Detection device for detecting analytes in liquid specimen

Abstract

A detection device for detecting analytes in liquid specimen is provided. The detection device comprises: a specimen chamber for collecting or storing a liquid specimen; a detecting chamber for containing a detecting element; and a through hole for transferring the liquid specimen between the specimen chamber and the detecting chamber. The through hole can be opened or self-sealed. The sealing or opening of the through hole controls whether or not the liquid specimen in the specimen chamber enters the detecting chamber via the through hole. Furthermore, a detection method is provided.

Claims

1. A method for detecting an analyte in a liquid sample, the method comprising: a) providing a detection device, the detection device comprising: a specimen chamber for collecting or storing the liquid sample; a detecting chamber for containing a detecting element; a liquid transferring chamber positioned between the specimen chamber and the detecting chamber; and a flexible nipple element positioned between the detecting chamber and the liquid transferring chamber, the flexible nipple element having a shrinkable through hole for passing the liquid specimen between the liquid transferring chamber and the detecting chamber, wherein the flexible nipple element comprises a first and a second status, the through hole being self-sealed when in the first status, and the through hole being open when in the second status, wherein the flexible nipple element is reversibly movable between the first and second status such that the through hole is resealable, wherein when the flexible nipple element is in the first status, the specimen chamber is in liquid communication with the liquid transferring chamber, the detecting chamber is not in liquid communication with the liquid transferring chamber, and the through hole is positioned inside the liquid transfer chamber and outside of the detecting chamber, and wherein when the flexible nipple element is in the second status, the detecting chamber is in liquid communication with the liquid transferring chamber via the through hole, the specimen chamber is not in liquid communication with the liquid transferring chamber, and the through hole is positioned inside the detecting chamber and outside of the liquid transferring chamber; b) shifting the flexible nipple element from the first status to the second status, thereby allowing the liquid specimen to flow into the detecting chamber from the collecting chamber via the through hole.

2. The method of claim 1, further comprising applying a rod to the flexible nipple element, wherein when the rod is moved from a first position to a second position, the flexible nipple element is changed to the second status from the first status.

3. The method of claim 2, further comprising, allowing the flexible nipple element to change from the second status to the first status.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a stereostructural schematic diagram of the detection device described in a specific example of the present invention.

(2) FIG. 2 is a schematic diagram of the exploded structure of the device shown in FIG. 1.

(3) FIG. 3A is a vertical sectional schematic diagram of the structure of the device shown in FIG. 1, wherein the through hole is in the first status and the piston push rod is in the first position; FIG. 3B is a cross sectional schematic diagram of the structure of the device in FIG. 3A, wherein the through hole is in the first status and the piston push rod is in the first position.

(4) FIG. 4A is a stereostructural schematic diagram of the device shown in FIG. 3A, wherein the through hole is the first status and the piston push rod is in the second position; FIG. 4B is a partial vertical sectional schematic diagram of the structure of the device shown in FIG. 4A; FIG. 4C is a cross sectional schematic diagram of the structure of the device shown in FIG. 4A.

(5) FIG. 5A is a stereostructural schematic diagram of a device described in a specific example of the present invention, wherein the through hole is in the second status and the piston is in the second position; FIG. 5B is a partial vertical sectional schematic diagram of the structure of the device shown in FIG. 5A; FIG. 5C is a cross sectional schematic diagram of the structure of the device shown in FIG. 5A.

(6) FIG. 6A is a stereostructural schematic diagram when the nipple element is in the first status; FIG. 6B is a sectional schematic diagram of the structure of the nipple element in the first status.

(7) FIG. 7A is a stereostructural schematic diagram of the nipple element in a second status; FIG. 7B is a sectional schematic diagram of the structure of the nipple element in the second status.

(8) FIG. 8A is a sectional schematic diagram of the structure of the assembly of the piston and the piston push rod element shown in FIG. 8C.

