This invention relates to analytical sensors for the detection of bioanalytes in a small volume sample, and methods of making and using the sensors.
Analytical sensors are useful in chemistry and medicine to determine the presence and concentration of a biological analyte. Such sensors are needed, for example, to monitor glucose in diabetic patients and lactate during critical care events.
Currently available technology measures bioanalytes in relatively large sample volumes, e.g., generally requiring 3 microliters or more of blood or other biological fluid. These fluid samples are obtained from a patient, for example, using a needle and syringe, or by lancing a portion of the skin such as the fingertip and “milking” the area to obtain a useful sample volume. These procedures are inconvenient for the patient, and often painful, particularly when frequent samples are required. Less painful methods for obtaining a sample are known such as lancing the arm or thigh, which have a lower nerve ending density. However, lancing the body in the preferred regions typically produces submicroliter samples of blood, because these regions are not heavily supplied with near-surface capillary vessels.
It would therefore be desirable and very useful to develop a relatively painless, easy to use blood analyte sensor, capable of performing an accurate and sensitive analysis of the concentration of analytes in a small volume of sample.
It would also be desirable to develop methods for manufacturing small volume electrochemical sensors capable of decreasing the errors that arise from the size of the sensor and the sample.
The sensors of the present invention provide a method for the detection and quantification of an analyte. In general, the invention includes a method and sensor for analysis of an analyte in a sample, e.g., a small volume sample, by, for example, coulometry, amperometry and/or potentiometry. A sensor of the invention may utilize a non-leachable or diffusible electron transfer agent and/or a redox mediator. The sensor also includes a sample chamber to hold the sample in electrolytic contact with the working electrode.
In one embodiment, the working electrode faces a counter electrode, forming a measurement zone within the sample chamber, between the two electrodes, that is sized to contain no more than about 1 μL of sample, e.g., no more than about 0.5 μL, e.g., no more than about 0.32 μL, e.g., no more than about 0.25 μL, e.g., no more than about 0.1 μL of sample.
In one embodiment of the invention, a sensor, configured for insertion into an electronic meter, is provided with a working electrode and a counter electrode, and a conductive insertion monitor which provides electrical contact with the electronic meter if the sensor is properly inserted into the meter. The conductive insertion monitor is configured and arranged to close an electrical circuit when the sensor is properly inserted into the electronic connector.
In another embodiment of the invention, a sensor is provided with a plurality of contacts, each contact having a contact pad, which is a region for connection with an electronic meter. The plurality of contacts and contact pads are on a substrate having a length and a width, and each contact pad has a contact pad width taken parallel to the width of the substrate. The sum of the contact pad widths is greater than the width of the substrate. In one embodiment, six electrical connections are made with six contact pads on the sensor but in a width that is approximately the width of four contact pads. For example, a working electrode, three counter electrodes (e.g., one counter electrode and two indicator electrodes), and two insertion trace connections each have a contact pad; connection can be made to each of these six contact pads in the same width of the contact pads of the working electrode and three counter electrodes.
The present invention also includes an electrical connector, for providing electrical contact between a sensor and an electrical meter or other device. The electrical connector has a plurality of contact structures, each which has a proximal contact end for electrical connection to a sensor contact, and a distal end for electrical connection to the electrical device. In one embodiment, a plurality of first contact structures extend longitudinally parallel from the distal to the proximal end. Additionally, one or more second contract structures extend longitudinally next to the first contact structures, from the distal end past the proximal end of the first contact structures, and angle toward a longitudinal center line of the connector. Contact to the sensor is then made via the proximal contact ends.
In some embodiments, the electrical connector has at least two second contact structures extending longitudinally past the proximal end of the first contact structures and angling toward the longitudinal center line of the connector. After the angled or bent portion, the proximal contact ends of the second contact structures of one embodiment make electrical contact with a single conductive surface of a sensor, such as a conductive insertion monitor. In another aspect, the first contact structures can be configured and arranged to contact one or more working and/or counter electrodes of a sensor, and the second contact structures are configured and arranged to contact one or more conductive insertion monitors.
The sensors of the present invention can be configured for side-filling or tip-filling. In addition, in some embodiments, the sensor may be part of an integrated sample acquisition and analyte measurement device. The integrated sample acquisition and analyte measurement device can include the sensor and a skin piercing member, so that the device can be used to pierce the skin of a user to cause flow of a fluid sample, such as blood, that can then be collected by the sensor. In at least some embodiments, the fluid sample can be collected without moving the integrated sample acquisition and analyte measurement device.
In one embodiment, the sensor is connected with an electrical device, to provide a processor coupled to the sensor. The processor is configured and arranged to determine, during electrolysis of a sample in the sample chamber, a series of current values. The processor determines a peak current value from the series of current values. After the current values decrease below a threshold fraction of the peak current values, slope values are determined from the current values and represent a linear function of the logarithm of current values over time. The processor determines, from the slope values, an extrapolation slope. From the extrapolated slope and the measured current values, the processor determines an amount of charge needed to electrolyze the sample and, from that amount of charge, the concentration of the analyte in the sample.
One method of forming a sensor, as described above, includes forming at least one working electrode on a first substrate and forming at least one counter or counter/reference electrode on a second substrate. A spacer layer is disposed on either the first or second substrates. The spacer layer defines a chamber into which a sample can be drawn and held when the sensor is completed. A redox mediator and/or second electron transfer agent can be disposed on the first or second substrate in a region that will be exposed within the sample chamber when the sensor is completed. The first and second substrates are then brought together and spaced apart by the spacer layer with the sample chamber providing access to the at least one working electrode and the at least one counter or counter/reference electrode. In some embodiments, the first and second substrates are portions of a single sheet or continuous web of material. The invention includes particularly efficient and reliable methods for the manufacture of these sensors.
One such efficient and reliable method includes providing an adhesive having first and second surfaces covered with first and second release liners and then making detailed cuts through the first release liner and the adhesive but not through the second release liner. These cuts define one or more sample chamber regions. A portion of the first release liner is removed to expose a portion of the first adhesive surface, which leaves a remaining portion of the first release liner over the sample chamber regions. This exposed first adhesive surface is applied to a first substrate having one or more conductive traces disposed thereon. The second release liner is removed together with the adhesive and the first release liner of the sample chamber regions in order to expose the second adhesive surface. The second adhesive surface is then applied to a second substrate having one or more conductive traces disposed thereon. This method forms a sensor having a sample chamber corresponding to one of the sample chamber regions.
These and various other features which characterize the invention are pointed out with particularity in the attached claims. For a better understanding of the invention, its advantages, and objectives obtained by its use, reference should be made to the drawings and to the accompanying description, in which there is illustrated and described preferred embodiments of the invention.
Referring now to the drawings, wherein like reference numerals and letters indicate corresponding structure throughout the several views:
As used herein, the following definitions define the stated term:
“Amperometry” includes steady-state amperometry, chronoamperometry, and Cottrell-type measurements.
A “biological fluid” is any body fluid in which the analyte can be measured, for example, blood (which includes whole blood and its cell-free components, such as, plasma and serum), interstitial fluid, dermal fluid, sweat, tears, urine and saliva.
“Coulometry” is the determination of charge passed or projected to pass during complete or nearly complete electrolysis of the analyte, either directly on the electrode or through one or more electron transfer agents. The charge is determined by measurement of charge passed during partial or nearly complete electrolysis of the analyte or, more often, by multiple measurements during the electrolysis of a decaying current and elapsed time. The decaying current results from the decline in the concentration of the electrolyzed species caused by the electrolysis.
A “counter electrode” refers to one or more electrodes paired with the working electrode, through which passes an electrochemical current equal in magnitude and opposite in sign to the current passed through the working electrode. The term “counter electrode” is meant to include counter electrodes which also function as reference electrodes (i.e. a counter/reference electrode) unless the description provides that a “counter electrode” excludes a reference or counter/reference electrode.
An “electrochemical sensor” is a device configured to detect the presence of and/or measure the concentration of an analyte via electrochemical oxidation and reduction reactions. These reactions are transduced to an electrical signal that can be correlated to an amount or concentration of analyte.
