US20080294029A1 - System to Measure Blood Coagulation Related Parameters - Google Patents

System to Measure Blood Coagulation Related Parameters Download PDF

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Publication number
US20080294029A1
US20080294029A1 US12/091,953 US9195306A US2008294029A1 US 20080294029 A1 US20080294029 A1 US 20080294029A1 US 9195306 A US9195306 A US 9195306A US 2008294029 A1 US2008294029 A1 US 2008294029A1
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channel
blood
layer
expandable
activated
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US12/091,953
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Laurent-Dominique Piveteau
Veronique Vallet
Frederic Neftel
Lynda Metref
Nicolas Blanc
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Debiotech SA
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Debiotech SA
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Assigned to DEBIOTECH S.A. reassignment DEBIOTECH S.A. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: METREF, LYNDA, PIVETEAU, LAURENT-DOMINIQUE, VALLET, VERONIQUE, BLANC, NICOLAS, NEFTEL, FREDERIC
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures 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
    • B01L3/50273—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures 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 characterised by the means or forces applied to move the fluids
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures 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
    • B01L3/502738—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures 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 characterised by integrated valves
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures 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
    • B01L3/502746—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures 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 characterised by the means for controlling flow resistance, e.g. flow controllers, baffles
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04B—POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
    • F04B43/00—Machines, pumps, or pumping installations having flexible working members
    • F04B43/02—Machines, pumps, or pumping installations having flexible working members having plate-like flexible members, e.g. diaphragms
    • F04B43/04—Pumps having electric drive
    • F04B43/043—Micropumps
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K99/0001—Microvalves
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K99/0001—Microvalves
    • F16K99/0003—Constructional types of microvalves; Details of the cutting-off member
    • F16K99/0026—Valves using channel deformation
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K99/0001—Microvalves
    • F16K99/0034—Operating means specially adapted for microvalves
    • F16K99/0036—Operating means specially adapted for microvalves operated by temperature variations
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K99/0001—Microvalves
    • F16K99/0034—Operating means specially adapted for microvalves
    • F16K99/0036—Operating means specially adapted for microvalves operated by temperature variations
    • F16K99/004—Operating means specially adapted for microvalves operated by temperature variations using radiation
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K99/0001—Microvalves
    • F16K99/0034—Operating means specially adapted for microvalves
    • F16K99/0055—Operating means specially adapted for microvalves actuated by fluids
    • F16K99/0061—Operating means specially adapted for microvalves actuated by fluids actuated by an expanding gas or liquid volume
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0809—Geometry, shape and general structure rectangular shaped
    • B01L2300/0816—Cards, e.g. flat sample carriers usually with flow in two horizontal directions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0809—Geometry, shape and general structure rectangular shaped
    • B01L2300/0825—Test strips
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0887—Laminated structure
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00—Moving or stopping fluids
    • B01L2400/04—Moving fluids with specific forces or mechanical means
    • B01L2400/0475—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
    • B01L2400/0481—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure squeezing of channels or chambers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00—Moving or stopping fluids
    • B01L2400/06—Valves, specific forms thereof
    • B01L2400/0633—Valves, specific forms thereof with moving parts
    • B01L2400/0655—Valves, specific forms thereof with moving parts pinch valves
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00—Moving or stopping fluids
    • B01L2400/06—Valves, specific forms thereof
    • B01L2400/0633—Valves, specific forms thereof with moving parts
    • B01L2400/0672—Swellable plugs
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K2099/0073—Fabrication methods specifically adapted for microvalves
    • F16K2099/008—Multi-layer fabrications
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K2099/0082—Microvalves adapted for a particular use
    • F16K2099/0084—Chemistry or biology, e.g. "lab-on-a-chip" technology
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00—Subject matter not provided for in other groups of this subclass
    • F16K2099/0082—Microvalves adapted for a particular use
    • F16K2099/0086—Medical applications
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28—Electrolytic cell components
    • G01N27/30—Electrodes, e.g. test electrodes; Half-cells
    • G01N27/327—Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
    • G01N27/3271—Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483—Physical analysis of biological material
    • G01N33/487—Physical analysis of biological material of liquid biological material
    • G01N33/49—Blood
    • G01N33/4905—Determining clotting time of blood
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T137/00—Fluid handling
    • Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
    • Y10T137/218—Means to regulate or vary operation of device
    • Y10T137/2191—By non-fluid energy field affecting input [e.g., transducer]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T137/00—Fluid handling
    • Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
    • Y10T137/218—Means to regulate or vary operation of device
    • Y10T137/2191—By non-fluid energy field affecting input [e.g., transducer]
    • Y10T137/2196—Acoustical or thermal energy

