US20160069832A1

US20160069832A1 - Co-facial analytical test strip with stacked unidirectional contact pads

Info

Publication number: US20160069832A1
Application number: US14/939,135
Authority: US
Inventors: Scott Sloss; Russell Bain; Graeme WEBSTER
Original assignee: Cilag GmbH International
Current assignee: Cilag GmbH International
Priority date: 2012-03-02
Filing date: 2015-11-12
Publication date: 2016-03-10
Also published as: AU2013224918A1; WO2013128021A1; CN104160035A; CN104160035B; ES2623505T3; US9217723B2; IN2014DN07232A; CA2865458C; US20130228474A1; EP2820143B1; RU2014139824A; HK1205766A1; JP2015508900A; CA2865458A1; EP2820143A1; KR20140137410A; AU2013224918B2

Abstract

An analytical test strip (“ATT”) for use with a test meter includes a first insulating layer, with a first insulating layer upper surface, and a first electrically conductive layer (“ECL”) disposed thereon. The first ECL includes a first electrode portion (“EP”) and an electrical contact pad in electrical communication with the first EP. The ATT also includes a patterned spacer layer disposed above the first ECL that includes (i) a distal portion defining a bodily fluid sample-receiving chamber therein that overlies the first EP and (ii) an insulating proximal portion with a second ECL disposed thereon. The second ECL includes an interlayer contact portion and an electrical contact pad. A third ECL of the ATT includes a second EP and a proximal portion that overlies the interlayer contact portion. The second EP is disposed overlying and exposed to the sample-receiving chamber in an opposing relationship to the first EP.

Description

CROSS-REFERENCE

This DIVISIONAL application claims the benefits of priority under 35 USC §§120 and 121 from prior filed U.S. application Ser. No. 13/410,609 filed on Mar. 2, 2012, allowed, in which prior filed application is incorporated by reference in its entirety into this application.

BACKGROUND OF THE INVENTION

1. Field of the Invention
The present invention relates, in general, to medical devices and, in particular, to test meters and related methods.
2. Description of Related Art
The determination (e.g., detection and/or concentration measurement) of an analyte in a fluid sample is of particular interest in the medical field. For example, it can be desirable to determine glucose, ketone bodies, cholesterol, lipoproteins, triglycerides, acetaminophen and/or HbA1c concentrations in a sample of a bodily fluid such as urine, blood, plasma or interstitial fluid. Such determinations can be achieved using a hand-held test meter in combination with analytical test strips (e.g., electrochemical-based analytical test strips).

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings, in which like numerals indicate like elements, of which:

FIG. 1 is a simplified exploded perspective view of an analytical test strip according to an embodiment of the present invention;

FIG. 2 is a simplified perspective view of the analytical test strip of FIG. 1;

FIG. 3 is a simplified perspective view of a distal portion of the analytical test strip of FIG. 1 in contact with test meter electrical connector pins;

FIG. 4 is a simplified side view of the distal portion of FIG. 3;

FIG. 5 is a top view of a patterned spacer layer of the analytical test strip of FIG. 1;

FIG. 6 is a top view of a third electrically conductive layer of the analytical test strip of FIG. 1;

FIG. 7 is a simplified top view of the analytical test strip of claim 1 with an integrated carrier sheet;

FIG. 8 is a simplified distal end view of the analytical test strip and integrated carrier sheet of FIG. 5

FIG. 9 is a simplified cross-sectional view of the analytical test strip and integrated carrier sheet of FIG. 5; and

FIG. 10 is a flow diagram depicting stages in a method for determining an analyte in a bodily fluid sample according to an embodiment of the present invention.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

