US20120322086A1 - Testing device for identifying antigens and antibodies in biofluids - Google Patents

Testing device for identifying antigens and antibodies in biofluids Download PDF

Info

Publication number
US20120322086A1
US20120322086A1 US13/497,704 US201013497704A US2012322086A1 US 20120322086 A1 US20120322086 A1 US 20120322086A1 US 201013497704 A US201013497704 A US 201013497704A US 2012322086 A1 US2012322086 A1 US 2012322086A1
Authority
US
United States
Prior art keywords
antibody
blood
antigen
testing device
detection zone
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/497,704
Inventor
Gil Garnier
Wei Shen
Mohidus Samad Khan
Xu Li
George Thouas
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monash University
Original Assignee
Monash University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2009904643A external-priority patent/AU2009904643A0/en
Application filed by Monash University filed Critical Monash University
Assigned to MONASH UNIVERSITY reassignment MONASH UNIVERSITY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GARNIER, GIL, SHEN, WEI, LI, XU, KHAN, MOHIDUS SAMAD, THOUAS, GEORGE
Publication of US20120322086A1 publication Critical patent/US20120322086A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • 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
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/80—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood groups or blood types or red blood cells
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/82—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a precipitate or turbidity
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/90—Plate chromatography, e.g. thin layer or paper chromatography
    • 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
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • G01N33/54366—Apparatus specially adapted for solid-phase testing
    • G01N33/54386—Analytical elements
    • G01N33/54387—Immunochromatographic test strips
    • G01N33/54388—Immunochromatographic test strips based on lateral flow
    • G01N33/54389—Immunochromatographic test strips based on lateral flow with bidirectional or multidirectional lateral flow, e.g. wherein the sample flows from a single, common sample application point into multiple strips, lanes or zones
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N2021/752—Devices comprising reaction zones
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N2021/757—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated using immobilised reagents
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/82—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a precipitate or turbidity
    • G01N2021/825—Agglutination

