|Publication number||USRE32089 E|
|Application number||US 06/235,093|
|Publication date||Mar 4, 1986|
|Filing date||Feb 17, 1981|
|Priority date||Aug 25, 1970|
|Publication number||06235093, 235093, US RE32089 E, US RE32089E, US-E-RE32089, USRE32089 E, USRE32089E|
|Inventors||William F. Blatt, Edward A. Agranat, Peter N. Rigopulos|
|Original Assignee||Amicon Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (6), Non-Patent Citations (2), Referenced by (81), Classifications (18), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation of Ser. No. 940,969, filed Sept. 11, 1978, now abandoned, and a reissue of Ser. No. 05/066,675, filed Aug. 25, 1970, now U.S. Pat. No. 3,750,100..Iaddend.
This application is a continuation-in-part of U.S. Ser. No. 828,935, filed May 29, 1969, now abandoned, and of Ser. No. 833,090, filed June 13, 1969, now abandoned.
When obtaining blood from a blood donor, it is very often desirable to be able to return the cellular components to the donor so that more frequent bleedings can be made. When only the plasma component of the blood is desired for emergency use, the formed elements of the blood (which include the red blood cells, white blood cells and platelets) can be discarded or used for other purposes or can profitably be returned to the donor. Such a return is particularly important because (1) it allows the donor to recuperate to a state where he can donate again within two weeks rather than in about 2 months as is the case when the non-plasma component of the blood is not returned to him, and (2) it avoids the temporary weakness suffered by some donors after they donate a pint of blood. The importance of a donor's being able to contribute blood at relatively frequent intervals is obvious in circumstances such as those wherein injuries are incurred during military operations or wherein a donor bears a rare blood-type for which an emergency need exists.
However, blood fractionating of the type described is not used as frequently as desirable because no really convenient means for carrying out the process has been available. In general, this type of blood-fractionating has been done by
(1) transferring the blood from a donor into a blood bag by means known to most blood donors, then
(2) transferring the blood bag into a centrifugal separating apparatus, then
(3) "spinning" the blood at a rate which optimizes the separation of plasma from other blood components, but substantially avoids damage to blood cells, then
(4) separation of plasma by bag compression or withdrawal to a receiving vessel, and finally
(5) returning the formed elements back into the patient by the usual transfusion techniques.
Not only does this process involve relatively expensive apparatus, but it also comprises a sufficiently large number of handling steps to significantly increase the chance of contamination and/or cellular damage in the relatively crude environments of the type that may be encountered at accident scenes, in military operations, etc.
Moreover, there are many situations in which it is desirable to separate blood components without returning any of them to the donor in order to use diagnostic tests without interference from either the formed cell or plasma components thereof.
The present invention provides a process and apparatus for simple fractionation of whole blood into a plasma component and a cellular component while subjecting the components to only very slight stress. The present invention is furthermore readily applicable to blood-donation procedures, making it possible to return the non-plasma component or fraction to the donor virtually simultaneously with the donation.
The process of the present invention comprises conducting the whole blood in a flow path parallel to one face of a porous filter membrane having effective pore diameters from 0.1 to 0.8 micron, the path having a maximum depth of 20 mils measured vertically from the face of the membrane, collecting from the opposite face of the membrane the plasma component, and collecting from the end of said flow path the cellular component while maintaining the pressure differential between opposite faces of the membrane from 1 to 15 p.s.i. For best results the rate of flow of the whole blood across the face of the membrane is maintained from 2 to 50 ft. per minute and the pore diameter is from 0.4 to 0.7 micron. The precise diameter of the pores within the stated ranges of size which gives best results depends upon the precise pressure differential employed, higher pressure differentials within the stated range requiring smaller pore diameters. The pressure differential is critical because it provides the driving force for controlling the velocity of the blood across, and plasma through the membrane, and also affects the degree of hemolysis which occurs during filtration.
It is essential that the blood being filtered travel in a path substantially parallel to and within 20 mils of the membrane surface. Attempts to utilize the same membranes under conditions whereby the whole blood is forced through the membrane by conventional filtration techniques (i.e., putting the blood in a reservoir over filtration membrane and applying a pressure difference across the membrane to push or pull the plasma fraction through the membrane) results in almost immediate "plugging" of the membrane.
