PERFUSION DEVICE, CORRESPONDING APPARATUS USING SAID PERFUSION DEVICE AND METHOD TO ANALYZE THE THROMBOTIC-ISCHEMIC AND HEMORRHAGIC PATHOLOGY

• US 20160018387A1
• Filed: 02/21/2013
• Published: 01/21/2016
• Est. Priority Date: 02/21/2012
• Status: Abandoned Application

• Current Assignee: SediciDodici S.r.l.
• Original Assignee: Sedicidodic SRL
• Inventors: Selmi, Ilaria, Mazzuccato, Mario
• Application Number:
  US14/378,826
• Publication Number:
  US 20160018387A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: B01L 2200/10 Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept
• CPC Class Codes: B01L 2200/146 Employing pressure sensors
• CPC Class Codes: B01L 2300/041 Connecting closures to device or container
• CPC Class Codes: B01L 2300/0654 Lenses; Optical fibres
• CPC Class Codes: B01L 2300/0867 Multiple inlets and one sample wells, e.g. mixing, dilution
• CPC Class Codes: B01L 2300/0874 Three dimensional network
• CPC Class Codes: B01L 2300/0877 Flow chambers
• CPC Class Codes: B01L 2300/16 Surface properties and coatings
• CPC Class Codes: B01L 2300/168 Specific optical properties, e.g. reflective coatings
• CPC Class Codes: B01L 2400/0478 pistons
• CPC Class Codes: B01L 2400/0622 distribution valves, valves having multiple inlets and/or outlets, e.g. metering valves, multi-way valves
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: B01L 3/502715 characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• CPC Class Codes: B01L 3/502723 characterised by venting arrangements
• CPC Class Codes: B01L 3/50273 characterised by the means or forces applied to move the fluids micropumps F04B19/006, of the membrane type F04B43/043
• CPC Class Codes: B01L 9/527 for microfluidic devices, e.g. used for lab-on-a-chip
• CPC Class Codes: G01N 2800/224 Haemostasis or coagulation
• CPC Class Codes: G01N 2800/226 Thrombotic disorders, i.e. thrombo-embolism irrespective of location/organ involved, e.g. renal vein thrombosis, venous thrombosis
• CPC Class Codes: G01N 33/4905 Determining clotting time of blood by chemical methods G01N33/86, C12Q1/56
• CPC Class Codes: G01N 33/86 involving blood coagulating time or factors, or their receptors

Abstract

Perfusion device for the dynamic analysis of the thrombotic-ischemic and hemorrhagic pathology, comprising at least one micro-channel (54) able to be connected to a circuit (13) and in which a fluid is able to flow, such as a biological fluid, like blood or other hematic fluids, whether they are animal or human fluids and mixtures of said fluids with additive substances, or a non-biological fluid, and in which at least one reactive substrate is present, intended for the analysis to be carried out, such as a cytoadhesive substrate, in order to simulate a damaged vasal surface and to reproduce hemostasis phenomena and processes. The perfusion chamber is made of a material which allows the optical acquisition in fluorescence light and/or in visible light of images or videos of the flow of fluid inside the at least one micro-channel (54).

Claims

1. Perfusion device for the dynamic analysis of the thrombotic-ischemic and hemorrhagic pathology, comprising a perfusion chamber provided with at least one micro-channel configured to be connected to a feed circuit of a fluid to be analyzed, in said at least one micro-channel a reactive substrate being present, suitable to simulate a damaged vasal surface and to reproduce hemostasis phenomena and processes, said perfusion chamber being made of a material which allows the optical acquisition, in fluorescence light and/or visible light, of images or videos of the flow of fluid inside said at least one micro-channel, wherein said perfusion chamber is defined by a cartridge coupled to a covering plate between which at least one micro-groove, in the micrometrical size range, is provided, said at least one micro-groove being made open on at least one of either said cartridge or said covering plate in order to define said at least one micro-channel;

wherein said cartridge comprises, integrated therewith in a single body;

a plurality of containing elements connected to said at least one micro-channel and configured to contain a biological fluid to be analyzed and/or one or more auxiliary fluids;

a selection valve configured to selectively put in fluidic communication one or the other of the containing elements with said at least one micro-channel;

a suction pump device located downstream of said at least one micro-channel and configured to aspirate the flow of fluid through said at least one micro-channel in controlled and selectively variable fluid-dynamic conditions.

2. Device as in claim 1, wherein said cartridge comprises, integrated in a single body, a light wave guide configured to be positioned facing toward said at least one micro-channel.

3. Device as in claim 1, wherein said at least one micro-groove has a mainly rectilinear development.

4. Device as in claim 1, wherein the cartridge is provided with at least one coupling surface on which, during use, a coordinated adhesion surface of the covering plate is suitable to be disposed, wherein said at least one micro-groove is made on said surface of the cartridge or on said coordinated adhesion surface and is provided with two ends respectively an entry end and an exit end for the fluidic connection to said feed circuit, wherein said adhesion surface and/or said surface of the cartridge are configured to close said at least micro-groove and to delimit said micro-channel.

