Abstract: A floating element for separating components of a physiological fluid comprises two parts that are relatively movable. The two parts define a prescribed volume between them when at their maximum separation, and one of the parts may be moved toward the other to express the fluid contained in the volume between the parts. The parts are made of materials having densities so that they assume a desired position in the fluid to allow selected components to be easily obtained and expressed.

Abstract: A floating separating element for use in centrifugal separation of components of a physiological fluid comprises a positioning part and a separating part, where the positioning part is designed to automatically assume a position in a supernatant and a separating part is positioned at a desired location with respect to the interface between the supernatant and heavier components. In preferred embodiments the physiological fluids are blood or bone marrow aspirate, and the heavier components comprise red blood cells. The positioning part comprises the majority of the mass of the separating element and is thin so that differences in the position of the separating element with respect to the interface are small compared to differences in the densities of the separated compoments, particularly the component comprising red blood cells. A method allows red blood cells to move the separating element during decanting to ensure complete decant of the supernatant.

Abstract: A centrifuge has a rotor for receiving a disposable processing unit. The centrifuge is configured such that the motor is attached to an enclosure and the enclosure is supported on a base. The connection between the base and the enclosure is a vibration isolator, and the isolator is positioned such that its effective line of action aligns with the effective plane of rotation of the rotor. In accordance with another feature of the invention, the processing units are held in a decanting position by a decant ring that moves vertically but does not rotate. The ring engages the top of the processing unit during decant and the abrasion is minimal.

Abstract: A method for aspirating bone marrow includes the step of injecting anticoagulant into the area Of the bone marrow cavity surrounding the entry site of the aspiration needle. The amount of anticoagulant may be relatively small because the primary objective is to address the damage caused by entry of the needle into and through regions of the bone marrow cavity. As little as 0.5 ml heparin is injected prior to aspiration. Additional anticoagulant is provided in the collection syringe to facilitate further processing, as by centrifugal fractionation of the marrow to obtain desired components.

Abstract: A separator disk for use in centrifugal separation of components is designed to automatically position itself during separation at the interface between the supernatant and the remaining components. Preferably the interface is between plasma and red blood cells.

Abstract: A separator disk for use in centrifugal separation of components is designed to automatically position itself during separation at the interface between the supernatant and the remaining components. Preferably the interface is between plasma and red blood cells.

Abstract: A floating element for separating components of a physiological fluid comprises two parts that are relatively movable. The two parts define a prescribed volume between them when at their maximum separation, and one of the parts may be moved toward the other to express the fluid contained in the volume between the parts. The parts are made of materials having densities so that they assume a desired position in the fluid to allow selected components to be easily obtained and expressed.

Abstract: A floating element for separating components of a physiological fluid comprises two parts that are relatively movable. The two parts define a prescribed volume between them when at their maximum separation, and one of the parts may be moved toward the other to express the fluid contained in the volume between the parts. The parts are made of materials having densities so that they assume a desired position in the fluid to allow selected components to be easily obtained and expressed.

Abstract: A container designed for use as a disposable processing unit in a centrifuge includes first and second chambers connected by a bridge that allows transfer of fluid between the chambers. One of the chambers has a sloped floor that directs fluids to a smaller bottom portion for providing greater depth in the collected fluids. The container also includes cam surfaces that facilitate insertion of the container in a centrifuge in the desired orientation. As well, a key may be provided to ensure that the container is used in the correct centrifuge.

Abstract: A floating element for separating components of a physiological fluid comprises two parts that are relatively movable. The two parts define a prescribed volume between them when at their maximum separation, and one of the parts may be moved toward the other to express the fluid contained in the volume between the parts. The parts are made of materials having densities so that they assume a desired position in the fluid to allow selected components to be easily obtained are expressed.

Abstract: One or more chemicals are added to a physiological fluid to alter the density and/or shape of cells in the fluid to provide a desired sedimentation rate of the cells. In a preferred embodiment, the chemical to be added is an anticoagulant, preferably ACD.

Abstract: A separator disk (4) for use in centrifugal separation of components is designed to automatically position itself during separation at the interface between the supernatant and the remaining components. Preferably the interface is between plasma and red blood cells.

Abstract: A centrifuge has a rotor for receiving a disposable processing unit. The centrifuge is configured such that the motor is attached to an enclosure and the enclosure is supported on a base. The connection between the base and the enclosure is a vibration isolator, and the isolator is positioned such that its effective line of action aligns with the effective plane of rotation of the rotor. In accordance with another feature of the invention, the processing units are held in a decanting position by a decant ring that moves vertically but does not rotate. The ring engages the top of the processing unit during decant and the abrasion is minimal.

Abstract: A system for the collection of physiological fluids includes a vacuum source (14) that is controlled to provide low vacuum as a function of whether fluids are entering the system. The suction wand and associated tubing are made of thin flexible materials, and the pressures employed do little damage to the collected fluids.

Abstract: A separator disk (4) for use in centrifugal separation of components is designed to automatically position itself during separation at the interface between the supenatant and the remaining components. Preferably the interface is between plasma and red blood cells.

Abstract: A method for washing collected blood uses an inert anticoagulant during collection of the blood. The inert anticoagulant does not interfere with agglomeration of the red blood cells so that gravity sedimentation separation is facilitated. The preferred inert anticoagulant is CPD.

Abstract: A system for the collection of physiological fluids includes a vacuum source (14) that is controlled to provide low vacuum as a function of whether fluids are entering the system. The suction wand and associated tubing are made of thin flexible materials, and the pressures employed do little damage to the collected fluids.

Abstract: A filter bag (200) and connector cartridge are used for collection of physiological fluids. The bag (200) includes an internal filter (206) and two seals (218, 220) on the perimeter. An inner seal (218) bonds the outer sheets (202, 204) of the bag and the filter, while the outer seal (220) bonds only the two outer sheets (202, 204) and acts as a safety seal. The bag includes a verification element that cooperates with a verification connector to ensure that the bag is properly attached to the fluid supply line before a fluid pump is enabled.

Abstract: A system for the collection of physiological fluids includes a vacuum source (14) that is controlled to provide low vacuum as a function of whether fluids are entering the system. The suction wand and associated tubing are made of thin flexible materials, and the pressures employed do little damage to the collected fluids.