WO1994013203A1 - Method and apparatus for in vivo determination of the concentration in a body fluid of metabolically significant substances - Google Patents

Method and apparatus for in vivo determination of the concentration in a body fluid of metabolically significant substances Download PDF

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Publication number
WO1994013203A1
WO1994013203A1 PCT/DK1993/000416 DK9300416W WO9413203A1 WO 1994013203 A1 WO1994013203 A1 WO 1994013203A1 DK 9300416 W DK9300416 W DK 9300416W WO 9413203 A1 WO9413203 A1 WO 9413203A1
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WIPO (PCT)
Prior art keywords
needle
sensor
vial
concentration
aqueous solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/DK1993/000416
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French (fr)
Inventor
Henrik Egesborg Hansen
Henrik Ege
Thomas Munk Plum
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novo Nordisk AS
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Novo Nordisk AS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Novo Nordisk AS filed Critical Novo Nordisk AS
Priority to DE69324376T priority Critical patent/DE69324376T2/en
Priority to US08/448,351 priority patent/US5680858A/en
Priority to AU56940/94A priority patent/AU5694094A/en
Priority to JP51369394A priority patent/JP3345422B2/en
Priority to EP94902646A priority patent/EP0674494B1/en
Publication of WO1994013203A1 publication Critical patent/WO1994013203A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/1468—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means
    • A61B5/1486—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue using chemical or electrochemical methods, e.g. by polarographic means using enzyme electrodes, e.g. with immobilised oxidase
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6846—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive
    • A61B5/6847—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be brought in contact with an internal body part, i.e. invasive mounted on an invasive device
    • A61B5/6848—Needles

