Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS3513976 A
Publication typeGrant
Publication dateMay 26, 1970
Filing dateMar 19, 1968
Priority dateMar 19, 1968
Publication numberUS 3513976 A, US 3513976A, US-A-3513976, US3513976 A, US3513976A
InventorsWilliam C James
Original AssigneeWilliam C James
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Leukocyte flask and method of obtaining white cells from whole blood
US 3513976 A
Abstract  available in
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

y 6, 1970 w. c. JAMES 3,513,976

LEUKOCYTE FLASH AND METHOD OF OBTAINING WHITE CELLS FROM WHOLE BLOOD Filed March 19, 1968 INVENTOR WILLIAM C. JAMES ATTORNEY US. Cl. 21078 2 Claims ABSTRACT OF THE DISCLOSURE This specification discloses a flask forpse in obtaining leukocyte from whole blood containing an ant1coagulant with the flask including a lower portion of substantially horizontal extent that receives the red blood cells, a narrow vertical column of small horizontal crosssectional area upstanding from the lower portion and which receives the leukocyte or white cells and an upper portion of large horizontal cross section that receives blood plasma. A tube is provided at one side of the lower portion for introducing mercury into the bottom thereof to raise the blood components to a desired level. A pipette is inserted through the plasma into the narrow column to withdraw the white cells aspiration.

The present invention relates to the harvesting of white blood cells from heparinized whole blood and is concerned primarily with a novel method and apparatus for achieving the harvest.

Present day practice in this field may be characterized as requiring two centrifugations of the blood with a substance of high molecular weight being added before the first centrifugation.

The present invention has as a highly important object the provision of a method and apparatus whereby the white cells of heparinized whole blood may be separated and harvested in a pure state with but a single centrifugation and without the addition of any susbtances to the blood.

Red blood cells constitute about forty percent of whole blood. Leukocyte or white blood cells are present in a proporotion of about one-half of one percent. Plasma makes up the remaining fifty-nine to sixty percent. When heparinized whole blood is centrifuged in accordance with present day practice, the small percentage of white cells forms a thin layer commonly known as a buify coat immediately over the top of the red blood cells. An important object of the present invention is to provide in a method of the type noted the step of transforming this thin layer into a narrow vertical column of leukocytes which may be readily harvested by aspiration.

In more detail, the invention has as an object the provision of a method of the character indicated which includes the step of centrifuging heparinized whole blood to form a mass of red blood cells at the bottom, a narrow column of white blood cells upstanding from the red blood cells, and a mass of plasma above the column and then harvesting the white blood cells by aspiration through the plasma.

Another object is to provide in a method of the type noted the step of accurately controlling the level constituting the line of demarcation between the red and white cells so that the latter may be harvested with the definite assurance that they will be in a pure state. This step may be carried out by introducing a required amount of a liquid of high density and chemically inert with respect to the blood, such as mercury, beneath the red blood cells.

As mentioned above, it is of course important to maintain a clear line of demarcation between the red blood United States Patent 3,513,976 Patented May 26, 1970 cells and the leukocytes. To this end, the method of this invention provides for the gradual diminution of the horizontal cross-sectional area of the red blood cells to their uppermost level at which point the narrow column of white blood cells begins.

Another important object in view is to provide apparatus for carrying out the above method with the apapparatus taking the form of a flask of what might be called a vertical dumbbell like formation. This flask comprises a bottom portion having an upper conical wall, the narrow end of which is joined to a tubular neck having a small bore with the upper end of the neck being joined into the small end of the lower conical section of an upper portion. The upper and lower portions and the intermediate neck are preferably integrally formed from any suitable transparent material such as glass.

Another object is to provide in a flask of the character aforesaid a lower portion or member the conical wall of which is formed with a passage through which extends a vertically disposed tube the lower free end of which is spaced slightly from the bottom of the flask. This tube is adapted to receive the mercury aforesaid.

In accordance with the present invention, the upper flask member terminates in an open top. A pipette of an external diameter less than the bore of the neck is passed through this open top and plasma in the upper portion into the neck with the lower end of the pipette being disposed slightly above the joinder of the neck to the conical end of the bottom section. Leukocytes are aspirated through this pipette.