The term "filtration membrane" is used in this application to means that class of filters normally supplied in thin sheet form and capable of effecting separation of very small particulate or molecular components from suspensions or solutions. Both anisotropic and depth-filter membranes are included within this description. The former type of membrane is preferred when conveniently availble, but a particularly surprising feature of the invention is that homogeneous depth filters may be utilized in the blood separation process.
The filtration process of the invention is carried out at relatively low pressure differentials, e.g., from 1 to 15 p.s.i, as measured both from one side of the filter membrane to the other and as measured from the inlet of the whole blood passage to the outlet for the blood fraction which fails to pass through the filter membrane. As a matter of convenience, both the receptable for the filtrate (plasma) and for the rejected blood (non-plasma fraction) are preferably maintained at atmospheric pressure. Pressure differentials near the lower end of this range, i.e., from 1.5 to 5 p.s.i. are most advantageous, in part because they can be utilized in equipment which is less rigorously designed to avoid undue stress on the cells contained in the blood being fractionated. Likewise the velocity across the face of the membrane is relatively low, i.e., in the range of from 2 to 50 feet per minute. Under these conditions, the flow is substantially laminar. In the more preferable embodiments of the invention the blood, after passing over the surface of the membrane, is recycled back to the whole blood reservoir. The velocity of the stream being dissipated in the contents of the reservoir aids in keeping the blood mixed well.
In order to point out more fully the nature of the present invention, the following specific example is given as an illustrative embodiment of the present process and products produced thereby.
FIG. 1 shows a view in elevation, partly in section, of a thin channel ultrafiltration cell useful for carrying out the process of the invention.
FIG. 2 is a perspective view from the bottom of the reservoir and flow-directing means showing the apparatus of FIG. 1.
FIG. 3 is an exploded view in perspective showing a novel apparatus useful in the process of another embodiment of the invention which comprises a means to attach a hypodermic needle thereto.
FIG. 4 is a view in elevation showing the apparatus of FIG. 3 in operation.
Referring to FIGS. 1 and 2, it is seen that an ultrafiltration cell 10 comprises a top cap 12, a bottom cap 14 and a cylinder assembly 16. The cylinder is compressed and sealed between caps 12 and 14 by means of toggle clamping assembly 18, top O-ring seal 20, and bottom O-ring seal 22.
Top cap 12 comprises a pressure relief valve 24 and a means to drive fluid across the membrane comprising a port 25 adapted for connection to a pressurized gas source for pressurizing liquid in reservoir 28.
Resting on bottom cap 14 is a macroporous support plate 30 formed of sintered polypropylene. Over plate 30 is a cellulosic ester filtration membrane 32 having a mean pore size of 0.45±0.02 micron and available from Millipore Corporation under the trade designation HAW PO 9025. Lower O-ring seal 22 is compressed against the outer periphery of membrane 32, thereby providing an efficient edge sealing means.
Cylinder assembly 16 comprises reservoir 28 and an aperture 34 leading from reservoir 28 into a spiral flow path 36 which is formed by spiral grooves 38 on the bottom surface 39 of assembly 16. This flow path 36 is 0.125 inch wide and 0.010 inch (10 mils) high. It follows a spiral path in a plane parallel to the membrane surface, terminating at a fluid outlet port 40 through which the retained liquid may, via conduit 41, be collected or recycled for another concentrating step. Filtrate, i.e., that fraction of material which comes through the filter is carried out of the cell through conduit 42 which is machined into bottom cap 14.
A sample of whole blood (treated with ACD) was inserted into reservoir 28 and, under a 2 p.s.i.g. driving force, was divided into a plasma fraction and a cellular fraction. The whole blood was forced through aperture 34 in cylinder assembly 16, and thereupon is caused to follow spiral flow path 36 over the surface of membrane 32. The blood plasma fraction passed through the filtration membrane, and was collected through conduit 41 at atmospheric pressure. About 60% of the plasma content of the blood was recovered and there was no evidence of hemolysis in the plasma so collected.