Definitions

  • the present invention is directed to the identification of antigens and antibodies within a biofluid. While the invention will be described with specific reference to its use in determining a person's blood type, it is to be appreciated that other applications of the invention are also envisaged.
  • Blood is essential for sustaining living tissue, with the most important roles of supplying oxygen and other soluble nutrients, immune protection and metabolic turnover. While it is a tissue in its own right, blood in a chemical sense can be considered as a stable, highly packed colloid suspension made of red blood cells (erythrocytes, 4-6 million/mL, 6-8 ⁇ m), white cells (leukocytes, 4000-6000/mL, 10-21 ⁇ m), platelets (150,000-400,000/mL, 2-5 ⁇ m) carried within a fluid solution (serum) containing a host of biomolecules (eg albumins, fatty acids, hormones), metabolites and electrolytes.
  • red blood cells erythrocytes, 4-6 million/mL, 6-8 ⁇ m
  • white cells leukocytes, 4000-6000/mL, 10-21 ⁇ m
  • platelets (150,000-400,000/mL, 2-5 ⁇ m) carried within a fluid solution (serum) containing a host of biomolecules (eg albumins,
  • biomolecules such as the binding proteins responsible for tissue immunity (antigens) and blood type
  • tissue immunity antigens
  • blood type A subset of these biomolecules, such as the binding proteins responsible for tissue immunity (antigens) and blood type, are directly adsorbed onto the surface of blood cells.
  • Common portable testing methods for blood include analysis of glucose content, cholesterol, metabolic panel (sodium, potassium, bicarbonate, blood urea nitrogen, magnesium, creatine, calcium, triglycerides), microbial and disease markers and protein molecular profile (liver, prostate).
  • a testing device for identifying an antigen or antibody within a biofluid sample including;
  • the surface including a collection zone, and at least one detection zone extending therefrom;
  • biofluid sample can be mixed with a specific antigen or antibody, and deposited on the collection zone and transferred by capillary action to the detection zone;
  • the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen thereby resulting in a visual indication within the detection zone.
  • a testing device for identifying an antigen or antibody within a biofluid sample including;
  • the surface including a collection zone, and at least one detection zone extending therefrom;
  • the detection zone having an antibody or antigen immobilised therein;
  • biofluid sample can be deposited on the collection zone and transferred by capillary action to the detection zone;
  • the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen within the detection zone thereby resulting in a visual indication therein.
  • the substrate may be formed from paper or other cellulosic materials.
  • the substrate may include a chromographic layer thereon or may be a wettable porous medium.
  • the biofluid sample being tested may preferably be blood, and the visual indication may be due to an agglutination of the blood upon reaction with a specific antibody resulting in reduced wicking and/or separation of the blood in the detection zone.
  • the substrate surface may have a hydrophilic microfluidic channel pattern thereon defining the collection zone and the detection zone.
  • a plurality of detection zones may extend from the collection zone.
  • red blood cell agglutination triggered by specific antigen interaction, drastically decreases blood wicking and dispersion on paper or chromatographic media.
  • the agglutination process also considerably enhances the chromatographic separation (elution) of the individual blood components, especially the red blood cells from the serum.
  • the testing device according to the present invention can allow direct analysis of blood cells because of this visual indication. This can be performed instantaneously, either with a detection/reporting system built-in to the device or in conjunction with other off-line analytical equipment.
  • the testing device may also allow for the identification and quantification of specific biomolecules (eg antigens and antibodies) based on induced coagulation, followed by the wicking and elution (separation) of the soluble protein fraction from the blood sample onto the porous substrate.
  • the blood colloids whose coagulation directly affects their wicking/separation, can either be present in the fluid of interest, such as the red blood cells of blood, or introduced as nanoparticles (gold, silver, micro-silica, zeolite, titanium dioxide and the like). In the latter case, the nanoparticle is typically covered with the specific counter-biomolecule or molecule of interest used as sensitive reporter component.
  • the colloid particles may be of a size ranging from 1 nm to 100 ⁇ m and may be introduced into the biofluid being analysed.
  • the present invention may determine the antigens present within a blood sample, the antigens determining whether the blood type is type A, B, O, AB and Rhesus+/ ⁇ .
  • Antibodies A, B and D are deposited into separate detection zones. It may also be preferable to include an untreated control zone in one of the detection zones. A drop of blood is then deposited on the central collection zone, the blood sample being transferred by capillary action to each of the detection zones. When the blood sample contacts an appropriate antibody, the reaction of the red blood cells antigen with its corresponding antibody results in agglutination or coagulation of the red cells.
  • This agglutination results in a drop in velocity of the movement of the blood sample along the microfluidic channel providing the detection zone and separation of the red blood cells from the serum.
  • the velocity of the blood samples travelling along other detection zones with non-specific antibodies is unaffected. This visual contrast facilitates easy and rapid identification of the blood type of the blood sample.
  • microfluidic systems described in this application utilise a paper based substrate, with the described fabrication methods producing hydrophilic microfluidic channels on the paper based substrates.
  • paper is used in this application to refer to all cellulosic materials including woven fabrics and non-woven cellulosic material as well as paper.
  • the microfluidic systems described in these applications can be readily adapted for the purpose of the present invention.
  • the testing device according to the present invention may also be used to detect illness as a result of blood cell malfunction on the blood cells being of abnormal shape as is the case with malaria.
  • the testing device according to the present invention may be used to detect illness by identifying the presence of an antigen, antibody, virus (such as HIV, influenza) or protein.
  • the microfluidic channels are fabricated by printing a hydrophobic agent on the substrate surface to define a peripheral edge of the microfluidic channels.
  • the antibody or antigen may also be printed within the microfluidic channels.
  • the technology used, namely ink jet printing technology, may also be used to print the antigen or antibody within the microfluidic channels.
  • a method for identifying an antigen or antibody within a biofluid sample including:
  • a testing device including a substrate having a hydrophilic surface thereon, the surface including said collection zone and at least one detection zone extending therefrom, the biofluid sample being transferred by capillary action to the detection zone;
  • a method for identifying an antigen or antibody within a biofluid sample including:
  • a testing device including a substrate having a hydrophilic surface thereon, the surface including said collection zone and at least one detection zone extending therefrom, the detection zone having an antibody or antigen immobilised therein, the biofluid sample being transferred by capillary action to the detection zone;
  • FIG. 1 shows a testing device according to the present invention used to determine B+ blood
  • FIG. 2 shows a testing device according to the present invention used to determine O+ blood
  • FIG. 3 shows the testing device according to the present invention using AB+ and B+ blood
  • FIG. 4 is the testing device according to the present invention showing blood wicking and blood separation as a function of time
  • FIG. 5 shows a testing device according to the present invention incorporating a valve
  • FIG. 6 A-F shows the operation of a testing device according to the present invention incorporating valves and switches
  • FIG. 7 are schematic representations of testing devices according to the present invention adapted for testing different blood types.
  • FIG. 8 shows the testing device of FIG. 7 showing the separation of red blood cells from the blood serum.
  • the applicants have discovered that blood agglutination mediated by specific antibody-antigen interactions drastically affects its separation behaviour on contact with paper or any thin layer chromatographic surface.
  • the invention relies on this biochemical phenomenon to control the rate of wicking and separation, which enables (i) identification and quantitative assessment of a specific antibody/antigen, (ii) blood typing, and potentially (iii) identification of blood-borne pathogens as a disease diagnostic.
  • the present invention is intended predominantly for applications in human and veterinary medicine and biotechnology.
  • Standard techniques for detection of blood agglutination are traditionally manual, involve dispensing of antibodies on a glass slide and microscopic visualization.
  • visualisation of agglutination is often subjective, and its automation requires a bank of sophisticated analytical equipment.
  • the present invention provides a single-step blood test that simplifies and circumvents these difficulties.
