CA2226857C - Test apparatus, system and method for the detection of test samples - Google Patents

Abstract

The invention concerns a test apparatus (10) for the testing of a test sampl e on or in a material, such as body fluids or food, particularly adapted to a bioluminescent test, such as for the detection of ATP or phosphatase or other materials. The test apparat us (10) includes a transparent tube having at one end a sample unit (14), at the other end a detachable or nondetachable test unit (16) which are connected, and which includes a cover (12) with a probe containing a swab (18) at one end. The test apparatus (10) includes probe positioning marks (22) on the exterior of the sample unit (14), so that the probe may be moved between selected test positions, and as it moves from a non-use to a use position, various test reagents which are sealed within the test unit (16) are punctured by the probe, and t he test sample and the test reagents are reacted together in the test unit (10).

Description

Test Apparatus, System and Method for the Detection of Test Samples Description Background of the Invention It is desired to provide for a rapid and efficient test for the detection of various test samples from materials or surfaces. Various test apparatuses and test methods have been developed for that purpose. For example, it is widely desirable to determine or to test through quantitative and qualitative tests body fluids, such as blood, urine, milk and the like, as well as food, such as meat products, fruit, vegetables, and to detect for alkaline phcsphatase, salmonella, drugs, and antibiotics, such as; for example, sulfa drugs, beta-lactam drugs, organophosphates, carbamates and active metabolites, various bacteria and pathogenic combinations, either in materials or on the surface of materials, or both.
For illustration only, the detection and characterization, quantitatively and qualitatively, through the employment of a color change or a bioluminescence test, for the detection of the alkaline phosphatase, such as for example, the detection of ATP on or in materials, is most desirable for providing a measure of immunoeffectiveness, so that a rapid determination can be made of whether a processing or surface area is adequately hygienically clean and free of, for example, alkaline phosphatase, so that corrective or disinfectant action can be instituted.

Typically, the detection of ATP is by bioluminescence assay, which is a standard test which will detect food residue, bacteria, yeast, mold, by measuring the ATP on a surface. The method comprises obtaining a test sample, for example, on the surface of the material, such as by non-laboratory or out-of-laboratory or at field locations, the activating of the test sample in the presence of test reagents, and then later employing a luminometer to determine test results, which can be compared with a controlled sample or controlled environment.

The detection of a phosphatase, like ATP, may be made in a dimensional color test and method. However, such a test is time consuming and requires laboratory trained personnel.
The present commercial tests are generally directed to a bioluminescence test, which ordinarily takes less than five minutes and employs premeasured and prepackaged separate test reagents and employs a luminometer to detect test results.
Generally, a portable luminometer, as used in the field, with the use of test containers, such as various test tubes or plates. The concentration of the phosphatase has been determined by measuring or counting of the bioluminescence, determined by the reagents mixing with the test sample, and comparing the count against certain accepted control standards, or a threshold of a control standard.

There are various ATP tests available in the field, and one bioluminescent ATP monitoring test in present use is described in "The Handbook of ATP-Hygiene Monitoring" by Bio-Orbit Oy of Turku, Finland. Another luminescent ATP hygiene monitoring test in use is called the Charm ABC Swab TestTM, sold by Charm Sciences, Inc., of Malden Massachusetts, and described in the technical note published by Charm Sciences, Inc. on March 10, 1994.

Another portable swab-type device for use in an ATP
bioluminescent test for measuring cleaning effectiveness is distributed under the mark LightningTM swab device by Idexx Laboratories, Inc., of Westbrook, Maine. (LightningTM is a trademark of Idexx). The LightningTM device consists of an integral swab design, which contains a unit dose of reagents in use with a portable luminometer. The device employs an elongated tube with a cover on it at one end and an elongated, extended premoistened wetting agent on a premoistened swab, and with such end containing a buffer in a bulb, while the opposite read chamber end, where the test results are read, comprises a glass ampoule. The ampoule contains a luciferin and luciferase reagent material, with a glass ampoule separating the read chamber from the buffer end. The swab is removed from the tube and is used to obtain a test sample from a surface to be tested for ATP, and then the swab is reinserted within the tube.

The cover end of the device is then met and squeezed to force out the buffer solution, while the opposite end containing the glass ampoule with the reagents, is crushed by the user so that the buffer solution and the crushed luciferin-luciferase test reagents are then admixed within the tube with the test sample to form the reaction mixture, which would provide for the appropriate bioluminescence. The read chamber at one end is inserted into and read by the portable luminometer. Thus, the LightningTM device provides a swab-type test probe requiring the bending and squeezing of the one end and the crushing of a glass ampoule at another end of the device, then the admix of the materials prior to inserting the read chamber into a luminometer and then reading the test results.

