DEVICE AND METHOD FOR REMOVING UNDESIRABLE BIOLOGICAL AND/OR CHEMICAL ENTITIES FROM BIOLOGICAL FLUIDS

Abstract

A device for removing a biological and/or chemical entity (C) from extracorporeal blood (B) is disclosed. The device has a hollow capture chamber with an inlet for the entry of the extracorporeal blood (B) and an outlet for the outflow of the extracorporeal blood (B) and a capture element inside the capture chamber having a reactant surface placed in contact with the extracorporeal blood (B) and a plurality of binding agents (A) for the biological and/or chemical entity to be removed (C) such that the biological and/or chemical entity (C), upon exiting the capture chamber, is removed from the extracorporeal blood (B) as linked to the reactant surface.

Claims

1. Device for the removal of a biological and/or chemical entity (C) from an extracorporeal blood volume (B) comprising: a hollow capture chamber having an inlet for the entry of the extracorporeal blood (B) and an outlet for the outflow of the extracorporeal blood (B) and a capture element inside the capture chamber and movable relative to the capture chamber, the capture element having a reactant surface placed in contact with the extracorporeal blood (B) and comprising a plurality of binding agents (A) for the biological and/or chemical entity to be removed (C) such that at the outlet of the capture chamber the biological and/or chemical entity (C) is removed from the extracorporeal blood (B), the biological and/or chemical entity (C) being bonded to the reactant surface, wherein the total volume of extracorporeal blood (B) flowing inside the capture chamber is between 1 and 6 TBVs and wherein each TBV consists of up to 5 litres of blood.

2. The device according to claim 1, wherein the biological and/or chemical entity to be removed (C) is a circulating tumour cell.

3. The device according to claim 1, wherein the binding agents (A) comprise one or more antibodies, or adhesion proteins, or aptamers, thereby providing the removal of epithelial, mesenchymal, hybrid epithelial-mesenchymal, and stem-like CTCs, singly and/or in clusters.

4. The device according to claim 1, wherein the capture chamber has a cylindrical shape and the movable capture element extends longitudinally within the capture chamber.

5. The device according to claim 1, wherein the movable capture element is rotatable about a longitudinal axis (a) of the capture chamber.

6. The device according to claim 1, wherein the movable capture element is removable from the capture chamber.

7. The device according to claim 1, wherein the reactant surface of the movable capture element is shaped like a helix or the like.

8. The device according to claim 1, further comprising one or more conical structures having each a filtering mesh surface made of holes with a diameter equal or greater than 100 m.

9. The device according to claim 1, wherein the plurality of binding agents (A) is distributed evenly over the entire reactant surface of the movable capture element.

10. The device according to claim 1, wherein the plurality of binding agents (A) consists of binding agents of a different nature, which are concentrated in specific areas of the reactant surface of the movable capture element.

11. The device according to claim 1, wherein the binding agents (A) are evenly distributed or concentrated in specific areas on the inner surface of the capture chamber.

12. The device according to claim 1, wherein the total volume of extracorporeal blood (B) flowing inside the capture chamber is up to 14 TBVs that consists of up to 70 litres of blood.

13. Extracorporeal circulation system comprising: extraction means for extracting venous blood (B) from the vascular system of a patient (P); input means for introducing the extracted blood (B) into the device according to claim 1, output means for extracting the blood (B) from the device and re-entry means for reintroducing the blood (B) extracted from the device into the vascular system of the patient (P).

14. The system according to claim 13, further comprising: a means for introducing an anticoagulant upstream of the device and a temperature control unit downstream of the device.

15. Ex-vivo method for the removal of at least one biological and/or chemical entity (C) from an extracorporeal blood volume (B) comprising: a) introducing the extracorporeal blood (B) into a hollow capture chamber comprising in its interior a capture element, the capture element being movable relative to the capture chamber; b) filtering the extracorporeal blood (B) by contact with a reactant surface of the movable capture element comprising a plurality of binding agents (A) for the biological and/or chemical entity (C) to be removed; and c) extracting the extracorporeal blood (B) devoid of said biological and/or chemical entity (C) from the capture chamber; wherein the total volume of extracorporeal blood (B) flowing inside the capture chamber is between 1 and 6 TBVs and wherein each TBV consists of up to 5 litres of blood.

