Abstract: Methods of separating selected blood components separate blood by centrifugation in a rotating chamber into a first separated blood component, a residual blood fluid, and an interface between the first separated blood component and the residual blood fluid. The methods withdraw the first separated blood component out of the rotating chamber through a first outlet port, and withdraw the residual blood fluid out of the rotating chamber through a second outlet port. During the separation step, the methods accumulate a second separated blood component in the interface without withdrawal from the rotating chamber by controlling the position of the interface within the rotating chamber at a location spaced away from flow communication with both the first and second outlet ports.

Abstract: A blood processing system and associated method include a first variable volume chamber to hold blood and a second variable volume chamber to hold additive solution for blood. The system and method further employ a separation device to remove undesired material from blood. An actuated element exerts external force simultaneously upon both first and second variable volume chambers to expel a first flow of blood from the first variable volume chamber and a second flow of additive solution from the second variable volume chamber. The system and method mix outside the first and second variable volume chambers the blood flow with the flow of additive solution to create a mixed flow comprising blood and additive solution. The system and method direct the mixed flow of blood and additive solution through a filter to remove undesired matter from the blood.

Abstract: Systems and methods for separating platelets from blood derive the yield of platelets in real time as processing is accomplished. The systems and method determine an incremental blood volume processed during a succession of incremental time periods during the separation step. The systems and methods also estimate a separation efficiency for the separation device during each incremental time period, while also estimating a current count of platelets available from the donor during each incremental time period. The systems and methods multiply the determined incremental blood volume for each incremental time period by the estimated current count of platelets for each incremental time period by the estimated separation efficiency for each incremental time period, to derive an incremental platelet yield for each incremental time period. The systems and methods sum the incremental platelet yields over the succession of incremental time periods to obtain the derived yield of platelets.

Abstract: Blood separation systems and methods separate mono nuclear cells from whole blood. The systems and methods introduce whole blood into a rotating chamber for separation into red blood cells, a plasma constituent, and an interface carrying mono nuclear cells between the red blood cells and the plasma constituent. The systems and methods convey whole blood into the chamber while removing red blood cells and the plasma constituent and while maintaining the interface at a set location within the chamber. At an appropriate processing time, the systems and methods move the interface from the set location for removal from the chamber through an outlet path. The outlet path includes a sensing element to locate mono nuclear cells in the outlet path outside the chamber.

Abstract: Systems and methods separate whole blood containing leukocytes in a first separation chamber into a first layer comprising red blood cells, a second layer comprising a suspension of platelets, and an interface between the first and second layers. The systems and methods convey the suspension of platelets into a second separation chamber while simultaneously filtering the suspension of platelets to reduce the number of leukocytes. The systems and methods separate the filtered suspension of platelets in the second separation chamber into a platelet-rich concentrate and platelet-poor component.

Abstract: A separation zone for separating platelets from a platelet-rich suspension establishes a relationship between its radial thickness (h) and axial height (Z) that, taking into account the given angular velocity of rotation and the given kinematic viscosity of the platelet-rich suspension introduced through the inlet, represents a (.lambda.) value that is less than 700,where ##EQU1## where: .OMEGA. is the angular velocity (in rad/sec);h is the radial depth (or thickness) of the chamber (in cm);.nu. is the kinematic viscosity of the fluid being separated (in cm.sup.2 /sec); andZ is the axial height of the chamber (in cm).

Abstract: A system for separating at least one constituent from a liquid suspension such as blood induces high velocity flow by viscous drag about the circumference of a spinner having a filtration membrane with pore sized selected for the desired constituent. The high velocity circumferential flow is bounded by a spaced apart shear wall, with a spacing selected relative to the diameter of the spinner and its rotational velocity, also with respect to the viscosity of the suspension, to establish a flow within the shear gap, as substantial centrifugal forces are exerted upon the suspension. Under these conditions, in contact with the membrane and filtrate passes through the membrane is replenished with minimal adverse effects from deposition and concentration polarization, and with high efficiency because of high shear levels that are maintained. The filtrate is collected within the interior of the spinner in a conduit system and passed to an outlet orifice.

Abstract: A container has first and second walls, each formed of a thermoplastic sheet having a peripheral edge. A peripheral seal joins the peripheral edges together to form an interior chamber enclosed by the first and second walls. A port communicates with the interior chamber. The port is spaced from and does not extend through the peripheral seal. The port comprises a hollow thermoplastic tube, which extends through a slit in one of the first and second sheets and is oriented tangentially thereto. The slit is fused by heat about the tube, forming a heat fused junction. A medical product or a blood filter material can be housed in the interior chamber.

Abstract: Blood separation systems and methods utilize a membrane separation device comprising a gap between a microporous membrane and a surface facing the microporous membrane, one of the microporous membrane and the surface being rotatable relative to the other to cause separation of whole blood in the gap into plasma and concentrated red blood cells. The systems and methods include an inlet pump element coupled to the membrane separation device to convey whole blood having a known beginning hematocrit value into the gap for separation. The systems and methods also include a drive element coupled to the membrane separation device to cause rotation of the rotatable one of the microporous membrane and the facing surface. The systems and methods command the inlet pump element and the drive element as a function of the known beginning hematocrit value.

Abstract: A blood component separating device comprises a centrifuge bowl adapted for rotation about its axis in a centrifuge. The bowl defines an outer circumferential wall plus an inner circumferential wall, spaced from the outer wall, to define a circumferential slot adapted for receiving blood components. Access tubing is adapted for communication with the slot. Preferably, an elongated, flexible, collapsible inner liner is provided in the slot. Individual access tubing also may communicate with an elongated container interior between the ends of the elongated, collapsible container. Furthermore, a portion of the slot may define the shape of an outwardly extending spiral, to provide an increasing gravitational field upon fluids therein as the fluid moves along the slot.