It is desirable to provide for a new and improved test apparatus, system and method adapted for use with a wide variety of known and unknown test methods for the detection of test materials on a material or_ on a surface. The improved test apparatus is greatly simplified in structure and is effective in use, eliminates possible operational mistakes by personnel in the field, does not require separate pipettes and test tubes, does not provide for the crushing of =
glass ampoules with its inherent danger, and provides excellent separate stability of test reagents which may be employed with the test results by specifically prepackaging the reagents, so that the test apparatus may be stored for long periods of time prior to use.
The device is particularly adapted for in-field or out of the laboratory testing by unsophisticated personnel, as well as the use by laboratory personnel, and further and importantly may have the test results determined by using the IS entire test results in one end thereof, or removing one end of the test unit for testing in a test instrument, which may be, for example, a visual change of color, or other property, in some tests, a use of a portable luminometer, or the use of other types of test instruments including radioactive detection devices, either alone or in any combination. The improved test device is particularly adaptable as a disposable, inexpensive, transparen "_plastic pocket test apparatus.
Suvnmary of the Invention The present invention concerns a test apparatus and a test system employing the test apparatus, and a test method employing the test apparatus and system, and in particular in one embodiment is directed to a bioluminescent type test for the detection of test samples from a material or material 20 surface, by employing known test techniques.
The invention comprises a test apparatus composed of a sample unit and a test unit, which sample and test units may =
be generally longitudinally aligned and secured together generally in tubular form, and which may be integral or may be disposed for the removable detachment of the test unit by the user. The test apparatus is employed for the detection of the qualitative or quantitative, or for any analytical test of one or more test samples from or on a material or on a material surface.
The test apparatus comprises a sample unit having a probe means, such as an elongated element having a first and second end, with the first end adapted to obtain a test sample with a test collection swab or means at one end, used to be collected from or on a material, and generally would comprise a probe-type collection means at one end, by which a test sample may be collected, and a sterile chamber having a first and second end and adapted to receive and retain IS therein prior to use, and optionally after use, the said probe means, and having a cover for the first end of said chamber to seal the end of the chamber.
The sample unit also includes means to retain said probe means within said chamber prior to use; that is, to render the test apparatus sterile prior to use, and without indiscriminate movement of the probe means within the chamber. The sample unit also includes a probe positioning means, comprising a plurality of selected identification positions between the probe means and the chamber in order to identify the relative position of the probe means, and particularly the first test end of the probe means, within said chamber or within said test units, both before and after use. The sample unit also includes means to move a cover end, having the probe means move generally longitudinally to 20 the first end of the probe means, in relationship to said chamber, typically over or within said chamber for use, to one, or typically a plurality of, selected identification positions as required in the particular test method and apparatus.
The test apparatus also includes a test unit attached to a sample unit, generally longitudinally aligned and attached =
to the sample unit and having at its bottom end a reagent housing, which is optionally generally transparent, so that =
a luminometer or visual test result observation may be made, and having a first end and second bottom end, the first end attached to said second end of the chamber in the sample unit, and the housing adapted for use alone or integrally with the test apparatus, so that the test results may be observed in the reagent housing, or the reagent housing may be detached and used in a test instrument, or to conduct tests on the admixture therein, or the entire test apparatus, together with the reagent housing, employed in a test instrument, such as the bottom end placed in a luminometer or other instruments for the detection of the test sample.
The test unit also includes a test sample reagent means, which comprises preselected reagents depending on the desired test to be carried out, and when one or more tests may be carried out alone or in any sequence as desired, with the test reagent means designed to contact the test sample collected. The reagent means generally comprises at least one sealed reagent package containing a test reagent, which may be solid, liquid, powder, emulsion suspension tablet or substantially any combination separately or admixtured thereof.
There may be and usually is a plurality of separate sealed reagent packages, depending on the particular test method selected for the test sample. The test sample reagent means is characterized as being adapted, arranged and constructed, so as to be displaced, punctured penetrated or unsealed by the longitudinal movement of the first end of the =
probe means to a selected identification position so as to permit the admixture or combination reaction or otherwise contacting the test sample on the probe means, and the one or more reagents which have been released from the sealed reagent action of the reagent means.
S Generally, the reagent means is characterized by a package having a puncturable foil seal or membrane, which is adapted to be penetrated by the movement of the probe means, or by other means after collection of the test sample by the probe means, and with the one end of the probe means moved to a selected identification position, so as to generally sequentially, puncture the aligned, sealed reagent packages in the desired sequence as desired. The puncturing occurs at progressive, selected identification positions, usually which positions are marked on the outside of the chamber for easy observation by the user. In some test methods, as desired or required, sequentially contacting of test reagents is desired, while in other tests the sequence is not of importance. Generally the reagents are also packaged and separated in order to provide for better storage life.
Generally, two, three, four, or five or more test reagents or combinations in a package are employed, and would include, for example, at least one liquid reagent, either water or a buffer solution or a neutralizing solution, and then one or more powdered or tablet type packages, so that as the test -sample as the probe means is pushed downwardly, it comes in contact with each of the selected reagents, with the test reagents.and test samples admixed at the bottom end of the test unit. A test reagent, packaged or unpackaged, may also be placed in the bottom end of the test unit, such as a solution or tablet to be admixed with the other reagents and test samples.
The test apparatus, containing the sample and test units, is composed, for example, of an elongated thermoplastic, transparent, flexible, plastic (like polyethylene) tube, having a cover, with an elongated semi-rigid probe exposed within the sterile chamber of the tube, =
and a transparent test unit end at the other end and containing therein the prepackaged test reagents. This apparatus is well adapted for use in the field by generally untrained personnel to obtain test samples from or in a wide variety of materials. The test apparatus may be composed of a disposable, transparent tube material that is easily carried by a user in a pocket or briefcase to the field or plant as required, and usually may be disposed of in toto, or where the test unit is removed from the bottom and then is sealed, may be used in a portable luminometer, which thus makes disposal of the test apparatus quite easy, without undue contamination of the atmosphere.
Generally, the probe means comprises an elongated, somewhat flexible, usually semi-rigid plastic element secured at second end to said cover, and which cover is mounted over the one end of the chamber, typically slidably but also for removable, helical or other longitudinal movement within the chamber. The probe means contains a test sample collection material secured at the one end, such as, for example, a fibrous type material such as a cotton swab, which may, if desired, be premoistened, such as by a water or an aqueous wetting solution, or with other compositions such as color indicators, dyes, reagents or test reagents, or merely may contain chemicals which physically or chemically bind to the material to which the test is directed. Generally, the first test end of the probe means is liquid-moistened, such as by water or a wetting agent solution, particularly when it is used for the collection of test samples on materials or surfaces, to determine hygiene cleanliness, in order to aid in the collection of the test sample on the surface.

The test apparatus is provided to the user with a sample and test units together and with the sterile probe means within the sterile chamber of the sample unit. The probe means is originally in a non-use position, so it does not longitudinally move until after the collection of the test sample by the user. The probe means is then moved sequentially to the selected identification positions.
Optionally and preferably the test apparatus includes some means to retain the probe means in the original, selected non-use position, prior to use by the user, such as the use of an adhesive tape wrapped about the one end of the cover and the chamber, which is user removable, and the use of an easily breakable adhesive, or the use of a heat shrinkable material, such as a transparent plastic material which may be shrunk around the one end of the cover and the chamber or the entire test apparatus to render it sterile until use, to preposition the probe means within the sterile chamber prior to use.
The test apparatus includes probe position means, in relationship between the sterile chamber and the one end of the cover containing the probe means, in one acceptable and preferential method of use. The probe position means generally would comprise any type of means by which the one end of the cover containing the probe means is moved longitudinally in relationship to the test unit which contains the reagent means. Thus, in one example and preferably, the chamber may contain a series of spaced-apart, generally parallel identification lines or marks, either marked by colors or numbers or both, or by some identification means, whereby the bottom portion of the cover containing the probe means and prior to the removal of the retaining means is prepositioned, and then user-moved relative to the marks on the chamber.

The test instructions then permits the obtaining of the test sample using the probe means on a material or a surface, and reinserting the probe means within the chamber, to a selected, usually first non-use, non-reagent identification mark, or in the one end of the probe chamber, and does not extend beyond the second end of the chamber, that is, the test end is above the test unit. The probe position means then provides for the longitudinal, slidable or helical movement of the cover means with the test probe, to say, a second position, third or fourth or multiple positions, whereby the one end of the probe means then contacts the respective reagent test means positioned in the test unit.
This provides for contact of the test_ sample of the probe means with the test reagents, so that all of the test samples or reagents are then contained and admixed within the test unit at the one bottom end of the test apparatus. Generally, the final probe position means is such that all of the test reagent unit means have been punctured down at the one end, and the one end of the probe means is disposed slightly within the test unit. The probe may then be twirled to ensure good contact with the reagents, and then withdrawn to the original or a non-use position within the chamber for later use or disposal. Typically, the sample unit is within the chamber, so that the test apparatus, the sample unit, or the 2S sample and test unit all together may be readily and easily disposed of in an acceptable manner.
The- position probe means should be well-marked and typically uncomplicated, so that the probe position means may be easily understood and used by people in the field.
s0 The means to move the one end of --the probe means may vary; so long as the probe means is moved longitudinally within the chamber between non-use and selected use positions, and from the one end of the chamber into the test .