Definitions

  • the invention relates to portable devices and methods for measuring coagulation time, such as for example prothrombin time or activated partial thromboplastine time.
  • Heparin is administrated subcutaneously or intravenously. Heparin activates a plasmatic protein, the antithrombin III that is a natural inhibitor of protease implicated in the coagulation cascade (factors VIIa, XIa, IXa, Xa, IIa). The rate of inactivation of these proteases by AT-III increases 1000-fold due to the binding of heparin.
  • Warfarin decrease blood coagulation by interfering with vitamin K metabolism by inhibiting the effective synthesis of biologically active forms of the Vitamin-K-dependent clotting factors II, VII, IX and X, as well as the regulatory factors protein C, protein S and protein Z. Warfarin has the advantage that it may be taken orally. However dosing warfarin is complicated by the fact that it is known to interact with many commonly used medications and other chemicals that may be present in appreciable quantities in food. But with both medications, dangerous side effects such as bleeding exist. Therefore in order to optimize the therapeutic effect and minimize risks for the patient, close monitoring of the degree of anticoagulation is required by blood testing. Two coagulation test measures are routinely used: the prothrombin time and the activated partial thromboplastin time.
  • the present invention simultaneously concerns an alternative and an improvement with respect to state-of-the-art coagulometers.
  • a system to measure blood coagulation related parameters comprising one first channel adapted to contain a blood sample, the system containing, at least partially, an expandable material which is able to increase its volume when activated by an exciting source, said system furthermore comprising several excitable regions distributed close to said first channel, in such a way that, when one of said excitable region is activated, said expandable material increases to such an extend that the channel cross section is reduced at a location situated at or near to said excitable region.
  • the invention furthermore relates to the use of a system to measure blood coagulation related parameters as defined above.
  • the coagulation time is based on the distance made by the liquid along the channel before being stopped, said liquid being moved by a sequential activation of the exciting elements.
  • the inventive concept is based on the measurement of the displacement of blood along a channel.
  • the displacement is driven by the closing of a channel located in a material that can change its volume when activated by an exciting factor.
  • the device includes a permanent and a disposable part.
  • the disposable part is in contact with blood and contains the channel in which the blood will move.
  • the permanent part contains an electronic that will trigger the activation of the material and measure the displacement. It also contains a screen to read the result of the test.
  • expansible material will be described as PDMSXB, i.e. Expancel beads dispersed into a PDMS matrix, and activation mean as heat produced by the resistance of an electric circuit. Naturally this description can apply to any material having the property to change its volume when activated by an exciting factor.
  • FIG. 1 is an illustration of the entire device (permanent +disposable part)
  • FIG. 2 is a side view of disposable part with the channel molded in the PDMS layer
  • FIG. 3 is a side view of disposable part with the channel molded in the PDMSXB layer
  • FIG. 4 is a top view of the disposable part
  • FIG. 5 is a detailed view of a resistance
  • FIG. 6 is an illustration of the functioning of the device from a front view
  • FIG. 7 is an illustration of the functioning of the device from a side view
  • FIG. 8 is an illustration of the functioning of the device with a non miscible fluid pushing the blood, from a side view
  • the disposable part 12 is formed by the superposition of the following layers: a PCB layer 1 , a PDMS layer 2 , a PDMSXB layer 4 , a protective layer 4 and a cover layer 5 .
  • the resistances 9 producing heat to activate the material are printed on the PCBlayer 1 .
  • the channel network in which the blood is displaced is molded in the POMS or in the PDMSXB layer.
  • the protective layer is preferably biocompatible with blood and/or ensure thermal isolation of the blood against the heated material.
  • the protective layer can consist of the superposition of two layers, one ensuring thermal isolation and the other biocompatibility.
  • the protective layer covering the PDMS and the one covering the PDMSXB are not necessarily the same.
  • the cover layer closes the channel but preferably contain an inlet hole that connect the channel to the outside in order to let the blood enter the device and an outlet hole
  • the disposable part is preferably adapted to the sensing mean incorporated to the permanent part, for example, if optical mean is used, the disposable is preferably transparent to the light used by, for example, containing a window.
  • the channel network preferably has the following properties:
  • the channel network may also have the following properties:
  • the resistance printed on the PCB preferably has the following properties:
  • sample of blood is taken from the patient, for example with a lancet.
  • the sample is placed on the cover hole and is aspired inside the device by capillary forces or by a pumping mechanism (FIGS. 6 . b & 7 . a ).
  • the sample of blood fills the different channel until their narrowing where it is stopped due to change in fluidic resistance. At this stage, it may be mixed with chemical reactive needed to perform the test.
  • the resistances placed upstream the narrowing are heated and this part of the channels is progressively closed and a volume of blood corresponding to the size of the resistance is push forward in the channel (FIGS. 6 . c & 7 . b ). This allows controlling the volume of blood to be analyzed.
  • the resistances are then heated one after the other along a channel, with a controlled amount of time between each successive heating (FIGS. 6 . d - e & 7 . c ).
  • the resistances are heated simultaneously along the different channels, in order to compare the coagulation time in the different channel, i.e. the coagulation time of blood mixed with different chemical. As long as blood has not coagulated, it may be push forward by the closing of the channel, but once coagulated it stays in place and the channel may not be closed (FIGS. 6 . f & 7 . d ).
  • Coagulation time is calculated by determining, for example optically, where the clot stays and at what time the corresponding resistance was heated.
  • Another fluid that is non miscible with blood may be placed upstream of the blood in the channel.
  • This other fluid is therefore the one that is displaced by the closing of the channel, and its displacement induces blood displacement ( FIG. 8 ).

