U.S. patent application number 14/176690 was filed with the patent office on 2014-06-26 for immunoassay test strip for use in a diagnostic system.
This patent application is currently assigned to HOLOGIC, INC.. The applicant listed for this patent is HOLOGIC, INC.. Invention is credited to Lina Baydoun.
Application Number | 20140178976 14/176690 |
Document ID | / |
Family ID | 44863217 |
Filed Date | 2014-06-26 |
United States Patent
Application |
20140178976 |
Kind Code |
A1 |
Baydoun; Lina |
June 26, 2014 |
IMMUNOASSAY TEST STRIP FOR USE IN A DIAGNOSTIC SYSTEM
Abstract
An immunoassay test strip includes a sample pad for receiving a
liquid patient sample; a conjugate pad fluidly coupled to the
sample pad, wherein the conjugate pad contains a substantially
uniform application of conjugate reagent; a contact pad fluidly
coupled to the conjugate pad; a porous or bibulous member, e.g.,
made from nitrocellulose, fluidly coupled to the contact pad which
is capable or transporting a liquid sample along the test strip,
wherein the porous or bibulous member serves as the solid support
upon which immunoreactions occur, and an absorbent pad fluidly
coupled to the porous or bibulous member, which serves to draw
sample fluid introduced onto the sample pad through the respective
conjugate pad, contact pad and porous or bibulous member.
Inventors: |
Baydoun; Lina; (Gilroy,
CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
HOLOGIC, INC. |
Marlborough |
MA |
US |
|
|
Assignee: |
HOLOGIC, INC.
Marlborough
MA
|
Family ID: |
44863217 |
Appl. No.: |
14/176690 |
Filed: |
February 10, 2014 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
13250028 |
Sep 30, 2011 |
8647888 |
|
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14176690 |
|
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61389171 |
Oct 1, 2010 |
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Current U.S.
Class: |
435/287.2 ;
422/421 |
Current CPC
Class: |
G01N 33/558 20130101;
G01N 33/5302 20130101; G01N 2333/78 20130101; G01N 33/6887
20130101 |
Class at
Publication: |
435/287.2 ;
422/421 |
International
Class: |
G01N 33/53 20060101
G01N033/53; G01N 33/68 20060101 G01N033/68 |
Claims
1. An immunoassay test strip, wherein results of an immunoassay
test of a patient sample are detectable by a change in color or
other property of the resulting immunoassay test strip using a
reflectance reader, and wherein the immunoassay test strip is
manufactured by performing the steps of applying a porous or
bibulous member to a substrate, wherein the porous or bibulous
member is capable of transporting a liquid sample and serves as a
solid support upon which immunoreactions may occur; adhering a
contact pad to the substrate adjacent a first end of the porous or
bibulous member, with an edge of the contact pad overlaying, so as
to be fluidly coupled with, the porous or bibulous member; adhering
a conjugate pad to the substrate adjacent the contact pad, with an
edge of the conjugate pad overlaying, so as to be fluidly coupled
with, the contact pad; applying a conjugate reagent to the
conjugate pad through a striping process, so that the conjugate pad
thereafter contains a substantially uniform application of
conjugate reagent; attaching a sample pad to the substrate adjacent
the conjugate pad, with an edge of the sample pad overlaying, so as
to be fluidly coupled with, the conjugate pad, the sample pad
comprising material suitable for receiving a liquid patient sample;
and attaching an absorbent pad to the substrate adjacent a second
end of the porous or bibulous member opposite the first end, with
an edge of the absorbent pad overlaying, so as to be fluidly
coupled with, the porous or bibulous member, wherein the absorbent
pad serves to draw sample fluid introduced onto the sample pad
through the respective conjugate pad, contact pad, and porous or
bibulous member, wherein the presence of the contact pad during the
striping process prevents excess liquid conjugate reagent from
wicking from the conjugate pad into the porous or bibulous
material, while still allowing for a combination of patient sample
liquid and conjugate reagent to flow from the conjugate pad,
through the contact pad, into the porous or bibulous material
during a subsequent immunoassay test.
2. The test strip of claim 1, wherein the conjugate pad comprises a
pretreated hydrophilic material.
3. The test strip of claim 1, wherein the conjugate reagent applied
during the striping process was allowed to dry prior to attaching
the sample pad.
4. The test strip of claim 1, wherein the porous or bibulous member
comprises nitrocellulose.
5. The test strip of claim 1, wherein the manufacture of the test
strip further included applying an immobilized binding partner of
an analyte of interest in a sample fluid to the porous or bibulous
member.
6. The test strip of claim 5, wherein the immobilized binding
partner comprises a capture antibody that binds to the analyte of
interest.
7. The test strip of claim 1, wherein the conjugate pad is adhered
to the substrate such that the contact pad is longitudinally
between the conjugate pad and the porous or bibulous member.
8. The test strip of claim 1, wherein the sample pad is attached to
the substrate comprises such that the conjugate pad is
longitudinally between the sample pad and the contact pad.
9. The test strip of claim 1, wherein the porous or bibulous member
comprises an antibody immobilized thereon.
10. The test strip of claim 1, wherein the results of the
immunoassay test are qualitative.
11. The test strip of claim 1, wherein the results of the
immunoassay test are quantitative.
12. The test strip of claim 1, wherein the immunoassay test detects
a presence of fetal fibronectin in the sample.
Description
RELATED APPLICATION DATA
[0001] The present application is a continuation of pending U.S.
patent application Ser. No. 13/250,028, filed Sep. 30, 2011, which
claims the benefit under 35 U.S.C. .sctn.119 to U.S. Provisional
Patent Application Ser. No. 61/389,171, filed on Oct. 1, 2010,
which are hereby incorporated by reference into the present
application in their entirety.
FIELD OF THE DISCLOSED INVENTIONS
[0002] The inventions disclosed in the present application pertain
to systems and methods that aid in providing a medical diagnosis or
risk assessment for a patient using biochemical and historic
patient data, including data from point of care diagnostic tests or
assays, and processing the information to give an indication of a
medical condition or risk. In particular, the present application
discloses and describes an improved immunoassay test strip for use
in a diagnostic system and related methods, such as the diagnostic
systems and methods disclosed and described in U.S. Pat. Nos.
6,267,722, 6,394,952 and 6,867,051, each of which is fully
incorporated herein by reference.
