Abstract:Near-infrared
surface plasmon resonance imaging (SPRI) microscopy
is used to detect and characterize the adsorption of single polymeric
and protein nanoparticles (PPNPs) onto chemically modified gold thin
films in real time. The single-nanoparticle SPRI responses, Δ%RNP, from several hundred adsorbed nanoparticles
are collected in a single SPRI adsorption measurement. Analysis of
Δ%RNP frequency distribution histograms
is used to provide information on the size, material content, and
interparticle interactions… Show more
“…For nanobubbles, since their refractive index is nearly one, ψ is near π, and the center of the pattern is dark. This result was confirmed by the plasmonic imaging of gas vesicles with a 2 nm protein shell …”
Section: Figurementioning
confidence: 99%
“…Recently,r esearchers attempted to characterize patterns by measuring the intensity of selected particles along and across the direction of the plasmonic wave. [9,13] Although the intensity fluctuations along these lines profiled the width and shape of the pattern, the parabolic patterns were found to be almost identical for nanoparticles with different refractive indices and sizes. [13a] Therefore,t he knowledge gap between the features of parabolic patterns and the scattering properties of particles has led to al ack of methods for accurately extracting information from patterns.…”
The development of optical imaging techniques has led to significant advancements in single‐nanoparticle tracking and analysis, but these techniques are incapable of label‐free selective nanoparticle recognition. A label‐free plasmonic imaging technology that is able to identify different kinds of nanoparticles in water is now presented. It quantifies the plasmonic interferometric scattering patterns of nanoparticles and establishes relationships among the refractive index, particle size, and pattern both numerically and experimentally. Using this approach, metallic and metallic oxide particles with different radii were distinguished without any calibration. The ability to optically identify and size different kinds of nanoparticles can provide a promising platform for investigating nanoparticles in complex environments to facilitate nanoscience studies, such as single‐nanoparticle catalysis and nanoparticle‐based drug delivery.
“…For nanobubbles, since their refractive index is nearly one, ψ is near π, and the center of the pattern is dark. This result was confirmed by the plasmonic imaging of gas vesicles with a 2 nm protein shell …”
Section: Figurementioning
confidence: 99%
“…Recently,r esearchers attempted to characterize patterns by measuring the intensity of selected particles along and across the direction of the plasmonic wave. [9,13] Although the intensity fluctuations along these lines profiled the width and shape of the pattern, the parabolic patterns were found to be almost identical for nanoparticles with different refractive indices and sizes. [13a] Therefore,t he knowledge gap between the features of parabolic patterns and the scattering properties of particles has led to al ack of methods for accurately extracting information from patterns.…”
The development of optical imaging techniques has led to significant advancements in single‐nanoparticle tracking and analysis, but these techniques are incapable of label‐free selective nanoparticle recognition. A label‐free plasmonic imaging technology that is able to identify different kinds of nanoparticles in water is now presented. It quantifies the plasmonic interferometric scattering patterns of nanoparticles and establishes relationships among the refractive index, particle size, and pattern both numerically and experimentally. Using this approach, metallic and metallic oxide particles with different radii were distinguished without any calibration. The ability to optically identify and size different kinds of nanoparticles can provide a promising platform for investigating nanoparticles in complex environments to facilitate nanoscience studies, such as single‐nanoparticle catalysis and nanoparticle‐based drug delivery.
“…A variety of nanoscale particles, such as metallic nanoparticles [129], dielectric nanoparticles [130,131], protein nanoparticles [132,133] and single DNA molecules [134,135] have been observed with this system. In addition, orthogonal and complementary measurement techniques, such as electrochemistry [129,136,137] and local thermal measurement [138], have also be incorporated into the system.…”
“…SPR imaging microscopy is especially powerful in the field of polymeric and protein nanoparticle (PPNP) detection, where high throughput and high sensitivity real-time characterization of dielectric nanoparticles is required. Corn et al recently utilized SPR imaging microscopy to characterize the size, material content and the inter-particle interactions of PPNPs, in which changes in the intensity of average single-nanoparticle surface plasmon resonance image (SPRI) response (∆%R NP ) at the center of the diffraction pattern is used to quantify the bioaffinity uptake of polypeptides and proteins by a variety of solid, porous PPNPs [133]. Figure 5h shows the frequency distribution histogram of the SPR responses of NIPAm-based hydrogel nanoparticles (d = 272 nm) in both the absence and presence of melittin.…”
Section: Nanoparticle Sizing and Specificationmentioning
Abstract:The interaction between nanoparticles and the electromagnetic fields associated with optical nanostructures enables sensing with single-nanoparticle limits of detection and digital resolution counting of captured nanoparticles through their intrinsic dielectric permittivity, absorption, and scattering. This paper will review the fundamental sensing methods, device structures, and detection instruments that have demonstrated the capability to observe the binding and interaction of nanoparticles at the single-unit level, where the nanoparticles are comprised of biomaterial (in the case of a virus or liposome), metal (plasmonic and magnetic nanomaterials), or inorganic dielectric material (such as TiO 2 or SiN). We classify sensing approaches based upon their ability to observe single-nanoparticle attachment/detachment events that occur in a specific location, versus approaches that are capable of generating images of nanoparticle attachment on a nanostructured surface. We describe applications that include study of biomolecular interactions, viral load monitoring, and enzyme-free detection of biomolecules in a test sample in the context of in vitro diagnostics.
“…SPRM has been successfully employed to probe individual cells [13], bacteria and viruses [14,15], DNA [16,17], and protein structures. [18] The ultimate sensitivity of SPRM is limited by various factors. [19][20][21] One limitation is related to the fact that SPR methods are not background-free, as small changes in the light intensity need to be discriminated against a bright background.…”
We describe the development and performance of a new type of optical sensor suitable for registering the binding/dissociation of nanoscopic particles near a gold sensing surface. The method shares similarities with surface plasmon resonance microscopy but uses a completely different optical signature for reading out binding events. This new optical read-out mechanism, which we call confined optical field enhanced fluorescence emission (Cofefe), uses pulsed surface plasmon polariton fields at the gold/liquid interface that give rise to confined optical fields upon binding of the target particle to the gold surface. The confined near-fields are sufficient to induce two-photon absorption in the gold sensor surface near the binding site. Subsequent radiative recombination of the electron-hole pairs in the gold produces fluorescence emission, which can be captured by a camera in the far-field. Bound nanoparticles show up as bright confined spots against a dark background on the camera. We show that the Cofefe sensor is capable of detecting gold and silicon nanoparticles, as well as polymer nanospheres and sub-μm lipid droplets in a label-free manner with average illumination powers of less than 10 μW/μm.
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