Definitions

  • the invention relates to a method and a meter for in vivo determination of the concentration in a body fluid of etabolically significant substances.
  • Knowledge of deviations from the accepted normal values in the concentration of metabolically significant substances in the body fluids is of great clinical importance. Especially excursions in the blood glucose concentration must be counteracted without delay by proper adjustments of the diet or the insulin injection regime. Diabetics must therefore have easy access to means for determining the concentration of glucose in their blood or other body fluids.
  • a number of devices for in vitro determination of the concentration of glucose in blood are known. The devices can be based on optical, chemical or electrochemical properties of glucose, but they all depend on the withdrawal of a small blood sample (about 25 ⁇ l ) .
  • the blood sample can be obtained e.g.
  • the device used for the analysis will be contaminated with blood which must be wiped off, or the sample receiving part of the device can be disposable, in which case it must be disposed of with care because of the possible contamination with infectious agents.
  • the measurement takes place in the subcutaneous tissue of the patient, preferably in the interstitial fluid, making it unnecessary to take a blood sample.
  • the insertion of the needle may cut a few small blood vessels, but especially if the needle is blunt, bleeding and pain associated with the insertion of the needle are usually insignificant.
  • Body areas with low sensitivity, i.e the abdomen or the thigh, can be chosen for the insertion of the needle thus minimizing the pain.
  • Electrochemical sensors usually require some conditioning time in a suitable buffer before their output signal is stable. It is convenient to let the sterilizing solution serve this purpose. Further, the solution may be used, for calibrating the sensor when the solution contains a suitable and constant quantity of the substance which should be determined.
  • the time the needle is inserted in the patient should be as short as possible e.g. 1- 100 seconds, preferably less than 5 seconds.
  • Some types of sensors may need a longer time for reaching equilibrium, but even when such sensors are used, an insertion time of less than 100 seconds, preferably less than 5 seconds, may be sufficient because the concentration of the substance in question can be calculated from the data recorded when the signal is converging towards the state of equilibrium.
  • the signals from the sensor, before and after it has been used can be compared, and a difference between the signals by more than a set quantity indicates an error, and the measurement should be discarded.
  • the invention also relates to an apparatus for carrying out the method.
  • Such an apparatus is characterized in that it comprises a needle with a sensor, a vial containing an aqueous solution (which may be suitable for sterilizing, conditioning or calibrating the sensor) , the vial being closed by membranes opposite each other, which membranes are leak proof when penetrated by the needle, an electronic unit receiving data from the sensor and having means for storing and processing these data on the basis of set criterions, and means driving the needle to protrude from the vial for a set time and thereafter withdrawing it into the vial.
  • aqueous solution which may be suitable for sterilizing, conditioning or calibrating the sensor
  • the sensor may be an electrochemical needle glucose sensor.
  • the shelf life of such a sensor is relatively long, more than one year, when stored in the dry state. In actual use, however, the life time of the sensor is only about a month. It is therefore appropriate that the needle with the sensor and the vial with the aqueous solution are independently disposable, several times usable devices, which are not brought together until some time before the first measurement is made.
  • the closures of the vial may be rubber membranes which are pierced by the needle. If the membrane is always pierced at the same spot, it will remain leak proof even when it is pierced numerous times.
  • the rubber membrane may be covered by a metal foil as a seal preventing evaporation of water. This is important in order to prolong the shelf life of the vial unit. Especially when the solution in the vial shall be used for calibrating the sensor, only a minute loss of water can be tolerated during the shelf life of the vial.
  • the life time of the vial unit is limited to about one month after it is first used and the membranes and the foils are perforated.
  • Figure 1 shows schematically a needle unit and a vial with solution for a measuring apparatus according to the invention
  • Figure 2 shows an embodiment of a measuring apparatus
  • Figure 3 shows a graph illustrating the current through a glucose oxidase based glucose sensor during an amperometric measuring sequence.
  • Figure 1 is shown schematically a needle unit with a needle 5 penetrating a membrane 3 which is closing one end of a vial 1 with solution 2.
  • the other end of the vial is closed by a membrane 4.
