Abstract: Microfluidic devices that are configured to use centrifugal forces to bias particles into one or more capture regions based on their individual sizes are described.

Abstract: Apparatus and methods for analyzing single molecule and performing nucleic acid sequencing. An apparatus can include an assay chip that includes multiple pixels with sample wells configured to receive a sample, which, when excited, emits emission energy; at least one element for directing the emission energy in a particular direction; and a light path along which the emission energy travels from the sample well toward a sensor. The apparatus also includes an instrument that interfaces with the assay chip. The instrument includes an excitation light source for exciting the sample in each sample well; a plurality of sensors corresponding the sample wells. Each sensor may detect emission energy from a sample in a respective sample well. The instrument includes at least one optical element that directs the emission energy from each sample well towards a respective sensor of the plurality of sensors.

Abstract: A method of transfer printing comprises globally heating an array of stamps, where each stamp comprises a shape memory polymer with a light absorbing agent dispersed therein, and pressing the array of stamps to a donor substrate comprising a plurality of inks. Each stamp is thereby compressed from an undeformed adhesion-off configuration to a deformed adhesion-on configuration. The array of stamps is then cooled to rigidize the shape memory polymer and bind the plurality of inks to the stamps in the deformed adhesion-on configuration. The plurality of inks remain bound to the stamps while the array of stamps is positioned in proximity with a receiving substrate. A selected stamp in the array is then locally heated using a concentrated light source. The selected stamp returns to the undeformed adhesion-off configuration, and the ink bound to the selected stamp is released and transfer printed onto the receiving substrate.

Abstract: A microfluidic device includes a block having at least one reservoir, a base layer attached to the bottom of the block and a microfluidic channel formed in the base layer or at the interface between the block and base layer. The microfluidic channel is in fluid communication with the at least one reservoir. A static pressure source is operatively coupleable to the reservoir. A flow path extends from the reservoir to the microfluidic channel. The flow path has a first portion which extends upwardly away from the base layer over a barrier and into a second portion which extends downwardly towards the base layer and leads to the microfluidic channel. The flow path is configured such that it prevents flow from the reservoir to the microfluidic channel under the influence of gravity alone when the reservoir is filled to a level below the level of the top of the barrier.

Abstract: A microfluidic device and method for fabrication includes a microfluidic channel that has a closed portion, which comprises: a liquid pathway formed by a wetting area; and an anti-wetting area extending along and contiguously with the liquid pathway. The anti-wetting area is configured so as to provide a vent to evacuate gas along the anti-wetting area.

Abstract: A capacitive autocoding circuit is provided herein. A test strip may include an embedded code comprising one or more individually electrically isolated contacting pads associated with one of a plurality of predefined capacitive states. The respective capacitive states associated with each of the contacting pads together form a capacitive state sequence such that when the test strip is inserted into a diagnostic meter the sequence is read to identify data particular to the capacitive sequence and the test strip.

Abstract: A preprocessing kit includes a separation device, a collecting container, and a skirt part. The skirt part is integrated with the separation device, and is provided to surround an outer circumferential surface of the separation device with a clearance being left from the outer circumferential surface so that a space having a closed upper side and an open lower side is formed between the outer circumferential surface of the separation device and the skirt part. The skirt part is provided in such a way that a lower end of the skirt part comes into intimate contact with a peripheral surface of an opening of the recess part when the collecting container containing the lower end of the separation device is fitted into the recess part.

Abstract: Provided is a testing device, including: a porous flow path member in which a flow path for flowing a sample is formed; and a resin layer provided at one position or a plurality of positions over the flow path member, wherein a reagent reactive with the sample is provided as a solid phase over a surface of the resin layer facing the flow path member.

Abstract: A microfluidic diagnostic chip may comprise a main fluid channel comprising a main pump, a secondary fluid channel branching off from the main fluid channel, and a secondary pump within the secondary fluid channel wherein the secondary pump is to pull a particle of analyte of a first size from a fluid passing through the main channel, the fluid comprising particles of analyte of the first size and of a number of larger sizes. A method of analyzing an analyte on a microfluidic chip may comprise pumping, with a main microfluidic pump, a fluid comprising an analyte particle through a main microfluidic channel fluidly coupled to a fluid slot and sorting the analyte particle within the fluid through a secondary microfluidic channel by pulling the analyte particle into the secondary microfluidic channel with a secondary microfluidic pump.

