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Emulsion Droplets (emulsion + droplet)
Selected AbstractsPhotonic Crystals: Patterned Polymeric Domes with 3D and 2D Embedded Colloidal Crystals using Photocurable Emulsion Droplets (Adv. Mater.ADVANCED MATERIALS, Issue 37 200937/2009) The inside cover shows a scheme for the preparation of photonic dome patterns, SEM images of a dome pattern, and a single dome decorated with 2D colloid array, as fabricated in work reported on p 3771 by Seung-Man Yang and co-workers. The background is an optical microscopy image of patterned photonic domes, which can be used as a near-field microlens array. The greenish color of the domes corresponds to the photonic bandgap. [source] Patterned Polymeric Domes with 3D and 2D Embedded Colloidal Crystals using Photocurable Emulsion DropletsADVANCED MATERIALS, Issue 37 2009Shin-Hyun Kim Hierarchical dome patterns are prepared via a novel single-step patterning process. Photonic domes with isotropic reflection colors are patterned on a prepatterned glass substrate with a hydrophobic moiety using photocurable emulsion droplets of all-equal size, which contain concentrated silica particles. Furthermore, embossed domes are patterned with PS particle-stabilized photocurable emulsion droplets, which can act as a near-field microlens array. [source] CMR2009: 1.02: Increasing ultrasound sensitivity to perfluorcarbon emulsion dropletsCONTRAST MEDIA & MOLECULAR IMAGING, Issue 6 2009R. F. Mattrey No abstract is available for this article. [source] Monodisperse Polymer Capsules: Tailoring Size, Shell Thickness, and Hydrophobic Cargo Loading via Emulsion TemplatingADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Jiwei Cui Abstract The preparation of monodisperse polymer (polydopamine, PDA) capsules by a one-step interfacial polymerization of dopamine onto dimethyldiethoxysilane (DMDES) emulsion droplets and removal of the DMDES templates with ethanol is reported. The diameters of the PDA capsules can be tailored from 400,nm to 2.4,µm by varying either the DMDES emulsion condensation time or the emulsion concentration used for templating. Further, capsules with defined nanometer-scale shell thicknesses (ranging from ,10 to 30,nm) can be prepared by adjusting the emulsion concentration. This shell thickness can be increased by repeated interfacial polymerization of dopamine, with three cycles yielding capsules with a shell thickness of up to 140,nm (for a 0.6% v/v suspension). Functional substances, such as organically stabilized magnetic (Fe3O4) nanoparticles, quantum dots (CdSe/CdS), and hydrophobic drugs (thiocoraline), can be preloaded in the emulsion droplets, and following PDA coating and DMDES removal, these materials remain encapsulated in the polymer capsules. All of the unloaded and loaded PDA capsules are monodisperse and do not aggregate. This work provides new avenues for the preparation of polymer capsules with defined size and shell thickness and for the encapsulation of a range of hydrophobic substances. [source] Liquid Crystal Emulsions as the Basis of Biological Sensors for the Optical Detection of Bacteria and VirusesADVANCED FUNCTIONAL MATERIALS, Issue 14 2009Sri Sivakumar Abstract A versatile sensing method based on monodisperse liquid crystal (LC) emulsion droplets detects and distinguishes between different types of bacteria (Gram +ve and ,ve) and viruses (enveloped and non-enveloped). LCs of 4-cyano-4'-pentylbiphenyl transition from a bipolar to radial configuration when in contact with Gram ,ve bacteria (E. coli) and lipid-enveloped viruses (A/NWS/Tokyo/67). This transition is consistent with the transfer of lipid from the organisms to the interfaces of the micrometer-sized LC droplets. In contrast, a transition to the radial configuration is not observed in the presence of Gram +ve bacteria (Bacillus subtilis and Micrococcus luteus) and non-enveloped viruses (M13 helper phage). The LC droplets can detect small numbers of E. coli bacteria (1,5) and low concentrations (104,pfu mL,1) of A/NWS/Tokyo/67 virus. Monodisperse LC emulsions incubated with phosholipid liposomes (similar to the E. coli cell wall lipid) reveal that the orientational change is triggered at an area per lipid molecule of ,46,Å2 on an LC droplet (,1.6,×,108 lipid molecules per droplet). This approach represents a novel means to sense and differentiate between types of bacteria and viruses based on their cell-wall/envelope structure, paving the way for the development of a new class of LC microdroplet-based biological sensors. [source] Patterned Polymeric Domes with 3D and 2D Embedded Colloidal Crystals using Photocurable Emulsion DropletsADVANCED MATERIALS, Issue 37 2009Shin-Hyun Kim Hierarchical dome patterns are prepared via a novel single-step patterning process. Photonic domes with isotropic reflection colors are patterned on a prepatterned glass substrate with a hydrophobic moiety using photocurable emulsion droplets of all-equal size, which contain concentrated silica particles. Furthermore, embossed domes are patterned with PS particle-stabilized photocurable emulsion droplets, which can act as a near-field microlens array. [source] Colloid Surfactants for Emulsion Stabilization,ADVANCED MATERIALS, Issue 17 2008Jin-Woong Kim Colloid surfactants are fabricated with precisely controlled geometry and used for emulsion stabilization. These amphiphilic dimer particles (left) combine the benefits of emulsion stabilization of particles and the amphiphilicity of molecular surfactants to afford better emulsion stabilization. Remarkably, these colloidal surfactants stabilize not only spherical emulsion droplets but also nonspherical ones (right). [source] Phase Reorganization in Self-Assembled Systems Through Interparticle Material Transfer,ADVANCED MATERIALS, Issue 10 2007C. Moitzi Transfer of material occurs when internally nanostructured emulsion droplets of different composition are mixed. This happens without droplet fusion. As the internal structure is dependent on the composition, the transfer can be followed by monitoring these