Various other more detailed objects and advantages of the invention such as arise in connection with carrying out the above noted ideas in a practical embodiment will in part become apparent and in part be hereinafter stated as the description of the invention proceeds.

For a more complete understanding of the invention, reference may be had to the following description and accompanying drawing, wherein:

FIG. 1 is a side elevation of a leukocyte flask designed in accordance with the principles of this invention.

FIG. 2 is a vertical section through the flask of FIG.

1 with the components of blood illustrated as being received therein and the pipette in position for harvesting the leukocytes.

FIG. 3 is a horizontal section taken about on the plane represented by the line 33 of FIG. 1.

Referring now to the drawing, the leukocyte flask of this invention is referred to in its entirety by the reference character F. It comprises three main portions or elements which are integrally connected. It may be made of glass or any other material having the required property of transparency so that a user may readily ascertain the condition of the blood components which obtain therewithin.

The flask F comprises a lower section 10, an intermediate neck 11, and an upper section 12.

The lower section 10 includes a flat bottom wall 13, the peripheral edge of which is integrally joined to a cylindrical wall portion 14. Integrally joined to the upper edge of the latter along the line represented at 15 is a conical section 16 having a small end at 17.

The neck 11 is joined to the conical section 16 at 17 and has a small bore 18. By way of example, it is noted that this bore 18 may have a diameter of 2.5 to 3 mm.

The neck 11 will have a vertical extent that is related to the volume of blood that is handled in any single operation. Thus, with a cylindrical portion 14 having a vertical extent of 27 mm. and the conical portion 16 a vertical extent of 18 mm., the neck 11 should have an extent of about 45 mm.

The upper end of the neck 11 is indicated at 19 and integrally joined thereto is the smaller end of the conical section 20 constituting a part of the upper member 12."'

The wider end of the conical section 20 is represented by the line 21 and integrally joined thereto is a cylindrical portion 22. The upper end of the latter is rounded as indicated in 23 and joined to a cylindrical portion 24 of reduced diameter. The latter terminates in a bead 25 which defines an open top.

To complete the specifications for the flask, it is noted that with the dimensions for the lower member 10 and neck 11 as given, the conical section 20 should have a vertical extent of 18 mm., the cylindrical portion 22 a vertical extent of 31 mm., and the reduced cylindrical portion 24 a vertical extent of 11 mm. Thus, with the flask F having an overall vertical extent of about 160 mm., the neck 11 has an extent of about 45 mm. It is also notable that the cylindrical sections 14 and 22 have outside diameters of about 35 mm. and a wall thickness of about 2 mm.

The conical section 16 of the bottom member 10 is formed with a vertical passage 26 through which passes a tube 27, the lower free end 28 of which is spaced slightly above the bottom wall 13.

In use, whole blood containing an anticoagulant, such as heparin or sodium citrate, is introduced into the flask F and centrifuged. This results in red blood cells such as represented at 29, in FIG. 2, filling the lower member 10 substantially up to the line 17. Luekocytes or white blood cells indicated at 30 fill the bore 18 of the neck 11 substantially up to the point 19, and plasma represented at 31 fills the upper section 12 up to the level represented at 32.

Before this separation is achieved, mercury is introduced through the tube 27 to build up a layer 33 of mercury of about one centimeter in thickness. After the blood is centrifuged, mercury may be added or withdrawn so that the lower level of the white cells 30 in the neck 11 will be positioned substantially at the line 17. A pipette 34 is then passed through the open top defined by the bead 25 and plasma 37 is passed into the bore 18 so that the lower end of the pipette 34 is represented at 35 and is disposed just above the line 17. The white blood cells 30 may then be withdrawn by aspiration and harvested in a substantially pure state.

While a preferred specific embodiment of the invention is hereinbefore set forth, it is clearly understood that the invention is not to be limited to the exact constructions, inventions and steps illustrated and described, because various modifications of these details may be provided the lower mass, the white blood cells assume the position of the narrow column, and plasma occupies the space of the upper mass, adjusting the line of demarcation between the 'red blood cells and the white blood cells by varying 'the quantity of mercury, and then withdrawing the white blood cells from the narrow column by aspiration.

