Method and Apparatus for Collecting and Preparing Biological Samples for Testing

Abstract

A kit and a method are disclosed for collecting and preparing a biological sample for testing where the sample is to be mixed with a buffer prior to being tested.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is related to co-owned U.S. Pat. No. 7,189,522, entitled “Dual Path Immunoassay Device,” the complete disclosure of which is hereby incorporated by reference herein.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates broadly to the testing of biological samples such as blood, oral fluids, epithelia, urine, stool, etc. More particularly, this invention relates to methods and apparatus for collecting and preparing such samples prior to testing.

2. State of the Art

Many types of ligand-receptor assays have been used to detect the presence of various substances, often generally called ligands, in body fluids such as blood, urine, or saliva. These assays involve antigen antibody reactions, synthetic conjugates comprising radioactive, enzymatic, fluorescent, or visually observable polystyrene or metal sol tags, and specially designed reactor chambers. In all these assays, there is a receptor, e.g., an antibody, which is specific for the selected ligand or antigen, and a means for detecting the presence, and in some cases the amount, of the ligand-receptor reaction product. Some tests are designed to make a quantitative determination, but in many circumstances all that is required is a positive/negative qualitative indication. Examples of such qualitative assays include blood typing, most types of urinalysis, pregnancy tests, and AIDS tests. For these tests, a visually observable indicator such as the presence of agglutination or a color change is preferred.

U.S. Pat. No. 6,485,982 discloses what may be called a single path immunoassay device. The device has an elongate outer casing which houses an interior permeable material, e.g., glass fiber, capable of transporting an aqueous solution by capillary action, wicking, or simple wetting. The casing defines a sample inlet, and interior regions which, for ease of description, can be designated as a test volume and a reservoir volume. The reservoir volume is disposed in a section of the test cell spaced apart from the inlet, and preferably is filled with sorbent material. The reservoir acts to receive liquid transported along a flow path defined by the permeable material and extending from the inlet and through the test volume. In the test volume is a test site comprising a first protein having a binding site specific to a first epitope of the ligand immobilized in fluid communication with the flow path, e.g., bound to the permeable material or to latex particles entrapped in or bonded to the permeable material. A window such as a hole or transparent section of the casing permits observations of the test site through the casing wall. The method requires that the test sample be mixed with a conjugate or buffer before it is dispensed into the inlet.

Previously incorporated U.S. Pat. No. 7,189,522 discloses both dry and liquid conjugate immunoassay device systems. The systems include test cells with a first sorbent having a first location for receiving a buffer solution (in the case of a dry conjugate system) or a conjugate solution (in the case of a liquid conjugate system) with the first sorbent defining a first horizontal flow path, a second sorbent having a second location for receiving a sample with the second sorbent defining a second horizontal flow path distinct from the first flow path, and a test line or test site with immobilized antigens or antibodies or other ligand binding molecules such as aptamers, nucleic acids, etc. located in a test zone at a junction of the first and second sorbents.

Where the test cell is provided in a housing, such as the housing 1 show in prior art FIG. 1, the housing is provided with a first opening 2 adjacent the first location and a second opening 3 adjacent the second location. A viewing window 4 is provided in the housing above the test line 5.

In the preferred embodiment, the first sorbent and second sorbent are separate pieces which overlie one another and the test line is printed on one or both of the sorbent materials at the junction. Alternatively, although not preferred, the first and second sorbents can be integral with each other. The systems preferably also include a control line 6 or site which may be seen from the viewing window 4.

According to one set of embodiments, the sorbents (and the housing in which the sorbents are provided) are laid out in a T shape, where the first location 2 for receiving the buffer or buffer-conjugate solution is located near one end of the top bar of the T, the second location 3 for receiving the sample is located near the end of the stem of the T, and the sorbents overlie each other at the intersection.

