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Biomedical subjects

Dayang Wang

Publications and source records attributed to Dayang Wang.

11 recordsLinked to original sources

Manipulation of aqueous growth of CdTe nanocrystals to fabricate colloidally stable one-dimensional nanostructures.

The present article is devoted to systematically exploring the influence of various experimental variables, including the precursor concentration, the ligand nature, the counterion type, the Cd-to-Te molar ratio, pH, and temperature, on the aqueous growth of CdTe nanocrystals. The growth may be divided into two stages: the early fast growth stage and the later slow growth stage. The later stage is found to be dominated by Ostwald ripening (OR), being strongly dependent on all experimental conditions. In contrast, the early stage is dominated by adding monomers to nanocrystals, which may be dramatically accelerated by lowering precursor concentrations and using ligands with a molecular structure similar to that of thioglycolic acid (TGA). This fast growth stage is similar to that observed during organometallic growth of nanocrystals in hot organic media. On the basis of this finding, one-dimensional wurtzite CdTe nanostructures can be directly prepared in aqueous media by storing rather dilute precursor solution (2.4 mM with reference to ligand) in the presence of TGA at lower temperature (from room temperature to 80 degrees C). A low growth temperature is used to suppress OR during crystal growth. In addition, the simultaneous presence of both TGA-like ligand and 1-thioglycerol or 2-mercaptoethylamine leads to formation of colloidally stable 1D CdTe nanostructures with controlled aspect ratios.

Journal Article↗

Directing the self-assembly of nanocrystals beyond colloidal crystallization.

This article gives an overview of recent progress in the self-assembly of nanocrystals. Classic self-assembly of nanocrystals, so-called colloidal crystallization driven by van der Waals interactions, is highlighted first with an emphasis on the recent realization of binary colloidal crystals. Next, new developments in the integration of nanocrystals into clusters based on electrostatic interactions, hydrogen bonding and dipole-dipole interactions are summarized, shedding light on the defined control of the interactions between the nanocrystals. Finally, the fabrication of heterogenous nanocrystals, obtained via either phase selective modification at the water/oil interface or facet-selective crystal growth on non-spherical nanocrystals is discussed. These last materials may provide significant building blocks for mimicking molecular self-assembly.

Adsorption↗

Chitosan-mediated synthesis of gold nanoparticles on patterned poly(dimethylsiloxane) surfaces.

Synthesis of gold nanoparticles on surfaces has been accomplished by the incubation of poly(dimethylsiloxane) (PDMS) films in tetrachloroauric(III) acid and chitosan solution at room temperature and 4 degrees C. One important point in the present study is that the synthesis selectively occurred on the PDMS surface. These observations are substantially different from the reaction in solution, in which no particles can be formed at room temperature. Computation of surface plasmon bands (SPBs) based on Mie theory suggests that the particles are partially coated by chitosan molecules, and the experimental results confirm the theoretical calculations. The proposed mechanism is that chitosan molecules adsorbed or printed on the PDMS surfaces act as reducing/stabilizing agents. Furthermore, PDMS films patterned with chitosan could induce localized synthesis of gold nanoparticles in regions capped with chitosan only. In this way, colloidal patterns were fabricated on the surfaces with high spatial selectivity simultaneously with the synthesis of the particles. Surface-induced fluorescence quenching was observed in the regions capped with gold nanoparticles as well.

Chitosan↗

pH-responsive capsules derived from nanocrystal templating.

In the current work we demonstrate a facile and versatile way to create hydrophilic polymeric capsules by integration of Au nanocrystal templating, surface-initiated atom-transfer radical polymerization, and selective chemical cross-linking of polymer shells. Capsules of the homopolymer of 2-(dimethylamino)ethyl methacrylate and its copolymers with 2-(diethylamino)ethyl methacrylate and poly(ethylene glycol) methyl ether methacrylate were constructed. They swell at low pH and shrink at high pH. On the basis of the pH sensitivity of the resulting capsules, encapsulation and release of a drug model, rhodamine 6G, were realized. Furthermore, by cleaving Au-S bonds between Au cores and polymer shells, capsules containing free Au cores were generated, paving a simple pathway to introduce more functionality to the polymeric capsules.

Journal Article↗

Fabrication of superhydrophobic surfaces from binary colloidal assembly.

In this work, superhydrophobic surfaces were derived from binary colloidal assemblies. CaCO(3)-loaded hydrogel spheres and silica or polystyrene ones were consecutively dip-coated on silicon wafers. The former assemblies were recruited as templates for the latter self-assembly. Due to the hydrophilicity difference between silicon wafers and CaCO(3)-loaded hydrogel spheres, the region selective localization of silica or polystyrene spheres leads to irregular binary structures with a hierarchical roughness. The subsequent modification with low surface energy molecules yields a superhydrophobic surface. The heating treatment may largely enhance the mechanical stability of the resulting binary structures, which allows regeneration of the surface superhydrophobicity, providing a good durability in practice.

Journal Article↗

Patterning microsphere surfaces by templating colloidal crystals.

By using the upper single or double layers in colloidal crystals as masks during Au vapor deposition, various Au patterns have been successfully constructed on the surfaces of the lower spheres. The dimension and geometry of the Au patterns obtained are dependent on the orientation of the colloidal crystal templates. Our patterning procedure is independent of the curvature and chemical composition of the surfaces, which definitely pave a promising way to pattern highly curved surfaces.

Journal Article↗

Magnetic colloidosomes derived from nanoparticle interfacial self-assembly.

Based on the interfacial self-assembly of magnetite nanoparticles, we demonstrate the formation of colloidosomes with shells predominantly composed of monolayers of liquid-like, close-packed nanoparticles. The gelation of aqueous phase with agarose leads to robust and water-dispersible nanoparticle colloidosomes, allowing encapsulation of various water soluble materials. The cutoff of the nanoparticle colloidosomes obtained is primarily defined by the nanoparticle size. This controllable permeability should be of great importance for the encapsulation application.

Colloids↗