Abstract: An apparatus for non-invasive glucose monitoring includes a first light source for emitting at least one ray of first light; a first beam splitter with a focusing function; a set of photo detectors for measuring optical rotatory distribution (ORD) information and absorption energy information of the first light reflected from the eyeball and transmitted through the first beam splitter to the set of photo detectors, and the first light emitted from the first light source being transmitted to the set of photo detectors by the first beam splitter and the eyeball to form an optical path; a processing unit receiving and processing the ORD information and the absorption energy information to obtain glucose information; and an eye positioning device including a second beam splitter disposed on the optical path between the first beam splitter and the eyeball and a camera for receiving image information transmitted from the second beam splitter.

Abstract: An apparatus for non-invasive glucose monitoring includes a light source for emitting at least one ray of light; a first beam splitter, a set of photo detectors for measuring optical rotatory distribution (ORD) information and absorption energy information; a reference component receiving the light from the first beam splitter, and the light reflected by the reference component being transmitted to the set of photo detectors by the first beam splitter, wherein the light emitted from the light source is transmitted to the set of photo detectors by the first beam splitter and the eyeball to form a first optical path, the light emitted from the light source is transmitted to the set of photo detectors by the first beam splitter and the reference component to form a second optical path; and a processing unit receiving and processing the ORD information and the absorption energy information to obtain a glucose information.

Abstract: A projection lens, a projection device and an optically-induced microparticle device are provided. The projection lens includes an aperture, a first and a second lens groups. The aperture, the first and the second lens groups are disposed on a projection path of an image. The aperture is between the first and the second lens groups. The first and the second lens groups are suitable for interchanging with each other to switch the magnification ratio. When in a first state, the first lens group is between the object and the aperture and the second lens group is between the aperture and a projection surface, herein the projection lens has a first magnification ratio. When in a second state, the first lens group is between the aperture and the projection surface, and the second lens group is between the object and the aperture, herein the projection lens has a second magnification ratio.

Abstract: A particle manipulation system and a projection device are provided. The projection device includes an image source and a projection lens. The image source provides an image beam. The projection lens is disposed on a light path of the image beam and includes a zoom lens set and a focusing lens set. The zoom lens set is disposed on the light path of the image beam from the image source and includes at least two lens groups disposed in sequence on the light path of the image beam. The focusing lens set is disposed on the light path of the image beam. The zoom lens set is disposed between the image source and the focusing lens set. A photoconductor chip is disposed on the light path of the image beam from the projection lens.

Abstract: A detecting device includes at least one detecting module. In the detecting module, a light source unit is configured to emit a first beam and a second beam. The wavelength of the first beam is different from that of the second beam. A packaging unit is disposed on the light source unit and a light detecting unit and on transmission paths of the first beam and the second beam from the light source unit. An optical microstructure unit is disposed on the transmission paths of the first beam and the second beam. The first beam and the second beam emitted from the light source unit pass through the packaging unit to pass the optical microstructure unit to be transmitted to a biological tissue, and then pass through the optical microstructure unit to pass the packaging unit to be transmitted to the light detecting unit in sequence.

Abstract: A retinal prosthesis including a microelectrode array, a polymer layer and a layer of bioactive molecule is provided. The microelectrode includes a plurality of microelectrodes. The polymer layer partly encapsulates the microelectrode array, in which the microelectrodes are exposed on the surface of the polymer layer. The layer of bioactive molecules is immobilized on the surface of the microelectrode.

Abstract: An optically-induced dielectrophoresis device includes a first substrate, a first conductive layer, a first patterned photoconductor layer, a first patterned layer, a second substrate, a second conductive layer, and a spacer. The first conductive layer is disposed on the first substrate. The first patterned photoconductor layer is disposed on the first conductive layer. The first patterned layer is disposed on the first conductive layer. The first patterned photoconductor layer and the first patterned layer are distributed alternately over the first conductive layer. Resistivity of the first patterned photoconductor layer is not equal to resistivity of the first patterned layer. At least one of the first substrate and the second substrate is pervious to a light. The second conductive layer is disposed on the second substrate and between the first substrate and the second substrate. The spacer connects the first substrate and the second substrate.

Abstract: A carrier with the optical registration function is disclosed. The carrier allows the registration of inspected results of the sampling images of the sample to the corresponding address codes of the address coding site of the carrier.

Abstract: A method for manufacturing a bioabsorbable stent and an apparatus for doing the same are disclosed. The method includes providing a polymer resin, melting the polymer resin to form a molten hollow parison, cooling the molten hollow parison to form a hot hollow parison, elongating the hot hollow parison, expanding the hot hollow parison by feeding a compressed gas into the hot hollow parison to form a stent preform, and patterning the stent preform to form a bioabsorbable stent.

Abstract: A method for non-invasive blood glucose monitoring includes the following steps. At least one ray of light is emitted from at least one light source. The light emitted from the light source is leaded into an eyeball and focused on the eyeball through a first beam splitter. The reflected light reflected from the eyeball is transmitted through the first beam splitter to a set of photo detectors. Optical rotatory distribution (ORD) information and absorption energy information of the reflected light transmitted to the set of photo detectors are measured. ORD difference and absorption energy difference resulting from the light emitted from the light source and the reflected light transmitted to the set of photo detectors are obtained. Glucose information is obtained by analyzing the ORD difference and the absorption energy difference, and since glucose information has a corresponding relationship with blood glucose information, blood glucose information may be read.

Abstract: An apparatus for non-invasive blood glucose monitoring includes a light source for generating at least one ray of light, a beam splitter with a focusing function leads the light into an eyeball and focuses on the eyeball, a set of photo detectors for measuring optical rotatory distribution (ORD) information and absorption energy information of the reflected light reflected from the eyeball and transmitted through the first beam splitter to the set of photo detectors, and a processing unit. The processing unit receives and processes the ORD information and the absorption energy information to obtain an ORD difference and an absorption energy difference resulting from the light emitted from the light source and the reflected light transmitted to the set of photo detectors, and analyzes the ORD difference and the absorption energy difference to obtain a glucose information to read the blood glucose information.

Abstract: A chemical or biochemical analysis apparatus includes: a computer processor; at least one controller electrically coupled to the computer processor; at least one first base configured with a plurality of dispensing tube assemblies arranged in alignment and electrically coupled to the at least one controller, independently; at least one second base configured with a plurality of the detectors arranged in alignment and electrically coupled to the at least one controller; and a stage, for carrying the at least one multi-well strip having a plurality of wells arranged in alignment and for transporting the multi-well strip to pass through and underneath the plurality of dispensing tube assemblies and the plurality of the detectors arranged in order, electrically coupled to the at least one controller.