  • One application of the invention involves a two step process in which the blood sample is first coagulated/agglutinated by combining it with the specific antibody/antigen of interest, followed by its deposition on the analytical substrate (eg Non-woven paper or porous mesh) on which the sample wicking and separation by elution/chromatography is measured, directly or indirectly.
  • the analytical substrate eg Non-woven paper or porous mesh
  • a second application of the invention involves a single-step process in which the biofluid/sample is deposited directly on the substrate/device which has previously been treated with the specific antigen/antibody.
  • the analyte samples simultaneously coagulate and elude on the same substrate.
  • the measured elution velocity and the extent of sample separation are directly related to the extent of coagulation, enabling the concentration of the biomolecule to be detected and quantified at the same time.
  • Both applications of the invention can be applied to a test device made of paper or any non-woven chromatographic surface, which are relatively cost effective.
  • These substrates are also able to be modified with the use of advanced printing techniques to create microfluidic features composed of hydrophobic materials, as previously described in the applicant's International application no. PCT/AU2009/000889. Combined with methods of direct antibody deposition using printing, manufacture and placement of antibody reagent can enable very accurate spatial control of blood flow within the paper substrate.
  • Antibody A and B (EpicloneTM Anti-A, Anti-B, and Anti-D; CSL, Australia) solutions were used. Anti-A and Anti-B come as blue and yellow colour reagents, respectively.
  • ‘B+’ blood was used in this study. The blood sample was supplied into plastic vials with anti-coagulant. ‘B+’ blood was separately mixed with pure Anti-A and Anti-B (as received) to prepare 100 ⁇ L solution. Paper strips (70 mm ⁇ 2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. The paper strips were soaked into phosphate buffer saline (PBS). Excess PBS was removed from the paper strips using standard blotting papers (Drink Coster Blotting, 280 GSM). The paper strips were then placed on Reflex Paper (80 GSM). 20 ⁇ L of every mixed solution was dispensed at the centre of paper strip using a calibrated micro-pipette. Pictures were taken after 4 minutes wicking.
  • PBS phosphate
  • a blood sample agglutinated/coagulated upon contact with its specific antibodies separated/eluded upon contact with paper here Blood B+ with Anti-B and Anti-D antibodies.
  • a blood sample upon contact with non-specific antibody does not agglutinate and does not separate/elute upon contact with paper.
  • Antibody A and B (EpicloneTM Anti-A, Anti-B and Anti-D; CSL, Australia) solutions were used. Anti-A and Anti-B come as blue and yellow colour reagents, respectively.
  • ‘O+’ blood was used in this study. The blood sample was supplied into plastic vials with anti-coagulant. ‘O+’ blood was separately mixed with Anti-A and Anti-B to prepare 100 ⁇ L solution. Paper strips (70 mm ⁇ 2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. The paper strips were soaked into phosphate buffer saline (PBS). Excess PBS was removed from the paper strips using standard blotting papers (Drink Coster Blotting, 280 GSM). The paper strips were then placed on Reflex Paper (80 GSM). 20 ⁇ L of every mixed solution was dispensed at the centre of paper strip using a calibrated micro-pipette. Pictures were taken after 4 minutes wicking.
  • PBS phosphate buffer saline
  • a blood sample agglutinated/coagulated upon contact with its specific antibodies separated/eluded upon contact with paper here Blood O+ with Anti-D antibodies.
  • a blood sample upon contact with non-specific antibody does not agglutinate and does not separate/elute upon contact with paper.
  • the paper is first treated with specific antibodies, dried or conditioned before been exposed to a sample of pure blood.
  • This example provides a single step treatment in which the only requirement is to deposit a drop of blood on the paper.
  • This example also illustrates the effect of diluting the antibody solution on the wicking and separation performance of blood on paper.
  • Antibody dilution affects the ratio blood (with its antigen) antibody.
  • Antibody A and B (EpicloneTM Anti-A and Anti-B; CSL, Australia) solutions were used. Anti-A and Anti-B come as blue and yellow colour reagents, respectively. “AB+” and ‘B+’ blood were used in this study. The blood sample was supplied into plastic vials with anti-coagulant. Paper strips (70 mm ⁇ 2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. Paper strips were soaked into antibody solutions of different concentrations (Anti-A@1.0 ⁇ , 0.8 ⁇ , 0.6 ⁇ , 0.4 ⁇ , 0.2 ⁇ and 0.0 ⁇ ); phosphate buffer saline (PBS) was used as diluent. Excess antibody was removed from the paper strips with blotting papers.
  • PBS phosphate buffer saline
  • the antibody (Anti-A) active paper strips were then placed on Reflex Paper. Blood drops of 20 ⁇ L were dispensed at the centre of paper strip using a calibrated micro-pipette. The wicking distance was measured from centre to either direction. Pictures were taken after 10 minutes.
  • Blood separation is a non-linear function of the antibody concentration on the treated paper. The higher the antibody concentration, the more abrupt is the cell separation from the serum.
  • Coagulation of red cell upon contact with its specific antibody drastically reduces its wicking/diffusion speed on the chromatographic surface, which promotes separation of cells from the serum. This drastic reduction and differentiation of elution speeds can serve as direct indicator of the type of blood.
  • the paper is first treated with specific antibodies, dried or conditioned before been exposed to a sample of pure blood.
  • This example illustrates the effect of contact time blood-antibody treated paper on the wicking and separation performance of blood on paper.
  • Antibody A and B (EpicloneTM Anti-A; CSL, Australia) solutions were used. Anti-A comes as a blue colour reagent. “AB+” blood was used in this study. The blood sample was supplied into plastic vials with anti-coagulant. Paper strips (70 mm ⁇ 2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. Paper strips were soaked into antibody solutions (Anti-A@); phosphate buffer saline (PBS) was used as diluent. Excess antibody was removed from the paper strips with blotting papers. The antibody (Anti-A) active paper strips were then placed on Reflex Paper. Blood drops of 20 ⁇ L were dispensed at the centre of paper strip using a calibrated micro-pipette. The wicking distance was measured from centre to either direction. Pictures were taken after different intervals of time.
  • paper-based microfluidic reactors can be used to conduct blood type tests. Specific antibodies are printed into the reactor designed on paper. Then blood cell suspension is introduced into the same reactor. The required period of time is allowed so that the antibodies and cell suspension can contact and mix. After a preset period of time, the valve of the reactor is closed to facilitate penetration of blood across the valve. If only the penetration of serum is observed, the test is positive because of agglutination of blood during the mixing time. If the penetration of blood is observed, the test is negative. Thus paper-based microfluidic reactor can provide a rapid visual test of blood type.
  • Paper microfluidic devices can be designed to increase the ratio of blood/antibody and to provide the required time delay to allow blood and antibody interactions before the test. This example shows that all these steps can be performed using a paper device.
  • FIG. 6 shows the design of the paper device.
  • a filter paper sheet is printed and cut as shown, and specific antibodies are either printed or deposited in the circled region.
  • a paper switch is made on the right hand side of the device.
  • B Blood sample is introduced onto the indicated region.
  • C The cut paper is folded towards the blood sample as shown.
  • D Blood sample is allowed to stay in contact with the antibody loaded paper for a set time.
  • E After a short period of contact time, the switch is closed as shown.
  • test If the test is positive, blood will agglomerate and only serum will wick out along the switch. (F) After a short period of contact, the switch is closed as shown. If the test is negative, blood will not agglomerate and will wick out along the switch.
  • a microfluidic system is printed on paper or a chromatographic medium and antibodies A, B and D (Rhesus) are printed into each of the 3 detection arms.
  • Blood typing is analysed by placing a blood droplet in the middle reservoir and reading the results. All the different combinations of blood type and their representations are represented in FIG. 7 .
  • FIG. 8 illustrates blood group detection using chromatographic separation of red blood cells (RBC) and blood serum on antibody active paper surface;
  • RBC red blood cells
  • FIG. 8 illustrates blood group detection using chromatographic separation of red blood cells (RBC) and blood serum on antibody active paper surface;
  • (b) and (c)(I) are trial 1 and 2 using A+ blood sample, respectively;
  • (b)(II), (c)(II) are the converted images of (b)(I), (c)(I) (RGB colour to BRG colour), respectively, for better resolution.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Hematology (AREA)
  • Physics & Mathematics (AREA)
  • Molecular Biology (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Pathology (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Plasma & Fusion (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Sampling And Sample Adjustment (AREA)

