IP Library Granted Patent US 12,709,631
Granted Patent B2
US 12,709,631 · App. 18/251,412 · Granted Aug 18, 2026

Filtration unit and a method for biomaterial purification

Inventors: Kristopher E. Richardson (Inver Grove Heights, MN); Daniel J. O'Neal (St. Paul, MN); Jerald K. Rasmussen (Woodville, WI); Andrew W. Vail (Bayport, MN); Alexei M. Voloshin (Woodbury, MN)
Assignee: Life Technologies Corporation
C07K1/32B01D37/00B01D39/1623B01D71/56C07K1/34C07K1/36C07K16/065B01D2239/0618B01D2239/0622B01D2239/1216B01D2239/1233B01D2239/1266
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,709,631
App. No.
18/251,412
Granted
Aug 18, 2026
Kind
B2
Abstract

Described herein is a method of purifying a target molecule from an aqueous biological composition, the method comprising: (a) contacting a cationic polymer and the aqueous biological composition to form a mixture, the mixture comprising a bio-polymer complex and the target non-binding molecule in a liquid, wherein the bio-polymer complex has an average particle diameter of at least 50 micrometers; (b) providing a filtering unit comprising (i) a housing having an inlet and an outlet, (ii) a porous, continuous filter medium which is fluidly connected to the inlet and the outlet, and (iii) a collection region upstream from the porous, continuous filter medium; (c) adding the mixture to the inlet; and (d) allowing the mixture to separate in the filtering unit, whereby the bio-polymer complex collects in the collection region and the target non-binding molecule passes through the filter medium, and wherein the majority of flow of the liquid through the porous, continuous filter medium is not substantially parallel with the direction of gravity.

Claims (31)

1 . A method of purifying a target non-binding molecule from an aqueous biological composition containing a binding species, the method comprising:

(a) contacting a cationic polymer and the aqueous biological composition to form a mixture, the mixture comprising a bio-polymer complex and the target nonbinding molecule in a liquid, wherein the bio-polymer complex has an average particle diameter of at least 50 micrometers;

(b) providing a filtering unit comprising (i) a housing having an inlet and an outlet, (ii) a porous, continuous filter medium which is fluidly connected to the inlet and the outlet, and (iii) a collection region disposed upstream from the porous, continuous filter medium; and

(c) adding the mixture to the inlet; and

(d) allowing the mixture to be separated in the filtering unit, whereby the bio-polymer complex collects in the collection region and the target non-binding molecule passes through the filter medium, and wherein a majority of flow of the liquid through the filter medium is at least partially parallel to the direction of gravity.

2 . The method of claim 1 , wherein the average diameter of the pores in the porous, continuous filter medium is symmetric in the direction of liquid flow.

3 . The method of claim 1 , wherein the porous, continuous filter medium has a pore size of at least 0.1 micrometers and at most 200 micrometers.

4 . The method of claim 1 , wherein the porous, continuous medium has a frontal surface area and wherein the collection region has a volume of at least 40 L per 1 m2 of frontal surface area.

5 . The method of claim 1 , wherein the flow of the liquid through the porous, continuous filter medium is in a direction counter to gravity.

6 . The method of claim 1 , wherein the flow of the liquid through the porous, continuous filter medium is in a direction from 30 to 90 degrees from the direction of gravity.

7 . The method of claim 1 , wherein the net direction of the fluid flow is not parallel to the direction of gravity.

8 . The method of claim 1 , wherein the cationic polymer is a water soluble or water dispersible polymer.

9 . The method of claim 1 , wherein the cationic polymer is functionalized with at least one of (a) guanidinyl groups, optionally according to the formula:

[C(R1)=N−R2]−N(R3)−[C(=NR4)N(R4)] m —R5,

wherein

R1 is a H, C1-C12 alkyl, C5-C12 (hetero) aryl, or a residue of the polymer chain;

R2 is a covalent bond, a C2-C12 (hetero)alkylene, or

a C5-C12 (hetero) arylene; each R3 is independently H, C1-C12 alkyl, or C5-C12 (hetero) aryl;

each R4 is H, C1-C12 alkyl or alkylene, C5-C12 (hetero) aryl or (hetero) arylene, cyano, or —C(═NH) N (R2)-Polymer;

n is 0 or 1; and

m is 1 or 2; and

(b) quaternary ammonium groups.

10 . The method of claim 1 , wherein the cationic polymer is derived from an amino polymer.

11 . The method of claim 1 , wherein the cationic polymer is derived from a carbonyl polymer.

12 . The method of claim 1 , wherein 0.1 to 10.000 micrograms of cationic polymer is added per mL of the aqueous biological composition.

