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.

Claims

1-8. (canceled)

9. A kit for collecting and preparing a biological sample for testing, said kit consisting of: a sterile swab having a stick with a sorbent fixed to the stick 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 consisting of a dropper cap having a spout and a threaded base and a first bottle with a threaded neck, said first bottle containing a liquid buffer and said dropper cap being coupled to said threaded neck, wherein the weakened portion of the stick located a distance from the end of the sorbent, the distance being 90% to 100% of the height of the first bottle without the dropper cap.

10. A kit for collecting and preparing a biological sample for testing, said kit consisting of: a sterile swab having a stick with a sorbent fixed to the stick 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 consisting of a dropper cap having a spout and a threaded base and a first bottle with a threaded neck, said first bottle containing a liquid buffer and said dropper cap being coupled to said threaded neck, wherein the weakened portion of the stick located a distance from the end of the sorbent, the distance being 90% to 100% of the height of the first bottle-without the dropper cap; and any one or more items selected from the group consisting of an alcohol swab, a safety lancet, a bandage, a blood collection loop, an immunoassay device having a first opening identified for receiving drops from said first bottle, and a second dropper bottle containing a liquid buffer, wherein said immunoassay device has a second opening identified for receiving drops from said second bottle.

11-13. (canceled)

14. A kit according to claim 9, wherein: said dropper cap has a hinged cover which covers said spout.

15. A kit according to claim 9, wherein: said dropper cap has a threaded cover which covers said spout.

16. A method for collecting and preparing a biological sample to be tested, comprising: obtaining a kit according to claim 9; obtaining the sample with the sterile swab, the swab having the sorbent mounted on the end of the stick; 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 at the pre-selected location 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; rotating the bottle so that the mixed sample-buffer solution reaches the spout; and dispensing at least a portion of the mixed sample-buffer solution contents of the bottle through the spout onto a first location of a test device.

17. A method according to claim 16, wherein: said agitating is accomplished by shaking the bottle multiple times.

18. A method according to claim 16, wherein: the stick has a weakened portion at a particular place to facilitate said breaking.

19. A method according to claim 16, wherein: said dropper cap has a hinged cover and said opening the dropper cap comprises rotating the hinged cover.

20. A method according to claim 16, wherein: said dropper cap has a threaded cover, and said opening the dropper cap comprises rotating said threaded cover to remove the threaded cover from the dropper cap.

21. A method according to claim 16, 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 the test device.

22. A method according to claim 16, wherein: said sample is a blood sample.

23. A method according to claim 16, wherein: said sample is one of oral fluid, blood, urine, stool, and epithelia.

24. A system for collecting and preparing a biological sample for testing, said system comprising: a dropper bottle assembly, said assembly consisting of a dropper cap having a spout and a threaded base and a first bottle with a threaded neck, said dropper cap being connected to said threaded neck; a sterile swab contained in said first bottle, wherein said sterile swab includes a broken stick having a broken end and an opposite end fixed to a sorbent, wherein said sorbent is in contact with said liquid buffer, and wherein a total length of the sterile swab is 90% to 100% of the height of the first bottle without the dropper cap.

25. A system according to claim 24, further comprising: an immunoassay device having a first opening identified for receiving drops from said first bottle.

26. A system according to claim 24, further comprising: a second dropper bottle containing a liquid buffer, wherein said immunoassay device has a second opening identified for receiving drops from said second bottle.

