CA2186743A1

CA2186743A1 - Detection of analytes

Info

Publication number: CA2186743A1
Application number: CA002186743A
Authority: CA
Inventors: Philip Robert Goodwin
Original assignee: Individual
Current assignee: Cortecs Ltd
Priority date: 1994-03-29
Filing date: 1995-03-29
Publication date: 1995-10-05
Also published as: NZ282861A; FI963862L; AU693181B2; CN1147855A; NO964083L; ZA952583B; MX9604416A; FI963862A7; FI963862A0; BR9507228A; GB9406209D0; WO1995026504A1; AU2078395A; JPH09511057A; EP0753150A1; NO964083D0

Abstract

The invention relates to an improved method of detecting analytes in a sample of body fluid. In this method, the sample is contacted with a specific binding agent capable of forming a specific binding complex with the analyte wherein the specific binding agent is immobilised on a porous solid substrate. The presence of specific binding complex is then detected. The method of the invention has the additional step of wiping the surface of the substrate before detection takes place in order to remove unadsorbed contaminants. The unadsorbed contaminants may be visualised on the surface of the substrate using a colouring agent so that it is easy to tell when the contaminants have been removed.

Description

,~ DETECTION OF ANALYTES
The present invention relateæ to an improved method f or the detection of analytes on a solid substrate. In particular, the method of the invention is ~rPl; r~hl e to samples of body fluids such as saliva, serum, whole blood and urine.
The detection of substances in various body fluids by ; n~say methods is well known and is frequently used for a variety of different purposes. Examples include the detection of antibodies in blood, saliva, urine or other body fluid samples as an indication of the presence of pathogens and thus for the diagnosis of various diseases and conditions . Other assays of ~body f luids include pregnancy tests and tests to determine the amount of alcohol in the blood.
Although such tests can be carried out as bulk lir~uid assays, it is often easier and more convenient to carry out the test by spotting the sample onto a solid substrate on which a specific binding agent for the analyte is immobilised and then detecting the presence of the specific binding complex. Such tests are popular since they are relatively clean and simple to operate.
However, there are certain disadvantages associated with the carrying out of tests on solid substrates. Firstly, in many assays carried out on a solid substate there is an unacceptable number of false positive results which indicate the presence of an analyte in a sample even if none is present.
The second problem is associated with the use of porous W09s/26504 r~"..~ /13 2 1 ~6743 solid substrates . This type of substrate is, in theory, particularly useful since it enables the bulk of the sample to be removed from the surface of the substrate whilst the analyte remains at the surface bound to the immobilised specific binding molecule. However, in pr~tiCP there are considerable difficulties because the flow of the sample through the substrate is often very slow 80 that the assay can sometimes take 20 to 30 minutes. This is a particular disadvantage for tests where the results are required very ~[uickly, for example tests that could otherwise be carried out by a general pract~ t; r~nP~ during a consultation .
The disadvantages discussed above have been ascribed to the presence in many samples of llnw-ntefl particulate matter ; n] ll.1; n~ cell debris, large proteins, mucopoly6accharides and other macromolecules. P.ttempts have been made to UY~l~ the problem of such unwanted material in the sample by filtering the sample before attempting to detect the presence of a specific binding complex.
However, surprisingly, this did not appear to be particularly ef f ective and an unacceptable number of false positive results was still obtained and the flow through time of the sample was still unacceptably long even when the sample was filtered twice before adding it to the substrate. It thus seemed that the presence of mucins and particulate material was not the whole cause o~ the false positive results and long sample flow through time.
After many attempts to solve the problem of false positive ~esults a~d slow sample flow, however, the WO95126504 2 1 8 6 1 1,. r~ 3 , inventors have discovered that when the assay involves the detection of a specific binding complex between an analyte and a specific binding molecule immobilised on a porous solid substrate, the rPl i ~h; l; ty of the test can be significantly improved simply by wiping the surface of the substrate af ter: the sample has been added to it .
This was most unexpected because it had been thought that all r~r~nt~m;n~ntR had been removed by the filtration steps which had been attempted previously whereas it now seems that this was not the case.
Therefore, in the present invention there is provided a method for detecting the presence of an analyte in a sample of body fluid, the method comprising contacting the sample with a specif ic binding agent capable of forming a specific biIlding complex with the analyte wherein the specific binding agent is ; Ih; 11 Red on a porous solid substrate; and detecting the presence of specific binding complex; characterised in that before detecting the specific binding complex, the surface of the substrate is wiped to remove lln~flRQrhPd rnnr~m;n~ntR
The simple step of wiping the substrate before attempting to detect the presence of specific binding complex has a remarkable effect on the success of the assay. The time taken for the sample to flow through the substrate can be reduced from 20 to 30 minutes to as little as 1 to 2 minutes and false positive results can be almost completely eliminated whilst still retaining the sensitivity of the assay to true positive results.
The wiping may be carried out manually or, alternatively, the process may be automated. Generally an ~hRnrhPnt r-tP~; ~l will be used to wipe the substrate and examples of suitable materials are cotton, cotton wool and absorbent paper.
The wiping step should be carried ~ out sufficiently vigorously tQ remove from the surface of the substrate any material which is not bound to a Gpecific binding molecule. In order to make it clear to the practitioner that all of the I tPr1 material has been removed, a colouring agent may be added to the sample. In cases where a buffer or surfactant sn1l~t;nn is added to the ~ample before transferring the sample to the substrate, the colouring agent may be inr~ pd in the buffer or surfactant solution but this will not nprpcs~rily be the case .
The colouring agent may be an agent such as a stain which is specific for mucins,, _ ^nt~ of cell debris or other cnnt~min~tc which remain on the substrate and are a cause of many of the problems of: false positives which occur with assays of body fluids. However, it is often simpler to provide as a colouring agent a coloured particulate material such as latex, agarose, polystyrene or another polymer which does not bind to the cr~ntr~in~ntq but which 6imply remains on the surface of the substrate because the particles are too large to pass through the pores of the substrate. The particles should thus o~ course be larger than the pore size of the substrate but must also be smaller than the pore size of any pre-filters which may be used. It has been found appropriate in many cases to use particles of diameter of about 3 llm since, as discussed in more detail below, the filters used in any initial purification steps can be chosen to have a pore size larger than this. The coloured particles will remain on the surface of the WO 95l26504 2 1 8 6 7 4 3 r~ . s 1l3 s - substrate along with the mucins and particulate impurities which appear to be causing the problem of false positives when smaller particles pass through the substrate .

