US2017336424A1PendingUtilityA1
Method for separating target molecules or particles from fibrinogen-containing samples including blood components
Est. expirySep 15, 2030(~4.2 yrs left)· nominal 20-yr term from priority
C12Q 1/56G01N 33/56938G01N 2333/75G01N 2333/974G01N 33/86C12Q 1/14C12Q 1/04
59
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Claims
Abstract
A method for separating target molecules or particles from a fibrinogen containing sample comprises: (a) trapping the said target molecules or particles in a fibrin network by converting at least partially the fibrinogen contained in the sample into fibrin; (b) retracting the said fibrin network to form a fibrin clot; (c) separating the said fibrin clot from the surrounding sample medium,
Claims
exact text as granted — not AI-modified1 .- 27 . (canceled)
28 . A sample collection device for separating target molecules or particles from a sample comprising: (i) an identification code; (ii) a container for containing the sample; and (iii) a dry reagents formulation in the container, the device being operable to form a fibrin clot that traps in a separable manner the target molecules or particles upon the exposure of the sample to thrombin or a thrombin-like enzyme within the device in the presence of fibrinogen that is native to the sample and/or artificially added, wherein the formulation comprises thrombin or a thrombin-like enzyme.
29 . The device according to claim 28 , wherein the volume of the sample container is between 0.1 and 20 ml.
30 . The device according to claim 28 , wherein the concentration of fibrinogen within the sample is between 0.1 to 10 mg/ml.
31 . The device of claim 28 wherein said fibrinogen is native to the sample.
32 . The device according to claim 28 wherein said fibrinogen is initially included within the device, prior to adding the sample into the device.
33 . The device according to claim 28 wherein said thrombin or thrombin-like enzyme is included within the device in a lyophilized format.
34 . (canceled)
35 . The device according to claim 28 , which further includes additives selected from the group consisting of calcium, chelating agents; activated platelet cells, activated platelet cell lysate, and factor XIII.
36 . The device according to claim 28 , which further includes magnetic particles.
37 . The device according to claim 36 , wherein the magnetic particles are coated with a fibrinogen/fibrin binding moiety.
38 . The device according to claim 37 , which further comprises molecules having: (I) fibrin/fibrinogen-binding moiety and (II) a substance-capturing moiety directed against said target molecules or particles.
39 . The device according to claim 28 , wherein the fibrinogen in the sample is recombinant.
40 . The device according to claim 39 , wherein the fibrinogen in the sample is a fibrinogen fusion protein with a capturing moiety domain directed against said target molecules or particles.
41 . A device according to claim 28 , wherein the target molecules or particles comprise bacteria, virus, yeast, proteins, peptides and/or nucleic acids.
42 . (canceled)
43 . The device according to claim 28 , wherein the dry formulation further comprises fibrinogen.Cited by (0)
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