Abstract

A testing device for identifying an antigen or antibody within a biofluid sample including: a substrate having a hydrophilic surface thereon; the surface including a collection zone, and at least one detection zone extending therefrom; wherein the biofluid sample can be mixed with a specific antigen or antibody, and deposited on the collection zone and transferred by capillary action to the detection zone; the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen thereby resulting in a visual indication within the detection zone.

Description

    FIELD OF THE INVENTION
  • The present invention is directed to the identification of antigens and antibodies within a biofluid. While the invention will be described with specific reference to its use in determining a person's blood type, it is to be appreciated that other applications of the invention are also envisaged.
    • BACKGROUND TO THE INVENTION
  • Blood is essential for sustaining living tissue, with the most important roles of supplying oxygen and other soluble nutrients, immune protection and metabolic turnover. While it is a tissue in its own right, blood in a chemical sense can be considered as a stable, highly packed colloid suspension made of red blood cells (erythrocytes, 4-6 million/mL, 6-8 μm), white cells (leukocytes, 4000-6000/mL, 10-21 μm), platelets (150,000-400,000/mL, 2-5 μm) carried within a fluid solution (serum) containing a host of biomolecules (eg albumins, fatty acids, hormones), metabolites and electrolytes. A subset of these biomolecules, such as the binding proteins responsible for tissue immunity (antigens) and blood type, are directly adsorbed onto the surface of blood cells. Common portable testing methods for blood include analysis of glucose content, cholesterol, metabolic panel (sodium, potassium, bicarbonate, blood urea nitrogen, magnesium, creatine, calcium, triglycerides), microbial and disease markers and protein molecular profile (liver, prostate). Surprisingly, and in spite of its vital importance, there are no convenient low cost disposable tests available for “on the spot” analysis of blood type. Blood samples are typically outsourced to an analytical laboratory. Reliable low cost tests which are able to instantaneously and reliably provide critical blood analysis without the requirement of sophisticated laboratory analytical instrumentation such as chromatographic and spectroscopic methods, would be invaluable for improving human health in developing countries, where economic resources are limited. Blood analysis is also important in non-human applications, such as veterinary medicine, where there is a demand for low cost and versatile devices suitable for field use.
    • DESCRIPTION OF INVENTION
  • With this in mind, according to one aspect of the present invention, there is provided a testing device for identifying an antigen or antibody within a biofluid sample including;
  • a substrate having a hydrophilic surface thereon;
  • the surface including a collection zone, and at least one detection zone extending therefrom;
  • wherein the biofluid sample can be mixed with a specific antigen or antibody, and deposited on the collection zone and transferred by capillary action to the detection zone;
  • the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen thereby resulting in a visual indication within the detection zone.
  • According to another aspect of the present invention there is provided a testing device for identifying an antigen or antibody within a biofluid sample including;
  • a substrate having a hydrophilic surface thereon;
  • the surface including a collection zone, and at least one detection zone extending therefrom;
  • the detection zone having an antibody or antigen immobilised therein;
  • wherein the biofluid sample can be deposited on the collection zone and transferred by capillary action to the detection zone;
  • the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen within the detection zone thereby resulting in a visual indication therein.
  • The substrate may be formed from paper or other cellulosic materials. Alternatively, the substrate may include a chromographic layer thereon or may be a wettable porous medium.
  • The biofluid sample being tested may preferably be blood, and the visual indication may be due to an agglutination of the blood upon reaction with a specific antibody resulting in reduced wicking and/or separation of the blood in the detection zone.
  • The substrate surface may have a hydrophilic microfluidic channel pattern thereon defining the collection zone and the detection zone. Preferably, a plurality of detection zones may extend from the collection zone.
  • It has been found that red blood cell agglutination, triggered by specific antigen interaction, drastically decreases blood wicking and dispersion on paper or chromatographic media. The agglutination process also considerably enhances the chromatographic separation (elution) of the individual blood components, especially the red blood cells from the serum. The testing device according to the present invention can allow direct analysis of blood cells because of this visual indication. This can be performed instantaneously, either with a detection/reporting system built-in to the device or in conjunction with other off-line analytical equipment. The testing device may also allow for the identification and quantification of specific biomolecules (eg antigens and antibodies) based on induced coagulation, followed by the wicking and elution (separation) of the soluble protein fraction from the blood sample onto the porous substrate. The blood colloids, whose coagulation directly affects their wicking/separation, can either be present in the fluid of interest, such as the red blood cells of blood, or introduced as nanoparticles (gold, silver, micro-silica, zeolite, titanium dioxide and the like). In the latter case, the nanoparticle is typically covered with the specific counter-biomolecule or molecule of interest used as sensitive reporter component. The colloid particles may be of a size ranging from 1 nm to 100 μm and may be introduced into the biofluid being analysed.
  • In the application of the present invention for determining the type of blood group, the present invention may determine the antigens present within a blood sample, the antigens determining whether the blood type is type A, B, O, AB and Rhesus+/−. Antibodies A, B and D (Rhesus) are deposited into separate detection zones. It may also be preferable to include an untreated control zone in one of the detection zones. A drop of blood is then deposited on the central collection zone, the blood sample being transferred by capillary action to each of the detection zones. When the blood sample contacts an appropriate antibody, the reaction of the red blood cells antigen with its corresponding antibody results in agglutination or coagulation of the red cells. This agglutination results in a drop in velocity of the movement of the blood sample along the microfluidic channel providing the detection zone and separation of the red blood cells from the serum. The velocity of the blood samples travelling along other detection zones with non-specific antibodies is unaffected. This visual contrast facilitates easy and rapid identification of the blood type of the blood sample.
  • The applicant has developed a low cost paper based microfluidic system which is described in International patent application no. PCT/AU2009/000889 details of which are incorporated herein by reference. The microfluidic systems described in this application utilise a paper based substrate, with the described fabrication methods producing hydrophilic microfluidic channels on the paper based substrates. It should be noted that the term paper is used in this application to refer to all cellulosic materials including woven fabrics and non-woven cellulosic material as well as paper. The microfluidic systems described in these applications can be readily adapted for the purpose of the present invention.
  • The testing device according to the present invention may also be used to detect illness as a result of blood cell malfunction on the blood cells being of abnormal shape as is the case with malaria. Alternatively, the testing device according to the present invention may be used to detect illness by identifying the presence of an antigen, antibody, virus (such as HIV, influenza) or protein.
  • In the International application, the microfluidic channels are fabricated by printing a hydrophobic agent on the substrate surface to define a peripheral edge of the microfluidic channels. According to the present invention, the antibody or antigen may also be printed within the microfluidic channels. The technology used, namely ink jet printing technology, may also be used to print the antigen or antibody within the microfluidic channels.
  • According to a further aspect of the present invention, there is provided a method for identifying an antigen or antibody within a biofluid sample, including:
  • mixing the biofluid sample with a specific antigen or antibody,
  • depositing the mixed biofluid sample on a collection zone of a testing device including a substrate having a hydrophilic surface thereon, the surface including said collection zone and at least one detection zone extending therefrom, the biofluid sample being transferred by capillary action to the detection zone; and
  • identifying the antigen or antibody by a resultant visual indication within the detection zone arising where the antigen or antibody in the biofluid sample reacts with an appropriate said antibody or antigen.
  • According to yet another aspect of the present invention, there is provided a method for identifying an antigen or antibody within a biofluid sample, including:
  • depositing the biofluid sample on a collection zone of a testing device including a substrate having a hydrophilic surface thereon, the surface including said collection zone and at least one detection zone extending therefrom, the detection zone having an antibody or antigen immobilised therein, the biofluid sample being transferred by capillary action to the detection zone; and
  • identifying the antigen or antibody by a resultant visual indication arising where the antigen or antibody in the biofluid sample reacts with an appropriate said antibody or antigen within the detection zone.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • It will be convenient to further describe the invention with respect to the accompanying drawings which illustrate preferred embodiments of the testing device according to the present invention. Other embodiments of the invention are possible, and consequently, the particularity of the accompanying drawings is not to be understood as superseding the preceding description of the invention.
  • In the drawings:
  • FIG. 1 shows a testing device according to the present invention used to determine B+ blood;
  • FIG. 2 shows a testing device according to the present invention used to determine O+ blood;
  • FIG. 3 shows the testing device according to the present invention using AB+ and B+ blood;
  • FIG. 4 is the testing device according to the present invention showing blood wicking and blood separation as a function of time;
  • FIG. 5 shows a testing device according to the present invention incorporating a valve;
  • FIG. 6 A-F shows the operation of a testing device according to the present invention incorporating valves and switches;
  • FIG. 7 are schematic representations of testing devices according to the present invention adapted for testing different blood types; and
  • FIG. 8 shows the testing device of FIG. 7 showing the separation of red blood cells from the blood serum.
    •  DETAILED DESCRIPTION OF THE INVENTION
  • The applicants have discovered that blood agglutination mediated by specific antibody-antigen interactions drastically affects its separation behaviour on contact with paper or any thin layer chromatographic surface. The invention relies on this biochemical phenomenon to control the rate of wicking and separation, which enables (i) identification and quantitative assessment of a specific antibody/antigen, (ii) blood typing, and potentially (iii) identification of blood-borne pathogens as a disease diagnostic. The present invention is intended predominantly for applications in human and veterinary medicine and biotechnology.