According to one disclosed method, a sample of interest is provided to the second opening or location 3. After a desired amount of time, a liquid such as a buffer solution is added to the first opening or location 2. If the sorbent is supporting a conjugate (i.e., in a dry conjugate system), the liquid is preferably simply a buffer solution. If the sorbent is not supporting a conjugate (i.e., in a liquid conjugate system), the liquid is preferably a buffer-conjugate liquid subsystem. In any event, after sufficient time to permit the conjugate to migrate to the test site 5 (and control site 6 if provided), the test site (and control site if provided) is inspected in order to determine whether the sample is “positive” or not.

The disclosed system can be used in conjunction with different types of samples such as blood, urine, saliva, and feces, and can be used to test for the presence of any ligand. Where blood, saliva or feces is to be provided, the blood, saliva or feces may be diluted or mixed with buffer prior to being added through the second hole 3. Alternatively, in some cases, the sample may be added through the hole and then a diluent may be added through the same hole 3.

SUMMARY OF THE INVENTION

The present invention provides a kit and a method for collecting and preparing a biological sample for use with an immunoassay device where the sample is to be mixed with a buffer prior to being added to the device. The kit includes a sterile swab and a dropper bottle assembly containing the buffer solution to which the sample is added. The dropper bottle assembly includes a dropper cap having a hinged cover and a threaded base and a bottle having a threaded neck. When the kit is delivered for use, the dropper cap is threadably connected to the threaded neck of the bottle and the hinged cover is closed. The sterile swab includes a sorbent mounted on the end of a stick. The stick is preferably long enough so that a sample can be obtained without the person taking the sample contaminating it. The stick is provided with a weakened portion where the stick can be readily broken.

A method according to the invention includes opening the dropper bottle assembly by unscrewing the cap, inserting the swab into the bottle, snapping the swab stick to break it, and screwing the cap back on the bottle. The bottle containing the sorbent end of the swab is then agitated by shaking it. Now the mixed sample and buffer are ready to dispense into the testing device. This is done by opening the hinged cover of the dropper cap, inverting the bottle and dispensing the appropriate number of drops onto the device by gently squeezing the bottle.

From the foregoing, it will be appreciated that the location of the weakened portion of the swab stick is such that when the swab is placed into the bottle and touching the bottom of the bottle, the weakened portion of the stick is directly adjacent to the upper lip of the bottle neck. In this manner, the stick can be broken simply by bending it against the bottle neck with the sorbent end in the bottle.

According to a presently preferred embodiment, the hinged cover on the dripper cap has a lock which prevents it from being inadvertently opened. This prevents contamination and loss of buffer solution. The kit according to the invention preferably also contains a second bottle of buffer solution for use with a test device employing a dual path immunoassay system. Optionally, the kit includes an alcohol swab, a safety lancet, and a bandage. The kit may, and preferably does contain an immunoassay device, preferably a dual path immunoassay device. A method of testing a blood sample includes using the alcohol swab to clean the area of the skin from which the sample will be taken, pricking the skin with the safety lancet, and collecting blood using the collection swab. The method then proceeds as described above.

Additional objects and advantages of the invention will become apparent to those skilled in the art upon reference to the detailed description taken in conjunction with the provided figures.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a plan view of a prior art immunoassay test device;

FIG. 2 is a side elevation view of a swab according to the invention;

FIG. 3 is a side elevation view of a dropper bottle assembly according to the invention;

FIG. 4 is a front elevation view of the dropper bottle assembly;

FIG. 5 is a rear elevation view of the dropper bottle assembly;

FIG. 6 is a side elevation view of the dropper bottle assembly with the cap removed and the swab inserted into the bottle;

FIG. 7 is a side elevation view of the dropper bottle with the sorbent end of the swab and the stick broken;

FIG. 8 is a side elevation view of the dropper bottle assembly with the sorbent end of the swab contained therein and the hinged cover opened;

FIG. 9 is a flow chart illustrating the method steps of the invention; and

FIG. 10 is a plan diagram of an expanded kit containing a dual path test device and related sampling items.