BACKGROUND
[0003] The above-incorporated U.S. Pat. Nos. 6,267,722, 6,394,952
and 6,867,051 disclose and describe objective techniques that
reduce the error associated with interpreting
immunochromato-graphic and other assay test results, including
providing systems, methods, devices and instruments for objectively
assessing data from biochemical and other tests and to use such
data for diagnosis and risk assessment, including the incorporation
of decision-support methodologies into such systems and thereby
enhance the diagnostic and risk assessment capabilities
thereof.
[0004] More specifically, the above-incorporated U.S. Pat. Nos.
6,267,722, 6,394,952 and 6,867,051 disclose and describe systems
and methods for detecting and measuring levels of a target analyte
in a patient sample, analyzing the resulting data, and providing a
diagnosis or risk assessment. The systems and methods include an
assay device in combination with a reader, particularly a
computer-assisted reader, such as a reflectance reader, and data
processing software employing data reduction and curve fitting
algorithms, optionally in combination with a trained neural network
for accurately determining the presence or concentration of analyte
in a biological sample. The methods include performing an
immunoassay assay on a patient sample using a specially constructed
test strip, reading the data using a reflectance reader, and
processing the reflectance data using data processing software
employing data reduction algorithms. Software, including curve
fitting algorithms, optionally in combination with a trained neural
network, is used to determine the presence or amount of analyte in
a given sample. The data obtained from the reader then can be
further processed by the medical diagnosis system to provide a risk
assessment or diagnosis of a medical condition as output.
[0005] In an exemplary embodiment, the assay device is a lateral
flow test strip encased in a housing designed to be read by the
reader, and the assay is a sandwich immunoassay. A patient sample
is contacted with an antibody for a selected target analyte
indicative of a disease, disorder or risk thereof. The antibody is
labeled by conjugation to a physically detectable label, and upon
contact with the sample containing the target analyte forms a
complex, wherein the antibody-analyte complex is then contacted
with a second antibody for the antigen, which is immobilized on a
solid support. The second antibody captures the antibody-analyte
complex to form an antibody-analyte-antibody sandwich complex, and
the resulting complex, which is immobilized on the solid support,
is detected by virtue of the label. The test strip is then inserted
into a reader, where the signal from the label in the complex is
measured. Additionally, the test strip may be enclosed within a
housing that includes an identifying symbol, such as a bar code,
which is also read by the reader and contains data related to the
assay device and/or test run.
[0006] The signal obtained is processed using data processing
software employing data reduction and curve fitting algorithms,
optionally in combination with a trained neural network, to give
either a qualitative (i.e., a positive or negative) result, or a
quantitative determination of the concentration of analyte in the
sample, which is correlated with a result indicative of a risk or
presence of a disease or disorder. The result can optionally be
input into a decision support system, and processed to provide an
enhanced assessment of the risk of a medical condition as output.
The entire procedure may be automated and/or
computer-controlled.
[0007] The analyte to be detected may be fetal fibronectin (fFN)
and the result obtained is a positive or negative indication of
pregnancy or the risk of certain pregnancy-related conditions or
fertility and infertility-related conditions, including ectopic
pregnancy, preterm labor, pre-eclampsia, imminent delivery, term
induction and fetal membrane rupture. Thus, the above-incorporated
U.S. Pat. Nos. 6,267,722, 6,394,952 and 6,867,051 disclose and
describe a rapid fFN test using a lateral flow test device, which
provides a means to detect and to quantitate concentrations of fFN
throughout pregnancy and to assess the risk and detect conditions
associated therewith. Because of the sensitivity of the combination
of the reader and devices provided herein, fFN may be monitored
throughout pregnancy, including times when it is not detected by
less sensitive systems.
[0008] Point of Care Diagnostic and Risk Assessment Systems
[0009] The above-incorporated U.S. Pat. Nos. 6,267,722, 6,394,952
and 6,867,051 disclose and describe systems for diagnosing and
assessing certain medical risks. The systems are designed for use
on site at the point of care, where patients are examined and
tested, as well as for operation remote from the site. The systems
are designed to accept input in the form of patient data,
including, but not limited to biochemical test data, physical test
data, historical data and other such data, and to process and
output information, such as data relating to a medical diagnosis or
a disease risk indicator. The patient data may be contained within
the system, such as medical records or history, or may be input as
a signal or image from a medical test or procedure, for example,
immunoassay test data, blood pressure reading, ultrasound, X-ray or
MRI, or introduced in any other form. Specific test data can be
digitized, processed and input into the medical diagnosis expert
system, where it may be integrated with other patient information.
The output from the system is a disease risk index or medical
diagnosis.
[0010] Point of care testing refers to real time diagnostic testing
that can be done in a rapid time frame so that the resulting test
is performed faster than comparable tests that do not employ this
system. For example, the exemplified fFN immunoassay disclosed and
described in the above-incorporated U.S. Pat. Nos. 6,267,722,
6,394,952 and 6,867,051 is performed in significantly less time
than the fFN ELISA assay, e.g., in less than half an hour. In
addition, point of care testing refers to testing that can be
performed rapidly and on site, such as in a doctor's office, at a
bedside, in a stat laboratory, emergency room or other such
locales, particularly where rapid and accurate results are
required. In general, "diagnosis" refers to a predictive process in
which the presence, absence, severity or course of treatment of a
disease, disorder or other medical condition is assessed. For
purposes herein, diagnosis will also include predictive processes
for determining the outcome resulting from a treatment. As used
herein, risk refers to a predictive process in which the
probability of a particular outcome is assessed.
[0011] In an exemplary embodiment, a point of care diagnostic and
risk assessment system includes a reader, such as a reflectance or
transmission reader, such as a reflectance reader, for reading
patient data, a test device designed to be read in the reader, and
software for analysis of the data. A test strip device in a plastic
housing is designed for use with the reader, optionally including a
symbology, such as an alphanumeric character bar code or other
machine-readable code, and software designed for analysis of the
data generated from the test strip are also provided.
