Device for whole blood cross flow filtration using a cannula needle

Patent metadata

Field	Value
Publication number	US-12023158-B2
Application number	US-202016891426-A
Country	US
Kind code	B2
Filing date	Jun 3, 2020
Priority date	Jul 31, 2013
Publication date	Jul 2, 2024
Grant date	Jul 2, 2024

Abstract

A whole blood filtration device is provided with a filter membrane separating a feeding volume and a clean side of the filter membrane from each other. The feeding volume communicates with a first feeding side opening and with a second feeding side opening. The filter membrane has pores with a pore size that ensures permeability of the filter membrane to blood plasma/serum and that retains blood cells. The first feeding side opening can be coupled to a first blood pump for feeding blood from the first feeding side opening into the feeding volume so that blood plasma/serum permeates the filter membrane and blood cells, retained by the filter membrane, exit from the feeding volume through the second feeding side opening.

First claim

What is claimed is:

1. A whole blood filtration device separating blood plasma/serum from blood cells and collecting the separated plasma/serum in a connection container for analysis, the whole blood filtration device comprising:
a filter housing having a tubular outer wall and elongated in an axial direction, the filter housing, comprising:
a first feeding side opening at a first axial end of the filter housing, the first feeding side opening having a first opening orientation;
a second feeding side opening at an opposite second axial end of the filter housing, the second feeding side opening having a second opening orientation;

two manual blood pumps of a resilient elastic material, comprising:
a first blood pump configured as a first resilient elastic balloon having a hollow interior compressible by squeezing, the first blood pump fixedly connected to the first feeding side opening; and
a second blood pump configured as a second resilient elastic balloon having a hollow interior compressible by hand squeezing, the second blood pump fixedly connected to the second feeding side opening;
wherein the first blood pump is coupled onto the first feeding side opening by a lock connection, the first blood pump having opposing pump actuation sides configured to compress together in a direction transverse to the axial direction;
wherein the second blood pump is coupled onto the second feeding side opening by a lock connection, the second blood pump having opposing pump actuation sides configured to compress together in a direction transverse to the axial direction;

wherein the filter housing further comprises a sample inlet opening in communication with a feeding volume to feed a blood sample into the feeding volume;
wherein the sample inlet opening comprises a cannula needle in communication with the feeding volume;
a filter membrane separating the feeding volume and a clean side of the filter membrane from each other, the filter membrane arranged in an interior of the filter housing;
wherein the filter membrane comprises at least one hollow fiber membrane made of a ceramic material, comprising a lumen including a first terminal opening and a second terminal opening;
the sample inlet opening arranged at the first axial end of the filter housing, the sample inlet opening projecting radially outward from an outer surface of the filter housing, the sample inlet opening in fluid communication with the feeding volume;
wherein the lumen in an interior of the at least one hollow fiber membrane forms the feeding volume,
the first feeding side opening in communication with the first terminal opening and the sample inlet opening, and
the second feeding side opening is in communication with the second terminal opening;

wherein the at least one hollow fiber membrane comprises a hydrophilicity-reducing coating;
wherein the term “hydrophilicity-reducing” is defined to refer to a water or blood droplet contact angle of the at least one hollow fiber membrane which is larger than a water or blood droplet contact angle of the at least one hollow fiber membrane prior to coating;
the filter membrane including pores with a pore size that ensures permeability of the filter membrane to blood plasma/serum and that retains blood cells, the pore size is between 100 nanometers and 1,000 nanometers, the filter membrane having a roughness lower than 10 microns;
wherein the first and/or the second blood pump, when released from compression, is configured to apply a vacuum to the sample inlet opening to draw blood through the sample inlet opening and into the feeding volume adjacent to the first feeding side opening;
wherein the first blood pump is operable, by compression, to feed blood from the first feeding side opening into the first feeding side and the feeding volume so that blood plasma/serum permeates the filter membrane and blood cells, retained by the filter membrane, exit from the feeding volume through the second feeding side opening;
wherein the second blood pump is operable, by compression, to feed blood from the second feeding side opening into the feeding volume so that a blood plasma/serum permeates the filter membrane and blood cells, retained by the filter membrane, exit from the feeding volume through the first feeding side opening;
wherein the interior of the filter housing at the clean side is hydrophobically coated; and
wherein the filter housing further comprises:
a plasma/serum outlet opening in communication with the clean side of the and arranged on the filter housing between the first axial end and the second axial end;

wherein one of the first blood pump and the second blood pump when de-coupled from the filter housing is configured to be removably coupled to a cannula needle to take blood from a patient.

2. The whole blood filtration device according to claim 1 , wherein
the at least one hollow fiber membrane is a membrane pre-treated by pre-flushing with an ionic solution.

3. The whole blood filtration device according to claim 2 , wherein
the ionic solution is a NaCl solution.

4. The whole blood filtration device according to claim 1 , wherein
the hydrophilicity-reducing coating is a hydrophobic coating.

5. The whole blood filtration device according to claim 1 , wherein
the material of the at least one hollow fiber membrane is a ceramic material comprising the pores with the pore size that ensures permeability of the filter membrane to blood plasma/serum and that retains blood cells.

6. The whole blood filtration device according to claim 1 , wherein
the filter housing tapers toward the plasma/serum outlet opening.

7. The whole blood filtration device according to claim 1 , further comprising: a blood container detachably plugged to the cannula needle.

8. The whole blood filtration device according to claim 1 , further comprising:
a plasma or serum container detachably connected to the plasma/serum outlet opening.

9. The whole blood filtration device according to claim 7 , wherein the blood container has a septum seal which is perforated by the cannula needle.

10. A whole blood filtration device separating blood plasma/serum from blood cells and collecting the separated plasma/serum in a connection container for analysis, the whole blood filtration device comprising:
a filter housing having a tubular outer wall and elongated in an axial direction, the filter housing, comprising:
a first feeding side opening at a first axial end of the filter housing, the first feeding side opening having a first opening orientation;
a second feeding side opening at an opposite second axial end of the filter housing, the second feeding side opening having a second opening orientation;

two manual blood pumps of a resilient elastic material, comprising:
a first blood pump configured as a first resilient elastic balloon having a hollow interior compressible by squeezing, the first blood pump fixedly connected to the first feeding side opening; and
a second blood pump configured as a second resilient elastic balloon having a hollow interior compressible by squeezing, the second blood pump fixedly connected to the second feeding side opening;
wherein the first blood pump is coupled onto the first feeding side opening by a lock connection, the first blood pump having opposing pump actuation sides configured to compress together in a direction transverse to the axial direction;
wherein the second blood pump is coupled onto the second feeding side opening by a lock connection, the second blood pump having opposing pump actuation sides configured to compress together in a direction transverse to the axial direction;

wherein the filter housing further comprises a sample inlet opening in com

Assignees

• Mann & Hummel Gmbh

Inventors

• Winkler Dagmar
• Rupp Heike
• Schuetz Steffen
• Talmon-Gros Dietmar
• Fasold Michael
• Schwinghammer Alfons-Alois
• Bartel Frank
• Bauer Sascha
• Nytz Patrick

Classifications

• B01D63/0233

  forming the bundle · CPC title

• B01D63/031

  Two or more types of hollow fibres within one bundle or within one potting or tube-sheet · CPC title

• B01D2313/901

  Integrated prefilter · CPC title

• G01N2800/22

  Haematology · CPC title

• G01N2201/0221

  Portable; cableless; compact; hand-held · CPC title