Abstract: An electrophoretic medium that may be incorporated into an electrophoretic display includes a dispersion that may be contained in a plurality of microcapsules or microcells or a polymeric continuous phase. The dispersion may include a non-polar fluid, a plurality of first charged particles; and an inhibitor of photo-thermally induced polymerization that inhibits potential cross-linking between the particles and/or the microcells or polymeric continuous phase. The inhibitor may be a compound having an unsaturated hydrocarbon ring and at least one of a hydroxyl group, a carbonyl group, and a nitroso group. The plurality of microcells or polymeric continuous phase and a coating of the particles may include a polymeric material that includes (meth)acrylates.

Abstract: Apparatus for intravascular access device displacement detection, where an intravascular access device is inserted into a blood vessel through the skin at an access site. The apparatus comprises electrodes located on either side of the intravascular access device which electrodes are mobile with the intravascular access device and attachable to the skin about the access site. The electrodes have a micro-current flow therebetween, which is sufficient to induce a current through the skin between the electrodes and the current persists as long as the electrodes are connected. If the device moves then one or more of the electrodes are disconnected and the micro-current is interrupted. A displacement alert device issues an alert signal upon interruption of the micro-current.

Abstract: The present invention is directed to an active molecule delivery system comprising a plurality of microcells wherein each of the microcells has a bottom, the panel has a first area and a second area, and the microcells in the first area have substantially the same bottom thickness and the microcells in the second area have added bottom thicknesses. Such a panel is useful for many applications, such drug administrations.

Abstract: An active molecule delivery system whereby active molecules can be released on demand and/or a variety of different active molecules can be delivered from the same system and/or different concentrations of active molecules can be delivered from the same system. The active delivery system includes a plurality of microcells, wherein the microcells are filled with a medium including an active ingredient and charged or magnetic particles. The microcells include an opening, and the opening is spanned by a porous diffusion layer. Because the porous diffusion layer can be blocked with the charged or magnetic particles, the rate at which the active ingredient is dispensed can be controlled with an electric or magnetic field, respectively.

Abstract: An active molecule delivery system whereby active molecules can be released on demand and/or a variety of different active molecules can be delivered from the same system and/or different concentrations of active molecules can be delivered from the same system. The active delivery system includes a plurality of microcells, wherein the microcells are filled with a medium including active molecules. The microcells include an opening, and the opening is spanned by a porous diffusion layer. The microcell arrays may be loaded with different active ingredients, thereby providing a mechanism to deliver different, or complimentary, active ingredients on demand.

Abstract: An electrophoretic medium that may be incorporated into an electrophoretic display includes a dispersion that may be contained in a plurality of microcapsules or microcells or a polymeric continuous phase. The dispersion may include a non-polar fluid, a plurality of first charged particles; and an inhibitor of photo-thermally induced polymerization that inhibits potential cross-linking between the particles and/or the microcells or polymeric continuous phase. The inhibitor may be a compound having an unsaturated hydrocarbon ring and at least one of a hydroxyl group, a carbonyl group, and a nitroso group. The plurality of microcells or polymeric continuous phase and a coating of the particles may include a polymeric material that includes (meth)acrylates.

Abstract: A writeable system that includes pen-like visual feedback and digitization of the stylus strokes. The system incorporates disappearing ink into a stylus (i.e., pen) that is configured to interact with a digitizing layer of an electrophoretic display. The electrophoretic display includes a clear protective sheet that can be written on with the disappearing ink. As the stylus is moved over the display, an ink trail is left on the display, however, after a short amount of time, the ink fades as the writing in replaced with an updated image corresponding to the stylus motion.

Abstract: Methods for improving the performance of electrophoretic media with the addition of acetylene surfactants comprising hydroxyl groups. In particular, the described acetylene surfactants reduce ghosting while improving the contrast ratio in electrophoretic displays.

Abstract: The object of the present invention is to provide a method for producing a micro-plasma with biocompatibility. The produced micro-plasma is a low temperature, adjustable micro-plasma with low energy consumption. The method provides a device comprising a first gas storage unit, a second gas storage unit, a unit for producing the micro-plasma, and a power supply unit.

Abstract: Additives for electrophoretic media comprising esters of branched polyols and fatty acids, such as esters of pentaerythritol propoxylate (5/4 PO/OH) and stearic acid. The fatty acids may be saturated or unsaturated, branched or unbranched. In some embodiments, the fatty acids are perfluorinated, or partially fluorinated. In some embodiments, the branched polyol will include oligomers of polypropylene oxide or polyethylene oxide. When the additives are included in an electrophoretic medium in a display, the resulting display has an improved contrast ratio and reducing ghosting.