  • the needle for an amperometric glucose sensor is typically made from a stainless steel tubing as used for injection needles.
  • a platinum wire inserted in the bore of the needle, and electrically insulated from the needle, is serving as the anode, while the stainless steel tube can be used as the cathode.
  • the elliptical surface of the obliquely cut and ground end of the needle 6 is coated with a glucose sensitive membrane containing glucose oxidase.
  • the electrodes are via leads 7 and 8 connected to an electronic unit providing the voltage, measuring the current, and performing the calculations.
  • the vial 1 containing the solution and being closed by the two rubber membranes 3 and 4 is manufactured as an independent unit.
  • the ends of the vial 1 may further be provided with not shown metal foils covering the rubber membranes and being adhered to the circumferential edge of the vial to provide a vapour tight sealing of the vial, enhancing the shelf life of the vial when filled with an aqueous solution.
  • the metal foils may either be removed before the vial is mounted in the meter, or they may be perforated by the needle.
  • the needle with the sensor is manufactured as another independent unit.
  • the needle unit and the vial When the needle unit and the vial are put into service, they are placed in a not disposable apparatus comprising a mechanism controlling the insertion and the retraction of the needle and comprising an electronic unit providing the voltage measuring the current and performing the calculations.
  • the needle is provided with a member 9 for engagement with a mechanism in the apparatus, which mechanism governs insertion and retraction of the needle.
  • the vial unit and the needle unit are mounted in the apparatus, the needle penetrates one of the membranes so that its pointed end with the glucose sensor is positioned in the solution in the vial.
  • Some electrochemical glucose sensors need a relatively long conditioning time, i.e. several hours, before they can be used for measuring. The conditioning may start when the electrode is brought into contact with the solution, and the conditioned state will be maintained as long as the electrode is stored in the solution and the voltage is applied to the anode.
  • FIG 2 shows an embodiment of a measuring apparatus having a housing 11 with a disposable unit 10 comprising a needle unit mounted in a vial as shown in Figure 1.
  • the housing 11 contains appropriate mechanical and electronic parts for performing a measuring sequence when such a sequence is triggered by operating a button 12. The result of the measurement is displayed on a display 13.
  • the needle 5 from its position shown in Figure 1 is moved forward to also penetrate the closure membrane 4 to protrude from the unit 10. This protruding position is maintained for a set time whereafter the needle is retracted to the position with the sensor stored in the aqueous solution in the vial 1.
  • FIG. 3 shows the course of the current during a measurement.
  • a reference current is recorded when the needle is located with its sensor membrane inside the vial with the aqueous solution.
  • the needle is shot with its pointed end carrying the sensor through the membrane 4 into the skin of the patient.
  • the needle remains in its inserted position until the time T2, whereafter it is retracted to its position inside the vial 1.
  • the current will begin to approach the equilibrium value corresponding to the actual glucose content in the blood/interstitial fluid in which the sensor is now situated. This is shown by the dotted graph.
  • the needle is retracted into the vial 1, and the current will now rapidly return to the reference value, as shown by the fully drawn graph.
  • the vial 1 with the aqueous solution and the needle 5 carrying the sensor may be marketed as individual items which may easily be electrically and mechanically coupled to a measuring apparatus.
  • the rubber membranes 3 and 4 should be manufactured from a material which can be pierced multiple times without producing debris and without loosing its leak proof properties.
  • the sealing must be very tight to allow the unit to be stored for say a couple of years before it is put into service.
  • the lifetime of the unit, after at least one of the membrane closures of the vial has been pierced, is estimated to be about one month or about 100 measurements.
  • the lifetime of the disposables is limited by the needle sensor or the aqueous solution deteriorating to a point where their performances are no longer within their specifications.
  • the apparatus is here described as using a sensor based on enzymatic oxidation of glucose.
  • a sensor based on the measurement of some optical characteristics of glucose, or the optical characteristics of a molecule formed by a chemical reaction between glucose and an auxiliary substance can be used.
  • the sensor need not be placed in the needle, but may be located in the not disposable part of the apparatus, and optical signals may be sent from the needle through a light conducting fibre which is coupled to the reusable part of the apparatus when the disposable needle unit is mounted.

