The field of this invention is fluidic medical diagnostic devices for measuring the concentration of an analyte in or a property of a biological fluid.
A variety of medical diagnostic procedures involve tests on biological fluids, such as blood, urine, or saliva, and are based on a change in a physical characteristic of such a fluid or an element of the fluid, such as blood serum. The characteristic can be an electrical, magnetic, fluidic, or optical property. When an optical property is monitored, these procedures may make use of a transparent or translucent device to contain the biological fluid and a reagent. A change in light absorption of the fluid can be related to an analyte H concentration in, or property of, the fluid.
In many such devices, fluid is introduced into the device at one location but analyzed at another. In such devices, movement of the introduced fluid from the introduction location to the measurement location is necessary. As such, these devices require a means for moving fluid from the introduction site to the measurement site.
A variety of different design configurations have been developed to provide for this fluid movement. One type of device relies on capillary action to move fluid through the device, where the fluid paths through the device are dimensioned to provide for this capillary action. Other designs include those intended for use with gravity, those intended for use with injection of the sample under pressure, and the like.
In one class of fluidic test devices or strips that find use in various assay applications, fluid is moved through the device from the point of introduction by negative pressure, where the negative pressure is typically provided by a compressible bladder. Such devices include those described in U.S. Pat. No. 3,620,676; U.S. Pat. No. 3,640,267 and EP 0 803 288.
With these types of devices, there is a need to be able to actuate the bladder in a reproducible and uniform manner, such that errors in the assay are not introduced through variations in bladder volume through the compression and decompression cycle.
Relevant Literature
References of interest include: U.S. Pat. Nos. 3,620,676; 3,640,267; 4,088,448; 4,426,451; 4,868,129; 5,104,813; 5,230,866; 5,700,695; 5,736,404; 5,208,163; and European Patent Application EP 0 803 288.
Gimbaled bladder actuators and methods for their use in compressing bladders present on fluidic devices or test strips are provided. The actuators are characterized by the presence of a gimbaled compression pad under movement control of an actuating means, preferably an automated actuating means. Also provided are meters for reading test strips that include bladders, where the meters include the subject gimbaled bladder actuators.
Gimbaled bladder actuators and methods for their use in compressing bladders present on test strips are provided. The subject actuators are characterized by the presence of a gimbaled compression pad under movement control of an actuating means, preferably an automated actuating means. Also provided are meters for reading bladder including test strips, where the meters include the subject gimbaled bladder actuating devices. In further describing the subject invention, the subject gimbaled bladder actuators are described first in greater detail, followed by a description of the test strip/meter systems with which the subject gimbaled bladder actuator find use, as well as methods for using the same.
Before the subject invention is described further, it is to be understood that the invention is not limited to the particular embodiments of the invention described below, as variations of the particular embodiments may be made and still fall within the scope of the appended claims. It is also to be understood that the terminology employed is for the purpose of describing particular embodiments, and is not intended to be limiting. Instead, the scope of the present invention will be established by the appended claims.
In this specification and the appended claims, singular references include the plural, unless the context clearly dictates otherwise. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood to one of ordinary skill in the art to which this invention belongs.
As summarized above, the subject invention provides bladder compressing devices or actuators that find use in compressing bladders on fluidic devices or test strips that include bladders. In further describing the subject devices, the subject bladder actuators will be described first in general terms, followed by a detailed discussion of a representative actuator in terms of the figures.
A feature of the subject bladder compressing devices or actuators is that they include a gimbaled compression pad. As such, the subject bladder actuators are gimbaled bladder actuators. By gimbaled compression pad is meant a planar compression element that is suspended from a holder in a manner such that the planar compression element becomes parallel to the surface it contacts during actuation. By planar compression element is meant a rigid piece having a substantially planar surface. The view normal to the planar surface of this element may have varying area configurations, including circular, square, rectangular, trapezoidal, oval, triangular, irregular, etc., and in many embodiments is selected so as to contact substantially all of the upper surface of a bladder of a test strip or fluidic device with which the gimbaled bladder actuator is employed. The actual area of the planar surface may vary, but is generally at least about 0.008 square inches, usually at least about 0.15 square inches and more usually at least about 0.2 square inches, where the actual area may be as great as 0.4 square inches or greater, but generally does not exceed about 0.6 square inches and usually does not exceed about 0.8 square inches. In certain embodiments, the actual area ranges from about 0.15 to 0.25 square inches, usually from about 0.19 to 0.21 square inches.
