IP Library Granted Patent US 12,458,925
Granted Patent B2
US 12,458,925 · App. 17/472,659 · Granted Nov 4, 2025

Membrane devices for filtration and extraction

Inventors: William E. Brewer (Columbia, SC); Matthew G. Fitts (Columbia, SC)
Assignee: DPX Technologies, Inc.
B01D61/18B01D69/108G01N1/4077G01N2001/4088
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 12,458,925
App. No.
17/472,659
Granted
Nov 4, 2025
Kind
B2
Abstract

A device for filtration or extraction using at least one filtration membrane is disclosed. The device is shaped like a Buchner funnel, but small enough to fit with wide bore pipette tips, slip tip syringes or an adaptor of a robotic liquid handler or pipettor. It also houses one or more filtration membranes and or a separation resin. A reservoir adaptor can be added to the top in a fluid tight manner to provide a removable large volume container where needed for larger samples, and a gasket adaptor allows the reservoir to be connected to other devices in a fluid tight manner.

Claims (50)

1 . A membrane device, said device comprising:

a) an upper portion having an open ended tubular shape with 0-2° taper and an internal diameter that is wide enough to fit over a separate device with a fluid tight fit, said separate device selected from a wide bore pipette tip, a slip tip syringe or a robotic liquid handler (RLH) adaptor;

b) a lower portion below said upper portion, said lower portion being an open ended tubular shape with 0-3° taper;

c) an intermediate portion having 45-180° of taper between said upper portion and said lower portion;

d) said upper, intermediate and lower portions being in fluidic connection;

e) a ridge on an inner surface between said upper portion and said intermediate portion;

f) at least one circular filtration membrane located on top of said ridge;

g) an optional removable reservoir adaptor that is an open ended tubular element having a distal end configured to fit inside said upper portion and provide a fluid tight fit therewith and an upper end configured to fit over said separate device in a fluid tight fit; and

h) an optional removable gasket adaptor that is an open ended tube having a gasket coating on a bottommost outer surface and sized to fit inside said optional removable reservoir adaptor and provide a fluid tight interface therewith and an upper end configured to fit over said separate device.

2 . The device of claim 1 , wherein said upper portion has a 1° taper and said lower portion has a 2° taper.

3 . The device of claim 1 , wherein said upper portion has a 1° taper and said lower portion has a 2° taper and having said reservoir adaptor, said reservoir adaptor having a 1° taper at a lower end thereof.

4 . The device of claim 1 , having said gasket adaptor, a bottommost edge of said gasket adaptor having an elastomeric coating.

5 . The device of claim 1 , wherein said ridge is annular and has one or more support ribs protruding internally from said ridge for further supporting said at least one filtration membrane.

6 . The device of claim 1 , further comprising a locking washer in the shape of an annular disk located above said at least one filtration membrane for holding said at least one filtration membrane in place.

7 . The device of claim 1 , said device having a plurality of circular filtration membranes located on top of said ridge.

8 . The device of claim 1 , said device having two circular filtration membranes and a separation resin therebetween.

9 . The device of claim 1 , wherein said at least one filtration membrane comprises silica, nylon, cellulose, nitrocellulose, polypropylene, polyethylene, polytetrafluoroethylene, polyvinylidenefluoride, ceramics, metal, immobilized streptavidin, immobilized biotin, immobilized protein A, immobilized protein G, or combinations thereof.

10 . The device of claim 1 , wherein said device has a total length of about 2 cm, wherein said upper tubular portion has an internal diameter of 6-7 mm and a length of about 5 mm; wherein said lower tubular portion is about 1.5 to 2 cm, and the outer diameter of the lower tubular portion is 0.1-2 mm.

11 . The device of claim 1 , wherein said device has a total length of about 2 cm, wherein said upper tubular portion has an internal diameter of 4-5 mm and a length of about 5 mm; wherein said lower tubular portion is about 1.5 cm in length and is 1.6 mm or less in outer diameter.