unit, for example, by the employment of a slidable longitudinal movement when the cover is placed in a snug, close-fitting sliding position over the one open upper end of the chamber of the sample unit, or where there are helical or spiral grooves placed on the inside of the cover, or on the outside of -the chamber unit or both, to provide for the spiral movement to a selected probe position means, or where merely bumps or other means are employed so that the user may move the probe means easily to the selected positions.
Of course, it is also recognized that where there is only a test sample at the end of a probe and only one reagent, it may well be that no probe position means are required, other than for use or non-use, and the probe merely, after a test sample is placed in the chamber, and merely longitudinally moved downwardly to contact a single reagent to force the reagent then to contact the test sample directly into the test unit for test or observation. This would indicate the use of a very simple test method, and typically would not lend itself, for example, to the bioluminescent-type method for determining enzymes like phosphatase, or for the use of beta-lactams, or in processing of meat, or for determining sulfa, drug residues or organophosphate residue on products.
In another embodiment, the test apparatus may comprise a single tube with a cover, wherein the entire test apparatus, after the test sample on the longitudinal movement of the probe means, is employed in its entirety in determining the test results, that is, the test unit is not either made or detached or removable from the one end of the sample unit, but is for example, securely attached thereto, for example, by being integrally molded therewith. In such a situation, the test unit at the one end can still be inserted into a luminometer, or other test instrument, and the color or other change affected by the test results observed or read. Thus, as desired, the entire test apparatus can be disposed of in an effective and environmentally non-toxic manner.
In another embodiment, which will be illustrated, the test unit at the one end of the test apparatus can be detachably removed in any manner thereto, such as employing threads, or slidably fit, or a weakened mechanical section or other means, or merely just taping the units together, so that after movement of the probe to selected identification positions, then the removal of the probe means to the non-use position, the test unit at the one end of the test apparatus may be easily twisted or removed by the user, and would then contain therein the test samples of the various reagents, in an admixture. In this particular method of operation and structure, the test unit, which occupies only a small volume at one end, may then be detached and inserted, for example, into a portable field-type luminometer, so this test method lends itself quite readily to the use of portable test instruments and use in the field or non-laboratory environments. Where this test method is employed it is often desirable to provide a means to seal the one open end of the test unit after removal from the test apparatus. This can be accomplished by a variety of means; fcr example, by employing a screw-type or plug-in type cap secured to the test apparatus, or by more conveniently using a removable adhesive detachable seal, for example, which may be secured to the test apparatus and readily removed .by the user after detachment of the test unit, and then placed over the open end of the test unit and wrapped around to cap the open end of the test unit. Such a seal, for example, may comprise but not be limited to: an aluminum foil, which is adhesively sealed on one side, or any other means to cap, seal or otherwise secure the one open end of the test unit.
It is sometimes desired to provide, rather than a generally cylindrical tube for the test apparatus, a tube wherein the plastic is flexible, particularly toward or near the one of the test unit, so that a user may then squeeze the one end of the tube generally intermediate the test unit and the sample unit, so as to insure the test sample on the probe means is squeezed out together, for example, with the premoistened reagent liquid and contacts the test reagents fully before the one end of the squeezed, used probe means is withdrawn into the chamber.
The reagent housing which is used generally is transparent, particularly where a visual observation is desired; however, it is recognized that the reagent housing IS may be non-transparent, particularly where the particular test to be carried out does not require transparency of the housing or test unit. The test sample reagent means, which is placed generally in the test unit or in the chamber adjacent the open end of the test unit, is adapted to be punctured or pushed by one end of the probe, and provides powdered, liquid, tablet or suspensions of one or more or a combination of chemicals, materials and reagents to the test unit as desired by any particular test.
Usually, the test reagents would generally comprise from two to five separate sealed reagent packages, at least one or more of which packages would be a liquid package, such as a water or buffer solution or a saline solution. It is desirable to place in at least one of the test sealed reagent packages an individual dye or combinations in each package, 20 so that the user is insured that the test probe punctures each package and that the dye color is present in the reagent housing.
Generally, for example, the sealed reagent package, particularly where the test unit is generally cylindrical, would comprise a plurality of spaced apart, separately sealed test reagents containing one or more test reagents, the package so designed, so as to be penetrated, punctured or dispersed by one end of the probe means on longitudinal movement, to provide for contact between the contents of the package and the test sample. The probe means penetrates a puncturable or rupturable membrane, which is placed on at least one side, and typically on opposing sides of a generally cylindrical package, or in fact where a tablet is used, is designed to break up a powdered tablet, in contact with the liquid solution and the test sample.
Generally, the sealed reagent package comprises a plurality of generally separate, individual packages with one or more test reagents having puncturable sealed membranes and opposite radial sides thereof, all selected to be punctured at selected identification positions by the probe positions, to provide for adequate contact between the test sample at the end of the probe means and each of the reagents, so that the entire mixture or content thereof;- would end up in the reagent. -The number, type, material concentration and form of the test reagents in each package, or alone, may widely vary.
For example, the test reagents may contain a dried microorganism or other microorganisms,-growth and enhancing indicators, such as detergents, ethylene diamine, tetraacetic acid, enhancing reagents to enhance the test results, such as pH or dye color indicators, buffer solutions, saline solutions, water solutions, enzymes, material which 20 bioluminesces, such as luciferin alone and in combination with a luciferin derivative, or with other materials which provide biolumination, as well as low level radioactive isotopes, for example a beta-lactam test, stabilizers, antioxidants, phosphatates and phosphatase substrates, various biological buffers, material such as a chromogen which acts in the presence of an enzyme, and a wide variety of other materials.
The test apparatus, for example, may be used in test methods to determine phosphatase, ATP, beta-lactams, pesticides, bacteria such as coliform and E. coli, etc (see, for example, tests described in U.S. Patents 4,239,745, 4,239,852, 5,200,311, 5,283,180, 5,354,663, and 5,374,535).

The invention comprises a method for the detection of a test sample from or on a material, which method includes providing a test apparatus with a sample and test units, collecting a test sample by use of a probe means which is stored in a sterile chamber within a sample unit, and thereafter using the probe means, for example, containing a test swab with an end thereof, which may be premoistened so as to collect a test sample. Thereafter, the method includes using the probe means within a chamber to puncture one or more test reagent means, so as to provide for contact within a test unit at one end of the test apparatus of the test samples with one or more test reagents, so that the test method can be carried out, and with the probe moved longitudinally between selected probe positions within the test apparatus.

The method also includes employing a test unit, either individually or by the use of instruments, either alone or as an integral part of the test apparatus, to do the test detection. Any test method may be typically employed in the test apparatus, the selection of a particular test and test reagents known to persons skilled in the art depending on the particular test.

The apparatus is composed of two units, the sample unit 15a and the test unit. In one embodiment, the test unit is an integral part of the apparatus and does not need to be removed for final reading of results. Instead, the whole apparatus is inserted to the luminometer for reading.
Another embodiment, which calls for removal of the test tube unit for analysis, may be used because of the portable luminometer constraints. The analyzer, e.g. luminometer, can accommodate the whole apparatus, and therefore better and more simply contain all chemicals in the apparatus for disposal. The cover/chamber sliding mechanism can be controlled after testing by a spiral or raised portion on the plastic in order to control the position and/or speed of or stop the downward motion of the probe, and control the timing for each chemical reaction. Some tests will require the use f5 of a timer to allow the full reaction to take place on a timed basis.
The sample unit contains a sterile_chamber housing the probe, made of disposable plastic and composed of a chamber cover that holds the probe and the chamber for the probe, which can be made of metal or other materials. The cover and chamber are sealed prior to use to prevent downward movement of the cover, moving the probe into the chamber. A simple sealing mechanism is used, such as heat shrink plastic or paper that can be torn by a simple twist, to open the chamber and cover and retrieve the probe for sampling.
The chamber is comprised of a waterproof housing to enable the probe material to be maintained moist with the proper solution and ready to use.
The probe may be a swab-type device, made of plastic, 20 wood or metal, with the tip made of absorbent material such as cotton, or synthetic material (plastic) , or a hollow tube;
e.g., a disposable pipette. The tip may be used to obtain a sample by a capillary or vacuum suction, or an affinity probe that can adsorb the analyte by bioaffinity binding; e.g., antibodies or receptors, may also be used.
The unit may also contain instructions and a control mechanism, by which the probe, after the sampling step, is inserted into the testing unit and longitudinally moved to puncture the membranes and allow penetration of each reagent container.
In an optional embodiment, a squeezing mechanism may be desired for full recovery of the sample and products of the interaction of the sample and the reagents. In this embodiment, the chamber's opening is narrowed to enable the swab, when withdrawn to the non-use position, to squeeze out all liquids into the test microtube for best recovery of color/luminescence products, or a flexible plastic tube squeezed about the probe means capping the apparatus.
The test unit is essentially a transparent test tube (plastic or glass) that contains the active components of a selected test with the test sample. Each chemical is contained within a small cylinder; e.g. a reagent chamber, and inserted in the housing and both top and bottom are sealed with a water- and chemical-resistant membrane made of aluminum foil, plastic or waxed paper, or a combination of the above.
The membrane is thin enough to be fractured, burst, or punctured by the probe with a slight pressure by the user.
The reagents are packaged in the reagent chamber in liquid, dried powder or tablet forms. The number of reagents may vary as required for each test method selected; for example, from one to five ingredients, depending on the test requirements.
Optionally, indicator dye is included with the early reagent (e.g. in the first Reagent A), the first penetrable reagent. This helps to verify that all the chemical interactions during the test are working properly. When the dye is visible in the test housing, it is an indicator of a used device.