13 . The method of claim 1 , wherein the bio-polymer complex has an average particle diameter of at most 200 micrometers.

14 . The method of claim 1 , wherein the liquid comprises water.

15 . The method of claim 1 , further comprising suspending the bio-polymer complex in the liquid prior to addition to the filtering unit.

16 . The method of claim 1 , wherein immediately following step (a), the mixture is added to the inlet.

17 . The method of claim 1 , wherein the porous, continuous filter medium is grafted.

18 . The method of claim 17 , wherein the porous, continuous filter medium has a modified surface layer comprising a grafted acrylic polymer comprising 10 to 100 percent by weight of a cationic or catatonically-ionizable monomer unit and optionally, a divalent residue of a polyether (meth) acrylate.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066432/0206 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2023
From: RICHARDSON, KRISTOPHER E.; O'NEAL, DANIEL J.; RASMUSSEN, JERALD K.; VAIL, ANDREW W.; VOLOSHIN, ALEXEI M.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 063501/0751 →
Continuity (2)
Provisional Application 63121269 · Dec 4, 2020
Related Publication 20240010674A1 · Jan 11, 2024
References Cited (40)
US 3876738A · Marinaccio et al. · 1975 [cited by applicant]
US 3928517A · Knight et al. · 1975 [cited by applicant]
US 4118531A · Hauser · 1978 [cited by applicant]
US 4529256A · Kretzschmar et al. · 1985 [cited by applicant]
US 4707265A · Barnes, Jr. et al. · 1987 [cited by applicant]
US 4726989A · Mrozinski · 1988 [cited by applicant]
US 4867881A · Kinzer · 1989 [cited by applicant]
US 5120594A · Mrozinski · 1992 [cited by applicant]
US 5260360A · Mrozinski et al. · 1993 [cited by applicant]
US 5458782A · Hou et al. · 1995 [cited by applicant]
US 5962544A · Waller, Jr. · 1999 [cited by applicant]
US 6056529A · Meyering et al. · 2000 [cited by applicant]
US 6267916B1 · Meyering et al. · 2001 [cited by applicant]
US 6413070B1 · Meyering et al. · 2002 [cited by applicant]
US 6464084B2 · Pulek · 2002 [cited by applicant]
US 6712966B1 · Pulek · 2004 [cited by examiner]
US 6776940B2 · Meyering et al. · 2004 [cited by applicant]
US 6779411B1 · Spurgeon · 2004 [cited by applicant]
US 6939466B2 · Pulek et al. · 2005 [cited by applicant]
US 7178676B2 · Pulek et al. · 2007 [cited by applicant]
US 7338692B2 · Smith et al. · 2008 [cited by applicant]
US 8945896B2 · Rasmussen et al. · 2015 [cited by applicant]
US 9296847B2 · Rasmussen et al. · 2016 [cited by applicant]
US 10005814B2 · Rasmussen et al. · 2018 [cited by applicant]
US 10087405B2 · Swanson et al. · 2018 [cited by applicant]
US 10722848B2 · Hester · 2020 [cited by examiner]
US 20080023385A1 · Baker, Jr. · 2008 [cited by examiner]
US 20110259812A1 · Marks et al. · 2011 [cited by applicant]
US 20180265542A1 · Rasmussen et al. · 2018 [cited by applicant]
WO 1997012901A1 · 1997 [cited by applicant]
WO 2013009491A2 · 2013 [cited by applicant]
WO 2016153915A1 · 2016 [cited by applicant]
WO 2017217930A1 · 2017 [cited by applicant]
WO 2021105864A1 · 2021 [cited by applicant]
Amersham Biosciences, “8-1165-29AA Selecting Hollow Fiber Cartridges and Systems”, 2003, 116 pages. [cited by applicant]
Davies, C.N., “The Separation of Airborne Dust and Particles” in the Institution of Mechanical Engineers, London, Proceedings, 1B, 1952, pp. 185-213. [cited by applicant]
International Search Report received for PCT International Application No. PCT/IB2021/060323, mailed on Feb. 23, 2022, 5 pages. [cited by applicant]
Tarleton, et al. “Solid Liquid Separation: Equipment Selection and Process Design”, 2007, Elsevier Science, pp. 64-66, 75, 142 and 143. [cited by applicant]
Wente, “Manufacture of Superfine Organic Fibers” Naval Research Laboratories Report No. 4364 (111437), May 1954, 19 pages. [cited by applicant]
Wente, “Superfine Thermoplastic Fibers”, Industrial and Engineering Chemistry, Aug. 1956, vol. 48, No. 8, pp. 1342-1346. [cited by applicant]