The following detailed description should be read with reference to the drawings, in which like elements in different drawings are identically numbered. The drawings, which are not necessarily to scale, depict exemplary embodiments for the purpose of explanation only and are not intended to limit the scope of the invention. The detailed description illustrates by way of example, not by way of limitation, the principles of the invention. This description will clearly enable one skilled in the art to make and use the invention, and describes several embodiments, adaptations, variations, alternatives and uses of the invention, including what is presently believed to be the best mode of carrying out the invention.
As used herein, the terms “about” or “approximately” for any numerical values or ranges indicate a suitable dimensional tolerance that allows the part or collection of components to function for its intended purpose as described herein.
In general, analytical test strips for use with a test meter (such as a hand-held test meter) according to embodiments of the present invention include a first insulating layer with a first insulating layer upper surface and a first electrically conductive layer disposed on the first insulating layer upper surface. The first electrically conductive layer includes a first electrode portion (such as a working electrode portion) and an electrical contact pad in electrical communication with the first electrode portion. The analytical test strips also include a patterned spacer layer disposed above the first electrically conductive layer. The patterned spacer layer includes (i) a distal portion defining a bodily fluid sample-receiving chamber therein that overlies the first electrode portion and (ii) an insulating proximal portion with an upper surface having a second electrically conductive layer disposed thereon. The second electrically conductive layer includes an interlayer contact portion and an electrical contact pad in electrical communication with the interlayer contact portion.
The analytical test strips further include a second insulating layer that is disposed above the patterned spacer layer and has a second insulating layer lower surface with a third electrically conductive layer disposed thereon. The third electrically conductive layer includes a second electrode portion (such as, for example, a reference/counter electrode) and a proximal portion that overlies the interlayer contact portion.
In addition, the second electrode portion of the analytical test strips is disposed overlying and exposed to the sample-receiving chamber in an opposing (i.e., co-facial) relationship to the first electrode portion. Moreover, the proximal portion is operatively juxtaposed with the interlayer contact portion such that there is an electrical connection between the second electrode portion of the third electrically conductive layer and the electrical contact pad of the patterned spacer layer during use of the analytical test strip.
The electrical contact pad of the first electrically conductive layer and the electrical contact pad of the second electrically conductive layer are referred to as stacked unidirectional contact pads. They are “stacked” since the electrical contact pad of the second electrically conductive layer is elevated with respect to the electrical contact pad of the first electrically conductive layer. They are “unidirectional” since both are on upper surfaces and can, therefore, be accessed and contacted from the same direction.
Analytical test strips according to the present invention are beneficial in that, for example, their configuration and, in particular, the stacked unidirectional nature of the contact pads, is amenable to high-volume, high-yield mass production without dedicated and complex tight-alignment die cutting steps to expose the contact pads.
FIG. 1 is a simplified exploded perspective view of an analytical test strip 100 according to an embodiment of the present invention. FIG. 2 is a simplified perspective view of the electrochemical-based analytical test strip of FIG. 1. FIG. 3 is a simplified perspective view of a portion of the electrochemical-based analytical test strip of FIG. 1 in contact with test meter electrical connector pins (ECP). FIG. 4 is a simplified side view of the portion of FIG. 3. FIG. 5 is a top view of a patterned spacer layer of the analytical test strip of FIG. 1. FIG. 6 is a top view of a third electrically conductive layer of the analytical test strip of FIG. 1.
Referring to FIGS. 1-6, analytical test strip 100 for use with a test meter in the determination of an analyte (such as glucose) in a bodily fluid sample (e.g., a whole blood sample) according to an embodiment of the present invention includes a first insulating layer 102 with a first insulating layer upper surface 104 and a first electrically conductive layer 106 disposed on first insulating upper surface 104. First electrically conductive layer 106 includes a first electrode portion 108 and an electrical contact pad 110 in electrical communication with first electrode portion 108.
Analytical test strip 100 also includes a patterned spacer layer 112 disposed above first electrically conductive layer 106. Patterned spacer layer 112 has a distal portion 114 defining a bodily fluid sample-receiving chamber 116 therein that overlies first electrode portion 108. Patterned spacer layer 112 also has an insulating proximal portion 118 with an upper surface 120 and a second electrically conductive layer 122 disposed thereon. Moreover, second electrically conductive layer 122 has an interlayer contact portion 124 and an electrical contact pad 126.
Analytical test strip 100 further includes a second insulating layer 128 disposed above patterned spacer layer 112. Second insulating layer 128 has a second insulating layer lower surface 130. Analytical test strip 100 yet further includes a third electrically conductive layer 132 disposed on second insulating layer lower surface 130 that includes a second electrode portion 134 and a proximal portion 136 that overlies interlayer contact portion 124. Second electrode portion 134 is disposed overlying and exposed to bodily fluid sample-receiving chamber 116 and in an opposing (i.e., co-facial) relationship to first electrode portion 108. Analytical test strip 100 also includes a reagent layer 138 (see FIG. 1 in particular).
In analytical test strip 100, the proximal portion of the third electrically conductive layer is operatively juxtaposed with the interlayer contact portion of the second electrically conductive layer such that there is an electrical connection between the second electrode portion of the third electrically conductive layer and the electrical contact pad of the patterned spacer layer during use of the analytical test strip. This electrical connection provides for unidirectional stacked electrical contact pads even though the first and second electrode portions are in an opposing (i.e., co-facial) arrangement.
