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Publication numberUS3862715 A
Publication typeGrant
Publication dateJan 28, 1975
Filing dateMay 26, 1972
Priority dateMay 26, 1972
Publication numberUS 3862715 A, US 3862715A, US-A-3862715, US3862715 A, US3862715A
InventorsCarl J Remenyik
Original AssigneeCarl J Remenyik
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Centrifuge for the interacting of continuous flows
US 3862715 A
Abstract
A liquid centrifuge rotor for inducing the interaction of a plurality of substances flowing continuously therethrough, separating products that result from this interaction and continuously removing these products. Plural flow passages, arranged as concentric cylinders near the periphery of the rotor, are interconnected with either porous walls or open portions in the walls for controlling velocities of radial flow between flow passages. The design thus permits countercurrent axial flow as well as radial cross-flow. Applications of this rotor are described for the continuous separation of particulate blood components via centrifugation combined with plasma cross-flow, and the oxygenation of blood as in a heart-lung machine.
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Description  (OCR text may contain errors)

United States Patent [1 1 Remenyik 1 Jan. 28, 1975 1 1 CENTRIFUGE FOR THE lNTERACTlNG OF CONTINUOUS FLOWS 211 Appl. No.: 257,081

Primary Examiner-George H. Krizmanich Attorney, Agent, or FirmMartin .1. Skinner [57] ABSTRACT A liquid centrifuge rotor for inducing the interaction of a plurality of substances flowing continuously therethrough, separating products that result from this interaction and continuously removing these products. Plural flow passages, arranged as concentric cylinders near the periphery of the rotor, are interconnected with either porous walls or open portions in the walls for controlling velocities of radial flow between flow passages. The design thus permits countercurrent axial flow as well as radial cross-flow. Applications of this rotor are described for the continuous separation of particulate blood components via centrifugation combined with plasma cross-flow, and the oxygenation of blood as in a heart-lung machine.

CENTRIFUGE FOR THE INTERACTING OF CONTINUOUS FLOWS BACKGROUND OF THE INVENTION The art of continuous-flow liquid centrifuges has been advanced substantially in recent years whereby rather intricate analytical-type methods may be easily accomplished. Typical of the centrifuges for these purposes are described in U.S. Pat. Nos. 3,536,253, 3,547,547 and 3,556,967. Additional information is described in the National Cancer Institute Monograph 2 l. The Development of Zonal Centrifuges and Ancilliary Systems for Tissue Fractionation and Analysis, US Dept. of Health, Education and Welfare, Public Health Service. Other pertinent references are: The Ultracentrifuge, T. Svedberg and K. O. Pedersen, Oxford University Press, Oxford, England (1940); and Counter-Streaming Centrifuge for the Separation of Cells or Cell Fragments of Different Sizes," P. E. Lindahl and E. Nyberg, IVA; Tidskrift For Teknisk-Vetenskaplig Forskning, 26, p. 309 (I955).

Centrifuges for separating the particulate components of blood are described in reports submitted by Abcor, Inc., Cambridge, Mass, to the National Cancer Institute, N.I.H., under Contract NIH-20-2239. The fundamental centrifuge for these studies is Model CL manufactured by International Equipment Corporation. A similar centrifuge was utilized in a research contract between International Business Machine Corp. and the National Cancer Institute.

Continuous flow centrifuge rotors of the prior art generally fall into one of three classes. In all of these types, entrance and exit is made at or near the axis of rotation. frequently at both ends. In one class of rotor, the separation chamber is essentially parallel to the axis of rotation, often a cylindrical chamber located at some distance from the axis. During passage of fluid through this chamber, dense suspensions tend to concentrate at or near the outer wall of the chamber and less dense ones. closer to the axis of rotation. One or more of these fractions may be individually removed by several conventional techniques after separations have been completed.

In the second class of rotors, the reaction vessel or chamber is essentially oriented in a radial position within the rotor. Usually the more dense fractions are left at the position farthest from the axis, and the less dense fractions leave with the carrier liquid at or near the axis. The more dense fractions may later be removed by a separate flow of fluid through the rotor.