  • Standard techniques for detection of blood agglutination are traditionally manual, involve dispensing of antibodies on a glass slide and microscopic visualization. However, the visualisation of agglutination is often subjective, and its automation requires a bank of sophisticated analytical equipment. The present invention provides a single-step blood test that simplifies and circumvents these difficulties.
  • One application of the invention involves a two step process in which the blood sample is first coagulated/agglutinated by combining it with the specific antibody/antigen of interest, followed by its deposition on the analytical substrate (eg Non-woven paper or porous mesh) on which the sample wicking and separation by elution/chromatography is measured, directly or indirectly. These two mixing steps can be enhanced and more accurately performed by mixing on paper substrates using built-in valving and channelling control features.
  • A second application of the invention involves a single-step process in which the biofluid/sample is deposited directly on the substrate/device which has previously been treated with the specific antigen/antibody. For this process, the analyte samples simultaneously coagulate and elude on the same substrate. The measured elution velocity and the extent of sample separation are directly related to the extent of coagulation, enabling the concentration of the biomolecule to be detected and quantified at the same time.
  • Both applications of the invention can be applied to a test device made of paper or any non-woven chromatographic surface, which are relatively cost effective. These substrates are also able to be modified with the use of advanced printing techniques to create microfluidic features composed of hydrophobic materials, as previously described in the applicant's International application no. PCT/AU2009/000889. Combined with methods of direct antibody deposition using printing, manufacture and placement of antibody reagent can enable very accurate spatial control of blood flow within the paper substrate.
    • EXAMPLES Example 1 Sequential Agglutination/Coagulation of Blood Followed by Wicking on Paper: B+ (Two Step Process) (See FIG. 1)
  • Antibody A and B (Epiclone™ Anti-A, Anti-B, and Anti-D; CSL, Australia) solutions were used. Anti-A and Anti-B come as blue and yellow colour reagents, respectively. ‘B+’ blood was used in this study. The blood sample was supplied into plastic vials with anti-coagulant. ‘B+’ blood was separately mixed with pure Anti-A and Anti-B (as received) to prepare 100 μL solution. Paper strips (70 mm×2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. The paper strips were soaked into phosphate buffer saline (PBS). Excess PBS was removed from the paper strips using standard blotting papers (Drink Coster Blotting, 280 GSM). The paper strips were then placed on Reflex Paper (80 GSM). 20 μL of every mixed solution was dispensed at the centre of paper strip using a calibrated micro-pipette. Pictures were taken after 4 minutes wicking.
  • It can be seen that:
  • B+ blood mixed with the solution of antibody A wicked and did not separate upon mixing and paper elution/wicking.
  • B+ blood mixed with the solution of antibody B wicked and STRONGLY separated (red cells from serum) and showed wicking.
  • B+ blood mixed with the solution of antibody D (Rhesus+) wicked and STRONGLY separated (red cells from serum).
  • A blood sample agglutinated/coagulated upon contact with its specific antibodies separated/eluded upon contact with paper (here Blood B+ with Anti-B and Anti-D antibodies).
  • A blood sample upon contact with non-specific antibody (here Blood B+ with Anti-A) does not agglutinate and does not separate/elute upon contact with paper.
  • This dramatic difference in elution/separation of blood/antibody mixing can be used to communicate specific agglutination and therefore can be used to identify blood typing.
    • Example 2 Sequential Agglutination/Coagulation of Blood Followed by Wicking on Paper: O+ (Two Step Process) (See FIG. 2)
  • Antibody A and B (Epiclone™ Anti-A, Anti-B and Anti-D; CSL, Australia) solutions were used. Anti-A and Anti-B come as blue and yellow colour reagents, respectively. ‘O+’ blood was used in this study. The blood sample was supplied into plastic vials with anti-coagulant. ‘O+’ blood was separately mixed with Anti-A and Anti-B to prepare 100 μL solution. Paper strips (70 mm×2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. The paper strips were soaked into phosphate buffer saline (PBS). Excess PBS was removed from the paper strips using standard blotting papers (Drink Coster Blotting, 280 GSM). The paper strips were then placed on Reflex Paper (80 GSM). 20 μL of every mixed solution was dispensed at the centre of paper strip using a calibrated micro-pipette. Pictures were taken after 4 minutes wicking.
  • It can be seen that:
  • O+ blood mixed with the solution of antibody A wicked and did not separate upon mixing and paper elution/wicking.
  • O+ blood mixed with the solution of antibody B wicked and did not separate (red cells from serum) and showed wicking.
  • O+ blood mixed with the solution of antibody D (Rhesus+) wicked and STRONGLY separated (red cells from serum).
  • A blood sample agglutinated/coagulated upon contact with its specific antibodies separated/eluded upon contact with paper (here Blood O+ with Anti-D antibodies).
  • A blood sample upon contact with non-specific antibody (here Blood O+ with Anti-A and Anti-B) does not agglutinate and does not separate/elute upon contact with paper.
  • This dramatic difference in elution/separation of blood/antibody mixing can be used to communicate specific agglutination and therefore can be used to identify blood typing.
    • Example 3 Simultaneous Agglutination/Coagulation of Blood Followed by Wicking on Paper: Effect of Antigen Concentration (One Step Process) (See FIG. 3)
  • In another embodiment of the invention, the paper is first treated with specific antibodies, dried or conditioned before been exposed to a sample of pure blood. This example provides a single step treatment in which the only requirement is to deposit a drop of blood on the paper. This example also illustrates the effect of diluting the antibody solution on the wicking and separation performance of blood on paper. Antibody dilution affects the ratio blood (with its antigen) antibody.
  • Antibody A and B (Epiclone™ Anti-A and Anti-B; CSL, Australia) solutions were used. Anti-A and Anti-B come as blue and yellow colour reagents, respectively. “AB+” and ‘B+’ blood were used in this study. The blood sample was supplied into plastic vials with anti-coagulant. Paper strips (70 mm×2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. Paper strips were soaked into antibody solutions of different concentrations (Anti-A@1.0×, 0.8×, 0.6×, 0.4×, 0.2× and 0.0×); phosphate buffer saline (PBS) was used as diluent. Excess antibody was removed from the paper strips with blotting papers. The antibody (Anti-A) active paper strips were then placed on Reflex Paper. Blood drops of 20 μL were dispensed at the centre of paper strip using a calibrated micro-pipette. The wicking distance was measured from centre to either direction. Pictures were taken after 10 minutes.
  • The results are shown in FIG. 3. It can be seen that:
  • Blood separates upon wicking with its specific antibody treated paper.
  • Blood separation is a non-linear function of the antibody concentration on the treated paper. The higher the antibody concentration, the more abrupt is the cell separation from the serum.
  • There is an optimum concentration to maximize wicking/separation/visualization.
  • Coagulation of red cell upon contact with its specific antibody drastically reduces its wicking/diffusion speed on the chromatographic surface, which promotes separation of cells from the serum. This drastic reduction and differentiation of elution speeds can serve as direct indicator of the type of blood.
    • Example 4 Effect of Time on the Wicking/Separation of Blood on Bioactive Antibody Paper (see FIG. 4)
  • In another embodiment of the invention, the paper is first treated with specific antibodies, dried or conditioned before been exposed to a sample of pure blood. This example illustrates the effect of contact time blood-antibody treated paper on the wicking and separation performance of blood on paper.
  • Antibody A and B (Epiclone™ Anti-A; CSL, Australia) solutions were used. Anti-A comes as a blue colour reagent. “AB+” blood was used in this study. The blood sample was supplied into plastic vials with anti-coagulant. Paper strips (70 mm×2 mm) were made from Whatman#4 filter paper on which 2 mm unit marks were printed. Paper strips were soaked into antibody solutions (Anti-A@); phosphate buffer saline (PBS) was used as diluent. Excess antibody was removed from the paper strips with blotting papers. The antibody (Anti-A) active paper strips were then placed on Reflex Paper. Blood drops of 20 μL were dispensed at the centre of paper strip using a calibrated micro-pipette. The wicking distance was measured from centre to either direction. Pictures were taken after different intervals of time.
  • It can be seen that:
  • blood wicking/separation levels off after about 4 minutes.
  • There is a minimum time of contact of antibody-blood required to allow proper blood coagulation/agglutination and wicking/separation.
  • There is an optimum time of contact of blood-antibody-paper. Too short, the blood does not properly coagulate; too long, the separation of red cell and serum can loose some of its sharpness.
    • Example 5 Paper Microfluidic System to Control Flow, Reaction and Dilution (See FIG. 5)
  • In the embodiment of the invention, paper-based microfluidic reactors can be used to conduct blood type tests. Specific antibodies are printed into the reactor designed on paper. Then blood cell suspension is introduced into the same reactor. The required period of time is allowed so that the antibodies and cell suspension can contact and mix. After a preset period of time, the valve of the reactor is closed to facilitate penetration of blood across the valve. If only the penetration of serum is observed, the test is positive because of agglutination of blood during the mixing time. If the penetration of blood is observed, the test is negative. Thus paper-based microfluidic reactor can provide a rapid visual test of blood type.
    • Example 6 Microfluidic System with Valves (See FIG. 6)
  • Paper microfluidic devices can be designed to increase the ratio of blood/antibody and to provide the required time delay to allow blood and antibody interactions before the test. This example shows that all these steps can be performed using a paper device. FIG. 6 shows the design of the paper device. (A) A filter paper sheet is printed and cut as shown, and specific antibodies are either printed or deposited in the circled region. A paper switch is made on the right hand side of the device. (B) Blood sample is introduced onto the indicated region. (C) The cut paper is folded towards the blood sample as shown. (D) Blood sample is allowed to stay in contact with the antibody loaded paper for a set time. (E) After a short period of contact time, the switch is closed as shown. If the test is positive, blood will agglomerate and only serum will wick out along the switch. (F) After a short period of contact, the switch is closed as shown. If the test is negative, blood will not agglomerate and will wick out along the switch.
    • Example 7 Paper Microfluidic System for Blood Typing (See FIG. 7)
  • In another embodiment of the invention, a microfluidic system is printed on paper or a chromatographic medium and antibodies A, B and D (Rhesus) are printed into each of the 3 detection arms. Blood typing is analysed by placing a blood droplet in the middle reservoir and reading the results. All the different combinations of blood type and their representations are represented in FIG. 7.
    • Example 8 Chromatographic Separation of RBC/Blood Serum on Paper (See FIG. 8)
  • FIG. 8 illustrates blood group detection using chromatographic separation of red blood cells (RBC) and blood serum on antibody active paper surface; (a) schematic of chromatographic separation on paper bioassay; (b) and (c)(I) are trial 1 and 2 using A+ blood sample, respectively; (b)(II), (c)(II) are the converted images of (b)(I), (c)(I) (RGB colour to BRG colour), respectively, for better resolution.
  • Modifications and variations as would be deemed obvious to the person skilled in the art are included within the ambit of the present invention as claimed in the appended claims.