[0012] Assays
[0013] The above-incorporated U.S. Pat. Nos. 6,267,722, 6,394,952
and 6,867,051 disclose and describe systems for performing assays,
including but are not limited to: nucleic acid detection, including
using amplification and non-amplification protocols, any assay that
relies on calorimetric or spectrometric detection, including
fluorometric, luminescent detection, such as creatine, hemoglobin,
lipids, ionic assays, blood chemistry. Immunoassays, including
competitive and non-competitive immunoassays, are among those
preferred for determination of the presence or amount of analyte in
a patient sample. An immunoassay may be any method using a
preferential binding of an antigen with a second material, a
binding partner, usually an antibody or another substance having an
antigen binding site, which binds preferentially with an epitope of
the fetal restricted antigen. Preferential binding, as used herein,
refers to binding between binding partners that is selective and
generally specific, and demonstrates less than 10%, preferably less
than 5%, cross-reactive nonspecific binding. Such immunoassay
methods include any known to those of skill in the art, including,
but not limited to, sandwich, competition, agglutination or
precipitation. Any known immunoassay procedure, particularly those
that can be adapted for use in combination with lateral flow
devices as described herein, can be used in the systems and methods
provided in the above-incorporated U.S. Pat. Nos. 6,267,722,
6,394,952 and 6,867,051, and also further provided herein.
[0014] Test Device
[0015] Any device which is compatible for use with a reader, such
as a reflectance reader, for determining the assay result is
contemplated for use herein. As used herein, a "test strip" refers
to any means on which patient test data or other data is generated,
recorded or displayed in a manner that forms an image or from which
an image can be generated. Such strips, include, but are not
limited to, immunochromatographic test strips, such as lateral flow
devices, X-ray films, such as X-rays and films produced from
sequencing gels, EKG printouts, MRI results and other such means
that generate or from which an image can be generated. The strip is
may be adapted for scanning or reading by a reader. Although
referred to as a "strip", a test strip can be of any shape or
geometry, including rectangular, three dimensional, circular, and
so forth. Test strips that may be adapted for use in combination
with a reader are disclosed and described in the above-incorporated
U.S. Pat. Nos. 6,267,722, 6,394,952 and 6,867,051.
[0016] Typically these test devices are intended for use with
biological samples, such as saliva, blood, serum, cerebral spinal
fluid, cervico-vaginal samples, for example. Other biological
samples, such as food samples, which are tested for contamination,
such as by bacteria or insects, are also contemplated. Target
analytes include, but are not limited to: nucleic acids, proteins,
peptides, such as human immunodeficiency virus (HIV) antigens,
antigens indicative of bacterial, such as Salmonella and E. coli,
yeast or parasitic infections, apolipoprotein(a) and
lipoprotein(a), environmental antigens, human chorionic
gonadotropin (hCG), E-3-G, interleukins and other cytokines and
immunomodulatory proteins, such as IL-6 and interferon, small
nuclear ribonuclear particles (snRNP) antigens, fFN and other
indicators, such as IGF binding protein-1, of pregnancy related
disorders.
[0017] Immunoassay Test Strip
[0018] An exemplary prior art immunoassay test strip disclosed and
described in the above-incorporated U.S. Pat. Nos. 6,267,722,
6,394,952 and 6,867,051 includes a membrane system that defines a
liquid flow pathway, as shown in FIGS. 1A and 1B, which are
described below in detail. Such lateral flow test immunoassay
devices are among those preferred for performing immunoassays,
wherein a membrane system forms a single fluid flow pathway along
the test strip. The membrane system includes components that act as
a solid support for immunoreactions. For example, porous or
bibulous or absorbent materials may be placed on a strip such that
they partially overlap, or a single material can be used, in order
to conduct liquid along the strip. The membrane materials may be
supported on a backing, such as a plastic backing. In an exemplary
prior art embodiment, the test strip includes a glass fiber pad, a
nitrocellulose strip and an absorbent cellulose paper strip
supported on a plastic backing
[0019] Antibodies that react with the target analyte and/or a
detectable label system are immobilized on the solid support. A
"solid support" refers to the material to which the antibody is
linked. A variety of materials can be used as the solid support.
The support materials include any material that can act as a
support for attachment of the molecules of interest. Such materials
are known to those of skill in this art. These materials include,
but are not limited to, organic or inorganic polymers, natural and
synthetic polymers, including, but not limited to, agarose,
cellulose, nitrocellulose, cellulose acetate, other cellulose
derivatives, dextran, dextran-derivatives and dextran co-polymers,
other polysaccharides, glass, silica gels, gelatin, polyvinyl
pyrrolidone, rayon, nylon, polyethylene, polypropylene,
polybutylene, polycarbonate, polyesters, polyamides, vinyl
polymers, polyvinylalcohols, polystyrene and polystyrene
copolymers, polystyrene cross-linked with divinylbenzene or the
like, acrylic resins, acrylates and acrylic acids, acrylamides,
polyacrylamides, polyacrylamide blends, co-polymers of vinyl and
acrylamide, methacrylates, methacrylate derivatives and
co-polymers, other polymers and co-polymers with various functional
groups, latex, butyl rubber and other synthetic rubbers, silicon,
glass, paper, natural sponges, insoluble protein, surfactants, red
blood cells, metals, metalloids, magnetic materials, or other
commercially available media.
[0020] The antibodies may be bound to the test strip by adsorption,
ionic binding, van der Waals adsorption, electrostatic binding, or
by covalent binding, by using a coupling agent, such as
glutaraldehyde. In the prior art test strip shown in FIGS. 1A and
1B, the antibodies are applied to the conjugate pad and
nitrocellulose strip using a volumetric ceramic piston pump
dispenser to stripe antibodies that bind the analyte of interest,
including a labeled antibody conjugate, onto the glass fiber
conjugate pad and the nitrocellulose strip. The test strips may or
may not be otherwise treated, for example, with sugar to facilitate
mobility along the test strip or with water-soluble non-immune
animal proteins, such as albumins, including bovine (BSA), other
animal proteins, water-soluble polyamino acids, or casein to block
non-specific binding sites.
[0021] An anti-fFN antibody is an antibody that binds selectively
with fFN. Such antibodies are known to those of skill in the art
and also may be readily isolated. Fetal restricted antigens refers
to antigen that are present in pregnant women uniquely, or in
substantially elevated amounts compared to non-pregnant women in
maternal serum, plasma, urine, saliva, sweat, tears and other
bodily fluids. Fetal fibronectin is a fetal restricted antigen
found in placenta, amniotic fluid and fetal connective tissue,
which differs structurally from adult fibronectins. Fetal
fibronectin is not present in significant quantities in maternal
plasma or serum, and may be captured with a general binding
antibody, such as an anti-fibronectin antibody, or an anti-fetal
restricted antigen antibody, such as anti-fetal fibronectin
antibody.