The proximal portion of the third electrically conductive layer can be operatively juxtaposed with the inter layer contact portion by, for example, attachment with an electrically conductive adhesive or by compression of a gap therebetween (in the direction of arrow A of FIG. 4) upon insertion into the test meter. Such a compression can be achieved, for example, by the application of a force in the range of 3 pounds per square-inch to 30 pounds per square inch. The operative juxtaposition can be provided by any known means including an electrically fused joint or an electrically conductive foil connection.
Electrical contact pads 126 and 110 are each configured to operatively interface with a test meter via electrical contact with separate electrical connector pins (labeled ECP in FIGS. 3 and 4) of the test meter.
First insulating layer 102, insulating proximal portion 118, and second insulating layer 128 can be formed, for example, of a plastic (e.g., PET, PETG, polyimide, polycarbonate, polystyrene), silicon, ceramic, or glass material. For example, the first and second insulating layers can be formed from a 7 mil polyester substrate.
In the embodiment of FIGS. 1-6, first electrode portion 108 and second electrode portion 134 are configured to electrochemically determine analyte concentration in a bodily fluid sample (such as glucose in a whole blood sample) using any suitable electrochemical-based technique known to one skilled in the art.
The first, second and third electrically conductive layers, 106, 122 and 132 respectively, can be formed of any suitable conductive material such as, for example, gold, palladium, carbon, silver, platinum, tin oxide, iridium, indium, or combinations thereof (e.g., indium doped tin oxide). Moreover, any suitable technique can be employed to form the first, second and third conductive layers including, for example, sputtering, evaporation, electro-less plating, screen-printing, contact printing, or gravure printing. For example, first electrically conductive layer 106 can be a sputtered palladium layer and third electrically conductive layer 132 can be a sputtered gold layer.
Distal portion 114 of patterned spacer layer 112 serves to bind together first insulating layer 102 (with first electrically conductive layer 106 thereon) and second insulating layer 128 (with third electrically conductive layer 132 thereon), as illustrated in FIGS. 1, 2, 3 and 4. Patterned spacer layer 112 can be, for example, a double-sided pressure sensitive adhesive layer, a heat activated adhesive layer, or a thermo-setting adhesive plastic layer. Patterned spacer layer 112 can have, for example, a thickness in the range of from about 50 micron to about 300 microns, preferably between about 75 microns and about 150 microns. The overall length of analytical test strip 100 can be, for example, in the range of 30 mm to 50 mm and the width can be, for example, in the range of 2 mm to 5 mm.
Reagent layer 134 can be any suitable mixture of reagents that selectively react with an analyte such as, for example glucose, in a bodily fluid sample to form an electroactive species, which can then be quantitatively measured at an electrode of analyte test strips according to embodiments of the present invention. Therefore, reagent layer 138 can include at least a mediator and an enzyme. Examples of suitable mediators include ferricyanide, ferrocene, ferrocene derivatives, osmium bipyridyl complexes, and quinone derivatives. Examples of suitable enzymes include glucose oxidase, glucose dehydrogenase (GDH) using a pyrroloquinoline quinone (PQQ) co-factor, GDH using a nicotinamide adenine dinucleotide (NAD) co-factor, and GDH using a flavin adenine dinucleotide (FAD) co-factor. Reagent layer 134 can be formed using any suitable technique.
Referring to FIGS. 6, 7 and 8, if desired, analytical test strip 100 can further include at least one integrated carrier sheet configured solely as a user handle. In the embodiment of FIGS. 6-8, analytical test strip 100 includes a first integrated carrier sheet 140 and a second integrated carrier sheet 142. Moreover, a portion of the first insulating layer, first electrically conductive layer, patterned spacer layer, second insulating layer and second electrically conductive layer are disposed between first integrated carrier sheet 140 and second integrated carrier sheet1 142. First integrated carrier sheet 140 is configured such that the electrical contact pad of the first electrically conductive layer and the electrical contact pad of the patterned spacer layer are exposed. Such exposure enables electrical contact to a test meter during use.
The first and second integrated carrier sheets can be formed of any suitable material including, for example, paper, cardboard, or plastic materials. Since the first and second integrated carrier sheets are configured solely as a user handle in the present embodiments, they can be formed of relatively inexpensive materials.
FIG. 10 is a flow diagram depicting stages in a method 1000 for determining an analyte (such as glucose) in a bodily fluid sample (for example, a whole blood sample). Method 1000 includes introducing a bodily fluid sample into a sample-receiving chamber of an analytical test strip that has a first electrode portion of a first electrically conductive layer and a second electrode portion of a third electrically conductive layer therein (see step 1010 of FIG. 10). In addition, the first electrode portion and the second electrode portion are in an opposing relationship.
At step 1020 of method 1000, an electrical response of the first electrode portion and the second electrode portion is measured via an electrical contact pad of the first electrically conductive layer and via an electrical contact pad of a second electrically conductive layer of a patterned spacer layer of the analytical test strip. The patterned spacer layer is disposed between the first electrically conductive layer and the third electrically conductive layer. Furthermore, the electrical contact pad of the first electrically conductive layer and the second electrically conductive layer are configured in a unidirectional stacked relationship and the second electrode portion is in electrical communication with the electrical contact pad of the second electrically conductive layer.
Method 1000 also includes, at step 1030, determining the analyte based on the measured electrical response.
Once apprised of the present disclosure, one skilled in the art will recognize that method 1000 can be readily modified to incorporate any of the techniques, benefits and characteristics of analytical test strips according to embodiments of the present invention and described herein.
While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that devices and methods within the scope of these claims and their equivalents be covered thereby.

