Repairable Macroscopic Monodomain Arrays from Block Copolymers Enabled by Photoplastic and Photodielectric Effects.

Upon exposure to UV light (120 mW/cm2, λ = 365 nm), a trans-cis isomerization occurs in a cylinder-forming, azobenzene-containing block copolymer of polydimethylsiloxane-b-poly((4(phenyldiazenyl)phenoxy)hexyl acrylate) (PDMS-b-PPHA) that enables the generation of monodomains of healable, long-range ordered arrays of nanoscopic domains over macroscopic distances. The trans-cis isomerization gives rise to a significant increase in the dielectric constant (from 6.52 to 19.8 at 100 Hz, photodielectric behavior) and a dramatic decrease in the Tg (from 54 to 1 °C, photoplastic behavior) of the PPHA block. By combining these characteristics with an in-plane electric field, macroscopic monodomains of near-perfectly aligned cylindrical microdomains are achieved at low temperatures, and a damage repair is clearly uncovered, where the 300 nm wide scratches can be completely healed at 40 °C, leaving a smooth, uniformly thick film where the continuity and orientation of the aligned microdomains are restored. Subsequent exposure to visible light causes a cis-trans isomerization, increasing the matrix Tg to 54 °C, producing highly oriented and aligned PDMS cylindrical microdomains in a PPHA matrix.

A Sarcopenia Detection System Using an RGB-D Camera and an Ultrasound Probe: Eye-in-Hand Approach.

Skeletal muscle mass deficiency and quality degradation constitute sarcopenia for elderly people. Sarcopenia can result in musculoskeletal damage and accompany various metabolic problems, which make early sarcopenia diagnosis important. Various modalities, such as computed tomography (CT) and magnetic resonance imaging (MRI), have been developed for screening sarcopenia. Recently, ultrasound scanning was suggested for screening sarcopenia because of its safety, usability, and cost effectiveness. However, there has been no standardized assessment methodology for screening sarcopenia with ultrasound scanning. Therefore, prior to this study, we developed a four-degrees-of-freedom (DOF) sarcopenia detection system using an RGB-D camera and an ultrasound probe to automatically scan the human thigh without operator dependency. However, due to the eye-to-hand approach with the RGB-D camera, the system has limited usability for clinical trials. Therefore, in this study we modified the system such that it became eye-in-hand by attaching the RGB-D camera to the upper part of the system with an enhanced arc fitting algorithm. The modified system and enhanced algorithm were verified by an in-vitro test with bean curd-gelatin phantom. The results showed that the thickness of bean curd in the gelatin phantom was maintained at approximately 12.7 ± 0.35 mm over the 71.5∘ scanning range with 2.49 ± 0.15 N radial force at various thickness measuring points.

Free Volume Effect via Various Chemical Structured Monomers on Adhesion Property and Relative Permittivity in Acrylic Pressure Sensitive Adhesives.

Acrylic pressure-sensitive adhesives (PSAs) are used as fixatives between layers of a display. PSAs' function is an important factor that determines the performance of the display. Of the various display types available, the touch screen panel (TSP) of smart devices is firmly related to the relative permittivity of the elementals. Therefore, adjusting the relative permittivity of the PSA is indispensable for driving the TSP. Accordingly, selected acrylic pre-polymers were polymerized and the pre-polymer was blended and cross-linked with monomers with different chemical structure to adjust the relative permittivity. The monomers were hexametyldisiloxane (HMDS), N-vinylcaprolactam (NVC), tert-butyl acrylate (TBA), and isooctadecyl acrylate (ISTA). The gel fraction and transmittance as a function of the monomers show a similar result to the pure acrylic PSA. However, the gel fraction value decreased to about 90% and the transmittance decreased to about 85%, due to the immiscibility between nonpolar HMDS and acrylic PSA. On the other hand, the adhesion properties were improved when NVC was added because of the polarity of the nitrogen group. In addition, the relative permittivity of the PSA decreased regardless of the monomer chosen. There was, however, a difference in the optimal content of each monomer, and NVC decreased from 4 phr content to about 3.4 in reducing relative permittivity. Through the above results, it was confirmed that NVC having a nitrogen group is most advantageous in lowering adhesion properties and relative permittivity, and necessitates further research based on the findings.

Mesoporous silica thin films as a spatially extended probe of interfacial electric fields for amplified signal transduction in surface plasmon resonance spectroscopy.

A new simpler concept about the signal amplification of surface plasmon resonance (SPR) that is based on the utilization of mesoporous silica thin films is demonstrated. As compared to monolayer based coatings, mesoporous silica thin films of approximately 200 nm extend the interaction arena away from the metal, thus permitting the integration of the change in optical contrast at different distances from the sensor surface.

In situ sensing of metal ion adsorption to a thiolated surface using surface plasmon resonance spectroscopy.