Thus, when the colouring agent is used, it will be a simple matter f or a practitioner to wipe the c~louring agent from the surface of the substrate and thus to ensure that all surface debris has been removed from the substrate.
The sample may comprise any body fluid, for example, saliva, whole blood, serum or urine but the greatest uv~ ~ are seen for saliva and whole blood since, on the whole, these tend to contain greater amounts of cell debris, high molecular weight proteins, mucopolysaccharides and other high molecular weight substances which cannot pass through the pores of the substrate .
The analyte may be any specif ic binding molecule capable of reacting with the specific binding agent to form a specif ic binding complex . Examples of specif ic binding _ l ~YPq include antibody-antigen complexes and thus the analyte may be either an antibody or an antigen.
In the case where the analyte is an antibody, it may be of any isotype and may be an antibody against any pathogen. Analysis of saliva or whole blood samples is particularly useful in the diagnosis of gut infections caused by pathogens such as Helicobacter pylori (formerly known as Campylobacter pylori). The presence of ~.
pylori infection is indicated by the presence in saliva of IgG or in the blood and therefore, if the aim of the .
WO 95/26504 2 1 8 6 7 4 3 . ~
test is to detect H. pylorl infection, the analyte may be IgG specific-to H. pylori antigen.
The expression "antigen" is used in its broadest sense and includes whole pathogen cells or homogeneous, near homogeneous or heterogeneous extracts from a pathogen, all of which are capable of binding to specific antibody in samples of a body f luid .
When the specif ic binding agent is an antigen, it may be a protein, polysaccharide or lipid or any combination thereof. Preferred specific binding agents which are antigens include protein, lipopolysaccharide or cell extract of p~th~ n prepared by, for example, sonication, pressure disintegration, detergent extraction or f ractionation .
When the method of the invention is used to detect infection with H. pylori, the specific bi~ding agent may be an antigen derived from H. pylori. Antigens derived from ~{. pylori suitable for use a6 specific binding agents in the method of the present invention are disclosed in WO-A-9322682. However, any H. pylori derived antigen could be used as a specif ic binding agent.
As ~1; CCllCRf'(~ above, the substrate is porous 50 as to allow the majority of the sample to flow through it whilst retaining the analyte on the surface where it is bound specifically to the specific binding agent. The substrate may be formed from nitrocellulose or other substances, for example polymers such as cellulose, polyacrylamide, nylon, polystyrene, polyvinyl chloride or polypropylene, but the invention is not limited to these.