2. In a leukocyte flask for separating white blood cells from whole blood containing an anticoagulant, a lower section having an upper conical portion, a vertical neck having a bore with its lower end integrally joined to the upper end of said conical portion, and an upper section having a lower conical portion, the smaller end of which is integrally joined to the upper end of said neck of said upper and lower portions and said neck being proportioned so that after blood received therein is centrifuged, red blood cells will substantially fill the lower portion, white blood cells will fill the bore of the neck, and plasma will be contained in the upper portion, the said lower section having a flat bottom wall together with a tube passing through the conical portion of said lower section and terminating substantially near above said bottom wall.

References Cited UNITED STATES PATENTS 2,854,143 9/1958 Novak 2l0 36l X 2,928,591 3/1960 Deaver 233-26 X 3,291,693 12/1966 Brown 23326 X OTHER REFERENCES German printed application No. 1,014,348, Aug. 22, 1957, Beyerle.

JAMES L. DECESARE, Primary Examiner US. Cl. X.R.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2854143 *Sep 16, 1957Sep 30, 1958Ohio Commw Eng CoCentrifugal stratifier with plural filter means
US2928591 *Dec 27, 1956Mar 15, 1960Lee Deaver GeorgeMethod and apparatus for separating particles in a fluid dispersion
US3291693 *Jul 14, 1959Dec 13, 1966American Optical CorpMethod for determining values of components of whole blood
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3750645 *Oct 20, 1970Aug 7, 1973Becton Dickinson CoMethod of collecting blood and separating cellular components thereof
US3914985 *Mar 29, 1974Oct 28, 1975American Hospital Supply CorpCentrifuging device and method
US3977598 *Apr 17, 1975Aug 31, 1976Mcdonald BernardCentrifuge tube
US4027660 *Apr 2, 1976Jun 7, 1977Wardlaw Stephen CMaterial layer volume determination
US4040959 *Jun 22, 1976Aug 9, 1977Berman Irwin RMulti-purpose blood bag
US4077396 *Dec 2, 1976Mar 7, 1978Wardlaw Stephen CMaterial layer volume determination
US4082085 *Sep 20, 1976Apr 4, 1978Wardlaw Stephen CBlood constituent testing methods
US4255256 *Nov 23, 1979Mar 10, 1981Antonio FerranteMedium for the separation of human blood leucocytes
US4511349 *Feb 27, 1984Apr 16, 1985Beckman Instruments, Inc.Ultracentrifuge tube with multiple chambers
US4639242 *Feb 4, 1985Jan 27, 1987Babson Arthur LVessel and procedure for automated assay
US4663032 *May 14, 1985May 5, 1987Npbi Nederlands Produktielaboratorium Voor Bloedtransfusieapparatuur En Infusievloeistoffen B.V.Apparatus for decanting of a blood-plasma layer and a buffy-coat layer from a centrifuge-blood bag
US4824560 *Apr 4, 1986Apr 25, 1989Assaf Pharmaceutical Industries Ltd.Separation of materials from a liquid dispersion by sedimentation
US4861477 *Apr 21, 1988Aug 29, 1989Shiro KimuraTubular container for centrifugal separation
US5152905 *Nov 6, 1990Oct 6, 1992Pall CorporationMethod for processing blood for human transfusion
US5360545 *Aug 3, 1993Nov 1, 1994Pall CorporationFilter for obtaining platelets
US5399268 *Jul 6, 1994Mar 21, 1995Pall CorporationMethod for processing blood for human transfusion
US5445736 *Apr 25, 1994Aug 29, 1995Pall CorporationDevice and filter element for processing blood for human transfusion