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  • Life Sciences & Earth Sciences (AREA)
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  • General Health & Medical Sciences (AREA)
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  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
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Abstract

A method for in vivo determination of the concentration in a body fluid of metabolically significant substances comprises storing of a needle with a sensor in a liquid-filled ampoule, brief insertion of the needle into a patient, recording of the output signal from the sensor, withdrawal of the needle, and calculation of the concentration looked for on the basis of the recorded signals. The method is preformed using an apparatus comprising a needle (5) with a sensor (6), an ampoule (1) containing a solution (2) and closed by two membranes (3, 4). The needle (5) is stored with its sensor (6) in the solution. The apparatus further comprises a mechanical unit for driving the needle (5) to protrude from the ampoule for a set moment, and an electronic unit storing the output signal from the sensor (6) and performing calculations on the basis of the stored signal values. The needle with its sensor (6) and the ampoule with the solution (2) are independent disposable parts mounted in a durable part containing the mechanical and electronic parts.

Description

Method and Apparatus for in Vivo Determination of the Concentration in a Body Fluid of Metabo- lically Significant Substances
The invention relates to a method and a meter for in vivo determination of the concentration in a body fluid of etabolically significant substances. Knowledge of deviations from the accepted normal values in the concentration of metabolically significant substances in the body fluids is of great clinical importance. Especially excursions in the blood glucose concentration must be counteracted without delay by proper adjustments of the diet or the insulin injection regime. Diabetics must therefore have easy access to means for determining the concentration of glucose in their blood or other body fluids. A number of devices for in vitro determination of the concentration of glucose in blood are known. The devices can be based on optical, chemical or electrochemical properties of glucose, but they all depend on the withdrawal of a small blood sample (about 25 μl ) . The blood sample can be obtained e.g. by a finger prick or by a cut in the ear lobe. Taking a blood sample is unpleasant and can be painful for many people, because the fingers and the ear lobes are rather sensitive areas. Further, the device used for the analysis will be contaminated with blood which must be wiped off, or the sample receiving part of the device can be disposable, in which case it must be disposed of with care because of the possible contamination with infectious agents.
Consequently, it is the object of the invention to provide a method of analysis and a meter by which a determination of the concentration of metabolically significant substances in the blood is performed using known principles but without the need for taking a blood sample.
It is known to implant a glucose sensor subcutaneously and to monitor the glucose concentration during a period. Such sensor devices may determine the glucose concentration in the blood or in the interstitial fluid, the latter being only slightly lower than that in blood. No blood sample is taken when using this technique, but it is a disadvantage that the sensor must be implanted for some time before the signal representing the glucose concentration is sufficiently stable. A long (hours) insertion time of the needle is, however, not compatible with the requirements to a personal blood analysing device. A technique with a very short implantation time of the needle can, however, be practised by a method in accordance to the invention and characterized by the steps
store a needle with a sensor. move the needle temporarily so it is inserted into the tissue of the person who's body fluid shall be analysed. withdraw the needle and calculate the concentration of the significant substance on the basis of the recorded signals.
With this technique the measurement takes place in the subcutaneous tissue of the patient, preferably in the interstitial fluid, making it unnecessary to take a blood sample. The insertion of the needle may cut a few small blood vessels, but especially if the needle is blunt, bleeding and pain associated with the insertion of the needle are usually insignificant. Body areas with low sensitivity, i.e the abdomen or the thigh, can be chosen for the insertion of the needle thus minimizing the pain.
When the needle with the sensor is used more than once it must be disinfected after each use. This is accomplished by storing the needle in an aqueous solution which contains a disinfecting agent e.g. merthiolate. Electrochemical sensors usually require some conditioning time in a suitable buffer before their output signal is stable. It is convenient to let the sterilizing solution serve this purpose. Further, the solution may be used, for calibrating the sensor when the solution contains a suitable and constant quantity of the substance which should be determined.
For practical reasons, the time the needle is inserted in the patient should be as short as possible e.g. 1- 100 seconds, preferably less than 5 seconds. Some types of sensors may need a longer time for reaching equilibrium, but even when such sensors are used, an insertion time of less than 100 seconds, preferably less than 5 seconds, may be sufficient because the concentration of the substance in question can be calculated from the data recorded when the signal is converging towards the state of equilibrium.
If the sensor is stored in a calibration solution, the signals from the sensor, before and after it has been used, can be compared, and a difference between the signals by more than a set quantity indicates an error, and the measurement should be discarded.
The invention also relates to an apparatus for carrying out the method. Such an apparatus is characterized in that it comprises a needle with a sensor, a vial containing an aqueous solution (which may be suitable for sterilizing, conditioning or calibrating the sensor) , the vial being closed by membranes opposite each other, which membranes are leak proof when penetrated by the needle, an electronic unit receiving data from the sensor and having means for storing and processing these data on the basis of set criterions, and means driving the needle to protrude from the vial for a set time and thereafter withdrawing it into the vial.
The sensor may be an electrochemical needle glucose sensor. The shelf life of such a sensor is relatively long, more than one year, when stored in the dry state. In actual use, however, the life time of the sensor is only about a month. It is therefore appropriate that the needle with the sensor and the vial with the aqueous solution are independently disposable, several times usable devices, which are not brought together until some time before the first measurement is made.