W0 95/26504 2 1 ~ 6 7 4 3 r The substrate will, however, preferably be a nitrocellulose membrane and may have a pore size of from about 0 . 5 to 3 llm with from about 1 to 2 llm being pref erred .

It is greatly pre~erred that the solid support is backed by an absorbent wicking material. Z~hs~rhl~nt paper will often be the material of choice, generally for reasons of cost, but any absorbent material can be used for this purpose.
The specific binding molecules useful in this invention may be either covalently or non-covalently ("passively") bound to the solid surface. Suitable binding processes are well known in the art and generally consist of cross-linking, covalently binding or physically adsorbing the antigen to the solid support.
The presence of the analyte is diagnosed by means of the present invention by detecting the ~ormation of a complex between the analyte and the specific binding agent. Some form of detecting means is therefore n~c~RRAry to identify the presence (or, if required, amount) of the specific binding complex.
The r1~tect;r~n means may be an antibody, conjugated with a reporter molecule, and which is capable of binding specifically to the specific binding complex.

3 0 In the case where an antibody is to be detected, the detection means may comprise a labelled second antibody specific for all Ant;ho~l;es of the isotype of the analyte antibody. In tests for H. pylori in humans, the analyte antibody will often be of the IgG isotype and in that W095/26~04 ~1 867~3 1~l,. /13 case the second antibody may be anti-human IgG.
A ~reporter molecule" is a molecule or group which, by its chemical nature, has an analytically identifiable S characteristic or provides an analytically i~f~nt; ~iAhl P
Gignal which allows the detection of antigen-bound antibody. Detection may be either .~ualitative or .~uantitative. Reporter molecules used in this type of assay may be either enzymes, fluorophores or radionuclide cnnt=;n;n~ molecules (ie radioisotopes). In the case of an eLzyme; n=Rc=y~ an enzyme ig conjugated to the second antibody, generally by means of glutaraldehyde or p~r; o~=t~ . A8 will be readily recognised, however, a wide variety of different conjugation techniques exist, which are readily available to those skilled in the art.
Commonly used enzymes include horseradish peroxidase, glucose oxidase, ~-galactosidase and =1 k=l; nf~
rh~Rrh~t~Re~ among others. The cl~.r- ~hnres to be used with the specific enzymes are generally chosen ~or the production, upon hydrolysis by the corresponding enzyme, of a detectable colour change. C11L~ ~1 ' res can be soluble or _ insoluble, ~Pr~nrl;n~ upon the chosen ~rrl;~'~t;nn For example, 5-bromo-4-chloro-3-indolyl phosphate/nitroblue tetrazolium is suitable for use with ;~lk=l in~ rhnsrh~t~Re conjugates; for peroxidase conjugates, 1,2-phenyll~n.sri;~m;nf~-5-Am;nnR=l;cylic acid, 3,3,5,5-tetramethylhPn7;ri;n~, tolidine or rl;=n;Riri;n~ are commonly used. It is also possible to employ fluorophores, which yield a fluorescent product, rather than the _l~u,,-u~hu~ c8 noted above. Examples of fluorophores are fluorescein and rhnrl=m;nF~. When activated by illumination with light of a particular wavelength, the fluu~uu~ hPll,od antibody absorbs the light energy, inducing a state of excitability in the .

WO gs/26504 2 1 8 6 7 4 3 r~ 3 molecule, ~ollowed by emission of the light at a characteristic colour which is usually visually detectable with a light microscope.
However, the present invention is particularly well adapted for use as an 'instant ~ gnnS;q' test from which the results will be available in a few minutes and which may be carried out by a general practitioner during a consultation. For this reason, it is greatly preferred that the method of detection is as simple as possible and requires no s~eci~l; R~ equipment . Therefore, the reporter molecules preferred in the present invention are colour reagents such as colloidal gold or carbon, polystyrene or latex particles.
When this type of reporter substance is used, it is important that unbound second antibody be removed so that the bound second antibody with the attached colour agent is clearly visible. It is thus particularly suited to the porous membrane backed by an absorbent pad which is used in the present invention since any surplus second antibody will pass through the membrane and be absorbed in the pad leaving only bound second antibody and associated colour agent on the surface of the nitro~ e membrane.
Although, as discussed above, it does not completely solve the problems of slow sample flow and false positive results, it will often be advantageous to include in the method of the invention one or more initial filtration steps .
Typically, a f ilter useful in the method will have an effective pore size of from about 1 to 15 ~Lm, preferably WO9S/26s04 2 t ~ 6743 r ~

