Method of filtering solids from a solution derived from plasma
AssigneeCsl Behring (Australia) Pty Ltd
InventorsKarl MCCANN, Zhenghui XU, Per HANSEN, Jiaxi ZHANG
Life of this patent
Estimating the term…
Loading patent…
AssigneeCsl Behring (Australia) Pty Ltd
InventorsKarl MCCANN, Zhenghui XU, Per HANSEN, Jiaxi ZHANG
Estimating the term…
A method (100) of filtering solids (41) from a solution (44) derived from blood plasma is disclosed. The method (100) comprises feeding (102) the solution (44) into a hollow fibre filter (12) at a feed rate, the hollow fibre filter (12) comprising a plurality of hollow fibres (38), each hollow fibre (38) comprising a membrane (36) defining an elongate hollow fibre channel (32). The method (100) further comprises filtering (104) the solution (44) using the hollow fibre filter (12) to produce a permeate (46) and a retentate (45), the permeate (46) passing through pores (37) of the membrane (36) at a trans-membrane pressure and the retentate (45) flowing from respective outlets of the elongate hollow fibre channels (32), wherein the permeate (46) has a reduced solids content with respect to the solution (44) fed into the hollow fibre filter (12).
A method of filtering solids from a solution derived from blood plasma, the method comprising:
The method of any one of the preceding claims, wherein the pores of the membrane have an average pore size of from about 0.1 microns to about 4 micron.
The method of any one of the preceding claims, wherein the trans-membrane pressure is from about 20 kilopascals to about 300 kilopascals.
The method of any one of the preceding claims, further comprising measuring a permeate flux during filtering.
The method of any one of the preceding claims, wherein the method comprises multiple filtering steps, and wherein the method further comprises feeding a backwash solution through the hollow fibre filter between filtering steps.
The method of any one of the preceding claims, wherein the solution has a conductivity of about 2 mS/cm to about 40 mS/cm.
The method of any one of the preceding claims, wherein the solution has a conductivity of about 8 mS/cm to about 15 mS/cm.
The method of any one of the preceding claims, wherein the solution is at a temperature of from about 4° C. to about 37° C.
The method of any one of the preceding claims, wherein the solution comprises a blood plasma fraction.
The method of any one of the preceding claims, wherein the solution comprises a buffer.
The method of any one of the preceding claims, wherein the solution comprises hemopexin.
The method of any one of the preceding claims, wherein the solution comprises a filter aid.
The method of any one of the preceding claims, wherein the solution has a pH of between about 4 and about 9.
The method of any one of the preceding claims, wherein a recovery of the permeate is at least 30%.
The method of any one of the preceding claims, wherein a recovery of the permeate is at least 50%.
The method of any one of the preceding claims, wherein a recovery of the permeate is at least 75%.
The method of any one of the preceding claims, wherein a recovery of the permeate is at least 90%.
The method of any one of the preceding claims, wherein a turbidity of the permeate is less than about 400 nephelometric turbidity units.
A blood plasma product produced using the method of any one of the preceding claims.
Dependencies are inferred from the claim text.