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T1 - Overgrowth of gold nanorods by using a binary surfactant mixture

T1 - Immobilization of gold nanorods onto acid-terminated self-assembled monolayers via electrostatic interactions

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Extinction spectra of silica-coated gold nanorods are shown in

Since silica shells were first coated onto gold nanoparticles using amino-terminated silane coupling agents as the primer to make the gold surface vitreophilic,34 various routes have been reported to prepare such silica-coated nanocomposites.35-38 When coating CTAB-capped gold nanorods, it is well-known thatthe concentrationofthe CTAB surfactantusedmust beclose to its critical micelle concentration.39 However, large amounts of CTAB in the system make the displacement by surface-coupling silane agents difficult due to the strong binding of CTAB molecules to the gold surface. Thus, with the CTAB-based approach, it has been a challenge to develop effective methods to coat gold nanorods with uniform silica shells in a controlled fashion.39-43 These problems tend to amplify for nanorods with the comparatively large aspect ratio needed for a near-IR plasmon band.

T1 - The stabilization and targeting of surfactant-synthesized gold nanorods

For a typical aggregation test, an aqueous dispersion of gold nanorods (0.5 mL, 2.72 nM, 1.6 OD) was incubated with either BaCl2 (0.5 mL, 66 mM, IS=200 mM) or NaCl (0.5 mL, 0.2 mM, IS=200 mM). Directly after addition of the salt, UV-VIS absorption spectra were recorded at 20 s time intervals.

Silica-Coated Gold Nanorods with a Gold Overcoat

T1 - Library approach for reliable synthesis and properties of DNA-gold nanorod conjugates

Silica-Coated Gold Nanorods with a Gold Overcoat: Controlling Optical Properties by Controlling the Dimensions of a Gold-Silica-Gold Layered Nanoparticle

We report the immobilization of gold nanorods onto self-assembled monolayers (SAMs) of 16-mercaptohexadecanoic acid (16-MHA). The simple two step protocol involves formation of a SAM of 16-MHA molecules onto gold-coated glass slides and subsequent immersion of these slides into the gold nanorod solution. The nanorods, formed by a seed-mediated, surfactant-assisted synthesis protocol, are stabilized in solution due to surface modification by the surfactant cetyltrimethylammonium bromide (CTAB). Attractive electrostatic interactions between the carboxylic acid group on the SAM and the positively charged CTAB molecules are likely responsible for the nanorod immobilization. UV-vis spectroscopy has been used to follow the kinetics of the nanorod immobilization. The nature of interaction between the gold nanorods and the 16-MHA SAM has been probed by Fourier transform infrared spectroscopy (FTIR). The surface morphology of the immobilized rods is studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM) measurements. SEM was also used to determine the density of the immobilized nanorods as a function of the pH of immobilization. Control over the surface coverage of the immobilized gold nanorods has been demonstrated by simple pH variation. Such well-dispersed immobilized gold nanorods with control over the surface coverage could be interesting substrates for applications such as surface-enhanced Raman spectroscopy (SERS).

Fig. 1. TEM image of gold nanorods.

Fig. 1. TEM image of gold nanorods.

We can conclude that iodide impurities can vary significantly from lot to lot within a product, to such an extent that there is no guarantee that gold nanorods can be synthesized with one or other CTAB product.

If the gold nanorods were washed several times, silica deposition was not ideal. Specifically, under these conditions, we tended to make more gold-free silica particles and nonspherical particles with a core of aggregated gold nanorods (see Supporting Information). If the gold nanorods were not washed, a large amount of aggregated precipitate appeared in the course of the sol-gel process. Therefore, we conclude that a single wash is an effective pretreatment step conducive for silica deposition from TEOS on CTAB-coated gold nanoparticles.

3. Manohar S. Gold nanorods as molecular contrast agents in photoacoustic imaging: the promises and the caveats.  2011;6:389-400
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  • Photochemical Synthesis of Gold Nanorods - Journal of …

    KW - plasmonic gold nanorod

  • Plasmonic sensing of CTAB in gold nanorods ..

    Keywords: gold nanorods, optoacoustic, dendritic polyglycerolsulfate, inflammation, polyanion, MSOT.

  • a history of gold nanorod synthesis.

    7. Zhang Z, Wang J, Chen C. Gold nanorods based platforms for light-mediated theranostics. 2013;3:223-38

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Gold nanorods: Synthesis, characterization and applications

PEGylation was performed by incubating the AuNR-CTAB with 1.24·105 eq. of mPEG1000 -SH as this ratio was identified to result in the highest possible degree of functionalization by a simple ligand exchange as the binding process is relatively slow []. The ligand exchange was confirmed macroscopically due to the perfect dispersability of the AuNRs in ethanol. As additional proof, an evenly spaced gold nanorod assembly with an interparticle diameter approximately resembling twice the length of an extended mPEG1000-SH chain was visualized by transmission electron microscopy (TEM) (: Figure S1B). Attenuated total reflectance - fourier transform infrared spectroscopy (ATR-FTIR) measurements further confirmed the functionalization with mPEG1000-SH due to the appearance of the characteristic (C-O-C) stretching vibration at 1100 cm-1 (Figure ).

Gold Nanorod Synthesis - Osujilab Wiki

(A) Synthesis of thioctic acid functionalized dendritic polyglycerolsulfate amide coupling. (B) Functionalization of CTAB double-layer coated gold nanorods with mPEG1000-SH followed by a partial replacement of mPEG1000-SH with TA-dPGS 10 kDa thermally induced ligand exchange reaction. Note: Elements in the scheme are not drawn to scale.

Synthesis of silica-coated gold nanorod as Raman tags …

The removal of unbound TA-dPGS from the colloidal solution after purification is essential for an accurate determination of the AuNR-dPGS targeting potential. Unfortunately, zeta potential measurements only give cumulative information about the colloidal solution and thus prohibit identification of unbound ligands. Even though altering SPR bands due to plasmon-plasmon interactions upon reduction of the interparticle diameter by cross-linking has been reported in literature [,-], this has not been used as an analytic tool to assess colloidal purity. We employed BaCl2 to induce agglomeration of sulfate functionalized gold nanorods, which confirmed a successful functionalization with dPGS when the plasmon resonance was altered. The nanorod dispersion was purified to BaCl2 incubation several times by centrifugation. After each purification cycle, a small sample of the redispersed colloidal dispersion was removed for the BaCl2 agglomeration assay. The respective samples were incubated with BaCl2 and their absorption monitored time-resolved UV-VIS spectroscopy. Surprisingly, no change in plasmon resonance, and thus agglomeration, was observed for samples of unpurified AuNR-dPGS after incubation with BaCl2. There was also no agglomeration for samples of AuNR-dPGS after four purification cycles (: Figure S7). Only samples of five-fold purified AuNR-dPGS exhibited a dramatic change of their plasmon resonance seconds after the addition of BaCl2 (Figure ).

NanoComposix’s gold nanorods are CTAB free where all ..

Figure 1. (a, b) TEM images of gold nanorods grown in aqueous solution indicate an average length and width of 59.2 ( 4.8 and 19.9 ( 2.4 nm, respectively, for the preparative conditions employed (see Experimental Section). (c) Normalized extinction spectrum obtained from an aqueous dispersion of these gold nanorods.

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