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  • Chemical & Material Sciences (AREA)
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  • General Engineering & Computer Science (AREA)
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  • Health & Medical Sciences (AREA)
  • Mechanical Engineering (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Hematology (AREA)
  • Clinical Laboratory Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Toxicology (AREA)
  • Micromachines (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Materials For Medical Uses (AREA)

Abstract

System to measure blood coagulation related parameters comprising one first channel (6) adapted to contain a blood sample; said system containing, at least partially, an expandable material which is able to increase its volume when activated by an exciting source; said system furthermore comprising several excitable regions distributed close to said first channel (6), in such a way that, when one of said excitable region is activated, said expandable material increases to such an extend that the channel cross section is reduced to a location situated at or near to said excitable region.

Description

    FIELD OF INVENTION
  • The invention relates to portable devices and methods for measuring coagulation time, such as for example prothrombin time or activated partial thromboplastine time.
    • STATE OF THE ART
  • In case of atrial fibrillation, deep venous thrombosis, pulmonary embolism or after replacement of cardiac valve, taking medication is necessary to maintain normal blood fluidity. The most commonly used drugs are heparin and warfarin. Heparin is administrated subcutaneously or intravenously. Heparin activates a plasmatic protein, the antithrombin III that is a natural inhibitor of protease implicated in the coagulation cascade (factors VIIa, XIa, IXa, Xa, IIa). The rate of inactivation of these proteases by AT-III increases 1000-fold due to the binding of heparin. Warfarin decrease blood coagulation by interfering with vitamin K metabolism by inhibiting the effective synthesis of biologically active forms of the Vitamin-K-dependent clotting factors II, VII, IX and X, as well as the regulatory factors protein C, protein S and protein Z. Warfarin has the advantage that it may be taken orally. However dosing warfarin is complicated by the fact that it is known to interact with many commonly used medications and other chemicals that may be present in appreciable quantities in food. But with both medications, dangerous side effects such as bleeding exist. Therefore in order to optimize the therapeutic effect and minimize risks for the patient, close monitoring of the degree of anticoagulation is required by blood testing. Two coagulation test measures are routinely used: the prothrombin time and the activated partial thromboplastin time. Both tests measure clotting time to evaluate a patient's baseline haemostatic state or to monitor the response to anticoagulant therapy as well as the overall function and status of the coagulant system. Prothrombin time is tested when warfarin is used and activated partial thromboplastin time when heparin is used. These tests are mainly done in hospital with relatively large laboratory instrument of complex technology and therefore must be done by qualified personnel. These types of tests are expensive and can be done only once a month approximately. Another possibility is to use point-of-care device. In this case the patient can perform the test by himself. This allows a better control over time as the test can be done daily. However, even if it has been shown self-management improves the quality of oral anticoagulation [1], this method is little used. This is mainly due to the cost of the test strips and to the complexity of use of the actual devices. Therefore new easy of use and inexpensive point-of-care devices and methods for blood coagulation testing are needed.
  • Methods for coagulation measurement using portable device are described in the following patents
      • U.S. Pat. No. 5,908,786: measurement of blood displacement using liquid crystal and heat
      • U.S. Pat. No. 6,673,622 BI: measurement of change in impedance
      • WO 2005/114140: measurement of blood displacement using magnetic beads
      • U.S. Pat. No. 5,302,348: measurement of blood displacement speed.
      • U.S. Pat. No. 4,964,728: measurement of blood turbidity by optical means
      • US 2005/0233466: measurement of blood viscosity using ferromagnetic agitator
    REFERENCE
    • [1] C. Heneghan, Self-monitoring of oral anticoagulation: a systematic review and meta-analysis, Lancet 2006, 367:404-11
    GENERAL DESCRIPTION OF THE INVENTION
  • The present invention simultaneously concerns an alternative and an improvement with respect to state-of-the-art coagulometers.
  • To this effect it relates to a system to measure blood coagulation related parameters comprising one first channel adapted to contain a blood sample, the system containing, at least partially, an expandable material which is able to increase its volume when activated by an exciting source, said system furthermore comprising several excitable regions distributed close to said first channel, in such a way that, when one of said excitable region is activated, said expandable material increases to such an extend that the channel cross section is reduced at a location situated at or near to said excitable region.
  • Preferred embodiments of the system according to the invention are defined in the dependent claims.
  • The invention furthermore relates to the use of a system to measure blood coagulation related parameters as defined above. Wherein the coagulation time is based on the distance made by the liquid along the channel before being stopped, said liquid being moved by a sequential activation of the exciting elements.