Claims (26)

1. A testing device for identifying an antigen or antibody within a biofluid sample including:
a substrate having a hydrophilic surface thereon;
the surface including a collection zone, and at least one detection zone extending therefrom;
wherein the biofluid sample can be mixed with a specific antigen or antibody, and deposited on the collection zone and transferred by capillary action to the detection zone;
the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen thereby resulting in a visual indication within the detection zone.
2. A testing device for identifying an antigen or antibody within a biofluid sample including:
a substrate having a hydrophilic surface thereon;
the surface including a collection zone, and at least one detection zone extending therefrom;
the detection zone having an antibody or antigen immobilised therein;
wherein the biofluid sample can be deposited on the collection zone and transferred by capillary action to the detection zone;
the antigen or antibody in the biofluid sample reacting with an appropriate said antibody or antigen within the detection zone thereby resulting in a visual indication therein.
3. A testing device according to claim 1, wherein the substrate is formed from paper or other cellulosic materials.
4. A testing device according to claim 1, wherein the substrate includes a chromographic layer thereon or other wettable porous media.
5. A testing device according to claim 1, wherein the substrate surface has a hydrophilic microfluidic channel pattern thereon defining the collection zone and the detection zone.
6. A testing device according to claim 5, including a plurality of detection zones extending from the collection zone.
7. A testing device according to claim 1, wherein biofluid sample being tested is blood, and the visual indication is due to an agglutination of the blood upon reaction with a specific antibody resulting in reduced wicking and/or separation of the blood in the detection zone.
8. A testing device according to claim 7, wherein the testing device includes at least one valve for controlling the wicking of biofluid to the detection zone from the collection zone.
9. A testing device according to claim 7, wherein the testing device includes a switch for controlling the contact of the biofluid with the antibody or antigen.
10. A method for identifying an antigen or antibody within a biofluid sample, including:
mixing the biofluid sample with a specific antigen or antibody;
depositing the mixed biofluid sample on a collection zone of a testing device including a substrate having a hydrophilic surface thereon, the surface including said collection zone and at least one detection zone extending therefrom, the biofluid sample being transferred by capillary action to the detection zone; and
identifying the antigen or antibody by a resultant visual indication within the detection zone arising where the antigen or antibody in the biofluid sample reacts with an appropriate said antibody or antigen.
11. A method for identifying an antigen or antibody within a biofluid sample, including:
depositing the biofluid sample on a collection zone of a testing device including a substrate having a hydrophilic surface thereon, the surface including said collection zone and at least one detection zone extending therefrom, the detection zone having an antibody or antigen immobilised therein, the biofluid sample being transferred by capillary action to the detection zone; and
identifying the antigen or antibody by a resultant visual indication arising where the antibody or antigen in the biofluid sample reacts with an appropriate said antigen or antibody within the detection zone.
12. A method according to claim 10, including mixing nanoparticles within the biofluids sample to facilitate said reaction in the detection zone.
13. A method according to claim 10, wherein biofluid sample being tested is blood, and the visual indication is due to an agglutination of the blood upon reaction with a specific antibody resulting in reduced wicking and/or separation of the blood in the detection zone.
14. A method according to claim 13, including detecting blood type from the visual indication.
15. A method according to claim 13 including detecting illness from the visual indication.
16. A testing device according to claim 2, wherein the substrate is formed from paper or other cellulosic materials.
17. A testing device according to claim 2, wherein the substrate includes a chromographic layer thereon or other wettable porous media.
18. A testing device according to claim 2, wherein the substrate surface has a hydrophilic microfluidic channel pattern thereon defining the collection zone and the detection zone.
19. A testing device according to claim 18, including a plurality of detection zones extending from the collection zone.
20. A testing device according to claim 2, wherein biofluid sample being tested is blood, and the visual indication is due to an agglutination of the blood upon reaction with a specific antibody resulting in reduced wicking and/or separation of the blood in the detection zone.
21. A testing device according to claim 20, wherein the testing device includes at least one valve for controlling the wicking of biofluid to the detection zone from the collection zone.
22. A testing device according to claim 20, wherein the testing device includes a switch for controlling the contact of the biofluid with the antibody or antigen.
23. A method according to claim 11, including mixing nanoparticles within the biofluids sample to facilitate said reaction in the detection zone.
24. A method according to claim 11, wherein biofluid sample being tested is blood, and the visual indication is due to an agglutination of the blood upon reaction with a specific antibody resulting in reduced wicking and/or separation of the blood in the detection zone.
25. A method according to claim 24, including detecting blood type from the visual indication.
26. A method according to claim 24 including detecting illness from the visual indication.
US13/497,704 2009-09-24 2010-09-24 Testing device for identifying antigens and antibodies in biofluids Abandoned US20120322086A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AU2009904643 2009-09-24
AU2009904643A AU2009904643A0 (en) 2009-09-24 Testing Device for Identifying Antigens and Antibodies in Biofluids
PCT/AU2010/001255 WO2011035385A1 (en) 2009-09-24 2010-09-24 Testing device for identifying antigens and antibodies in biofluids

