|Title of Invention||
COMPOUND METAL ANALYTE SENSOR
|Abstract||A sensing element adapted to, at least in part, be inserted into a mammalian body. The sensing element is made up of a core of a structurally robust metal and a plated portion made of an electrochemically active metal conjoined to at least a portion of the core. This sensing element may be used as part of a method for the continuous monitoring of an analyte within a mammalian body. The method includes inserting at least a portion of sensing element into a mammalian body and measuring any electric current produced by at least of portion of the Sensor.|
|Full Text||COMPOUND METAL ANALYTE SENSOR TECHNICAL FIELD
With the advent of indwelling wire sensors has come the danger to the patient of having a wire sensor fatigue from the flexure caused by bodily movement and break off inside the body. Under such circumstances a wire sensor can move through tissue relatively quickly and in an unpredictable manner, potentially posing a threat to the delicate internal organs.
In the background art, the typical metal used for such a wire sensor is platinum, which is electrochemically active and generally very useful in sensing applications. Platinum, however, is a weak metal that is easily broken with only a little flexure. Moreover, the electrochemical nature of platinum surfaces is only imperfectly understood. Efforts to make sensors from very thin platinum wires that are stranded together, there by providing greater flex resistance, have encountered negative effects on the biochemical reactivity of the more complex platinum surface.
Also, platinum is very expensive costing on the order of $ 25 - $30 per gram. For a multiple use sensing assembly incorporating a multiplicity of single use sensing elements, this may be a considerable expense. Also, for sensing elements that double as skin piercing lancets, greater strength is needed than may be available from small diameter platinum wire. Even for sensors that are to be worn for a few days, the cost of the platinum portion of the sensor can place a strain on the overall budget for a production run of sensors.
DISCLOSURE OF THE INVENTION
In a first separate aspect, the present invention is a sensor adapted to, at least in part, be inserted into a mammalian body. The sensor comprises a core of a structurally robust material and a plated portion, comprising an electrochemically active metal plated onto at least a portion of the core.
In a second separate aspect, the present invention is a method for the continuous monitoring of an analyte within a mammalian body. The method includes inserting at least a portion of a sensor into the mammalian body, continuously monitoring any electric current produced by at least a portion of the sensor. The sensor, in turn, includes a core of
structurally robust material and a plated portion, comprising an electrochemically active metal plated onto at least a portion of the core.
In a third separate aspect, the present invention is a method of producing a sensor that is adapted to, at least in part, be inserted into a mammalian body and dwell within the mammalian body for at least an hour. The method comprises applying a layer of an electrochemically active metal plated onto at least a portion of a core made of a structurally robust material.
The forgoing and other objectives, features and advantages of the invention will be more readily understood upon consideration of the following detailed description of the invention, taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a side cross-sectional view of a sensing element according to the present invention.
PREFERRED METHODS OF PRACTICING THE INVENTION
Referring to FIG. 1. sensing element 12 includes a bimetallic wire 20 that, when a voltage is placed on wire 20 relative to a reference electrode, in conjunction with a membrane system 22 reacts to the presence of glucose and oxygen (in some preferred embodiments, glucose only) by creating a current. Wire 20 is coated with a protective layer 23, made of durable, non-toxic material such as polyimide, except for where coated by membrane system 22. In production, protective layer 23 is dip-coated onto wire 20 and then removed, preferable with an excimer or ND: YAG laser in the area in which membrane system 22 is to be applied. In other preferred embodiments there is no protective layer 23 and the entire wire 20 is coated with membrane assembly 22.
Wire 2o may have a diameter on the order of 227 microns and has a wire core 24 of structurally robust metal such as stainless steel or tantalum that is 226 microns thick and an electrochemically active layer 26, such as platinum, that is less than a micron thick. In an alternative preferred embodiment, wire 20 is 177 microns in diameter, core 24 is 157 microns in diameter and is made of tantalum and layer 26 is 10 microns thick and is a platinum foil that has been joined to core 24.
To expand somewhat on the specific construction, wire core 24 may be of any structurally robust metal, such as tantalum, stainless steel or nitinol, which is an alloy of
nickel and titanium. Tantalum and nilinol, although both fairly expensive, are desirable because they are both naturally flexible. This is of particular importance if sensing element 12 is to be inserted in a patient and worn for a period of days. In addition, core 24 could be made of polymeric material or a glass fiber. Electrochemically active layer 26 may be made of one of the noble metals, such as platinum, palladium, gold or a combination of any of the aforesaid with iridium. In a set of preferred embodiments, other noble metals are uses in layer 26.