  • The inventive concept is based on the measurement of the displacement of blood along a channel. The displacement is driven by the closing of a channel located in a material that can change its volume when activated by an exciting factor. The device includes a permanent and a disposable part. The disposable part is in contact with blood and contains the channel in which the blood will move. The permanent part contains an electronic that will trigger the activation of the material and measure the displacement. It also contains a screen to read the result of the test. In the rest of this document, expansible material will be described as PDMSXB, i.e. Expancel beads dispersed into a PDMS matrix, and activation mean as heat produced by the resistance of an electric circuit. Naturally this description can apply to any material having the property to change its volume when activated by an exciting factor.
    • DETAILED DESCRIPTION OF THE INVENTION
  • The invention will be better understood below with an example illustrated by the following figures:
  • FIG. 1 is an illustration of the entire device (permanent +disposable part)
  • FIG. 2 is a side view of disposable part with the channel molded in the PDMS layer
  • FIG. 3 is a side view of disposable part with the channel molded in the PDMSXB layer
  • FIG. 4 is a top view of the disposable part FIG. 5 is a detailed view of a resistance
  • FIG. 6 is an illustration of the functioning of the device from a front view
  • FIG. 7 is an illustration of the functioning of the device from a side view
  • FIG. 8 is an illustration of the functioning of the device with a non miscible fluid pushing the blood, from a side view
    •
  • The following numerical references are used in the figures
      • 1. PCB
      • 2. PDMS layer
      • 3. PDMSXB layer
      • 4. protective layer
      • 5. coverlayer
      • 6. channel
      • 7. inlet hole
      • 8. outlet hole
      • 9. resistance
      • 10. region of narrowing
      • 11. permanent part
      • 12. disposable part
      • 13. measurement window
      • 14. screen for result reading
      • 15. blood
      • 16. non miscible fluid
  • The disposable part 12 is formed by the superposition of the following layers: a PCB layer 1, a PDMS layer 2, a PDMSXB layer 4, a protective layer 4 and a cover layer 5. The resistances 9 producing heat to activate the material are printed on the PCBlayer 1. The channel network in which the blood is displaced is molded in the POMS or in the PDMSXB layer. The protective layer is preferably biocompatible with blood and/or ensure thermal isolation of the blood against the heated material. The protective layer can consist of the superposition of two layers, one ensuring thermal isolation and the other biocompatibility. The protective layer covering the PDMS and the one covering the PDMSXB are not necessarily the same. The cover layer closes the channel but preferably contain an inlet hole that connect the channel to the outside in order to let the blood enter the device and an outlet hole The disposable part is preferably adapted to the sensing mean incorporated to the permanent part, for example, if optical mean is used, the disposable is preferably transparent to the light used by, for example, containing a window.
  • The channel network preferably has the following properties:
      • The channel network contains at least two identical channels to be able to perform the coagulation test and a control test in the same time (FIG. 4).
      • Each small channel in the network is able to contain chemical species necessary for the test to be performed and allow them to be mixed with blood.
      • Each small channel in the network contains a narrowing allowing to stop the blood entering the device and therefore to control the volume of blood displaced in each channel (FIG. 4)
  • The channel network may also have the following properties:
      • Each small channel may contain several narrowing to stop the blood.
      • The chemical species necessary for the test to be performed are contained in reservoirs linked to the channel network
  • The resistance printed on the PCB preferably has the following properties:
      • Under each channel a first resistance is placed upstream of the narrowing. The size of this resistance determines the volume of blood that will be displaced in the channel.
      • Downstream of the narrowing, identical resistance are placed in series along a channel and in parallel along the different channels.
      • Each resistance consists in a folded line. The foldings are more and more distant along the resistance to allow a progressive heating and therefore a progressive closing of the channel (FIG. 5).
  • Description of the functioning: sample of blood is taken from the patient, for example with a lancet. The sample is placed on the cover hole and is aspired inside the device by capillary forces or by a pumping mechanism (FIGS. 6.b & 7.a). The sample of blood fills the different channel until their narrowing where it is stopped due to change in fluidic resistance. At this stage, it may be mixed with chemical reactive needed to perform the test. The resistances placed upstream the narrowing are heated and this part of the channels is progressively closed and a volume of blood corresponding to the size of the resistance is push forward in the channel (FIGS. 6.c & 7.b). This allows controlling the volume of blood to be analyzed. The resistances are then heated one after the other along a channel, with a controlled amount of time between each successive heating (FIGS. 6.d-e & 7.c). The resistances are heated simultaneously along the different channels, in order to compare the coagulation time in the different channel, i.e. the coagulation time of blood mixed with different chemical. As long as blood has not coagulated, it may be push forward by the closing of the channel, but once coagulated it stays in place and the channel may not be closed (FIGS. 6.f & 7.d). Coagulation time is calculated by determining, for example optically, where the clot stays and at what time the corresponding resistance was heated.
  • In order to avoid direct contact of the blood with the activated region, another fluid that is non miscible with blood may be placed upstream of the blood in the channel. This other fluid is therefore the one that is displaced by the closing of the channel, and its displacement induces blood displacement (FIG. 8).
  • Of course the present invention is not limited to the embodiments discussed above.