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2010/001255 A-371-Of-International WO2011035385A1 (en) 2009-09-24 2010-09-24 Testing device for identifying antigens and antibodies in biofluids

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US15/175,477 Division US11391746B2 (en) 2009-09-24 2016-06-07 Testing device for identifying antigens and antibodies in biofluids

Publications (1)

Publication Number Publication Date
US20120322086A1 true US20120322086A1 (en) 2012-12-20

Family

ID=43795228

Family Applications (2)

Application Number Title Priority Date Filing Date
US13/497,704 Abandoned US20120322086A1 (en) 2009-09-24 2010-09-24 Testing device for identifying antigens and antibodies in biofluids
US15/175,477 Active 2031-05-16 US11391746B2 (en) 2009-09-24 2016-06-07 Testing device for identifying antigens and antibodies in biofluids

Family Applications After (1)

Application Number Title Priority Date Filing Date
US15/175,477 Active 2031-05-16 US11391746B2 (en) 2009-09-24 2016-06-07 Testing device for identifying antigens and antibodies in biofluids

Country Status (6)

Country Link
US (2) US20120322086A1 (en)
EP (1) EP2480885B1 (en)
CN (1) CN102576017B (en)
AU (1) AU2010300092B2 (en)
NZ (2) NZ599044A (en)
WO (1) WO2011035385A1 (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9180449B2 (en) 2012-06-12 2015-11-10 Hach Company Mobile water analysis
US9182353B2 (en) 2010-07-22 2015-11-10 Hach Company Lab-on-a-chip for alkalinity analysis
USD768872S1 (en) 2012-12-12 2016-10-11 Hach Company Cuvette for a water analysis instrument
US20160327460A1 (en) * 2013-11-08 2016-11-10 Espci Method and support for storing and concentrating a non-volatile compound
WO2017123668A1 (en) * 2016-01-12 2017-07-20 Trustees Of Tufts College Separation of cells based on size and affinity using paper microfluidic device
US9949671B2 (en) 2013-03-13 2018-04-24 Orthoaccel Technologies, Inc. Diagnostic mouthpieces
US20180120232A1 (en) * 2015-03-27 2018-05-03 University Court Of The University Of St Andrews Pharmaceutical detection
WO2019246207A1 (en) * 2018-06-22 2019-12-26 Trustees Of Tufts College Patterned dried blood spot cards and related articles and methods
CN113514646A (en) * 2021-08-26 2021-10-19 深圳市亚辉龙生物科技股份有限公司 Microfluidic chip, method, kit and system for detecting protein antigen
US11391746B2 (en) * 2009-09-24 2022-07-19 Monash University Testing device for identifying antigens and antibodies in biofluids

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012083361A1 (en) * 2010-12-24 2012-06-28 Monash University Method and system for detection of blood types
WO2012142763A1 (en) * 2011-04-21 2012-10-26 Siemens Aktiengesellschaft Blood typing devices and methods for testing blood type
US20140295472A1 (en) * 2011-11-10 2014-10-02 The Administrators Of The Tulane Educational Fund Paper Based Diagnostic Test
EP2845001B1 (en) 2012-05-03 2016-12-14 Qualigen, Inc. Whole blood analytic device and method therefor
CN103575728B (en) * 2012-08-01 2016-12-21 中国科学院大连化学物理研究所 Based on filter paper, colorimetric sensor array is used for trace heavy metal ion detection method
JP6120518B2 (en) * 2012-10-10 2017-04-26 公益財団法人かずさＤｎａ研究所 Simple measuring instrument
CN104020300A (en) * 2013-02-28 2014-09-03 西门子公司 Detection device and method and equipment for detecting by using device
US20180021773A1 (en) * 2014-07-25 2018-01-25 Loughborough University Assay devices, methods for carrying out assays, assay kits and method for manufacturing assay devices
PL410603A1 (en) 2014-11-28 2016-06-06 Geomobile Spółka Z Ograniczoną Odpowiedzialnością Method for detection of agglutination
CN106076445B (en) * 2016-07-18 2018-06-15 天津德祥生物技术有限公司 Micro-fluidic reagent card and its detection method and application
US11642669B2 (en) 2017-10-18 2023-05-09 Group K Diagnostics, Inc. Single-layer microfluidic device and methods of manufacture and use thereof
USD879999S1 (en) 2018-11-02 2020-03-31 Group K Diagnostics, Inc. Microfluidic device
MX2019004935A (en) * 2019-04-26 2020-10-27 Unima Diagnosticos De Mexico S De R L De C V Reservoir, test, kit and method for detecting, analysing and identifying substances.
CN113295859B (en) * 2021-05-21 2023-08-22 中国科学技术大学 Paper-based microfluidic chip detection system comprising gyroscopic sample microcentrifuge and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005098439A2 (en) * 2004-03-30 2005-10-20 Whatman, Inc. Lateral flow format, materials and mehtods
WO2011000047A1 (en) * 2009-06-30 2011-01-06 Monash University Quantitative and self-calibrating chemical analysis using paper-based microfluidic systems

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5164598A (en) * 1985-08-05 1992-11-17 Biotrack Capillary flow device
DE3686474T2 (en) * 1985-10-11 1993-02-11 Abbott Lab DIAGNOSTIC SAMPLE.
US4851210A (en) 1986-05-22 1989-07-25 Genelabs Incorporated Blood typing device
US4943522A (en) * 1987-06-01 1990-07-24 Quidel Lateral flow, non-bibulous membrane assay protocols
IT1227293B (en) * 1988-10-06 1991-04-05 Boehringer Biochemia Srl DEVICE AND METHOD FOR PREGNANCY DIAGNOSIS
US5585278A (en) * 1994-10-27 1996-12-17 Bayer Corporation Method for coupling antibody to novel latex substrate and its use in immunoassay
US5904824A (en) * 1997-03-07 1999-05-18 Beckman Instruments, Inc. Microfluidic electrophoresis device
AU3494600A (en) * 1999-02-19 2000-09-04 Medical Analysis Systems, Inc. Rapid assay for arthropod-borne disease vectors and pathogens
ES2228234B1 (en) * 2002-11-06 2006-05-16 Eduardo Jaime Cadorniga Martinez METHOD FOR SELF-EXECUTION OF THE ABO SANGUINEO GROUP.
GB0306098D0 (en) * 2003-03-18 2003-04-23 Platform Diagnostics Group Ltd Sample testing device
GB0329220D0 (en) * 2003-12-17 2004-01-21 Inverness Medical Switzerland System
GB0423885D0 (en) * 2004-10-28 2004-12-01 Platform Diagnostics Ltd Blood analysis
US20100089529A1 (en) 2005-01-12 2010-04-15 Inverness Medical Switzerland Gmbh Microfluidic devices and production methods therefor
AU2006313611B2 (en) * 2005-11-12 2013-01-31 Platform Diagnostics Limited Agglutination assay
US7598091B2 (en) * 2006-04-04 2009-10-06 Micropoint Bioscience, Inc. Micromachined diagnostic device with controlled flow of fluid and reaction
EP2101917A1 (en) * 2007-01-10 2009-09-23 Scandinavian Micro Biodevices A/S A microfluidic device and a microfluidic system and a method of performing a test
US20100062414A1 (en) * 2007-04-05 2010-03-11 Panasonic Corporation Sample liquid analytical chip
NZ616821A (en) * 2008-07-11 2015-08-28 Univ Monash Method of fabricating microfluidic systems
CN102483410A (en) * 2009-03-25 2012-05-30 莱泽尔诊断公司 Apparatus and methods for analyzing fluid variables
WO2011035385A1 (en) 2009-09-24 2011-03-31 Monash University Testing device for identifying antigens and antibodies in biofluids
US20150323525A1 (en) * 2012-12-19 2015-11-12 Stichting Sanquin Bloedvoorziening Methods and means for detecting cells using surface plasmon resonance
WO2017123668A1 (en) * 2016-01-12 2017-07-20 Trustees Of Tufts College Separation of cells based on size and affinity using paper microfluidic device