“Electrolysis” is the electrooxidation or electroreduction of a compound either directly at an electrode or via one or more electron transfer agents (e.g., redox mediators and/or enzymes).
The term “facing electrodes” refers to a configuration of the working and counter electrodes in which the working surface of the working electrode is disposed in approximate opposition to a surface of the counter electrode. In at least some instances, the distance between the working and counter electrodes is less than the width of the working surface of the working electrode.
An “indicator electrode” or “fill indicator electrode” is an electrode that detects partial or complete filling of a sample chamber and/or measurement zone with sample.
A “layer” is one or more layers.
The “measurement zone” is defined herein as a region of the sample chamber sized to contain only that portion of the sample that is to be interrogated during an analyte assay.
A “non-diffusible,” “non-leachable,” or “non-releasable” compound is a compound which does not substantially diffuse away from the working surface of the working electrode for the duration of the analyte assay.
A “redox mediator” is an electron transfer agent for carrying electrons between the analyte and the working electrode, either directly or through another electron transfer agent.
A “reference electrode” includes a reference electrode that also functions as a counter electrode (i.e., a counter/reference electrode) unless the description provides that a “reference electrode” excludes a counter/reference electrode.
A “working electrode” is an electrode at which analyte is electrooxidized or electroreduced with or without the agency of a redox mediator.
Referring to the Drawings in general and
Sensor Strips
Referring to
The dimensions of a sensor may vary. In certain embodiments, the overall length of sensor strip 10, 10′ may be no less than about 20 mm and no greater than about 50 mm. For example, the length may be between about 30 and 45 mm; e.g., about 30 to 40 mm. It is understood, however that shorter and longer sensor strips 10, 10′ could be made. In certain embodiments, the overall width of sensor strip 10, 10′ may be no less than about 3 mm and no greater than about 15 mm. For example, the width may be between about 4 and 10 mm, about 5 to 8 mm, or about 5 to 6 mm. In one particular example, sensor strip 10, 10′ has a length of about 32 mm and a width of about 6 mm. In another particular example, sensor strip 10, 10′ has a length of about 40 mm and a width of about 5 mm. In yet another particular example, sensor strip 10, 10′ has a length of about 34 mm and a width of about 5 mm.
Substrates
As provided above, sensor strip 10, 10′ has first and second substrates 12, 14, non-conducting, inert substrates which form the overall shape and size of sensor strip 10, 10′. Substrates 12, 14 may be substantially rigid or substantially flexible. In certain embodiments, substrates 12, 14 are flexible or deformable. Examples of suitable materials for substrates 12, 14 include, but are not limited, to polyester, polyethylene, polycarbonate, polypropylene, nylon, and other “plastics” or polymers. In certain embodiments the substrate material is “Melinex” polyester. Other non-conducting materials may also be used.
Spacer Layer
As indicated above, positioned between substrate 12 and substrate 14 can be spacer 15 to separate first substrate 12 from second substrate 14. Spacer 15 is an inert non-conducting substrate, typically at least as flexible and deformable (or as rigid) as substrates 12, 14. In certain embodiments, spacer 15 is an adhesive layer or double-sided adhesive tape or film. Any adhesive selected for spacer 15 should be selected to not diffuse or release material which may interfere with accurate analyte measurement.
In certain embodiments, the thickness of spacer 15 may be at least about 0.01 mm (10 μm) and no greater than about 1 mm or about 0.5 mm. For example, the thickness may be between about 0.02 mm (20 μm) and about 0.2 mm (200 μm). In one certain embodiment, the thickness is about 0.05 mm (50 μm), and about 0.1 mm (100 μm) in another embodiment.
Sample Chamber
The sensor includes a sample chamber for receiving a volume of sample to be analyzed; in the embodiment illustrated, particularly in
Sample chamber 20 is configured so that when a sample is provided in chamber 20, the sample is in electrolytic contact with both the working electrode and the counter electrode, which allows electrical current to flow between the electrodes to effect the electrolysis (electrooxidation or electroreduction) of the analyte.
Sample chamber 20 is defined by substrate 12, substrate 14 and spacer 15; in many embodiments, sample chamber 20 exists between substrate 12 and substrate 14 where spacer 15 is not present. Typically, a portion of spacer 15 is removed to provide an area between substrates 12, 14 without spacer 15; this volume of removed spacer is sample chamber 20. For embodiments that include spacer 15 between substrates 12, 14, the thickness of sample chamber 20 is generally the thickness of spacer 15.
Sample chamber 20 has a volume sufficient to receive a sample of biological fluid therein. In some embodiments, such as when sensor strip 10, 10′ is a small volume sensor, sample chamber 20 has a volume that is preferably no more than about 1 μL, for example no more than about 0.5 μL, and also for example, no more than about 0.25 μL. A volume of no more than about 0.1 μL is also suitable for sample chamber 20, as are volumes of no more than about 0.05 μL and about 0.03 μL.
A measurement zone is contained within sample chamber 20 and is the region of the sample chamber that contains only that portion of the sample that is interrogated during the analyte assay. In some designs, the measurement zone has a volume that is approximately equal to the volume of sample chamber 20. In some embodiments the measurement zone includes 80% of the sample chamber, 90% in other embodiments, and about 100% in yet other embodiments.
As provided above, the thickness of sample chamber 20 corresponds typically to the thickness of spacer 15. Particularly for facing electrode configurations, this thickness is small to promote rapid electrolysis of the analyte, as more of the sample will be in contact with the electrode surface for a given sample volume. In addition, a thin sample chamber 20 helps to reduce errors from diffusion of analyte into the measurement zone from other portions of the sample chamber during the analyte assay, because diffusion time is long relative to the measurement time, which may be about 5 seconds or less.
Electrodes
As provided above, the sensor includes a working electrode and at least one counter electrode. The counter electrode may be a counter/reference electrode. If multiple counter electrodes are present, one of the counter electrodes will be a counter electrode and one or more may be reference electrodes. Referring to
Working Electrode
At least one working electrode is positioned on one of first substrate 12 and second substrate 14. In all of
Working electrode 22 can be a layer of conductive material such as gold, carbon, platinum, ruthenium dioxide, palladium, or other non-corroding, conducting material. Working electrode 22 can be a combination of two or more conductive materials. An example of a suitable conductive epoxy is ECCOCOAT CT5079-3 Carbon-Filled Conductive Epoxy Coating (available from W.R. Grace Company, Woburn, Mass.). The material of working electrode 22 typically has relatively low electrical resistance and is typically electrochemically inert over the potential range of the sensor during operation.
Working electrode 22 may be applied on substrate 12 by any of various methods, including by being deposited, such as by vapor deposition or vacuum deposition or otherwise sputtered, printed on a flat surface or in an embossed or otherwise recessed surface, transferred from a separate carrier or liner, etched, or molded. Suitable methods of printing include screen-printing, piezoelectric printing, ink jet printing, laser printing, photolithography, and painting.
As provided above, at least a portion of working electrode 22 is provided in sample chamber 20 for the analysis of analyte, in conjunction with the counter electrode.
Counter Electrode
The sensor includes at least one counter electrode positioned within the sample chamber. In
Counter electrode 24 may be constructed in a manner similar to working electrode 22. Suitable materials for the counter/reference or reference electrode include Ag/AgCl or Ag/AgBr on a non-conducting base material or silver chloride on a silver metal base. The same materials and methods may be used for counter electrode 24 as are available for working electrode 22, although different materials and methods may also be used. Counter electrode 24 can include a mix of multiple conducting materials, such as Ag/AgCl and carbon.
Electrode Configurations
Working electrode 22 and counter electrode 24 may be disposed opposite to and facing each other to form facing electrodes. See for example,
Working electrode 22 and counter electrode 24 can alternately be disposed generally planar to one another, such as on the same substrate, to form co-planar or planar electrodes. Referring to
Sensing Chemistry
In addition to working electrode 22, sensing chemistry material(s) are preferably provided in sample chamber 20 for the analysis of the analyte. Sensing chemistry material facilitates the transfer of electrons between working electrode 22 and the analyte in the sample. Any sensing chemistry may be used in sensor strip 10, 10′; the sensing chemistry may include one or more materials.
