The present invention relates to a dialysis machine having a hydraulic system that is intended for providing a dialysis solution or an element of the dialysis solution, wherein the hydraulic system has a degassing pump for degassing the dialysis solution or an element of the dialysis solution, and having a pneumatic system in which a vacuum is present at least at times for operating a component of the dialysis machine, wherein there is a connection line between the suction side of the degassing pump and the pneumatic system for a vacuum generation in the pneumatic system.

A crossflow filter includes a rigid cylindrical inner wall and a rigid cylindrical outer wall inner with an inelastic filter membrane positioned therebetween defining a retentate channel inside the filter membrane and a permeate channel outside the filter membrane. Further, the filter includes transition channels shaped and connected to the inner and outer walls to deliver a flow of fluid from an inlet port to the retentate channel and to capture flow flowing longitudinally along the cylindrical inner and outer walls from both the retentate and permeate channels to respective outlet ports.

The present disclosure is to provide a method for producing polyurethane (PU) nanofibers with significantly improved hydrophilicity by producing water-soluble polymer/PU blend nanofiber by coaxial-electrospinning water-soluble polymer and hydrophobic PU, and, subsequently, dissolving and removing the water-soluble polymer from the blend nanofiber in water.

A blood filtering device comprises a casing defining a containment volume and provided with at least a first inlet for the venous blood, at least a second inlet for the intracavitary blood, at least a third inlet for the extra cavitary blood and at least an outlet mouth for the blood; blood filtering means which are housed inside the containment volume and delimiting at least one filtering volume communicating with the blood inlets and at least one collecting volume communicating with the outlet mouth; where filtering means comprise: at least a first filtering element defining a closed profile and delimiting a first filtering volume communicating with the first inlet; at least a second filtering element defining a closed profile and delimiting a second filtering volume communicating with the second inlet; at least a third filtering element defining a closed profile and delimiting a third filtering volume communicating with the third inlet.

An apparatus for isolating stems cells from extracted mammalian tissue comprising: a portable hollow casing having fixed dimensions and a sized internal spatial volume; a filter housed and contained within said sized internal spatial volume, wherein said filter captures particles in said extracted mammalian tissue having a diameter of about 5 to 10 microns or more and allows particles in said extracted mammalian tissue having a diameter of less than about 5 to 10 microns to pass through; a first channel to which a container holding said extracted mammalian tissue can attach, and through which said extracted mammalian tissue is input into the hollow casing; wherein a stem cell collection chamber can attach to said first channel, and the particles having a diameter of about 5 to 10 microns or more are output from the hollow casing through said first channel and collected in the stem cell collection chamber; and a second channel to which a remnant collection chamber can attach, and through which the particles having a diameter of less than about 5 to 10 microns are output from the hollow casing and collected in the remnant collection chamber.

Filtering systems, methods, and devices, particularly adapted for apheresis of cellular bodies and more specifically for apheresis of circulating tumor cell bodies (CTCs) employs a cross-flow channel. Systems and methods as well as devices for such a system are described. Embodiments include a cylindrical filter that employs a thin micro-machined porous filter membrane with a regular array of pores and reliably pass blood while trapping CTCs.

A filtration device includes a first channel member, a second channel member, and a filter. The first channel member has a recess recessed inward from an outer wall surface. A groove is formed is the recess and has an opening in a recessed surface of the recess. First and second channels, each defined by a through-hole, are formed in the first channel member and are connected to the groove. A first connection part connects the groove with the first channel. The second channel member has a projection that detachably mates with the recess. The second channel member includes a discharge channel that has an opening in a projecting surface of the projection, the opening being located over the groove. The filter is disposed along the groove, and positioned at the opening of the discharge channel. When the first and second channel members are placed in a operative relationship, a third channel is formed by the projecting surface of the projection and the opening of the groove. The third channel is connected to the first channel via the first connection part. The third channel at which the filter is positioned has a smaller cross-sectional area than the first channel.

The invention relates to an apparatus for extracorporeal blood treatment, comprising a blood treatment unit 1 that comprises at least one compartment 3. The invention further relates to an apparatus 15A, 15B for collecting blood clots for a blood line 5, 7 for supplying blood to or removing blood from a blood treatment unit 1 of an extracorporeal blood treatment apparatus, and to a method for determining a hemodynamic parameter during extracorporeal blood treatment using an extracorporeal blood treatment apparatus. In order to determine the hemodynamic parameter, the conveying direction of the blood pump 10 is reversed from a normal blood flow to a reversed blood flow. It has been found in practice that, in the event of a reversal in the conveying direction of the blood pump in order to carry out a measurement for determining a hemodynamic parameter, there is a risk of blood clots reaching the patients, although the dialyser traps blood clots. The apparatus according to the invention provides an apparatus 15A for catching blood clots, at least in the blood line of the extracorporeal blood circuit I that leads to the blood treatment unit 1 during a normal blood flow. The blood treatment unit traps blood clots during blood treatment having a normal blood flow. In the case of a reversed blood flow, the apparatus for catching blood clots in the blood line that leads to the blood treatment unit 1 during a normal blood flow traps blood clots that may have previously accumulated at the inlet of the blood treatment unit.

A blood filtering device has a filtration section with filter medium separating raw side and clean side. A first communication path connects raw side and a first variable blood reservoir volume; a second communication path connects raw side and a second variable blood reservoir volume coupled to a receptacle. When varying the first variable blood reservoir volume, blood contained therein flows through first communication path to raw side, plasma/serum passes through the filter medium from raw side to clean side, and residual blood flows from raw side through second communication path into the second variable blood reservoir volume. When varying the second variable blood reservoir volume, blood contained therein flows through second communication path to raw side, plasma/serum passes through the filter medium from raw side to clean side, and residual blood flows from raw side through first communication path into first variable blood reservoir volume.

A blood separation method using a blood separation filter (10A) includes: an arrangement step of arranging a housing (18) such that a blood inflow chamber (20) is positioned below a filter member (24) and the blood outflow chamber (22) is positioned above a filter medium (38); a blood treatment step of allowing blood to flow in the filter medium (38) upward from vertically below; and a post residual treatment blood collection step of arranging the housing (18) such that an outflow port (28) is positioned vertically below the blood outflow chamber (22) so as to guide the post-separation residual blood in the housing (18) to the outflow port (28).