Blood phase separator device

Claim 2

A blood collection device for receiving a sample of whole blood adapted to be centrifuged into a phase of lighter specific gravity and a phase of heavier specific gravity comprising: a collection container having an open end and a closed end; a stopper in said open end sealing same closed and being penetrable by a needle for delivering blood to said container; a separator assembly positioned inside said container intermediate said open and closed ends adapted to move along a longitudinal axis therein and including a receptacle with a thixotropic barrier material in said receptacle, said receptacle having an aperture facing said closed end of the container, the size of said aperture and the viscosity of said thixotropic barrier material cooperating to prevent said barrier material from flowing out of said aperture under normal gravity conditions; said separator assembly having a specific gravity greater than the specific gravity of the heavier blood phase and adapted to move toward said closed end during centrifugation of said device, said barrier material having a specific gravity intermediate the specific gravities of the lighter and heavier phases of blood and adapted to flow under its own influence through said aperture during centrifugation of said device, travel to a position intermediate the lighter and heavier phases of blood separated during centrifugation and adhere to the inside wall of said container to form a barrier between said phases to maintain the separation therebetween; and said receptacle having a smaller transverse dimension than the inside wall of said container to provide annular clearance therebetween for blood passage toward the closed end of said container during the blood collection procedure and for the passage of barrier material toward the interface of the phases separated during centrifugation.

Claim 3

The device of claim 1 wherein the interior of said container is evacuated.

Claim 4

The device of claim 1 wherein said receptacle alone has a specific gravity greater than the specific gravity of the heavier blood phase.

Claim 5

The device of claim 1 wherein said assembly further includes a plurality of circumferentially spaced ribs around said receptacle slidably engaging the inside wall of said container.

Claim 6

The device of claim 1 wherein said assembly further includes a removable blood clotting activator at least on its surfaces bordering the annular clearance so that whole blood contacting said activator during passage through said clearance picks up said activator and rapid blood clotting is induced.

Claim 7

The device of claim 5 wherein said activator is silica.

Claim 8

The device of claim 1 wherein said receptacle is made of plastic.

Claim 9

The device of claim 1 wherein said barrier material includes a polyester material.

Claim 10

The device of claim 1 wherein said receptacle has an access opening opposite said aperture for facilitating the deposit of barrier material into said receptacle.

Claim 11

The device of claim 1 wherein said receptacle further includes means across said access opening for preventing flow of the barrier material out of said access opening and assuring flow out of said aperture during centrifugation of said device.

Claim 12

The device of claim 10 wherein said means is an open mesh screen.

Claim 13

The device of claim 10 wherein said means is a flexible diaphragm.

Claim 14

The device of claim 10 wherein said means is a piston slidable toward said aperture to assist the flow of said barrier material through said aperture during centrifugation.

Claim 15

A blood collection device for receiving a sample of whole blood adapted to be centrifuged into a serum phase of lighter specific gravity and a clotted phase of heavier specific gravity comprising: an elongate, evacuated collection container having an open end and a closed end; a stopper in said open end sealing same closed and being penetrable by a needle for delivering blood to said container; and a separator assembly positioned inside said container intermediate said open and closed ends adapted to move along the longitudinal axis of said container and including a receptacle with a thixotropic barrier material therein, said receptacle having a smaller cross-sectional dimension than the inside wall of said container to provide an annular clearance therebetween for blood passage toward the closed end of said container during the blood collection procedure and to provide for the passage of barrier material toward the interface of the phases separated during centrifugation, said receptacle having a plurality of circumferentially spaced ribs around its periphery slidably engaging the inside wall of the container, said receptacle including an aperture facing said closed end of the container and an access opening opposite said aperture for facilitating the deposit of barrier material into said receptacle, the size of the aperture and the viscosity of the thixotropic barrier material cooperating to prevent said barrier material from flowing out of said aperture under normal gravitational conditions, said separator assembly including a removable blood clotting activator on its surfaces bordering the annular clearance so that whole blood contacting said activator during passage through said clearance picks up said activator and rapid blood clotting is induced, said separator assembly and said receptacle alone each having a specific gravity greater than the specific gravity of clotted blood, said assembly adapted to move toward said closed end during centrifugation of said device, said barrier material having a specific gravity intermediate the specific gravities of the serum and clotted phases of blood and adapted to flow under its own influence through said aperture during centrifugation of said device, travel to a position intermediate the serum and clotted phases of blood separated during centrifugation and adhere to the inside wall of said container to form a barrier between said phases to maintain the separation therebetween.

Claim 16

A blood collection device for receiving a sample of whole blood adapted to be centrifuged into a serum phase of lighter specific gravity and a clotted phase of heavier specific gravity comprising: an elongate, evacuated collection container having an open end and a closed end; a stopper in said open end sealing same closed and being penetrable by a needle for delivering blood to said container; and a separator assembly positioned inside said container intermediate said open and closed ends adapted to move along the longitudinal axis of said container and including a receptacle with a thixotropic barrier material therein, said receptacle having a smaller cross-sectional dimension than the inside wall of said container to provide an annular clearance therebetween for blood passage toward the closed end of said container during the blood collection procedure and to provide for the passage of barrier material toward the interface of the phases separated during centrifugation, said receptacle having a plurality of circumferentially spaced ribs around its periphery slidably engaging the inside wall of the container, said receptacle including an aperture facing said closed end of the container and an access opening opposite said aperture for facilitating the deposit of barrier material into said receptacle, the size of the aperture and the viscosity of the thixotropic barrier material cooperating to prevent said barrier material from flowing out of said aperture under normal gravitational conditions, said separator assembly including a removable blood clotting activator on its surfaces bordering the annular clearance so that whole blood contacting said activator during passage through said clearance picks up said activator and rapid blood clotting is induced, said separator assembly and said receptacle alone each having a specific gravity greater than the specific gravity of clotted blood, said assembly adapted to move toward said closed end during centrifugation of said device, said barrier material having a specific gravity intermediate the specific gravities of the serum and clotted phases of blood and adapted to flow under its own influence through said aperture during centrifugation of said device, travel to a position intermediate the serum and clotted phases of blood separated during centrifugation and adhere to the inside wall of said container to form a barrier between said phases to maintain the separation therebetween.