The sensing chemistry can be diffusible or leachable, or non-diffusible or non-leachable. For purposes of discussion herein, the term “diffusible” will be used to represent “diffusible or leachable” and the term “non-diffusible” will be used to represent “non-diffusible or non-leachable” and variations thereof. Placement of sensing chemistry components may depend on whether they are diffusible or not. For example, both non-diffusible and/or diffusible component(s) may form a sensing layer on working electrode 22. Alternatively, one or more diffusible components may be present on any surface in sample chamber 20 prior to the introduction of the sample to be analyzed. As another example, one or more diffusible component(s) may be placed in the sample prior to introduction of the sample into sample chamber 20.
Electron Transfer Agent
The sensing chemistry generally includes an electron transfer agent that facilitates the transfer of electrons to or from the analyte. The electron transfer agent may be diffusible or non-diffusible, and may be present on working electrode 22 as a layer. One example of a suitable electron transfer agent is an enzyme which catalyzes a reaction of the analyte. For example, a glucose oxidase or glucose dehydrogenase, such as pyrroloquinoline quinone glucose dehydrogenase (PQQ), is used when the analyte is glucose. Other enzymes can be used for other analytes.
The electron transfer agent, whether it is diffusible or not, facilitates a current between working electrode 22 and the analyte and enables the electrochemical analysis of molecules. The agent facilitates the transfer electrons between the electrode and the analyte.
Redox Mediator
This sensing chemistry may, additionally to or alternatively to the electron transfer agent, include a redox mediator. Certain embodiments use a redox mediator that is a transition metal compound or complex. Examples of suitable transition metal compounds or complexes include osmium, ruthenium, iron, and cobalt compounds or complexes. In these complexes, the transition metal is coordinatively bound to one or more ligands, which are typically mono-, di-, tri-, or tetradentate. The redox mediator can be a polymeric redox mediator, or, a redox polymer (i.e., a polymer having one or more redox species). Examples of suitable redox mediators and redox polymer are disclosed in U.S. Pat. No. 6,338,790, for example, and in U.S. Pat. Nos. 6,605,200 and 6,605,201.
If the redox mediator is non-diffusible, then the redox mediator may be disposed on working electrode 22 as a layer. In an embodiment having a redox mediator and an electron transfer agent, if the redox mediator and electron transfer agent are both non-leachable, then both components are disposed on working electrode 22 as individual layers, or combined and applied as a single layer.
The redox mediator, whether it is diffusible or not, mediates a current between working electrode 22 and the analyte and enables the electrochemical analysis of molecules which may not be suited for direct electrochemical reaction on an electrode. The mediator functions as an agent to transfer electrons between the electrode and the analyte.
Sorbent Material
Sample chamber 20 can be empty before the sample is placed in the chamber, or, in some embodiments, the sample chamber can include a sorbent material to sorb and hold a fluid sample during the measurement process. The sorbent material facilitates the uptake of small volume samples by a wicking action which can complement or, e.g., replace any capillary action of the sample chamber. Suitable sorbent materials include polyester, nylon, cellulose, and cellulose derivatives such as nitrocellulose. In addition to or alternatively, a portion or the entirety of the wall of the sample chamber may be coated by a surfactant, which is intended to lower the surface tension of the fluid sample and improve fluid flow within the sample chamber.
Methods other than the wicking action of a sorbent can be used to transport the sample into the sample chamber or measurement zone. Examples of such methods for transport include the application of pressure on a sample to push it into the sample chamber, the creation of a vacuum by a pump or other vacuum-producing method in the sample chamber to pull the sample into the chamber, capillary action due to interfacial tension of the sample with the walls of a thin sample chamber, as well as the wicking action of a sorbent material.
Fill Indicator Electrode
In some instances, it is desirable to be able to determine when the sample chamber is filled. Sensor strip 10, 10′ can be indicated as filled, or substantially filled, by observing a signal between an indicator electrode and one or both of working electrode 22 or counter electrode 24 as sample chamber 20 fills with fluid. When fluid reaches the indicator electrode, the signal from that electrode will change. Suitable signals for observing include, for example, voltage, current, resistance, impedance, or capacitance between the indicator electrode and, for example, working electrode 22. Alternatively, the sensor can be observed after filling to determine if a value of the signal (e.g., voltage, current, resistance, impedance, or capacitance) has been reached indicating that the sample chamber is filled.
Typically, the indicator electrode is further downstream from a sample inlet, such as inlet 21, than working electrode 22 and counter electrode 24.
For side-fill sensors, an indicator electrode can be present on each side of the counter electrode. This permits the user to fill the sample chamber from either the left or right side with an indicator electrode disposed further upstream. This three-electrode configuration is not necessary. Side-fill sensors can also have a single indicator electrode and may include some indication as to which side should be placed in contact with the sample fluid.
The indicator electrode can also be used to improve the precision of the analyte measurements. The indicator electrode may operate as a working electrode or as a counter electrode or counter/reference electrode. Measurements from the indicator electrode/working electrode can be combined (for example, added or averaged) with those from the first counter/reference electrode/working electrode to obtain more accurate measurements.
The sensor or equipment that the sensor connected is with (e.g., a meter) can include a sign (e.g., a visual sign or auditory signal) that is activated in response to the indicator electrode to alert the user that the measurement zone has been filled. The sensor or equipment can be configured to initiate a reading when the indicator electrode indicates that the measurement zone has been filled with or without alerting the user. The reading can be initiated, for example, by applying a potential between the working electrode and the counter electrode and beginning to monitor the signals generated at the working electrode.
Insertion Monitor
In accordance with this invention, the sensor includes an indicator to notify when proper insertion of sensor strip 10, 10′ into receiving equipment, such as a meter, has occurred. As seen in
Insertion monitor 30 is used to encode information regarding sensor strip 10, 10′. The encoded information can be, for example, calibration information for that manufacturing lot or for that specific strip. Such calibration information or code may relate to, e.g., the sensitivity of the strip or to the y-intercept and/or slope of its calibration curve. The calibration code is used by the meter or other equipment to which sensor strip 10, 10′ is connected to provide an accurate analyte reading. For example, based on the calibration code, the meter uses one of several programs stored within the meter.
In some embodiments, a value indicative of the calibration code is manually entered into the meter or other equipment, for example, by the user. In other embodiments, the calibration code is directly read by the meter or other equipment, thus not requiring input or other interaction by the user.
In one embodiment, illustrated, for example in
The calibration code can be designed into insertion monitor 30, for example, either by the resistance or other electrical characteristic of insertion monitor 30, by the placement or position of insertion monitor 30, or by the shape or configuration of insertion monitor 30.
Insertion monitor 30 may alternately or additionally carry other information regarding the sensor strip 10, 10′. This other information that could be encoded into insertion monitor 30 include the test time needed for accurate analyte concentration analysis, expiration date of the sensor strip 10, 10′, various correction factors, such as for environmental temperature and/or pressure, selection of the analyte to be analyzed (e.g., glucose, ketone, lactate), and the like.
The resistance of insertion monitor 30, such as that of single stripe 130 or area or of a conductive path between the two or more contact pads, is related to the encoded information. As an example of discrete calibration values, resistance values in a given range can correspond to one calibration setting, and resistance values in a different range can correspond to a different calibration setting. Thus, when a meter or other equipment receives a sensor strip, indicator monitor 30 will notify the meter or equipment which assay calculation to use.
In addition to varying the resistance of indicator monitor 30 by varying the conductive or semi-conductive material used, the resistance of indicator monitor 30 can be varied by cutting or scoring some or all of the conductive pathways so that they do not carry charge. The resistance can additionally or alternately be controlled by the width or length of the conductive path. An example of a material suitable for indicator monitor 30 is a combination of carbon and silver; the resistance of this mixture will vary, based on the ratio of the two materials.
The placement or position of insertion monitor 30 can additionally or alternately be related to the encoded calibration information. For example, the calibration code can be directly related to the location of indicator monitor 30. For example, the position of indicator monitor 30 can be varied so that is makes electrical contact with different contact structures. (Contact structures are described below in “Sensor Connection to Electrical Device”). Depending on the contact structures engaged, the meter will recognize the calibration code and thus know what parameter to use to calculate an accurate analyte level.