from 3 to ~ ~m. This may be achieved usin~ any type of 3 filter but a preferred type is a frit made from a plastics material and having a typical actual pore size of about 5 to lO~m. In this type of frit, the effective pore size is smaller than the actual pore size because the frit is relatively deep and the pores are out of alignment .
A further step which may be ;nrl~ tl before the filtration step is a primary separation step in which the sample is passed through a coarse filter such as a cotto~
or cotton wool pad. This step is particularly useful in reducing the viscosity of saliva samples, probably because it_ removes a large proportion of the mucopolysaccharides which are present in saliva samples but it may also be helpful in assays of other types of body f luid .
A further rPf;r ' of the method which assists in the elimination of false positive results is the provis~on on the substrate of a control reagent which is capable of reacting with the detection reagent. The control reagent will be present in a different location from the specific binding molecule and will be capable of sper;fir~lly binding the detection agent. Thus, for example, if the detection reagent is anti-human IgG, the control reagent will be human IgG. The presence o~ the control reagent is a means of monitoring the viability o~ the method of the invention since if its presence is not rl~-tert~, then clearly, the detection method is not working correctly.
Before addi~g the sample to the substrate, it is often preferable ~to treat it with a col--t;nn rnnt~;n;nrJ a buffer and/or a surfactant. For whole blood samples, a W095l26504 2 1 8 6 7 4 3 r~ .. '0~ /l3 3~
lysing buffer may be used. The buffer will usually have a pH of f rom about 6 . 8 to 7 . 8 and pref erably about pH
7.2. The buffer will generally contain a surfactant such as the non- ionic polyoxyethylene ether sold under the trade mark TRITON X_100 (Union Carbide Chemicals and Plastics Co, Inc) which may be present in an amount of from 0.05~ to 1~ and preferably about 0.19~ by volume.
The combined use of the wiping step and the buf f er has allowed the flow through time of whole blood samples to be reduced from 20 to 30 minutes to 120 to 180 seconds.
When the body fluid i3 saliva, it will, for preference, be treated with a solution comprising polyoxyethylenesorbitan derivatives of palmitic and/or stearic acids and buf f ered to pH about 6 . 8 to 7 . 8, pref erably about pH 7 . 4 .
Suitable surfactants are available under the trade marks 2 0 TWEEN 4 0, TWEEN 6 0, TWEEN 6 1, TWEEN 6 5 and TWEEN 8 0 .
It is particularly preferred that the surfactant ~ntAlnR
from 40% to 659~ stearic acid derivatives and TWEEN 60 which r~ntA;nR about 55~ stearic acid derivatives with the balance being palmitic acid derivatives is particularly pref erred and provides signif icantly more reliable results than most other surf actants .
The amount of surfactant present will for preference be chosen so as to maximise the flow of sample through the substrate. The flow is usually maximised when the surfactant is present in an amount of from 0.1~ to 1~ by volume, typically about 0.59~. This amount of surfactant give the best results for ~l;m;nAt;n~ non-specific Wo95/26504 21 86743 r~ /13 ~

binding without greatly affecting the specific binding and thus the threshold of detection obtainable using the method of the invention.
other agents may be present in the solution in order to minimise the non-specific binding of mucins and particulate material in the test sample to the teat reagents. Such agents include inorganic salts such as sodium chloride and proteins such as bovine serum albumin (BSA) .
Sodium chlo~ide may be present in a concentration of from about 0.1 to 0.2 M. It i8 greatly preferred that the upper concen~ration limit of 0 . 2 M is not ~Yr~ d since this would tend to discourage specific binding.
Typically, the concentration of sodium chloride present in the Snl l~t; nn is about 0 .125 M.
BSA, if present will typically be included in an amount of about 0.05~ to 0.596 by weight, preferably of 0.1~.
Phosphate is a particularly preferred bui~fer for the LLeal.,~ L of both blood samples and saliva samples but other ~ of buffers which could be used to ensure that the pH of the solution i8 within the preferred range are f ;~ r to those skilled in the art .
Any water soluble salt such as a sodium, potassium or salt may be used for the preparation of the buffer solution although sodium salts often give the best results. It has been found that effective buffering is rht~in~l using a 0.001 - 0.05 M, preferably about 0.02 M, solution of 8O.1;l~m phosphate.