In accordance with another embodiment, there is provided a test apparatus for the luminescent or color determination of a test sample, which test apparatus comprises: (a) an elongated tubular sample unit having:
(i) a probe means having a first and a second end with said first end comprising a swab to obtain a test sample; (ii) a chamber having a first end and a second end and adapted to retain and receive after obtaining the test sample, the said probe means having a cover for the first end of the probe with the second end of the probe means attached thereto; and (iii) threadable means to move longitudinally said first end of said probe means within said chamber to selected sequential non-use, use, and non-use positions; and (b) a tubular test unit longitudinally aligned and attached to the second end of the chamber having: (i) a transparent housing with a closed bottom end adapted for use with a test instrument to measure emitted bioluminescence within the housing; and (ii) test sample reagent means and comprising in sequence sealed reagents characterized by a swab puncturable membrane to include: a release solution for the release of the sample in the test sample on the swab; a buffer solution; and a detectable reagent composition, the reagent means with the test sample on the swab combined in the bottom end of the housing unit.

In accordance with yet another embodiment, there is provided a method for the luminescent determination of a test sample, which method comprises: (a) providing a test apparatus with a sample unit having an enclosed chamber and a top cover with a probe means of a swab at one end within the chamber and a transparent test unit at another end of the sample unit containing one or more separate membrane puncturable sealed test reagent means and having a closed bottom end and a top end and means to move the top cover and probe means; (b) removing the probe means from the chamber;

5(c) collecting a test sample from a material or surface to be tested; (d) inserting the swab with the test sample back into the chamber; (e) moving longitudinally the cover with the swab and collected test sample in the chamber to puncture with the swab sequentially the membrane sealed reagent means of a release solution and, a buffer solution, to permit the resulting admixed test sample with release solution and buffer solution to contact a luciferin-luciferase composition which provides a luminescent test; and (f) measuring the amount of luminescence in the test unit.

In accordance with yet another embodiment, there is provided a unit dose reagent chamber for use in a test apparatus for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in a test sample, and wherein a moveable probe is employed to obtain a test sample and to release reagents from the reagent chamber to a test unit, which unit dose chamber comprises: (a) a cylinder having a one open end and an other opposite open end; (b) a probe-puncturable membrane seal over the one end and the other end of the cylinder to form a sealed compartment; and (c) a reagent composition for use in the detection of the test sample and sealed within the sealed compartment, which composition is selected from the group consisting of: (i) a detergent-containing buffered solution to release adenosine triphosphate (ATP) or alkaline phosphatase (AP) from the test sample into the solution for testing; (ii) a reaction stopping solution; and (iii) a luciferin-luciferase or phosphatase substrate reagent.

18a In accordance with yet another embodiment, there is provided a test apparatus for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in a test sample, by luminescence or color, which test apparatus comprises: (a) a longitudinal test apparatus housing having a one end and an other end; (b) a moveable probe within the housing to collect a test sample and arranged to puncture a membrane seal; (c) a transparent test unit having a one end and a closed bottom end extending from the one end of the housing for use in detecting luminescence or color in the test sample, and a reagent to detect adenosine triphosphate (ATP) or alkaline phosphatase (AP), by color or luminescence, at the closed bottom end; and (d) one or more unit dose reagent chambers longitudinally-positioned in the test unit, which reagent chamber comprises: (i) a cylinder having a one open end and an other opposite open end; (ii) a probe-puncturable membrane seal at and over the one end and the other end of the cylinder to form a sealed compartment; and (iii) a reagent composition for use in the detection of adenosine triphosphate (ATP) or alkaline phophatase (AP) in the test sample and sealed within the sealed compartment, which reagent composition comprises a buffered solution to release adenosine triphosphate (ATP) or alkaline phosphatase (AP) from the test sample into the solution for subsequent reaction with the reagent.

In accordance with yet another embodiment, there is provided a transparent test unit for use in a test apparatus, for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP), and which test unit comprises: a one open end; a closed bottom end; a probe-puncturable membrane over the one end; and the one end having threads for threadable attachment of the test unit to the test apparatus, and the test unit having one or more separate, longitudinally-aligned 18b unit dose reagent chambers, which unit dose chamber comprises:
(a) a cylinder having a one open end and an other opposite open end; (b) a probe-puncturable membrane seal over the one end and the other end of the cylinder to form a sealed compartment; (c) a reagent composition for use in the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in the test sample and sealed within the sealed compartment, which comprises a solution to release adenosine triphosphate (ATP) or alkaline phosphatase (AP) from the test sample into the solution; and (d) a reagent at the bottom end to detect the adenosine triphosphate (ATP) or alkaline phosphatase (AP) in the solution by luminescence or color.

The test apparatus system and method will be described for the purposes of illustration only in connection with a series of illustrative test apparatus and test method employing various test apparatus. However, it is recognized that those persons skilled in the art may make various modifications, changes, additions, and improvements to the test apparatus, system and methods without departing from the spirit and scope of the invention.

Brief Description of the Drawings Fig. 1 is an elevational view of the test wand apparatus of the invention.

Fig. 2 is a sectional view along line 2-2 of the apparatus of Fig. 1.

Fig. 3 is an elevational view of the apparatus of Fig. 1 with the plunger removed.

Fig. 4 is an elevational view of the apparatus of Fig. 1 with the microtube removed and capped.

18c Fig. 5, with schematic illustrations 5A-G, shows the steps of the test method employing the apparatus of Fig. 1.
Fig. 6 is an enlarged, fragmented, sectional view of the lower section of the apparatus of Fig. 1 in the non-use position.

Fig. 7 is an enlarged, exploded, fragmented view of the microtube and reagent packages of the apparatus of Fig. 1.
Fig. 8 is an elevational view of another embodiment of a threadable test wand apparatus of the invention, with Fig. 8A showing the apparatus with the cover removably secured to the chamber, and Fig. 8B showing the apparatus with the cover removed.

18d Description of the Embodiments Fig. 1 shows the test wand apparatus 10, comprised of transparent, semi-rigid molded polyethylene, with cover/plunger 12 being secured around and outside of elongated sterile sample unit cylinder 14. A microtube test unit 16 is attached to the bottom end of the sample unit cylinder 14, the microtube test unit 16 having indentations 26 and finger grips 24 to enable a user to manually grasp and remove the microtube test unit 16 from the sample unit cylinder 14.

A swab 18 (shown in broken line) is inserted into the interior top end 15 of the cover 12 and removably secured therein. A generally circular aluminium foil seal 20 is positioned on the exterior surface of the microtube test unit 16 and is removably adhered by self-adhesive backing to the microtube 16. Indicator lines 22 are shown on the upper end of the sample unit cylinder 14. The bottom end of the cover 12 and the top end of the sample unit cylinder 14 are secured together with a heat-shrunk plastic seal, and removably secured around the periphery of the cover 12 and sample unit cylinder 14, to prevent downward movement of the cover 12 when the apparatus is in a non-use position.