Claims

What is claimed is:

1. A method for determining an analyte in a bodily fluid sample, the method comprising:

introducing a bodily fluid sample into a sample-receiving chamber of an analytical test strip, the sample receiving chamber having a first electrode portion of a first electrically conductive layer and a second electrode portion of a third electrically conductive layer therein, the first electrode portion and the second electrode portion being in an opposing relationship;

measuring an electrical response of the first electrode portion and the second electrode portion via an electrical contact pad of the first electrically conductive layer and via an electrical contact pad of a second electrically conductive layer of a patterned spacer layer of the analytical test strip, the patterned spacer layer being disposed between the first electrically conductive layer and the third electrically conductive layer and

wherein the electrical contact pad of the first electrically conductive layer and the second electrically conductive layer are configured in a unidirectional stacked relationship, and

wherein the second electrode portion is in electrical communication with the electrical contact pad of the second electrically conductive layer; and

determining the analyte based on the measured electrical response.

2. The method of claim 1 wherein the analytical test strip is an electrochemical-based analytical test strip.

3. The method of claim 2 where the analyte is glucose.

4. The method of claim 2 wherein the bodily fluid sample is a whole blood sample.

5. The method of claim 1 wherein the analytical test strip includes at least one integrated carrier sheet configured solely as a user handle.

6. The method of claim 5 wherein the analytical test strip includes a first integrated carrier sheet and a second integrated carrier sheet.

7. The method of claim 6 wherein one of the first integrated carrier sheet and the second integrated carrier sheet is configured such that the electrical contact pad of the first electrically conductive layer and the electrical contact pad of the patterned conductor layer are exposed.

8. The method of claim 1 wherein the electrochemical-based analytical test strip is configured for the determination of an analyte in a bodily fluid sample.