Claims (24)

1. System to measure blood coagulation related parameters comprising one first channel adapted to contain a blood sample; said system containing, at least partially, an expandable material which is able to increase its volume when activated by an exciting source; said system furthermore comprising several excitable regions distributed close to said first channel, in such a way that, when one of said excitable region is activated, said expandable material increases to such an extend that the channel cross section is reduced at a location situated at or near to said excitable region.
2. System according to claim 1 furthermore comprising at least a second channel, said second channel being parallel to and communication at one of its end with said first channel.
3. System according to claim 1 wherein said material is adapted to be activated by heat, light, pH variation or by a chemical, electromagnetic or radioactive element as exciting factor.
4. System according to claim 1 wherein said material is a mixture comprising Expancel®.
5. System according to claim 1 in combination with an exciting source, such as a laser, which is distinct from said system.
6. System according to claim 1 furthermore comprising an exciting source such as an electrical resistance.
7. System according to claim 1 wherein said channel is defined by two horizontal and two lateral walls.
8. System according to claim 7 wherein at least one of said horizontal walls is made of said expandable material.
9. System according to claim 1 wherein said channel cross section is adapted to be reduced along a vertical direction.
10. System according to claim 7 wherein both lateral walls are made of said expandable material.
11. System according to claim 10 wherein said channel cross section is adapted to be reduced along a horizontal direction.
12. System according to claim 1 wherein the said material is expandable and is a mixture comprising PDMS or a biocompatible material.
13. System according to claim 1 wherein said channel(s) comprise(s) at least a region of narrowing.
14. System according to claim 1, said system having a multilayered structure comprising successively a substrate layer, an expandable layer, a rigid layer and a cover layer, said substrate layer incorporating said exciting source and said channel(s) being defined in said rigid layer.
15. System according to claim 14 wherein said substrate layer is made of PCB, said expandable layer is made of PDMSXB et said rigid layer is made of PDMS.
16. System according to claim 1 furthermore comprising sensing means.
17. System according to claim 16 wherein said sensing means are diodes, optical density or impedance measuring means.
18. System according to claim 16 wherein said sensing means are adapted to locate where the blood stops.
19. System according to claim 16 wherein said sensing means are adapted to detect blood displacement.
20. Assembly comprising a system as defined in claim 1 in combination with at least one reservoir communicating with said channel(s), said reservoir(s) being adapted to contain reactive which are used in the coagulation tests.
21. Use of a system or an assembly as defined in claim 1 for determining the coagulation time based on the distance made by the liquid along the channel before being stopped, said liquid being moved by a sequential activation of said exciting sources.
22. Use of a multi-channel system or an assembly as defined in claim 1 wherein each channel is used for a test.
23. Use according claim 22 wherein all channels are used for carrying out the same test.
24. Use of a system or an assembly as defined in claim 1 characterized by the use of a pushing fluid which is non miscible with blood and located between blood and the region of the channel being closed.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010048020A1 (en) * 2008-10-20 2010-04-29 Epitome Pharmaceuticals Limited Methods and systems for improved pharmaceutical intervention in coagulation control
US20120064552A1 (en) * 2010-09-14 2012-03-15 California Institute Of Technology Using blood clot in microfluidic valving applications
CN104062207A (en) * 2014-07-15 2014-09-24 中国科学院苏州生物医学工程技术研究所 Monitoring device for viscoelastic strength of blood
WO2016122559A1 (en) * 2015-01-30 2016-08-04 Hewlett-Packard Development Company, L.P. Microfluidic chip for coagulation sensing
US9649436B2 (en) 2011-09-21 2017-05-16 Bayer Healthcare Llc Assembly method for a fluid pump device for a continuous multi-fluid delivery system
US10507319B2 (en) 2015-01-09 2019-12-17 Bayer Healthcare Llc Multiple fluid delivery system with multi-use disposable set and features thereof
US11112400B2 (en) 2016-01-16 2021-09-07 Hewlett-Packard Development Company, L.P. Blood characteristic measurement
US12019041B2 (en) 2018-11-20 2024-06-25 Xatek, Inc. Portable dielectric spectroscopy device