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005098439A2 (en) * 2004-03-30 2005-10-20 Whatman, Inc. Lateral flow format, materials and mehtods
WO2011000047A1 (en) * 2009-06-30 2011-01-06 Monash University Quantitative and self-calibrating chemical analysis using paper-based microfluidic systems

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
Anderson et al. ("Analytical Techniques for Cell Fractions XVIII. Use of Cellulose Wicks to Monitor Agglutination Reactions" Analytical Biochemistry, 38, 175-189, 1970) *
Carrilho et al. ("Understanding Wax Printing: A Simple Micropatterning Process for Paper-Based Microfluidics" Anal. Chem. 2009, 81, 7091-7095). *
Li et al. ("Paper-Based Microfluidic Devices by Plasma Treatment" Anal. Chem. 2008, 80, 9131-9134). *
Martinez et al. ("Three-Dimensional Microfluidic Devices Fabricated in Layered Paper and Tape" PNAS, Vol. 105, No. 50, Dec. 16, 2008, pp. 19606-19611). *
Pelton et al. ("Bioactive paper provides a low-cost platform for diagnostics" Trends in Analytical Chemistry, Volume 28, Issue 8, September 2009, Pages 925-942 Available online 26 June 2009). *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11391746B2 (en) * 2009-09-24 2022-07-19 Monash University Testing device for identifying antigens and antibodies in biofluids
US9182353B2 (en) 2010-07-22 2015-11-10 Hach Company Lab-on-a-chip for alkalinity analysis
US9180449B2 (en) 2012-06-12 2015-11-10 Hach Company Mobile water analysis
USD768872S1 (en) 2012-12-12 2016-10-11 Hach Company Cuvette for a water analysis instrument
US9949671B2 (en) 2013-03-13 2018-04-24 Orthoaccel Technologies, Inc. Diagnostic mouthpieces
US20160327460A1 (en) * 2013-11-08 2016-11-10 Espci Method and support for storing and concentrating a non-volatile compound
US20180120232A1 (en) * 2015-03-27 2018-05-03 University Court Of The University Of St Andrews Pharmaceutical detection
WO2017123668A1 (en) * 2016-01-12 2017-07-20 Trustees Of Tufts College Separation of cells based on size and affinity using paper microfluidic device
US10758846B2 (en) 2016-01-12 2020-09-01 Trustees Of Tufts College Separation of cells based on size and affinity using paper microfluidic device
US11772017B2 (en) 2016-01-12 2023-10-03 Trustee Of Tufts College Separation of cells based on size and affinity using paper microfluidic device
WO2019246207A1 (en) * 2018-06-22 2019-12-26 Trustees Of Tufts College Patterned dried blood spot cards and related articles and methods
CN113514646A (en) * 2021-08-26 2021-10-19 深圳市亚辉龙生物科技股份有限公司 Microfluidic chip, method, kit and system for detecting protein antigen

Also Published As

Publication number Publication date
WO2011035385A1 (en) 2011-03-31
NZ599044A (en) 2014-06-27
CN102576017A (en) 2012-07-11
AU2010300092B2 (en) 2016-02-04
NZ625421A (en) 2015-09-25
EP2480885A4 (en) 2013-04-03
AU2010300092A1 (en) 2012-04-19
CN102576017B (en) 2015-09-23
EP2480885B1 (en) 2016-11-30
EP2480885A1 (en) 2012-08-01
US20160291039A1 (en) 2016-10-06
US11391746B2 (en) 2022-07-19

Similar Documents

Publication Publication Date Title
US11391746B2 (en) Testing device for identifying antigens and antibodies in biofluids
CA2469935C (en) Diagnostic testing process
US9857365B2 (en) Freeze-dried conjugate structure for point-of-care testing (POCT) immunochromatography, immunoassay kit comprising the same, and method for analysis using the kit
US10058867B2 (en) Sample metering device and assay device with integrated sample dilution
JP4216838B2 (en) Non-continuous immunoassay device and immunoassay method using the same
US20110229913A1 (en) Method for Amplification of Signal in Immunochromatographic Assay and Immunochromatographic Kit Using the Method
CA2819195A1 (en) Sample metering device and assay device with integrated sample dilution
US9795962B2 (en) Ratiometric immunoassay method and blood testing device
JP4653574B2 (en) Method for measuring hemoglobin A1c
Raj et al. Semi-enclosed microfluidic device on glass-fiber membrane with enhanced signal quality for colorimetric analyte detection in whole blood
KR102346178B1 (en) Strips, kits for immunochromatography and competitive immunochromatographic assays using the same
Ardakani et al. Pronounced Effect of lamination on plasma separation from whole blood by microfluidic paper-based analytical devices
US10670586B2 (en) Test instrument for measuring analyte in sample by an aggregation assay using a metal colloid and using a reagent attached in a dry state in a reaction chamber, and method for measuring analyte using same
JPH11133027A (en) Instrument for analyzing component in red blood corpuscle
DE69024936T2 (en) Device for the determination and semi-quantitative measurement of components
JP6738066B2 (en) Extraction filter and immunochromatographic analysis kit including the same
JP2003194818A (en) Specific binding analyzing method and device used therefor
KR20220047198A (en) Strips, kits for immunochromatography and sandwich immunochromatographic assays for measuring tryptase using the same
CN116018207A (en) System and method for sample analysis
WO2024126727A1 (en) Method of producing an analysis device, analysis device, analysis arrangement and analysis method

Legal Events

Date Code Title Description
AS Assignment

Owner name: MONASH UNIVERSITY, AUSTRALIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:GARNIER, GIL;SHEN, WEI;KHAN, MOHIDUS SAMAD;AND OTHERS;SIGNING DATES FROM 20120419 TO 20120508;REEL/FRAME:028316/0652

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION