A liquid evaluation system can include a cartridge including a channel configured to pull a liquid into the channel by capillary action. The cartridge can include an upper plate and a lower plate located in close proximity to the upper plate. The lower plate includes a deposition region for dispensing liquid. The extent of the deposition region in one or more directions can be defined by a repellant barrier, such as a boundary with a set of areas configured to be repellant to the liquid. An internal facing surface of each plate can include a corresponding region forming the channel. Each of the regions can be configured to have an affinity for the liquid. The close proximity of the plates and the regions having an affinity for the liquid cause the liquid to be pulled into the channel by capillary action.

A pipette controller for aspirating and dispensing multiple aliquots of a fluid from a reservoir of fluid. The pipette controller can include a pipette holder adapted to operatively connect a pipette to the pipette holder; a pump having a vacuum port and a pressure port, the pump pneumatically connected to the pipette holder; an aspirate valve that controls airflow between the vacuum port and the pipette holder; a dispense valve that controls airflow between the pressure port and the pipette holder; a piston chamber; an aliquot dispense pump including a piston having a shaft that extends into the piston chamber, the shaft defining a stroke length; and an aliquot check valve that connects the pipette holder and the aliquot dispense pump; wherein the aliquot valve opens to allow airflow into the pipette holder upon engagement of the aliquot dispense valve. The pipette controller can also include a piston pump pneumatically connected to the pipette holder configured to deliver a bolus of air to the pipette holder.

An object of the present invention is to provide a blood test kit and a blood analysis method, which are for performing quantitative analysis of components by precisely obtaining a dilution factor. According to the present invention, provided is a blood test kit for analyzing a concentration of a target component in a blood sample using a normal component which is homeostatically present in blood, the kit including a diluent solution for diluting the blood sample, a first storing instrument for storing the diluent solution, a separation instrument for separating and recovering blood plasma from the blood sample diluted with the diluent solution, a holding instrument for holding the separation instrument, a second storing instrument for storing the recovered blood plasma, and a sealing instrument for keeping the stored blood plasma within the second storing instrument, in which the separation instrument is composed of glass fiber coated with a resin.

The present invention relates to a kit with which a user can conveniently and hygienically collect bio-samples using a collecting rod. A collection kit for collecting a bio-sample using a collection rod according to the present invention comprises: a cap on the lower part of the central part of which a filter is detachably mounted, wherein a cover is formed on the upper part of the filter; a collection rod having a collection unit and a handle part; and a tube fastened with the cap and for accommodating the extraction solution.

A system and method for handling a sample comprising particles (CE) bound to ferromagnetic particles (FP); a magnetic field is created in a container (3) inside which the sample (TS) is arranged so that the particles (CE) are attracted against a side wall (4) of the container (3); part of the sample (TS) is sucked through a cannula (8), kept in position by an alignment device (10) so as not to be in contact with the side wall (4) of the container (3), without withdrawing the particles (CE) that remain in contact with the side wall (4).

Unitary measuring pipettes include a tubular body of biaxially oriented thermoplastic material, together with size reduction, elimination, and/or reorientation of longitudinally spaced, raised circumferential witness features, to mitigate or avoid interference between such witness features and graduated volumetric markings on an outside surface of the tubular body. Methods and apparatus for vacuum forming of unitary measuring pipettes are also provided. Gas permeable apertures or pores having a maximum width of no greater than 150 microns, in ranges of 10-100 microns, 10-50 microns, or subranges thereof, may be defined in face plates or inserts received by mold blanks, or defined in molding surface of cooperating mold bodies, and may be used to produce a tubular pipette body having reduced height witness features. Cooperating mold bodies may each be produced from multiple mold body sections with gas passages defined therein and/or therebetween.

A qualitative and quantitative heavy metal analysis device and, more particularly, a qualitative and quantitative heavy metal analysis device implemented by a rotary platform are provided. The rotary platform device includes a main injection part which is positioned near a rotating shaft of a rotary platform, wherein the main injection part is configured to receive a fluid sample containing heavy metals, a pH adjusting part configured to adjust pH of the fluid sample, a detecting part coated with a chelating agent configured to initiate a color reaction with heavy metals in the fluid sample by spreading the pH-adjusted fluid sample into the detecting part, and a ruler for measuring a spreading distance of the color reaction, wherein the fluid sample moves from the main injection part through the pH adjusting part to the detecting part by a rotation of the rotary platform device.

A method of reducing or preventing bubbles in a microfluidic sample liquid is provided. The method comprises providing a microfluidic sample holder comprising an enclosed fluid channel for holding at least part of the sample liquid, and filling at least part of the fluid channel with a sample liquid. The method further comprises: a step of pressurizing the sample liquid in the fluid channel to raise a sample liquid pressure to an elevated pressure higher than an ambient pressure and an operating pressure, a step of maintaining the sample liquid pressure at least at the elevated pressure for a predetermined period to cause dissolving of gas into the sample liquid, and a step of reducing the sample liquid pressure from the elevated pressure to the operating pressure. An associated system is also provided.

The invention, is directed to devices and methods for low cost and convenient separation, of plasma from whole blood. In some embodiments, devices of the invention comprise an integrated collection of channels and chambers m a body that permit acquisition of a blood sample by capillary action, centrifugal separation of cells from plasma, and manual dispensing of purified plasma by simple pinching of a bellows chamber to force air into plasma-holding channels which thereby expels a predetermined volume of the purified plasma.

Unitary measuring pipettes include a tubular body of biaxially oriented thermoplastic material, together with size reduction, elimination, and/or reorientation of longitudinally spaced, raised circumferential witness features, to mitigate or avoid interference between such witness features and graduated volumetric markings on an outside surface of the tubular body. Methods and apparatus for vacuum forming of unitary measuring pipettes are also provided. Gas permeable apertures or pores having a maximum width of no greater than 150 microns, in ranges of 10-100 microns, 10-50 microns, or subranges thereof, may be defined in face plates or inserts received by mold blanks, or defined in molding surface of cooperating mold bodies, and may be used to produce a tubular pipette body having reduced height witness features. Cooperating mold bodies may each be produced from multiple mold body sections with gas passages defined therein and/or therebetween.