(9) FIG. 8B is a schematic diagram of another section of the structure of the assembly of the piston and the piston push rod element shown in FIG. 8C; FIG. 8C is a stereostructural schematic diagram of the assembly of the piston and the piston push rod element (the piston rod is in the first position, the piston is in the first position).

(10) FIG. 9A is a sectional schematic diagram of the structure of the assembly of the piston and the piston push rod element shown in FIG. 9C; FIG. 9B is a schematic diagram of another section of the structure of the assembly of the piston and the piston push rod element shown in FIG. 9C; FIG. 9C is a stereostructural schematic diagram of the assembly of the piston and the piston push rod element (the piston rod is in the second position).

(11) FIG. 10A is a sectional schematic diagram of the structure of the detection device in a specific example of the present invention, wherein the flexible element is in the first status and the through hole is self-sealed or closed; FIG. 10B is a stereostructural schematic diagram when the flexible element is in the first status; FIG. 10D is a stereostructural schematic diagram when the flexible element is in the second status and the through hole is opened; FIG. 10C is a sectional schematic diagram of the structure of the device shown in FIG. 10A, wherein the flexible element is in the second status and the through hole is opened; FIG. 10E is a stereostructural schematic diagram when the flexible element is in the third status, wherein the flexible element goes back to be self-sealed or closed, as it is in the first status.

(12) FIG. 11A is a sectional schematic diagram of the structure of the detection device in a specific example of the present invention, wherein the flexible element is in the first status and the through hole is self-sealed or closed; FIG. 11B is a stereostructural schematic diagram wherein the flexible element is in the first status; FIG. 11C is a sectional schematic diagram of the structure of the device shown in FIG. 11A, wherein the flexible element is in the second status and the through hole is opened; FIG. 11D is a stereostructural schematic diagram wherein the flexible element is in the second status and the through hole is opened.

DESCRIPTION OF REFERENCE INDEXES

(13) Detection device 10; detecting element 700; cover 800, 80; detecting chamber 400, 40; flexible element 30, 13; cutting slot 33; small hole 133; cup body 600; collecting chamber 601, 61; seat base 602 of the cup body, opening 606 of the cup body; transferring chamber 500; opening 501 at one end of the transferring chamber, opening 502 at the other end of the transferring chamber; annular convex edge 503 at the base of the transferring chamber; channel 603; nipple element 300; nipple seat base 301; side wall 304 of nipple; nipple cutting slot 303; nipple chamber 305; nipple top 304; rod 204, 24, 14; rod top 205; nipple groove 306; piston 200; outside wall 203 of piston; a first sealing ring 201; a second sealing ring 202; a first clamp strip 207, end 208 of the first clamp strip; a second clamp strip 206; end 209 of the second clamp strip, first pair of clamp slots 105, 105; second pair of clamp slots 104, 104′; piston push rod 100; push rod head 101; piston push rod body 103; outside wall 108 of the push rod body; chamber 210 of the piston 200.

DETAILED DESCRIPTION OF THE INVENTION

(14) In the following detailed description, the figures and the corresponding description are used to explain the particular specific embodiments of the present invention. These specific embodiments are just used as examples for illustrating the invention. Skilled artisans understand that any other specific embodiments that comply with the scope of the claims in the present invention should also be included in the present invention.

(15) On one hand, the present invention provides a detection device for detecting analytes in liquid specimen. The device can detect and test the liquid specimen without contaminating the remaining liquid specimen. Further, the detecting is completed in one step without involving complicated operational steps.

