DEVICES AND METHODS FOR EXTRACTING BLOOD PLASMA

1 . A method comprising:

(a) providing or obtaining a blood sample obtained from an individual;

(b) applying a positive pressure to a starting volume of the blood sample such that the blood sample is pushed or forced into a filter or a membrane, wherein the starting volume of the blood sample is not more than about 1 milliliter (mL);

(c) filtering the blood sample through the filter or the membrane to separate plasma from the blood sample, and

(d) collecting the plasma in a collection vessel, wherein a volume of the plasma is greater than about 25% of the starting volume of the blood sample.

2 . The method of claim 1 , wherein the volume of the plasma is greater than about 30%, greater than about 35%, or greater than about 40% of the starting volume of the blood sample.

3 . The method of claim 1 , wherein at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, or greater, of the total amount of plasma present in the blood sample is collected.

4 . The method of claim 1 , wherein the plasma comprises cell-free nucleic acids.

5 . The method of claim 4 , wherein the method results in an enrichment of cell-free nucleic acids.

6 . The method of claim 1 , wherein the starting volume of the blood sample is not more than about 500 microliters (μL), not more than about 250 μL, not more than about 150 μL, not more than about 100 μL, not more than about 80 μL, not more than about 60 μL, not more than about 50 μL, not more than about 40 μL, or not more than about 25 μL.

7 . The method of claim 1 , wherein cellular nucleic acids are reduced in the plasma, or wherein the plasma is substantially free of cellular nucleic acids.

8 . The method of claim 1 , wherein cells, cell fragments, microvesicles, or any combination thereof, are reduced in the plasma.

9 . The method of claim 1 , wherein the blood sample is or comprises capillary blood.

10 . The method of claim 1 , wherein the blood sample is or comprises whole blood or one or more blood components.

11 . The method of claim 1 , wherein a volume of plasma collected in (d) is greater than a volume of plasma collected using an equivalent method using negative pressure or vacuum, such as at least about 10%, at least about 25%, at least about 50%, at least about 75%, at least about 100%, or greater than a volume of plasma collected using an equivalent method using negative pressure or vacuum.

12 . The method of claim 1 , wherein the positive pressure is of an amount of less than about 4 psi, an amount of 4 psi to about 11 psi, or an amount greater than about 11 psi.

13 . The method of claim 1 , wherein the method is performed in 1 minute or less.

14 . The method of claim 1 , wherein the method does not result in substantial lysis or disruption of white blood cells.

15 . The method of claim 1 , wherein the positive pressure is selected such that hemolysis of red blood cells may occur, but white blood cells are not lysed or disrupted.

16 . The method of claim 1 , wherein the cell-free nucleic acids are deoxyribonucleic acid.

17 . The method of claim 1 , wherein the cell-free nucleic acids comprise cell-free nucleic acids from a tumor, cell-free nucleic acids from a fetus, or cell-free nucleic acids from a tissue or an organ.

18 . The method of claim 1 , wherein the cell-free nucleic acids comprise from about 10 4 to about 10 9 cell-free nucleic acid molecules.

19 . The method of claim 1 , wherein the blood sample is obtained from the individual by a finger prick.

20 . The method of claim 1 , wherein the method is performed on a point-of-care or point-of-need device.