16. The method according to claim 15, further comprising: d) stopping the introduction of extracorporeal blood (B) into the capture chamber after introducing a predetermined volume of blood (B) and removing the capture element to analyse the nature and quantity of the biological and/or chemical entity (C) removed and present on the reactant surface.

17. The method according to claim 15, wherein the total volume of extracorporeal blood (B) flowing inside the capture chamber is up to 14 TBVs that consists of up to 70 litres of blood.

18. (canceled)

19. The method according to claim 15, further comprising diagnosing and/or monitoring the progression of a tumour disease present in the extracorporeal blood wherein the extracorporeal blood is obtained from a patient suspected of having circulating tumour cell.

Description

[0079] These and other aspects of the present invention will become more apparent in the light of the following description of a few preferred embodiments described below.

[0080] FIGS. 1a and 1b are schematic representations of the device according to the present invention in a longitudinal view (a) and in cross section (b);

[0081] FIG. 2 is a schematic representation of a capture element according to an embodiment of the present invention;

[0082] FIG. 3 is a schematic representation of the capture element of FIG. 2 with a progressive distribution of the binding agents on the reactant surface;

[0083] FIGS. 4a, 4b, 4c and 4d are schematic representations of a capture element according to a second (a, b) and a third (c, d) embodiment of the present invention in a longitudinal view (a, c) and in cross section (b, d);

[0084] FIG. 5 is a representation of an extracorporeal circulation system according to the present invention;

[0085] FIG. 6 shows a detail of the extracorporeal circulation system according to an embodiment of the present invention;

[0086] FIG. 7 shows a detail of the extracorporeal circulation system according to another embodiment of the present invention; and

[0087] FIG. 8 schematically shows a flow diagram of a method according to the present invention.

[0088] FIG. 1 is a schematic representation of the device 1 for the removal of at least one undesirable biological and/or chemical element C (not shown in the figure) from an extracorporeal blood volume B. In particular, the device is suitable for the removal of circulating tumour cells. The device 1 essentially consists of a capture chamber 10 having an inlet 12 for the entry of the extracorporeal blood B and an outlet 14 for the outflow of the blood B. As can be seen from the comparison of FIGS. 1a and 1b, the capture chamber has a hollow cylindrical shape and the blood B flows through the cavity of circular cross-section.

[0089] Inside the capture chamber 10 there is the capture element 20; 20; 20, which, thanks to the presence of a reactant surface (not shown in the figure) placed in contact with the blood B, is able to capture and remove the undesirable biological and/or chemical entity C from the bloodstream B.

[0090] FIG. 2 shows an embodiment of a capture element 20 to be placed inside the capture chamber 10. This consists of a longitudinal element 24 parallel to the longitudinal axis a of the capture chamber 10 around which a helical-shaped reactant surface 22 is wound. Specifically, the reactant surface 22 has the shape of an Archimedes' screw. The binding agents A (represented in the figure by arrows) are distributed on the reactant surface 22, the which agents are used to capture the biological and/or chemical entity C to be removed, represented by a circulating tumour cell. As can be seen in the figure, the capture element 20 can rotate around the longitudinal axis a of the capture chamber 10. This rotation is caused by the blood flow B which drives the reactant surface 22 into a helical motion. In this way, each part of the reactant surface 22 can come into contact with the blood flow B.

[0091] FIG. 3 shows the particular case in which the binding agents are distributed in a circumscribed manner in certain regions of the reactant surface 22 of the capture element 20. In particular, the figure shows six different rectangular regions defined on the helical-shaped reactant surface 22, which in FIG. 3 is arranged on a single plane for reasons of clarity. Each of the six regions displays a binding agent A of a different nature (A.sub.1, A.sub.2, A.sub.3, A.sub.4, A.sub.5 and A.sub.6), so that different subpopulations of tumour cells C (in this case six) associated with different antigens may be simultaneously captured and localized on the reactant surface 22 in an easier and faster way. Alternatively, the different types of binding agents can be adhered to the central device with an even concentration but not located on specific surfaces, i.e. by distributing them homogeneously over the entire surface of the device or on the internal wall of the capture chamber.