A third, or intermediate, class of rotors has separation chambers in the rotors such that the principal flow directions are inclined at angles, to the axis, between and 90.

In most continuous flow centrifuges, only the fluid carrying the unseparated mixture of suspensions is flowing continuously through the rotor. The various separated suspensions band in zones and remain there until the flow of the mixture is turned off. The position of the zones is determined by the densities and fluid mechanical properties of the suspended particles. These separated components of the mixture are removed from the rotor after the flow of the mixture has been interrupted.

Present centrifuges from which separated blood components (red blood cells, white blood cells and plasma) are removed continuously have unsatisfactory efficiencies, usually less than about 20%. Furthermore, may types of desired interactions are not possible in these prior art devices.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. I is a vertical sectional drawing, in schematic form, of a centrifuge rotor to accomplish the interacting of at least two continuous flows of fluids; and

FIG. 2 is an enlarged sectional drawing of a portion of the rotor of FIG. 1 taken at 22 thereof.

SUMMARY OF THE INVENTION My improved centrifuge rotor is an elongate cylinder having a plurality of slender concentric vessels arranged near the periphery thereof. Plural inlet and outlet ports are provided at one or both ends of the rotor, near to and concentric with the axis of rotation, whereby two or more fluids may be passed continuously through adjacent vessels. Small openings between the concentric vessels permit radial flow, inward or outward, to control the radial velocity of fluids to induce the interaction between the plural fluids and the removal of certain products of the interaction. Separation of the products is achieved by the combined centrifugal field acting upon components of differing densities and by drag forces produced by the cross-flow.

DETAILED DESCRIPTION Referring now to FIG. 1, a rotor body 10 is caused to be rotated about axis of revolution 11 by any suitable means including conventional bearings, seals and drive motor (not shown). A first fluid inlet 12 is positioned on the axis at either end of body 10 (shown here at the bottom) and communicates with radially-extending passageway 13 leading to a primary slender cylindrical reaction vessel 14. By slender I mean having a radial dimension that is small with respect to the axial dimension. The upper end of reaction vessel 14 connects to radial passageway 15 which, in turn, connects with outlet 16 on the axis 11 at the top of body 10. A second fluid inlet 17 is concentric with outlet 16 and communicates with passageway 18 leading to slender cylindrical chamber 19. The vessel 14 and chamber 19 are separated by a wall 22. Small interconnections 20, 21 in wall 22 between chamber 19 and reaction vessel 14 join chamber 19 to reaction vessel 14 on either side of a constriction formed by ridge 23 projecting into vessel 14. The ridge 23 may extend into reaction vessel 14 from either the inner or outer wall thereof. Similar small interconnections 24, 25 through a wall 37 join reaction vessel 14 to an inwardly disposed slender cylindrical chamber 26 for purposes discussed below.

An outer slender concentric channel 27 is connected to reaction vessel 14, by passageway 28, on the upstream side of the ridge 23, and additional channels 29, 30 connect to vessel 14 for purposes described hereinafter. Channel 27 and channel 29 connect to a common passageway 31 leading to an outlet 32 concentric with outlet 16. Channel 30 connects with passageway 33 which, in turn, connects with concentric outlet 34.

The rotor of my design may be fabricated from any material which is compatible with the fluids to be utilized in the separations. Since the rotor is not intended for high-speed operation, even certain inert plastics may be utilized to simplify fabrication procedures. Alternatively, the bulk of the rotor may be fabricated of either metal or plastic, with all cavity surfaces coated with unreactive materials. Typically, the rotor may be fabricated in several portions to produce the required cavities and thereafter the portions joined to create the entire rotor. In order to minimize the number of rotary seals, all inlets and outlets for the rotor preferably may be at one end of the rotor. Theppenings or pores 20, 21 24 and 25 are in the form of inserts of sheets of porous materials or like materials. The pore size is greater than the size of red blood cells which is about 7-8;.L. Thus the pore size is about 101.1. or greater.