[0022] Test Strip Housing
[0023] The test strip optionally may be contained within a
customized housing shaped for insertion into the reflectance
reader. The housing may be made of plastic or other inert material
that does not interfere with the assay procedure. An exemplary
prior art assay device, including a test strip and housing assembly
disclosed and described in the above-incorporated U.S. Pat. Nos.
6,267,722, 6,394,952 and 6,867,051, FIGS. 2-5, which are described
in detail below.
[0024] The test strip housing may include a symbology, such as a
bar code that can be associated with data related to the assay
device, patient data and/or test run. For example, information
associated with the device, such as lot number, expiration date,
analyte and intensity value, or information related to the test
run, such as date, reflectance value or other such information, can
be encoded and associated, such as in a database with a bar code
imprinted on the device. FIGS. 2A, 2B and 3 depict assay devices
that optionally include bar codes, 216 and 316, respectively.
[0025] Antibodies
[0026] Any antibody, including polyclonal or monoclonal antibodies,
or any fragment thereof, such as the Fab fragment, that binds the
analyte of interest, is contemplated for use with the test strips
disclosed and described herein. Monoclonal and/or polyclonal
antibodies may be used. For example, a mouse monoclonal anti-fetal
fibronectin antibody may be used in a labeled antibody-conjugate
for detecting fetal fibronectin, and a polyclonal goat anti-mouse
antibody may also be used to bind fetal fibronectin to form a
sandwich complex. An antibody that binds to the labeled antibody
conjugate that is not complexed with fetal fibronectin may be
immobilized on the test strip and used as a control antibody. For
example, when fetal fibronectin is the analyte, a polyclonal goat
anti-mouse IgG antibody may be used.
[0027] An antibody that will bind the analyte of interest is
conjugated to a detectable label. In a particular embodiment, where
fetal fibronectin is to be detected, a mouse monoclonal anti-fFN
antibody (see, e.g., U.S. Pat. No. 5,281,522), conjugated to latex
particles containing a blue dye may be used. In one embodiment, a
goat polyclonal antibody to human fibronectin is conjugated to a
colloidal gold label. In an exemplary embodiment, an antibody that
binds the labeled antibody conjugate that is not complexed with
fetal fibronectin is used as a control antibody. For example, where
the labeled conjugate includes a monoclonal anti-fetal fibronectin
antibody, a polyclonal goat anti-mouse IgG antibody is used. The
antibodies may be raised and purified using methods known to those
of skill in the art or obtained from publicly available
sources.
[0028] Conjugation of the Antibody to a Label
[0029] An antibody conjugate containing a detectable label may be
used to bind the analyte of interest. The detectable label used in
the antibody conjugate may be any physical or chemical label
capable of being detected on a solid support using a reader, such
as a reflectance reader, and capable of being used to distinguish
the reagents to be detected from other compounds and materials in
the assay. Suitable antibody labels are well known to those of
skill in the art. The labels include, but are not limited to
enzyme-substrate combinations that produce color upon reaction,
colored particles, such as latex particles, colloidal metal or
metal or carbon sol labels, fluorescent labels, and liposome or
polymer sacs, which are detected due to aggregation of the label.
An exemplary label is a colored latex particle. Colloidal gold may
also be used in the labeled antibody conjugate.
[0030] The label may be derivatized for linking antibodies, such as
by attaching functional groups, such as carboxyl groups to the
surface of a particle to permit covalent attachment of antibodies.
Antibodies may be conjugated to the label using well known coupling
methods. Coupling agents such as glutaraldehyde or carbodiimide may
be used. The labels may be bonded or coupled to the antibodies by
chemical or physical bonding. A carbodiimide coupling reagent,
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDAC), may be used
to link antibodies to latex particles.
[0031] Measurement of Analytes
[0032] Any analyte that can be detected in any assay, particularly
colorimetric assays, including immunoassays, and that can be
associated with a disorder is contemplated for as a target.
Suitable analytes are any which can be used, along with a specific
binding partner, such as an antibody, or a competitor, such as an
analog, in an assay. Analytes may include, but are not limited to
proteins, haptens, immunoglobulins, enzymes, hormones (e.g., hCG,
LH, E-3-G estrone-3-glucuronide and P-3-G
(progestrone-3-glucuronide)), polynucleotides, steroids,
lipoproteins, drugs, bacterial or viral antigens, such as
Streptococcus, Neisseria and Chlamydia, lymphokines, cytokines, and
the like. A number of suitable analytes are described in U.S. Pat.
No. 5,686,315, which is fully incorporated herein by reference.
Although examples are provided for the determination of fetal
fibronectin in cervicovaginal samples, the systems and methods
disclosed and described in the above-incorporated U.S. Pat. Nos.
6,267,722, 6,394,952 and 6,867,051, and further provided herein,
are not limited to the detection and measurement of fetal
fibronectin, but apply to any biochemical test, particularly those
for which test strips can be developed or for which test strips are
known.
[0033] Test Strip for Measuring fFN and Cellular Fibronectin
[0034] Methods for measuring fetal fibronectin and cellular
fibronectin levels in cervicovaginal samples are known, (see, e.g.,
U.S. Pat. Nos. 5,096,830, 5,185,270, 5,223,440, 5,236,846,
5,281,522, 5,468,619 and 5,516,702, which are fully incorporated by
reference herein), and diagnostic tests for various
pregnancy-related disorders are available (see, e.g., U.S. Pat.
Nos. 5,096,830 and 5,079,171, which are also fully incorporated by
reference herein). These methods can be adapted for use with the
immunoassay test strips and devices described herein.
[0035] Fetal Fibronectin Assay Procedure
[0036] In conducting the assay, a patient sample is obtained. The
sample may include fluid and particulate solids, and, thus, can be
filtered prior to application to the assay test strip. The sample
may be removed from the patient using a swab having a fibrous tip,
an aspirator, suction or lavage device, syringe, or any other known
method of removing a bodily sample, including passive methods for
collecting urine or saliva. In particular, the sample may be
extracted into a buffer solution, and optionally heated, for
example, at 37.degree. C., and filtered. Where fetal fibronectin is
to be detected in a sample, the sample is obtained from in the
vicinity of the posterior fornix, the ectocervix or external
cervical os using a swab having a dacron or other fibrous tip.