[0092] FIG. 4 shows another embodiment of a capture element 20; 20 to be placed inside the capture chamber 10. According to this embodiment, the capture element 20; 20 has a conical structure and is positioned inside the capture chamber 10 so that the blood flow enters through the base of the conical structure. The capture element may comprise a single conical structure 20 (FIGS. 4a and 4b) or a plurality of conical structures 20. Specifically, FIGS. 4c and 4d show the case in which two conical structures are placed in series in the direction of the blood flow B. The conical structure 20; 20 of this embodiment, in particular, consists of thin cables made of biocompatible material onto which the binding agents A adhere. The conical structure 20; 20 has a circular base and extends symmetrically around a longitudinal element 24; 24 parallel to the longitudinal axis a of the capture chamber 10.

[0093] FIG. 5 shows an extracorporeal circulation system 100 according to the present invention. Through a system of cannulae 2 the blood B can be extracted from the vascular circuit of a patient P and through another system of cannulae 3 it can be introduced into the removal device 1. A means 6 for the introduction of an anticoagulant is inserted between the two systems of cannulae 2 and 3. After passing inside the device 1, the blood B can be extracted through suitable dedicated means 4, and by passing through a temperature control unit 7, reintroduced through a new system of cannulae 5 into the body of the patient P. An appropriate means 8 for the reintegration of fluids, for example for neutralizing the effect of the anticoagulant, is inserted in the vicinity of the system of cannulae 5 for reintroducing the blood B.

[0094] FIG. 6 shows a detail of the system 100 with regard to the inlet 12 and the outlet 14 of the capture chamber 10 of the device 1. Specifically, the system comprises a pump for the extracorporeal circulation 30, an inlet valve 32 and outlet valve 34 for the entry into and the exit from the capture chamber 10, two manifolds 34 at the inlet 12 and the outlet of the capture chamber 10, an air detector 37 downstream of the device 1 and a detector for the inlet pressure 38 and a detector for the outlet pressure 39. FIG. 6 shows, inside the system 100, a device 1 comprising a capture element 20 with a helical reactant surface 22. However, this is removable and replaceable by a different capture element 20 comprising a plurality of conical structures 22.

[0095] FIG. 7 shows a detail of the system 100 with regard to the inlet 12 and the outlet 14 of the capture chamber 10 of the device 1 according to an alternative embodiment. In particular, the disclosed system is very similar to the one shown in FIG. 6, the only difference being that the capture element 20 consists of a helical structure followed by a plurality of conical structures. Therefore, the reactant surface 22 is defined by a combination of conical and helical surfaces, thus increasing the chances of capture of the cells to be removed by the device 1. Moreover, the combined presence of conical structures increases the clinical safety of the device 1 since it may block potential clots and emboli.

[0096] Lastly, FIG. 8 shows a block diagram describing the method 200 for the removal of at least one biological and/or chemical entity C from an extracorporeal blood volume (B) according to the present invention.

[0097] The method 200 comprises the step of introducing 210 the extracorporeal blood B into the capture chamber 10 of the device 1 having in its interior at least one capture element 20; 20; 20. Subsequently, the method comprises the step of screening 220 the extracorporeal blood B by contact with the reactant surface 22; 22; 22 of the capture element 20; 20; 20 comprising a plurality of binding agents A for the biological and/or chemical entity C to be removed. Finally, the method comprises the step of extracting 230 the extracorporeal blood B devoid of said biological and/or chemical entity C from the capture chamber 10.

[0098] The steps 210, 220 and 230 may be carried out after analysing a predetermined volume of blood B. Above this value of blood volume B, the method 200 comprises the step of stopping 240 the introduction of extracorporeal blood B into the capture chamber 10 and removing the capture element 20; 20; 20 to analyse the nature and quantity of the biological and/or chemical entity C removed and present on the reactant surface 22; 22; 22. Finally, in a subsequent step 250, the capture element 20; 20; 20, once cleared of the entities previously captured, can be reintroduced into the capture chamber 10 and the method 200 can be restarted from step 210. It should be noted that on the basis of the analysis of the entities captured in step 240, the capture element 20; 20; 20 may be replaced with a different one in terms of shape and/or configuration of the reactant surfaces 22; 22; 22 or in terms of quantity, nature and distribution of the binding agents A.

[0099] A person skilled in the art, in order to meet further and contingent requirements, may effect several further modifications and variations to the device, the system and the method described above, all however comprised within the scope of protection of the present invention as defined by the appended claims.