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Kafe 바로가기국가/구분 | United States(US) Patent 등록 |
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국제특허분류(IPC7판) |
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출원번호 | US-0569075 (2009-09-29) |
등록번호 | US-8118993 (2012-02-21) |
발명자 / 주소 |
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출원인 / 주소 |
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대리인 / 주소 |
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인용정보 | 피인용 횟수 : 1 인용 특허 : 450 |
A sensor utilizing a non-leachable or diffusible redox mediator is described. The sensor includes a sample chamber to hold a sample in electrolytic contact with a working electrode, and in at least some instances, the sensor also contains a non-leachable or a diffusible second electron transfer agen
A sensor utilizing a non-leachable or diffusible redox mediator is described. The sensor includes a sample chamber to hold a sample in electrolytic contact with a working electrode, and in at least some instances, the sensor also contains a non-leachable or a diffusible second electron transfer agent. The sensor and/or the methods used produce a sensor signal in response to the analyte that can be distinguished from a background signal caused by the mediator. The invention can be used to determine the concentration of a biomolecule, such as glucose or lactate, in a biological fluid, such as blood or serum, using techniques such as coulometry, amperometry; and potentiometry. An enzyme capable of catalyzing the electrooxidation or electroreduction of the biomolecule is typically provided as a second electron transfer agent.
1. A method for determining a concentration of an analyte in a sample, comprising the steps of: contacting a sample with a sensor, wherein the sensor comprises: a first electrode, a second electrode, and a third electrode;a sample chamber for holding the sample fluid, the sample chamber comprising t
1. A method for determining a concentration of an analyte in a sample, comprising the steps of: contacting a sample with a sensor, wherein the sensor comprises: a first electrode, a second electrode, and a third electrode;a sample chamber for holding the sample fluid, the sample chamber comprising the first electrode, the second electrode, and the third electrode; andan analyte-responsive enzyme and a redox mediator disposed in the sample chamber;applying a first potential between the first and second electrodes to determine when the sample chamber is beginning to fill with sample;applying a second potential between the first and third electrodes to determine when the sample chamber is substantially filled with sample;applying a third potential between the first and second electrodes to electrolyze the analyte, thereby generating an analyte signal; anddetermining the concentration of the analyte using the analyte signal. 2. The method according to claim 1, wherein determining when the sample chamber is beginning to fill with sample comprises observing a signal between the first and second electrodes. 3. The method according to claim 2, wherein observing a signal between the first and second electrodes comprises observing a voltage, current, resistance, impedance, capacitance, or combination thereof between the first and second electrodes. 4. The method according to claim 1, wherein determining when the sample chamber is substantially filled with sample comprises observing a signal between the first and third electrodes. 5. The method according to claim 4, wherein observing a signal between the first and third electrodes comprises observing a voltage, current, resistance, impedance, capacitance, or combination thereof between the first and third electrodes. 6. The method according to claim 1, wherein determining the concentration of the analyte comprises determining the concentration of the analyte by coulometry using the analyte signal. 7. The method according to claim 1, wherein determining the concentration of the analyte comprises determining the concentration of the analyte by amperometry using the analyte signal. 8. The method according to claim 1, wherein determining the concentration of the analyte comprises determining the concentration of the analyte by potentiometry using the analyte signal. 9. The method according to claim 1, further comprising: providing calibration data on a batch of the electrochemical sensors to a measurement instrument, said calibration data comprising information related to a magnitude of a background charge for the batch of the electrochemical sensors;wherein the step of determining the concentration of the analyte comprises determining the concentration of the analyte using the sensor signal and the calibration data. 10. The method according to claim 1, wherein the sensor is configured and arranged so that a background signal generated by the redox mediator is no more than 25% of the signal generated by oxidation or reduction of the analyte. 11. The method according to claim 1, wherein the sensor is configured and arranged so that a background signal generated by the redox mediator is no more than 10% of the signal generated by oxidation or reduction of the analyte. 12. The method according to claim 1, wherein the sample chamber is sized to contain a volume of no more than about 1 μL of the sample. 13. The method according to claim 1, wherein the analyte is glucose or a ketone body. 14. The method according to claim 1, wherein the analyte is glucose and the analyte-responsive enzyme is selected from the group consisting of: glucose oxidase and glucose dehydrogenase. 15. The method according to claim 1, wherein the first, second and third electrodes are coplanar. 16. The method according to claim 1, wherein the sensor is a tip-fill sensor. 17. The method according to claim 1, wherein the sample is a blood sample, and wherein the method further comprises obtaining the blood sample from a finger of a subject. 18. The method according to claim 1, wherein the sample is a blood sample, and wherein the method further comprises obtaining the blood sample from a region of a subject having a lower nerve end density as compared to a fingertip. 19. The method according to claim 18, wherein the region of a subject having a lower nerve end density as compared to a fingertip is selected from the group consisting of: a forearm region, and a thigh region.
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