(16) Referring to FIG. 10, a detection device of the present invention comprises a specimen chamber 61 for collecting or storing liquid specimen; and a detecting chamber 40 comprising a detecting element 700; the detecting element can be a lateral flow immunoassay reagent strip; a flexible element 30 is disposed between the detecting chamber and the specimen chamber, and the flexible element is a rubber flake, and the detecting chamber and the specimen chamber are separated by the sheet-like rubber flake so that they are not in liquid communication, i.e., there is no liquid exchange between them (such as in FIG. 10A). A cross-shaped cutting slot 33 is cut on the rubber flake with a sharp knife in advance. When there is no external force or the external force is not sufficient, the cutting slot 33 is still in the first status of self-closed or sealed (such as in FIG. 10B) when a certain amount of liquid specimen 66 is collected in the specimen chamber. At this time, the liquid specimen 66 in the specimen chamber cannot flow into the detecting chamber via the cross-shaped cutting slot. When the rubber flake receives external forces, for example, rubber flake 30 is pressed by a rod like subject 14, the rubber flake 30 undergoes elastic deformation, and the self-closed cutting slot 33 is opened and is in the second status; at this time, part of the liquid specimen 67 in the specimen chamber flows into the detecting chamber via the opened cutting slot and has contact with the detecting element 700, and whether the liquid specimen contains the particular analytes (such as in FIGS. 10C and 10D) can be detected through the detecting element. When part of the liquid specimen enters the detecting chamber, it allows the external force forcing the rubber flake 30 to disappear, for example, the rod like subject 14 is no longer in contact with the rubber flake. At this time, the cutting slot 33 that is originally opened goes back to the self-closed or self-sealed status because of the flexibility, and the liquid that originally flows to the detecting chamber is blocked (such as in FIG. 10E). The rubber flake of the flexible element may have a thickness of 0-30 millimeters, preferably 1-15 millimeters, and even more preferably 2-5 millimeters; for example, it can be such as 1 millimeter, 2 millimeters, 3 millimeters, 5 millimeters, or 10 millimeters. The cutting slot may have an area of 1-10 cm.sup.2 or 2-5 cm.sup.2. What material to use and how to choose suitable thickness or size of the cutting slot can be determined according to requirements, which can be accomplished by a person skilled in the art according to teachings of the present invention combining the prior art. In examples in the present application, a small hole can be opened on the detecting chamber and the detecting chamber is in communication with the environmental pressure so that the liquid specimen can flow into the detecting chamber through the cutting slot 33 more naturally and fluently from the specimen chamber. In addition, the specimen chamber can also be in communication with the environmental pressure. When the cutting slot 33 is opened, part of the liquid specimen may be forced to flow into the detecting chamber via the opened cutting slot with the aid of the pressure of the liquid specimen itself or the pressure difference between the liquid specimen and the detecting chamber.

(17) FIGS. 11A-11D is a detection device in another specific example of the present invention. The detection device comprises a specimen chamber 61, and the opening at one end of the specimen chamber is for receiving liquid specimen such as urine, with another end closed. A hole (not shown) is opened at the closed end and is sealed with a rubber sheet 13 having the same size as that of the hole. Further, the detection device also comprises a chamber 40, and part of the chamber 401 is at the closed end of the specimen chamber and is beneath the rubber sheet 13, and another part of the chamber 402 comprises a detecting element 700. A small hole 133 is opened on the rubber sheet 13 in advance, and when the rubber sheet is in natural status or only the specimen chamber contains the liquid specimen, the small hole 133 is the first status, i.e., the self-closed or sealed status, and is in the “—” liked shape; at this time, the liquid specimen in the specimen chamber cannot get into the detecting chamber 40 via the small hole, as shown in FIG. 11B. When the opening of the specimen chamber 61 is sealed by a cover 80 having a push rod 24, the push rod moves from the top to bottom to have contact with the rubber sheet and presses the opening or other places of the rubber sheet 13 gradually when the lid is rotating down. Because of the self flexibility, the small hole 133 that is self-sealed originally now gradually opens and is in the second status, and the liquid in the liquid specimen chamber enters the detecting chamber via the small hole 133 and is in contact with the detecting element, as shown in FIGS. 11C and 10D.

