U.S. patent number RE34,405 [Application Number 07/120,455] was granted by the patent office on 1993-10-12 for determination of analytes in particle-containing medium.
This patent grant is currently assigned to Abbott Laboratories. Invention is credited to Dennis R. Gould, Robert F. Zuk.
United States Patent |
RE34,405 |
Gould , et al. |
October 12, 1993 |
Determination of analytes in particle-containing medium
Abstract
Methods and compositions are provided for concentrating
particles in a minute area on a solid surface. The method permits
the detection of small amounts of analytes by providing for an
observable signal in relation to the concentration of particles in
the area.
Inventors: |
Gould; Dennis R. (San Gregorio,
CA), Zuk; Robert F. (Burlingame, CA) |
Assignee: |
Abbott Laboratories (Abbott
Park, IL)
|
Family
ID: |
26818390 |
Appl.
No.: |
07/120,455 |
Filed: |
November 12, 1987 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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Reissue of: |
519300 |
Aug 1, 1983 |
04552839 |
Nov 12, 1985 |
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Current U.S.
Class: |
435/7.1; 422/400;
435/7.2; 435/7.22; 435/7.31; 435/7.32; 435/7.9; 435/805; 435/810;
435/975; 436/536; 436/541; 436/810; 436/824 |
Current CPC
Class: |
G01N
33/558 (20130101) |
Current International
Class: |
G01N
33/558 (20060101); G01N 033/535 (); G01N 033/536 ();
G01N 033/538 (); G01N 033/52 () |
Field of
Search: |
;422/56
;435/7,805,810,7.1,7.2,7.2,7.31,7.32,7.9,975
;436/536,541,810,824 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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0141547A1 |
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0000 |
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EP |
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0021214A1 |
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Jan 1981 |
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EP |
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2421035 |
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Nov 1974 |
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DE |
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Other References
Derwent Abstract 59604C/34 Asahi Chemical Ind KK J5 5090-858. .
Derwent Abstract 57601A/32 Eisai KK J5 3075-322. .
Derwent Abstract 88490B/49 Mitsubishi Chem Ind KK (Teik) J5
4139-595. .
Abstract 58-755(A) Olympus Kogaku Kogyo K.K. "Vessel for Decision
of Particle Cohesion and Decision Apparatus of Particle Cohesion
Using This Vessel". .
Abstract 58-223758(A) Olympus Kogaku Kogyo K.K. "Immunoassay Method
and Reaction Vessel Used for Same Method". .
Derwent Abstract 04835 J/49 Knapp "Capillary tube for radio
immunoassay investigations-has fine filter and suction nozzle at
end". .
N. G. Anderson, Analytical Biochemistry, vol. 38, 1970, pp.
175-189..
|
Primary Examiner: Nucker; Christine M.
Assistant Examiner: Kim; Kay
Attorney, Agent or Firm: Schmidt; Richard D.
Claims
What is claimed is:
1. A method for detecting the presence of a member of a specific
binding pair ("sbp member") in a .[.liquid assay medium.].
.Iadd.sample.Iaddend., said specific binding pair consisting of
ligand and homologous receptor, where said method involves
particles to which are bound at least one member of a specific
binding pair, a solid bibulous member and a signal-producing system
which involves at least one label which is bound to said particles
or an sbp member,
said method comprising:
combining in an aqueous assay medium, .[.said.]. a sample
.Iadd.suspected of containing an sbp .Iaddend.member and at least
one .Iadd.of the group consisting .Iaddend.of said particles and
.Iadd.said .Iaddend.labeled sbp members, with the proviso that
particles are added when said sample lacks particles having an sbp
member; under conditions where particles only within a
predetermined size.[.,.]. range and charge will concentrate in an
area on said bibulous member adjacent the air/liquid interface,
when said bibulous member is contacted with said assay medium;
contacting said bibulous member with said assay medium whereby said
assay medium is wicked past said area and particles within said
predetermined size .Iadd.range .Iaddend.and charge concentrate at a
small site in said area; and
detecting the signal as a result of said signal-producing system,
wherein said signal is related to the amount of label in said area
and the amount of label in said area is related to the amount of
said sbp member in said sample.
2. A method according to claim 1, wherein said sample has particles
within said predetermined size .Iadd.range .Iaddend.to which are
bound an sbp member.
3. A method according to claim 1, wherein said sample has particles
below said predetermined size .Iadd.range .Iaddend.to which are
bound an sbp member and said label is joined to a polyvalent
homologous sbp member.
4. A method according to claim 1 wherein said particles are labeled
with a member of said signal producing system.