The gimbaled compression pad is characterized by being capable of applying uniform pressure to the bladder upon actuation. By uniform pressure is meant that the pressure applied by the planar compression element at any two different locations on the bladder that is contacted by the compression element is substantially the same or identical. Where there is pressure variance, the magnitude of the variance at any two given locations typically does not exceed about 18 lbs per square inch, usually does not exceed about 7 lbs per square inch and more usually does not exceed about 2 lbs per square inches. The amount of force applied by the gimbaled pad to the bladder during use typically ranges in many embodiments from about 0.25 to 10, usually from about 0.5 to 5 and more usually from about 1.0 to 1.5 lbs.
Also present in the subject bladder compressing devices is an actuating means for actuating or moving the gimbaled compression pad onto and off of a bladder of present on a test strip. In principal, any convenient actuating means may be employed that is capable of contacting the gimbaled compression pad against the bladder surface in a manner that applies substantially uniform pressure across the bladder surface, as described supra. Thus, the actuation means may be manual or automatic. Manual actuation means may simply be a compression button that can be pushed by an operator to achieve contact of the gimbaled compression pad and the bladder surface. In many preferred embodiments, the actuation means is an automated actuation means that is capable of contacting the bladder surface with the gimbaled compression pad in a reproducible manner.
While any convenient automated actuation means may be employed, one convenient automated actuation means includes the following elements: (i) a lever arm; (ii) a chassis; and (iii) a solenoid. In this representative automated actuation means, at one end of the lever arm the gimbaled compression pad (i.e. the planar compression element and the holder) is attached. The lever arm is such that it is capable of holding the gimbaled compression pad over, the bladder such that, upon actuation, the gimbaled compression pad contacts the bladder in a manner sufficient to compress the bladder, as described supra. The other end of the lever arm is connected to a chassis or analogous element. The length of the lever arm generally ranges from about 0.3 inches to 0.4 inches, usually from about 0.345 inches to 0.355 inches.
The chassis or analogous element provides for operative communication between the lever arm and the solenoid. The chassis may have any convenient configuration, where a representative configuration is provided in the figures, described infra.
Connected to the chassis is a solenoid actuator which is capable of moving the lever arm and therefore the gimbaled compression pad in the desired manner upon actuation. The solenoid is generally a dual action solenoid capable of moving the gimbaled compression pad in two directions: a first direction onto the bladder and a second direction off of the bladder. Generally, the solenoid is under the control of a solenoid actuation means, where the means may be manual (i.e. may actuate the solenoid following direct input from a human user) or automated (i.e. may automatically actuate the solenoid following detection of an event by a sensor in a device, such as a sample placement detecting sensor).
Turning now to the figures,
FIG. 7A and
Systems
The above described gimbaled bladder compressing devices or actuators find use in systems made up of test strips and meters, as described in greater detail below.
Test Strips
The test strips with which the subject gimbaled bladder actuators find use are fluidic devices that generally include a sample application area; a bladder, to create a suction force to draw the sample into the device; a measurement area, in which the sample may undergo a change in an optical parameter, such as light scattering; and a stop junction to precisely stop flow after filling the measurement area. Preferably, the test strip is substantially transparent over the measurement area, so that the area can be illuminated by a light source on one side and the transmitted light measured on the opposite side.
A representative test strip with which the subject gimbaled bladder actuators find use is shown in
As shown in
As shown in
The test strip pictured in FIG. 2 and described above is preferably formed by laminating thermoplastic sheets 26 and 28 to a thermoplastic intermediate layer 24 that has adhesive on both of its surfaces. The cutouts that form the elements shown in
Other fluidic device configurations are also possible, where such alternative device configurations include those that have: (a) a bypass channel; (b) multiple parallel measurement areas; and/or (c) multiple in series measurement areas; etc. In addition, the above described laminated structures can be adapted to injection molded structures. A variety of alternative fluidic devices with which the subject gimbaled bladder compressing devices may find use are described in co-pending application Ser. Nos. 09/333,765, filed Jun. 15, 1999; and Ser. No. 09/356,248, filed Jul. 16, 1999, the disclosures of which are herein incorporated by reference.