(18) Alternatively, the self-closed rubber sheet can be pressed to open rather than be opened by the push rod directly. The specimen chamber can be allowed to be sealed by the cover, and the pressure on the surface of the liquid in chamber 61 can be increased in relative to the atmosphere pressure, consequently, the increased pressure can force the small hole that is self-closed to open indirectly, and the liquid specimen to enter into the detecting chamber. In addition, the pressure on the surface of the liquid in the specimen chamber can be adjusted to the same as the atmosphere pressure again, and at this time, the opened small hole goes back to the self-closed or sealed status due to disappearing of the external force, whereby blocking the liquid specimen from flowing into the detecting chamber. The method of adjusting the pressure on the surface of the liquid in the specimen chamber to the atmosphere pressure includes: opening a small hole on the cover, and sealing the small hole by a plastic soft cork, and allowing the pressure in the specimen chamber to increase; when the pressure needs to be reduced, taking out the cork and allowing the specimen chamber to connect with the atmosphere. The method and structure of increasing pressure are disclosed in the published Chinese Patent Application No. 200480033286.8. All the examples therein are cited and enclosed herein as specific examples of the present invention.

(19) FIGS. 1-7 illustrate the detection device and the method of using it in another specific example of the present invention. As shown in FIG. 1 and FIG. 2, the device comprises a specimen chamber 601, a detecting chamber 400, and a nipple-shaped flexible element 300. The specimen chamber 601 and the nipple element 300 are in the cup body 600, an opening 606 of which collects the liquid specimen to the specimen chamber 601, the bottom of which comprises a channel 603 that is in communication with a transferring chamber 500, and the specimen chamber 601 is in communication with the transferring chamber 500 via a channel 603, and the bottom of the collecting chamber 601 and the transferring chamber share a wall, and the channel 603 is on this wall. Two ends of the transferring chamber 500 are open, and on the opening 502 close to the detecting chamber 400 a nipple-shaped flexible element 300 is disposed, and on the opening far from the detecting chamber and near the channel 603 a piston 200 is comprised, and the piston is within the empty chamber of the transferring chamber, and the piston can move left and right in the transferring chamber 500. The piston 200 comprises flexible sealed elements 201, 202, and the sealed elements are for sealing the inside wall of the transferring chamber and the outside wall 203 of the piston. Therefore, a chamber 900 is defined between the nipple element 300 and the piston 200 that receives the liquid specimen in the specimen chamber via the channel 603.

(20) Referring to FIGS. 6A-6B and 7A-7B, the nipple-shaped flexible element 300 comprises a convex portion and a seat base 301, and the convex portion comprises the side wall 304 and the top 302, and a through hole 303 is opened on the side wall 304; the side wall 304 and the top 302 enclose a nipple chamber 305. The base part 301 comprises a groove 306, which cooperate with the annular convex edge 503 of the transferring chamber to allow the seat base of the nipple element to be installed and sealed on the opening 502 at one end of the transferring chamber. When the nipple-shaped flexible element 300 is in the first status, the convex portion of the nipple, i.e., the chamber of the nipple, is towards right, and the hole 303 is self-sealed at the time due to the self flexibility of the nipple chamber 305. When the nipple chamber 305 is forced to turn over and the top 302 is on left of the seat base part 301, the through hole 303 that is in the sealed or closed status is forced to opened. In one specific example, a push rod 204 is integrated with the piston as one piece and is right on the top of the top 302 of the nipple-shaped flexible element 300, and the push rod 204 moves from right to left when the piston moves from right to left in the transferring chamber. Therefore, the push rod can force the top 302 moves from the right of the seat base part 301 to the left of the seat base part 301. Certainly, in other alternative embodiments, the through hole can also be opened at other places rather than on the side wall, such as on other positions of the top or the side wall.

(21) By reference to the figures, the operating mechanism of the detection device is further described in details as follows.