The space between walls in vessel 14 and chambers 19, 26 may vary typically between 1 mm and mm. To meet external constraints, rotor lengths may be 15 to 50 cm and diameters 10 to cm. A typical rotor speed is 1000 rpm. It will be recognized that exact parameters of size and speed are determined by particular applications of my rotor design.

The concentric relationship of the various chambers with the reaction vessel 14 is illustrated also in FIG. 2 which is an enlarged portion of a transverse section taken through the rotor at 22 of FIG. 1 perpendicular to the axis of rotation of rotor 10. The details of the passages are more clearly illustrated in this enlargement. The wall 22 between channel 19 and reaction vessel 14 is made up of a plurality of generally teardrop shaped sections 35 to thereby form radiallyoriented channels 36 running in an axial direction. The portion of channels 36 most distant from the axis of rotor 10 are narrow, and interconnections or pores 21 communicate to these channels at that point. The shape of channel 36 is chosen to produce the proper radial (inward) velocity gradient to fluids entering the periphery of the channel whereby drag forces are produced on particles attempting to move radially outwardly. The pores 21 act as diffusers to give the high initial velocity. Reduced velocity and thus drag forces exist inward from that radius due to the widening of channel 36, as shown. The effect of this construction will become more apparent from the hereinafterdescribed separation of particulate blood components.

In the figures, reaction vessel 14 and concentric chambers 19, 26, and channel 27 are illustrated as being completely annular in rotor 10. While this may be preferred for high volume flow through the rotor, these elements may also be subdivided by axiallyextending septa if desired for fabrication requirements. Likewise, the radially-extending passageways, e.g., 13, may be subdivided.

The rotor of my design may be utilized for inducing many interaction reactions such as those between whole blood and blood components. Typical is the separation of particulate blood components from whole blood by centrifugation with plasma cross-flow. For this separation, and referring to FIGS. 1 and 2, whole blood is introduced into reaction vessel 14 through inlet I2 and passageway 13, while plasma is fed through inlet 17 and passageway 18 into chamber 19. Plasma flows through the openings (small pores) 21 to mix with the whole blood in vessel 14. Due to the centrifugal effects and the counter-acting radial component of the plasma stream, large rouleaux (aggregate) of red blood cells separate from the whole blood stream and collect along the outer wall of reaction vessel 14 (in channels 36) in a band designated as A in FIG. 2. These then move axially and are withdrawn through passageway 28 into channel 27 where they later leave the rotor 10 through outlet 32. Concurrently, plasma, platelets,

single red blood cells and small rouleaux of red blood cells pass through pores 25 into chamber 26.

The remaining portion of the blood stream in reaction vessel 14, as in band B of FIG. 2 which is primarily white blood cells and intermediate rouleaux of red blood cells, passes ridge 23 where remaining rouleaux are broken by shear forces. Additional plasma enters the stream through pores 20 and additional separation occurs as a function of centrifugation and drag forces. The white cells are the fastest sedimenting component in this region and are thus drawn off into channel 30 so as to leave rotor 10 thorugh outlet 34. Since the red cells are more dense than plasma, they sediment and are removed through channel 29 and flow, with the large rouleaux and some plasma, through passageway 31 and outlet 32. Remaining plasma then leaves through outlet 16.

' The separation and collection of white blood cells, as described above, is highly useful in the treatment of persons afflicted with leukemia. These persons often require the addition of the order of 10 white blood cells per day. This quantity of cells necessitates the processing, with presently available efficiencies of the prior art, of the order of 10 liters of blood or the equivalent of about 20 donors if batches of collected blood are to be processed. However, a healthy donor can spare that quantity of white blood cells if there is no substantial loss of red blood cells. Accordingly, my rotor can be utilized to continuously separate the particulate components of a donors blood and return the plasma and red blood cells to the donor without contact with any deleterious substance such as gases or chemicals.

For this separation, a whole blood flow rate into the rotor is about ml/min. and the recirculating plasma feed rate is about 200 ml/min. These fluids are subjected to a centrifugal acceleration force of about 50G I to bring about the intereaction and the subsequent separation of the components as described above.