5. A method for detecting cells that have at least one
predetermined determinant site, where said method involves labeled
receptors which bind to said determinant site or to receptors
binding to said determinant site, and a solid bibulous member,
where the label of said labeled receptor by itself or in
combination with other members of a signal producing system
produces a detectable signal, said method comprising:
combining in an aqueous assay medium, a sample suspected of
containing said cells, labeled receptors to said determinant site
or receptors for said determinant site and labeled receptors for
said receptors, under conditions where individual cells migrate
along a bibulous member away from an air-liquid interface when said
medium is contacted with said bibulous member, but receptor linked
cells concentrate at .[.the.]. .Iadd.an .Iaddend.area of .Iadd.said
.Iaddend.bibulous member at the air-liquid interface;
contacting said bibulous member with said assay medium, whereby
linked cells concentrate in said area; and
detecting the signal as a result of said signal producing system
wherein said signal is related to the amount of label in said
area.
6. A method according to claim 5, wherein said cell is a bacterial
cell, fungal .Iadd.cell.Iaddend., protozoan .Iadd.cell.Iaddend., or
other parasitic or infectious agent.
7. A method according to claim 5, wherein said label is an
enzyme.
8. A method according to claim 5, wherein said bibulous member has
a small orifice surrounded .[.on one side of said bibulous
member.]. with a water impermeable layer and said assay medium is
contacted with said bibulous member at said orifice.
9. A method according to claim 5, wherein said bibulous member is
supported by a plastic support having a centrally located orifice.
.Iadd.10. A method according to claim 1 wherein after said
contacting of said bibulous member with said assay medium, said
area on said bibulous member is contacted with an aqueous medium
containing a labeled sbp member when said labelled sbp member is
not included in said assay medium. .Iaddend. .Iadd.11. A method
according to claim 1 wherein said contacting is carried out by
introducing a portion of said bibulous member into said assay
medium. .Iaddend. .Iadd.12. A method according to claim 1 wherein
said contacting is carried out by introducing a portion of said
assay medium onto said bibulous member. .Iaddend. .Iadd.13. A
method according to claim 1 wherein said combining is carried out
by combining said sample in an aqueous medium with said particles
and said contacting is carried out by contacting said assay medium
with a portion of said bibulous member. .Iaddend. .Iadd.14. A
method for detecting the presence of an analyte, said method
comprising:
combining a medium suspected of containing said analyte, which is a
member of a specific binding pair (sbp), with particles having
bound thereto an sbp member reciprocal to said analyte,
contacting said medium with an area of a bibulous member under
conditions where said medium wicks away from said area and at least
a portion of said particles concentrate in a localized site on said
bibulous member, and
examining said site to determine the presence of said analyte.
.Iaddend.
.Iadd.15. The method of claim 14 wherein said particles have a
label. .Iaddend. .Iadd.16. The method of claim 14 wherein said
examining is carried out by (1) contacting said site with a medium
containing a labeled receptor for said analyte and (2) determining
the presence of said labeled receptor at said site to determine the
presence of said analyte. .Iaddend. .Iadd.17. The method of claim
14 wherein said examining is carried out by (1) contacting said
site with a medium containing a labeled receptor for said
reciprocal sbp member and (2) determining the presence of said
labeled receptor at said site to determine the presence of said
analyte. .Iaddend. .Iadd.18. The method of claim 14 wherein said
site is examined by contacting said site with members of a signal
producing system and then examining said site for the presence of a
detectable signal to determine said analyte. .Iaddend. .Iadd.19.
The method of claim 14 wherein said medium wicks away from said
area by migrating outward along said bibulous member. .Iaddend.
.Iadd.20. A method for detecting the presence of an epitopic site
on particles, said method comprising:
contacting a spot on a bibulous member with a medium containing a
labelled antibody reciprocal to said epitopic site and particles
suspected of having said epitopic site under conditions where
excess of said labelled antibody will wick away from said spot;
and
detecting the presence of said labelled antibody at said spot.
.Iaddend. .Iadd.21. The method of claim 20 wherein said antibody is
labelled with an enzyme or a fluorescer. .Iaddend. .Iadd.22. A
method for detecting the presence of an analyte, said method
comprising:
providing in combination an aqueous medium suspected of containing
said analyte, which is a member of a specific binding pair (sbp),
particles having bound thereto an sbp member reciprocal to said
analyte, and an area of a bibulous member under conditions where
said medium wicks away from said area and at least a portion of
said particles concentrate in a localized site on said bibulous
member, and
examining said site to determine the presence of said analyte.