The shape and/or configuration of insertion monitor 30 can additionally or alternatively be related to the encoded calibration code. For example, the calibration code can be directed related to which and/or the number of contact structures that make electrical contact with indicator monitor 30. For example, a pattern of discrete and unconnected indicator monitors can be present on the sensor; the calibration code will be directly related to the arrangement of those monitors. The pattern could be parallel lines, orderly arranged dots or squares, or the like.
While it is preferred to provide this encoded information on the insertion monitor, it should be recognized that the insertion monitor function and the encoding of information can also be implemented separately using separate conductive traces on the strip.
Conductive insertion monitor 30 is positioned on the non-conductive base substrate and has a contact pad for electrical contact with a connector. Insertion monitor 30 is configured and arranged to close an electrical circuit when sensor 10, 10′ is properly inserted into the connector.
Insertion monitor 30 may have any suitable configuration, including but not limited to, a stripe extending across sensor strip 10, 10′ from a side edge to a side edge, such as stripe 130, a stripe extending across the sensor strip, although not the entire width, and an array of unconnected dots, strips, or other areas. Other suitable configurations for insertion monitor 30 are illustrated in
Sensor Connection to Electrical Device
Referring to
Sensor strip 100 is configured to couple to a meter or other electrical device by electrical connector 500 which is configured to couple with and contact the end of sensor 100 at contact pads 123, 124, 125, 126. The sensor meter typically includes a potentiostat or other component to provide a potential and/or current for the electrodes of the sensor. The sensor reader also typically includes a processor (e.g., a microprocessor or hardware) for determining analyte concentration from the sensor signals. The sensor meter also includes a display or a port for coupling a display to the sensor. The display displays the sensor signals and/or results determined from the sensor signals including, for example, analyte concentration, rate of change of analyte concentration, and/or the exceeding of a threshold analyte concentration (indicating, for example, hypo- or hyperglycemia).
One example of a suitable connector is shown in
Leads 223, 224, 225, 226, have proximal ends to physically contact pads 123, 124, 125, 126, respectively, and to connect to any attached meter. Each pad 123, 124, 125, 126 has its respective lead 223, 224, 225, 226. The end of sensor 100 having the contact pads can be slid into or mated with connector 500 by placing sensor 100 into slide area 530, which provides a support for and retains sensor 100. It is typically important that the contact structures of the connector 500 make electrical contact with the correct pads of the sensor so that the working electrode and counter electrode(s) are correctly coupled to the meter.
Connector 500 includes leads or contact structures 51, 52 for connection to insertion monitor 30. Insertion monitor 30 is configured and arranged to close an electrical circuit between contact structures 51 and 52 when the sensor is properly inserted into the connector. Proper insertion into connector 500 means that the sensor strip 100 is inserted right side up, that the correct end of strip 100 is inserted into connector 500, and that sensor strip 100 is inserted far enough into connector 500 that reliable electrical connections are made between the electrode contact pads 123, 124, 125, 126 and the corresponding contacts leads 223, 224, 225, 226. Preferably, no closed circuit is made unless all electrode pads have properly contacted the contact structures of connector 500. The insertion monitor may have shapes other than a stripe across the width of the sensor; for example, other designs include an individual dot, a grid pattern, or may include stylistic features, such as words or letters.
Because this insertion monitor 30 is not at the end with the contact regions for the electrodes, the insertion monitor 30 does not require additional width space on the sensor. The width of the contact pads 123, 124, 125, 126 is defined as the width on which a lead could be placed that would result in an electrical connection; typically, the contact width is the width of the exposed contact area. In one embodiment, six contact lead structures on the connector (e.g., 52, 223, 224, 225, 226, 51) can contact sensor 100 in the same width as the four contact pads (e.g., 123, 124, 125, 126). This concept of having contact points on the sensor that occupy more width than the width of the sensor may be used for any number of contact points; this may be used with or without an insertion monitor 30.
As a particular example, four leads 223, 224, 225, 226 make contact with contact pads 123, 124, 125, 126. If each lead and/or contact pad is one millimeter wide, a sensor of at least 4 mm wide is needed to make contact. Additional leads, such as those for insertion monitor 30 (i.e., contact leads 51, 52), can make contact by having leads 51, 52 extend along the side of leads 223, 226 and then angle in toward the center of strip 100 after the point where leads 223, 224, 225, 226 contact strip 100. The insertion monitor leads 51, 52 cross side edges of sensor 100 to make contact with the sensor, thus not requiring additional sensor width.
The contact structures are generally parallel and non-overlapping. The lead structures 223, 224, 225, 226 terminate in close proximity to the proximal end of sensor strip 100 (e.g., on contact pads 123, 124, 125, 126), but lead structures 51, 52 continue longitudinally past the proximal end of lead structures 223, 224, 225, 226 further toward the distal end of sensor strip 100. Once past the proximal end and past lead structures 223, 224, 225, 226, lead structures 51, 52 angle in toward the center of the sensor strip.
In an optional embodiment to ensure proper insertion of a sensor into a meter, the meter may include a raised area or bump that prevents or hinders the insertion of the sensor in an improper direction. Objects other than a raised area can also be used to guide the user in correct introduction of the sensor into the meter.
General Method for Manufacturing Sensors
Referring now to
In
Carbon or other electrode material (e.g., metal, such as gold or platinum) is formed on substrate 1000 to provide a working electrode 22 for each sensor. The carbon or other electrode material can be deposited by a variety of methods including printing a carbon or metal ink, vapor deposition, and other methods. The printing may be done by screen printing, gravure roll printing, transfer printing, and other known printing methods. The respective trace and contact pad 23 could be applied together with working electrode 22, but may be applied in a subsequent step.
Similar to the working electrode 22, counter electrode 24 is formed on substrate 1000. The counter electrode(s) are formed by providing carbon or other conductive electrode material onto substrate 1000. In one embodiment, the material used for the counter electrode(s) is a Ag/AgCl ink. The material of the counter electrode(s) may be deposited by a variety of methods including printing or vapor deposition. The printing may be done by screen printing, gravure roll printing, transfer printing, and other known printing methods. The respective trace and contact pad 25 could be applied together with counter electrodes 24, but may be applied in a subsequent step.
Preferably, multiple sensors 10 are manufactured simultaneously; that is, the working electrodes, including their traces and contact pads, for a plurality of sensors are produced (e.g., printed) on a polymer sheet or web, and simultaneously or subsequently, the counter electrodes, and their traces and contact pads, for a plurality of sensors are produced (e.g., printed). The working electrode(s) and counter electrode(s) can be formed on separate substrates that are later positioned opposite one another so that the electrodes face each other. Alternately, to simplify registration of the substrates, the working electrodes can be formed on a first half of a substrate sheet of web and the counter electrodes are formed on a second half of the substrate sheet or web so that the sheet or web can be folded to superimpose the working and counter electrodes in a facing arrangement.
To provide sample chamber 20, spacer 15 is formed over at least one of the substrate/working electrode and substrate/counter electrode(s). Spacer 15 can be an adhesive spacer, such as a single layer of adhesive or a double-sided adhesive tape (e.g., a polymer carrier film with adhesive disposed on opposing surfaces). Suitable spacer materials include adhesives such as urethanes, acrylates, acrylics, latexes, rubbers and the like.
A channel, which will result in the sample chamber, is provided in spacer 15, either by cutting out a portion of the adhesive spacer or placing two adhesive pieces in close proximity but having a gap therebetween. The adhesive can be printed or otherwise disposed on the substrate according to a pattern which defines the channel region. The adhesive spacer can be optionally provided with one or more release liners prior to its incorporation into the sensor. The adhesive can be cut (e.g., die-cut or slit) to remove the portion of the adhesive corresponding to the channel prior to disposing the spacer on the substrate.