changes using time-resolved small angle X-ray scattering (SAXS; see figure). [source] Synthesis of Monodisperse Colloidal Spheres, Capsules, and Microballoons by Emulsion Templating,ADVANCED MATERIALS, Issue 7 2005I. Zoldesi New types of monodisperse, micrometer-sized, hollow particles (see Figure) are obtained by encapsulation of emulsion droplets in solid shells and dissolution of the cores. A facile fabrication method is used in which, by simply tuning the thickness of the shells, different types of particles with tunable properties are obtained. [source] Synthesis by a single-step swelling process and characterization of micrometer-sized polychloromethylstyrene/poly(butyl methacrylate) hemispherical composite particles of narrow size distributionJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2008Sigal Baruch-Sharon Abstract Polychloromethylstyrene (PCMS) micrometer-sized particles of narrow size distribution were prepared by the dispersion polymerization of chloromethylstyrene in a mixture of ethanol and dimethyl sulfoxide. Micrometer-sized PCMS/poly(butyl methacrylate) hemispherical composite particles of narrow size distribution were prepared by a single-step swelling process of the uniform PCMS template particles with emulsion droplets of butyl methacrylate (BMA) containing benzoyl peroxide, followed by the polymerization of BMA at 73°C within the swollen template particles. The effects of various polymerization parameters, for example, BMA volume, initiator type and concentration, and toluene as the swelling solvent, on the properties (size and size distribution, morphology, polymerization yield, and composition) of the hemispherical composite particles were elucidated. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Micropipette manipulation: A technique to evaluate the stability of water-in-oil emulsions containing proteinsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 12 2004Lene Jorgensen Abstract The interfacial properties and stability of water-in-oil emulsions containing protein were studied using micromanipulation. Micropipettes were used to produce individual water droplets in oil in a controlled manner on the micron scale. The pipettes were then used to bring two droplets into contact in order to observe fusion. The occurrence of fusion was investigated as a function of the compositions of both the continuous (oil) and dispersed (aqueous) phases. Various proteins, i.e., insulin, growth hormone, or serum albumin, were dissolved in the dispersed phase. When low concentrations of surfactants or no surfactant were present in the oil phase, a condensed protein film was formed at the surface of the droplets, which was revealed by the irregular topology of the droplet surface viewed with contrast microscopy. At higher surfactant concentrations, this topology was not observed nor was the stability apparently affected; emulsion droplets coalesce immediately upon contact with each other. There seems to be a limiting surfactant concentration, which stabilizes the droplets toward fusion and prevents formation of a condensed surface film, when the droplets contain protein. The technique exhibits potential for examination of the effects of various excipients on the coalescence stability of emulsion droplets. © 2004 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 93:2994,3003, 2004 [source] Development of New Microencapsulation Techniques Useful for the Preparation of PLGA MicrospheresMACROMOLECULAR RAPID COMMUNICATIONS, Issue 21 2006Hongkee Sah Abstract Summary: Intensive efforts were made to develop an efficient, novel microencapsulation system useful to encapsulate a model drug, risperidone, to PLGA microspheres. Methyl dichloroacetate was used as a dispersed solvent for the first time, since it possessed excellent solvency power on PLGA and readily underwent ammonolysis. A dispersed phase composed of methyl dichloroacetate, risperidone, and PLGA was emulsified in an aqueous phase to form an O/W emulsion. Adding ammonia solution into the emulsion rapidly converted methyl dichloroacetate into water-soluble dichloroacetamide and methanol. As a result, emulsion droplets were immediately transformed into hardened microspheres. The new microencapsulation system allowed us to make PLGA microspheres with a drug payload of >40 wt.-% and attain almost complete encapsulation efficiencies. In summary, preparing an O/W emulsion and subjecting the emulsion to ammonolysis led to development of an efficient, novel microencapsulation system. It was anticipated that the new system could make it possible to load other bioactive materials into microspheres made of various types of hydrophobic polymers. SEM micrographs of the external and internal morphology of PLGA/risperidone microspheres. [source] Cell-free Protein Synthesis through Solubilisate Exchange in Water/Oil Emulsion CompartmentsCHEMBIOCHEM, Issue 8 2004Adriana V. Pietrini Dr. Abstract This work is aimed at finding conditions under which synthetic compartments used as cell models can fuse with each other and allow reagents contained in the different compartments to react. This goal seems to be best achieved by the use of water in oil emulsions (w/o) with dimensions in the range of 30,60 ,m. In particular, cell-free EGFP (enhanced green fluorescent protein) synthesis takes place in Tween 80/Span 80 w/o emulsions, and the extent of the reaction can be monitored directly by fluorescence. The medium is mineral oil, containing 0.5,% v/v aqueous solution. Different premixing configurations of the components (plasmid, amino acids, E. Coli extract) are used and compared. The in vitro synthesis of EGFP in emulsion droplets proceeds for 1 h, and the yield is 7.5 ng,,L,1protein. EGFP synthesis in aqueous solution takes place for at least 5 h. The yield is 10.5 ng,,L,1protein after 1 h and 15.8 ng,,L,1protein after 5 h.The results with the w/o emulsions show that solubilisate exchange takes place among the different water droplets, but it is not possible to demonstrate clearly that a true fusion takes place. [source] | |||||||||||||||||||||||||