In the sectional diagram of Fig. 2, the apparatus of the invention 10 is shown with the cover 12 having the swab 18 removably inserted into the interior of top end 15 of the cover 12. The top of the sample unit cylinder 14 is shown with an angular, elliptical cut 19 thereon. A swab 18 is inserted into the interior top end 15 of the cover 12 and removably secured therein. Fig. 2 also shows the microtube test unit 16 with inner containment system having units 30 and 32 and space at the bottom 34, the units containing Reagent A 36, Reagent B 38, and Tablet C 40 respectively. Puncturable membranes 74, which separate each unit of the inner containment system, are also shown.

Fig 3 shows the apparatus 10 with the cover 12 removed from the sample unit cylinder 14, the microtube test unit 16 still attached to the end of the sample unit cylinder 14. A swab 18 is inserted into the interior top,end 15 of the cover 12 and removably secured therein.

Fig. 4 shows the apparatus 10 with the microtube test unit 16 detached from the sample unit cylinder 14 and sealed with the adhesive-back, aluminium foil seal 20.

Fig. 5 shows the apparatus 10 of Figs. 1-4 in use.
Fig. 5A shows the apparatus 10 prior to use, with cover 12, sample unit cylinder 14 and microtube test unit 16 attached.
Fig. 5B shows the cover 12 withdrawn from the sample unit cylinder 14, with the swab 18 obtaining a test sample from the surface area 48. Fig. 5C shows the cover 12 being reinserted into the sample unit cylinder 14, and being moved downwardly longitudinally to the first of the indicator marks 22. Fig. 5D
shows the cover 12 being further depressed into the sample unit cylinder 14 at the second of the indicator marks 22.

Fig. 5E illustrates the cover 12 being depressed in a downwardly longitudinal manner fully within the sample unit cylinder 14 to moisten the tablet at the bottom of the microtube test unit 16. Fig. SF shows the microtube test unit 16 after removal from the sample unit cylinder 14, with the adhesive-backed aluminium foil seal 20 being sealed over the microtube test unit 16. Fig. 5G shows the microtube test unit of Fig. 5F being inserted into a luminometer 44 and counted with a counter 46 for testing of the sample.

Fig. 6 depicts an enlarged view of the bottom end of the apparatus 10 with the microtube test unit 16. The swab 18, premoistened with swabbing solution, is moving longitudinally and downwardly toward the first prepackaged containment unit with a microbial lysis solution and ATP stabilizer. The second prepackaged containment unit contains buffer optimized for luciferin-luciferase reaction, and the luciferin-luciferase Reagent tablet 40 is shown in the bottom of the microtube test unit 16.

Fig. 7 shows in further detail the single use sequential unit dose containment system 49, with plastic cylinders 30 and 32 containing Reagent A 36 and Reagent B 38.
Tablet 40 is shown in position below the units. Puncturable membrane seals 74 for the separation of the containment units are also illustrated. The system 49 is shown prior to insertion into the microtube test unit 16. While in the preferred embodiment for the detection of ATP the above-mentioned reagents are utilized, it is recognized that other combinations of reagents and detection products may be used for specific alternate applications of the test apparatus as shown and described.

Fig. 8 illustrates another embodiment of the test apparatus 50, with cover/plunger 52 having a rounded top end and threads 56 on the interior surface of the open bottom end of the cover 52. These threads 56 are threadably fit to the threads 58 on the outside of the open upper end of the sample unit cylinder 54. A swab 18 is removably inserted into the interior of the top end of the cover 52. This embodiment also depicts a microtube test unit 60 removably secured to the sample unit cylinder 54 with a peripheral indentation 66 and finger grip 64 to enable the user to detach the microtube test unit 60 from the sample unit cylinder 54. A plastic heat shrunk seal secures the sample unit cylinder 54 and cover 52, and an adhesive-backed aluminium foil seal is removably secured to the exterior surface of the microtube test unit 60.

The aluminium foil seal is used to cap the microtube test unit 60 in a secure fashion after it is detached from the sample unit cylinder 54 for testing. Indicator lines allow the user to control the turning of the cover 52 with the threads 56 to enable the swab 70 to be longitudinally downwardly inserted into the prepackaged reagent containment system 60.

Fig. 8A illustrates the apparatus 50 in a non-use position, and Fig. 8B shows the apparatus 50 in a use position with the cover 52 removed for obtaining a test sample. The reagent containment system 60 in Fig. 8 may be comprised of the same reagent combinations as illustrated in Figs. 1-4, or may be any other combination of reagents and chemicals as desired for testing.

In use, the test apparatus is used by removing the heat-shrunk plastic seal 17 securing the cover 12 to the sample unit cylinder 14, and removing the cover 12, which cover has a premoistened swab 18 removably secured into the interior of the top 15 of the cover 12. After swabbing/sampling the affected area being tested, the cover 12 and swab 18 with the sample are re-inserted into the sample unit cylinder 14. The sample unit cylinder 14 has three indicator markings 22 on its exterior surface. When the cover 12 with swab 18 is re-inserted into the sample unit cylinder 14, it is moved downwardly longitudinally to the second mark, and the cover is twirled twice, breaking into the first containment unit 30 with Reagent A 36. The cover 12 is then moved downwardly longitudinally to the third mark and twirled twice more, breaking into the second containment unit 32 with reagent B 38. The plunger is then depressed fully in a downwardly longitudinal manner, breaking into the bottom chamber 34 with Reagent tablet C, and is then twirled, moistening the reagent tablet C 42 at the bottom of the microtube test unit 16. The cover 12 with swab 18, having all three reagents thereon and mixed with the sample on the swab, is withdrawn upwardly and longitudinally into the sample unit cylinder 14.

22a The microtube test unit 16 is then detached, if desired, from the sample unit cylinder 14 at break point 26 by means of the finger grips 24. After removing the adhesive-backed aluminum foil seal 20, the microtube test unit 16 is then covered with the adhesive cap 20 and counted, such as by a luminometer 44 (see Fig. 5). To ensure proper reacting of all samples, the semi-rigid plastic sample unit cylinder may also be squeezed by hand.
After testing, the entire apparatus 10 may be easily disposed of. Further, before use, the entire test apparatus 10 may be easily carried and stored in the user's pocket or a portable, lightweight carrying case. The unique single use sequential unit dose containment system 49 within the microtube test unit 16 allows for easy storage and portability, without mixing of the reagent chemicals and possible spoilage of the chemicals therein.
The following examples are provided to illustrate optional uses of the sample and test kit apparatus and method:

Total Hygienic Test - Total sanitation ATP monitoring test kit: Pocket SwabT"', (a trademark of Charm Sciences, Inc., Malden, Massachusetts) The swab contains water or cleaning solution (e.g. detergent, such as an anionic-like sodium lauryl sulfate, a non-ionic like Triton X-100, a quaternary ammonium like benzalkonium chloride at 0.01-0.30, for swabbing biofilm and dried microbial film.
20 The chamber's ingredients are Buffer A: (0.1-0.3 ml) buffer containing phosphoric acid 0.05o and anionic detergents (0.10) for rapid release of ATP from microorganisms. The buffers could be acids: e.g., trichloroacetic acid or phosphoric acid at 0.01-0.5%, pH 1-3 (e.g. 0.1% phosphoric acid pH 2 and 0.5% Triton X-100), or neutral to alkaline pH buffers such as tris, tricine or carbonate. Detergents can be anionic (sodium lauryl sulfate), neutral (Triton* X-100) or cationic (like quaternary ammonium).
The indicator dye: pH indicator such as phenol red (PR) or bromocresol purple (BCP) at 0.0001-0.001%, just enough to be visible to the naked eye. The BCP is yellow in buffer A, it changes to blue in step 2 when B and A are mixed, and remains blue in step 3 when A and B are mixed with Reagent C.
Buffer B is comprised of a neutralizer buffer to optimize the luciferin-luciferase reaction, e.g. 0.05-0.2M of tris, tricine or other biological buffers. Optionally, it is possible to combine Buffer A with Buffer B.