The closures of the vial may be rubber membranes which are pierced by the needle. If the membrane is always pierced at the same spot, it will remain leak proof even when it is pierced numerous times. The rubber membrane may be covered by a metal foil as a seal preventing evaporation of water. This is important in order to prolong the shelf life of the vial unit. Especially when the solution in the vial shall be used for calibrating the sensor, only a minute loss of water can be tolerated during the shelf life of the vial. The life time of the vial unit is limited to about one month after it is first used and the membranes and the foils are perforated.
In the following the invention will be further explained with references to the drawings, wherein
Figure 1 shows schematically a needle unit and a vial with solution for a measuring apparatus according to the invention,
Figure 2 shows an embodiment of a measuring apparatus, and
Figure 3 shows a graph illustrating the current through a glucose oxidase based glucose sensor during an amperometric measuring sequence.
In Figure 1 is shown schematically a needle unit with a needle 5 penetrating a membrane 3 which is closing one end of a vial 1 with solution 2. The other end of the vial is closed by a membrane 4. Thereby the pointed end of the needle is positioned in the solution. The needle for an amperometric glucose sensor is typically made from a stainless steel tubing as used for injection needles. A platinum wire inserted in the bore of the needle, and electrically insulated from the needle, is serving as the anode, while the stainless steel tube can be used as the cathode. The elliptical surface of the obliquely cut and ground end of the needle 6 is coated with a glucose sensitive membrane containing glucose oxidase. When glucose diffuses into the membrane, and a voltage difference (600-700 mV) is applied between the anode and the cathode, an electric current, which in principle is proportional to the glucose concentration in the membrane, will pass from the anode to the cathode. The electrodes are via leads 7 and 8 connected to an electronic unit providing the voltage, measuring the current, and performing the calculations. The vial 1 containing the solution and being closed by the two rubber membranes 3 and 4 is manufactured as an independent unit. The ends of the vial 1 may further be provided with not shown metal foils covering the rubber membranes and being adhered to the circumferential edge of the vial to provide a vapour tight sealing of the vial, enhancing the shelf life of the vial when filled with an aqueous solution. When the vial is put into service, the metal foils may either be removed before the vial is mounted in the meter, or they may be perforated by the needle.
The needle with the sensor is manufactured as another independent unit. When the needle unit and the vial are put into service, they are placed in a not disposable apparatus comprising a mechanism controlling the insertion and the retraction of the needle and comprising an electronic unit providing the voltage measuring the current and performing the calculations. The needle is provided with a member 9 for engagement with a mechanism in the apparatus, which mechanism governs insertion and retraction of the needle. When the vial unit and the needle unit are mounted in the apparatus, the needle penetrates one of the membranes so that its pointed end with the glucose sensor is positioned in the solution in the vial. Some electrochemical glucose sensors need a relatively long conditioning time, i.e. several hours, before they can be used for measuring. The conditioning may start when the electrode is brought into contact with the solution, and the conditioned state will be maintained as long as the electrode is stored in the solution and the voltage is applied to the anode.
Figure 2 shows an embodiment of a measuring apparatus having a housing 11 with a disposable unit 10 comprising a needle unit mounted in a vial as shown in Figure 1. The housing 11 contains appropriate mechanical and electronic parts for performing a measuring sequence when such a sequence is triggered by operating a button 12. The result of the measurement is displayed on a display 13. When a measuring sequence is triggered, the needle 5 from its position shown in Figure 1 is moved forward to also penetrate the closure membrane 4 to protrude from the unit 10. This protruding position is maintained for a set time whereafter the needle is retracted to the position with the sensor stored in the aqueous solution in the vial 1.
The apparatus with the unit 10 is pressed against the skin in the place where the measurement should be performed, and the apparatus is activated by pressing the trigger button 12. Figure 3 shows the course of the current during a measurement. Before the apparatus is activated, a reference current is recorded when the needle is located with its sensor membrane inside the vial with the aqueous solution. Thereafter, at the time Tl the needle is shot with its pointed end carrying the sensor through the membrane 4 into the skin of the patient. The needle remains in its inserted position until the time T2, whereafter it is retracted to its position inside the vial 1. At the time Tl, when the sensor is passed into the patient, the current will begin to approach the equilibrium value corresponding to the actual glucose content in the blood/interstitial fluid in which the sensor is now situated. This is shown by the dotted graph. Before the equilibrium value is reached, the needle is retracted into the vial 1, and the current will now rapidly return to the reference value, as shown by the fully drawn graph.
As it is seen from the graph, the insertion of the needle is terminated before the equilibrium value of the current is attained, but the initial part of the current graph will contain sufficient information for extrapolating the equilibrium value.
The vial 1 with the aqueous solution and the needle 5 carrying the sensor may be marketed as individual items which may easily be electrically and mechanically coupled to a measuring apparatus. The rubber membranes 3 and 4 should be manufactured from a material which can be pierced multiple times without producing debris and without loosing its leak proof properties. The sealing must be very tight to allow the unit to be stored for say a couple of years before it is put into service. The lifetime of the unit, after at least one of the membrane closures of the vial has been pierced, is estimated to be about one month or about 100 measurements. The lifetime of the disposables is limited by the needle sensor or the aqueous solution deteriorating to a point where their performances are no longer within their specifications.
The apparatus is here described as using a sensor based on enzymatic oxidation of glucose. Another possibility is to use a sensor based on the measurement of some optical characteristics of glucose, or the optical characteristics of a molecule formed by a chemical reaction between glucose and an auxiliary substance. In this case the sensor need not be placed in the needle, but may be located in the not disposable part of the apparatus, and optical signals may be sent from the needle through a light conducting fibre which is coupled to the reusable part of the apparatus when the disposable needle unit is mounted.

