Embodiments in accordance with the present disclosure are directed to sample collecting and dispensing methods and apparatuses. An example apparatus includes a capillary sampler disposed on a device first end, wherein the capillary sampler is configured to collect a fluid sample via an opening and a capillary body. The apparatus further includes a reagents chamber in fluid communication with the capillary sampler, and a barrier assembly disposed between the capillary sampler and the reagents chamber, wherein the barrier assembly is configured to separate fluid in the reagents chamber from the capillary sampler. A plunger assembly disposed on a device second end opposite the device first end, may modify the barrier assembly to dispense the fluid from the reagents chamber to the capillary sampler responsive to application of a force in the direction of the device first end.

A blood sample collection and/or storage device includes a two-piece housing that encompasses a port at which a fingertip blood sample is collected. After the sample is taken, the two-piece housing is moved to a closed position to protect the sample for storage and optionally process the sample within the housing. The housing may also be opened to access the stored sample for further processing.

A method of obtaining a numerical model is disclosed. The numerical model correlates estimated line width values to minimum pressure for gas bubble generation (MPGBG) values. An MPGBG value of each capillary tube in the reference group is measured for a liquid. A nanoparticle composition is deposited, under standard conditions, on substrate(s) from each respective reference capillary tube, to form nanoparticle lines. A line width of each of the nanoparticle lines deposited using each respective reference capillary tube is measured by a microscope apparatus. A numerical model that correlates estimated line width values to MPGBG values for the liquid is calculated.

A suction tip that sucks a biological subject includes a base tip and a sub-tip. The base tip includes a distal end portion having a distal end opening, and a tubular passage connected to the distal end opening. The sub-tip includes a suction port that sucks the biological subject, and a guide passage having one end connected to the suction port and the other end that receives the distal end portion of the base tip. The base tip and the sub-tip are coupled and integrated by externally fitting the other end of the guide passage to the distal end portion, the integration forming one suction path in which the tubular passage and the guide passage communicate with each other. The suction port has a size smaller than a size of the distal end opening.

An automated pipetting system includes a pipettor. The pipettor includes a pipetting channel, a first plunger mechanism operable to change a pressure in the pipetting channel to aspirate or dispense a liquid, and a second plunger mechanism operable to change the pressure in the pipetting channel to aspirate or dispense the liquid.

An automated pipetting system includes a pipettor. The pipettor includes a pipetting channel, a first plunger mechanism operable to change a pressure in the pipetting channel to aspirate or dispense a liquid, and a second plunger mechanism operable to change the pressure in the pipetting channel to aspirate or dispense the liquid.

A pipette includes a capillary, a pressure chamber, a drive unit, and a control unit. The capillary has a first end and a second end that are two ends in a length direction and that are open. The pressure chamber communicates with an inside of the capillary via the second end. The drive unit changes a volume of the pressure chamber. The control unit controls the drive unit. The control unit outputs a vibrational movement signal that drives the drive unit so that a liquid moves from a mid-position in the capillary to a finish position that is located closer to the second end than the mid-position. The vibrational movement signal has a waveform that drives the drive unit so that the volume of the pressure chamber alternately increases and decreases repeatedly.

Described are exemplary embodiments of a syringe for use with a handheld positive displacement pipette, the syringe being releasably retainable by the pipette. Syringe embodiments may be configured to hold different material volumes. At least certain syringe embodiments may include a cooperative adapter that is used to releasably couple the syringe to the pipette.

A positive displacement pipette tip for motorized control automation or liquid handling instrument system is disclosed. The positive displacement pipette tip includes a pipette tip and a pipette plunger. An interface portion of the pipette tip of the positive displacement pipette tip is designed to be used in combination with a zero-insertion force pipette tip clamping mechanism in, for example, a liquid handling instrument. Further, the pipette plunger of the positive displacement pipette tip is designed to be used in combination with a zero-insertion force pipette plunger clamping mechanism in, for example, a liquid handling instrument.

A testing assembly for the rapid detection of a desired chemical from a sample, the testing assembly having a sample collection device for obtaining the sample and depositing the sample into a chemical capture cartridge that operably engages with a sensing device, the chemical capture cartridge utilizing the microdiffusion of reagents to isolate the desired chemical from the sample and react the desired chemical to form a detectible complex that can be detected and measured. The testing assembly can be portable and can rapidly diagnose a toxic industrial chemical exposure in just a few minutes, preferably about a minute or less for cyanide exposure using a blood sample from a subject onsite. The testing assembly can be used to determine the presence and/or concentration of a toxic industrial chemical in a variety of samples, including biological, environmental, and industrial samples.