360-degree mixed reality volumetric display using an asymmetric diffusive holographic optical element.

Volumetric display technique has a great advantage of displaying realistic three-dimensional contents with a 360-degree viewing angle. However, most volumetric displays cannot provide mixed reality because their screens inside the displays obstruct the external scene. We design a 360-degree mixed-reality volumetric display using an asymmetric diffusive holographic optical element (ADHOE). The ADHOE has wavelength selectivity, and it diffuses the light with the only specific wavelength for the virtual object, so it is possible to optically combine the virtual object and the real scene. Also, the ADHOE has different vertical and horizontal diffusing angles, and it is suitable for a horizontal-parallax-only application. In our system, the parallax images are generated by the DMD, and they are projected sequentially on the ADHOE. The ADHOE is shaped as a slanted curved surface with respect to the optical axis, and some annoying color dispersion is observed due to the mismatch between the diffraction peak points of two different wavelengths. In order to solve this problem, the carrier frequency is applied to green elemental images and the proper Fourier filter cuts off the unwanted diffraction peak points. The Fourier transform with 2f optics is built to record the ADHOE where the angular spectral bandwidth is determined by adjusting the width of the incident object light. A 360-degree see-through display with ADHOE is implemented and the feasibility of mixed reality is verified successfully.

Spread spectrum SERS allows label-free detection of attomolar neurotransmitters.

The quantitative label-free detection of neurotransmitters provides critical clues in understanding neurological functions or disorders. However, the identification of neurotransmitters remains challenging for surface-enhanced Raman spectroscopy (SERS) due to the presence of noise. Here, we report spread spectrum SERS (ss-SERS) detection for the rapid quantification of neurotransmitters at the attomolar level by encoding excited light and decoding SERS signals with peak autocorrelation and near-zero cross-correlation. Compared to conventional SERS measurements, the experimental result of ss-SERS shows an exceptional improvement in the signal-to-noise ratio of more than three orders of magnitude, thus achieving a high temporal resolution of over one hundred times. The ss-SERS measurement further allows the attomolar SERS detection of dopamine, serotonin, acetylcholine, γ-aminobutyric acid, and glutamate without Raman reporters. This approach opens up opportunities not only for investigating the early diagnostics of neurological disorders or highly sensitive biomedical SERS applications but also for developing low-cost spectroscopic biosensing applications.

Design of Bio-Impedance Electrode Topologies for Specific Depth Sensing in Skin Layer.

Bio-impedance analysis provides non-invasive estimation of body composition. Recently, applications based on bio-impedance measurement in skin tissue such as skin cancer diagnosis and skin composition monitoring have been studied. For scanning the electrical properties along the skin depth, the relationship between the electrode topologies and the depth sensitivity should be clarified. This work reports a systematic analysis on designing line electrode topologies to measure the bio-impedance of the skin layer at specific depth using a finite element method (FEM). Four electrodes consisting of two outer current electrodes and two inner voltage electrodes in the form of Wenner-Schlumberger array were employed on the top of a collagen layer as a skin model. The numerical results demonstrate a change in the effective depth of measurement depending on the electrode topologies, which also have a good agreement with an analytic solution. This study suggests a decision guideline for designing the electrode topologies to achieve target depth sensitivity in bio-impedance measurement of skin tissue.Clinical Relevance-This establishes the effect of electrode topologies on depth sensitivity in bio-impedance measurements in skin layer.

Nanoplasmonic Alloy of Au/Ag Nanocomposites on Paper Substrate for Biosensing Applications.

Plasmonic alloy has attracted much interest in tailoring localized surface plasmon resonance (LSPR) for recent biosensing techniques. In particular, paper-based plasmonic substrates allow capillary-driven lateral flow as well as three-dimensional metal nanostructures, and therefore they become actively transferred to LSPR-based biosensing such as surface-enhanced Raman spectroscopy (SERS) or metal-enhanced fluorescence (MEF). However, employing plasmonic alloy nanoislands on heat-sensitive substrate is still challenging, which significantly inhibits broad-range tailoring of the plasmon resonance wavelength (PRW) for superior sensitivity. Here we report paper-based plasmonic substrate with plasmonic alloy of Au/Ag nanocomposites for highly sensitive MEF and SERS biosensing applications. The nanofabrication procedures include concurrent deposition of Au and Ag below 100 °C without any damage on cellulose fibers. The Au/Ag nanocomposites feature nanoplasmonic alloy with single plasmon peak as well as broad-range tunability of PRW by composition control. This paper-based plasmonic alloy substrate enables about twofold enhancement of fluorescence signals and selective MEF after paper chromatography. The experimental results clearly demonstrate extraordinary enhancement in SERS signals for picomolar detection of folic acid as a cancer biomarker. This new method provides huge opportunities for fabricating plasmonic alloy on heat-sensitive substrate and biosensing applications.

Plasmonic Schirmer Strip for Human Tear-Based Gouty Arthritis Diagnosis Using Surface-Enhanced Raman Scattering.

Biomarkers in tear fluid have attracted much interest in daily healthcare sensing and monitoring. Recently, surface-enhanced Raman scattering (SERS) has enabled highly sensitive label-free detection of small molecules. However, a highly stable straightforward tear assay with superior sensitivity is still under development in tear collection and analysis. Here we report a plasmonic Schirmer strip for on-demand, rapid, and simple identification of biomarkers in human tears. The diagnostic strip features gold nanoislands directly and evenly formed on the top surface of cellulose fibers, which maintain a hygroscopic nature for an efficient collection of tear production as well as provide plasmonic enhancement in SERS signals for identification of tear molecules. The uric acid in human tears was quantitatively detected at physiological levels (25-150 µM) by using SERS. The experimental results also clearly reveal a strong linear correlation between uric acid level in both human tears and blood for gouty arthritis diagnosis. This functional paper strip enables noninvasive diagnosis of disease-related biomarkers and healthcare monitoring using human tears.

Silver nanoislands on cellulose fibers for chromatographic separation and ultrasensitive detection of small molecules.

High-throughput small-molecule assays play essential roles in biomedical diagnosis, drug discovery, environmental analysis, and physiological function research. Nanoplasmonics holds a great potential for the label-free detection of small molecules at extremely low concentrations. Here, we report the development of nanoplasmonic paper (NP-paper) for the rapid separation and ultrasensitive detection of mixed small molecules. NP-paper employs nanogap-rich silver nanoislands on cellulose fibers, which were simply fabricated at the wafer level by using low-temperature solid-state dewetting of a thin silver film. The nanoplasmonic detection allows for the scalable quantification and identification of small molecules over broad concentration ranges. Moreover, the combination of chromatographic separation and nanoplasmonic detection allows both the highly sensitive fluorescence detection of mixed small molecules at the attogram level and the label-free detection at the sub-nanogram level based on surface-enhanced Raman scattering. This novel material provides a new diagnostic platform for the high-throughput, low-cost, and label-free screening of mixed small molecules as an alternative to conventional paper chromatography.

Electrokinetic preconcentration of small molecules within volumetric electromagnetic hotspots in surface enhanced Raman scattering.

The on-chip integration of a preconcentration chamber for ultrasensitive surface-enhanced Raman scattering (SERS) is shown. Small molecules are preconcentrated using 3D volumetric electromagnetic hotspots. The experimental results demonstrate an enhancement of the SERS signals of over two orders of magnitude, which allows the fingerprinting of neurotransmitter molecules at the nanomolar level and furthers the selective detection of oppositely charged molecules. This on-chip integration will provide new directions for ultrasensitive SERS applications.