[0037] A volume of the test sample is then delivered to the test
strip using any known means for transporting a biological sample,
for example, a standard plastic pipet. Any analyte in the sample
binds to the labeled antibody and the resulting complex migrates
along the test strip. Alternatively, the sample may be pre-mixed
with the labeled conjugate prior to applying the mixture to the
test strip. When the labeled antibody-analyte complex encounters a
detection zone of the test strip, the immobilized antibody therein
binds the complex to form a sandwich complex, thereby forming a
colored stripe. Any unbound latex-conjugated antibody continues to
migrate into a control zone where it is captured by a second
immobilized antibody or other agent capable of binding the
conjugate, and thereby forms a second colored stripe due to the
aggregation of the dye-containing latex beads. This indicates that
the assay run has completed.
[0038] Reader
[0039] A reader refers to an instrument for detecting and/or
quantitating data, such as on test strips. The data may be visible
to the naked eye, but does not need to be visible. Such readers are
disclosed and described in the above-incorporated U.S. Pat. Nos.
6,267,722, 6,394,952 and 6,867,051. As disclosed and described
therein, a reflectance reader refers to an instrument adapted to
read a test strip using reflected light, including fluorescence, or
electromagnetic radiation of any wavelength. Reflectance can be
detected using a photodetector or other detector, such as charge
coupled diodes (CCD). A exemplary reflectance reader includes a
cassette slot adapted to receive a test-strip, light-emitting
diodes, optical fibers, a sensing head, including means for
positioning the sensing head along the test strip, a control
circuit to read the photodetector output and control the on and off
operation of the light-emitting diodes, a memory circuit for
storing raw and/or processed data, and a photodetector, such as a
silicon photodiode detector. It will be appreciated that a color
change refers to a change in intensity or hue of color or may be
the appearance of color where no color existed or the disappearance
of color.
[0040] In an exemplified embodiment disclosed and described in the
above-incorporated U.S. Pat. Nos. 6,267,722, 6,394,952 and
6,867,051, a sample is applied to a diagnostic immunoassay test
strip, and colored or dark bands are produced. The intensity of the
color reflected by the colored label in the test region (or
detection zone) of the test strip is, for concentration ranges of
interest, directly proportional or otherwise correlated with an
amount of analyte present in the sample being tested. The color
intensity produced is read, in accordance with the present
embodiment, using a reader device, for example, a reflectance
reader, adapted to read the test strip. The intensity of the color
reflected by the colored label in the test region (or detection
zone) of the test strip is directly proportional to the amount of
analyte present in the sample being tested. In other words, a
darker colored line in the test region indicates a greater amount
of analyte, whereas a lighter colored line in the test region
indicates a smaller amount of analyte. The color intensity
produced, i.e., the darkness or lightness of the colored line, is
read using a reader device, for example, a reflectance reader,
adapted to read the test strip.
[0041] A reflectance measurement obtained by the reader device is
correlated to the presence and/or quantity of analyte present in
the sample. The reader takes a plurality of readings along the
strip, and obtains data that are used to generate results that are
an indication of the presence and/or quantity of analyte present in
the sample. The system may correlate such data with the presence of
a disorder, condition or risk thereof.
[0042] As mentioned above, in addition to reading the test strip,
the reader may (optionally) be adapted to read a symbology, such as
a bar code, which is present on the test strip or housing and
encodes information relating to the test strip device and/or test
result and/or patient, and/or reagent or other desired information.
Typically the associated information is stored in a remote computer
database, but can be manually stored. Furthermore, the symbology
can be imprinted when the device is used and the information
encoded therein.
SUMMARY
[0043] An immunoassay test strip is provided, wherein results of an
immunoassay test of a patient sample are detectable by a change in
color or other property of the test strip that can be detected
using a reflectance reader. In one embodiment, the immunoassay test
strip includes a sample pad for receiving a liquid patient sample;
a conjugate pad fluidly coupled to the sample pad, wherein the
conjugate pad contains a substantially uniform application of
conjugate reagent; a contact pad fluidly coupled to the conjugate
pad; a porous or bibulous member, e.g., made from nitrocellulose,
fluidly coupled to the contact pad which is capable or transporting
a liquid sample along the test strip, wherein the porous or
bibulous member serves as the solid support upon which
immunoreactions occur, and an absorbent pad fluidly coupled to the
porous or bibulous member, which serves to draw sample fluid
introduced onto the sample pad through the respective conjugate
pad, contact pad and porous or bibulous member.
[0044] The porous or bibulous member may include an immobilized
capture antibody that binds to an analyte of interest in the sample
fluid in a detection zone. For example, the porous or bibulous
member may have an antibody diffusively bound thereto. The results
of the immunoassay test may be qualitative and/or quantitative. In
one embodiment, the immunoassay test detects a presence of fetal
fibronectin in the sample.
[0045] Other and further aspects and embodiments of the disclosed
inventions will be apparent to those skilled in the art upon
reviewing the following Detailed Description in conjunction with
the accompanying figures.
BRIEF DESCRIPTION OF THE DRAWINGS
[0046] It will be appreciated that the system and apparatus shown
in the drawings are not necessarily drawn to scale, with emphasis
instead being placed on illustrating the various aspects and
features of the illustrated embodiments, in which:
[0047] FIG. 1A is a top view of a prior art immunoassay test
strip;
[0048] FIG. 1B is a side view of the immunoassay test strip of FIG.
1A;
[0049] FIG. 2A is a perspective view of a prior art assay device,
including the assay test strip of FIG. 1A and FIG. 1B and housing
assembly and showing a bar code, which can optionally be affixed to
the housing;
[0050] FIG. 2B is a perspective view of an alternative embodiment
of a prior art assay device, including the assay test strip of FIG.
1A and FIG. 1B and housing assembly and showing a bar code, which
can optionally be affixed to the housing;
[0051] FIG. 3 is a perspective view of the assay device of FIG. 2B
showing the individual components of the device;
[0052] FIG. 4 is a top view of an exemplary prior art housing
assembly for the assay test strip of FIGS. 1A and 1B;
[0053] FIG. 5 is a side assembly view of the housing assembly of
FIG. 4;
[0054] FIG. 6A is a top view of an improved immunoassay test strip
constructed according to one embodiment of the disclosed
inventions;
[0055] FIG. 6B is a side view of the immunoassay test strip of FIG.
