DEVICE FOR SEPARATING AND RECOVERING BLOOD FRACTIONS

Abstract

A device for separating and recovering blood fractions includes two conical chambers communicating via their bases, the first chamber having a duct for supplying the fluid to be treated and means for recovering at least one component, the second chamber comprising an elastically deformable flexible membrane that transversely separates a space opening into the duct for communicating with the second chamber, and a bag having a volume that varies according to the deformation of the membrane.

Claims

1. A device for separating and recovering blood fractions, comprising: two conical chambers communicating via their bases, a first chamber of the two conical chambers having a duct for supplying a fluid to be treated, and recovery means for recovering at least one component of the blood, wherein a second chamber of the two conical chambers comprises an elastically deformable flexible membrane transversely separating a space opening into a duct for communicating between the two conical chambers, and a bag having a volume that varies according to deformation of the elastically deformable flexible membrane.

2. The device of claim 1, wherein the recovery means comprises at least one float having a determined density and positioned in a channel at an interface between the two conical chambers.

3. The device of claim 1, wherein the recovery means comprises a three-way valve positioned in a channel at an interface between the two conical chambers, the three-way valve comprising an outlet nozzle.

4. Equipment for separating and recovering blood fractions, comprising a centrifuge having a plate, wherein the plate has at least one recess configured to receive a device according to claim 1.

5. The equipment of claim 4, wherein the at least one recess is configured to receive a device according to claim 3, and wherein the equipment further comprises an image sensor, a field of vision of the image sensor corresponding to a passage zone during rotation of a segment for communicating between the two conical chambers and a part at least adjacent to each of the two conical chambers, the plate comprising a control means for controlling a position of the three-way valve of the device when the device is received in the at least one recess of the plate.

6. The equipment of claim 5, further comprising a computer configured to control the control means depending on development of images acquired by the image sensor.

7. A device for separating and recovering blood fractions, comprising: a first conical chamber having a narrow base; a second conical chamber having a narrow base adjacent the narrow base of the first conical chamber; a fluid pathway defined between the narrow base of the first conical chamber and the narrow base of the second conical chamber; a duct for supplying a fluid to be treated into the first conical chamber; a flexible membrane covering an opening of the second conical chamber; and a conduit for selectively recovering at least one component of the blood from a location proximate the narrow base of the first conical chamber and the narrow base of the second conical chamber.

8. The device of claim 7, further comprising a float valve in the conduit for selectively recovering the at least one component of the blood.

9. The device of claim 7, further comprising a three-way valve positioned in the conduit for selectively recovering the at least one component of the blood, the three-way valve comprising an outlet nozzle.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The present disclosure will be more clearly understood upon reading the following description, which refers to the accompanying drawings and relates to a non-limiting embodiment of the disclosure, in which drawings:

[0018] FIG. 1 is a longitudinal cross-sectional view of a device according to an embodiment of the disclosure;

[0019] FIG. 2 is a longitudinal cross-sectional view of a variant of the device according to an embodiment of the disclosure comprising a three-way valve;

[0020] FIG. 3 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the blood-charging step;

[0021] FIG. 4 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the centrifugation step;

[0022] FIG. 5 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the separating step;

[0023] FIG. 6 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the deceleration step;

[0024] FIG. 7 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the crank pin rotation step;

[0025] FIG. 8 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the step of resuming the deceleration; and

[0026] FIG. 9 is a longitudinal cross-sectional view of the variant comprising a three-way valve at the step of re-establishing communication between two cones of the device.

DETAILED DESCRIPTION

First Application Context of the Disclosure

[0027] Embodiments of the present disclosure are described below with reference to the figures, in the more specific context of cell therapies using blood components.

[0028] The embodiments described below relate to a device, preferably single-use, intended for an automated system that makes it possible to treat and to concentrate the stem cells without losing or altering their functionality, in particular, for the transplantation of hematopoietic progenitor stem cells.

[0029] The fraction rich in stem cells is isolated from the peripheral blood taken in the circulatory system.

[0030] In order to isolate the stem cells from the buffy coat, density-gradient products are used, such as those available under the names FICOLL and PERCOLL (trademarks). The density-gradient product is first introduced into the treatment device, followed by the introduction of whole blood, then a component of biological fluid is separated by centrifugation and collected by pipetting, for example.