Claims

1. A method for in vivo determination of the concentration in a body fluid of metabolically significant substances characterized by the following steps:
- store a needle with a sensor.
- move the needle temporarily so it is inserted into the tissue of the person whose body fluid shall be analysed.
record the output signal from the needle sensor.
- withdraw the needle and
- calculate the concentration of the significant substance on the basis of the recorded signals.
2. A method according to claim 1, characterized in, that the needle is inserted for 1-100 seconds, preferably less than 5 seconds.
3. A method according to claim 1 or 2, characterized in, that the needle with the sensor is stored in one or more aqueous solution(s) .
4. A method according to claim 3, characterized in, that the aqueous solution(s) is/are used for sterilizing the sensor.
5. A method according to claim 4, characterized in, that the sterilizing agent is Merthiolate.
6. A method according to claim 3, 4 or 5 characterized in, that the aqueous solution(s) is/are used for calibrating the sensor.
7. A method according to claim 6, characterized in, that the output signal from the needle is measured during the storage of the needle in the calibrating solution(s) and is compared with the output signal from the sensor when the needle returns to the calibrating solution(s) , and an error is registered if these signals differ by more than a set amount.
8. A method according to any of the claims 1 - 7, characterized in, that the metabolically significant substance is glucose.
9. An apparatus for carrying out the method of claims
1 - 8, characterized in, that it comprises a needle with a sensor, a vial containing aqueous solution(s) , the vial being closed by membranes opposite each other, which membranes are leak proof when penetrated by the needle, an electronic unit receiving a signal from the sensor and having means for storing and processing this signal on the basis of set criterions, and means of driving the needle to protrude from the vial for a set time and thereafter withdraw it into the vial.
10. An apparatus according to claim 10, characterized in, that the sensor is an electrochemical or optical needle glucose sensor.
11. An apparatus according to claim 9 or 10, characterized in, that the needle with the sensor and the vial with the aqueous solution(s) are independently disposable, several times usable devices.
12. An apparatus according to any of claims 9 - 11 characterized in, that the closing membranes of the vial are rubber membranes covered by a metal foil.
PCT/DK1993/000416 1992-12-10 1993-12-10 Method and apparatus for in vivo determination of the concentration in a body fluid of metabolically significant substances Ceased WO1994013203A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
DE69324376T DE69324376T2 (en) 1992-12-10 1993-12-10 DEVICE FOR IN-VIVO DETERMINING THE CONCENTRATION OF METABOLITES IN A BODY LIQUID
US08/448,351 US5680858A (en) 1992-12-10 1993-12-10 Method and apparatus for in vivo determination of the concentration in a body fluid of metabolically significant substances
AU56940/94A AU5694094A (en) 1992-12-10 1993-12-10 Method and apparatus for in vivo determination of the concentration in a body fluid of metabolically significant substances
JP51369394A JP3345422B2 (en) 1992-12-10 1993-12-10 Apparatus for in vivo measurement of the concentration of metabolically significant substances in body fluids
EP94902646A EP0674494B1 (en) 1992-12-10 1993-12-10 Apparatus for in vivo determination of the concentration in a body fluid of metabolically significant substances

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DK1485/92 1992-12-10
DK921485A DK148592D0 (en) 1992-12-10 1992-12-10 APPARATUS

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EP (1) EP0674494B1 (en)
JP (1) JP3345422B2 (en)
AT (1) ATE178472T1 (en)
AU (1) AU5694094A (en)
DE (1) DE69324376T2 (en)
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WO (1) WO1994013203A1 (en)

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WO1998058250A3 (en) * 1997-06-16 1999-04-01 Elan Corp Plc Methods of calibrating and testing a sensor for in vivo measurement of an analyte and devices for use in such methods
US6014577A (en) * 1995-12-19 2000-01-11 Abbot Laboratories Device for the detection of analyte and administration of a therapeutic substance
WO2002030488A2 (en) 2000-10-12 2002-04-18 Abbott Laboratories Device and method for obtaining interstitial fluid from a patient for diagnostic tests
WO2004091693A3 (en) * 2003-03-31 2005-06-02 Rosedale Medical Inc Body fluid sampling constructions and techniques
EP1862116A2 (en) * 1996-05-17 2007-12-05 Roche Diagnostics Operations, Inc. Disposable element for use in a body fluid sampling device
US8919605B2 (en) 2009-11-30 2014-12-30 Intuity Medical, Inc. Calibration material delivery devices and methods
US8969097B2 (en) 2005-06-13 2015-03-03 Intuity Medical, Inc. Analyte detection devices and methods with hematocrit-volume correction and feedback control
US9060723B2 (en) 2005-09-30 2015-06-23 Intuity Medical, Inc. Body fluid sampling arrangements
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JPH08504337A (en) 1996-05-14
DK148592D0 (en) 1992-12-10
AU5694094A (en) 1994-07-04
EP0674494A1 (en) 1995-10-04
DE69324376D1 (en) 1999-05-12
US5680858A (en) 1997-10-28
JP3345422B2 (en) 2002-11-18
EP0674494B1 (en) 1999-04-07
DE69324376T2 (en) 1999-12-30
ATE178472T1 (en) 1999-04-15

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