Tablet C contains luciferase and luciferin substrate for detection of ATP. These ingredients are stabilized in a tablet format (see U.S. Patents 4,239,745, 4,239,852, 5,200,311, 5,283,180, 5,354,663, and 5,374,535).

EXAMPLE OF RESULTS ENCLOSED AS APPENDIX 1: Sanitation results (RLU) vs. the presence of various microorganism on surfaces in a processing food plant.

*Trade-mark T'able Example of resufts for the PocketSwab in processing food plant SPC - standard plate count for total aerobic bactena CFU - colony forming unit COLI - coiiforms bacteria ATP - adeninenudeotide triphosphate RLU - relative light unit LOCATIO Sanitation PoclcetSw SPC YEASJ MOLD COLI Total level ATP microbia t Good 0 0 0 0 2 Good 0 140 6 0 0 146 3 Good 0 0 0 0 0 0 4 Good 0 0 0 4 0 4 Good 0 0 0 0 0 0 6 Good 0 0 0 0 0 0 7 Good 0 0 0 0 0 0 8 Good 0 0 0 0 0 0 9 Good 0 0 0 0 0 0 Good 0 20 2 3 0 25 11 Good 0 0 0 0 0 0 12 Good 0 0 0 0 0 0 13 Good 0 0 0 0 0 0 14 Good 0 0 0 0 0 0 Good 0 0 0 0 0 0 16 Good 0 0 0 0 0 0 17 Good 0 0 0 0 0 0 18 Gooa 0 0 0 0 0 0 19 Good 0 10 0 0 0 10 Good 0 0 0 0 0 0 21 Good 0 0 0 0 0 0 22 Good 0 10 0 0 0 10 23 low 594 50 0 0 0 50 24 low 647 10 16 4 0 30 low 1347 210 8 0 0 218 26 low 2292 110 0 0 10 120 27 low 2437 388 0 0 0 388 28 low 2969 100 0 0 0 t 00 29 bw 3267 2440 23 11 0 2464 low 3959 0 0 0 0 0 31 low 3989 0 0 0 280 280 32 low 4460 0 0 0 975 975 33 med 4889 13000 5 0 24 13029 34 med 6697 30 15 0 0 45 med 6975 13000 0 0 26 13026 36 med 7174 580 8 32 36 656 37 med 7275 10 123 10 0 143 38 med 8075 460 101 72 0 633 39 med 10625 190 0 S2 0 242 med 10972 180 2 4 0 186 41 med 15830 300 187 2 0 489 n2 med 28067 30 9 164 32 235 43 med 32009 3900 0 0 2 3902 44 med 42685 112 0 3 0 115 high 53712 6500 650 455 17 7622 46 high 59019 19500 0 1300 0 20800 47 high 1308.'i7 16250 520 178 46 16994 48 hiqh 175154 19500 0 6500 0 26000 Testing residual raw milk/meat/fish. This test measures the activity of phosphatase as indicative of raw tissue, milk or serum in cooked produce (e.g. pasteurized milk, cooked meat salami, cold cuts, smoked fish) . It also can be used to detect cross-contamination from raw material in processing surfaces and equipment intended for finishing products.
Commercial name - CHEF TestTM (a trademark of Charm Sciences, Inc., af Malden, Massachusetts) . ALK TestT"", Cross-contamination test.
The swab can be dry for sampling wet surfaces, or is moistened with water/buffer for meat products and solid dairy products, like cheese.
The chamber ingredients include in Chamber A, a water or saline buffer, pH 6-10 with preservatives (e.g. benzoic acid, sorbate) , and a pH indicator such as phenol red at 0.0010.
The second chamber contains tablet MP, with Tropix phosphatase substrate (CPD, a product of Tropix, Mass.), freeze dried and made into a tablet.
Chamber 3 contains a stopping solution (0.0025-0.025M
EDTA, 0.05-0.2M Tris base or other biological buffers, 0.1-0.3 NaCl, pH 8-11).
2S EXAMPLE OF RESULTS AS ENCLOSED IN APPENDIX 2: Study of CHEF
TestT"" Performance in testing cooked ground beef hamburgers.

Study of CHEF Test'" Performance in Heat Processing of Ground Beef Purpose: To demonstrate the CHEF (Cooking Heat Efficiency) Test""'s performance, precision and accuracy in predicting doneness of cooked ground beef. Inadequate cooking has been the major cause of stomach poisoning from pathogenic bacteria like E.coli and salmonella.

Introduction: The CHEF TestTM uses the presence of phosphatase activity to determine whether cooked meats have met CFR specified cooking temperatures. Acid phosphatase as an indicator for cooking has been reported in previous literature.

Principle: The CHEF TestTM uses a chemiluminescent substrate for rapid determination of phosphatase activity. The procedure includes the sampling step, which includes using a wet swab to sample the core of the meat (after splitting the meat sample to expose the inner core) . Also, it can be used to swab an equipment surface (e.g., a slicing machine), or other surfaces to test for residual raw meat/milk. In the incubation step, the swab is brought into contact with the chemiluminescent substrate, e.g., CSPD, a Tropix product, for one to ten minutes at a temperature range from room temperature to 65 C, for example, 55 C for one minute. At the reading step, the reaction is terminated and stabilized by adding a stopping solution and immediately counting relative light units using a luminometer.

Results: The average CHEF TestTM for raw beef is in the range of 15,000 to 20,000 RLU, while fully cooked beef gives results in the range of 0-300 RLU (see Table 3).
Results for ground beef heated to various temperatures and hold times are listed in Table 2.

Discussion: Using the results for fully cooked meat, a cut off for determining incompletely cooked meat can be set at the upper range (e.g. 300 RLU). In our field samples (Table 3) all the hamburgers were properly cooked (all results below 300 RLU). In our own cooking experiment, (Table 2), we effectively screen low temperature cooked products (Samples 1-4) from adequately processed and cooked products (Samples 5 and 6 ) .
f5 Conclusion: The CHEF Test accurately detects raw meat and also can distinguish fully cooked meats from incompletely cooked meats. Meat processed at a temperature 2 C below CFR
specifications and for thirty seconds too short a time (Sample 4), was identified as positive in this study.
Samples properly processed, and hamburgers purchased from a local restaurant, were negative for residual raw meat.

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-fl co Q F-Example 3 Chemical and antibiotic residue test - Testing of residual antibiotics in milk, urine, and meats.

The swab is dry for sampling of water, milk, meat serum or urine.

The chamber ingredients are comprised of water or 0.005-0.1 phosphate buffer pH 5-8 in Chamber One. In Chamber Two, the tablet contains dried microorganisms, such as naturally luminescent bacteria such as P. phosphoreum, (Canadian Pat #1103050) or, genetically modified bacteria (e.g.
E. coli mutant used in the Toxi-Chromotest* EBPI, Ontario, Canada); a growth and maintenance nutrient (see USP 5,354,663 incorporated herein by reference), and a growth or activity indicator like chromogen, which in the presence of an enzyme, such as D-galactosidase or phosphatase, can produce colour or luminescence (e.g., Tropix luminescence substrates: CSPD, Galacton-Plus).

