Microfluidic devices and nanobiosensors comprising a magnetic nanoparticle attached to a reporter molecule via a release unit for microfluidic-based detection of a target analyte in a biological sample. The nanobiosensors can be magnetically manipulated or guided through the microfluidics channels for incubation with the biological sample, concentration of the nanobiosensors, and detection of target analytes, without having to pump the entire initial sample through a microfluidic channel of the microfluidic device. The magnetic nanoparticles are separated from the reporter molecules before detection and can be re-used.

Disclosed is a measurement apparatus for analyzing a cell contained in a specimen, comprising: a chamber for preparing a measurement sample in which the cell is stained with first and second fluorescent dyes contained in a reagent supplied from at least one reagent container; a liquid feeding section for feeding the reagent from the reagent container to the chamber via a liquid feeding tube provided between the reagent container and the chamber; and a detection section that acquires first and second signals each corresponding to fluorescence of a first wavelength and fluorescence of a second wavelength emitted from the cell stained with the first and second fluorescent dyes in response to irradiation of the measurement sample flowing in a flow cell with light; and an analysis section that analyzes the cell on the basis of the first and second signals.

A pathogen detection apparatus includes a collector that collects a pathogen in air; a reactor that causes the pathogen collected by the collector to react with a labeled substance; a time measurer that measures time from start of reaction in the reactor; a detector that detects a quantity of labeled substance that has reacted with the pathogen; and a controller. The controller calculates a gradient value on the basis of a predetermined time period from the start of reaction measured by the time measurer and the quantity of labeled substance detected by the detector, and determines, on the basis of the gradient value, a time interval to next collection that is to be performed by the collector.

Multi-omic analysis (analysis of proteins, lipids, and metabolites) is a powerful and increasingly utilized approach to gain insight into complex biological systems. One major hindrance with multi-omics, however, is the lengthy sample preparation process. Preparing samples for mass spectrometry (MS)-based multi-omics broadly involves extraction of metabolites and lipids with organic solvents, precipitation of proteins, and overnight digestion of proteins. The existing workflows are disparate and laborious, requiring multiple complex operation steps typically taking 1-2 days to perform. The present invention provides methods for preparing multi-omic samples that are faster and simpler than conventional methods, making it easier for a single lab or researcher to collect quality multi-omic data. A monophasic extraction solvent is used to efficiently extract biomolecules from a sample, including lipids and both polar and non-polar metabolites, and is paired with on-bead protein aggregation and rapid protein digestion.

A method of marking a hydrated tissue specimen for mechanical testing is provided. The method includes adding a metal nanoparticle precursor solution to a reducing agent solution to form a mixture; incubating the mixture to form a plurality of aggregated metal nanoparticles, where each of the aggregated metal nanoparticles includes a plurality of individual metal nanoparticles; separating the plurality of aggregated metal nanoparticles from a supernatant by means of centrifugation or gravitational settling; resuspending the plurality of aggregated metal nanoparticles in a buffer solution to form a colloidal metal nanoparticle suspension; and soaking the hydrated tissue specimen in the colloidal metal nanoparticle suspension, where at least a portion of the plurality of aggregated metal nanoparticles adhere to the hydrated tissue specimen in a random pattern of speckles.

Single dye fluorescent staining, microscopic imaging, and the combination of differences in both intensity and spectral emission permit determination of the minimum concentration of an antibiotic needed to inactivate bacteria (Minimum Inhibitory Concentration (MIC)), thereby providing a means for rapid Antibiotic Susceptibility Testing (AST). By use of microscopic imaging, such as confocal imaging, this allows for a quick and easy means for clinicians to determine a suitable treatment regimen for patients suffering from bacterial infections, including those that eventually lead to sepsis.

Among other things, the present invention is related to the field of bio/chemical sampling, sensing, assays and other applications.

A method for quantitatively and indirectly measuring non-fluorine anti-soil chemistry in carpet applications, is based on a known amount of FI trace to be added along with anti-soil chemistry in formulation prior to application to a carpet surface. The anti-soil chemistry with the trace amount of FI is then applied to the carpet through a topical foam or spray applicator during a precoating process. After completion of the precoat process, a carpet sample is collected, carpet face fiber is shaved, and FI is extracted using water. The extracted water solution is used to measure the fluorescence intensity (in counts per second or CPS) using a Fluorimeter.

A pathogen detection apparatus includes a collector that collects a pathogen in air; a reactor that causes the pathogen collected by the collector to react with a labeled substance; a time measurer that measures time from start of reaction in the reactor; a detector that detects a quantity of labeled substance that has reacted with the pathogen; and a controller. The controller calculates a gradient value on the basis of a predetermined time period from the start of reaction measured by the time measurer and the quantity of labeled substance detected by the detector, and determines, on the basis of the gradient value, a time interval to next collection that is to be performed by the collector.

Disclosed herein is a system of measuring contamination of a water sample. The system may include a mixture container comprising a mixture chamber, a sample opening, and a reagent opening. Further, the system may include a light emitting device disposed proximal to the mixing chamber. Further, the system may include a light sensing device disposed proximal to the mixing chamber. Further, the system may include a processing device communicatively coupled with each of the light emitting device and the light sensing device. Further, the processing device may be configured for analyzing the at least one predetermined attribute and the at least one attribute. Further, the system may include a storage device configured for storing the notification. Further, the system may include a presentation device communicatively coupled with the processing device. Further, the presentation device is configured for presenting the notification.