Any sensing chemistry is disposed onto the substrate in at least the sample chamber regions. If any of the sensing chemistry component(s) is non-leachable, that component is preferably disposed on the working electrode. If any of the sensing chemistry component(s) is diffusible, that component can be disposed on any surface of the substrate in the channel region. The redox mediator and/or electrode transfer agent can be disposed independently or together on the substrate prior to or after placement of the spacer. The redox mediator and/or electrode transfer agent may be applied by a variety of methods including, for example, screen printing, ink jet printing, spraying, painting, striping along a row or column of aligned and/or adjacent electrodes, and the like. Other components can be deposited separately or together with the redox mediator and/or electrode transfer agent; these components can include, for example, surfactants, polymers, polymer films, preservatives, binders, buffers, and cross-linkers.
After disposing the spacer, redox mediator, second electron transfer agent, sensing layers, and the like, the first and second substrates (having the working and counter electrodes thereon) are positioned opposite each other to form the sensor. The faces of the substrate are joined by the adhesive of the spacer. After bringing the faces together, individual sensors can be cut out from the web of sensors using a variety of methods including, for example, die cutting, slitting, or otherwise cutting away the excess substrate material and separating the individual sensors. In some embodiments, a combination of cutting or slitting methods is used. As another alternative, the individual sensor components can first be cut out of the substrates and then brought together to form the sensor by adhesively joining the two components, such as by using the spacer adhesive.
The sides of the sensor can be straight to allow the sensor to be cut out from the remainder of the substrate and/or from other sensors by slitting the substrate in parallel directions using, for example, a gang arbor blade system. The edges of the sensor can define edges of the sample chamber and/or measurement zone. By accurately controlling the distance between cuts, variability in sample chamber volume can often be reduced. In some instances, these cuts are parallel to each other, as parallel cuts are typically the easiest to reproduce.
Application of the Sensor
A common use for the analyte sensor of the present invention, such as sensor strip 10, 10′, 100 is for the determination of analyte concentration in a biological fluid, such as glucose concentration in blood, interstitial fluid, and the like, in a patient or other user. Sensor strips 10, 10′, 100 may be available at pharmacies, hospitals, clinics, from doctors, and other sources of medical devices. Multiple sensor strips 10, 10′, 100 may be packaged together and sold as a single unit; e.g., a package of 25, 50, or 100 strips.
Sensor strips 10, 10′, 100 can be used for an electrochemical assay, or, for a photometric test. Sensor strips 10, 10′, 100 are generally configured for use with an electrical meter, which may be connectable to various electronics. A meter may be available at generally the same locations as sensor strips 10, 10′, 100 and sometimes may be packaged together with sensor strips 10, 10′, 100, e.g., as a kit.
Examples of suitable electronics connectable to the meter include a data processing terminal, such as a personal computer (PC), a portable computer such as a laptop or a handheld device (e.g., personal digital assistants (PDAs)), and the like. The electronics are configured for data communication with the receiver via a wired or a wireless connection. Additionally, the electronics may further be connected to a data network (not shown) for storing, retrieving and updating data corresponding to the detected glucose level of the user.
The various devices connected to the meter may wirelessly communicate with a server device, e.g., using a common standard such as 802.11 or Bluetooth RF protocol, or an IrDA infrared protocol. The server device could be another portable device, such as a Personal Digital Assistant (PDA) or notebook computer, or a larger device such as a desktop computer, appliance, etc. In some embodiments, the server device does have a display, such as a liquid crystal display (LCD), as well as an input device, such as buttons, a keyboard, mouse or touch-screen. With such an arrangement, the user can control the meter indirectly by interacting with the user interface(s) of the server device, which in turn interacts with the meter across a wireless link.
The server device can also communicate with another device, such as for sending glucose data from the meter and/or the service device to a data storage or computer. For example, the service device could send and/or receive instructions (e.g., an insulin pump protocol) from a health care provider computer. Examples of such communications include a PDA synching data with a personal computer (PC), a mobile phone communicating over a cellular network with a computer at the other end, or a household appliance communicating with a computer system at a physician's office.
A lancing device or other mechanism to obtain a sample of biological fluid, e.g., blood, from the patient or user may also be available at generally the same locations as sensor strips 10 and the meter, and sometimes may be packaged together with sensor strips 10 and/or meter, e.g., as a kit.
Integrated Sample Acquisition and Analyte Measurement Device
An analyte measurement device constructed according to the principles of the present invention typically includes a sensor strip 10, 10′, 100, as described hereinabove, combined with a sample acquisition apparatus to provide an integrated sampling and measurement device. The sample acquisition apparatus typically includes, for example, a skin piercing member, such as a lancet, that can be injected into a patient's skin to cause blood flow. The integrated sample acquisition and analyte measurement device can comprise a lancing instrument that holds a lancet and sensor strip 10, 10′, 100. The lancing instrument might require active cocking. By requiring the user to cock the device prior to use, the risk of inadvertently triggering the lancet is minimized. The lancing instrument could also permit the user to adjust the depth of penetration of the lancet into the skin. Such devices are commercially available from companies such as Boehringer Mannheim and Palco. This feature allows users to adjust the lancing device for differences in skin thickness, skin durability, and pain sensitivity across different sites on the body and across different users.
In one embodiment, the lancing instrument and the meter are integrated into a single device. To operate the device the user need only insert a disposable cartridge containing a sensor strip and lancing device into the integrated device, cock the lancing instrument, press it against the skin to activate it, and read the result of the measurement. Such an integrated lancing instrument and test reader simplifies the testing procedure for the user and minimizes the handling of body fluids.
In some embodiments, sensor strips 10, 10′ may be integrated with both a meter and a lancing device. Having multiple elements together in one device reduces the number of devices needed to obtain an analyte level and facilitates the sampling process.
For example, embodiments may include a housing that includes one or more of the subject strips, a skin piercing element and a processor for determining the concentration of an analyte in a sample applied to the strip. A plurality of strips 10, 10′, 100 may be retained in a cassette in the housing interior and, upon actuation by a user, a single strip 10, 10′ may be dispensed from the cassette so that at least a portion extends out of the housing for use.
Operation of the Sensor Strip
In use, a sample of biological fluid is provided into the sample chamber of the sensor, where the level of analyte is determined. The analysis may be based on providing an electrochemical assay or a photometric assay. In many embodiments, it is the level of glucose in blood that is determined. Also in many embodiments, the source of the biological fluid is a drop of blood drawn from a patient, e.g., after piercing the patient's skin with a lancing device, which could be present in an integrated device, together with the sensor strip.
The analyte in the sample is, e.g., electrooxidized or electroreduced, at working electrode 22, and the level of current obtained at counter electrode 24 is correlated as analyte concentration.
Sensor strip 10, 10′, 100 may be operated with or without applying a potential to electrodes 22, 24. In one embodiment, the electrochemical reaction occurs spontaneously and a potential need not be applied between working electrode 22 and counter electrode 24. In another embodiment, a potential is applied between working electrode 22 and counter electrode 24.
The invention has been described with reference to various specific and preferred embodiments and techniques. However, it will be apparent to one of ordinarily skill in the art that many variations and modifications may be made while remaining within the spirit and scope of the invention.
All patents and other references in this specification are indicative of the level of ordinary skill in the art to which this invention pertains. All patents are herein incorporated by reference to the same extent as if each individual patent was specifically and individually incorporated by reference.