(22) When in the first status, referring to FIGS. 1-3, the top 302 of the nipple flexible element is towards right, and the piston that is in its first position is within the transferring chamber (or called the piston chamber) 500 and defines a chamber 900 together with the nipple-liked flexible element, and the side wall of the chamber 900 comprises a channel 603, the sealing element of the piston, such as sealing rings 201 and 202, seals the outside wall of the piston with the inside wall of the transferring chamber 500. Moreover, the piston does not seal the channel 603, as shown in FIGS. 1 and 3A-3B. At this time, when the liquid specimen is collected with the device, if the specimen chamber is full of the liquid specimen, part of the liquid specimen flows into the chamber 900 via the channel 603. However, as the through hole 303 on the nipple-liked flexible element 300 is in the self-closed or sealed first status, the liquid specimen cannot flow into the detecting chamber 400 via the through hole on the nipple-liked flexible element. Although the liquid specimen in the liquid specimen chamber generates some stress or pressure on the through hole 303 on the nipple flexible element 300, as well as on the top 302 of the nipple, the stress or pressure is not sufficient to force the self-closed or sealed through hole to open. In addition, the piston 200 seals another end of the transferring chamber 500, and therefore, the volume of the liquid specimen inside the chamber 900 is fixed. Of course, the volume of the chamber can be freely chosen, such as 1-5 milliliters, or 2-10 milliliters, etc.

(23) When in use, referring to FIGS. 4A-4C, the piston push rod 100 that is in movable connection with the piston 200 is pulled away and the head 101 of the piston push rod is pushed, which moves the piston from a first position to a second position. During the moving process, the outside wall 203 of the piston seals the channel 603, and one end 205 of the top of the push rod 204 contacts with the top 302 of the nipple-liked flexible element 300. The chamber 900 is sealed completely at the time, which neither exchanges liquid with the specimen chamber nor with the detecting chamber.

(24) Referring to FIGS. 5A-5C, when the piston further moves to a second position, the push rod 204 that is integrated with the piston as one piece forces the chamber 305 of the nipple element to turn over, from towards right to towards left, and the top 304 of the nipple element 300 is changed from within the chamber 900 to within the detecting chamber 400. Since the side wall of the nipple element 300 is turned inside out, the through hole 303 that is on the side wall 304 of the nipple element 300 is now in its opened second status, and moving of the piston forces the liquid specimen in the chamber 900 enters the detecting chamber 400 via the through hole 303 to have contact with the detecting element 700, and whether the liquid specimen contains the analyte can then be detected through the detecting element. At this time, the chamber 900 is in liquid communication with the detecting chamber, but is not in liquid communication with the specimen chamber 601.

(25) In one embodiment, the piston 200 and the piston push rod 100 are a moveable connection. When it needs to push the piston to move in the transferring chamber 500 through the piston push rod 100, the piston push rod 100 is pulled out from the piston chamber 210, and then fixed with the piston 200 through a fixing mechanism so that there will be no relative movement between the piston 200 and the piston push rod 100; consequently, the piston and the piston push rod are integrated as one piece. When pushing the piston push rod 100, the piston and the piston push rod move together, driving the push rod 204 that is integrated with the piston as one piece to move together. Therefore, the nipple flexible element that is in the self-closed or sealed first status is changed to the second status by position moving of the push rod 204. See the following description for more details.

