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The plasmonic properties of noble metals facilitate their use for in-vivo bio-applications such as targeted drug delivery and cancer cell therapy. Nanosilver is best suited for such applications as it has the lowest plasmonic losses among all such materials in the UV-visible spectrum. Its toxicity, however, can destroy surrounding healthy tissues and thus, hinders its safe use. Here, that toxicity against a model biological system (Escherichia coli) is "cured" or blocked by coating nanosilver hermetically with a about 2 nm thin SiO2 layer in one-step by a scalable flame aerosol method followed by swirl injection of a silica precursor vapor (hexamethyldisiloxane) without reducing the plasmonic performance of the enclosed or encapsulated silver nanoparticles (20 - 40 nm in diameter as determined by X-ray diffraction and microscopy). This creates the opportunity to safely use powerful nanosilver for intracellular bio-applications. The label-free biosensing and surface bio-functionalization of these ready-to-use, non-toxic (benign) Ag nanoparticles is presented by measuring the adsorption of bovine serum albumin (BSA) in a model sensing experiment. Furthermore, the silica coating around nanosilver prevents its agglomeration or flocculation (as determined by thermal annealing, optical absorption spectroscopy and microscopy) and thus, enhances its biosensitivity, including bioimaging as determined by dark field illumination.

The crystallization of PbS in aqueous solutions containing the surfactant sodium dodecyl sulfate (SDS) and hydrophilic polymers resulted in a novel type of metastable nanotubes, the walls of which consist of layers of ordered PbS nanoparticles, apparently separated by layers of surfactant molecules. Information on the mechanism of formation of these structures was obtained by focusing on the roles of the polymer, and of the insoluble lead dodecyl sulfate (Pb(DS)2) present in the system. TEM investigations of the early stages of crystallization revealed the coexistence of PbS and Pb(DS)2 precipitates, the latter being surprisingly important for nanotube formation, and allowed to follow the evolution of layered structures from combination of the two types of crystals. Six different hydrophilic polymers have been used, which interact with SDS with varying strengths. Surprisingly, and in contrast to previous hypotheses, layered nanostructures were observed in all polymer solutions, regardless of the strength of polymer-surfactant interactions. This indicates that, although the presence of a polymer is necessary, polymer-SDS interactions are not a driving force for the formation of the layered structures and nanotubes. On the contrary, the interactions between the polymer chains and the growing particles appear to be of the utmost importance. Results presented here can be interpreted in terms of two alternative mechanisms for layered nanostructure and nanotube formation. © 2006 Elsevier Inc. All rights reserved. 302 1 170 177 Cited By :7

In this work, we examine the rich crystallization behavior that occurs in PbII/S-II/poly(ethylene oxide) (PEO)/sodium dodecyl sulfate (SDS) systems, in which the anionic surfactant interacts strongly with the polymer molecules, forming micellar aggregates attached to the polymer chains above the critical association concentration. Lead sulfide crystallites are formed in the vicinity of polymer-bound micelles by adding lead and sulfide ions to the polymer-surfactant solution. Surfactant-stabilized inorganic particles adsorbed on the polymer chains combine through a polymer-mediated bridging flocculation mechanism to produce characteristic rodlike colloidal aggregates. Under certain conditions, these evolve into a range of metastable structures, composed of lead sulfide, PbS, and lead dodecyl sulfate, Pb(DS)2. XRD analysis of the metastable reaction products allows us to follow the slow kinetics of their formation and reveals a well-defined layered structure, based on lead dodecyl sulfate, the thickness of which is determined by the length of the surfactant chains. Elemental analysis, 13C- and 207Pb-NMR spectroscopy, FTIR spectroscopy, XPS, and HRTEM are used to characterize these superstructures. At other pH values and system compositions, the production of pure PbS or pure Pb(DS)2 is favored, by appropriate tuning of the concentrations of Pb2+ and S2- ions. The resulting unexpectedly rich crystallization behavior illustrates the complexity of colloidal aggregation phenomena in polymer-surfactant solutions and the significance of coupling colloidal aggregation to ionic equilibria. 105 19 4133 4144 Cited By :31