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Kafe 바로가기국가/구분 | United States(US) Patent 등록 |
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국제특허분류(IPC7판) |
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출원번호 | US-0569351 (2009-09-29) |
등록번호 | US-8449758 (2013-05-28) |
발명자 / 주소 |
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출원인 / 주소 |
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대리인 / 주소 |
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인용정보 | 피인용 횟수 : 1 인용 특허 : 455 |
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 glucose in a sample, comprising the steps of: (a) contacting a sample with an electrochemical sensor comprising: (i) a proximal end and a distal end, the distal end being configured and arranged for insertion into a sensor reader;(ii) a first electrode,
1. A method for determining a concentration of glucose in a sample, comprising the steps of: (a) contacting a sample with an electrochemical sensor comprising: (i) a proximal end and a distal end, the distal end being configured and arranged for insertion into a sensor reader;(ii) a first electrode, a second electrode, and a third electrode, wherein the first and second electrodes are separated by a closest distance in a range of 25 to 1000 μm;(iii) a sample chamber comprising the first electrode, the second electrode, and the third electrode, wherein the sample chamber is sized to contain a volume of no more than about 1 μL of the sample; and(iv) a glucose-responsive enzyme and a redox mediator disposed in the sample chamber;(b) applying a first potential between the first and second electrodes to determine when the sample chamber is beginning to fill with sample;(c) applying a second potential between the first and third electrodes to determine when the sample chamber is substantially filled with sample;(d) applying a third potential between the first and second electrodes to electrolyze the glucose, thereby generating a glucose signal; and(e) determining the concentration of the glucose using the glucose signal. 2. The method of claim 1, wherein the step of contacting a sample with an electrochemical sensor comprises contacting a sample with the electrochemical sensor, wherein the first electrode and the third electrode are separated by a closest distance in a range of 25 to 1000 μm. 3. The method of claim 1, wherein the first electrode is disposed on a first substrate and the second electrode is disposed on the first substrate. 4. The method of claim 1, wherein the step of determining the concentration of the glucose using the glucose signal comprises determining the concentration of the glucose by amperometry using the glucose signal. 5. The method of claim 1, wherein the step of determining the concentration of the glucose using the glucose signal comprises determining the concentration of the glucose by coulometry using the glucose signal. 6. The method of claim 1, wherein the step of determining the concentration of the glucose using the glucose signal comprises determining the concentration of the glucose by potentiometry using the glucose signal. 7. The method of claim 1, wherein the step of determining the concentration of the glucose using the glucose signal comprises determining the concentration of the glucose by voltammetry using the glucose signal. 8. The method of claim 1, wherein the sample chamber is sized to contain a volume of no more than about 0.5 μL of the sample. 9. The method of claim 1, wherein the sample chamber is sized to contain a volume of no more than about 0.2 μL of the sample. 10. The method of claim 1, wherein the sample chamber is sized to contain a volume of no more than about 0.1 μL of the sample. 11. The method of claim 1, wherein the sample is a blood sample, and wherein the method further comprises obtaining the sample from a finger of a subject. 12. The method of claim 1, wherein the sample is a blood sample, and wherein the method further comprises obtaining the sample from a region of a subject having a lower nerve end density as compared to a fingertip. 13. The method of claim 1, wherein the proximal end comprises a first extension positioned at a first sample entry port and a second extension positioned at a second sample entry port.
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