Device and method for determining analyte levels
Devices and methods for determining analyte levels are described. The devices and methods allow for the implantation of analyte-monitoring devices, such as glucose monitoring devices, that result in the delivery of a dependable flow of blood to deliver sample to the implanted device. The devices comprise a unique microarchitectural arrangement in the sensor region that allows accurate data to be obtained over long periods of time.
1. A device for measuring glucose in a bodily fluid, the device comprising:
a sensor operably connected to an electronic circuit and configured to continuously measure a signal associated with a glucose concentration in a host, the sensor comprising a working electrode and a reference electrode, wherein the working electrode and the reference electrode are configured for implantation in a subcutaneous tissue of the host; and
a membrane disposed on a portion of the sensor, configured to provide at least two phases of sensor function, wherein the at least two phases of sensor function comprise:
a first phase that occurs after implantation of the device in the subcutaneous tissue and during which the signal provides an unstable measurement of the glucose concentration in the host; and
a second phase that occurs after the first phase and during which the signal provides a stable measurement of the glucose concentration in the subcutaneous tissue of the host, wherein at least 95% of glucose concentration values measured by the signal are within 25% of one or reference glucose values over a period of time no less than 3 days in the subcutaneous tissue of the host, and wherein the one or more reference values are determined by analysis of the host's blood glucose;
wherein the device is configured to respond substantially linearly to changes in glucose concentration at a glucose concentration of up to about 400 mg/dL.
2. The device of claim 1 , wherein the membrane comprises an electrolyte layer, wherein the electrolyte layer comprises a flexible, hydrophilic material.
3. The device of claim 1 , wherein the membrane comprises a resistance layer comprising a semipermeable membrane configured to control a flux of oxygen and glucose therethrough.
4. The device of claim 1 , further comprising a housing filled with a material comprising a resin, wherein the resin secures the electronic circuit within the housing.
5. The device of claim 1 , further comprising an apparatus operatively connected to the electronic circuit and configured for transmitting data to a location external to the device.
6. The device of claim 5 , wherein the electronic circuit is configured to transmit data at intervals.
7. The device of claim 1 further comprising a housing comprising a cavity contained therewithin.
8. The device of claim 7 , wherein the sensor is situated within the housing cavity.
9. The device of claim 1 , wherein the membrane is configured to restrict passage of interfering species therethrough.
10. The device of claim 1 , wherein the membrane comprises a cross-linked polymer and is configured to control a flux of oxygen and glucose therethrough.
11. The device of claim 1 , wherein the sensor comprises an electrochemical mechanism.
12. The device of claim 1 , wherein the sensor comprises a non-enzymatic mechanism.
13. The device of claim 1 , wherein the sensor comprises a resonance mechanism.
14. The device of claim 1 , wherein the sensor comprises an acoustic wave mechanism.
15. The device of claim 1 , wherein the sensor comprises an optical mechanism.
16. The device of claim 1 , wherein the device is configured to provide stabilization of the membrane to reduce motion artifact.
17. A device for measuring glucose in a bodily fluid, the device comprising:
a sensor configured to generate a signal associated with a concentration of glucose in a host, wherein the sensor comprises a working electrode and a reference electrode, and wherein the working electrode and the reference electrode are configured for implantation in a subcutaneous tissue of the host; and
a membrane disposed on a portion of the sensor, wherein the membrane is configured to control a flux of oxygen and glucose therethrough;
wherein the device is configured, while implanted in the subcutaneous tissue of the host, to respond substantially linearly to changes in glucose concentration at a glucose level up to 400 mg/dL, wherein the membrane provides for at least 95% of glucose concentration values measured by the signal being within 25% of one or more reference glucose values for a useful life of the device of no less than 3 days in the subcutaneous tissue of the host, and wherein the reference values are determined by analysis of the host's blood glucose.
18. The device of claim 17 , wherein the device further comprises an apparatus configured to transmit data to a location external to the device.
19. The device of claim 17 , wherein the membrane comprises an electrolyte layer, wherein the electrolyte layer comprises a flexible, hydrophilic material.
20. The device of claim 17 , wherein the membrane is configured to restrict passage of interfering species therethrough.
21. The device of claim 17 , wherein the sensor comprises an electrochemical mechanism.
22. The device of claim 17 , wherein the sensor comprises a non-enzymatic mechanism.
23. The device of claim 17 , wherein the sensor comprises a resonance mechanism.
24. The device of claim 17 , wherein the sensor comprises an acoustic wave mechanism.
25. The device of claim 17 , wherein the sensor comprises an optical mechanism.
26. The device of claim 17 , wherein the device is configured to provide stabilization of the membrane to reduce motion artifact.