A further application of my rotor design, in a simplified form, is that of performing the functions ofa heartlung machine. For this application, the ridge 23 is not required nor are the majority of various channels to re ceive separated components. The whole blood is pumped into reaction vessel 14, as above. An oxygenrich liquid of lower density than the whole blood, such as oxygenated plasma, is admitted into chamber 19 where it then passes inwardly through pores 20, 21 to perfuse the blood, thereby exchanging oxygen to the red blood cells. Oxygen-depleted liquid leaves the blood stream through pores 24, 25 into chamber 26. Oxygenated blood then leaves the rotor through channel 29 (and outlet 32) and the oxygen depleted liquid is removed through outlet 16. In this manner the centrifugal field accelerates the exchange of oxygen by accelerating the transition of the oxygen-rich liquid (plasma) through the whole blood. This then reduces the amount of blood that is outside a patient at any one time.

In any treatment of blood, particularly where all or portions thereof are to be reinjected into patients, care must be exercised to minimize (preferably prevent) contact with an adverse environment such as gases, e.g., air. Otherwise there is a detrimental reaction between the blood and the gases, resulting in cell deterioration, as well as the entrapment of gas bubbles in the blood, causing embolism. In my rotor design, blood is not exposed to air or other gas interface at any time. Prevention of contact is accomplished by first filling (and flushing) the rotor passages with a fluid which is compatible with blood constituents. This fluid may be, for example, additional blood plasma. A flow of whole blood then displaces the plasma and the abovedescribed procedures are carried out. Thus, the desirable products from my rotor may be used directly for patients permitting a closed flow-path from the patient back to the patient or from a donor back to a patient and to the donor as desired. Appropriate pumps would be combined with my centrifuge to bring about the desired flow.

Although my rotor has been described for applications wherein there is interaction between whole blood and plasma or other second liquid, it is generally applicable to the interaction of other liquids where centrifugal and drag forces can be combined to sediment products of the interaction and provide for the continuous removal of the products.

I claim:

1. A centrifuge rotor for effecting interaction between continuously flowing first and second liquid streams and for continuously removing the products of the interaction, which comprises: a cylindrical rotor body symmetrical about an axis of rotation; a slender annular reaction vessel within the rotor body coaxial with the axis of rotation; a first liquid inlet to the rotor body; an axially-symmetrical first inlet passage peripherally connecting the first inlet with one end of the reaction vessel for uniformly and continuously admitting the first liquid; a slender annular first chamber within the body coaxial with the reaction vessel and spaced farther from the axis of rotation; a second liquid inlet to the rotor body; a second inlet passage peripherally connecting the second inlet with the first chamber for uniformly and continuously admitting the second liquid; a plurality of radially-oriented first openings interconnecting the first chamber and the reaction vessel whereby the second liquid is continuously in cross-flow relationship with the first liquid to bring about interaction therebetween; an axially-symmetrical first outlet passage connected to the second end of the reaction vessel to continuously remove one interaction product; an axially-symmetrical second outlet passage connected to the periphery of the reaction vessel at a greater distance from the axis of rotation to remove another interaction product; and outlets from the rotor body connected to the first and second outlet passages.

2. The rotor of claim 1 further comprising a plurality of axially-extending channels in the reaction vessel along a wall farthest removed from the axis of rotation, the peripheral width of these channels decreasing at increased distances from the axis of rotation; and wherein the first openings from the first chamber communicate with the most .convergent portion of the channels.

3. The rotor of claim 2 further comprising: an annular ridge extending radially from one wall of the reaction vessel in a plane perpendicular to the axis of rotation; and an axially-symmetrical third outlet passage peripherally connected to the reaction vessel at a position between the annular ridge and the first inlet passage, the third outlet being at a greater distance from the axis of rotation than the second outlet.

4. The rotor of claim 2 further comprising a slender annular second chamber coaxial with the reaction vesse] and spaced toward the axis of rotation from the reaction vessel, and a plurality of radially-oriented second openings interconnecting the reaction vessel and the second chamber.