6A;
[0056] FIG. 7 is a picture of the top surface of a card from which
test strips such as those shown in FIGS. 6A and 6B are cut, taken
after the conjugate striping process has visually saturated the
conjugate pad of the membrane system; and
[0057] FIG. 8 is a picture of the top surface of a test strip
similar to that shown in FIGS. 6A and 6B, taken with the conjugate
pad removed to reveal an underlying portion of the contact pad,
including conjugate material that is deposited in the contact pad
from the conjugate pad during the striping process.
DETAILED DESCRIPTION
[0058] Reference is initially made to Prior Art FIGS. 1-5, which
are taken from the above-incorporated U.S. Pat. No. 6,867,051.
[0059] As shown in FIGS. 1A and 1B, the prior art test strip 100
disclosed and described in the above-incorporated U.S. Pat. No.
6,867,051 includes a membrane system including three components: a
porous or bibulous member 102; a conjugate pad 108; and an
absorbent pad 110. The membrane system is mounted on a substrate or
backing 112, with the conjugate pad 108 and the absorbent pad 110
slightly overlapping the porous or bibulous member 102, which is
interposed therein between. As can be seen, the conjugate pad 108
overlaps the porous or bibulous member 102 so that a fluid sample
placed onto the conjugate pad 108 is communicated from the
conjugate pad 108 to the porous or bibulous member 102. Similarly,
the absorbent pad 110 overlaps with the porous or bibulous member
102 so that fluid samples introduced into the porous or bibulous
member 102 from the conjugate pad 108 are then be transmitted to
the absorbent pad 110. In this manner, the respective conjugate pad
108, absorbent pad 110 and porous or bibulous member 102 are in
fluid communication with one another, so that a fluid sample placed
on the conjugate pad 108 is able to propagate through the conjugate
pad 108 to the porous or bibulous member 102, and then from the
porous or bibulous member 102 to the absorbent pad 110.
[0060] The porous or bibulous member 102 is capable of transporting
a liquid sample along the test strip and serves as the solid
support upon which the immunoreactions occur. Antibodies which
react with the target analyte and/or label are immobilized on the
solid support. Possible solid supports include paper and cellulose
derivatives, such as cellulose esters and ethers, natural and
synthetic polymeric materials, such as vinyl polymers and partially
hydrolyzed derivatives, polycondensates, copolymers and inorganic
materials. One such solid support is a nitrocellulose membrane. As
can be seen in the figures, the porous or bibulous member 102
contains two distinct zones, a detection zone 104, and a control
zone 106, at which two different antibodies are immobilized. The
detection zone contains an immobilized capture antibody that binds
the analyte of interest, whereas the control zone contains an
immobilized antibody or other component, such as an antigen, that
binds labeled antibody conjugate that has not bound to analyte. The
conjugate pad 108 serves as a sample application component, and is
striped with an antibody to the analyte, which is conjugated to a
detectable label. In particular, the labeled antibody conjugate is
diffusively bound to the conjugate pad 108 and becomes mobile upon
application of the liquid sample and moves along the test strip
100. The conjugate pad 108 is made of a porous material, such as
glass fiber. The conjugate pad 108 may also act as a pre-filter for
the sample. The absorbent pad 110 serves to draw liquid
continuously through the device, and may be made of a material such
as cellulose paper or other material known to those of skill in the
art.
[0061] Referring now to FIG. 2A, the immunoassay device disclosed
and described in the above-incorporated U.S. Pat. No. 6,867,051
includes a test strip (100) and housing assembly 200, wherein the
housing 202 generally surrounds the test strip 100 (FIGS. 1A and
1B) and includes an opening through which test sample is applied
204, as well as an aperture above the detection and control zones
206 that permits measurement of the amount of label by the reader,
which is correlated with the amount of analyte in the test sample.
The housing 202 includes at its upper surface 208 a fattened end
210, used for gripping the housing 202, an application window 204
(or sample window) through which a sample is applied to a conjugate
pad 108 of an immunoassay test strip within the housing 202. The
housing 202 also includes a test window 214 through which the test
result of the immunoassay is viewed. In accordance with the
embodiments shown, no window material is mounted within the test
window 214 (or the sample window 212). Thus, an optical path from
outside the housing 202 through the test window 214 to the
immunoassay test strip is unobscured by even a transparent
material. Also, as shown in FIG. 2A and FIG. 2B, the housing may
include a symbology, exemplified as a bar code 216 or 316 that can
be read by the reader or a separate reading device and associated
with identifying information pertaining to the particular device
and/or test run or other information.
[0062] An alternative embodiment of the test device is shown in
FIG. 2B. The components of device are shown in FIG. 3 and include
the upper and lower members 302 and 320 of the housing and the test
strip 100. Also shown are the sample application port 304, test
window 306, and the optionally included bar code 316.
[0063] FIG. 4 is a top view is shown of the immunoassay test strip
housing 202 of FIG. 2A, showing the sample window 212, and the test
window 214, and the enlarged gripping portion 210. Also shown are
structures 402 for holding the immunoassay test assembly within the
housing 202 and structures 404 for securing upper and lower halves
of the housing 202 to one another.
[0064] FIG. 5 is a side cross-sectional assembly view of the test
strip housing 202, showing the sample window 212, the test window
214, and the structures 402 for holding the immunoassay test strip
assembly in place within the housing 202. As can be seen, an upper
half 502 of the housing 202 is mated with a lower half 504 of the
housing 202. The immunoassay test strip is sandwiched between the
upper and lower halves 502 and 504 of the housing 202 and is
secured in place by the structures 402 of the upper half 502. The
immunoassay test strip is positioned so as to be viewable through
the test window 214 when the immunoassay test strip assembly is
secured within the housing and the conjugate pad is positioned to
be contactable through the sample window 212.
[0065] These above-described and illustrated devices of FIGS. 1-5
are particularly adapted for use with the reflectance reader
disclosed and described in the above-incorporated U.S. Pat. No.
6,867,051.