.Iaddend. .Iadd.23. The method of claim 22 wherein said particles
have a label. .Iaddend. .Iadd.24. The method of claim 22 wherein
said examining is carried out by (1) contacting said site with a
medium containing a labeled receptor for said analyte and (2)
determining the presence of said labeled receptor at said site to
determine the presence of said analyte. .Iaddend. .Iadd.25. The
method of claim 22 wherein said examining is carried out by (1)
contacting said site with a medium containing a labeled receptor
for said reciprocal sbp member and (2) determining the presence of
said labeled receptor at said site to determine the presence of
said analyte. .Iaddend. .Iadd.26. The method of claim 22 wherein
said examining is carried out by (1) contacting said site with
members of a signal producing system and then (2) determining the
presence of a detectable signal at said site to determine the
presence of said analyte. .Iaddend. .Iadd.27. The method of claim
22 wherein said medium wicks away from said area by migrating
outward along said bibulous member. .Iaddend. .Iadd.28. A device
for conducting an assay, said device comprising a non-bibulous
member having an orifice and serving as a support for a bibulous
member, said bibulous member having an orifice that extends through
said bibulous member, said orifices corresponding in location.
.Iaddend. .Iadd.29. The device of claim 28 wherein said orifice of
said bibulous member and said orifice of said support are centrally
located. .Iaddend. .Iadd.30. The device of claim 28 wherein said
bibulous member is a circular disc.
.Iaddend. .Iadd.31. A kit comprising in packaged form:
a device comprising a non-bibulous member having an orifice and
serving as a support for a bibulous member such that, when said
device is used in conducting an assay, liquid containing particles
applied to said bibulous member through said orifice migrates away
from point of application and at least a portion of the particles
present in said liquid concentrate at said joint of application and
in a separate container particles which have bound irreversibly
thereto a member of a specific binding pair. .Iaddend. .Iadd.32.
The kit of claim 31 which further comprises in a separate container
a member of a signal producing system. .Iaddend. .Iadd.33. A method
for detecting the presence of a member of a specific binding pair
("sbp member") in a sample, said specific binding pair consisting
of ligand and homologous receptor, where said method involves
particles to which are bound at least one member of a specific
binding pair, a solid bibulous member and a signal-producing system
which involves at least one label which is bound to an sbp
member,
said method comprising:
combining in an aqueous assay medium, a sample suspected of
containing an sbp member and said particles and said labeled sbp
member under conditions where said particles concentrate in an area
on said bibulous member adjacent the air/liquid interface, when
said bibulous member is contacted with said assay medium;
contacting said bibulous member with said assay medium whereby said
assay medium is wicked past said area and particles concentrate at
a small site in said area; and
detecting the signal as a result of said signal-producing system,
wherein said signal is related to the amount of label in said area
and the amount of label in said area is related to the amount of
said sbp member in said sample. .Iaddend. .Iadd.34. The method of
claim 33 wherein said label is an enzyme. .Iaddend. .Iadd.35. The
method of claim 33 wherein said sbp member in said sample is an
antigen, said sbp member bound to said particles is an antibody for
said antigen and said sbp member bound to said label is an
antibody. .Iaddend. .Iadd.36. The method of claim 33 wherein said
sbp member in said sample is a hapten, said sbp member bound to the
particles is an antibody for said hapten and said sbp member bound
to said label is said hapten. .Iaddend. .Iadd.37. A method for
detecting the presence of an analyte, said method comprising:
combining a medium suspected of containing said analyte, which is a
member of a specific binding pair (sbp), with particles having
bound thereto an sbp member reciprocal to said analyte and with a
labeled sbp member wherein the amount of labeled sbp member which
binds to said particles is related to the amount of analyte in said
medium,
contacting said medium with an area of a bibulous member under
conditions where said medium wicks away from said area and said
particles concentrate in a localized site on said bibulous member,
and
examining said site for the presence of labeled sbp member to
determine the presence of said analyte. .Iaddend. .Iadd.38. The
method of claim 37 wherein said site is contacted with members of a
signal producing system and then is examined for the presence of a
detectible signal to determine the analyte. .Iaddend. .Iadd.39. The
method of claim 37 wherein said medium wicks away from said area by
migrating outward along said bibulous member. .Iaddend. .Iadd.40. A
method for performing an immunoassay for an analyte in a sample,
which method comprises providing a chromatographic medium, forming
a reaction mixture containing a specific binder for the analyte,
said specific binder being immobilized by attachment to a
particulate solid phase, and a labeled reagent partly in a form
which is mobile on said medium and partly in the form of a labeled
analyte/specific binder reaction product insolubilized so as to be
immobile on the medium, the proportions of the two forms being
determined by the amount of analyte in the sample, applying the
reaction mixture to a spot on the chromatographic medium, causing
the mobile form of the labeled reagent to migrate from the spot,
and thereafter, observing one or both of the mobile and immobile,
insolubilized forms of the labeled reagent. .Iaddend. .Iadd.41. The
method as claimed in claim 40, wherein the chromatographic medium
is in sheet form, with the reaction mixture being applied to a spot
on the sheet and the mobile form of the labeled reagent being
caused to migrate radially from the spot. .Iaddend. .Iadd.42. The
method as claimed in claim 40, wherein migration is assisted by
subsequent application to the spot of a solvent which causes mobile
species, but not immobile species, to migrate through the
chromatographic medium. .Iaddend. .Iadd.43. The method as claimed
in claim 42, wherein the solvent is an aqueous liquid. .Iaddend.
