Integrated testing devices with control vessel for fluid control

Abstract

An integrated testing device is described, for example for testing bodily fluids. The device has a test component, a reservoir containing a test fluid, and a control vessel. The reservoir discharges test fluid into the control vessel, which discharges the test fluid in a controlled way to the test component.

Claims

1. An integrated testing device comprising: a test component; a reservoir; and a fluid delivery actuator; the device further including a control vessel, and in operation the fluid delivery actuator causes a test fluid to be released from the reservoir into the control vessel, wherein the control vessel comprising one or more openings in its bottom wall and being positioned above the test component so as to provide a controlled volume discharge of test fluid directly onto the test component via the one or more openings.

2. An integrated testing device according to claim 1, wherein the control vessel is integrally formed with said device, and the reservoir and test component are formed separately.

3. An integrated testing device according to claim 1, wherein the control vessel and the reservoir are formed together as a separate component.

4. A testing device according to claim 3, wherein the reservoir and the control vessel are connected by a tube.

5. An integrated testing device according to claim 1, wherein the device further includes an interlock assembly so that operation of the interlock assembly causes the fluid delivery actuator to be inoperable until after a sample is delivered to the test component.

6. An integrated testing device according to claim 1, wherein the controlled volume discharge is controlled by the shape and disposition of one or more selected from the group consisting of the reservoir, the control vessel, the openings in the control vessel, and the fluid paths between and therefrom.

7. A testing device including a control vessel, and a test component, a test fluid being released from a separate or integral reservoir into the control vessel, the control vessel comprising one or more openings in its bottom wall and being positioned above the test component so as to provide a controlled volume discharge of test fluid directly onto the test component via one or more openings.

8. A testing device according to claim 7, wherein the device further includes an interlock assembly so that operation of the interlock assembly causes a fluid delivery actuator to be inoperable until after a sample is delivered to the test component, and the test fluid is discharged after the sample is delivered, such that the controlled volume discharge of test fluid reaches the test component after the sample is delivered to the test component.

9. A testing device according to claim 7, wherein the controlled volume discharge is controlled by the shape and disposition of one or more selected from the group consisting of the reservoir, the control vessel, the openings in the control vessel, and the fluid paths between and therefrom.

10. A testing device according to claim 7, wherein the control vessel and the reservoir are formed together as a separate component.

11. A testing device according to claim 10, wherein the reservoir and the control vessel are connected by a tube.

12. A testing device according to claim 7, wherein the control vessel is integrally formed with said device, and the reservoir and test component are formed separately.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Illustrative embodiments of the present invention will now be described with reference to the accompanying drawings, in which:

(2) FIG. 1 shows a perspective view of one implementation of the present invention;

(3) FIG. 2 is a longitudinal cross section a view of the implementation of FIG. 1;

(4) FIG. 3 is a more detailed cross sectional view;

(5) FIGS. 4A, 4B and 4C illustrate the operation of an interlock component in the implementation of FIG. 1;

(6) FIG. 5 is a plan view, with the cover removed, of the implementation of FIG. 1;

(7) FIGS. 6A and 6B are perspective views of one implementation of a fluid reservoir;

(8) FIGS. 7A, 7B and 7C illustrate in cross section the stages in discharge of test fluid; and

(9) FIGS. 8A and 8B illustrate an alternative reservoir with integral discharge vessel.

DETAILED DESCRIPTION OF THE INVENTION

(10) The present invention will be described with reference to a number of possible embodiments. It will be appreciated that the present invention is capable of being implemented in numerous ways, in addition to the examples provided. The embodiments are intended as illustrative, and are in no way limitative of the inventive concept or its possible implementations. Further, it will be understood that the features of different embodiments may be formed into different combinations, or added together, in order to provide further implementations of the present invention.

(11) The present invention is principally concerned with a specific aspect of the operation of a test device, relating to the discharge of a fluid which is intended to contact the test material. Accordingly, while specific examples of the remaining mechanical structures of a test unit will be provided and described, it will be understood that in principle the present invention can be used with any design of such a test unit. In particular, known test units, as well as those disclosed in the specifications incorporated by reference, may be modified so as to incorporate implementations of the present invention.

(12) FIGS. 1 and 2 illustrate one implementation of the present invention, in cross section in FIG. 2. The test unit 10 includes a cover 15, which includes a depressible section 26 for releasing the test fluid. The test fluid 41 is contained in a sachet 40. Test unit 10 further includes an arm 25 with a collection device 28 for a bodily fluid, in this case blood. Test unit 10 also has an opening 20 for a blood sample to be received, and an indicator opening 21, through which the result of the test can be seen.