Abstract: Systems and methods take into account that the spleen normally holds a number of platelets in reserve out of circulation. During blood processing, the spleen releases these platelets into the donor's circulatory system, making them available for collection. The systems and methods estimate the number of platelets N.sub.SPLEEN held in reserve by the spleen in a human body. The systems and methods derives a splenic mobilization function (Spleen), which can be expressed as a function of a precount of platelets Plt.sub.PRE. The systems and methods estimate N.sub.SPLEEN where:N.sub.SPLEEN =(Spleen-1).times.Plt.sub.PRE .times.DonVolwhere DonVol is blood volume in the body. The systems and methods can also estimate the total number of platelets N.sub.PLT in a human body, taking the Spleen function into account, where:N.sub.PLT =Plt.sub.PRE .times.Spleen.times.

Abstract: Systems and methods centrifugally separate mono nuclear cells from whole blood in a separation chamber. The systems and methods control the exit hematocrit value of red blood cells separated in the chamber by recirculating a portion of the red blood cells removed from the chamber for mixing whole blood entering the separation chamber. The systems and methods also control the entry hematocrit value of whole blood entering the separation chamber by recirculating a portion of the plasma constituent removed from the separation chamber for mixing whole blood entering the separation chamber.

Abstract: A peristaltic pump tube holder includes a body that supports a flexible tubing loop in an erect, outwardly bowed position extending from the body for engagement with a peristaltic pump rotor. The holder also includes a receptacle carrying the body. The receptacle includes a wall forming a chamber that covers the flexible tubing loop and at least partially shields it from contact. The chamber further serves, during engagement between the tubing loop and a peristaltic pump rotor, as a cover for the peristaltic pump rotor.

Abstract: A process for filtration of matter from a liquid suspension through a membrane uses a rotor within a concentric shell rotating with a surface velocity which, together with the rotor-shell gap and suspension viscosity, establishes vigorous vortex cells about the rotor. At least one of the rotor and shell surfaces include a filter membrane. Tangential velocity components at the membrane surface constantly sweep the membrane surface to limit cell deposition tendencies while constantly replenishing the medium to be filtered. The vortex cells are established along the length of the membrane despite the constant extraction of filtrate and the resultant change in physical characteristics of the suspension.

Abstract: Blood processing systems and methods separate whole blood into red blood cells and a plasma constituent within a rotating centrifugal separation device. The systems and methods convey whole blood into the separation device through an inlet path including a pump operable at a prescribed rate. The systems and methods remove plasma constituent from the separation device through an outlet path including a pump operable at a prescribed rate. The systems and methods derive a value H.sub.b representing an apparent hematocrit of whole blood entering the separation device, where: ##EQU1## and where H.sub.rbc is a value relating to hematocrit of red blood cells in the separation device. The systems and methods generate outputs and control commands based, at least in part, upon H.sub.b.

Abstract: The position of a rotating pump element is sensed by a reflective object sensor 406 in association with a view disk 412 coupled to the operative element for rotation in synchrony with the operative element. The view disk 412 has first 422 and second 420 surface portions that present themselves in succession to the reflective object sensor during rotation of the operative element. The first surface portion 422 is spaced at or near the optical focus of the reflective object sensor, whereas the second surface portion 422 is not. The reflective object sensor 406 thus generates different outputs, depending upon whether the first surface or second surface portions are in optical alignment with the reflective object sensor.

Abstract: A tube holder secures to the rotating processing chamber of a centrifuge tubing that conveys fluid to or from the chamber. The tube holder is part of a carrier that is connected by a pin to a support on the processing chamber. The support has walls defining an enclosure. The carrier swings about the pin on the support between an opened position free of the enclosure and a closed position captured within the enclosure. In the opened position, the tube holder is exposed for receiving tubing. In the closed position, the tubing is retained within the enclosure in the tube holder. The tube holder allows straightforward attachment and removal of the tubing, always in a prescribed manner and with a single hand. The tube holder securely retains the tubing during use in a closed, protected environment, safeguarding it against inadvertent dislodgement, removal, or damage.

Abstract: A squeezable, resilient pouch is used for collecting a blood sample. The walls of the pouch are moved together in response to the application of an external squeezing force. The squeezing force collapses the pouch and expels fluid from it. Upon removal of the squeezing force, the resilience of the pouch walls moves them apart. The resilient expansion of the pouch creates suction that draws a fluid sample into the pouch. The pouch can be attached to a blood collection and/or storage container by flexible tubing in a way that prevents communication with the atmosphere. By squeezing the pouch, the user obtain a sample of the blood without using special tools and with no danger of activating or damaging the blood component being sampled.

Abstract: Systems and methods of collecting blood cells, substantially free of undesired matter, use a first container, that forms a part of a blood collection system, to initially collect a quantity of blood cells. A filtration system is then attached to the first container. The filtration system includes a second container, a first fluid path that leads to the second container through a filtration device, and a second fluid path that leads to the second container bypassing the filtration device. The blood cells are conveyed from the first container through the first fluid path and filtration device and into the second container to separate the undesired matter from the blood cells. The blood cells, now substantially free of the undesired matter, are then conveyed from the second container through the second fluid path, bypassing the filtration device, and back into the first container. The filtration system is then detached from the blood collection system.