.Iadd.44. The method as claimed in claim 42 wherein the reaction
mixture is formed by causing the analyte in the sample, and a
labeled version of the analyte, to compete for reaction with a
limited amount of a specific binder for the analyte, the
analyte/specific binder complex being rendered insoluble. .Iaddend.
.Iadd.45. The method as claimed in claim 44, wherein the
analyte/specific binder complex is rendered insoluble by reaction
of the specific binder with its antibody, said reaction being
effected before, during and after incubation with the analyte.
.Iaddend. .Iadd.46. The method as claimed in claim 40, wherein the
reaction mixture is formed by causing the analyte in the sample to
bind to an excess of an immobilized specific binder and a labeled
specific binder for the analyte is caused to bind to vacant binding
sites of the analyte. .Iaddend.
Description
BACKGROUND OF THE INVENTION
The clinical laboratory has become an increasingly important
adjunct to medicine, both in diagnosis and therapy. As the variety
of situations in which determinations are desired have expanded,
there has been an increasing variety of approaches for measuring
the substance of interest. There are many considerations involved
in the development of the assay. One consideration is the
simplicity of the protocol. The more measurements and steps that
are required, the greater the likelihood for error. A second
consideration is the concentration range and absolute amount to be
measured. A third consideration is the nature of the sample
involved. A fourth consideration is the nature of pretreatments
which may be required. A fifth consideration is the nature of
interfering substances in the samples. A sixth consideration is the
intended environment in which the assay is performed and the
technical skill of the persons who will perform the assay. This
will also involve whether an instrument is to be used or only a
visual determination. Thus, each new development provides
advantages which find particular applications as to analytes,
preparation of reagents, nature of the users, and manner of
performance.
DESCRIPTION OF THE PRIOR ART
Anderson, Anal. Biochem. (1970) 38:175-189 describes the use of
cellulose wicks to monitor agglutination reactions.
SUMMARY OF THE INVENTION
Novel methods and compositions are provided for determining the
presence of analytes in a particle containing medium, where the
analyte of interest may be bound or unbound to the particle in a
sample. By contacting the assay medium with a bibulous material at
a liquid air interface, a small situs, usually a thin band or
concentrated point, of particles can be obtained adjacent the
interface, which site provides a signal which can be related to the
presence of analyte in the sample. The particles include synthetic
particles, cells, and immune complex aggregates. The size and
nature of the particles, as well as the nature of the aqueous
medium, can be used to modulate the formation of the small
site.
.Iadd.BRIEF DESCRIPTION OF THE DRAWING
FIG. 1 is a partial elevational view of a device in accordance with
the present invention.
FIG. 2 is a cross-sectional view of the device of FIG. 1.
.Iaddend.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS
The subject invention is based on the concentration of particles at
a small site, generally having one dimension less than about one mm
wide, on a bibulous solid support in relation to the presence or
absence of an analyte in a sample. The site may be a point, a
straight or curved band, or the like. The concentration of
particles at the predetermined site can be used to provide a
detectable signal at a site. The sample may influence the
concentration of the particles at the site and/or the production of
a detectable signal. The detectable signal will be determined in a
detection zone, which may or may not be the concentration site.
The particles which are involved in the assay may be present in the
sample, may be added as reagents or formed in situ. The nature of
the particle may vary widely, being naturally occurring or
synthetic, being a single material, a few materials, or a
combination of a wide variety of materials. Naturally occurring
particles include nuclei, mycoplasma, plastids, mammalian cells,
unicellular microorganisms, e.g., bacteria, etc. Synthetic
particles may be prepared from synthetic or naturally occurring
materials, such as metal colloids or latex particles made from
polystyrene polyacrylates or naturally occurring materials, such as
polysaccharides, e.g., agarose, or the like. Non-naturally
occurring particles may be varied depending upon the particular
assay, the protocol for the assay, or other considerations.