(13) As will be described in more detail below, in use, the operator according to this embodiment operates lancet 30 to release blood from a suitable site on the body, for example a finger. In this implementation lancet 30 is integrated with the unit, although in other implementations it could be a separately supplied device. The user may need to milk the blood from the lanced site.

(14) Collection device 28 is placed onto the exuded blood, and withdraws (in this case by capillary action) a sample. Other sample collection arrangements may be used in alternative implementations, for example a non-integral suction or capillary device, or direct placement of the fluid onto the test material 60.

(15) After the collecting device is filled, the arm 25 may then be rotated (as will be described in more detail below) into a delivery position. The collection device is then in contact, via opening 20, with test material 60, and the sample is discharged onto test material 60.

(16) The user may then depress section 26, which applies pressure to sachet 40 so that the test fluid 41 is released. Test fluid 41 flows into vessel 50. Vessel 50 has one or more openings (not shown in these views) which allow test fluid 41 to discharge at a controlled rate onto test material 60.

(17) It is emphasised that the present invention can be applied to any kind of test, where the rate of test fluid needs to be controlled. In this case, the test is illustratively a lateral flow test. However, any other desired type of chromatographic or other test may be used. Similarly, the test fluid may be water, a buffer solution, or any other required fluid to conduct, support or be otherwise used in conjunction with the test.

(18) FIGS. 6A and 6B illustrate one implementation of the sachet 40, in this case as a structure formed in a similar way to a blister pack. Fluid is contained in the blister section 42. An outlet tube 43 is closed by a seal 44 with a reduced strength relative to the rest of the device, for example by having a thinner wall. Such a sachet may be manufactured using conventional blister pack technology.

(19) When force is applied by depressible section 26, the pressure in the blister increases, until the seal 44 fails, and the fluid id discharged through tube 43. In FIG. 6B, it can be seen that blister 42 is depressed, all the fluid is discharged, through the now open tube 43.

(20) The operation of the overall system, and its discharge, can be better understood from FIGS. 3 and 5. In FIG. 3, the sachet 40 with test fluid 41 can be seen, under the depressible portion 26. The arm 25 which carried the collection device 28 can also be seen. When the fluid discharges from the sachet 40, it is collected in vessel 50, via discharge conduit 52. Vessel 50 has an opening 51 in its bottom wall, which discharges directly onto area 61 of the test material 60. Region 62 marks the point where the bodily fluid would be deposited via opening 20, and so it can be seen that the discharged test fluid is deposited so as to allow the test fluid to meet the sample after it is deposited.

(21) It will be understood that the sachet or reservoir may be provided using any suitable technology, preferably including a referred failure direction for discharge under pressure. However, it will be appreciated that other release mechanisms, for example cutting or puncturing, could be used to release the fluid.

(22) FIGS. 4A, 4B and 4C illustrate the operation of an interlock, which in a preferred implementation for a blood application ensures that the test fluid is only discharged onto the test material after the blood sample is deposited. In FIG. 4A, cam 32 can be seen. As will be explained in more detail, the rotational position of cam 32 determines whether the fluid in the reservoir can be released.

(23) In FIG. 4A, the lancet 30 is in a rest position, and so no blood has yet been drawn. Projection 33 on depressible portion 26 is engaged by cam 32, and cannot move downwards. In FIG. 4B, the lancet has been engaged and operated, and has moved to a safe rest position 31. Blood can now be collected in collection device 28. Cam 32 still blocks projection 33.

(24) In FIG. 4C, arm 25 has been rotated, so that blood can be deposited onto the test material 60 via opening 20. Cam 32 has now rotated so that recess 34 is located adjacent projection 33, and the depressible portion 26 can now be moved downward, so as to exert pressure on the sachet and release the fluid (not shown in this view). Thus, cam 32 acts as an interlock to prevent premature release of the test fluid. It will be appreciated that other mechanical system could be used to achieve this. Examples of such mechanisms are provided in the aforementioned patent applications. In many cases, the timing of the delivery of the fluid is critical to a proper result, and premature release will invalidate the test.

(25) FIGS. 7A, 7B and 7C illustrate in more detail the sequence of test fluid discharge in the illustrative device. In FIG. 7A, the sachet 40 contains the test fluid 41 and has yet to be discharged by pressure from depressible portion 26. It can be seen that some of the fluid 41 is also in the tube section 44.

(26) In FIG. 7B, depressible portion 26 has been depressed, and test fluid 41 has been discharged (as illustrated by the arrow) into vessel 50. Vessel 50 is more or less directly engaged with test material 60. It will be appreciated that in other implementations, different fluid flow paths and geometry could be employed.