12 . A kit comprising a container holding a plurality of membrane devices of claim 1 plus a plurality of wide bore pipette tips or slip fit syringes or reservoir adaptors or gasket adaptors that fit said membrane device.

13 . A kit comprising a container holding a plurality of membrane devices of claim 1 plus a plurality of reservoir adaptors that fit said membrane device and a plurality of gasket adaptors that fit said reservoir adaptors or pipette tips.

14 . A method for treating a chemical or biological sample, comprising:

a) dispensing a chemical or biological sample into the membrane device of claim 1 using said separate device;

b) trapping a first portion of said sample in or on said at least one circular filtration membrane;

c) passing a remaining portion of said sample out of said membrane device.

15 . The method of claim 14 , comprising a further step of eluting said first portion of said sample from said at least one circular filtration membrane after trapping step b).

16 . The method of claim 14 , said at least one circular filtration membrane being at least two membranes with a separation resin therebetween.

17 . The method of claim 14 , further including one or more washing steps comprising passing a wash solution through said membrane device.

18 . The method of claim 14 , said at least one circular filtration membrane being a plurality of membranes with decreasing pore size from a top membrane to a bottom membrane.

19 . A method for extracting nucleic acids from a sample, comprising:

a) dispensing a sample containing nucleic acid into the membrane device of claim 1 ;

b) trapping said nucleic acid in or on said at least one circular filtration membrane, said at least one circular filtration membrane comprising silica;

c) passing a remaining portion of said sample out of said membrane device;

d) passing an ethanol solution through said device;

e) drying said filtration membrane;

f) passing at least one elution buffer for unbinding the nucleic acids from said silica through said membrane device; and

g) collecting said elution buffer and nucleic acids into a separate sample collection vial.

20 . The method of claim 19 , further including a PCR amplification step to amplify said nucleic acid and a detection step to detect said amplified nucleic acid.

21 . A method of isolating DNA from a cell sample, said method comprising the steps of:

a) dispensing a sample containing cells into the membrane device of claim 1 ;

b) passing a lysis buffer through said membrane device to lyse cells and release nuclei and cell debris;

c) trapping said nuclei in or on said at least one circular filtration membrane, said membrane having a pore size of 0.4 to 5 microns;

d) passing a nuclear lysis buffer through said membrane device to lyse said nuclei and release DNA; and

e) collecting said nuclear lysis buffer and said DNA into a separate sample collection vial.

22 . The method of claim 21 , further including a PCR amplification step to amplify said DNA and a detection step to detect said amplified DNA.

23 . A method of isolating DNA from whole blood, said method comprising the steps of:

a) adding water to blood to lyse red blood cells while retaining white blood cells;

b) passing said white blood cells through the membrane device of claim 1 to trap said white blood cells in or on said filtration membrane;

c) passing lysing solution through said membrane device to lyse said white blood cells and release DNA;

d) collecting said lysate solution and said DNA.

Assignments (2)
CHANGE OF NAME Recorded Oct 3, 2025
From: BREWER, WILLIAM E.; FITTS, MATTHEW G.
To: DPX TECHNOLOGIES, INC.
Reel/Frame 072461/0392 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2021
From: BREWER, WILLIAM E; FITTS, MATTHEW G
To: DPX TECHNOLOGIES, LLC
Reel/Frame 057873/0975 →
Continuity (2)
Provisional Application 63080396 · Sep 18, 2020
Related Publication 20220088537A1 · Mar 24, 2022
References Cited (7)
US 4341635A · Golias · 1982 [cited by examiner]
US 8202693B2 · Guo · 2012 [cited by applicant]
US 20060182657A1 · Pathirana et al. · 2006 [cited by applicant]
US 20160103045A1 · Scott · 2016 [cited by examiner]
EP 1835020A1 · 2007 [cited by applicant]
WO 2018026886A1 · 2018 [cited by applicant]
Extended European Search Report issued in European Patent Application No. 21196765.8, dated Dec. 21, 2021 (9 pages). [cited by applicant]