[0066] Embodiments of the inventions disclosed herein are
illustrated in FIGS. 6-8, and are directed to an improved
immunoassay test strip for use in a diagnostic system and related
methods, and in particular for use in diagnostic systems and
methods such as those disclosed and described in the
above-incorporated U.S. Pat. No. 6,867,051. Specifically, exemplary
embodiments of an improved immunoassay test strip disclosed and
described herein are preferably sized and configured to be readily
substituted for the prior art test strip 100 of FIGS. 1A and 1B,
without requiring changes to the housing 200 or reader. However, it
will be appreciated by those skilled in the art that the improved
immunoassay test strips disclosed and described herein are not
limited to use in the diagnostic systems and methods disclosed and
described in the above-incorporated U.S. Pat. No. 6,867,051.
[0067] Referring now to FIGS. 6A and 6B, an exemplary embodiment of
an improved immunoassay test strip 600 includes a membrane system
having five main components: a sample pad 608; a conjugate pad 615;
a contact pad 617; a porous or bibulous portion comprising a thin
membrane of nitrocellulose 602; and an absorbent pad 610. The
membrane system (608, 615, 617, 602, 610) of the test strip 600 is
mounted on a suitable substrate or backing 612, wherein the sample
pad 108 overlaps the conjugate pad 615, the conjugate pad 615
(slightly) overlaps the contact pad 617, and the respective contact
pad 617 and absorbent pad 610 each overlap the nitrocellulose
membrane 602, which is interposed therein between. In particular,
and as can be seen in FIG. 6B, the sample pad 608 overlaps the
conjugate pad 615 so that a fluid sample placed onto the sample pad
608, e.g., through an open sample window in a housing (not shown)
that encases the immunoassay test strip 600 is readily communicated
from the sample pad 608 to the conjugate pad 615. Similarly, the
conjugate pad 615 slightly overlaps the contact pad 617, and the
respective contact pad 617 and absorbent pad 610 overlap the
nitrocellulose membrane 602, so that a fluid sample placed onto the
sample pad 608 will readily propagate from the sample pad 608 to
the conjugate pad 615, from the conjugate pad 615 to the contact
pad 617, from the contact pad 617 into the nitrocellulose membrane
602, and from the nitrocellulose membrane 602 into the absorbent
pad 610, respectively.
[0068] In this manner, the respective sample pad 608, conjugate pad
615, contact pad 617, nitrocellulose membrane 602 and absorbent pad
610 are all in fluid communication with one another. As explained
in greater detail below, the materials used to form the respective
membrane system components 602, 608, 610, 615 and 617, along with
their respective dimensions and amount of respective overlap
between adjacent components, will greatly influence the flow rate
of sample fluid introduced onto the sample pad 608 all the way to
the absorbent pad 610.
[0069] As with the porous or bibulous member 102 of the prior art
test strip 100 of U.S. Pat. No. 6,867,051, the nitrocellulose
membrane 602 of the present test strip 600 is capable of
transporting a liquid sample, and also serves as the solid support
upon which the immunoreactions occur. Antibodies which react with
the target analyte and/or label are immobilized on the solid
support. Possible solid supports include paper and cellulose
derivatives, such as cellulose esters and ethers, natural and
synthetic polymeric materials, such as vinyl polymers and partially
hydrolyzed derivatives, polycondensates, copolymers and inorganic
materials. As can be seen in FIGS. 6A and 6B, the nitrocellulose
membrane 602 contains a distinct detection zone 604, and a distinct
control zone 606, at which two different antibodies are
immobilized. The detection zone 604 contains an immobilized capture
antibody that binds the analyte of interest, whereas the control
zone 606 contains an immobilized antibody or other component, such
as an antigen, that binds labeled antibody conjugate that has not
bound to analyte.
[0070] In order to better understand the improved immunoassay test
strips, the individual components and an exemplary manufacturing
process will now be described.
[0071] Sample Pad
[0072] The sample pad 608 of test strip 600 is essentially
unchanged from the prior art test strip 100 of FIGS. 1A and 1B,
except that it is not striped with any conjugate, and functions
only as a sample fluid flow pathway.
[0073] Conjugate Pad
[0074] The conjugate pad 615 of test strip 600 has no counterpart
component in the prior art test strip 100. In the illustrated
embodiment, the conjugate pad is a pretreated hydrophilic material,
such as Nylon, supplied by Porex Technologies. During the
manufacturing process, after the respective nitrocellulose membrane
602 and (porous) contact pad 617 are applied (in the case of the
nitrocellulose membrane 602) or adhered (in the case of the contact
pad 617) to the substrate 612, the conjugate pad 615 is adhered to
the substrate 612, so as to have one edge very slightly overlapping
the contact pad 617 (as shown in FIG. 6B), with the other edge
being very slightly separated from a temporary release liner
covering over the adhesive substance on the substrate 612 to which
the sample pad 608 will subsequently be adhered. Thereafter, but
before the respective sample pad 608 and absorbent pad 610 are
adhered to the substrate 612 (which remains in the form of an
elongate card sized for making a large number, e.g., several dozen,
test strips) is "striped" according to a well-known process, in
which the respective antibodies and/or other components that form
the detection zone 604 and the control zone 606 are applied to the
nitrocellulose membrane 602, and the conjugate reagent material is
simultaneously applied (deposited into) the conjugate pad 615.
[0075] In particular, the conjugate reagent is applied to the
conjugate pad to the degree that the entire pad appears "visually
saturated" (meaning that, while it may technically be able to hold
additional volume, the reagent is evenly and completely distributed
throughout the conjugate pad. Because the conjugate pad 615 has one
edge slightly overlapping the contact pad 617, and another edge
isolated from the release liner covering over the adhesive
substance on the substrate 612 to which the sample pad 608 will
subsequently be adhered, any "back end" wicking of any excess
conjugate material will be prevented during the striping process,
with any such excess conjugate material instead being absorbed by
the contact pad 617. However, as seen in FIG. 8 (with the conjugate
pad removed after the striping process), the contact pad 617 is
sufficiently dense so that the excess conjugate does not wick into
the nitrocellulose membrane 602. This arrangement is believed to
provide a significant reduction in variability from test strip 600
to test strip 600 over the prior art test strips 100, because each
resulting conjugate covered (substantially square) portion of the
conjugate pad 615 holds a similar amount of conjugate. In addition,
the conjugate comes off the conjugate pad 615 very consistently
from test strip 600 to test strip 600.