W0 95/26504 2 18 6 7 4 3 r~l. .. /IJ

Aæ briefly mentioned above, a colouring agent for visualiæing the cnnt~m1n~ntq which are to be wiped from the surf ace of the 9ubstrate may be i n~ d in the buffer or surfactant solution. When it i8 included in a buffer or surfactant solution, a particulate colouring agent may be present in an amount of from about 0.005~ to 0.05~ and preferably from about 0.01% to 0.029~ by weight.
If a stain is uæed, however, the concentration may be " ' ~t higher than this.
The buffer and/or æurfactant solution comprising a colouring agent is new and itself forms a part of the invention .
Theref ore, in a second aspect of the invention there is provided a buffer solution for the treatment of a sample of body fluid to be assayed and comprising a surfactant and a colouring agent.
Aæ discussed above, the colouring agent may be specific for some ~nntAm;n~nt which it is desirable to remove but it will, for preference comprise a coloured particulate ."-t.ot~ 1 such as latex, agaroæe, polystyrene or another polymer. The particles should of course be larger than the pore size of the substrate but must also be smaller than the pore size of any pre-filters which may be used.
It has been found appropriate in many cases to use particles of diameter of about 3 ~m.
The buffer solution may be included in a kit for carrying out the method of the invention, which kit itself forms a further aspect of the invention.
In this aspect of the invention there iæ provided a kit Wo gs/26504 r~

comprising:
i. a buffer solution comprising a surfactant and a colouring agent;
ii. a ~ apecifi~ binding agent i ' ,; 7; qed on a porous substrate and capable of f orming a specif ic binding complex with the analyte; and iii . a detection reagent f or detecting the presence of specif ic bi~ding complex.
The present invention is particularly u~eful for the detection of antibodies against H. pyl ori which may be present in the saliva of H. pylori infected patients. As discussed above, N. pylori is unu~ual in that infection gives rise to antibodies of the IgG isotype present in the saliva.
Therefore i~ a fourth aspect of the invention there is provided a kit for the detection of IgG specific for H.
pylori, the kit comprising:
i. a 601ution comprising a surfactant and a colouri~g agent;
ii. an antigen derived from H. pylori immobilised on a porous substrate; and iii. a solution of a 1 ~h~ d antibody capable of binding specifically to human IgG.
When the kit is for the assay of whole blood or saliva samples, the preferred components of the solutions are those which are described for the method of the f irst Wo gs/26s04 ~ / 13 21 ~6743 aspect of the invention. The preferred substrates and detection reagents are also as described for the first aspect of the invention.
The kit may also contain a collection device appropriate to the body fluid to be assayed_ A coarse filter such as a cotton or cotton wool pad for preliminary filtration of the sample may also be included and may optionally form a part of a saliva collection device. Furthermore, the kit may include a filter for removing particulate material f rom the sample . As discussed above in relation to the method of the first aspect, the filter may have an effective pore size of from about 1 to 15 ~Lm, preferably from 3 to 8 llm. This may be achieved using any type of filter but a preferred type is a frit made from a plastics material and having a typical actual pore size of about 5 to lO~m.
The invention will now be described in detail with reference to the following examples.