This application is a continuation of U.S. Ser. No. 11/281,883, filed Nov. 17, 2005, which is a continuation-in-part of U.S. Ser. No. 10/866,477, filed Jun. 12, 2004 now abandoned, which is a continuation of U.S. Ser. No. 10/033,575, filed Dec. 28, 2001, issued as U.S. Pat. No. 6,749,740, which is a continuation of U.S. Ser. No. 09/434,026, filed Nov. 4, 1999, issued as U.S. Pat. No. 6,616,819, the entire disclosures of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3260656 | Ross, Jr. | Jul 1966 | A |
3653841 | Klein | Apr 1972 | A |
3719564 | Lilly, Jr. et al. | Mar 1973 | A |
3776832 | Oswin et al. | Dec 1973 | A |
3837339 | Aisenberg et al. | Sep 1974 | A |
3972320 | Kalman | Aug 1976 | A |
3979274 | Newman | Sep 1976 | A |
4008717 | Kowarski | Feb 1977 | A |
4016866 | Lawton | Apr 1977 | A |
4055175 | Clemens et al. | Oct 1977 | A |
4059406 | Fleet | Nov 1977 | A |
4076596 | Connery et al. | Feb 1978 | A |
4098574 | Dappen | Jul 1978 | A |
4100048 | Pompei et al. | Jul 1978 | A |
4151845 | Clemens | May 1979 | A |
4168205 | Danninger et al. | Sep 1979 | A |
4172770 | Semersky et al. | Oct 1979 | A |
4178916 | McNamara | Dec 1979 | A |
4206755 | Klein | Jun 1980 | A |
4224125 | Nakamura et al. | Sep 1980 | A |
4240438 | Updike et al. | Dec 1980 | A |
4240889 | Yoda et al. | Dec 1980 | A |
4247297 | Berti et al. | Jan 1981 | A |
4271119 | Columbus | Jun 1981 | A |
4318784 | Higgins et al. | Mar 1982 | A |
4340458 | Lerner et al. | Jul 1982 | A |
4356074 | Johnson | Oct 1982 | A |
4365637 | Johnson | Dec 1982 | A |
4366033 | Richter et al. | Dec 1982 | A |
4375399 | Havas et al. | Mar 1983 | A |
4384586 | Christiansen | May 1983 | A |
4392933 | Nakamura et al. | Jul 1983 | A |
4401122 | Clark, Jr. | Aug 1983 | A |
4404066 | Johnson | Sep 1983 | A |
4407959 | Tsuji et al. | Oct 1983 | A |
4418148 | Oberhardt | Nov 1983 | A |
4420564 | Tsuji et al. | Dec 1983 | A |
4427770 | Chen et al. | Jan 1984 | A |
4431004 | Bessman et al. | Feb 1984 | A |
4436094 | Cerami | Mar 1984 | A |
4440175 | Wilkins | Apr 1984 | A |
4444892 | Malmros | Apr 1984 | A |
4450842 | Zick et al. | May 1984 | A |
4461691 | Frank | Jul 1984 | A |
4469110 | Slama | Sep 1984 | A |
4477314 | Richter et al. | Oct 1984 | A |
4483924 | Tsuji et al. | Nov 1984 | A |
4484987 | Gough | Nov 1984 | A |
4522690 | Venkatasetty | Jun 1985 | A |
4524114 | Samuels et al. | Jun 1985 | A |
4526661 | Steckhan et al. | Jul 1985 | A |
4534356 | Papadakis | Aug 1985 | A |
4538616 | Rogoff | Sep 1985 | A |
4543955 | Schroeppel | Oct 1985 | A |
4545382 | Higgins et al. | Oct 1985 | A |
4552840 | Riffer | Nov 1985 | A |
4560534 | Kung et al. | Dec 1985 | A |
4571292 | Liu et al. | Feb 1986 | A |
4573994 | Fischell et al. | Mar 1986 | A |
4580564 | Andersen | Apr 1986 | A |
4581336 | Malloy et al. | Apr 1986 | A |
4595011 | Phillips | Jun 1986 | A |
4595479 | Kimura et al. | Jun 1986 | A |
4619754 | Niki et al. | Oct 1986 | A |
4633878 | Bombardieri | Jan 1987 | A |
4637403 | Garcia et al. | Jan 1987 | A |
4650547 | Gough | Mar 1987 | A |
4654127 | Baker et al. | Mar 1987 | A |
4654197 | Lilja et al. | Mar 1987 | A |
4655880 | Liu | Apr 1987 | A |
4655885 | Hill et al. | Apr 1987 | A |
4671288 | Gough | Jun 1987 | A |
4679562 | Luksha | Jul 1987 | A |
4680268 | Clark, Jr. | Jul 1987 | A |
4682602 | Prohaska | Jul 1987 | A |
4684537 | Graetzel et al. | Aug 1987 | A |
4685463 | Williams | Aug 1987 | A |
4703756 | Gough et al. | Nov 1987 | A |
4711245 | Higgins et al. | Dec 1987 | A |
4714874 | Morris et al. | Dec 1987 | A |
4717673 | Wrighton et al. | Jan 1988 | A |
4721601 | Wrighton et al. | Jan 1988 | A |
4726378 | Kaplan | Feb 1988 | A |
4750496 | Reinhart et al. | Jun 1988 | A |
4757022 | Shults et al. | Jul 1988 | A |
4758323 | Davis et al. | Jul 1988 | A |
4759371 | Franetzki | Jul 1988 | A |
4759828 | Young et al. | Jul 1988 | A |
4764416 | Ueyama et al. | Aug 1988 | A |
4776944 | Janata et al. | Oct 1988 | A |
4781798 | Gough | Nov 1988 | A |
4784736 | Lonsdale et al. | Nov 1988 | A |
4795707 | Niiyama et al. | Jan 1989 | A |
4805624 | Yao et al. | Feb 1989 | A |
4813424 | Wilkins | Mar 1989 | A |
4815469 | Cohen et al. | Mar 1989 | A |
4820399 | Senda et al. | Apr 1989 | A |
4822337 | Newhouse et al. | Apr 1989 | A |
4830959 | McNeil et al. | May 1989 | A |
4832797 | Vadgama et al. | May 1989 | A |
4840893 | Hill et al. | Jun 1989 | A |
4848351 | Finch | Jul 1989 | A |
4854153 | Miyagawa et al. | Aug 1989 | A |
4871351 | Feingold | Oct 1989 | A |
4871440 | Nagata et al. | Oct 1989 | A |
4890620 | Gough | Jan 1990 | A |
4894137 | Takizawa et al. | Jan 1990 | A |
4895147 | Bodicky et al. | Jan 1990 | A |
4897162 | Lewandowski et al. | Jan 1990 | A |
4897173 | Nankai et al. | Jan 1990 | A |
4909908 | Ross et al. | Mar 1990 | A |
4911794 | Parce et al. | Mar 1990 | A |
4919141 | Zier et al. | Apr 1990 | A |
4919767 | Vadgama et al. | Apr 1990 | A |
4923586 | Katayama et al. | May 1990 | A |
4927516 | Yamaguchi et al. | May 1990 | A |
4935105 | Churchouse | Jun 1990 | A |
4935345 | Guilbeau et al. | Jun 1990 | A |
4936956 | Wrighton | Jun 1990 | A |
4938860 | Wogoman | Jul 1990 | A |
4942127 | Wada et al. | Jul 1990 | A |
4945045 | Forrest et al. | Jul 1990 | A |
4950378 | Nagata | Aug 1990 | A |
4953552 | DeMarzo | Sep 1990 | A |
4954087 | Lauks et al. | Sep 1990 | A |
4968400 | Shimomura et al. | Nov 1990 | A |
4970145 | Bennetto et al. | Nov 1990 | A |
4974929 | Curry | Dec 1990 | A |
4986271 | Wilkins | Jan 1991 | A |
4994167 | Shults et al. | Feb 1991 | A |
4999582 | Parks et al. | Mar 1991 | A |
5026388 | Ingalz | Jun 1991 | A |
5034192 | Wrighton et al. | Jul 1991 | A |
5037527 | Hayashi et al. | Aug 1991 | A |
5053199 | Keiser et al. | Oct 1991 | A |
5070535 | Hochmair et al. | Dec 1991 | A |