The size of the particles will vary widely, generally ranging from
about 0.05 to 100 microns, more usually from about 0.1 to 75
microns. The particles may be charged, either positively or
negatively, may be amphoteric or lack any charge, being neutral.
The presence or absence of charge will affect other parameters
involved in the assay.
The means for detecting the detectable signal at or away from the
concentration site may or may not be an intrinsic property of the
particles. The particles may be labeled with a wide variety of
materials which allow for detection, such as radionuclides, dyes,
fluorescers, enzymes, or other convenient label providing for a
detectable signal, either visually observable or detectable by
instrumentation. The various labels would normally be covalently
bonded to the particle, using linking arms as appropriate. The
labels may be bound to the surface or, when feasible, extend
throughout the particle.
Any convenient bibulous absorbent solid material may be employed
which allows for capillary transport of a liquid away from the
interface between the air and liquid. Various materials include
paper, cellulose particles, silica gel, cellulosic beads, glass
fiber, filter paper, and the like. The surface should be relatively
smooth, so as to allow for the formation of a concentrated particle
site, for example, in the form of a sharp band or point. The size
and shape of the bibulous material may be varied widely considering
the purpose of the material. Namely, one wishes to form a fine
band, curve, circle, line, or point by concentrating small
particles which are relatively uniformly dispersed in a liquid
medium. The concentrating is best achieved by transporting a
relatively large volume through a relatively narrow area. The
bibulous material may be shaped, therefore, as a narrow strip of
from about one to about five millimeters in width, a triangular
shaped structure having a rounded tip or a circular disc having a
central small orifice or other structure. The size of the orifice
may vary depending on whether the orifice extends solely through a
non-bibulous support .Iadd.(such as, for example, depicted in FIGS.
1 and 2 wherein non-bibulous member 10 has an orifice 12).Iaddend.,
leaving the bibulous member underneath the orifice intact, or the
orifice extends through the bibulous member underneath .Iadd.(such
as, for example, depicted in FIGS. 1 and 2 wherein bibulous member
14 has orifice 16).Iaddend.. In the first situation, the orifice
will generally be about 0.10 to 2 mm, usually 0.25 to 1 mm. In the
second case, the orifice will generally be less than one
millimeter, ranging from about 0.1 to 0.5 mm. In each case, the
bibulous material will usually have a support which provides
structural strength. The non-bibulous material may be a water
impermeable layer or coating.
The liquid medium will normally be an aqueous medium, which may
have from about 0-40 volume percent of a miscible solvent such as
alkanols, ethers, sulfoxides, amides, etc., generally ranging from
about 1 to 6 carbon atoms.
In performing the subject invention, one usually wishes to
concentrate or collect particles at the air-liquid interface
depending upon the presence or absence of a predetermined
condition. The condition will be the presence in the sample, above
a predetermined amount, of an analyte which is a member of a
specific binding pair.
By appropriate choice of conditions in the aqueous medium, one can
modulate the size of particles which will concentrate at the
air-liquid interface as contrasted with following the solvent
front, so that no or few particles collect at the air-liquid
interface, resulting in the absence of an observable site.
The choice of conditions will vary, with the nature of the
particle, as to size, charge, polarity or other property which
affects the repulsion or attraction of the particles to each other.
In order to form the concentrated particle site, one wishes to
distinguish between particles of a particular size or between
different sized particles. In the former situation, the method
serves to concentrate particles present in the medium above a
predetermined size. In this situation, the particles do not undergo
a change in size distribution as a result of the presence of an
analyte. In the latter situation, the presence of an analyte will
result in the binding together of particles, where the original
sized particles would follow the solvent front, while particles
which are bound together will remain on the bibulous surface at the
air-liquid interface. Therefore, the conditions will be chosen so
that particles of above a certain size will be retained at the
air-liquid interface, while particles smaller than that size will
travel away from the air-liquid interface.
Factors that affect the size of the particle which will migrate
involve repulsive and attractive forces, which can be influenced by
pH and ionic strength. Where the particles are heavily charged with
the same charge, at a relatively high ionic strength, the charge
will be neutralized which will allow the particles to aggregate or
band together. Where the particles have acidic or basic groups, a
pH can be chosen, to reduce the number of charges present on the
particle. Conditions can be chosen so that the particles will not
aggregate unless a binding means is provided. The binding means
will be a member of a specific binding pair, which is polyvalent
and is, therefore, capable of binding to at least two
particles.
The pH will vary with the nature of the particle. For basic
particles, one may induce repulsive charges by lowering the pH,
while for acidic particles, one may induce repulsive charges by
raising the pH. The pH will be chosen so as to maintain mild
repulsion between particles, so as to encourage the transport of
the particles, except where a plurality of particles are joined
together.
