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Opportunities for near-infrared thermal ablation of colorectal metastases by guanylyl cyclase C-targeted gold nanoshells.

Colorectal cancer is the third most common malignancy and the second most common cause of cancer-related mortality worldwide. While surgery remains the mainstay of therapy, approximately 50% of patients who undergo resection develop parenchymal metastatic disease. Unfortunately, current therapeutic regimens offer little improvement to the survival of patients with parenchymal metastases in the liver and lung. In that context, there is a significant unrealized opportunity at the intersection of engineering and biology for the development of novel targeted therapeutic approaches to colorectal cancer metastases. This opportunity exploits the discovery that an intestinal receptor, guanylyl cyclase C, which mediates diarrhea induced by bacterial heat-stable enterotoxins (STs), is over-expressed by metastatic colorectal tumors only. Moreover, it leverages recent advances in the fabrication of metal nanoshells with defined thicknesses absorb near-infrared (NIR) light, resulting in resonance and transfer of thermal energies of more than 40 degrees C. Thus, the conjugation of ST to gold nanoshells, which can undergo resonance excitation by NIR light and emit heat, represents a previously unrecognized approach for the targeted therapy of parenchymal colorectal cancer metastases, specifically to the liver and lung. This article discusses the potential of ST-targeted nanoshells for NIR thermal ablation of metastatic colorectal tumors and highlights the significant challenges and solutions linked to the translation of this emerging technology to patient care.

Biomarkers, Tumor↗

Temperature-sensitive polymer-nanoshell composites for photothermally modulated drug delivery.

Composites of thermally sensitive hydrogels and optically active nanoparticles have been developed for the purpose of photothermally modulated drug delivery. Copolymers of N-isopropylacrylamide (NIPAAm) and acrylamide (AAm) exhibit a lower critical solution temperature (LCST) that is slightly above body temperature. When the temperature of the copolymer exceeds the LCST, the hydrogel collapses, causing a burst release of any soluble material held within the hydrogel matrix. Gold-gold sulfide nanoshells, a new class of nanoparticles designed to strongly absorb near-infrared light, have been incorporated into poly(NIPAAm-co-AAm) hydrogels for the purpose of initiating a temperature change with light; light at wavelengths between 800 and 1200 nm is transmitted through tissue with relatively little attenuation, absorbed by the nanoparticles, and converted to heat. Significantly enhanced drug release from composite hydrogels has been achieved in response to irradiation by light at 1064 nm. We have investigated the release of methylene blue and proteins of varying molecular weight. Additionally, the nanoshell-composite hydrogels can release multiple bursts of protein in response to repeated near-IR irradiation.

Acrylamides↗

Rapid detection of Escherichia coli by using antibody-conjugated silver nanoshells.

Silver shells of 20 nm thickness have been deposited on silica particles of 200 nm diameter with narrow size distribution. Silver nanoshells dispersed in water exhibit a strong surface plasmon resonance band at 443 nm. This band was found to be very sensitive to rabbit immunoglobulin G antibodies, which were anchored on the nanoshells. These in turn could be utilized to detect the presence of small (approximately 5) to large numbers (approximately 10(9)) of Escherichia coli in water. The protocol presented here proves to be a specific, rapid, reliable, and inexpensive method to detect E. coli.

Antigen-Antibody Complex↗

Synthesis and characterization of Ag nanoshells by a facile sacrificial template route through in situ replacement reaction.

A facile in situ replacement reaction route was successfully introduced for synthesizing Ag nanoshells with outer diameters of 40-50 nm and inner diameters of 20-30 nm using Co nanoparticles as sacrificial templates. The products were characterized by XRD, TEM, SAED, and UV-vis absorption spectra. The formation mechanism was also discussed. The reaction driving force comes from the large reduction potential gap between the Ag+/Ag and Co2+/Co redox couples, which results in the consumption of Co cores and the formation of a hollow cavity of Ag nanoshells. The UV-vis spectrum of this nanostructure exhibits a distinct difference from that of solid nanoparticles, which makes it a good candidate for application in photothermal materials.

Journal Article↗

Interfacial synthesis of dendritic platinum nanoshells templated on benzene nanodroplets stabilized in water by a photocatalytic lipoporphyrin.

Nanoscale metal shells have many potential uses and in some applications offer significant advantages over nanoparticles. The synthesis of platinum nanoshells using stabilized nanodroplets of benzene in water as growth templates is described; the nanodroplets are stabilized by a surfactant-like tin(IV)-porphyrin complex localized at the benzene-water interface. The porphyrin also acts as a photocatalyst that reduces the platinum complex and deposits metal onto the nanodroplets to form dendritic metal nanoshells. Below the solubility limit of benzene in water, the lipoporphyrin-stabilized nanodroplets have a reproducible number, size distribution, and surface area, which allows the thickness of the platinum shell walls to be controlled by changing the amount of platinum complex. Nanoscale platinum shells with magnetic interiors can be made by dispersing Fe3O4 nanoparticles in the benzene nanodroplets.

Journal Article↗

Cu nanoshells: effects of interband transitions on the nanoparticle plasmon resonance.