US5474687 *Aug 31, 1994Dec 12, 1995Activated Cell Therapy, Inc.Methods for enriching CD34+ human hematopoietic progenitor cells
US5543060 *Jun 6, 1995Aug 6, 1996Pall CorporationMethod for processing blood for human transfusion
US5577513 *Aug 31, 1994Nov 26, 1996Activated Cell Therapy, Inc.Centrifugation syringe, system and method
US5580465 *Dec 3, 1993Dec 3, 1996Pall CorporationMethod for preparing platelets
US5646004 *Aug 31, 1994Jul 8, 1997Activated Cell Therapy, Inc.Methods for enriching fetal cells from maternal body fluids
US5648223 *Aug 31, 1994Jul 15, 1997Activated Cell Therapy, Inc.Methods for enriching breast tumor cells
US5656154 *Jun 7, 1995Aug 12, 1997Organ, Inc.Method and apparatus for separating a fluid into components and for washing a material
US5663051 *Dec 11, 1995Sep 2, 1997Activated Cell Therapy, Inc.Separation apparatus and method
US5770069 *Feb 21, 1997Jun 23, 1998Organ, Inc.Collapsible container for holding a fluid during a centrifugation operation
US5840502 *Aug 31, 1994Nov 24, 1998Activated Cell Therapy, Inc.Methods for enriching specific cell-types by density gradient centrifugation
US6309606 *Oct 29, 1998Oct 30, 2001Giammaria SitarDevice and method for the separation of human or animal cells of different densities from cellular dispersions which contain them
US8048678 *Jun 29, 2010Nov 1, 2011Ecw Therapeutics, Inc.Cell separation method and apparatus
US8241592Sep 29, 2011Aug 14, 2012Endocellutions, Inc.Cell separation method and apparatus
US9168528 *Apr 1, 2014Oct 27, 2015Alliance Partners, LlcFluids concentration cup assembly with hourglass shape
US9573130Oct 26, 2015Feb 21, 2017Alliance Partners, LlcMethod of separating biological fluids into component parts using a fluids concentration cup assembly with hourglass shape
US20100120596 *May 8, 2008May 13, 2010Ge Healthcare Bio-Sciences AbSeparation device
US20110033925 *Jun 29, 2010Feb 10, 2011Duffy Jr Neil FCell Separation Method and Apparatus
US20150004080 *Apr 1, 2014Jan 1, 2015Alliance Partners LlcFluids concentration cup assembly with hourglass shape
CN102844121A *Dec 15, 2010Dec 26, 2012全玟墉Centrifuge tube
CN105289772A *Sep 22, 2015Feb 3, 2016烟台森森环保科技有限公司Special centrifugal tube for platelet rich plasma
CN105289772B *Sep 22, 2015Dec 28, 2016烟台森森环保科技有限公司一种富血小板血浆专用离心管
EP0069053A1 *May 26, 1982Jan 5, 1983Battelle Memorial InstituteTest tube for separating, by centrifugation, a physiological liquid, and for collecting one of the constituents with a given density
EP0742735A1 *Jan 23, 1995Nov 20, 1996Applied Imaging Corp.Centrifuge tube and adaptor
EP0742735A4 *Jan 23, 1995Jun 10, 1998Applied Imaging CorpCentrifuge tube and adaptor
WO1982004201A1 *May 25, 1982Dec 9, 1982Ringrose AnthonyTest-tube for the centrifuging and collecting of a liquid
WO1984000313A1 *May 16, 1983Feb 2, 1984Beckman Instruments IncUltracentrifuge tube with multiple chambers
WO1991004088A1 *Sep 11, 1990Apr 4, 1991Pall CorporationDevice and method for processing blood for human transfusion
WO2008143570A1 *May 8, 2008Nov 27, 2008Ge Healthcare Bio-Sciences AbSeparation device
WO2011071353A2Dec 15, 2010Jun 16, 2011Min-Yong JeonCentrifuge tube
WO2017025506A1 *Aug 8, 2016Feb 16, 2017Roth FelixMedical test tube
U.S. Classification210/782, 210/361, 494/16, 422/918, 494/902
International ClassificationG01N33/49, B01L3/14
Cooperative ClassificationG01N33/491, Y10S494/902, B01L3/5021
European ClassificationB01L3/5021, G01N33/49C