[0076] In particular, it has been found that using a visually
saturated pre-treated Porex material as the conjugate pad results
in the sample mixing with the conjugated beads in-process, with the
conjugate-sample mix coming off the conjugate pad 615 and moving
into the into the contact pad 617 within seconds of application. In
this manner, the conjugate pad 615 allows the test strip 600 to
perform similar to a liquid immunoassay system having a strip run
vertically (e.g., in a test tube), where a known amount of
conjugate is added to and allowed to mix with the sample prior to
adding to strip. The conjugate pads 615 are preferably square in
their length-width dimensions once the test strip 600 is cut from
the card. In one embodiment, the conjugate pads 615 of the final
test strip 600 are approximately 0.320'' by 0.320'' in their
length-width dimensions.
[0077] Contact Pad
[0078] Like the conjugate pad 615, the contact pad 617 of test
strip 600 also has no counterpart component in the prior art test
strip 100. As described above, insertion of the additional contact
pad 617 into the fluid path of the test strip 600 allows for using
a striping process to apply the conjugate reagent to the conjugate
pad 615 at the same time as the respective antibodies and/or other
components that form the detection zone 604 and the control zone
606 are applied to the nitrocellulose membrane 602, because the
contact pad 617 prevents any excess conjugate material from wicking
from the conjugate pad 615 into the nitrocellulose material 602.
Additionally, the contact pad 617 serves to gate the
conjugate/sample mixture in-process, and meters it for a few
minutes onto the nitrocellulose membrane 602. This in-process
metering of the conjugate/sample mixture allows more binding and
slows down the reaction, which in turn allows a more desired
reaction time and sensitivity.
[0079] Absorbent Pad
[0080] The absorbent pad 610 of the test strip 600 is essentially
unchanged from the prior art test strip 100 of FIGS. 1A and 1B, and
functions to draw the sample fluid flow through the fluid pathway,
and in particular through the nitrocellulose membrane 602.
[0081] Exemplary Manufacturing Process
[0082] In accordance with one embodiment, the lamination of the
solid phase is carried out on a vinyl backing card (i.e., substrate
612) that is approximately 0.010''.+-.0.0005'' thick, 2.7'' wide
and 17.73'' long, with release liners pre-scored at 10 mm, 18.25
mm, 23 mm and 56 mm. The 10 mm release liner will allow for a gap
between the liner (which is covering the eventual location of the
sample pad 608) and the conjugate pad 615. This gap is critical for
striping the conjugate reagent without causing leakage on the
back-end of the membrane 615.
[0083] The lamination sequence is as follows: [0084] 1.
Nitrocellulose Membrane--Unisart (PN: 1UN95E) from Sartorius with
33 mm width. The nitrocellulose should have a thickness of 240-270
um (including 100 um polyester backing film) and wicking speed
across the rolls of 90-135 s/4 cm (both based on manufacturers
Certificate of Analysis). [0085] 2. Contact Pad--Whatman, Grade:
S14, width: 5.8.+-.0.1 mm, length approx. 450 mm. [0086] 3.
Conjugate Pad--Porex [X-41210 (distributor #), X-4588 (Manufacturer
#)] thin hydrophilic membrane, 0.025''.+-.0.004'' thick, pore size
of 75-110 um. The pad is received in sheets of 10''.times.17.75''
and cut into 0.0320'' strips using the rotary cutter or it may also
be pre-cut by Interstate Specialty Products into
17.75''.times.0.32'' strips. It is important that Porex material
not be received in rolls due to the memory capacity of the material
and that it is stored in a dark environment.
[0087] Following the above first steps of the lamination process,
the following reagent application on the solid phase is carried out
using striping equipment: [0088] 4. Reagent Application--The
A137-MS Conjugate reagent is striped at appropriate % solids,
determined by titering the conjugate. Lot-to-lot variation in the
Porex conjugate membrane and overlap variability between the
conjugate pad and contact pad will influence the required conjugate
reagent volume and needle position to ensure an appropriate
saturation level.
[0089] FIG. 7 is a picture of the top surface of a card from which
test strips such as those shown in FIGS. 6A and 6B are cut, taken
after the conjugate striping process has visually saturated the
conjugate pad of the membrane system. In particular, FIG. 8 depicts
the conjugate pad 615 after it is completely covered with conjugate
on both ends after conjugate application.
[0090] FIG. 8 is a picture of the top surface of a test strip
similar to that shown in FIGS. 6A and 6B, taken with the conjugate
pad removed to reveal an underlying portion of the contact pad,
including conjugate material that is deposited in the contact pad
from the conjugate pad during the striping process. In particular,
FIG. 9 shows an example of a striped Rapid fFN 10Q strip with the
(previously visually saturated) conjugate pad 615 removed. The area
of the contact pad 617 where the respective conjugate pad 615
overlaps the contact pad 617 has a limited amount of conjugate
material that had leaked "controllably" from the conjugate pad 615
onto the contact pad 617 during the striping process. This is
representative of the ideal striped 10Q strip. In comparison, a
contact pad that has "white" areas or areas missing some conjugate
is less desirable and may contribute to higher variability. Both
the complete coverage of the Porex and the controlled leakage onto
the contact pad are necessary for acceptable striping.
[0091] After the reagent application onto the nitrocellulose
membrane 602 and the conjugate pad 615, the cards are preferably
left to dry overnight at controlled temperature. After drying,
cards are preferably stored flat, desiccated in coolers.
[0092] After striping, the lamination of the solid phase continues,
and includes placement of the sample pad 608 and the absorbent pad
610: [0093] 5. Sample Pad--Whatman, Grade: S14, width:
0.515''.+-.0.005'' [0094] 6. Absorbent Pad--Whatman Inc, width:
0.65'' with 684-753 um thickness and 13.9-16.2 s/300 ml/sq"
porosity, grade: C7218
[0095] The cards are preferably rolled after final lamination
(either at lamination step or at cutting step).
[0096] It will be appreciated by the skilled in the art that the
disclosed inventions may be embodied in other specific forms
besides and beyond those illustrated in FIGS. 6-8 and described
herein. The foregoing embodiments are therefore to be considered in
all respects illustrative rather than limiting.
* * * * *