5078854 | Burgess et al. | Jan 1992 | A |
5082550 | Rishpon et al. | Jan 1992 | A |
5082786 | Nakamoto | Jan 1992 | A |
5089112 | Skotheim et al. | Feb 1992 | A |
5094951 | Rosenberg | Mar 1992 | A |
5096560 | Takai et al. | Mar 1992 | A |
5096836 | Macho et al. | Mar 1992 | A |
5101814 | Palti | Apr 1992 | A |
5108564 | Szuminsky et al. | Apr 1992 | A |
5109850 | Blanco et al. | May 1992 | A |
5120420 | Nankai et al. | Jun 1992 | A |
5120421 | Glass et al. | Jun 1992 | A |
5126034 | Carter et al. | Jun 1992 | A |
5126247 | Palmer et al. | Jun 1992 | A |
5128015 | Szuminsky et al. | Jul 1992 | A |
5130009 | Marsoner et al. | Jul 1992 | A |
5133856 | Yamaguchi et al. | Jul 1992 | A |
5140393 | Hijikihigawa et al. | Aug 1992 | A |
5141868 | Shanks et al. | Aug 1992 | A |
5160278 | Johnson | Nov 1992 | A |
5161532 | Joseph | Nov 1992 | A |
5165407 | Wilson et al. | Nov 1992 | A |
5168046 | Hamamoto et al. | Dec 1992 | A |
5174291 | Schoonen et al. | Dec 1992 | A |
5185256 | Nankai et al. | Feb 1993 | A |
5192415 | Yoshioka et al. | Mar 1993 | A |
5192416 | Wang et al. | Mar 1993 | A |
5198367 | Aizawa et al. | Mar 1993 | A |
5200051 | Cozzette et al. | Apr 1993 | A |
5201324 | Swierczek | Apr 1993 | A |
5202261 | Musho et al. | Apr 1993 | A |
5205920 | Oyama et al. | Apr 1993 | A |
5206145 | Cattell | Apr 1993 | A |
5208154 | Weaver et al. | May 1993 | A |
5217595 | Smith et al. | Jun 1993 | A |
5227042 | Zawodzinski et al. | Jul 1993 | A |
5229282 | Yoshioka et al. | Jul 1993 | A |
5250439 | Musho et al. | Oct 1993 | A |
5262035 | Gregg et al. | Nov 1993 | A |
5262305 | Heller et al. | Nov 1993 | A |
5264103 | Yoshioka et al. | Nov 1993 | A |
5264106 | McAleer et al. | Nov 1993 | A |
5266179 | Nankai et al. | Nov 1993 | A |
5271815 | Wong | Dec 1993 | A |
5272060 | Hamamoto et al. | Dec 1993 | A |
5278079 | Gubinski et al. | Jan 1994 | A |
5282950 | Dietze et al. | Feb 1994 | A |
5286362 | Hoenes et al. | Feb 1994 | A |
5286364 | Yacynych et al. | Feb 1994 | A |
5288636 | Pollmann et al. | Feb 1994 | A |
5293546 | Tadros et al. | Mar 1994 | A |
5310885 | Maier et al. | May 1994 | A |
5320725 | Gregg et al. | Jun 1994 | A |
5320732 | Nankai et al. | Jun 1994 | A |
5326449 | Cunningham | Jul 1994 | A |
5337747 | Neftel | Aug 1994 | A |
5352348 | Young et al. | Oct 1994 | A |
5352351 | White et al. | Oct 1994 | A |
5356786 | Heller et al. | Oct 1994 | A |
5364797 | Olson et al. | Nov 1994 | A |
5366609 | White et al. | Nov 1994 | A |
5368028 | Palti | Nov 1994 | A |
5372133 | Hogen Esch | Dec 1994 | A |
5378628 | Gratzel et al. | Jan 1995 | A |
5380422 | Negishi et al. | Jan 1995 | A |
5382346 | Uenoyama et al. | Jan 1995 | A |
5384028 | Ito | Jan 1995 | A |
5387327 | Khan | Feb 1995 | A |
5390671 | Lord et al. | Feb 1995 | A |
5391250 | Cheney, II et al. | Feb 1995 | A |
5393903 | Gratzel et al. | Feb 1995 | A |
5395504 | Saurer et al. | Mar 1995 | A |
5410474 | Fox | Apr 1995 | A |
5411647 | Johnson et al. | May 1995 | A |
5413690 | Kost et al. | May 1995 | A |
5422246 | Koopal et al. | Jun 1995 | A |
5435735 | Wittig et al. | Jul 1995 | A |
5437973 | Vadgama et al. | Aug 1995 | A |
5437999 | Diebold et al. | Aug 1995 | A |
5438271 | White et al. | Aug 1995 | A |
5478751 | Oosta et al. | Dec 1995 | A |
5494562 | Maley et al. | Feb 1996 | A |
5496453 | Uenoyama et al. | Mar 1996 | A |
5497772 | Schulman et al. | Mar 1996 | A |
5501956 | Wada et al. | Mar 1996 | A |
5502396 | Desarzens et al. | Mar 1996 | A |
5507288 | Bocker et al. | Apr 1996 | A |
5508171 | Walling et al. | Apr 1996 | A |
5514253 | Davis et al. | May 1996 | A |
5520787 | Hanagan et al. | May 1996 | A |
5525511 | D'Costa | Jun 1996 | A |
5526120 | Jina et al. | Jun 1996 | A |
5531878 | Vadgama et al. | Jul 1996 | A |
5552027 | Birkle et al. | Sep 1996 | A |
5556524 | Albers | Sep 1996 | A |
5565085 | Ikeda et al. | Oct 1996 | A |
5567302 | Song et al. | Oct 1996 | A |
5568806 | Cheney, II et al. | Oct 1996 | A |
5569186 | Lord et al. | Oct 1996 | A |
5571132 | Mawhirt et al. | Nov 1996 | A |
5575895 | Ikeda et al. | Nov 1996 | A |
5580527 | Bell et al. | Dec 1996 | A |
5582184 | Erickson et al. | Dec 1996 | A |
5582697 | Ikeda et al. | Dec 1996 | A |
5582698 | Flaherty et al. | Dec 1996 | A |
5586553 | Halili et al. | Dec 1996 | A |
5589045 | Hyodo | Dec 1996 | A |
5589326 | Deng et al. | Dec 1996 | A |
5593852 | Heller et al. | Jan 1997 | A |
5596150 | Arndt et al. | Jan 1997 | A |
5599479 | Kimura et al. | Feb 1997 | A |
5617851 | Lipkovker | Apr 1997 | A |
5628890 | Carter et al. | May 1997 | A |
5650062 | Ikeda et al. | Jul 1997 | A |
5651869 | Yoshioka et al. | Jul 1997 | A |
5660163 | Schulman et al. | Aug 1997 | A |
5665215 | Bussmann et al. | Sep 1997 | A |
5670031 | Hintsche et al. | Sep 1997 | A |
5680858 | Hansen et al. | Oct 1997 | A |
5680872 | Sesekura et al. | Oct 1997 | A |
5682233 | Brinda | Oct 1997 | A |
5694932 | Michel | Dec 1997 | A |
5695623 | Michel et al. | Dec 1997 | A |
5708247 | McAleer et al. | Jan 1998 | A |
5711861 | Ward et al. | Jan 1998 | A |
5711862 | Sakoda et al. | Jan 1998 | A |
5720862 | Hamamoto et al. | Feb 1998 | A |
5727548 | Hill et al. | Mar 1998 | A |
5730753 | Morita | Mar 1998 | A |
5741211 | Renirie et al. | Apr 1998 | A |
5741688 | Oxenboll et al. | Apr 1998 | A |
5746217 | Erickson et al. | May 1998 | A |
5759364 | Charlton et al. | Jun 1998 | A |
5770028 | Maley et al. | Jun 1998 | A |
5780304 | Matzinger et al. | Jul 1998 | A |
5781455 | Hyodo | Jul 1998 | A |
5791344 | Schulman et al. | Aug 1998 | A |
5801057 | Smart et al. | Sep 1998 | A |
5804048 | Wong et al. | Sep 1998 | A |
5820570 | Erickson et al. | Oct 1998 | A |
5830341 | Gilmartin | Nov 1998 | A |
5834224 | Ruger et al. | Nov 1998 | A |
5837454 | Cozzette et al. | Nov 1998 | A |