Prep~ration of Buffcred gurfactant S~ t~n for Saliv~
S~nple A buffered surfactant solution was prepared from the following ingredients:
0 . 02M sodium phosphate solution 100 mL
sodium chloride o . 73 g 3 0 Bovine serum albumin 0 .1 g TWEEN 6 O~M O ~ g dark blue latex particles (3 . O ,um diameter) 0 .1 g by mixing at room temperature. The dark blue latex ~oss/26so4 P~ll~., "3 2~ 86743 particles are available from Polymer Laboratories, UK.
E;X~MPLE ~
Preparation of ~. pyl ori derived antigen An antigen derived from E. pylori was ~ L~:d according to the method set out in Example l of WO-A-9322682. In summary, a crude sonicate of H. pylori was prepared and fractionated~ A 440 kDa protein was removed leaving a mixture ~ nt;~;n;n~ 265 and 340 kDa proteins.
~x~P~E 3 Preparation o~ Test Device Between 1 and 5 ~L~ o~ a 0 . 05~ (w/w) solution of the antigen of Example 2 was spotted onto a substrate to form a test area. The substrate was a 1. 2 ~Lm SARTORIUSIM
nitrocellulose membrane supported upon a backing layer of Schleicher ~& Schuell chromatography paper ~o 3469 (available from Anderman & Co, Kinston upon Thames, UK) which acts as a wicking material.
From 1 to 5 ~L~ of a 0 . 005~6 (w/w) solution of purified normal human IgG (Sigma Chemical Company ~td, Poole, Dorset, UK) was spotted onto the substrate in a control area distinct from the test area.
~PI,E 4 ~
Prep~r~tion of n; ~ in5 Agent A disclosing agent was prepared by diluting colloidal gold conjugated to goat anti-human IgG (heavy and light chains) (Biocell Research Laboratories, Cardiff, IJK) in rhnsrh~t~ buffered saline (PBS) ~ ntilin;n~ 0.05~ by Wogs/26s04 2 1 8 6743 P~

volume of the surfactant available under the trade mark TWEEN 20 and Q.19~ by weight BSA to an i~hqnrh~nre at 520 nm, 1 cm path length of 0 . 5 optical density units .
EXAMP~E 5 Assay of Saliva Sa~nple Saliva (lm~) was collected using the collection device available under the trade mark O~NISAL (Saliva Diagnostic Systems, Vancouver, Washington, USA) in which the sample is collected in a pad which also acts as a coarse filter.
The collection device cnntA;n;nr the sample was then transferred to a tube cnn~A;n;nr l.0 mL of the solution - of Example 1. The collected saliYa was filtered using a Porex IJltrafine serum separator having an approximate exclusion of 5 llm and was then added to the test device prepared in Example 3.
.
After the diluted saliva sample had flowed through the nitrocellulose membrane into the chromatography paper backing layer, the blue latex particles formed a layer on the surface of the substrate. This layer was removed by wiping f irmly but gently with cotton wool until no blue colour Ll ; n~l.
o . 5 mL of the disclosing agent of Example 4 was then added to the test device. The disclosing agent was allowed to drain through the nitrocellulose membrane and then the test was read.
A single pink spot in the control area indicates a viable but negative test result whereas a test which results in a spot in the test area and a spot in the control area indicates a positive result.

4 r~.,~.~. ! /13 The test was capable of detectins levels of anti~
pylori IgG of as low as 0.8 units (on a scaIe of from 0 to 10) and did not give false positive results.

5 EX~AMPL13 6 Pr~paration of Buf~ered Surfactant Sol~l~;An ~or Blood gample A buffered s~urfactant solution was prepared from the following ingredients:
O . 02M sodium rh~ph~tP solution 100 mL
TRITON X 100 0.1 mL
dark blue latex particles (3 . O ~lm diameter) 0 .1 g by mixing at room temperature. The dark blue latex particles are available from Polymer Laboratories, UK.
lP~ 7 Aaa~y of Blood Sample The assay was carried out according to the method of Example 5 except that the blood sample was collected using a UNISTI~ 2T~ collection device and a VoLAclM
heparinised glass tube. The blood sample was treated with the solution of Example 6 rather than the solution of Example 1.
Again, a single pink spot in the control area indicates a viable but negative test result whereas a test which results in a spot in the test area and a spot in the control area indicates a positive result.
The test was capable of detecting levels of anti-H.
pylori IgG of as low as 0.8 units (on a scale of from 0 Wo ss/26 to 1~) and did r!ot give ialse po~litiv~ re/~lllt~.

Claims

1. A method for detecting the presence of an analyte in a sample of body fluid, the method comprising contacting the sample with a specific binding agent capable of forming a specific binding complex with the analyte wherein the specific binding agent is immobilised on a porous solid substrate; and detecting the presence of specific binding complex; characterised in that before detecting the specific binding complex, the surface of the substrate is wiped to remove unadsorbed contaminants.

2. A method as claimed in claim 1, wherein the wiping step is carried out manually.

3. A method as claimed in claim 1, wherein the wiping step is automated.

4. A method as claimed in any one of claims 1 to 3, wherein a colouring agent which will remain on the surface of the substrate is added to the sample before the wiping step.

