nanoparticles can easily be coated with a silica shell by exploiting the ability of the peptide coating to hydrolyze silica precursors such as TEOS or TMOS. The resulting silica layer protects the nanoparticles from chemical etching, allows their inclusion in other materials, and renders them biocompatible. Using electron and atomic force microscopy, we show that the silica shell thickness and the particle aggregation can be controlled simply by the reaction time. Small-angle X ray scattering confirms the Ag/peptide@silica core-shell structure. UV-vis and circular dichroism spectroscopy prove the conservation of the silver nanoparticle chirality upon silicification. Biological tests show that the biocompatibility in simple bacterial systems is significantly improved once a silica layer is deposited on the silver particles.
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Biomimética/métodos , Nanopartículas del Metal/química , Péptidos/química , Dióxido de Silicio/química , Plata/química , Diferenciación Celular/efectos de los fármacos , Línea Celular , Supervivencia Celular/efectos de los fármacos , Escherichia coli K12/efectos de los fármacos , Humanos , Macrófagos/citología , Macrófagos/efectos de los fármacos , Plata/farmacología , Plata/toxicidad , Análisis Espectral , Estereoisomerismo , Propiedades de SuperficieRESUMEN
Peptide-modified silver nanoparticles have been coated with an erbium-doped silica layer using a method inspired by silica biomineralization. Electron microscopy and small-angle X-ray scattering confirm the presence of an Ag/peptide core and silica shell. The erbium is present as small Er(2)O(3) particles in and on the silica shell. Raman, IR, UV-Vis, and circular dichroism spectroscopies show that the peptide is still present after shell formation and the nanoparticles conserve a chiral plasmon resonance. Magnetic measurements find a paramagnetic behavior. In vitro tests using a macrophage cell line model show that the resulting multicomponent nanoparticles have a low toxicity for macrophages, even on partial dissolution of the silica shell.
Asunto(s)
Materiales Biomiméticos , Erbio , Macrófagos/metabolismo , Nanopartículas/química , Péptidos , Dióxido de Silicio , Plata , Resonancia por Plasmón de Superficie/métodos , Materiales Biomiméticos/síntesis química , Materiales Biomiméticos/química , Materiales Biomiméticos/farmacocinética , Materiales Biomiméticos/farmacología , Línea Celular , Erbio/química , Erbio/farmacocinética , Erbio/farmacología , Humanos , Macrófagos/citología , Fenómenos Magnéticos , Péptidos/química , Péptidos/farmacocinética , Péptidos/farmacología , Dióxido de Silicio/síntesis química , Dióxido de Silicio/química , Dióxido de Silicio/farmacocinética , Dióxido de Silicio/farmacología , Plata/química , Plata/farmacocinética , Plata/farmacología , Análisis EspectralRESUMEN
Silver nanoparticles (SNP) are the subject of worldwide commercialization because of their antimicrobial effects. Yet only little data on their mode of action exist. Further, only few techniques allow for visualization and quantification of unlabeled nanoparticles inside cells. To study SNP of different sizes and coatings within human macrophages, we introduce a novel laser postionization secondary neutral mass spectrometry (Laser-SNMS) approach and prove this method superior to the widely applied confocal Raman and transmission electron microscopy. With time-of-flight secondary ion mass spectrometry (TOF-SIMS) we further demonstrate characteristic fingerprints in the lipid pattern of the cellular membrane indicative of oxidative stress and membrane fluidity changes. Increases of protein carbonyl and heme oxygenase-1 levels in treated cells confirm the presence of oxidative stress biochemically. Intriguingly, affected phagocytosis reveals as highly sensitive end point of SNP-mediated adversity in macrophages. The cellular responses monitored are hierarchically linked, but follow individual kinetics and are partially reversible.
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Macrófagos/química , Nanopartículas del Metal , Nanotecnología , Plata/análisis , Espectrometría de Masa de Ion Secundario/métodos , Toxicología , Humanos , Macrófagos/ultraestructura , Microscopía Electrónica de Transmisión , Estrés OxidativoRESUMEN
Silica is an important mineral in biology and technology, and many protocols have been developed for the synthesis of complex silica architectures. The current report shows that silsesquioxane nanoparticles carrying polymer arms on their surface are efficient templates for the fabrication of silica particles with a star- or raspberry-like morphology. The shape of the resulting particles depends on the chemistry of the polymer arms. With poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) arms, spherical particles with a less electron dense core form. With poly{[2-(methacryloyloxy)ethyl] trimethylammonium iodide} (PMETAI), star- or raspberry-like particles form. Electron microscopy, electron tomography, and small-angle X-ray scattering show that the resulting silica particles have a complex structure, where a silsequioxane nanoparticle carrying the polymer arms is in the center. Next is a region that is polymer-rich. The outermost region of the particle is a silica layer, where the outer parts of the polymer arms are embedded. Time-resolved zeta-potential and pH measurements, dynamic light scattering, and electron microscopy reveal that silica formation proceeds differently if PDMAEMA is exchanged for PMETAI.
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Nanopartículas , Compuestos de Organosilicio/química , Poliaminas/química , Microscopía Electrónica de Rastreo , Espectroscopía Infrarroja por Transformada de Fourier , Difracción de Rayos XRESUMEN
We have recently shown that the hydrated ionic liquid tetrabutylammonium hydroxide (TBAH) is an efficient ionic liquid precursor (ILP) for the fabrication of ZnO/carbohydrate materials (D. Mumalo-Djokic, W. B. Stern, A. Taubert, Cryst. Growth Des. 2008, 8, 330). The current paper shows that ZnO is just one example out of the large group of technologically important metal (hydr)oxides that can be made using TBAH. Simply by using different metal acetates as precursors in TBAH, it is possible to make a wide variety of metal (hydr)oxides with well-defined size, morphology, and chemical composition. It is also possible to dope metal oxide particles or to synthesize mixed metal oxide particles, and therefore to control properties like magnetism.