Ionic strength may also be used in a similar fashion to modulate
repulsion. By reducing or raising the ionic strength, one may
modulate the repulsive effect between particles, so that at low
ionic strength, one enhances the repulsive effect, while at high
ionic strength, one reduces the repulsive effect between charged
particles. Therefore, depending on the nature of the particles, one
will modify the conditions of the medium. The various conditions
will be optimized depending on the nature of the system.
The pH which is employed will generally be in the range of about 2
to 12, with the range varying from about 3 to 7 for positively
charged particles and from about 6 to 11 for negatively charged
particles. The ionic strength will generally vary from about
10.sup.-1 to 10.sup.-4. One may optimize these two parameters
empirically depending upon the size and nature of the particles
involved.
A further factor is the inclusion of surfactants in the assay
medium. The surfactants aid in the migration of the particles
through the bibulous support. By modifying the surface tension,
migration of the particles may be enhanced or diminished. The
surfactants may be anionic, cationic or non-ionic, preferably
non-ionic or combinations of non-ionic and anionic. Surfactants
will be used in minor amount, generally being present in from about
0 to 2 vol % of the assay medium, more usually from about 0.005-1.5
vol %, and preferably from about 0.01 to about 1 vol %. Various
surfactants may be used, such as Tween 20, QS44, PEG 1500, etc.
Other factors may also be employed to affect properties of the
assay medium. Chaotropic or antichaotropic agents may be employed.
Illustrative chaotropic agents include fluoride ion and
polyethylene glycol. Illustrative antichaotropic agents include
trichloroacetate, thiocyanate and dextran. Agents to modify the
viscosity of the medium may be employed. Elevated or reduced
temperatures may also find application.
Method
As indicated previously, the subject method is predicated on either
concentrating particles over a predetermined size at a localized
site or being able to distinguish two sets of particles: (a)
Particles which migrate with the solvent away from the air-liquid
interface and (b) particles which form a localized site at the
air-liquid interface. The latter situation will be the more common
one.
In the former case, the primary function is concentrating particles
which are present in a dilute solution. This situation may be
exemplified by a mixture of particles where only a small percentage
may be the particles of interest. For example, a clinical sample
which has a heterogeneous population of cells, where one wishes to
determine the presence of a particular species or strain. By
employing a labeled antibody in the medium, one could rapidly tag
any cells of interest. The presence of the tag at the localized
site would be diagnostic of the presence of the particular cells.
Any unbound label would follow the solvent front, minimizing any
background. The absence of an observable band would indicate the
absence of the cells of interest in the sample.
A particle is employed which migrates under the conditions of the
assay, but in the presence of analyte in the medium, can be
inhibited from migrating or permitted to migrate. In this way, one
can relate the presence of a detectable signal at a localized site
on a bibulous surface to the presence of the analyte of interest in
the assay medium.
The concentration of particles at the localized site is achieved by
providing bridges between particles of specific binding members.
Specific binding members can be broken up into two primary groups:
(1) ligands and receptors; and (2) complementary polynucleotides.
The ligands and receptors involve organic molecules, where the
ligand is any molecule for which a receptor is available or can be
made. The ligand is characterized by having a polar and spatial
organization which binds to a reciprocal or homologous receptor.
The receptor is conventionally a macromolecule which has a
structural organization complementary to the ligand so as to have a
high avidity for the particular structure of the ligand to provide
for a specific binding complex. Conventional receptors include
antibodies and fragments thereof, enzymes, naturally occurring
receptors, and the like.
In the subject invention, the ligands may be haptens or antigens,
but where the ligand is monovalent and has to serve as a bridge, it
will be provided in a polyvalent form. The polynucleotides may be
DNA or RNA, where the bridge will have a sufficiently extended
complementary sequence, for example, by repeating the same sequence
to allow binding to two different fragments of complementary
polynucleotide sequences.
In carrying out the method, one combines the sample, the assay
medium having the appropriate conditions for the particles,
particles, if particles are to be added, and the bridging system
for bridging the particles. Depending upon the manner in which the
localized site is to be detected, a signal producing system may
also be involved, where one or more labels are provided bound to
members of the bridging system or to binding members which bind to
the analyte. By having two different binding members involved in
the production of a detectable signal, one can provide for
detection of an analyte having two different reciprocal binding
members.
After combining the sample with the bridging members and any signal
producing members, as appropriate, in an appropriate assay medium,
one then contacts a small portion of the bibulous member with the
assay medium, where a major portion of the bibulous member does not
contact the assay medium and may act as a wick or well for
absorbing liquid, for example, by capillary or wicking action, so
as to draw liquid through the area at the air-liquid interface.