Abstract: Systems and methods for analysis of samples, and in certain embodiments, microfluidic sample analyzers configured to receive a cassette containing a sample therein to perform an analysis of the sample are described. The microfluidic sample analyzers may be used to control fluid flow, mixing, and sample analysis in a variety of microfluidic systems such as microfluidic point-of-care diagnostic platforms. Advantageously, the microfluidic sample analyzers may be, in some embodiments, inexpensive, reduced in size compared to conventional bench top systems, and simple to use. Cassettes that can operate with the sample analyzers are also described.

Abstract: Methods, devices, and systems for integrating extraction and purification of bio-sample regions and materials with patient analysis, diagnosis, follow up, and treatment. The invention provides a means to insert disclosed substrates, cartridges, and cartridge-processing instrument or instruments into a standard clinic or pathology laboratory workflow. Specifically, we disclose methods, devices, and systems for inserting standard pathology slides into disclosed cartridges and cartridge-processing instruments, either manually, semi-automatically, automatically, or by robotic means.

Abstract: Disclosed is an apparatus for simultaneous detection of amines and thiols.

Abstract: System and method of determining an amount of an analyte in a blood sample using a cartridge and blood collector are disclosed. The blood collector has a mounting surface, a capillary structure with a curved portion, and a capillary inlet. The cartridge has a receiving surface, a cartridge inlet, a microfluidic structure, and a measurement structure. The method includes placing the blood sample into the capillary inlet; attaching the mounting surface to the receiving surface; rotating the cartridge about a rotational axis to transport the blood sample from the capillary structure to the cartridge inlet and into the microfluidic structure; controlling the rotation of the cartridge to process the blood sample into the processed sample using the microfluidic structure; controlling the rotation of the cartridge to transfer the processed sample to the measurement structure; and measuring the amount of the analyte using the measurement structure and a measurement system.

Abstract: A device is adapted to identify and monitor a reagent kit adapted for insertion into an analytical system, the device is positioned in the reagent kit and includes: apparatus for measuring the temperature of the reagent kit; apparatus for measuring the light level to which the reagent kit is subjected; apparatus for measuring the electric conductivity level of the reagent kit; means for measuring the triaxial acceleration to which the reagent kit is subjected; a multiparameter data-logger for logging the data obtained from the temperature, light, conductivity and acceleration measuring apparatus; apparatus for storage and short-range transmission of data identifying the reagent kit and the data obtained from the temperature, light, conductivity and acceleration measuring apparatus, in order to detect operational or non-operational conditions of the kit.

Abstract: The present invention provides a feces sampling and detecting device and a method for detecting feces based on the feces sampling and detecting device. The device includes a detector, a casse with detecting strips provided in the detector, a collector accommodated in the detector detachably, a feces sampler for sealing the collector detachably, and at least one puncturing part arranged at a bottom of the detector facing one side of the collector. The feces sampling and detecting device can detect collected feces quickly, thereby avoiding feces sample from nature changing in an interval period, and preventing liquid in the collector from entering the detector to influence safety of the device of the present invention.

Abstract: This disclosure provides methods and apparatuses for sorting target particles. In various embodiments, the disclosure provides a cassette for sorting target particles, methods for sorting target particles, methods of loading a microchannel for maintaining sample material viability, methods of quantifying sample material, and an optical apparatus for laser scanning and particle sorting.

Abstract: A microfluidic device, including a matrix array of controllable shape-changing micropillars where a shape of the shape-changing micropillars is changed by a fluid.

Abstract: A method of applying a dielectric lubricant to an electrical connector of a consumer electronic device. The method includes inserting a dielectric lubricant delivery device apertures for delivering the dielectric lubricant to the electrical connector into a receptacle of the electronic device; applying pressure to a chamber including the dielectric lubricant, the chamber being fluidly coupled to the apertures of the lubricant delivery device such that the pressure causes the lubricant to enter the receptacle via the apertures and deposit on contacts of the electrical connector; and pulling vacuum using the lubricant delivery device to remove excess dielectric lubricant from the receptacle and the electrical connector.