DETAILED DESCRIPTION OF THE PRESENTLY PREFERRED EMBODIMENTS

Turning now to FIGS. 2-5, a kit according to the invention includes a sterile swab 10 and a dropper bottle assembly 12 containing the buffer solution 14 to which the sample is to be added. The sterile swab 10 includes a sorbent 16 mounted on the end of a stick 18. The stick 18 is preferably long enough so that a sample can be obtained without contaminating it. The stick is provided with a weakened portion 20 where the stick 18 can be readily broken. The dropper bottle assembly 12 includes a dropper cap 22 having a dropper spout 23, a hinged cover 24 and a threaded base 26 and a bottle 28 having a threaded neck 30 (FIGS. 6 and 7). When the kit is delivered for use, the dropper cap is threadably connected to the threaded neck of the bottle and the hinged cover is closed as shown in FIGS. 3-5.

Referring now to FIGS. 3-5 and 8, the dropper cap 22 includes a forward projecting finger 32 and two rearward projecting fingers 34, 36. The cover 24 has a rear slot which is bifurcated by a cross member 38 and a front slot which is either bifurcated or terminated by a cross member 40. As seen best in FIGS. 5, 6, and 8, the rearward projecting fingers extend into the rear slot and embrace the cross member 38 thereby forming a hinge. As seen best in FIG. 4, when the cover is closed, the forward projecting finger 32 engages the front slot above the cross member 40 and thereby prevents the cover from accidentally opening. The cover 24 is made of resilient material which can be deformed by squeezing the sides of the cover. Squeezing the sides of the cover deforms it in a manner that causes the cross member 40 to move forward and out from under the finger 32 thereby unlocking the cover and allowing it to be hingedly rotated about cross member 40 thereby opening the cover to the position shown in FIG. 8 with the spout 23 exposed. A dropper bottle assembly of the type described above is also described in U.S. Pat. No. 5,328,058, the complete disclosure of which is incorporated by reference herein.

A method according to the invention is illustrated in FIG. 9. The method is preferably performed in a clean room which is free from food, drink, and smoke as illustrated at 100. Optimally, the person performing the method may don protective clothing such as a face mask and rubber gloves as indicated at 102. Before beginning the method, the kit should be examined at 104 to determine whether it has expired or been contaminated through a broken package. The method then proceeds to opening the dropper bottle assembly at 106 by unscrewing the cap and preferably placing the bottle and the cap on a sterile surface. The swab is then removed from its sterile package (not shown) at 108 and is used to obtain a sample at 110. The sorbent end of the swab is then placed into the open bottle (FIG. 6) and the stick is broken at 112 (FIG. 7). The cap is then screwed back onto the bottle at 114 with the broken-stick-swab therein and the bottle is agitated at 116, preferably by shaking it a number of times, e.g. ten. The hinged cover is then opened (FIG. 8) at 118 and the bottle inverted at 120. The bottle is positioned over the test apparatus which has been removed from its sterile package (see 11 in FIG. 10) and an appropriate number of drops are dispensed at 122 through the dropper spout 23 by gently squeezing the bottle. When a dual path immunoassay device is used, at 124, pure buffer from a separate bottle (discussed below) is added to another location of the test apparatus.

The apparatus of the invention was tested on one hundred patients known to be infected with HIV. The tests involved collecting oral fluid and performing the procedure described above. Ninety-seven positive test results were obtained and one indeterminate result. This compared favorably with a currently (at the time of the tests) FDA approved test which obtained ninety-eight positive test results from the one hundred patients. The apparatus of the invention was tested on twenty-five patients known to be not infected with HIV. The tests involved collecting oral fluid and performing the procedure described above. All twenty-five patients tested negative for HIV. The FDA approved test achieved the same results.