A number of strategies are possible for making plated core or wire 20. In one method, a tube of platinum is prepared and molten stainless steel, tantalum or nitinol is poured inside of it, to form a filled tube. The filled tube is then drawn through progressively smaller apertures, until its diameter reaches the desired thickness. This produces a filled tube that typically is far longer than is necessary, but is available to be cut to whatever length is desired. Another issue with drawn filled tubes is that it is difficult to reduce the thickness of the layer of platinum to less than 20 microns. This increases the expense because it forces the use of a greater than otherwise necessary amount of platinum.
Another method starts with a robust metal wire that is then electroplated with platinum. In this method the robust metal wire is typically negatively charged to form a cathode. A plating solution bath is positively charged to form an anode. Typically the first step is to plate the stainless steel with an intermediate layer that bonds well to both stainless steel and platinum. Typically this layer is gold, although it has been found to be advantageous to plate a first intermediate layer of nickel, plate gold over this layer of nickel and finally plate the gold with platinum. The plating solution may be either acid or alkaline.
In one preferred method, a core of nitinol was used. In this method gold is plated over the nitinol. As nitinol oxidizes very rapidly, hydrofluoric acid is included in the gold bath to strip away any oxidation that may have formed on the nitinol.
In yet another preferred method, a core of robust metal is clad in platinum foil. Although with this method a 1 micron cladding cannot be achieved, cladding in the neighborhood of 5 to 15 microns is possible. One advantage of a thicker cladding is that it is harder for pinholes to extend all the way through.
Another possibility is coating by way of plasma vapor deposition, in which a metallic vapor is created and coats the core 24. First a wire of structurally robust metal 24, such as tantalum, is passivated meaning that a thin layer of oxide is created on the exterior of the wire. Then platinum is vaporized in a plasma environment, and deposition of layer 26 on the tantalum wire results. Using this technique a robust coating 26 of platinum (or another electrochemically active metal) can be created on an underlying tantalum (or other structurally robust metal) core. Moreover, the layer 26 of platinum is electrically isolated from the structurally sound metal 24 by a layer of oxide, which is non-conducting. Accordingly, if there is a pinhole in the platinum 26, there will nevertheless be no electrical contact between the body fluid and the underlying core 24 of structurally sound metal. If body fluid were to contact core 24, unpredictable electrical activity could result, potentially corrupting the measurement. In a similar manner, and electrochemically active metal may be deposited on a continuous wire of structurally sound metal, designed to host many sensing sites.
Also, sputtering, in which free metallic charged particles are created, may be used to perform the coating or cladding step. Both plasma vapor deposition and sputtering are well known in the art.
In yet another preferred method of producing a thin platinum coating over stainless steel, a strike, or extremely thin ( The membrane system 22 must perform a number of functions. First, it must provide an enzyme that reacts with glucose and oxygen (or glucose only in some preferred embodiments) to form an electrolyte. A reactive layer 30 of glucose oxidase, glutaraldehyde and albumin, which produces hydrogen peroxide when contacted by glucose and oxygen, performs this function. Other enzymes may be used for this process and fall within the scope of this invention.
Second, because glucose is far more prevalent in the blood and other body fluids than oxygen, system 22 must include a membrane placed over the reactive layer 30 to
permit a greater permeation of oxygen than glucose, so that the glucose concentration measurement is not limited by the oxygen concentration in the immediately surrounding tissue. This function is performed by a permselective hard block/soft block copolymer layer 32. This layer is of the type described in U.S. Patents 5,428,123; 5,589,563 and 5,756,632, which are hereby incorporated by reference as if fully set forth herein. Layer 32 is preferably less than 10 microns thick, to permit rapid permeation by glucose and oxygen.
Third, membrane system 22 must prevent interferents, such as acetaminophen, from corrupting the measurement by causing current flow unrelated to the presence of glucose. This Junction by an inner interferent reducing layer 34 of a compound such as sulfonated polyether sulfone, 3-amino-phenol, or polypyrrole, which quickly permits the permeation of the hydrogen peroxide, which causes the current flow indicative of the concentration of glucose. Persons skilled in the relevant arts will readily recognize that quick permeation is highly desirable in a briefly indwelling sensor so that a measurement may be quickly obtained.