Abstract: The invention is directed to a microfluidic device. The device includes an input microchannel, a set of m distribution microchannels, a set of m microfluidic modules and a set of m nodes. The m microfluidic modules (m?2) are in fluidic communication with the m distribution microchannels, respectively. The one or more nodes of the set of m nodes branch from the input microchannel, and further branch to a respective one of the set of m distribution microchannels. In addition, a subset, but not all, of the nodes are altered. The nodes of the set of m nodes have different liquid pinning strengths. As a result, the extent in which a liquid passes through one or more of the m microfluidic modules varies based on the different liquid pinning strengths, in operation. Additional sets of nodes may be provided to allow liquid to pass through ordered pairs of modules.

Abstract: A microfluidic system includes a substrate, a set of input ports coupled to the substrate, and a set of output ports coupled to the substrate. The microfluidic system also includes a microfluidic processing system coupled to the substrate and including a plurality of processing sites. The microfluidic processing system is coupled to the set of input ports and the set of output ports. The microfluidic system further includes one or more microfluidic logic devices coupled to the substrate and operable to control at least a portion of the microfluidic processing system.

Abstract: A device for processing a biological sample includes a first substrate having a first cavity, a second substrate having a second cavity, a filter element having a plurality of perforations, and an electrically conductive structure. The first cavity forms a first chamber segment of a chamber for accommodating the biological sample. The second cavity forms a second chamber segment of the chamber for accommodating the biological sample. The filter element is formed between the first cavity and the second cavity in order to hold back a plurality of organic cells of the biological sample on the plurality of perforations when the biological sample moves between the first cavity and the second cavity through the filter element. The electrically conductive structure is arranged on the filter element and is configured to cause lysis of the organic cells and/or to duplicate and/or detect defined segments of exposed DNA.

Abstract: A microfluidic device with reduced risk of bubble formation at a capillary junction between two conduits is provided. In some embodiments, the microfluidic device comprises a supply reservoir, a first conduit and a second conduit. The first conduit is configured such that liquid flows by capillary effect from the supply reservoir into the first conduit. The second conduit is connected to the first conduit through an opening in a wall of the first conduit and is configured such that liquid flows from the first conduit to the second conduit by capillary effect. A width of the second conduit, along a direction of liquid flow in the first conduit, is greater than a depth of the second conduit and a depth of the second conduit is less than a depth of the first conduit.

Abstract: A thin film valve includes at least one chamber for storing a fluid required for biological/chemical analysis, a plurality of chamber for performing a biological/biochemical reaction, or connecting, at least one chamber performing the biological or biochemical reaction to enable a movement of the fluid flow, a flow path arranged to communicate with the hole on the flow path, a thin film closing membrane for closing the fluid hole, a thin film valve including the hole and the fluid hole closing membrane, a multilayered plurality of substrates forming the fluid path, the fluid hole and the chamber, a rotatable disk forming the fluid path, fluid hole, the plurality of chambers, a heat generator, laser beam generator heating the thin film valves, a light detector for detecting amount of light passing through the membrane and closing the fluid hole, and a feedback controller for controlling the focusing actuator.

Abstract: We disclose a microfabricated device for both extracting and preconcentrating samples for gas chromatography analysis. The device includes a conduit with at least two sections and multiple ports which may be connected to multiple gas chromatography columns. The inner surface of the conduit may be coated with multiple sorbents which bind volatile analytes with different affinities. The sections of the conduit may be divided by a thermal barrier which inhibits heat transfer between sections. Consequently, each section may be independently heated to encourage desorption of volatile analytes. The disclosed device separates and concentrates volatile analytes into different pools according to their chemical and physical properties before they enter a gas chromatography column that is optimized for that pool. The device reduces the amount of heat and time needed to perform gas chromatography analysis as well as avoids the need for purified gas sources typically used for the moving phase.