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2901489A1 (en) * 2006-05-29 2007-11-30 Debiotech Sa Microfluidic device to produce a reactional mixture of two different liquids, comprises plates forming substrates and having perforations, activable materials for delimiting channel portions, and an anti-adhesive layer
EP2208530A1 (en) * 2008-12-23 2010-07-21 Debiotech S.A. On-Chip micro pumping system
DE102009035291B4 (en) * 2009-07-30 2011-09-01 Karlsruher Institut für Technologie Device for producing a microfluidic channel structure in a chamber, method for its production and its use
KR101130698B1 (en) * 2009-11-03 2012-04-02 삼성전자주식회사 Valve unit, microfluidic device including the same, and driving method of the valve unit
US8973613B2 (en) * 2011-04-27 2015-03-10 Google Inc. Electrorheological valve
GB201121269D0 (en) * 2011-12-12 2012-01-25 Vivacta Ltd A method forblood measurement
CN103932718B (en) * 2013-01-17 2015-12-02 北京怡成生物电子技术股份有限公司 The portable monitoring system of thing is analyzed in dynamic METHOD FOR CONTINUOUS DETERMINATION body fluid
US9441753B2 (en) 2013-04-30 2016-09-13 Boston Dynamics Printed circuit board electrorheological fluid valve
US10213140B2 (en) 2013-05-17 2019-02-26 Johnson & Johnson Vision Care, Inc. Ophthalmic lens with a microfluidic system
PL3007882T3 (en) * 2013-06-13 2020-06-01 Aspect Biosystems Ltd. System for additive manufacturing of three-dimensional structures and method for same
FR3015310B1 (en) * 2013-12-24 2020-09-11 Espci Innov DEVICE FOR HANDLING, SORTING, GENERATING AND STORING AN ELEMENT OF A NON-MISCIBLE FLUID AND DEVICE FOR MERGING TWO SUCH ELEMENTS
CN108698814A (en) * 2015-12-30 2018-10-23 伯克利之光生命科技公司 Microfluidic device, kit and its method of convection current and displacement for optical drive
US10497541B2 (en) 2016-05-19 2019-12-03 Nedal Saleh Apparatus and method for programmable spatially selective nanoscale surface functionalization
SG11201908329QA (en) 2017-03-15 2019-10-30 Aspect Biosystems Ltd Systems and methods for printing a fiber structure
WO2019209290A1 (en) 2018-04-25 2019-10-31 Hewlett-Packard Development Company, L.P. Selective release of material in thermally degradable capsule
JP7071641B2 (en) * 2018-10-18 2022-05-19 日本電信電話株式会社 Laminates, method of manufacturing laminates and shape control devices
CN109211729A (en) * 2018-10-29 2019-01-15 杨忠思 A kind of blood stagnation condition checkout gear and method for precisely medical treatment detection
CN111419207B (en) * 2020-03-12 2021-02-19 中山大学 Heart detection device and manufacturing method thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5302348A (en) * 1992-12-10 1994-04-12 Itc Corporation Blood coagulation time test apparatus and method
US5344754A (en) * 1993-01-13 1994-09-06 Avocet Medical, Inc. Assay timed by electrical resistance change and test strip
US5908786A (en) * 1997-12-12 1999-06-01 Akzo Nobel, N.V. Blood coagulation monitoring device with liquid crystal and gradient heater
US6273687B1 (en) * 1998-11-26 2001-08-14 Aisin Seiki Kabushiki Kaisha Micromachined pump apparatus
US20030175947A1 (en) * 2001-11-05 2003-09-18 Liu Robin Hui Enhanced mixing in microfluidic devices
US20040094733A1 (en) * 2001-08-31 2004-05-20 Hower Robert W. Micro-fluidic system
US20040189311A1 (en) * 2002-12-26 2004-09-30 Glezer Eli N. Assay cartridges and methods of using the same
US20050098435A1 (en) * 1998-02-04 2005-05-12 Jacobson Stephen C. Methods for forming small-volume electrical contacts and material manipulations with fluidic microchannels