To produce sensing element 12, first the interferent reducing layer 34 of 3-amino-phenol is solution-coated or electro polymerized onto the surface of platinum plating 26. Layer 34 may be from a few nanometers to 2 microns thick, to permit rapid permeation by JbOi ions, thereby reacting very quickly to glucose concentration. Over this the reactive layer 30 of glucose oxidase is dip-coated or electrodeposited. Glutaraldehyde is deposited on the glucose oxidase to immobilize the glucose oxidase. The sensor is dip coated in the soft block/hard block copolymer 32. In the finished product, the surface of the sensing region 22 is slightly depressed relative the remainder of the surface of sensing element 12.In the finished product, the surface of the sensing region 22 is slightly depressed relative the remainder of the surface of sensing element 12. In one embodiment, the glucose oxidase 30 is applied before layer 34, which is electrodeposited through layer 30. A voltage is placed between contacts 72 at the beginning of the measurement process. When electrical current flows between contacts 72, this indicates that body fluid has completely wet membrane system 22 and serves as a signal to place a voltage on conductor 24.
Jn one preferred embodiment, a layer of absorbent metal is included over membrane system 22. In use, sensing element 12 may be either inserted into the body of a number of days and may provide a multiplicity of glucose measurement or may be used as a single use sensing element. When used as for a single use, sensing element 12 may be part of a multiple sensing element assembly. The measurement of glucose concentration may occur when sensing element 12 is briefly indwelling, or may occur after it has been withdrawn, with retained body fluid being tested. A single use element 12 is typically optimized to provide a fast readout, whereas a sensing element that dwells within the body for days is typically optimized for accuracy over time and for to satisfy the greater safety challenge posed by an indwelling device.
The present invention has industrial applicability in the field of medical technology.
The terms and expressions which have been employed in the foregoing specification are used as terms of description and not of limitation, and there is no intention, in the use of such terms and expressions, of excluding equivalents of the features shown and described or portions thereof, it being recognized that the scope of the invention is defined and limited only by the claims which follow.
1. An analyte sensing element adapted to be, at least in part, inserted into a
mammalian body, said sensing element comprising a core of a structurally robust
material; wherein said core is structurally flexible; and a layer of electrochemically
active metal surrounding, covering and in contact with the outer surface of said core
to prevent said core Erom contact with body fluid.
2. The analyte sensing element as claimed in claim 1 wherein said electrochemically
active metal is a noble metal.
3. The analyte sensing element as claimed in claim 2 wherein said noble metal is gold or
platinum or palladium or a combination of any of the aforesaid with iridium.
4. The analyte sensing element as claimed in claim 1 wherein said structurally robust
material is stainless steel or tantalum or nitinol or polymeric material or glass fiber.
5. The analyte sensing element as claimed in claim I wherein said core is round in
cross-section and wherein said electrochemically active metal is applied to said core
6. The analyte sensing element as claimed in claim 1 wherein said outer surface of said
core comprises a passivated oxide.
7. The analyte sensing element as claimed in claim 1 wherein said layer of
electrochemically active metal is at least partially surrounded by a membrane system.
8. The analyte sensing element as claimed in claim 1, further being biocompatible so
that it may be implanted into a mammal for at least 24 hours.
9. A method for measuring the concentration of an analyte within a mammalian body
having body fluids by an analyte sensing element as claimed in claim 1 wherein;
placing at least a portion of said analyte sensing element into contact with said body
fluid; and measuring any electric current produced by said analyte sensing element
and forming a measurement of analyte concentration based on said current
10. The method as claimed in claim 1 wherein said sensor remains implanted for at least
24 hours and produces a multiplicity of analyte measurements.
|Indian Patent Application Number||378/DELNP/2007|
|PG Journal Number||11/2014|
|Date of Filing||15-Jan-2007|
|Name of Patentee||ISENSE CORPORATION|
|Applicant Address||27700 sw 95th avenue,willsonville, or 97070, USA|
|PCT International Classification Number||A61B 05/00|
|PCT International Application Number||PCT/US2004/019648|
|PCT International Filing date||2004-06-16|