The present disclosure provides modes of relative motion between a solid surface and a solution, and the related motion apparatuses. In an interaction between the solid surface and a target object, the target object is dissolved or dispersed in the solution, and the solid surface and the solution make a relative motion, with the relative motion including a relative movement perpendicular to the solid surface, in order to improve at least one of the following: binding rate, dissociation rate, binding uniformity, binding directionality and binding density of the target object to the solid surface. Compared with the traditional modes of relative motion in which the relative motion is parallel to a sensor surface, the modes of relative motion of the present disclosure can effectively improve the binding efficiency and dissociation efficiency between a ligand and an analyte given the same relative motion velocity between the sensor and the solution.

A colorimetric sensor for detecting bacteria and/or includes one or more layers having a photonic crystal structure a functional layer comprising a nanomaterial capable of generating bacteria- and/or viruses-bioresponsive surface plasmon overlapping the one or more layers having the photonic crystal structure. The bacteria- and/or viruses-bioresponsive nanomaterial of the functional layer is doped with proteinic substances or antibodies acting as virus receptors, or the colorimetric sensor comprises a receptor layer comprising proteinic substances or antibodies acting as virus receptors. The functional layer and receptor layer overlap each other. Alternatively, or in addition to, the colorimetric sensor comprises a plasmonic nanostructured layer comprising nanostructures such to generate plasmonic colors, overlapping the one or more layers having the photonic crystal structure.

Provided herein are methods of determining molecular binding kinetics on particles, such as magnetic nanoparticles. In some embodiments, the methods include introducing an incident light from a light source toward a sample container that comprises a particle-bound biomolecule-ligand composition comprising a plurality of particle-bound biomolecules and a plurality of ligands that binds, or is capable of binding, to biomolecules of the plurality of particle-bound biomolecules, detecting light scattered from particle-bound biomolecule-ligand complexes in the particle-bound biomolecule-ligand composition over a duration to produce a set of imaging data using the detector, and determining size or volume changes of one or more of the particle-bound biomolecule-ligand complexes during at least a portion of the duration from the set of imaging data to thereby determine the molecular binding kinetics on the particles. Related systems and computer readable media are also provided.

This disclosure presents a docking station into which a test card can be inserted for rapid analyte detection and reporting. This docking station has portable capability and can include wire or wireless transmission to a local server or cloud-based server. A test card that has a test structure located on the test structure that includes a modified waveguide can be inserted into the and a docking station that includes a laser and interferometer provides for accurate and rapid detection of a test sample.

Systems and methods for determining the osmolarity of a sample are provided. Aspects of the subject methods include contacting a sensing surface of a surface plasmon resonance based sensor with a sample, and generating one or more data sets at at least two wavelengths over a time interval, wherein the data sets are used to determine the osmolarity of the sample. The subject methods find use in determining the osmolarity of a sample, such as a biological sample (e.g., a tear fluid), and in the diagnosis and/or monitoring of various diseases and disorders, such as, e.g., dry eye disease.

A method for characterizing compounds of interest, introduced into a measuring chamber of an electronic nose, includes injecting a first gas sample formed from a carrier gas without the compounds of interest forming a second gas sample from the carrier gas with the compounds of interest; determining a measurement signal (S.sub.k(t.sub.i)); measuring values φ1, φ2 of the relative humidity; determining corrective parameter ({tilde over (S)}.sub.k.sup.ref|.sub.φ2; ΔS.sub.k.sup.ref|.sub.Δφ); and determining a useful signal (Su.sub.k(t.sub.iϵP2)) by correcting the measurement signal associated with the second gas sample using the determined corrective parameter, and characterizing the compounds of interest based on the useful signal.

A single ion imaging-based detection method and device are provided. After being reflected by an electromodulation singularity coupling differential imaging reaction unit, a probe beam from a total internal reflection ellipsometry imager converges on a CCD or CMOS detector, the acquired sensing surface image data is transmitted to a signal processing unit, the common mode noise is eliminated by performing spectral analysis on differential signals of a working sensing surface and a reference sensing surface, the peak intensity of a modulating signal is selected on the spectrum for wave filtering to obtain a real-time signal of interaction of single ions or charged molecules at a solid-liquid interface. Based on the singularity effect at a surface plasma resonance angle of an ellipsometry phase and a corresponding optical signal noise suppression scheme, the present application can achieve real-time observation of the adsorption of single ions or charged molecules at a solid surface.

Methods and systems for determining kinetic parameters are provided. The methods and systems may use a surface having a matrix attached thereto and probe molecules bound to the matrix. Target molecules may be introduced and bind reversibly to the probe molecules. As target molecules are introduced, a first amount of intermolecular complex is generated between the target molecules and the probe molecules and monitored. Once a threshold first amount intermolecular complex is exceeded, introduction of the target molecules may cease. At this point, competitive inhibitor molecules may be introduced and bind to free target molecules produced from continued dissociation of the intermolecular target-probe complex. An amount of the first intermolecular complex may be monitored. This amount may be indicative of the kinetics of a second intermolecular complex between the free target molecules and the competitive inhibitor molecules. In this manner, kinetic parameters of the second intermolecular complex may be estimated.

The present invention relates to a method for the measurement of at least one sample by the interaction with the surface in the field of at least one sensor surface, such as surface plasmon resonance measurement, comprising the steps of: i) sampling the sample and a buffer; ii) transporting the sample and the buffer to at least one flow cell which is in liquid contact with the sensor surface of at least one sensor for measuring a parameter of a sample by interaction of the sample at the sensor surface in the field of the sensor surface; iii) transporting the sample into the flow cell into contact with the sensor surface; iv) handling a separation fluidum by inserting and/or removing the separation fluidum by between the sample and the buffer upstream and/or downstream of the sensor surface; v) measuring the interaction of the sample at the sensor surface; and vi) dispensing the sample from the flow cell, and to a measuring system for such method.

The present application provides stable, carbene-functionalized composite materials, and methods and uses thereof. These carbene-functionalized composite materials comprise a material having a metal surface, and a carbene monolayer that is uniform, contaminant-free (metal oxide, etc), and more stable than thiol-functionalized monolayers. Uses of such carbene-functionalized composite materials include semi-conducting materials, microelectronic devices, drug delivery or sensing applications.