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6345502B1 (en) 1997-11-12 2002-02-12 California Institute Of Technology Micromachined parylene membrane valve and pump
US6167910B1 (en) * 1998-01-20 2001-01-02 Caliper Technologies Corp. Multi-layer microfluidic devices
WO1999039120A1 (en) * 1998-01-29 1999-08-05 University Of Pittsburgh Thermal expansion-induced fluid control for microfluidic devices
GB9804483D0 (en) 1998-03-02 1998-04-29 Central Research Lab Ltd Apparatus for and method of controlling the rate of flow of fluid along a pathway
DE19812436A1 (en) * 1998-03-22 1999-09-30 Univ Dresden Tech Functional component e.g. membrane, filter valve, dosing unit or pump
ATE215673T1 (en) 1999-06-28 2002-04-15 California Inst Of Techn ELASTOMERIC MICROPUMP AND MICROVALVE SYSTEMS
SE9902474D0 (en) 1999-06-30 1999-06-30 Amersham Pharm Biotech Ab Polymer valves
ATE340025T1 (en) * 2000-01-06 2006-10-15 Caliper Life Sciences Inc APPARATUS AND METHODS FOR HIGH-THROUGHPUT SAMPLING AND ANALYSIS
JP3333876B2 (en) 2000-07-24 2002-10-15 独立行政法人産業技術総合研究所 Light-driven integrated chemical system
JP2002066999A (en) 2000-08-30 2002-03-05 Kawamura Inst Of Chem Res Extremely small valve mechanism and manufacturing method of the same
EP1328346A2 (en) 2000-10-06 2003-07-23 Protasis Corporation Microfluidic substrate assembly and method for making same
DE60103924T2 (en) * 2000-11-06 2005-07-14 Nanostream, Inc., Pasadena MICROFLUID FLOW RATE DEVICE
GB0028647D0 (en) 2000-11-24 2001-01-10 Nextgen Sciences Ltd Apparatus for chemical assays
US6548895B1 (en) * 2001-02-21 2003-04-15 Sandia Corporation Packaging of electro-microfluidic devices
JP3696141B2 (en) 2001-09-27 2005-09-14 株式会社東芝 Chemical analyzer, analysis method
US20030156991A1 (en) * 2001-10-23 2003-08-21 William Marsh Rice University Optomechanically-responsive materials for use as light-activated actuators and valves
JP3777112B2 (en) 2001-11-02 2006-05-24 財団法人川村理化学研究所 Microfluidic device and manufacturing method thereof
DE10157317A1 (en) * 2001-11-23 2003-06-05 Gesim Ges Fuer Silizium Mikros A base element used for a microfluid processor in cell biology, comprises an actuator based on a swellable polymer network having volume phase transition behavior and an interface arranged close to the actuator
ATE370338T1 (en) 2002-03-23 2007-09-15 Starbridge Systems Ltd MICROMECHANICAL COMPONENTS
TW536524B (en) * 2002-09-17 2003-06-11 Fan-Gen Tzeng Network-type micro-channel device for micro-fluid
US20040086872A1 (en) 2002-10-31 2004-05-06 Childers Winthrop D. Microfluidic system for analysis of nucleic acids
JP2004291187A (en) * 2003-03-27 2004-10-21 Shimadzu Corp Electrostatic micro valve and micro pump
GB2400158B (en) 2003-04-02 2006-03-22 Starbridge Systems Ltd Fluidic devices
FR2856046B1 (en) * 2003-06-16 2005-07-29 Biomerieux Sa FLUIDIC MICROVANNE WITH OPENING BY ELECTRICAL CONTROL
WO2005036182A1 (en) * 2003-10-15 2005-04-21 Matsushita Electric Industrial Co., Ltd. Method of passing fluid in capillary chip
JP2005246203A (en) 2004-03-03 2005-09-15 Nippon Sheet Glass Co Ltd Microchemical system
US8961900B2 (en) 2004-04-28 2015-02-24 Yokogawa Electric Corporation Chemical reaction cartridge, method of producing chemical reaction cartridge, and mechanism for driving chemical reaction cartridge
US20060029808A1 (en) * 2004-08-06 2006-02-09 Lei Zhai Superhydrophobic coatings
US7832429B2 (en) * 2004-10-13 2010-11-16 Rheonix, Inc. Microfluidic pump and valve structures and fabrication methods
JP2005257695A (en) 2005-04-18 2005-09-22 Olympus Corp Small analyzer