(26) Referring to FIGS. 8A-8C and FIGS. 9A-92, the piston 200 is a cylinder, comprising a hollow chamber 210, and the outside wall 203 of the piston is disposed with two grooves for installing sealing elements 201, 202, and one end of the piston is sealed and has a rod-structured 204 protruding outward. The piston push rod 100 comprises a push rod body 103 and a head 101 connected with the body, and the outside wall 108 of the push rod body 103 comprises two pairs of clamping slots, the first pair of clamp slots 105, 105′ and the second pair of clamp slots 104, 104′. The clamp slot has an upside down “L” shape. Two clamp strips 207, 206 are fixed on the inside wall of the piston chamber 210, respectively. One end of the clamp strips has downward bending end 208, 209, respectively. When the push rod body 103 is within the piston chamber 210, the bending ends of the two clamp strips 207, 206 are just fitting in the pair of slots 105, 105′, and the pair of slots 104, 104′ are vacant and in the status of not clamped by the clamp strips (FIG. 8B). When in operation, the pushing head 101 is pulled out toward right with hand, and the push rod body 103 is pulled out from the piston chamber 210 and a “click” sound can be heard, indicating that the ends 208, 209 of the clamp strips 207, 206 are moved to the second pair of slots 104, 104′ from the first pair of slots 105, 105′, respectively, and are clamping in the slots 104, 104′ of the push rod body 103. Then the pushing head 101 is pushed toward left, because at this time the push rod body 103 is integrated with the piston 200 as one piece through the aforesaid clamp mechanism, and is no longer movable in relative to the piston, the piston is then pushed to its second position from its first position by the push rod body 103. Therefore, the rod 204 connected on the piston 200 moves from its first position to its second position, and the position moving of the push rod 204 changes the nipple-liked flexible element that is in the self-closed or sealed first status to the opened second status.

(27) The push rod that is in a moveable connection with the piston can be used not only in the detection device of the present invention but also in other detection devices, as an independent structure unit.

(28) The “specimen” in the present invention denotes any substances in which the presence and the concentration of the analyte need to be tested and/or analyzed, or one or more specimen in which the presence and the quantity of the analyte need to be tested and/or analyzed, or substances with which qualitative evaluation is needed. The specimen can be liquid specimen, such as liquid sample. Liquid samples comprise body fluids such as blood, serum, plasma, saliva, urine, tear, sperm and marrow; the liquid specimen can also be water samples such as seawater, lake water, river water, etc., or household water, municipal water uses or industrial water sources, runoff water or sewage water; the specimen can be food samples such as milk and wine. Mucus and semi-solid or solid specimen can be used to prepare samples such as liquid, eluate, suspension, or leaching solution. For example, samples of throat or genitalia can be soaked in liquid to prepare specimen. The specimen may comprise mixtures of liquid, solid and gas or any related mixtures, such as a cell suspension in a diluted fluid or a solution. The specimen comprises biomaterials such as cell, microorganism, organelle and biocomposite. The liquid specimen can be prepared and obtained from such as soil, dejecta, tissue, organ, biological body fluid or other non-liquid specimen in nature such as solid, semi-solid or highly viscous material. For example, these solid or semi-solid specimen can be mixed with suitable solutions such as diluted liquid. Specimen can be softened by soaking, frozen and unfrozen, or prepared to liquid samples by other extracting methods. The remaining particulate material can be removed with conventional methods such as filtering or depositing.

(29) The analytes denoted in the present invention can be “drugs of abuse” (DOA) or other interested substances contained in the specimen. “Drugs of abuse” (DOA) refers to using drugs not for medical purposes (normally for paralysis of nerves). Abuse of the drugs will lead to body and spirit damages, generate dependency, addiction and/or death. Examples of drugs of abuse include cocaine, amphetamine (such as black beauty, white amphetamine tablets, dexamphetamine, dextro-amphetamine, Beans); methamphetamine (crank, methamphetamine, crystal, speed); barbiturate (such as Valium, Roche pharmaceuticals, Nutley, N.J.); ataractic (drugs for assisting sleeping); lysergic acid diethylamide (LSD); depressor (downers, goofballs, barbs, blue devils, yellow jackets, methaqualone); tricyclic antidepressants (TCA, i.e., imipramine, amitriptyline and doxepin); phencyclidine (PCP), tetrahydrocannabinol (THC, pot, dope, hash, weed, etc.); opiates (i.e., morphia, opium, codeine, heroin, oxycodone); antianxiety drug and sedative-hypnotic drugs, antianxiety drug is mainly for reducing anxiety, tension, fears and stabilizing emotion as well as sedative-hypnotic, including benzodiazepines (BZs), non-typical BZs, fused-dinitrogen-NB23Cs, benzazepins, ligands of BZ acceptors, ring-opening BZs, diphenylmethane derivatives, piperazinecarboxylates, piperidinecarboxylates, quinazoline ketones, thiazine and thiazole derivatives, other heterocyclics, sedative/anodyne of imidazole type, propylene glycol derivatives—carbamates, aliphatic compounds, and anthracene derivatives. The device can also be used to detect drugs which are for medical purposes but are easily overdosed such as tricyclic antidepressants (imipramine or analogs) and acetaminophen. These drugs will be decomposed to different small molecules after absorbed by human body, and the small molecules are present in body fluids such as blood, urine, saliva, and perspiration.