Abstract: A membrane-based device for multi-step assays including one or more reagents pre-dried on the device, and one or more one fluid storage zones intended to enable the automated sequential delivery of the reagents to a test zone from addition of a fluid to the device. Addition of the fluid to the device may include a single addition of the fluid to the device. The fluid storage zones may fill with the fluid when the fluid with a sample is added to the device, and then the fluid may be released to the device at a later time. In some cases, the fluid from the sample zone is wicked into both the test zone and the fluid storage zones. Preferably, the device includes multiple layers. At least one porous membrane may be disposed between at least two of the layers. Also, associated methods are disclosed.

Abstract: An apparatus is configured to detect a beverage that is contaminated with a substance. The apparatus may include a testing material, wherein the testing material may comprise a cavity having a complementary shape to a molecule associated with the substance. The apparatus may include a taste substance filling the cavity, wherein the taste substance filling the cavity may bleed out into the beverage when the molecule associated with the substance in the beverage replaces the taste substance filling the cavity, wherein a taste of the beverage may change when the taste substance bleeds out into the beverage as an indicator that the substance is present in the beverage.

Abstract: Disclosed is a centrifugal microfluidic device comprising a piezoelectric substrate; a rotatable platform device on the substrate; and at least one transducer on the substrate, the transducer being configured to generate a surface acoustic wave that propagates on the surface of the substrate and contacts the rotatable platform device asymmetrically to transfer energy thereto with a lateral distribution to cause rotation of the rotatable platform device. The device may be a microfluidic valve, a microfluidic mixer or a microfluidic particle concentrator.

Abstract: An inspection apparatus is provided that comprises an optical target including a solid host material and a fluorescing material embedded in the solid host material. The solid host material has a predetermined phonon energy HOSTPE. The fluorescing material exhibits a select ground energy level and a target excitation (TE) energy level separated from the ground energy level by a first energy gap corresponding to a fluorescence emission wavelength of interest. The fluorescing material has a next lower lying (NLL) energy level relative to the TE energy level. The NLL energy level is spaced a second energy gap FMEG2 below the TE energy level, wherein a ratio of the FMEG2/HOSTPE is three or more.

Abstract: The present invention relates to a microparticle separation apparatus assembly comprising multiple separable panels, more specifically, to a microparticle separation apparatus assembly having a novel structure, comprising: a first panel comprising a magnetic microstructure for applying magnetophoretic force to microparticles; and a second panel, which can be separated from the first panel and through which a sample comprising microparticles passes, wherein the first panel comprising the magnetic microstructure can be recycled.

Abstract: This invention publicly announces a quantificational testing method of semen liquefaction ability. By following the steps of sample preparation, image collection, image quantificational analysis and curve analysis to analyze the quantificational testing of semen liquefaction ability; indirectly indicate the semen liquefaction ability by observing the color depth change in the sperm sampled cover black area; to analyze the quantification of semen liquefaction by observing the level of change in grey level value versus time; thus, to efficiently, subjectively and standardly test the semen liquefaction ability and avoid human errors.

Abstract: Chemical compositions and methods provide labeling, detection and measurement of target substances in exhaled human breath, and can be implemented in connection with a handheld device—much like a Breathalyzer portable breath testing unit for alcohol—to support rapid quantification of levels of cannabinoid compounds, such as tetrahydrocannabinol (THC), of suspected users at the roadside.

Abstract: Disclosed are apparatuses, systems, and methods for performing electroporation.

Abstract: This invention pertains to a new microfluidic device and the method of using it to sort droplets. The method comprises (a) providing a plurality of droplets flowing in a microfluidic channel, wherein the plurality of droplets comprise desired droplets and undesired droplet (b) identifying desired droplets in the plurality of droplets, (c) changing volume of the desired droplets relative to volume of the undesired droplets such that at least some of the desired droplets have a different volume than the undesired droplets, and (d) passively sorting the desired droplets having the different volume from the undesired droplets.