5. A method as claimed in claim 4, wherein the colouring agent comprises coloured particles of diameter smaller than the pore size of any filters used in filtration steps but larger than the pore size of the substrate.

6. A method as claimed in any one of claims 1 to 5, wherein the body fluid comprises saliva, whole blood, serum or urine.

7. A method as claimed in any one of claims 1 to 6, wherein the analyte is an antibody.

8. A method as claimed in claim 7, wherein the analyte is an antibody specific for an H. pylori antigen.

9. A method as claimed in claim 8, wherein the antibody is of the IgG isotype.

10. A method as claimed in any one of claims 1 to 9, wherein the specific binding molecule is an antigen.

11. A method as claimed in claim 10, wherein the antigen is derived from H. pylori.

12. A method as claimed in any one of claims 1 to 11, wherein the substrate is formed from nitrocellulose, cellulose, polyacrylamide, nylon, polystyrene, polyvinyl chloride or polypropylene.

13. A method as claimed in any one of claims 1 to 12, wherein the substrate has a pore size of from about 0.5 to 8 µm, preferably from about 1 to 2 µm.

14. A method as claimed in any one of claims 1 to 13, wherein the solid support is backed by an absorbent wicking material.

15. A method as claimed in any one of claims 1 to 14, wherein the specific binding complex is detected using an antibody, conjugated with a reporter molecule, the antibody being capable of binding specifically to the specific binding complex.

16. A method as claimed in claim 15, wherein the analyte is an H. pylori specific antibody of the IgG isotype and the specific binding complex is detected using an antibody capable of binding specifically to human IgG.

17. A method as claimed in claim 15 or claim 16, wherein the reporter molecule is an enzyme such as horseradish peroxidase, glucose oxidase, .beta.-galactosidase or alkaline phosphatase, a fluorophore such as fluorescein or rhodamine, a radionuclide containing molecule or a colour reagent such as colloidal gold or polystyrene particles.

18. A method as claimed in any one of claims 1 to 17, further including the step of filtering the sample before attempting to detect the presence of a specific binding complex.

19. A method as claimed in claim 18, wherein the filter has an effective pore size of from about 3 to 8 µm.

20. A method as claimed in any one of claims 1 to 19, further including an initial coarse filtration step.

21. A method as claimed in any one of claims 1 to 20 for the assay of whole blood samples, the method comprising the step of treating the sample with a buffered surfactant solution comprising a surfactant such as the non-ionic polyoxyethylene ether sold under the trade mark TRITON X-100 in an amount of from 0.05% to 1% by volume and buffered to a pH of about 6.8 to 7.8 before adding the sample to the substrate.

22. A method as claimed in any one of claims 1 to 21 for the assay of saliva samples, the method comprising the step of treating the sample with a buffered surfactant solution comprising polyoxyethylenesorbitan derivatives of palmitic and/or stearic acids and buffered to pH about 6.8 to 7.8 before adding the sample to the substrate.

23. A method as claimed in any one of claims 1 to 22, wherein there is immobilised on the substrate a control reagent capable of being detected by the same means as the specific binding complex.

24. A method as claimed in claim 23, wherein the control reagent is human IgG.

25. A buffer solution for the treatment of a sample of body fluid to be assayed and comprising a surfactant and a colouring agent which will remain on the surface of a substrate during an assay.

26. A buffer solution as claimed in claim 25, wherein the colouring agent comprises coloured particles of diameter smaller than the pore size of any filters used in filtration steps but larger than the pore size of the substrate.

27. A solution as claimed in claim 25 or claim 26, wherein the particles comprise latex, agarose, polystyrene or another polymer.

28. A kit comprising:
i. a buffer solution as claimed in any one of claims 25 to 27;
ii. a specific binding agent immobilised on a porous substrate and capable of forming a specific binding complex with the analyte; and iii. a detection reagent for detecting the presence of specific binding complex.

29. A kit comprising:
i. a buffer solution as claimed in any one of claims 25 to 27;
ii. an antigen derived from H. pylori immobilised on a porous substrate; and iii. a solution of a labelled antibody capable of binding specifically to human IgG.

30. A kit as claimed in claim 28 or claim 29, further including one or more of the following:
a body fluid collection device;
a coarse filter such as a cotton or cotton wool pad which may form a part of the collection device; and a filter for removing particulate material from the sample.