5. The rotor of claim 4 wherein the radial dimension of the reaction vessel and the first and second chambers is about 1 to 5 mm, wherein the rotor axial length is about 15 to 50 cm and wherein the size of the first and second openings is at least 10 u.

l= l l l=

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US935311 *Dec 4, 1908Sep 28, 1909Oscar Max KuchsCentrifugal concentrator and glassifier.
US3027390 *Mar 13, 1959Mar 27, 1962Benjamin H ThurmanApparatus and method for centrifugal purification of fatty oils
US3202347 *May 2, 1960Aug 24, 1965Benjamin H ThurmanCountercurrent flow centrifugal separator
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3955755 *Apr 25, 1975May 11, 1976The United States Of America As Represented By The United States Energy Research And Development AdministrationClosed continuous-flow centrifuge rotor
US4939087 *May 12, 1987Jul 3, 1990Washington State University Research Foundation, Inc.Method for continuous centrifugal bioprocessing
US5217426 *Aug 14, 1991Jun 8, 1993Baxter International Inc.Combination disposable plastic blood receiving container and blood component centrifuge
US5217427 *Oct 4, 1991Jun 8, 1993Baxter International Inc.Centrifuge assembly
US5571068 *Jul 20, 1994Nov 5, 1996Baxter International Inc.Centrifuge assembly
US5759147 *Jun 7, 1995Jun 2, 1998Baxter International Inc.Blood separation chamber
US6344489 *Jan 3, 1996Feb 5, 2002Wayne State UniversityWithout bubbles
US7008535Aug 4, 2000Mar 7, 2006Wayne State UniversityApparatus for oxygenating wastewater
US7294278Nov 4, 2005Nov 13, 2007Wayne State UniversityMethod for oxygenating wastewater
US7497351 *May 30, 2006Mar 3, 2009Kimberly-Clark Worldwide, Inc.Wet wipe dispensing system
US7517582May 10, 2007Apr 14, 2009Kimberly-Clark Worldwide, Inc.warming sensation on the skin when the wet wipe is used; contact sodium acetate, sodium sulfate, sodium sulfate activator in aqueous sugar solution, release heat to cause a warming sensation on the skin; personal care products
US7597954Dec 14, 2006Oct 6, 2009Kimberly-Clark Worldwide, Inc.warming sensation on the skin when the wet wipe is used; contact sodium acetate, sodium sulfate, sodium sulfate activator in aqueous sugar solution, release heat to cause a warming sensation on the skin; personal care products
US7654412May 30, 2006Feb 2, 2010Kimberly-Clark Worldwide, Inc.Wet wipe dispensing system for dispensing warm wet wipes
US7850041Nov 7, 2008Dec 14, 2010John David AmundsonWet wipes dispensing system
US7914891Dec 28, 2005Mar 29, 2011Kimberly-Clark Worldwide, Inc.Wipes including microencapsulated delivery vehicles and phase change materials
US8192841Dec 14, 2006Jun 5, 2012Kimberly-Clark Worldwide, Inc.Personal care products for the skin comprising an encapsulation layer surrounding an aqueous core composition of an encapsulating activator, a matrix, and an active agent where the microencapsule has a diameter of 5-5000 micrometers; stability; moisturizers, conditioners, cleaning compounds, wipes
DE3635300A1 *Oct 16, 1986Apr 23, 1987Cobe LabZentrifugal-separator
DE19634413A1 *Aug 26, 1996Mar 12, 1998Komanns AribertVerfahren und Vorrichtung zur Sortierzentrifugation oder Sortierdurchflußzentrifugation
DE19634413C2 *Aug 26, 1996Jul 30, 1998Komanns AribertVerfahren zur Sortierzentrifugation oder Sortierdurchflußzentrifugation und Vorrichtung zur Durchführung des Verfahrens
Classifications
U.S. Classification494/22, 494/43
International ClassificationB04B1/00, B04B5/04
Cooperative ClassificationB04B1/00, B04B2005/0464, B04B5/0442
European ClassificationB04B5/04C, B04B1/00