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5302348A (en) * 1992-12-10 1994-04-12 Itc Corporation Blood coagulation time test apparatus and method
US5344754A (en) * 1993-01-13 1994-09-06 Avocet Medical, Inc. Assay timed by electrical resistance change and test strip
US5908786A (en) * 1997-12-12 1999-06-01 Akzo Nobel, N.V. Blood coagulation monitoring device with liquid crystal and gradient heater
US20050098435A1 (en) * 1998-02-04 2005-05-12 Jacobson Stephen C. Methods for forming small-volume electrical contacts and material manipulations with fluidic microchannels
US6273687B1 (en) * 1998-11-26 2001-08-14 Aisin Seiki Kabushiki Kaisha Micromachined pump apparatus
US20040094733A1 (en) * 2001-08-31 2004-05-20 Hower Robert W. Micro-fluidic system
US20030175947A1 (en) * 2001-11-05 2003-09-18 Liu Robin Hui Enhanced mixing in microfluidic devices
US20040189311A1 (en) * 2002-12-26 2004-09-30 Glezer Eli N. Assay cartridges and methods of using the same

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010048020A1 (en) * 2008-10-20 2010-04-29 Epitome Pharmaceuticals Limited Methods and systems for improved pharmaceutical intervention in coagulation control
US20120064552A1 (en) * 2010-09-14 2012-03-15 California Institute Of Technology Using blood clot in microfluidic valving applications
US8845979B2 (en) * 2010-09-14 2014-09-30 California Institute Of Technology Thermal blood clot formation and use in microfluidic device valving applications
US9649436B2 (en) 2011-09-21 2017-05-16 Bayer Healthcare Llc Assembly method for a fluid pump device for a continuous multi-fluid delivery system
US9700672B2 (en) 2011-09-21 2017-07-11 Bayer Healthcare Llc Continuous multi-fluid pump device, drive and actuating system and method
CN104062207A (en) * 2014-07-15 2014-09-24 中国科学院苏州生物医学工程技术研究所 Monitoring device for viscoelastic strength of blood
US10507319B2 (en) 2015-01-09 2019-12-17 Bayer Healthcare Llc Multiple fluid delivery system with multi-use disposable set and features thereof
US11491318B2 (en) 2015-01-09 2022-11-08 Bayer Healthcare Llc Multiple fluid delivery system with multi-use disposable set and features thereof
WO2016122559A1 (en) * 2015-01-30 2016-08-04 Hewlett-Packard Development Company, L.P. Microfluidic chip for coagulation sensing
US10725019B2 (en) 2015-01-30 2020-07-28 Hewlett-Packard Development Company, L.P. Microfluidic chip for coagulation sensing
US11112400B2 (en) 2016-01-16 2021-09-07 Hewlett-Packard Development Company, L.P. Blood characteristic measurement
US12019041B2 (en) 2018-11-20 2024-06-25 Xatek, Inc. Portable dielectric spectroscopy device

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US20090044875A1 (en) 2009-02-19
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