Abstract: A supporting structure for supporting a plurality of sealed medical cartridges is disclosed, comprising a planar supporting plate having a plurality of receptacles for accommodating the sealed cartridges. Retaining protrusions are formed at the bottom ends of the receptacles protruding inward, which are mated with the shoulder portions of the sealed cartridges in such a manner that the shoulder portions of the sealed cartridges are supported on the retaining protrusions of the receptacles and that the upper ends of the sealed cartridges protrude from the upper ends of the receptacles at an upper side of the planar supporting plate, when the sealed cartridges are accommodated upside-down in the receptacles. The inventive nest will be suitable for any nested liquid filling machine without much changes in filling table and general settings.

Abstract: The invention describes a foil of polymeric material comprising a plurality of patch portions and a grid portion arranged between said patches. Each patch portion is connected to the grid portion by means of one or more connecting elements. Each patch portion is separated from the grid portion in the X-Y plane by means of a release portion, said release portion having a tensile strength in the X-Y plane which is lower than the tensile strength of both said patch portions and said grid portion, such that—upon exertion of a tensile force between said patch portions and said grid portion—said foil ruptures preferentially at said release portion. The invention relates to a method for the production of cell-capture chips using said foil, and a cell capture chip produced by said method.

Abstract: A system and method for augmenting or adding to the information used by an in-vitro diagnostic or other diagnostic device to generate results of a test is disclosed. A diagnostic device is capable of generating test results based on a sample, such as a sample provided by a patient, and is also capable of receiving additional information to enhance the results providable by the device. For example, an in-vitro diagnostic device is configured to read a lateral flow assay test, and is configured to receive additional diagnostic, network, test identification, or environmental information over a network. Using both the result of the diagnostic test and the additional information, the disclosed device provides more thorough, accurate, and reliable diagnostic information. The results generated by the device may be communicated to an appropriate remote device to enhance the results obtainable by such tests.

Abstract: Provided herein are methods and components for successive capture of nucleic acids using magnetic glass particles.

Abstract: The present invention provides methods for continuous measurement of triglyceride digestibility during a meal. A stable isotope labeled triglyceride and a free fatty acid tracer are added to the meal. The ratio between a ratio of isotope labeled fatty acid produced after digestion to free fatty acid tracer represents the percentage of digestion of triglycerides by lipase from the pancreas.

Abstract: Disclosed is a specimen processing apparatus for genetic testing. The apparatus includes: a mode setting section configured to receive a setting of an operation mode from: an emulsion preparation mode for preparing a water-in-oil type (W/O type) emulsion having dispersed therein a plurality of droplets, each droplet containing a specimen which contains DNA and a bead to which a reagent component necessary for amplifying a target DNA molecule is bound; and an emulsion breaking mode for breaking the emulsion and collecting beads from the droplets; and a controller programmed to control the transfer unit and the dispensing unit in accordance with the operation mode set by the mode setting section.

Abstract: The present invention is generally in the field of measuring and indicating techniques and relates to a time-temperature indicator and methods of manufacturing and use thereof. More specifically, the time-temperature indicator comprises a time temperature indicator comprising at least one metal layer or metal containing layer and in direct contact to the metal layer or to the metal containing layer at least one doped polymer layer, wherein the dopant is an acid, a base or a salt or a photolatent acid or a photolatent base which dopant is added to the polymer, and/or at least one polymer layer wherein a polymer is functionalized with acidic or latent acidic or basic or latent basic groups; or a time temperature indicator comprising at least one polymer layer containing metal particles and a photolatent acid or a photolatent base, or at least one polymer layer containing metal particles wherein the polymer is functionalized with latent acidic or latent basic groups.

Abstract: A control method and a control apparatus for a paraffin dispenser in an embedder, a paraffin dispenser and an embedder are provided. The control method includes: collecting information of a current mold so as to acquire an identification of the current mold; determining whether the identification of the current mold is correct; and controlling the paraffin dispenser to pour paraffin into the current mold, when it is determined that the identification of the current mold is correct.

Abstract: A cell culture bag is provided. The cell culture bag includes: an external film of the cell culture bag; at least one sensor chip arranged on a culture fluid side of the external film, the at least one sensor chip including a layer reacting to an object to be detected; and a permeable film that covers a culture fluid side of the sensor chip, the permeable film permeating the object to be detected.

