The device (100) comprises a cavity (101) and at least two microporous membranes (102), wherein the microporous membranes (102) are arranged in series in the cavity (101) and divide the cavity (101) into a plurality of chambers (1011); each of the microporous membranes (102) is provided with micropores (103), and two adjacent chambers (1011) are in communication via the micropores (103); and each of the chambers (1011) is provided with an electrode (1012).

A particle separating device includes at least three liquid chambers adapted to store a liquid therein; at least two liquid passages, each connecting adjacent two of the liquid chambers; an inlet adapted to introduce a liquid in which multiple particles of different sizes are dispersed into one of the liquid chambers; and at least two electrodes disposed inside at least two of the liquid chambers, respectively, the electrodes adapted to apply different electrical potentials to the liquid. The cross-sectional areas of the at least two liquid passages are different from each other.

A blood measuring apparatus includes: a liquid supply source storing a sheath liquid and applying a pressure to supply the sheath liquid to first and second chambers, pressures of the sheath liquids to be supplied to the first and second chambers different from each other; a sheath flow generator sending a blood sample supplied to the first chamber, to the aperture while causing the blood sample to be converged by a sheath flow due to the sheath liquid supplied from the liquid supply source; and a swirling flow generator causing the blood sample in the second chamber, to be converged by a swirling flow due to the sheath liquid supplied from the liquid supply source, thereby allowing the blood sample to flow in a direction separating from the aperture.

A system and method for the label-free analysis of cells includes a purification device configured to receive a heterogeneous population of cells, the purification device temporarily trapping therein a subpopulation of cells from the heterogeneous population of cells and a cell analysis device positioned downstream of the purification device and configured to measure one or more cellular parameters including cell count, measured cell size, and/or cell morphology. In an alternative embodiment, the subpopulation of cells is analyzed while they are trapped within the purification device.

Systems and methods to integrate electrical sensors comprising parallel electrodes into microfluidic devices that are manufactured using soft lithography are disclosed herein. With minimal fabrication complexity, more uniform electric fields than conventional coplanar electrodes are produced. The methods disclosed are also more suitable for the construction of complex electrical sensor networks in microfluidic devices due to greater layout flexibility and provide improved sensitivity over conventional coplanar electrodes.

A nanopore device includes a pore and an electrode pair. A current measurement unit applies a bias voltage that corresponds to a voltage setting command across an electrode pair and generates digital current data that corresponds to a current signal that flows through the nanopore device. A data processing apparatus generates the voltage setting command, acquires the current data and voltage data including information with respect to the waveform of the bias voltage Vb in a form in which they are associated on the time axis, and judges the kind of particles stored in the nanopore device based on the current data and the voltage data.