Disclosed are a biochip capable of detecting and analyzing multivalent bindings between target protein and binding mediator from monovalent bindings and a method for manufacturing the same. A biochip according to an embodiment comprises: a hydrogel functional layer on which a binding mediator is formed and of which physical properties are changed by a reaction between target protein to be introduced and the binding mediator; and a transducer configured to deliver a displacement signal corresponding to a change in the physical properties of the hydrogel functional layer to an analysis instrument, wherein the reaction is multivalent bindings between the target protein and the binding mediator, and de-swelling occurs in at least a portion of the hydrogel functional layer by the multivalent bindings.

Various embodiments are drawn to systems and methods for detecting an analyte of interest in a sample including an optical sensor, a capture probe attached to a surface of the optical sensor wherein the capture probe is capable of binding to the analyte to form a duplex or complex, and an antibody capable of binding to the analyte, duplex, or complex. In several embodiments, systems and methods further include a particle attached to the antibody or capable of binding to the antibody. In several embodiments, systems and methods for analyte detection feature one or more of the following: high detection sensitivity and specificity, scalability and multiplex capacity, ability to analyze large analytes, and ability to detect or measure multiple individual binding events in real-time.

A chemical sensor, including a porous optical waveguide. The loss or index of refraction, or both, of the porous waveguide is affected by the presence of one or more chemicals of interest.

The present disclosure concerns a photonic integrated circuit (10) and a method for interrogating a ring resonator (3) comprised therein. The circuit (10) comprises an optical port (4) for coupling light (L) into and out of the circuit (10). The circuit (10) further comprises a first waveguide (1) for receiving light (L1) from the optical port (4), and a second waveguide (2) for sending back light to the optical port (4). The ring resonator (3) is arranged between the first waveguide (1) and the second waveguide (2) for coupling a resonant wavelength () of the light therein between. The optical port (4) comprises a polarization splitting coupler for coupling light of a first polarization (P1) to and from the first waveguide (1) and coupling light of a second polarization (P2), orthogonal to the first polarization (P1), to and from the second waveguide (2).

Aspects of enhanced nanoscale gas chromatography are described. In one embodiment, a nano-scale gas chromatography (GC) module includes a light source, a light detector, and a sensor module having vertically-integrated photonic crystal slab (PCS) Fano resonance filter and GC channel layers. The PCS Fano resonance filter layer includes a hole lattice region, and the GC channel layer comprises a gas channel for separation of analytes in a gas mixture. The gas channel includes a coiled section and an extended length section, where the extended length section extends through a region in the GC channel layer that is stacked in proximity with the hole lattice region. The hole lattice region in the PCS Fano resonance filter layer provides local field enhancement of light generated by the light source for increased light-matter interaction with the analytes in the gas channel.

Optical analytical devices and their methods of use are provided. The devices are useful in the analysis of highly multiplexed optical reactions in large numbers at high densities, including biochemical reactions, such as nucleic acid sequencing reactions. The devices include integrated illumination elements and optical waveguides for illumination of the optical reactions. The devices further provide for the efficient coupling of optical excitation energy from the waveguides to the optical reactions. Optical signals emitted from the reactions can thus be measured with high sensitivity and discrimination using features such as spectra, amplitude, and time resolution, or combinations thereof. The devices of the invention are well suited for miniaturization and high throughput.

Disclosed are a biochip capable of detecting and analyzing multivalent bindings between target protein and binding mediator from monovalent bindings and a method for manufacturing the same. A biochip according to an embodiment comprises: a hydrogel functional layer on which a binding mediator is formed and of which physical properties are changed by a reaction between target protein to be introduced and the binding mediator; and a transducer configured to deliver a displacement signal corresponding to a change in the physical properties of the hydrogel functional layer to an analysis instrument, wherein the reaction is multivalent bindings between the target protein and the binding mediator, and de-swelling occurs in at least a portion of the hydrogel functional layer by the multivalent bindings.

A sensing apparatus includes a light source to transmit a light beam, an input switch, a first sensing element, a second sensing element, and a detector. The input switch receives the light beam and includes a phase change material having a first state and a second state. The first sensing element receives the light beam from the input switch when the phase change material is in the first state and produces a first change in the light beam in response to a presence of a first analyte. The second sensing element receives the light beam from the input switch when the phase change material is in the second state and produces a second change in the light beam in response to a presence of a second analyte. The detector detects the first change and/or the second change in the light beam.

An optical microtoroid resonator including one or more nanoparticles attached to a surface of the resonator and capable of receiving an input signal from a far-field source (via free-space transmission) and outputting light propagating within the optical apparatus. A method for coupling light into and out of an optical resonator using a nanoparticle or nanoparticles to interface with spatially separated far-field optical elements.

Disclosed are a sensor including a first metal layer and a second metal layer facing each other, and a volume changeable layer disposed between the first metal layer and the second metal layer and capable of absorbing a material to change the thickness thereof, wherein at least one of the first metal layer and the second metal layer is a semi-transmissive layer and the sensor indicates a color change by changing a resonance wavelength of light transmitted through the semi-transmissive layer according to a change in thickness of the volume changeable layer, and a sensor device, an electronic device, a smart window, and an IoT system including the same.