(30) Detecting Element 700

(31) The device of the present invention can use various test strips as its detecting element, depending on the analytes to be detected and the purpose of the detection. There are mainly two types of test strips: test strips for detecting and for preventing adulteration. The test strips for detecting include substances for detecting the components needed to be detected in the specimen. Test strips for preventing adulteration include substances for detecting the characteristic property of the specimen. Both types of strips comprise sample-adding area and detecting area.

(32) Test Strips for Detecting: various test strips for detecting can be used in the present invention. The test strips for detecting comprise immunoassay detecting or chemical detecting of the concerned analytes in specimen. These analytes comprise: drugs of abuse or metabolites that indicate the health situation.

(33) Take the “Drugs of Abuse” (DOA) described above as examples. The test strips of the present invention also can be used to detect drugs that are legal for medical purpose but are easily overdosed, which comprise: tricyclic antidepressants (imipramine and other analogs) and OTC products containing acetaminophen (such as drugs provided by McNeil-PPC Company located in Washington County, Pennsylvania, U.S.A. with the brand name of TYLENOL™). Such a detection may help emergency doctors to determine whether the patient overdoses certain drugs.

(34) The metabolites in urine that can indicate the health situation comprise, but are not limited to, creatinine, bilirubin, nitrite, protein (nonspecific), hormone (such as human chorionic gonadotropin, luteal hormone, follicle stimulating hormone, etc.), blood, white blood cells, sugar, heavy metal or toxin, bacteria components (such as specific proteins and carbohydrates of special type of bacteria, such as Escherichia coli 0157: H7, staphylococcus, salmonella, fusobacterium, Campylobacter, L. monocytogenes, vibrio, or Bacillus cereus) and the physical properties such as the pH value and the specific gravity. Any other clinical chemical analytes presented in urine and suitable for rapid detecting method can be used in the present invention.

(35) The test strips for detecting can be in various forms. Generally speaking, the test strips consist of water-absorbing materials. The water-absorbing materials comprise sample-adding area, test material area and detecting area. The specimen is added to the sample-adding area and migrates towards to the test material area due to the capillary effects. In the test material area, the specimen is dissolved and mixed with test materials needed for detecting the analytes (if present in the specimen). The specimen mixed with the test materials migrates to the detecting area subsequently. Additional test materials are fixed in the detecting area. These second group of test materials react with analytes (if present) or one of materials in the first group of test materials in the test material area. If the analyte exists in the specimen indeed, a signal will appear in the detecting are, and there will be no signal otherwise.

(36) As a more specific example, the test strips for detecting revealed in the following U.S. patents or materials disclosed in patent applications can be used in the present invention: U.S. Pat. Nos. 5,252,496, 5,415,994, 5,559,041, 5,602,040, 5,656,503, 5,712,170, 5,877,028, 5,965,458, 6,046,058, 6,136,610, 6,140,136, 6,183,972, 6,187,268, 6,187,598, 6,194,221, 6,194,224, 6,221,678, 6,228,660, 6,241,689, 6,248,598, 6,271,046, 6,297,020, 6,316,205, 6,372,514, 6,338,969, 6,368,873, 6,372,516, 6,375,896, 6,375,897, 6,391,652, 6,403,383, 6,418,606, 6,429,026, 6,464,939, 6,468,474, 6,485,982, 6,506,612, 6,514,769, 6,528,323, 6,548,019, 6,730,268, 2001/0004532, 2001/0021536, 2001/0023076, 2002/0001854, 2002/0004019, 2002/0031840, 2002/0031845, 2002/0052050, 2002/0085953, 2002/0137231, 2002/0173047, 2002/0132267, 2003/0129673, 2003/0207466, 2004/0018636 and 2004/0191760.