The optical properties of metals arise both from optical excitation of interband transitions and their collective electronic, or plasmon, response. Here, we examine the optical properties of Cu, whose strong interband transitions dominate its optical response in the visible region of the spectrum, in a nanoshell geometry. This nanostructure permits the geometrical tuning of the nanoparticle plasmon energy relative to the onset of interband transitions in the metal. Spectral overlap of the interband transitions of Cu with the nanoshell plasmon resonance results in a striking double-peaked plasmon resonance, a unique phenomenon previously unobserved in other noble or coinage metal nanostructures.

Copper↗

Optimization of plasmonic heating by gold nanospheres and nanoshells.

Gold nanoparticles have strong and tunable absorption peaks in their optical extinction spectra, a phenomenon that has recently been exploited to generate localized heating in the vicinity of these particles. However the optimum particle geometry and illumination regime to maximize these effects appears not to have been previously examined in any detail. Here we show that the interplay between the particles' absorption cross-sections, volume, and surface area lead to there being specific conditions that can maximize particle temperature and surface heat flux. Optical absorption efficiencies were calculated from the formulation of Mie, and radiative, convective, and conductive heat transfer models were used to model the thermal performance of particles in different situations. Two technologically relevant scenarios for illumination, namely, irradiation by sunlight at 800 W/m2 and by a monochromatic laser source of 50 kW/m2 tuned to the peak absorption wavelength, were considered. For irradiation by sunlight, the resultant heat flux is optimized for an 80 nm diameter nanoshell with an aspect ratio of 0.8, while for irradiation by laser the maximum heat flux is found for 50 nm nanoshells, with an aspect ratio of 0.9.

Journal Article↗

Surface-enhanced Raman scattering on nanoshells with tunable surface plasmon resonance.

Fabrication, characterization, and optical enhancement applications of bimetallic AgAu nanoparticles and nanoshells are reported. Nanoparticles with tunable surface plasmon resonances are synthesized at room temperature and characterized by transmission electron microscopy, X-ray photoelectron spectroscopy, and photon correlation spectroscopy. The collective electron oscillation of the nanoparticles shows a controllable tunability in the 400-990 nm spectral range, in agreement with plasmon absorption calculated using Mie theory, providing an optimum substrate for surface plasmon-assisted enhanced spectroscopy. Surface-enhanced Raman scattering experiments show that the average enhancement factor obtained with nanoshells could be higher than those obtained with silver sols.

Journal Article↗

Synthesis of tubular gold and silver nanoshells using silica nanowire core templates.

We report the synthesis of tubular gold and silver nanoshells on silica nanowire core templates in solution. Silica nanowires were synthesized and characterized with optical and NMR methods. Gold nanoparticle seeds (2 to 3 nm) with weak repulsive surfactants such as tetrakis-hydroxymethyl-phosphonium chloride (THPC) were conjugated to the surface of these nanowires. A regrowth process was initiated from these nanoparticles on the surface of the silica nanowires dispersed in gold or silver stock solutions in the presence of reducing agents. Micrometers-long gold and silver tubular nanoshells (80-150 nm o.d.) were made, fully covering the silica nanowires.

Journal Article↗

Plasmon hybridization in nanoshell dimers.

We extend the plasmon hybridization method to investigate the plasmon modes of metallic nanoshell dimers. The formalism is also generalized to include the effects of dielectric backgrounds. It is shown that the presence of dielectrics shifts the plasmon resonances of the individual nanoparticles to lower energies and screens their interaction in the dimer configuration. The net result is a redshift of dimer energies compared to the system without dielectrics and a weaker dependence of the dimer plasmon energies on dimer separation. We calculate the plasmon energies and optical absorption of nanoshell dimers as a function of dimer separation. The results are in excellent agreement with the results of finite difference time domain simulations.

Journal Article↗

Density-matrix calculation of surface-enhanced Raman scattering for p-mercaptoaniline on silver nanoshells.

A theoretical analysis of recent experiments measuring the 782 nm surface-enhanced Raman scattering of p-mercaptoaniline bound to silver nanoshells of different core and shell radii [J. B. Jackson and N. J. Halas, Proc. Natl. Acad. Sci. U.S.A. 101, 17930 (2004)] is performed. Electronic structure Hartree-Fock and density-functional theory calculations for Ag salts of p-mercaptoaniline are used to characterize observed vibrational modes and configuration-interaction singles calculations are carried out to examine excited states. Multimode vibronic density-matrix calculations are then made including one excited electronic state, using a classical description of the strong local fields and a phenomenological treatment of relaxations. The spectral behavior as a function of both nanoshell surface-plasmon resonance position and molecular electronic spacing is examined.

Journal Article↗

Atomic-focuser imaging in electron nanodiffraction from carbon nanoshells

When nanodiffraction patterns are obtained by transmission through the top and bottom walls of near-spherical, hollow carbon nano-shells, using the focused probe of a STEM instrument, a graphitic crystal in one wall may act as an atomic focuser to produce high-resolution images of small regions of the other wall within the central beam and the diffraction disks of the nanodiffraction pattern. A theoretical analysis of the imaging process is given. Images showing one- and two-dimensional periodicities, with fringe spacings as small as 0.124 nm, and also images showing non-periodic features have been obtained from carbon nanoshells having diameters of the order of 100 nm.