(27) In FIG. 7C, the test fluid 41 is discharging in a controlled way through opening 51 (not visible in this view) onto test component 60. Thus, test fluid 41 is discharged in a measured, controlled way onto test component 60 and not in an uncontained rush.

(28) It will be understood that while the fluid will discharge over time, it will not necessarily be at a constant rate. The rate will be determined in part by the sizes of the opening (or openings) in the vessel, as well as the absorption by the test material. Flow may slow as more or most of the fluid has left the vessel, for example.

(29) The fluid in the sachet may be any kind of fluid necessary or desired to perform or validate the test. It will be appreciated that the fluid may have different properties, for example density, viscosity and surface tension, and that appropriate changes to the sachet and frangible area may need to be made. The present invention is concerned with how the fluid is delivered, and is applicable to any desired fluid for use with a test.

(30) The test material may be, illustratively, a lateral flow test for a component of blood, electrolyte, blood sugar, cholesterol or any other blood component. It may adapted to detect specific biological or immunological responses, for example the presence of a pathogen or antibodies to a pathogen. Any kind of test on a body fluid which is suitable for this type of test unit can be used. The present invention is not specific to any type or form of test material, whether of lateral flow type or otherwise. Similarly, it is not constrained to blood, but could be applied to tests on any suitable bodily fluid, for example urine, interstitial fluid, faeces, or sputum, whether directly applied to the test unit or after pre-processing.

(31) It will be appreciated that the specific dimensions, shapes and parameters will need to be determined, in part by trial and error, for specific applications. The required volume of fluid will determine the size of the sachet. The properties of the specific fluid, and the required rate of flow will determine the size and nature of the outlets required in the vessel. The surface properties of the interaction between the specific fluid and the materials over which it will flow also need to be considered. For example, in an aqueous fluid, given the relatively high surface tension, smooth shapes are preferred over corners to ensure a smooth flow of the fluid. The detention vessel illustrated is contained wholly within the test unit, however, it will be appreciated that this could be partly open if desired. The required flow rate and volume are specific to the particular test material being used, and will generally be advised by the test material manufacturer.

(32) This implementation accordingly allows for the rate of delivery of a test fluid to be closely controlled. The fluid is first released into the detention vessel. The size, number, and shape of the outlets, as well as the shape of the vessel, will determine the rate (whether variable or constant) at which the fluid is released. For example, if the outlets are relatively small, the fluid will be released over a longer time period. The combination of controlling the volume of the fluid, and its fluid path, allows for relatively accurate control of the delivery of the fluid, and further ensures that it is delivered to the correct point on the test material.

(33) The present invention may be implemented in ways that do not incorporate all of the preferred features noted in relation to the example above. For instance, the sample of blood or other fluid could be placed directly into a suitable recess or opening in the test unit, without using the capillary or another mechanism. The buffer reservoir may not be integrated, but rather could be a separate bottle or sachet. The detention vessel in this instance would include an opening or passage for the entry of the fluid from the external container.

(34) The present invention includes within its scope a device in which all the fluid componentsthe reservoir, the vessel and any conduits between are integrally formed into a device. However, it is presently preferred, for reasons of practical manufacturing, that the reservoir be separately formed. This facilitates, for example, the sizing of different reservoirs or sachet for different test components, and the replacement during manufacture of these in tandem.

(35) Although a sachet has been described to retain the fluid, it will be appreciated that the present invention is by no means limited to such an arrangement. The sachet could be formed, for example, as a blister pack type unit, in a foil container, or in any other suitable way. The reservoir could be simply formed in the test unit, and filled during the process of manufacture. Another type of frangible container, which will open at a selected point under pressure or other stimulus, could be used. More than one fluid could be provided, either to be delivered at once, or sequentially, or in the alternative.

(36) FIGS. 8A and 8B illustrate an implementation in which the vessel is provided as part of the sachet unit. Unit 70 includes a reservoir 71, tube 72 and seal 73 similar to those in FIG. 6A. However, vessel 75 is also provided as part of the blister type structure, with an opening 74. It will be appreciated that this is shown upside down for illustrative purposes.

(37) Once the sachet is depressed, as shown in FIG. 8B, seal 73 fails and the test fluid passes into the vessel 75, where in operation it discharges in a controlled way onto the test material (not shown in this view). In this case, the test unit would not include an integrated reservoir, but rather have an appropriate recess for unit 70 under the depressible portion 26, so that opening 75 discharged directly onto the test component 60.

(38) It will be understood that the illustrative embodiments are only provided by way of example, and many other structures could be used to implement the invention, and in particular, the control vessel. These implementations will be necessarily varied in form and mechanism dependent upon the test system in which they are to be employed.