Closed loop control of microfluidic systems
US-2024293817-A1 · Sep 5, 2024 · US
US10413901B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10413901-B2 |
| Application number | US-201515507616-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 28, 2015 |
| Priority date | Aug 29, 2014 |
| Publication date | Sep 17, 2019 |
| Grant date | Sep 17, 2019 |
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Provided herein is technology relating to microfluidic devices and particularly, but not exclusively, to devices, methods, systems, and kits for imparting stresses on a fluid flowing through a microfluidic device that is designed to mimic a stress profile of a macrofluidic device or pathology.
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We claim: 1. A method for monitoring platelet activation state in a subject, the method comprising: a) modeling the shear stress profile of a pathology in a medical device, wherein the pathology is a cardiovascular pathology, wherein the medical device is a mechanical circulatory support device, wherein the modeling comprises one or more of device thrombogenicity emulation, producing a probability density function of the medical device, and determining individual particle trajectories for particles flowing through the medical device; b) reproducing the shear stress profile of the pathology in the device in a microfluidic device; c) flowing a sample from the subject through the microfluidic device, wherein the sample comprises platelets separated from a blood sampled obtained from the subject, wherein the sample has a volume of 1 to 100 nanoliters, 1 to 1000 nanoliters, 1 to 100 microliters, or 1 to 1000 microliters; and d) testing a platelet activation state of the sample. 2. The method of claim 1 wherein the pathology is a deviation from a normal geometry or flow characteristic. 3. The method of claim 1 wherein the pathology is an arterial narrowing, stenosis, outpouching, anurysm or pseudoaneurysm, dissection, flap, fistula, constriction, thrombus, intinal hyperplasia, or tumor. 4. The method of claim 1 wherein the medical device is a ventricular assist device, stent, total artificial heart, or valve. 5. The method of claim 1 further comprising adjusting the dose of a drug or other therapeutic agent administered to the subject and/or adjusting the dose of an anti-thrombosis drug administered to the subject. 6. The method of claim 1 wherein the sample is acquired from the patient 1 to 10 times a day.
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