5. Device as in claim 4, wherein said micro-groove is made on said surface of said cartridge and said adhesion surface of the covering plate closes said micro-groove

6. Device as in claim 5, wherein said entry end and said exit end are fluidically connected to said feed circuit by respective channels made at least transversely through the thickness of the cartridge.

7. Device as in claim 6, wherein the channel which is directly connected to said entry end is associated with an auxiliary pipe made in said cartridge for the introduction of additive substances into the fluid to be analyzed.

8. Device as in claim 7, wherein said channel which is directly connected to said entry end is provided with at least one mixing tank for mixing said fluid to be analyzed with said additive substances.

9. Device as in claim 4, wherein said micro-groove is defined by walls which extend substantially orthogonal and parallel with respect to the surface of said cartridge.

10. Device as in claim 4, wherein said surface of said cartridge and said adhesion surface of the covering plate are substantially coplanar with respect to each other.

11. Device as in claim 4, wherein said cartridge is provided with said suction pump device, at least partially integrated, which suction pump device is disposed downstream of the at least one micro-channel, and the suction pump device comprises at least one containing element of the fluid analyzed and a suction element suitable to aspirate the fluid making the fluid pass through said micro-channel, and to maintain said surface of the cartridge and said adhesion surface of the covering plate adherent with respect to each other.

12. Device as in claim 4, further comprising integrated pressure means suitable to maintain the surface of the cartridge in contact against the adhesion surface of the covering plate.

13. Device as in claim 1, wherein said suction pump device comprises a suction plunger positioned sliding in one containing element of said containing elements.

14. Apparatus for the dynamic analysis of the thrombotic-ischemic and hemorrhagic pathology comprising:

a circuit in which a fluid such as blood, hematic or biological fluids is able to flow, whether the fluids are animal or human fluids and mixtures of said fluids with additive substances;

a perfusion device as in claim 1, connected to said circuit;

a suction pump device suitable to move the fluid through the circuit and the perfusion device in controlled and selectively variable fluid-dynamic conditions;

optical acquisition means of images or videos and electronic processing means suitable to acquire in real time and to process images of the fluid flow from said perfusion device.

15. Apparatus as in claim 14, the suction pump device is disposed downstream of a perfusion chamber of said perfusion device and is suitable to aspirate the fluid making the fluid pass through said micro-channel, and to maintain a surface of the cartridge and an adhesion surface of the covering plate adherent with respect to each other.

16. Apparatus as in claim 14, further comprising pressure means suitable to maintain the surface of the cartridge in contact against the adhesion surface of the covering plate.

17. Apparatus as in claim 16, characterized in that said pressure means comprise a support element associated with an elastic element configured to accommodate the perfusion chamber, and a covering element configured to respectively maintain said covering plate pressed against said support element and said support element pressed against said elastic element.

18. Method for the dynamic analysis of the thrombotic-ischemic and hemorrhagic pathology, comprising a first step in which a fluid such as a biological fluid, such as blood or other hematic fluids, whether they are animal or human fluids and mixtures of said fluids with additive substances, or a non-biological fluid, is made to flow in controlled and variable fluid-dynamic conditions through a circuit by a suction pump device, said fluid being made to pass through at least one micro-channel of a perfusion chamber in which a reactive substrate is present, intended for the analysis to be carried out, such as a cytoadhesive substrate, in order to simulate a damaged vasal surface and to reproduce hemostasis phenomena and processes, and at least one second step of optical acquisition and processing of images or videos acquired, from said at least one micro-channel, by optical acquisition means of images or videos, and processed by electronic processing means, and in which said perfusion chamber is made of a material which allows the optical acquisition, in fluorescence light and/or visible light, of images or videos of the flow of fluid inside said at least one micro-channel by means of said optical acquisition means of images or videos, wherein during said first step said fluid is introduced into said perfusion chamber which is defined by at least one cartridge coupled to a covering plate between which at least one micro-groove is provided to define said micro-channel, said micro-groove being made open on at least one of either said cartridge or said covering plate, with a desired depth, in the micrometrical size range, wherein said cartridge comprises, integrated therewith in a single body:

a plurality of containing elements connected to said at least one micro-channel and configured to contain a biological fluid to be analyzed and/or one or more auxiliary fluids;

a selection valve configured to selectively put in fluidic communication one or the other of the containing elements with said at least one micro-channel;

a suction pump device, located downstream of said at least one micro-channel.

19. Method as in claim 18, wherein the flow of fluid is introduced and moved through said at least one micro-channel through suction, by means of said suction pump device which also provides to maintain a surface of the cartridge and an adhesion surface of the covering plate adherent with respect to each other.

20. Method as in claim 19, wherein during said first step the covering plate is compressed by pressure means against the cartridge to make said surface of the cartridge and said adhesion surface of the covering plate adhere.

21. Method as in claim 18, wherein before said first step of fluid flow, a priming step is provided in which a solution of biologically inert liquid, is introduced through said circuit and made to pass through said micro-channel of the perfusion chamber to flood said micro-channel and the areas surrounding the micro-channel.