Chamber Three contains an enhancing reagent, such as fluorescamine or Tropix enhancing reagent (Emerald, Sapphire).
The procedure for this test comprises obtaining a test sample with the probe means, inserting the swab into the buffer compartment, inserting it into the tablet compartment, and the inserting the swab into the chromogen. It should be noted that the tablet and chromogen can be contained in a single compartment.

The test samples should be incubated for 1-120 minutes and the luminescence then recorded. Inhibition of *Trademark luminescence indicates the presence of a chemical inhibitor in the sample. For example, using E. coli and Tropix Galacton-plus* substrate in E*Colite/ColiGeLTM media (a trade-mark of Charm Sciences, Inc., of Malden, Massachusetts), *Trade-mark 30a can be used to detect antibiotics such as quinolones, and others. Using Bacillus stearothermophius, a variety of antibiotics can be detected in about 60-120 minutes using color change or change in luminescence substrate.
Each test kit is fully packaged all in one device, including the reagents, which greatly simplifies the test, making it user-friendly. The test utilizes simple steps which are controlled by the plunger and indicator marks, and has puncturable seals, such as aluminum foil seals, that separate the various compartments. It eliminates the need to prepare reagents, and no pipettes or dispensers are needed.
This device eliminates operational mistakes due to inaccurate pipettes. Since-all the reagents, liquid and tablets, are individually packaged and sealed, under optimum conditions, -the test kit has excellent shelf l.i.fe- stability, with an expectation of over two month's stability at room temperature. The test device can be easily carried and used in any place,- for example, in a processing plant, without restrictions.
Thus, the test apparatus of the invention provides for a safe, convenient, lightweight and inexpensive test apparatus that may be stored for longer periods and easily transported for use. Further, the-invention is easy, neat and convenient to use. The prepackaged single use sequential unit dose containment system allows for fewer user errors in preparing reagent chemicals for use-. While the single use packaging system of the invention is shown.and described herein for the testing of ATP for sanitation purposes, it is recognized that the apparatus, system and method may be used for a wide variety of product applications.

Claims (57)

CLAIMS:

1. A test apparatus for the luminescent or color determination of a test sample, which test apparatus comprises:

(a) an elongated tubular sample unit having:

(i) a probe means having a first and a second end with said first end comprising a swab to obtain a test sample;

(ii) a chamber having a first end and a second end and adapted to retain and receive after obtaining the test sample, the said probe means having a cover for the first end of the probe with the second end of the probe means attached thereto; and (iii) threadable means to move longitudinally said first end of said probe means within said chamber to selected sequential non-use, use, and non-use positions; and (b) a tubular test unit longitudinally aligned and attached to the second end of the chamber having:

(i) a transparent housing with a closed bottom end adapted for use with a test instrument to measure emitted bioluminescence within the housing; and (ii) test sample reagent means and comprising in sequence sealed reagents characterized by a swab puncturable membrane to include: a release solution for the release of the sample in the test sample on the swab; a buffer solution; and a detectable reagent composition, the reagent means with the test sample on the swab combined in the bottom end of the housing unit.

2. The apparatus of claim 1 wherein said test unit and said sample unit are prepared from a thermoplastic material.

3. The apparatus of claim 1 or 2 wherein said probe means comprises an elongated element secured at said second end to said cover and having a test sample collection material at said first end.

4. The apparatus of any one of claims 1 to 3 wherein the chamber includes probe position identification means of a plurality of selected spaced-apart visual marks on the chamber.

5. The apparatus of any one of claims 1 to 4 wherein the apparatus includes a means for capping said first end of said test unit.

6. The apparatus of any one of claims 1 to 5 wherein the sample unit and test unit are longitudinally, threadably, detachedly secured together.

7. The apparatus of any one of claims 1 to 6 wherein said test sample reagent means comprises a plurality of sealed packages composed of test reagents which tend to prereact or to be less effective with time if directly admixed with said test sample.

8. The apparatus of any one of claims 1 to 6 wherein said test sample reagent means comprises a plurality of sealed, longitudinally aligned, separate packages of test reagents in generally cylindrical form and having opposing probe means-puncturable membranes.

9. The apparatus of any of one claims 1 to 8 wherein said test reagent means comprises a plurality of test reagents having at least one buffer test reagent and at least one test reagent for detection of said test sample in the presence of the buffer.

10. The apparatus of any one of claims 1 to 9 for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) from a material or surface and wherein said first end of said probe means is pre-moistened and said reagent means comprises a plurality of test reagents, said plurality of test reagents comprising:

(a) a buffer solution with a detergent; and (b) a tablet which comprises luciferase and a luciferin substrate for the detection of ATP or AP in the sample.

11. In combination, the test apparatus of any one of claims 1 to 10 and a photometer to measure the luminescence in said test unit for the detection of said test sample.

12. The apparatus of any one of claims 1 to 9 for the detection of alkaline phosphatase (AP) from a material or surface and wherein the first end of said probe means is pre-moistened and said test reagent means comprises a plurality of test reagents, said plurality of test reagents comprising:

(a) a water or saline buffer solution;

(b) a tablet which comprises a luminescent phosphatase substrate to measure the phosphatase on said test sample; and (c) a biological buffer solution to stop the reaction of the phosphatase with the test sample.

13. The apparatus of any one of claims 1 to 9 for the detection of chemical biocides or antibiotic test samples and wherein the test reagent means comprises a plurality of test reagents, said plurality of test reagents comprising:

(a) water or a buffer solution;

(b) a tablet which comprises a microorganism, a nutrient for the microorganism and a growth-activity indicator; and (c) an enhancing reagent to enhance the test results and permit test measurement for detection.

14. In combination, the apparatus of claim 13 with a means to incubate said test unit with said test sample and test reagents.

15. The apparatus of any one of claims 1 to 6 wherein the release solution and buffer solution are combined in a single membrane sealed reagent means.

16. The apparatus of any one of claims 1 to 9 wherein the detectable reagent composition is in stabilized tablet form at the said bottom end of the housing.

17. The apparatus of any one of claims 1 to 16 wherein the release solution comprises an acidic solution and the buffer solution neutralizes the test sample release solution.

18. The apparatus of any one of claims 1 to 17 wherein the release solution further comprises a visible dye.

19. A method for the luminescent determination of a test sample, which method comprises:

(a) providing a test apparatus with a sample unit having an enclosed chamber and a top cover with a probe means of a swab at one end within the chamber and a transparent test unit at another end of the sample unit containing one or more separate membrane puncturable sealed test reagent means and having a closed bottom end and a top end and means to move the top cover and probe means;

(b) removing the probe means from the chamber;

(c) collecting a test sample from a material or surface to be tested;

(d) inserting the swab with the test sample back into the chamber;

(e) moving longitudinally the cover with the swab and collected test sample in the chamber to puncture with the swab sequentially the membrane sealed reagent means of a release solution and, a buffer solution, to permit the resulting admixed test sample with release solution and buffer solution to contact a luciferin-luciferase composition which provides a luminescent test; and (f) measuring the amount of luminescence in the test unit.

20. The method of claim 19 which includes employing a probe position identification means which comprises a plurality of selected spaced-apart user-visual marks on the sample unit.

21. The method of claim 19 or 20 which includes threadably moving the probe means between non-use and use positions.

22. The method of any one of claims 19 to 21 which includes detaching the test unit with the test sample and test reagents therein from said sample unit for use in a photometric instrument.

23. The method of any one of claims 19 to 22 which includes detaching the transparent test unit from the sample unit and sealing said top end of the detached test unit with a cap means after detaching of said test unit from said sample unit.

24. The method of any one of claims 19 to 23 which includes providing the test reagent with a plurality of separate sealed packages of test reagents.

