In-vivo monitoring of molecular targets
The present disclosure provides devices, methods and systems for analyte detection and/or monitoring, e.g., the continuous and/or semi-continuous monitoring of in-vivo analyte concentrations in real time. Generally, the devices, methods and systems of the present disclosure make use of signaling probes; methods or devices for reducing interferent-based fouling of the signaling probes, non-specific binding to the signaling probes and/or occlusion of a sensor surface; and methods and/or devices for providing an adjusted signal based on a detected signal from the signaling probes. Compositions including conformation switching signaling probes are also provided.
1. A method of determining an in vivo concentration of an analyte in a biological fluid, the method comprising:
flowing the biological fluid from a living subject;
contacting the biological fluid or a component thereof with a signaling probe comprising a conformation switching aptamer and a detectable label, wherein the signaling probe is immobilized on a working electrode of an electrochemical sensor, wherein the working electrode generates a detectable signal based on a property of the detectable label, wherein specific binding of the analyte to the conformation switching aptamer causes a change in the detectable signal generated by the working electrode, wherein the detectable label is a redox reporter and the property is a change in the rate of charge transfer or impedance at the working electrode;
detecting detectable signals during a first period of time in response to a binding event between the analyte, when present in the biological fluid, and the signaling probe, wherein the detecting comprises:
voltammetrically interrogating the working electrode during the first period of time with a first waveform to obtain a first signal;
voltammetrically interrogating the working electrode during the first period of time with a second waveform to obtain a second signal;
combining the first signal and the second signal to obtain an adjusted signal for the first period of time, wherein the adjusted signal for the first period of time has a greater magnitude than the first signal and the second signal; and
determining the in vivo concentration of the analyte during the first period of time based on the adjusted signal for the first period of time.
2. The method of claim 1 , wherein the signaling probe is immobilized in a channel of a microfluidic device.
3. The method of claim 2 , wherein the channel is configured to receive a sample stream comprising the biological fluid and a buffer stream, and wherein the microfluidic device is further configured to provide a stacked laminar flow of the sample stream and buffer stream in the channel, when present in the microfluidic device, such that the sample stream is positioned adjacent to, and in contact with, the buffer stream.
4. The method of claim 3 , wherein the stacked laminar flow is a vertically stacked laminar flow.
5. The method of claim 3 , wherein the stacked laminar flow is a horizontally stacked laminar flow.
6. The method of claim 3 , wherein the height of the channel is from about 1 μm to about 1000 μm.
7. The method of claim 3 , wherein the sample stream has a first flow rate, the buffer stream has a second flow rate, and the ratio of the second flow rate to the sum of the first and second flow rates is from about 0.1:1 to about 1:1.
8. The method of claim 1 , comprising administering a pharmacologically active agent based on the determined in vivo concentration of the analyte.
9. The method of claim 8 , wherein the administering is automatic.
10. The method of claim 1 , wherein the analyte is a small molecule drug or a metabolite thereof, and the method further comprises:
administering a small molecule drug to the subject; and
following said determining, administering an adjusted dose of the small molecule drug to the subject based on the determined in vivo concentration of the analyte.
11. A method of determining a concentration of an analyte in a sample fluid, the method comprising:
flowing the sample fluid;
contacting the sample fluid or a component thereof with a signaling probe comprising a redox reporter, wherein the signaling probe produces a detectable signal based on specific binding of the signaling probe to the analyte when present in the sample fluid and change in the rate of charge transfer or impedance at a working electrode of an electrochemical sensor that the signaling probe is immobilized on, and wherein the signaling probe further comprises a conformation switching aptamer;
detecting detectable signals during a first period of time in response to a binding event between the analyte, when present in the sample fluid, and the signaling probe, wherein the detecting comprises:
voltammetrically interrogating the working electrode during the first period of time with a first waveform to obtain a first signal;
voltammetrically interrogating the working electrode during the first period of time with a second waveform to obtain a second signal;
combining the first signal and the second signal to obtain an adjusted signal for the first period of time, wherein the adjusted signal for the first period of time has a greater magnitude than the first signal and the second signal; and
determining the concentration of the analyte during the first period of time based on the adjusted signal for the first period of time.
12. The method of claim 1 , wherein voltammetrically interrogating the working electrode comprises square-wave voltammetry (SWV).
13. The method of claim 1 , wherein voltammetrically interrogating utilizes alternating current voltammetry, linear sweep voltammetry, or differential pulse voltammetry.
14. The method of claim 11 , wherein voltammetrically interrogating the working electrode comprises square-wave voltammetry (SWV).
15. The method of claim 11 , wherein voltammetrically interrogating utilizes alternating current voltammetry, linear sweep voltammetry, or differential pulse voltammetry.
16. The method of claim 1 , wherein the redox reporter comprises a redox-active metal center.
17. The method of claim 16 , wherein the redox reporter is a redox-active organic molecule.
18. The method of claim 1 , wherein the detectable label is covalently linked to the conformation switching aptamer.
19. The method of claim 1 , wherein the adjusted signal for the first period of time is the difference of the first signal and the second signal divided by the average of the first signal and the second signal.
20. The method of claim 1 , wherein the method further comprises:
continuing to flow the biological fluid from the living subject;
continuing to contact the biological fluid or a component thereof with the signaling probe;
detecting detectable signals during a second period of time in response to a binding event between the analyte, when present in the biological fluid, and the signaling probe, wherein the detecting comprises:
voltammetrically interrogating the working electrode during the second period of time with the first waveform to obtain a third signal;
voltammetrically interrogating the working electrode during the second period of time with the second waveform to obtain a fourth signal;
combining the third signal and the fourth signal to obtain an adjusted signal for the second period of time;
determining the in vivo concentration of the analyte during the second period of time based on the adjusted signal for the second period of time.
21. The method of claim 20 , wherein the second period of time begins at least 5 minutes after the first period of time ends.
22. The method of claim 21 , wherein the second period of time begins at least 1 hour after the first period of time ends.