Although the optimum operation of the illustrated device was realized with an operating pressure of from 2 to 4 p.s.i.g., it is stressed that higher operating pressures may be used when particular care is taken to smooth blood-contacting surfaces in such a way as to avoid excessive mechanical shear on the formed elements of the blood. For example, a stream-lined or smooth-surfaced wall 49 with gently rounded corners of aperture 34 is advantageous in this respect. In general, however, a low-pressure process is most desirable for use in emergency blood-donation procedures.
Another embodiment of the apparatus is disclosed in FIG. 3. In this apparatus, which is most useful in analytical work, a hypodermic syringe 50 has been utilized to withdraw a blood sample from a patient. The needle (not shown) of the syringe is then removed and the syringe is attached, by means of a fastening means 52, such as Luer lock 54, to filtration cell 56. Filtration cell 56 comprises a top retaining plate 58, filtration membrane 60, a sintered porous polyethylene support disk 62, and a bottom retaining plate 64.
Retaining plate 58 comprises a spiral ridge forming a shallow flow path 66 having a depth of 6 mils, a width of 0.5 cm. and a length of 70 cm. between inlet port 68 and outlet port 70. Retaining plate 64 comprises a filtration outlet port 71.
In order to achieve the most reproducible filtration results, it has been found more desirable to provide the above-described apparatus with a positive pressure control means rather than to rely upon the manual pressure exerted by a number of different operators. Therefore, a spring means 72 is mounted, at one end 74 thereof, on projecting outlet port 70. The other end 76 of the spring is adapted to press on plunger 78 of the hypodermic syringe 50. When spring means 72 is so mounted as to rest on plunger 78, a controlled amount of pressure, about 2.5 p.s.i., is generated for filtering the blood. Another advantage is that one operator can utilize a number of these devices at a single time since they do not require close attention during the filtration operation.
FIG. 4 shows a schematic diagram showing the analytical device of FIG. 3 in operation. A plasma fraction of the blood is being collected in vessel 82 while the other blood components are being collected in vessel 80.
Using the cellulosic ester membrane described above, less than 0.1% hemolysis was observed, and the plasma obtained was not detectably different from that obtained by conventional centrifugation. From a 10 ml. sample of fresh blood of normal hematocrit, there was obtained, in a filtering time of 15 to 20 minutes, approximately 3.0 to 3.4 ml. of plasma. Similar results were obtained using under the same conditions a polycarbonate membrane 1-10 mils thick) having a pore size of 0.5±0.06 microns available under the trademark Nuclepore from the General Electric Company.
Various other advantages and modifications will be apparent to those skilled in the art and fall within the scope of the appended claims.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3448041 *||Jun 14, 1965||Jun 3, 1969||Roy L Swank||Method and apparatus for treating blood preliminary to its use in transfusions|
|US3483867 *||Jun 13, 1968||Dec 16, 1969||Meyer Markovitz||Artificial glomerulus and a method for treating blood|
|US3488768 *||Feb 8, 1968||Jan 6, 1970||Amicon Corp||Self-cleaning ultrafilter|
|US3539300 *||Oct 23, 1967||Nov 10, 1970||Schering Corp||Body fluid collector and separator having improved flow rate|
|US3560377 *||Jan 21, 1969||Feb 2, 1971||Amicon Corp||Apparatus and process for filtering fluids|
|US3567031 *||May 29, 1969||Mar 2, 1971||Amicon Corp||Autoagitating ultrafiltration apparatus|
|1||Bixler et al., "The Development of a Diafiltration System for Blood Purification", from Trans. Amer. Soc. Artif. Int. Organs, vol. XIV, Jun. 14, 1968, 99-108.|
|2||*||Bixler et al., The Development of a Diafiltration System for Blood Purification , from Trans. Amer. Soc. Artif. Int. Organs, vol. XIV, Jun. 14, 1968, 99 108.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4964976 *||Feb 1, 1990||Oct 23, 1990||Lysaght Michael J||Optimized filter and method|