Abstract: The present invention provides a method for forming metal nanoparticle(s) onto an inner surface of one or more open volume defects within a substrate by providing the substrate containing the one or more open volume defects, depositing an immiscible metal on a surface of the substrate, and forming the metal nanoparticle(s) by diffusing the immiscible metal from the surface onto the inner surface of each open volume defect using a heat treatment. The method can be used to produce a substrate having at least one open volume defect with a metal nanoparticle formed onto an inner surface of the open volume defect, a solar cell, an optical switch, a radiation detector, or other similar device.

Abstract: Methods for improving the performance of electrophoretic media with the addition of acetylene surfactants comprising hydroxyl groups. In particular, the described acetylene surfactants reduce ghosting while improving the contrast ratio in electrophoretic displays.

Abstract: Additives for electrophoretic media comprising esters of branched polyols and fatty acids, such as esters of pentaerythritol propoxylate (5/4 PO/OH) and stearic acid. The fatty acids may be saturated or unsaturated, branched or unbranched. In some embodiments, the fatty acids are perfluorinated, or partially fluorinated. In some embodiments, the branched polyol will include oligomers of polypropylene oxide or polyethylene oxide. When the additives are included in an electrophoretic medium in a display, the resulting display has an improved contrast ratio and reducing ghosting.

Abstract: Polyhydroxy sealing formulations for the production of electrophoretic displays, and portions thereof, for example, front plane laminates. When the disclosed polyhydroxy compounds are included in a sealing layer (or in a binder layer), the layer has improved wetting properties, allowing for more consistent application of the layer in a roll-to-roll production process. Additionally, the polyhydroxy compounds can migrate into the electrophoretic medium, where they improve the contrast ratio and reduce ghosting.

Abstract: In one aspect, provided herein are set of primers and use of the same for the detection of SNPs associated with diabetes. In certain embodiments, the primers used to detect SNP sites associated with diabetes comprise Primer Set 1 to Primer Set 47. The experiments show: the genotyping results of the SNP sites associated with diabetes can be accurately detected by the primers disclosed herein, and the risk of individuals can be comprehensively evaluated and the result is more accurate than the single site analysis. In addition, SNPs disclosed herein are verified as associated with type 2 diabetes and its complications, which are especially suitable for the prevention and individualized treatment for type 2 diabetes in East Asian, for example, in China.

Abstract: The object of the present invention is to provide a method for producing a micro-plasma with biocompatibility. The produced micro-plasma is a low temperature, adjustable micro-plasma with low energy consumption. The method provides a device comprising a first gas storage unit, a second gas storage unit, a unit for producing the micro-plasma, and a power supply unit.

Abstract: The object of the present invention is to provide a method for producing a micro-plasma with biocompatibility. The produced micro-plasma is a low temperature, adjustable micro-plasma with low energy consumption. The method provides a device comprising a first gas storage unit, a second gas storage unit, a unit for producing the micro-plasma, and a power supply unit.

Abstract: The present invention provides a method for forming metal nanoparticle(s) onto an inner surface of one or more open volume defects within a substrate by providing the substrate containing the one or more open volume defects, depositing an immiscible metal on a surface of the substrate, and forming the metal nanoparticle(s) by diffusing the immiscible metal from the surface onto the inner surface of each open volume defect using a heat treatment. The method can be used to produce a substrate having at least one open volume defect with a metal nanoparticle formed onto an inner surface of the open volume defect, a solar cell, an optical switch, a radiation detector, or other similar device.

Abstract: A method for producing a royal jelly solution, comprising subjecting an aqueous royal jelly suspension to an enzymatic reaction catalyzed by an enzyme having cysteine protease activity at 20° C.˜70° C.

Abstract: The transfer of strained semiconductor layers from one substrate to another substrate involves depositing a multilayer structure on a substrate having surface contaminants. An interface that includes the contaminants is formed in between the deposited layer and the substrate. Hydrogen atoms are introduced into the structure and allowed to diffuse to the interface. Afterward, the deposited multilayer structure is bonded to a second substrate and is separated away at the interface, which results in transferring a multilayer structure from one substrate to the other substrate. The multilayer structure includes at least one strained semiconductor layer and at least one strain-induced seed layer. The strain-induced seed layer can be optionally etched away after the layer transfer.