After sufficient time to allow for a sufficient proportion of the
assay medium to be absorbed by the bibulous member, so that
concentrations of the particles at the localized site can form, as
appropriate, contact with the assay medium may be terminated.
Depending upon the signal producing system, the presence of the
site may be determined or additional members of the signal
producing system may be added to the area at which the site may
have formed to provide a detectable signal. If a quantitative
result is desired, the detectable signal may be measured by any
convenient means.
To further illustrate the subject invention, the following
illustrative examples will be described. In an assay for a hapten,
one could provide colored beads to which a hapten is covalently
bonded by an appropriate linking arm. The assay conditions and size
of beads, as well as the nature of the bibulous member, would be
chosen, so that the individual beads would migrate with the
solvent, and no band would be observed. One could then combine the
sample and antibodies, so that at a concentration of interest of
the analyte, a major proportion of the antibody sites would be
filled by the available hapten.
After sufficient time for binding to occur, one could then add the
particles to the assay medium and incubate a second time to allow
for binding of any available antibody binding sites to the hapten
on the colored beads. In the absence of hapten in the sample, there
would be a substantial amount of bridging between the beads by the
antibodies.
One would then contact the bibulous member with the assay medium
and allow a sufficient amount of the assay medium to be wicked into
the bibulous member so that a substantial number of particles may
traverse the air-liquid interface adjoining the bibulous member.
Based on the color of the beads, one would observe a sharp,
distinct band in the absence of hapten and substantially no beads
in the presence of hapten. Where one is interested in a range of
concentration of the hapten, a controlled amount of the assay
medium would be absorbed by the wick and the concentration of
particles determined by appropriate spectrophotometric
measurements, e.g., using a reflectometer. This result could be
compared with the result observed with a sample having a known
amount of the hapten.
A second illustrative example is the determination of an antigen.
Beads could be provided which are labeled with antibodies to the
antigen and an enzyme, for example, horseradish peroxidase. One
would combine the beads under conditions where individual beads
would migrate with the solvent, but linked beads would remain at
the juncture of the air-liquid interface. One would combine the
beads with the sample and incubate the mixture for sufficient time
to allow the antigen to bind to the antibodies to provide bridges
between the beads. One would then introduce the bibulous member as
before and allow a sufficient amount of the liquid medium to be
wicked by the bibulous member.
After a sufficient amount of the medium had been wicked through the
bibulous member to allow for the formation of a narrow band or
point, the bibulous member would be removed from the assay medium
and placed in a development solution containing hydrogen peroxide
and a substrate for horseradish peroxidase, which upon oxidation
forms a color, desirably forms an insoluble dye, which precipitates
onto the beads. In this manner, the band or point would become
visually observable where particles are present to which
horseradish peroxidase has become bound or retained.
A third illustrative example is where one is interested in a
particular bacterial strain. In this method one might choose a
bibulous member circle mounted on a non-bibulous plastic support
having a centrally located orifice of about 0.5 mm dia. A swab is
taken of a clinical sample and dispersed in PBS-0.05% Tween 20. To
the dispersion is added a monoclonal antibody conjugated to an
enzyme and the mixture is incubated. A few drops of the sample are
placed over a device comprising a lower bibulous disc bonded to an
upper hydrophobic plastic disc having a central orifice of about
0.5 mm dia. The liquid passes through the orifice and spreads
evenly outward from the orifice with the organisms concentrated to
the spot on the bibulous member underneath the orifice. The
monoclonal antibody-enzyme conjugate will bind to any organisms
which have the reciprocal epitopic site. Excess monoclonal
antibody-enzyme will wick away so that only specifically bound
enzyme will remain as the spot. To ensure removal of residual
enzyme which is not specifically bound, a few drops of the
PBS-Tween 20 solution may be placed over the orifice and allowed to
wick. About 0.05 ml of a developer solution is then added, e.g.,
H.sub.2 O.sub.2 +4-chloronaphthol with HRP as the enzyme and the
solution allowed to wick. Color will indicate the presence of the
organism.
A large number of patents have been issued which describe a wide
variety of labels which have found use in diagnostic assays.
Various protocols can be developed where these labels may be used
with advantage. Illustrative of such patents are U.S. Pat. Nos.
3,850,752; 4,255,329; 4,233,402; and 4,208,479.
For performing the method, kits can be provided where the various
reagents are combined in predetermined amounts in combination with
various ancillary materials for combination with the sample. In
view of the wide spectrum of protocols and reagents, a wide variety
of kits may be prepared. For the most part, where the method
involves the addition of particles, the kits will involve particles
which have a member of a specific binding pair substantially
irreversibly bound to the particle, either covalently or
non-covalently. Also, there may be a label bound to the surface of
the particle or dispersed therein, particularly a dye, which may be
colored in the visible range of fluorescent. In some instances, the
particle may also be labelled with an enzyme.