Meters
The subject gimbaled bladder actuators find use in meters, generally automated meters, that are designed for use with the above described test strips. A representative meter is depicted in
Methods of Use
The above described test strip/meter systems that include the subject gimbaled bladder actuators are suitable for use in a variety of analytical tests of biological fluids, such as determining biochemical or hematological characteristics, or measuring the concentration in such fluids of analytes such as proteins, hormones, carbohydrates, lipids, drugs, toxins, gases, electrolytes, etc. The procedures for performing these tests have been described in the literature. Among the tests, and where they are described, are the following: (1) Chromogenic Factor XIIa Assay (and other clotting factors as well): Rand, M. D. et al., Blood, 88, 3432 (1996); (2) Factor X Assay: Bick, R. L. Disorders of Thrombosis and Hemostasis: Clinical and Laboratory Practice. Chicago, ASCP Press, 1992; (3) DRVVT (Dilute Russells Viper Venom Test): Exner, T. et al., Blood Coag. Fibrinol, 1, 259 (1990); (4) Immunonephelometric and Immunoturbidimetric Assays for Proteins: Whicher, J. T., CRC Crit. Rev. Clin Lab Sci. 18:213 (1983); (5) TPA Assay: Mann, K. G., et al., Blood, 76, 755, (1990); and Hartshorn, J. N. et al., Blood, 78, 833 (1991); (6) APTT (Activated Partial Thromboplastin Time Assay): Proctor, R. R. and Rapaport, S. I. Amer. J. Clin. Path, 36, 212 (1961); Brandt, J. T. and Triplett, D. A. Amer. J. Clin. Path., 76, 530 (1981); and Kelsey, P. R. Thromb. Haemost. 52, 172 (1984); (7) HbAlc Assay (Glycosylated Hemoglobin Assay): Nicol, D. J. et al., Clin. Chem. 29, 1694 (1983); (8) Total Hemoglobin: Schneck et al., Clinical Chem., 32/33, 526 (1986); and U.S. Pat. No. 4,088,448; (9) Factor Xa: Vinazzer, H., Proc. Symp. Dtsch. Ges. Klin. Chem., 203 (1977), ed. By Witt, I; (10) Colorimetric Assay for Nitric Oxide: Schmidt, H. H., et al., Biochemica, 2, 22 (1995).
The above described test strip/meter systems are particularly well suited for measuring blood-clotting time—“prothrombin time” or “PT time,” as more fully described in U.S. Pat. No. 6,521,182, filed Jun. 15, 1999; and U.S. Pat. No. 6,261,519, filed Jul. 16, 1999; the disclosures of which are herein incorporated by reference. The modifications needed to adapt the device for applications such as those listed above require no more than routine experimentation.
In using the above systems that include the subject gimbaled bladder actuator, the first step the user performs is to turn on the meter, thereby energizing strip detector 40, sample detector 42, measurement system 44, and optional heater 46. The second step is to insert the strip. Preferably, the strip is not transparent over at least a part of its area, so that an inserted strip will block the illumination by LED 40a of detector 40b. (More preferably, the intermediate layer is formed of a non-transparent material, so that background light does not enter measurement system 44.) Detector 40b thereby senses that a strip has been inserted and triggers gimbaled bladder actuator 48 to compress bladder 14. A meter display 50 then directs the user to apply a sample to sample port 12 as the third and last step the user must perform to initiate the measurement sequence. The empty sample port is reflective. When a sample is introduced into the sample port, it absorbs light from LED 42a and thereby reduces the light that is reflected to detector 42b. That reduction in light, in turn, signals gimbaled bladder actuator 48 to release bladder 14. The resultant suction in channel 16 draws sample through measurement area 18 to stop junction 22. Light from LED 44a passes through measurement area 18, and detector 44b monitors the light transmitted through the sample as it is clotting. Analysis of the transmitted light as a function of time (as described below) permits a calculation of the PT time, which is displayed on the meter display 50. Preferably, sample temperature is maintained at about 39° C. by heater 46.
As described above, the detector senses a sample in sample port 12, simply by detecting a reduction in (specular) reflection of a light signal that is emitted by 42a and detected by 42b. However, that simple system cannot easily distinguish between a whole blood sample and some other liquid (e.g., blood serum) placed in the sample port in error or, even, an object (e.g., a finger) that can approach sample port 12 and cause the system to erroneously conclude that a proper sample has been applied. To avoid this type of error, another embodiment measures diffuse reflection from the sample port. This embodiment appears in
It is evident from the above results and discussion that the subject invention provides a means for applying uniform and reproducible bladder compression and decompression in test strips that include bladders. As such, the subject devices provide for the elimination of a source of error in analytical assays using such test strips. As such, the subject invention represents a significant contribution to the art.
All publications and patents cited in this specification are herein incorporated by reference as if each individual publication or patent were specifically and individually indicated to be incorporated by reference. The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention.
Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.
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