25. The method of any one of claims 19 to 24 which includes providing a plurality of packaged test reagents in said test unit having at least one buffer test reagent, an indicator dye therein and at least one test reagent for reacting with said test sample in the presence of the buffer and dye indicator.

26. The method of any one of claims 19 to 25 which includes providing a test method for the detection of ATP or AP
from a material surface and wherein the test reagent means comprises a plurality of test reagents to include:

(a) a buffer solution with a detergent;
(b) neutralizing buffer solution; and (c) a reagent which comprises luciferase and a luciferin substrate for the detection of ATP or AP in the sample.

27. The method of any one of claims 19 to 21 which includes placing said undetached test unit of the apparatus in a luminescent-measuring chamber of a photometer.

28. The method of any one of claims 19 to 25 for the detecting of phosphatase from a material, comprising a plurality of test reagents including:

(a) a water or saline buffer solution;

(b) a reagent which comprises a luminescent phosphatase substrate to measure the phosphatase of the test sample; and (c) a biological buffer solution to stop the reaction of the phosphatase with the test sample.

29. The method of any one of claims 19 to 25 for the detecting of chemicals and antibiotics from a material, comprising a plurality of test reagents to include:

(a) water or a buffer solution;

(b) a reagent which comprises a microorganism, a nutrient for the microorganism and a growth or activity indicator; and (c) an enhancing reagent to enhance the test results and permit test measurement.

30. The method of any one of claims 19 to 29 which includes timing and incubating said test unit with said test sample and test reagents.

31. The method of any one of claims 19 to 30 wherein the release solution is acidic and contains a visible dye and the buffer solution is a neutralizing buffer solution and the luciferin-luciferase composition comprises a stabilized luciferin-luciferase tablet.

32. The method of any one of claims 19 to 21 which includes inserting the test unit undetached from the sample unit into a luminometer test instrument to measure the ATP
bioluminescence.

33. The method of any one of claims 19 to 32 which includes the swab with the test sample penetrating and sequentially rupturing a first, second, and third thin rupturable seal membrane which membrane extends radially fully across the test unit.

34. The method of any one of claims 19 to 25 which comprises detecting ATP or AP.

35. A unit dose reagent chamber for use in a test apparatus for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in a test sample, and wherein a moveable probe is employed to obtain a test sample and to release reagents from the reagent chamber to a test unit, which unit dose chamber comprises:

(a) a cylinder having a one open end and an other opposite open end;

(b) a probe-puncturable membrane seal over the one end and the other end of the cylinder to form a sealed compartment; and (c) a reagent composition for use in the detection of the test sample and sealed within the sealed compartment, which composition is selected from the group consisting of:

(i) a detergent-containing buffered solution to release adenosine triphosphate (ATP) or alkaline phosphatase (AP) from the test sample into the solution for testing;

(ii) a reaction stopping solution; and (iii) a luciferin-luciferase or phosphatase substrate reagent.

36. The chamber of claim 35 wherein the membrane seal comprises aluminum foil.

37. The chamber of claim 35 or 36 wherein the reagent composition comprises a phosphoric acid buffer and an anionic or non-ionic detergent.

38. The chamber of any one of claims 35 to 37 wherein the reagent composition includes a pH indicator.

39. In combination, the chamber of any one of claims 35 to 38 in a test apparatus for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in a test sample, which test apparatus includes a luciferin-luciferase or phosphatase substrate reagent for reaction with the released adenosine triphosphate (ATP) or alkaline phosphatase (AP) in the solution.

40. The combination of claim 39 wherein the test apparatus includes a longitudinally moveable probe to puncture the membrane seals to carry out the test.

41. The combination of claim 39 or 40 wherein the test apparatus includes a closed bottom end, transparent test unit at the one end of the test apparatus, and wherein one or more unit dose reagent chambers are longitudinally positioned in the test unit.

42. The combination of claim 41 wherein the test unit has an open top end with threads and a closed bottom end, and the test unit is removedly, threadably secured to one end of the test apparatus.

43. The combination of claim 42 wherein the top end of the test unit is sealed with a probe-puncturable membrane seal.

44. The combination of any one of claims 41 to 43 wherein the sealed compartment comprises the buffered-detergent solution and a luciferase and a luciferin reagent in tablet form at the bottom end of the test unit.

45. A test apparatus for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in a test sample, by luminescence or color, which test apparatus comprises:

(a) a longitudinal test apparatus housing having a one end and an other end;

(b) a moveable probe within the housing to collect a test sample and arranged to puncture a membrane seal;

(c) a transparent test unit having a one end and a closed bottom end extending from the one end of the housing for use in detecting luminescence or color in the test sample, and a reagent to detect adenosine triphosphate (ATP) or alkaline phosphatase (AP), by color or luminescence, at the closed bottom end; and (d) one or more unit dose reagent chambers longitudinally-positioned in the test unit, which reagent chamber comprises:

(i) a cylinder having a one open end and an other opposite open end;

(ii) a probe-puncturable membrane seal at and over the one end and the other end of the cylinder to form a sealed compartment; and (iii) a reagent composition for use in the detection of adenosine triphosphate (ATP) or alkaline phophatase (AP) in the test sample and sealed within the sealed compartment, which reagent composition comprises a buffered solution to release adenosine triphosphate (ATP) or alkaline phosphatase (AP) from the test sample into the solution for subsequent reaction with the reagent.

46. The apparatus of claim 45 wherein the membrane seal comprises aluminum foil.

47. The apparatus of claim 45 or 46 wherein the reagent composition comprises a phosphoric acid and a detergent solution.

48. The apparatus of any one of claims 45 to 47 wherein the test unit has an open top end with threads, and a closed bottom end and is removedly, threadably secured to one end of the test apparatus.

49. The apparatus of any one of claims 45 to 48 wherein the one end of the test unit is sealed with a probe-puncturable membrane.

50. The apparatus of any one of claims 45 to 49 wherein the sealed compartment comprises a buffer-detergent solution and a luciferase and a luciferin substrate, as a reagent tablet, is at the bottom end of the test unit.

51. The apparatus of any one of claims 45 to 50 which includes two sequential reagent unit dose chambers comprising:
a first chamber containing the reagent solution to release phosphatase from the probe; and a second chamber containing a reagent for the detection of the phosphatase in the test sample.

52. A transparent test unit for use in a test apparatus, for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP), and which test unit comprises: a one open end; a closed bottom end; a probe-puncturable membrane over the one end; and the one end having threads for threadable attachment of the test unit to the test apparatus, and the test unit having one or more separate, longitudinally-aligned unit dose reagent chambers, which unit dose chamber comprises:

(a) a cylinder having a one open end and an other opposite open end;

(b) a probe-puncturable membrane seal over the one end and the other end of the cylinder to form a sealed compartment;

(c) a reagent composition for use in the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP) in the test sample and sealed within the sealed compartment, which comprises a solution to release adenosine triphosphate (ATP) or alkaline phosphatase (AP) from the test sample into the solution; and (d) a reagent at the bottom end to detect the adenosine triphosphate (ATP) or alkaline phosphatase (AP) in the solution by luminescence or color.

53. The test unit of claim 52 wherein the probe-puncturable membrane seal comprises aluminum foil.

54. The test unit of claim 52 or 53 wherein the test unit includes a luciferin-luciferase reagent tablet.

55. The chamber of claim 35 or 36 wherein the reagent composition includes a biological buffer solution to optimize a reaction for the detection of adenosine triphosphate (ATP) or alkaline phosphatase (AP).

56. The chamber of claim 55 wherein the biological buffer comprises tris(hydroxymethyl)aminomethane (TRIS) or tricine.

57. The combination of claim 39 wherein the test apparatus includes a threadable means to move the probe spirally and longitudinally to puncture the membrane seals.