Magnetic point-of-care systems and assays for determining GFAP in biological samples
Disclosed herein are systems and assays that employ magnetically susceptible beads and point-of-care devices comprising magnetic immunosensors to determine the amount of glial fibrillary acidic protein (GFAP) in a biological sample obtained from a subject.
1 . An assay for measuring an amount of glial fibrillary acid protein (GFAP) in a biological sample obtained from a subject, comprising:
performing an assay for GFAP, wherein the assay comprises: (a) contacting the sample with a cartridge comprising at least one magnetic immunosensor and (i) at least one first specific binding partner comprising at least one anti-GFAP antibody which is configured to specifically bind to GFAP in the sample, wherein the anti-GFAP antibody that is configured to be printed on the cartridge, wherein said at least one first specific binding partner is configured to be immobilized on at least one magnetically susceptible bead;
and (ii) at least one second specific binding partner comprising a detectable label that is configured to be printed on the cartridge, thereby producing one or more complexes comprising the first specific binding partner-GFAP-second specific binding partner;
(b) said assay configured for magnetically capturing and retaining the bead containing the complexes using the at least one magnetic immunosensor; and (c)) said assay configured for assessing a signal from the complexes, wherein the amount of detectable signal from the detectable label is configured to indicate the amount of GFAP in the sample, wherein the cartridge is used in a point-of-care device, and further wherein the assay is configured to exhibit at least a 5-fold increase in sensitivity compared to an assay that does not immobilize the first specific binding partner on a magnetically susceptible bead and magnetically capture and retain the bead containing the complexes on at least one magnetic immunosensor in a cartridge used in a point-of-care device.
2 . The assay of claim 1 , wherein the assay further comprises the step of washing unbound sample that is not magnetically captured and retained on the at least one magnetic immunosensor.
3 . The assay of claim 1 , wherein the magnetic immunosensor comprises a sensing electrode on a substantially planar chip and a magnetic layer on the chip.
4 . The assay of claim 3 , wherein the magnetic layer comprises high-field magnetic particles.
5 . The assay of claim 1 , wherein the assay further comprises measuring an amount of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) in the sample using a non-magnetic assay.
6 . The assay of claim 1 , wherein the assay exhibits at least a 7-fold, at least an 8-fold, at least a 9-fold, at least a 10-fold, at least a 11-fold, at least a 12-fold, at least a 13-fold, at least a 14-fold, or at least a 15-fold increase in sensitivity compared to an assay that does not immobilize the first specific binding partner on a magnetically susceptible bead and magnetically capture and retain the bead containing the complexes on at least one magnetic immunosensor in a cartridge contained in a point-of-care device.
7 . The assay of claim 1 , wherein the assay is used to aid in a diagnosis and evaluation of a subject that has sustained or may have sustained an injury to the head.
8 . The assay of claim 7 , wherein the subject is diagnosed as having a traumatic brain injury.
9 . The assay of claim 8 , wherein the subject is treated for the traumatic brain injury.
10 . The assay of claim 1 , wherein the sample is collected using a microsampling device or a fingerstick device.
11 . The assay of claim 1 , wherein the sample is venous blood, capillary blood, fingerstick blood, or a combination thereof.
12 . The assay of claim 1 , wherein the sample is processed prior to performing the assay.
13 . The assay of claim 12 , wherein the sample is processed by plasma separation.
14 . The assay of claim 13 , wherein the sample is processed using a plasma separation device.
15 . The assay of claim 14 , wherein the plasma separation device is: (a) incorporated into or operably linked to the point-of-care device; or (b) separate from the point-of-care device.
16 . The assay of claim 5 , wherein the amount of GFAP is communicated by displaying on the device.
17 . A system comprising: an assay for glial fibrillary acidic protein (GFAP), wherein the assay comprises contacting a biological sample from a subject with a cartridge comprising at least one magnetic immunosensor and (i) at least one first specific binding partner comprising at least one anti-GFAP antibody w which is configured to specifically bind to GFAP in the sample, wherein the anti-GFAP antibody that is configured to be printed on the cartridge, wherein said at least one first specific binding partner is configured to be immobilized on at least one magnetically susceptible bead;
and (ii) at least one second specific binding partner comprising a detectable label that is configured to be printed on the cartridge, thereby producing one or more complexes comprising the first specific binding partner-GFAP-second specific binding partner;
a point-of-care device comprising the cartridge, wherein the device (a) is configured to determines an amount of GFAP in a sample obtained from the subject by magnetically capturing and retaining the bead containing the complexes on the at least one magnetic immunosensor; and (b) is configured to assess a signal from the complexes, wherein the amount of detectable signal from the detectable label is configured to indicate the amount of GFAP in the sample, wherein the assay is configured to exhibit at least a 5-fold increase in sensitivity compared to an assay that does not immobilize the first specific binding partner on a magnetically susceptible bead and magnetically capture and retain the bead containing the complexes on at least one magnetic immunosensor in a cartridge contained in a point-of-care device.
18 . The system of claim 17 , wherein the magnetic immunosensor comprises a sensing electrode on a substantially planar chip and a magnetic layer on the chip.
19 . The system of claim 18 , wherein the magnetic layer comprises high-field magnetic particles.
20 . The system of claim 17 , wherein the system further comprises an assay for measuring an amount of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) in the sample using a non-magnetic assay.
21 . The system of claim 17 , wherein the assay exhibits at least a 7-fold, at least an 8-fold, at least a 9-fold, at least a 10-fold, at least a 11-fold, at least a 12-fold, at least a 13-fold, at least a 14-fold, or at least a 15-fold increase in sensitivity compared to an assay that does not immobilize the first specific binding partner on a magnetically susceptible bead and magnetically capture and retain the bead containing the complexes on at least one magnetic immunosensor in a cartridge contained in a point-of-care device.
22 . The system of claim 17 , wherein the assay is used to aid in a diagnosis and evaluation of a subject that has sustained or may have sustained an injury to the head.
23 . The system of claim 22 , wherein the subject is diagnosed as having a traumatic brain injury.
24 . The system of claim 23 , wherein the subject is treated for the traumatic brain injury.
25 . The system of claim 17 , wherein the sample is collected using a microsampling device or a fingerstick device.
26 . The system of claim 17 , wherein the sample is venous blood, capillary blood, fingerstick blood or a combination thereof.
27 . The system of claim 17 , wherein the sample is processed prior to performing the assay.
28 . The assay of claim 27 , wherein the sample is processed by plasma separation.
29 . The system of claim 28 , wherein the sample is processed using a plasma separation device.
30 . The system of claim 29 , wherein the plasma separation device is: (a) incorporated into or operably linked to the point-of-care device; or (b) separate from the point-of-care device.
31 . The system of claim 20 , wherein the amount of GFAP is communicated by displaying on the device.
32 . The assay of claim 16 , wherein the assay, prior to displaying the amount of the GFAP on the device, further comprises:
a. determining the amount or of GFAP in the capillary blood sample;
b. selecting a conversion factor for comparing the amount of GFAP in the sample with the amount of the GFAP in venous blood, wherein the conversion factor is a static correlation ratio, a dynamic ratio or a combination thereof; and
c. normalizing the amount of GFAP in the sample with the amount of GFAP from venous blood by applying the conversion factor selected in step b) to the amount of GFAP in the sample.
33 . The assay of claim 32 , wherein the normalized amount of GFAP is displayed by the device.
34 . The assay of claim 32 , wherein the conversion factor is from about 1.2:1.0 to about 1.0:0.5.
35 . The assay of claim 32 , wherein the conversion factor is from about 1.0:0.85.