(37) Test Strips for Preventing Adulteration: detecting strips for preventing adulteration are used for detecting characteristic property or material of specimen, such as temperature, specific gravity, pH value, as well as contamination of certain material, including contamination of oxidant, contamination of glutaconaldehyde, contamination of nitrite, contamination of ascorbic acid (vitamin C) and contamination of creatinine. For such a purpose, it is acceptable that the following test strips are used. The test strips combine reagents for detecting additional chemical substances or other reagents intending to frustrate detecting and testing intention. These test strips can be used in any forms, such as immunoassay or chemical reaction. In some examples, the test strips can include tests for creatinine and protein to detect whether the urine sample is diluted. The test strips for preventing adulteration also can detect vitamin B or other materials added to the urine sample to frustrate the detection. The materials comprise: glutaraldehyde, nitrite, chromate, vinegar, products with a “VISINE™” (provided by Pfizer Pharmaceuticals Limited located in the City of New York, N.Y., U.S.A.), sodium bicarbonate, products with a “DRANO™” (provided by S.C. Johnson Company located in Racine, Wis., U.S.A.), soft beverages, oxidants (such as bleaching reagent, hydrogen peroxide, pyridine, chlorinated chromate).

(38) The above test strips for detecting characteristic property of liquid specimen materials can be also used in the present invention. These test strips comprise water-absorbing materials for passing the liquid specimen through the strips, filtering element in liquid communication with the water-absorbing materials, and test material pad in liquid communication with the filtering element and an optional transparent lid. The test material pad comprises test materials for generating signals that can be detected, and the signals are related to the characteristic property of the specimen and are observable through the transparent lid or transparent pan of the device (if used). The filtering element can be made by materials inhibiting reflux of liquid from the raw material pad to the water-absorbing material. The term “inhibiting reflux” refers to the flowing amount from the test material pad to the water-absorbing material in such a small amount that it cannot change the detecting results, or that the test materials transferred from the test material pad to the water-absorbing material or the adjacent test material pad is in such a small amount that it cannot be detected or cannot make the detecting results unclear. The test strips also can comprise water repellent material disposed between part of the filtering material and the water-absorbing material. The water repellent material is for inhibiting reflux of specimen from the test material pad to the water-absorbing material. The liquid specimen migrates and passes the whole test strip due to capillary action. The term “capillary action” refers to the physical effect generated through internal interaction between liquid and wall or interior of material well known to a person skilled in the art, and the physical effect can result in that the liquid passes through the material. The term “water-absorbing material” refers to materials that can attract or absorb fluid easily and the materials are suitable for the capillary action for transmitting fluid from a place of the material to another place. The “filtering element” may even promote diffusion of the specimen during flowing to the test material pad, therefore facilitating formation of uniform and detectable signals on the test material pad. The filtering element also inhibits reflux of specimen from the test material pad to the water-absorbing material, and, therefore, inhibits chemical substances of the test materials transmitting from a test material pad to another test material pad. The “water repellent material” refers to the material that does not allow the amount of fluid that could change the detecting results to pass through. The “water repellent material” is typically a barrier of fluid flow.

(39) Other types of test strips for preventing adulteration can also be combined to the device of the present invention. For example, the test strips for preventing adulteration revealed in the following reference materials can be applied in the present application: 2002/0001845, 2002/0098512, 2002/0155028, 2003/0045003, U.S. Pat. Nos. 5,922,283, 6,248,598, 6,514,768, 6,537,823 and 6,548,019.