Abstract: The present invention relates to analytical testing devices comprising a single channel with micro-environment sensors and methods for assaying coagulation in a fluid sample applied to the micro-environment sensors, and in particular, to performing coagulation assays using a single channel with micro-environment sensors in a point of care test cartridge. For example, the present invention may be directed to a sample analysis cartridge including an inlet chamber configured to receive a biological sample and a conduit fluidically connected to the inlet chamber. The conduit includes a sensor chip including a first micro-environment sensor and a second microenvironment sensor, and a fluid lock valve.

Abstract: Devices are provided that include a plurality of microneedles that penetrate skin and that receive interstitial fluid from the skin tissue. The microneedles are further configured to direct the received interstitial fluid to nanosensors configured to change an optical property based on interaction with an analyte in the received interstitial fluid, allowing optical detection of the analyte. Direction of the received interstitial fluid to the nanosensors can be facilitated by a pump configured to control the flow rate of the interstitial fluid through the microneedles. Such devices could be configured to detect the analyte independently or in combination with a reader device configured to be periodically mounted to the devices and to detect the analyte. Further, such devices can include delivery systems configured to transdermally deliver a drug or other substance into or through the skin in response to a detected concentration, presence, or other property of the analyte.

Abstract: A measurement tool for circle area includes a cylinder, a rectangular container and a pipe. The cylinder is provided with a first opening and filled with a liquid. The rectangular container is provided with a second opening, and at least side surface of the rectangular container is provided with at least scale table. The pipe is arranged on the cylinder and the rectangular container and connected with the first opening and the second opening. When the cylinder is tilted, the liquid flows to the rectangular container through the pipe, and a volume of the liquid in the rectangular container is figured out according to a length, a width and a height of the rectangular container and the scale table. The volume equals an inner-cylinder volume of the cylinder. An inner-circle area of the cylinder is obtained according to the inner-cylinder volume and a height of the cylinder.

Abstract: Provided herein are compositions and methods for the assembly of a bioluminescent complex from two or more non-luminescent (e.g., substantially non-luminescent) peptide and/or polypeptide units. In particular, bioluminescent activity is conferred upon a non-luminescent polypeptide via structural complementation with another, complementary non-luminescent peptide.

Abstract: The invention relates to a process for preparing isocyanates by reacting primary amines with phosgene in a solvent, where the solvent comprises a dialkyl carbonate.

Abstract: Described is a method aiding in the assessment of rheumatoid arthritis (“RA”). The method is used in assessing RA in vitro. It is practiced by analyzing biochemical markers, including measuring the concentration of anti-CCP and anti-PIK 3CD and correlating the concentrations determined to the absence or presence of RA. Also disclosed is the use of a marker panel including anti-CCP and anti-PIK3CD in the diagnosis of RA and it teaches a kit for performing the method. Also described is the use of a marker panel comprising anti-CCP and anti-PIK3CD to differentiate RA from other autoimmune diseases, preferably osteoarthritis (OA).

Abstract: A method and system for optically inspecting parts are provided wherein the system includes a part transfer subsystem including a transfer mechanism adapted to receive and support a part at a loading station and to transfer the supported part by a split belt conveyor so that the part travels along a first path which extends from the loading station to an inspection station at which the part has a predetermined position and orientation for inspection. An illumination assembly simultaneously illuminates a plurality of exterior side surfaces of the part with a plurality of separate beams of radiation. A telecentric lens and detector assembly forms an optical image of at least a portion of each of the illuminated side surfaces of the part and detects the optical images. A processor processes the detected optical images to obtain a plurality of views of the part which are angularly spaced about the part.

Abstract: A method and system for optically inspecting parts are provided wherein the system includes a part transfer subsystem including a transfer mechanism adapted to receive and support a part at a loading station and to transfer the supported part by a split belt conveyor so that the part travels along a first path which extends from the loading station to an inspection station at which the part has a predetermined position and orientation for inspection. An illumination assembly simultaneously illuminates a plurality of exterior side surfaces of the part with a plurality of separate beams of radiation. A telecentric lens and detector assembly forms an optical image of at least a portion of each of the illuminated side surfaces of the part and detects the optical images. A processor processes the detected optical images to obtain a plurality of views of the part which are angularly spaced about the part.