Physical Description of the Device

[0031] The centrifugation device according to the present disclosure is formed by a molded part made of plastic material, in the general shape of an hourglass or bicone, comprising: [0032] a peripheral conical part (10) comprising, at the peripheral end thereof, a large base closed by a cover (11) and comprising a supply opening (12); and [0033] a central conical part (20), the central end of which is separated from a concave base (21) by a resilient membrane (22), and a connecting sleeve (30) between the base of the peripheral conical part (10) and the base of the central conical part (20).

[0034] The cover (11) of the peripheral conical part (10) comprises, at the central part thereof, a peripheral rib (13) that comes to rest on an annular seal (14) received in a peripheral groove (15) provided at the peripheral edge of the peripheral conical part (10). The peripheral rim (16) forms a hooking element in a chamber of a centrifuge (not shown).

[0035] The connecting sleeve (30) comprises two channels (31, 32) opening at the inside of the lower central conical part (20).

[0036] The first channel (31) establishes communication between the base of the peripheral conical part (10) and the central conical part (20). A first float (33) of density D1 is suitable.

[0037] The second channel (32) passes through the peripheral conical part (10) and opens outside the cover (11). It encloses a first float (34) of density D2 and a second float (35) of density D3.

[0038] The resilient membrane (22) is an elastically deformable biocompatible silicone membrane having an elasticity of approximately 450% and a thickness of between 1 and 2 millimeters, and a diameter of 50 millimeters. It ensures a toroidal peripheral edge that is enclosed in the annular grooves provided on the front part of the central conical part (20), and a closure cover.

[0039] The upper diameter of the peripheral (10) and central (20) conical parts is 50 millimeters, and the inside diameter of the communication channel is between 1 and 1.5 millimeters.

Description of a Three-Way Valve Variant

Description of the Centrifuge According to the Second Variant

[0040] Referring to FIG. 2, the centrifugation device according to this variant is also formed by a molded part made of plastic material, in the general shape of an hourglass or bicone, comprising: [0041] a peripheral conical part (10) closed by a cover (11) comprising a supply opening (12); [0042] a central conical part (20), the central end of which is separated from a concave base (21) by a resilient membrane (22); and [0043] a connecting sleeve (30) between the base of the peripheral conical part (10) and the base of the central conical part (20).

[0044] The connecting sleeve (30) comprises a channel (36). Channel (36) establishes communication between the base of the peripheral conical part (10) and the central conical part (20). It is provided with a crank pin that controls a three-way valve (37), which, according to its position, controls: [0045] the flow of fluid between the two conical parts (10, 20); [0046] the flow of fluid between the peripheral conical part (10) and a collection nozzle (38); and [0047] the closure of the channel (36).

[0048] The resilient membrane (22) is an elastically deformable biocompatible silicone membrane having an elasticity of approximately 450% and a thickness of between 1 and 2 millimeters, and a diameter of 50 millimeters. It comprises a toroidal peripheral edge (23) that is engaged between an annular groove (24) provided on the front edge of the central conical part (20) and a groove (25) formed in the concave base (21). The edge of groove (25) comprises a rib (26) that ensures the retention, by clipping, of the central conical part (20).

Functional Description

[0049] FIGS. 3 to 9 illustrate a sequence of centrifugation of a blood sample.

[0050] The blood sample is transferred from a sterile bag to the peripheral conical part (10) by a sterile tube that connects it to the filling nozzle of supply opening (12) (FIG. 3).

[0051] The device is then placed in a centrifuge, the peripheral conical part (10) being placed on the side of the center of the centrifuge, and the central conical part (20) being placed on the peripheral side. The three-way valve (37) is placed in the passage position, in order to allow the blood contained in the peripheral conical part (10) to flow toward the central conical part (20) under the effect of the centrifugal force (FIG. 4).

[0052] The centrifuge is then stopped in order to allow the different components of the blood to separate according to their density, increasingly the red blood cells, the white blood cells, the platelets and the plasma (FIG. 5).

[0053] A slow deceleration then takes place in order to raise the layer of interest to just below the separation zone. Once the layer of interest has arrived at the zone, to the centrifuge is rotated at a constant centrifugation speed. The layers are thus immobilized, and the resilient membrane equalizes the pressure (FIG. 6).

[0054] The three-way valve (37) is then changed into the position for establishing communication with the collection nozzle (38) in order to allow for the collection of platelets (FIG. 7).

[0055] The centrifuge is returned to slow deceleration—the layer of interest is evacuated via the lateral outlet nozzle or collection nozzle (38).

[0056] As soon as the platelet layer is recovered, the return to constant speed is commanded (FIG. 8).

[0057] The crank pin controlling the three-way valve is then returned to the passage position. The layer of interest is isolated (FIG. 9).