Continuous microfluidic dilatometry devices and methods are provided for activity monitoring with ultra-high sensitivity. Corner flow in capillary channels is used to detect the resistance change in microfluidic circuits filled with ionic liquids. The conversion of mechanical input (e.g. strain) to an intermediary domain, namely liquid displacement, allows a large enhancement in sensor performance. Embodiments are suitable for tracking skin deformations that occur as a result of human movements.

A microporous substrate for detection of surface bound target analyte molecules includes a microporous substrate material having opposed surfaces and tapered micropores extending through the substrate with the micropores having wider openings on one side of the substrate compared to the other side. The micropores have bound therein analyte specific receptors complementary to the target molecules. When a liquid sample containing the target analyte molecules with optical probes attached to the target molecules is flowed through the substrate, they bind to their complementary analyte specific receptors and emit light. This microporous substrate structure gives an increase in the collection efficiency of light emitted from optical probes when the light is detected by a light detector spaced from the side of the microporous substrate facing the larger micropores openings compared to a light collection efficiency of light emitted from the optical probes when the micropores are straight and not tapered.

A microfluidic device is disclosed which comprises a main flow channel and a partition chamber connected to a portion of same by a chamber inlet and chamber outlet. The device utilizes select cross sections to advantage capillary effects during filling and partitioning steps to isolate biological or other samples in the partition chamber for analysis and can be employed in a digital array.

A single device for testing each of total cholesterol, HDL, and triglyceride concentrations of a whole blood sample is disclosed. The device includes an inlet (10) for blood plasma and a transfer element (200) in fluid communication with the inlet (10), the transfer element (200) including a plurality of channels (210, 220, 230), each channel allowing capillary flow of blood plasma from the inlet (10) to a respective testing region (1, 2, 3). A channel (230) has a multiplicity of corners (235) which define a zigzag profile.

The present invention provides a diagnostic kit for detecting the presence or quantity of one or more test analytes within a test sample taken from a body surface of a mammal, the diagnostic kit comprising: a separate insert for a lateral flow device (200, 411) comprising a membrane (201) fixed to a rigid support (202) and, the separate insert being configured to obtain the test sample; a lateral-flow assay device configured (300, 400) to accept the separate insert (200, 411); a securing member (210) configured to releasably attach (211) the separate insert to a body surface of a mammal (213); wherein the securing member (210) comprise an expandable layer (212) configured to apply pressure to the separate insert (200, 411) thereby pressing the separate insert (200, 411) against the body surface of the mammal (213).

The present invention relates to a device (10) for use in fluid sample analysis. It is described to position (310) a top part (20) of the device (10) adjacent to a base part (30) of the device so as to define a fluidic receiving region in between, the top part being provided with a through opening fluidly connected to the fluidic receiving region, and the bottom part being provided with a radiation window adjacent to the fluidic receiving region. A fluidic sample is supplied (320) through the opening (24). The fluidic sample is moved laterally (330) in the fluid receiving region without the use of an intermediary membrane between the top part and the base part. A radiation is emitted (340) to the fluid receiving region. A radiation is detected (350) that is reflected by the device. A presence of the fluidic sample is determined (360) on the basis of a measured reflectance value based on the detected radiation.

A microfluidic detection strip chip for multiple indicator detection of microsample and method thereof are disclosed. The microfluidic detection strip chip includes a substrate, a plurality of microfluidic pipes, and a plurality of reagent blocks, the microfluidic pipes and the reagent blocks arranged in a lattice are arranged on the substrate for detection of enzyme, chemistry, protein, polypeptide, amino acid, nucleic acid, and exocrine components in samples. The microfluidic pipes and reagent blocks are made using micro processing technology, and the reagent blocks are printed to the lattice array grooves constructed by the substrate and microfluidic pipes, thus realizing an analysis and detection effect of multiple indicators of microsample.

A valve system for driving fluid and a method for using the same are provided. The valve system includes a fluid unit far away from the rotation center, a fluid unit close to the rotation center, a fluid transferring unit and a gas path pipeline for communicating the fluid unit close to the rotation center with the fluid unit far away from the rotation center. A rotation radius of a fluid outlet of the fluid unit far away from the rotation center is greater than that of a fluid inlet of the fluid unit close to the rotation center. The fluid outlet of the fluid unit far away from the rotation center is located at an end thereof away from the rotation center, and the fluid inlet of the fluid unit close to the rotation center is located at an end thereof close to the rotation center.

A droplet (415) is ejected from a surface (411) of a fluid sample containing an analyte using an ejector (420). A solvent is pumped into a solvent inlet (432) of an open port probe (OPP) (430) spaced apart from the surface using a pump (438). The solvent is pumped to send it from the solvent inlet (432) to a tip (431) of the OPP (430) through a solvent capillary (434) of the OPP (430), receive the droplet (415) at the tip (431) where the droplet is combined with the solvent to form an analyte-solvent dilution, and transport the dilution from the tip (431) to an output (435) of the OPP (430) through a sample capillary (436) of the OPP (430). The solvent is heated to a temperature above a threshold temperature using a heating element (437). The solvent is heated to reduce the viscosity of the solvent below a threshold viscosity and maintain the viscosity below the threshold viscosity as the dilution is transported from the tip (431) to the outlet (435).

Examples of the disclosure relate to an apparatus for analysing fluid samples. The apparatus is sized and shaped so that it can fit into an input port of an electronic device. The input port could be an existing port of the electronic device such as an input port for a memory card or a charger. The electronic device can be configured with a heat transfer means so that, when the apparatus is inserted into the electronic device, heat from the electronic device can be used to control the temperature of a fluid sample within the apparatus. This can enable the reaction conditions within the apparatus to be controlled.