The above described kit and method can be used with a single path assay device or with a dual path assay device. FIG. 10 shows a kit which is specifically intended for use with a dual path assay device (1 in FIG. 1) which is shown in a sterile package 11. The kit includes the swab 10 which is preferably contained in a sealed sterile package (not shown) and bottle assembly 12. In addition, a second dropper bottle 41 is provided containing the buffer solution to be added to hole 2 in FIG. 1 and as shown in phantom at 124 in FIG. 9. The kit further includes a safety lancet 42, a packaged alcohol swab 44 and a bandage 46. Thus, the kit contains all that is needed to test several different kinds of samples, including blood.

A method of testing a blood sample includes using the alcohol swab 44 to clean the area of the skin from which the sample will be taken, pricking the skin with the safety lancet 42, collecting blood using the collection swab 10, and bandaging the collection site with the bandage 46. The method then proceeds as described above with reference to FIG. 9. While the presently preferred embodiment of the kit and method are designed for use with a dual path immunoassay device, a kit and method for use with a single path device are also contemplated by the invention. When applied to a single path device, the kit need not contain the second dropper bottle 41.

There have been described and illustrated herein methods and apparatus for the collection and preparation of biological samples for testing. While particular embodiments of the invention have been described, it is not intended that the invention be limited thereto, as it is intended that the invention be as broad in scope as the art will allow and that the specification be read likewise. It will therefore be appreciated by those skilled in the art that yet other modifications could be made to the provided invention without deviating from its spirit and scope as claimed.

Claims

1. A method for collecting and preparing a biological sample to be tested, comprising:

obtaining the sample with a swab, the swab having a sorbent mounted on the end of a stick;

obtaining a dropper bottle assembly having a dropper cap with a spout, a threaded base and a bottle with a threaded neck, the bottle containing a buffer solution;

opening the dropper bottle assembly by unscrewing and removing the cap with the spout;

inserting the sorbent end of the swab into the bottle;

breaking the stick leaving the sorbent and a portion of the stick in the bottle;

closing the dropper bottle assembly by re-screwing the cap onto the threaded neck;

agitating the bottle to mix the sample with the buffer solution;

opening the dropper cap to expose the spout;

inverting the bottle; and

dispensing at least a portion of the mixed sample-buffer solution contents of the bottle through the spout onto a first location of said test device.

2. A method according to claim 1, wherein:

said agitating is accomplished by shaking the bottle multiple times.

3. A method according to claim 1, wherein:

the stick has a weakened portion at a particular place to facilitate said breaking.

4. A method according to claim 1, wherein:

said dropper cap has a hinged cover.

5. A method according to claim 4, wherein:

said opening the dropper cap comprises rotating the hinged cover.

6. A method according to claim 1, further comprising:

obtaining a second dropper bottle containing buffer solution; and

dispensing at least a portion of said buffer solution of said second dropper bottle onto a second location different than said first location on said test device.

7. A kit for collecting and preparing a biological sample for testing, said kit comprising:

a sterile swab having a stick with a sorbent at one end of the stick, said stick having a weakened portion to facilitate breaking the stick at a pre-selected location;

a dropper bottle assembly, said assembly including a screw cap having a spout, a locking hinged cover and a threaded base and a first bottle with a threaded neck, said first bottle containing a liquid buffer and said screw cap being coupled to said threaded neck, wherein

the weakened portion of the stick located a distance from the end of the sorbent approximately equal to the height of the first bottle.

8. A kit according to claim 7, further comprising:

a second dropper bottle containing a liquid buffer.

9. A kit according to claim 8, further comprising:

an alcohol swab, a safety lancet, and a bandage.

10. A kit according to claim 8, further comprising:

an immunoassay device having a first opening identified for receiving drops from said first bottle and a second opening identified for receiving drops from said second bottle.

11. A kit according to claim 7, further comprising:

an immunoassay device having an opening for receiving drops from said first bottle.