27. A system according to claim 24, wherein: said dropper cap has a hinged cover which covers said spout.

28. A system according to claim 24, wherein: said dropper cap has a threaded cover which covers said spout.

29. A system according to claim 24, wherein: said dropper cap is separate and disconnected from said swab.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] FIG. 1 is a plan view of a prior art immunoassay test device;

[0018] FIG. 2 is a side elevation view of a swab according to the invention;

[0019] FIG. 3 is a side elevation view of a dropper bottle assembly according to the invention;

[0020] FIG. 4 is a front elevation view of the dropper bottle assembly;

[0021] FIG. 5 is a rear elevation view of the dropper bottle assembly;

[0022] FIG. 5a is a front elevation view of an alternative dropper bottle assembly;

[0023] FIG. 6 is a side elevation view of the dropper bottle assembly with the cap removed and the swab inserted into the bottle;

[0024] FIG. 7 is a side elevation view of the dropper bottle with the sorbent end of the swab and the stick broken;

[0025] 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;

[0026] FIG. 9 is a flow chart illustrating the method steps of the invention; and

[0027] 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

[0028] 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 (e.g., six inches long) 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 dosed as shown in FIGS. 3-5.

[0029] 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 tiredly 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.

[0030] An alternative dropper bottle assembly 12a useful in of bottle assembly 12 is seen in FIG. 5a. Dropper bottle assembly 12a includes a bottle 28a having a threaded neck 30, a dropper cap 22 having internal threads (not shown) for mating with threaded neck 30 and a spout 23a having a neck 23b with external threads, and a cover 24a with internal threads (not shown) for mating with the threads of neck 23b. As will be appreciated, cap 22a and cover 24a can be removed together from bottle 28a, and cover 24a can be removed separately from cap 22a.

[0031] 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 by opening up the kit and then opening the, dropper bottle assembly at 106 by unscrewing the cap 22 (or cap 22a plus cover 24a) and preferably placing the bottle and the cap (or cap plus cover) 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 which may be oral fluid (e.g., saliva or sputum), blood, urine, stool (feces), epithelia, etc. The sorbent end of the swab is then placed into the open bottle (FIG. 6) and the stick is broken at 112 (FIG. 7) typically by leveraging the stick against the edge of the threaded neck 30 of the bottle 12 so that the weakened portion 20 of the stick is near the leveraged point and snaps. Thus, the weakened portion of the stick is preferably selected to be located at a distance from the end of the sterile swab which is approximately (i.e., plus or minus 10%) the same height as the dropper bottle assembly without its cap. The cap (or cap plus cover) 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 (or the cover 24a is removed from the cap 22a) and the bottle inverted at 120 so that the buffer reaches the spout (the bottle may be held at an angle). 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 (or 23a) 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.

[0032] 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 or HIV. The FDA approved test achieved the same results.

[0033] The above described kit (with bottle 12 or bottle 12a) and method can be used with a single path assay device or with a dual path assay device. FIG. 10 shows a kit which specifically intended for use with a dual path assay device (1 in FIG. 1) which is shown in a sterile package 1. The kit includes the swab 10 which is preferably contained in a sealed sterile package (not shown) bottle assembly 12 (which can be replaced with bottle assembly 12a). The kit may also include the assay device 1 and a second dropper bottle 41 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 preferably 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. If desired, the kit may also include a blood collection loop 48. All elements of the kit may be provided in a container or bag 50.

[0034] A method of testing a blood sample includes using the alcohol swab 44 to dean 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.

[0035] As previously mentioned, if desired the kit of FIG. 10 may also include a blood collection loop 48. If a blood collection loop is used to collect a blood sample, the blood sample in the loop may be transferred to the assay device by touching the loop with blood collected therein to the sample pad at the sample opening. One or more drops of buffer may then be added. If the assay device is a dual path assay device, the blood sample is applied at the sample opening 3. Buffer from the second dropper bottle 41 (i.e., the pure or running buffer) is then added to the sample pad at the sample opening 3. After a period of time, a desired number of drops of buffer from bottle 41 are then added to opening 2 of the assay device 1.

[0036] 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. Thus, depending upon the assay device which is included in the kit, or with which the kit is to be used, different numbers of bottles of buffer, and different types of buffers or different types of solutions might be utilized, and the methods of use might vary. Also, depending upon the technique of the technician using the kit, it will be appreciated that different steps can performed in different order. 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.