Journal Article↗

A whole blood immunoassay using gold nanoshells.

A rapid immunoassay capable of detecting analyte within complex biological media without any sample preparation is described. This was accomplished using gold nanoshells, layered dielectric-metal nanoparticles whose optical resonance is a function of the relative size of its constituent layers. Aggregation of antibody/nanoshell conjugates with extinction spectra in the near-infrared was monitored spectroscopically in the presence of analyte. Successful detection of immunoglobulins was achieved in saline, serum, and whole blood. This system constitutes a simple immunoassay capable of detecting sub-nanogram-per-milliliter quantities of various analytes in different media within 10-30 min.

Animals↗

Layer-by-layer deposition of bimetallic nanoshells on functionalized polystyrene beads.

Bimetallic nanoshells on functionalized polystyrene beads have been fabricated through a layer-by-layer deposition technique exploiting electrostatic interaction. The synthesis has been achieved through the immobilization and successive reduction of the corresponding precursor ions. It has been shown that the thickness of the shell can be controlled by a number of cyclic depositions of respective metals onto the surface of the polystyrene beads.

Journal Article↗

Dye-labeled silver nanoshell-bright particle.

Silica beads with average diameters of 40-600 nm were prepared, and Ru(bpy)3(2+) complexes were incorporated into the beads. These beads were coated by silver layer by layer to generate porous but continuous metal nanoshells. The thicknesses of these metal shells were 5-50 nm. The emission band from the dyes in the silica cores was more narrow and the intensity was enhanced with growth of silver shell thickness due to coupling of the emission light from Ru(bpy)3(2+) in the cores with the metal plasmon from the silver shells. The enhancement of emission intensity was also dependent on the size of the silica core, showing that the enhancement efficiency decreased with an increase in the size of the silica beads. Lifetime measurements support the coupling mechanism between the dye and metal shell. This study can be used to develop novel dye-labeled metal particles with bright and narrow emission bands.

Fluorescent Dyes↗

Layer-by-Layer electrostatic self-assembly of polyelectrolyte nanoshells on individual carbon nanotube templates.

Carbon nanotubes have been featured prominently in the nanotechnology research for some time, yet robust strategies for noncovalent chemical modification of the nanotube surface are still missing. Such strategies are essential for the creation of functional device architectures. Here, we present a new general procedure for carbon nanotube modification based on polyelectrolyte layer-by-layer assembly. We have built multilayer structures around individual carbon nanotube bridges by first modifying the nanotube surface with a pyrene derivative followed by layer-by-layer deposition of polyelectrolyte macroions on the nanotube. Transmission electron microscopy and scanning confocal fluorescence microscopy images confirm the formation of nanometer-thick amorphous polymer nanoshells around the nanotubes. These multilayer polyelectrolyte shells on individual carbon nanotubes introduce nearly unlimited opportunities for the incorporation of various functionalities into nanotube devices, which, in turn, opens up the possibility of building more complex multicomponent structures.

Journal Article↗

Gold nanoshells on polystyrene cores for control of surface plasmon resonance.

A method is presented for synthesizing core-shell structures consisting of monodisperse polystyrene latex nanospheres as cores and gold nanoparticles as shells. Use of polystyrene spheres as the core in these structures is advantageous because they are readily available commercially in a wide range of sizes, and with dyes or other molecules doped into them. Gold nanoparticles, ranging in size from 1 to 20 nm, are prepared by reduction of a gold precursor with sodium citrate or tetrakis(hydroxymethyl)phosphonium chloride (THPC). Carboxylate-terminated polystyrene spheres are functionalized with 2-aminoethanethiol hydrochloride (AET), which forms a peptide bond with carboxylic acid groups on their surface, resulting in a thiol-terminated surface. Gold nanoparticles then bind to the thiol groups to provide up to about 50% coverage of the surface. These nanoparticles serve as seeds for growth of a continuous gold shell by reduction of additional gold precursor. The shell thickness and roughness can be controlled by the size of the nanoparticle seeds as well as by the process of their growth into a continuous shell. By variation of the relative sizes of the latex core and the thickness of the gold overlayer, the plasmon resonance of the nanoshell can be tuned to specific wavelengths across the visible and infrared range of the electromagnetic spectrum, for applications ranging from the construction of photonic crystals to biophotonics. The position and width of the plasmon resonance extinction peak are well-predicted by extended Mie scattering theory.

Journal Article↗

Stabilized porous phospholipid nanoshells.

Chemically stabilized, porous phospholipid nanoshells (PPNs) were prepared via copolymerization of reactive monomers with unilamellar bis-Sorbyl phosphatidylcholine vesicles. The resulting PPN vesicular assemblies possess a highly porous membrane structure that allows passage of small molecules, which can react with encapsulated proteins and reporters. The unique combination of membrane stability and porosity will prove useful for preparing nanometer-sized sensor, container, and reactor platforms stable in harsh chemical and biological environments.

Genes, Reporter↗