5837546 | Allen et al. | Nov 1998 | A |
5839916 | Chishima | Nov 1998 | A |
5842883 | Igarashi et al. | Dec 1998 | A |
5842983 | Abel et al. | Dec 1998 | A |
5846702 | Deng et al. | Dec 1998 | A |
5846744 | Athey et al. | Dec 1998 | A |
5856195 | Charlton et al. | Jan 1999 | A |
5857983 | Douglas et al. | Jan 1999 | A |
5873990 | Wojciechowski et al. | Feb 1999 | A |
5879311 | Duchon et al. | Mar 1999 | A |
5902253 | Pfeiffer et al. | May 1999 | A |
5934933 | Kordecki et al. | Aug 1999 | A |
5951836 | McAleer et al. | Sep 1999 | A |
5964718 | Duchon et al. | Oct 1999 | A |
5968836 | Matzinger et al. | Oct 1999 | A |
5971941 | Simons et al. | Oct 1999 | A |
5997817 | Crismore et al. | Dec 1999 | A |
6004441 | Fujiwara et al. | Dec 1999 | A |
6015392 | Douglas et al. | Jan 2000 | A |
6033866 | Guo et al. | Mar 2000 | A |
6053930 | Ruppert | Apr 2000 | A |
6071391 | Gotoh et al. | Jun 2000 | A |
6120676 | Heller et al. | Sep 2000 | A |
6143164 | Heller et al. | Nov 2000 | A |
6153069 | Pottgen et al. | Nov 2000 | A |
6156173 | Gotoh et al. | Dec 2000 | A |
6162397 | Jurik et al. | Dec 2000 | A |
6168957 | Matzinger et al. | Jan 2001 | B1 |
6200442 | Markart | Mar 2001 | B1 |
6207000 | Schwobel et al. | Mar 2001 | B1 |
6258229 | Winarta et al. | Jul 2001 | B1 |
6283982 | Levaughn et al. | Sep 2001 | B1 |
6287451 | Winarta et al. | Sep 2001 | B1 |
6299757 | Feldman et al. | Oct 2001 | B1 |
6332871 | Douglas et al. | Dec 2001 | B1 |
6356774 | Bernstein et al. | Mar 2002 | B1 |
6377894 | Deweese et al. | Apr 2002 | B1 |
6461496 | Feldman et al. | Oct 2002 | B1 |
6464649 | Duchon et al. | Oct 2002 | B1 |
6503381 | Gotoh et al. | Jan 2003 | B1 |
6558402 | Chelak et al. | May 2003 | B1 |
6562625 | Modzelewski et al. | May 2003 | B2 |
6599406 | Kawanaka et al. | Jul 2003 | B1 |
6616819 | Liamos et al. | Sep 2003 | B1 |
6743635 | Neel et al. | Jun 2004 | B2 |
6749740 | Liamos et al. | Jun 2004 | B2 |
6766817 | da Silva | Jul 2004 | B2 |
6780645 | Hayter et al. | Aug 2004 | B2 |
6814844 | Bhullar et al. | Nov 2004 | B2 |
6827829 | Kawanaka et al. | Dec 2004 | B2 |
6866758 | Bhullar et al. | Mar 2005 | B2 |
6875327 | Miyazaki et al. | Apr 2005 | B1 |
7340309 | Miazga et al. | Mar 2008 | B2 |
D583691 | Wang | Dec 2008 | S |
D587142 | Wang | Feb 2009 | S |
20030159945 | Miyazaki et al. | Aug 2003 | A1 |
20040094432 | Neel et al. | May 2004 | A1 |
20040178066 | Miyazaki et al. | Sep 2004 | A1 |
20040178067 | Miyazaki et al. | Sep 2004 | A1 |
20040225230 | Liamos et al. | Nov 2004 | A1 |
20040244151 | Sakata et al. | Dec 2004 | A1 |
20050016845 | Groll et al. | Jan 2005 | A1 |
20060091006 | Wang et al. | May 2006 | A1 |
20060191787 | Wang et al. | Aug 2006 | A1 |
20080105024 | Creaven et al. | May 2008 | A1 |
20090029479 | Docherty et al. | Jan 2009 | A1 |
Number | Date | Country |
---|---|---|
2903216 | Aug 1979 | DE |
227029 | Sep 1985 | DE |
0048090 | Mar 1982 | EP |
0078636 | May 1983 | EP |
0080304 | Jun 1983 | EP |
0096288 | Dec 1983 | EP |
0136362 | Apr 1984 | EP |
0125139 | Nov 1984 | EP |
0127958 | Dec 1984 | EP |
0170375 | Feb 1986 | EP |
0184909 | Jun 1986 | EP |
0206218 | Dec 1986 | EP |
0230472 | Aug 1987 | EP |
0241309 | Oct 1987 | EP |
0245073 | Nov 1987 | EP |
0255291 | Feb 1988 | EP |
0278647 | Aug 1988 | EP |
0286084 | Oct 1988 | EP |
0359831 | Mar 1990 | EP |
0368209 | May 1990 | EP |
0390390 | Oct 1990 | EP |
0400918 | Dec 1990 | EP |
0453283 | Oct 1991 | EP |
0470290 | Feb 1992 | EP |
0537761 | Apr 1993 | EP |
0781406 | Jul 1997 | EP |
1394171 | May 1975 | GB |
2073891 | Oct 1981 | GB |
2154003 | Aug 1985 | GB |
2204408 | Nov 1988 | GB |
54-41191 | Apr 1979 | JP |
55-10581 | Jan 1980 | JP |
55-10583 | Jan 1980 | JP |
55-10584 | Jan 1980 | JP |
55-12406 | Jan 1980 | JP |
56-163447 | Dec 1981 | JP |
57-70448 | Apr 1982 | JP |
60-173457 | Sep 1985 | JP |
60-173458 | Sep 1985 | JP |
60-173459 | Sep 1985 | JP |
62-114747 | May 1987 | JP |
63-58149 | Mar 1988 | JP |
63-128252 | May 1988 | JP |
63-139246 | Jun 1988 | JP |
63-294799 | Dec 1988 | JP |
63-317758 | Dec 1988 | JP |
1-114746 | May 1989 | JP |
1-114747 | May 1989 | JP |
1-134244 | May 1989 | JP |
1-156658 | Jun 1989 | JP |
2-62958 | Mar 1990 | JP |
2-120655 | May 1990 | JP |
2-287145 | Nov 1990 | JP |
2-310457 | Dec 1990 | JP |
3-26956 | Feb 1991 | JP |
3-28752 | Feb 1991 | JP |
3-181850 | Aug 1991 | JP |
3-202764 | Sep 1991 | JP |
5-72171 | Mar 1993 | JP |
5-149910 | Jun 1993 | JP |
5-196595 | Aug 1993 | JP |
6-118057 | Apr 1994 | JP |
6-190050 | Jul 1994 | JP |
6-285855 | Oct 1994 | JP |
9-189675 | Jul 1997 | JP |
10-170471 | Jun 1998 | JP |
10-332626 | Dec 1998 | JP |
11-108875 | Apr 1999 | JP |
11-108879 | Apr 1999 | JP |
1281988 | Jan 1987 | SU |
WO 8505119 | Nov 1985 | WO |
WO 8908713 | Sep 1989 | WO |
WO 9005300 | May 1990 | WO |
WO 9104704 | Apr 1991 | WO |
WO 9213271 | Aug 1992 | WO |
WO 9420602 | Sep 1994 | WO |
WO 9427140 | Nov 1994 | WO |
WO 9502817 | Jan 1995 | WO |
WO 9700441 | Jan 1997 | WO |
WO 9718464 | May 1997 | WO |
WO 9719344 | May 1997 | WO |
WO 9742882 | Nov 1997 | WO |
WO 9742883 | Nov 1997 | WO |
WO 9742886 | Nov 1997 | WO |
WO 9742888 | Nov 1997 | WO |
WO 9743962 | Nov 1997 | WO |
9835225 | Aug 1998 | WO |
WO 9843073 | Oct 1998 | WO |
WO 9858250 | Dec 1998 | WO |
WO 9905516 | Feb 1999 | WO |
WO 9908106 | Feb 1999 | WO |
WO 9930152 | Jun 1999 | WO |
WO 0133216 | May 2001 | WO |
Number | Date | Country | |
---|---|---|---|
20080283396 A1 | Nov 2008 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 11281883 | Nov 2005 | US |
Child | 11932658 | US | |
Parent | 10033575 | Dec 2001 | US |
Child | 10866477 | US | |
Parent | 09434026 | Nov 1999 | US |
Child | 10033575 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 10866477 | Jun 2004 | US |
Child | 11281883 | US |