The kinetics of the adsorption of metal ions onto a thiolated surface and the selective and quantitative sensing of metal ions were explored using surface plasmon resonance (SPR) spectroscopy. The target metal ion was an aqueous solution of Pt2+ and a thin-gold-film-coated glass substrate was modified with 1,6-hexanedithiol (HDT) as a selective sensing layer. SPR spectroscopy was used to examine the kinetics of metal ion adsorption by means of the change in SPR angle. The selectivity of the thiolated surface for Pt2+ over other divalent metal ions such as Cu2+, Ni2+, and Cd2+ was evident by the time-resolved SPR measurement. SPR angle shift, deltatheta(SPR), was found to increase logarithmically with increasing concentration of Pt2+ in the range of 1.0 x 10(-5)-1.0 mM. The rate of Pt2+ adsorption on HDT observed at both 0.1 and 1 mM Pt2+ accelerates until the surface coverage reaches approximately 17%, after which the adsorption profile follows Langmuirian behavior with the surface coverage. The experimental data indicated that heavy metal ions were adsorbed to the hydrophobic thiolated surface by a cooperative mechanism. A mixed self-assembled monolayer (SAM) composed of HDT and 11-mercaptoundecanoic acid was used to reduce the hydrophobicity of the thiol-functionalized surface. The addition of hydrophilic groups to the surface enhanced the rate of adsorption of Pt2+ onto the surface. The findings show that the adsorption of metal ions is strongly dependent upon the hydrophilicity/hydrophobicity of the surface and that the technique represents an easy method for analyzing the adsorption of metal ions to a functionalized surface by combining SPR spectroscopy with a SAM modification.

Characterization of surface-confined alpha-synuclein by surface plasmon resonance measurements.

Urea-driven denaturation and renaturation of surface-bound alpha-synuclein are monitored by surface plasmon resonance (SPR) spectroscopy. The differential SPR angle shift (Delta Theta(SPR))(Net) enables us to estimate the Gibbs free energy change (DeltaG(o)) for the denaturation of the supported alpha-synuclein. DeltaG(o) for the denaturation of the supported alpha-synuclein, which is indirectly related to its biological activity can be increased significantly by the mixed self-assembled monolayers of 11-mercaptoundecanoic acid and 1,6-hexanedithiol. These SPR measurements of surface-bound biomolecules suggested herein can be further utilized to design effective biological scaffold for biosensor, biocatalyst, and possible diagnosis.

Investigation of adsorption behavior of bisphenol A on well fabricated organic surfaces using surface plasmon resonance spectroscopy.

Molecular adsorption of bisphenol A (BPA) on three types of self-assembled monolayers with different functionalities, such as -CH3, -SH, and -COOH, was examined using surface plasmon resonance (SPR) spectroscopy. BPA molecules in an aqueous solution were easily adsorbed onto a hydrophobic surface compared to a hydrophilic surface. Sorption behavior of BPA into poly(2-methoxyethyl acrylate) (PMEA) layer, which is known as a biocompatible polymer, was also investigated. Sorption and desorption dynamics of BPA into PMEA were found to be very rapid and quite reversible. The swelling of PMEA by sorption of BPA results in the change in SPR angle and allows one to quantify the BPA concentration below 100 ppm. In addition, the transport mechanism of BPA within the membrane of organ can be inferred by the experimental results.

Highly responsive sensor on a nanostructured surface via the self-assembly of a biomolecule with an evanescent wave technique.

A self-assembled biomolecule was used to create a highly sensitive sensor surface for detecting toxic chemical species (polychlorinated biphenyls, PCBs). We fabricated the nanostructured sensor surface via the self-assembly of cytochrome c on a Au thin film. Surface plasmon resonance (SPR), an evanescent wave technique possessing maximum sensitivity on the surface and characterized by an exponential decay of sensitivity with distance from the surface, was utilized as the principle for signal transduction. When this sensor surface was used for the detection of PCB, even trace amounts of PCB (from 0.1 ppb to 8.0 ppb) in an aqueous solution were readily detectable.

Fabrication of reusable sensor for detection of Cu2+ in an aqueous solution using a self-assembled monolayer with surface plasmon resonance spectroscopy.

The proposed procedure for recycling the sensor surface consists of (1) the self-assembly of 2-aminoethanethiol hydrochloride (AET) on the Au substrate, (2) the neutralization of zwitterion-like species, -NH3+Cl- to -NH2 by treatment with a NaOH solution (pH 11), (3) the detection of Cu2+ on the NaOH-treated AET-Au substrate, and finally (4) regeneration of the sensor surface from [-NH2--> Cu2+] to [-NH3+Cl-] by treatment with 1 M HCl.

Direct observation of a cooperative mechanism in the adsorption of heavy metal ions to thiolated surface by in-situ surface plasmon resonance measurements.

S-type adsorption kinetics, obtained by surface plasmon resonance spectroscopy measurements, suggest that the rate of Pt2+ adsorption on 1,6-hexanedithiol (HDT) on gold increases until the surface coverage reaches ca. 17%, after which, the adsorption profile of Pt2+ follows Langmuirian behavior for the surface coverage.