Where particles are not to be included, the reagents will normally
involve labelled receptors or ligands, where the labels provide for
a detectable signal and may provide for the inhibition of migration
of the particles present in the assay medium. In addition to the
labelled reagents, there will be ancillary reagents such as
buffers, stabilizers, detergents, and as appropriate substrates for
enzymes, bulking agents, and the like. Also included in such kits
would be the wicking material--prepared as strips or discs--with
precut orifices, etc.
The following examples are offered by way of illustration and not
by way of limitation.
EXPERIMENTAL
In the following experiment, a variety of beads of different colors
and sizes were combined to demonstrate that one could achieve bands
of different colors depending upon the sizes of the beads and their
color and the effect of the combination of the beads in a band. The
protocol was to combine 0.05 ml of each 2% bead preparation plus 20
ml of a 1% solution of normal sheep serum in PBS containing 0.05%
QS44 and 0.05% Tween 20. The paper which was employed was
triangular-shaped Millipore membrane paper with a rounded tip,
where the tip was inserted into the assay medium. This shape
provides for enhanced concentration of the particles, while
providing a large wicking reservoir.
The following table indicates the beads that were employed, the
expected color and the observed color.
TABLE 1 ______________________________________ Bead Color Red Blue
Yellow Color Size, .mu. Expected Observed
______________________________________ 1. .15 .5 .5 green green 2.
.5 .25 .5 orange orange 3. .5 .5 .25 purple purple 4. .15 .25 .5
yellow yellow 5. .5 .25 .25 red red 6. .15 .5 .25 blue blue 7. .5
.5 .5 brown brown 8. .15 .25 .25 white No color
______________________________________
The colors were predicted based on the 0.5 micron particles being
retained on the surface adjacent the interface, while the small
particle migrated with the solvent front; thus, the complementary
color of the larger beads is seen.
In the next experiment, an assay was performed to detect the
presence of Streptococcus pyogenes (Lancefield Group A) in a
mixture of Group A and Group B. The assay medium was prepared by
removing cells of the two organisms from agar growth by loop and
suspending them in 1 ml of PBS plus 0.05% Tween 20. A mouse
monoclonal antibody against Group A (anti-A) at about 5 mg/ml was
employed. Also employed was goat antibodies against mouse IgG
(G-anti-IgG) which was conjugated to horseradish peroxidase. As a
developing solution, a solution was employed containing 200
.mu.g/ml of sodium 4-chloro-2-naphthol, 50 mM glucose, 2 mg/ml
bovine serum albumin and excess hydrogen peroxide. The protocol was
to combine 100 ml of the organism solution (about 10.sup.7
cells/ml), 20 .mu.l of the antibody-horseradish peroxidase
conjugate and 20 .mu.l of the anti-A, incubate the mixture and then
wick 50 ml on a cellulose strip (cellulose strips used for tlc).
The strip was then placed in the substrate solution and a dark band
formed indicating the presence of Group A organisms.
A similar experiment was carried out, where enzyme channeling was
involved, demonstrating a rapid antibiotic sensitivity assay.
Group A strep. pyogenes (0.2 ml of 10.sup.8 cells/ml) were
incubated for 23/4 hrs. at 37.degree. C. in the presence or absence
of penicillin at 2 units/ml. This solution was then combined with
0.8 ml of phosphate buffered saline (0.02 ml phosphate plus 0.05%
Tween 20 - pH 7.2) followed by the addition of 0.01 ml of a
monoclonal anti-Group A antibody conjugated to horseradish
peroxidase (HRP). 0.2 ml of this mixture was wicked for 7 min. with
a cellulose TLC paper strip. The wick was then transferred into
developer (0.2 ml of the above-described 4-chloronaphthyl substrate
solution plus 0.5 .mu.l glucose oxidase). The wick was developed
for 30 min.
RESULTS
Bacterial cells exposed to the penicillin formed a less intense
blue-purple band than did the unexposed cells. The difference was
easily detectable by the eye.
It is evident from the above results, that a simple rapid method is
provided for detecting the presence of an analyte. The method can
be qualitative or quantitative and can be used with a variety of
protocols which can be adapted to particular samples. Furthermore,
simple equipment is employed and the results can be obtained by
visual observation.
Although the foregoing invention has been described in some detail
by way of illustration and example for purposes of clarity of
understanding, it will be obvious that certain changes and
modifications may be practiced within the scope of the appended
claims.
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