|US5045195 *||Jan 16, 1990||Sep 3, 1991||Accuventure, Inc.||Personal drinking water purification tube|
|US5232437 *||Mar 21, 1990||Aug 3, 1993||Baxter International Inc.||Mobile, self-contained blood collection system and method|
|US5674394 *||Mar 24, 1995||Oct 7, 1997||Johnson & Johnson Medical, Inc.||Single use system for preparation of autologous plasma|
|US5691453 *||Jun 7, 1995||Nov 25, 1997||Biopure Corporation||Separation of polymerized hemoglobin from unpolymerized hemoglobin on hydroxyapatite using HPLC|
|US6197194||Sep 24, 1999||Mar 6, 2001||Elaine Whitmore||Single use system for preparing autologous plasma and fibrin gel|
|US6214338 *||Apr 25, 2000||Apr 10, 2001||Plasmaseal Llc||Plasma concentrate and method of processing blood for same|
|US6241886 *||Jun 7, 1996||Jun 5, 2001||Toyo Boseki Kabushiki Kaisha||Plasma separation filter|
|US6695803||Oct 15, 1999||Feb 24, 2004||Mission Medical, Inc.||Blood processing system|
|US6817984||Oct 3, 2002||Nov 16, 2004||Mission Medical, Inc.||Blood processing system|
|US7008393||Oct 3, 2002||Mar 7, 2006||Mission Medical, Inc.||Blood processing system|
|US7374678||Sep 2, 2004||May 20, 2008||Biomet Biologics, Inc.||Apparatus and method for separating and concentrating fluids containing multiple components|
|US7384549||Dec 22, 2006||Jun 10, 2008||Spf Innovations, Llc||Method and apparatus for the filtration of biological solutions|
|US7682511||May 3, 2008||Mar 23, 2010||Spf Innovations, Llc||Method and apparatus for the filtration of biological solutions|
|US7708152||Jan 30, 2006||May 4, 2010||Hanuman Llc||Method and apparatus for preparing platelet rich plasma and concentrates thereof|
|US7780860||May 19, 2008||Aug 24, 2010||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US7806276||Apr 11, 2008||Oct 5, 2010||Hanuman, Llc||Buoy suspension fractionation system|
|US7824559||Jan 30, 2006||Nov 2, 2010||Hanumann, LLC||Apparatus and method for preparing platelet rich plasma and concentrates thereof|
|US7832566||May 25, 2006||Nov 16, 2010||Biomet Biologics, Llc||Method and apparatus for separating and concentrating a component from a multi-component material including macroparticles|
|US7837884||Dec 29, 2008||Nov 23, 2010||Hanuman, Llc||Methods and apparatus for isolating platelets from blood|
|US7845499||May 25, 2006||Dec 7, 2010||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US7866485||Jul 31, 2007||Jan 11, 2011||Hanuman, Llc||Apparatus and method for preparing platelet rich plasma and concentrates thereof|
|US7871528 *||Mar 15, 2007||Jan 18, 2011||Elfo Ag||Water filter|
|US7914689||May 19, 2008||Mar 29, 2011||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US7967987||Jan 11, 2010||Jun 28, 2011||Spf Innovations, Llc||Method and apparatus for the filtration of biological solutions|
|US7987995||May 3, 2010||Aug 2, 2011||Hanuman, Llc||Method and apparatus for preparing platelet rich plasma and concentrates thereof|
|US7992725||Apr 11, 2008||Aug 9, 2011||Biomet Biologics, Llc||Buoy suspension fractionation system|
|US8012077||May 23, 2008||Sep 6, 2011||Biomet Biologics, Llc||Blood separating device|
|US8048321||Aug 11, 2010||Nov 1, 2011||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US8062534||Dec 6, 2010||Nov 22, 2011||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US8096422||Nov 1, 2010||Jan 17, 2012||Hanuman Llc||Apparatus and method for preparing platelet rich plasma and concentrates thereof|
|US8105495||Jan 10, 2011||Jan 31, 2012||Hanuman, Llc||Method for preparing platelet rich plasma and concentrates thereof|
|US8119013||Oct 4, 2010||Feb 21, 2012||Hanuman, Llc||Method of separating a selected component from a multiple component material|
|US8133389||Jul 29, 2011||Mar 13, 2012||Hanuman, Llc||Method and apparatus for preparing platelet rich plasma and concentrates thereof|
|US8157999||May 15, 2011||Apr 17, 2012||Spf Innovations, Llc||Method and apparatus for the filtration of biological solutions|
|US8163184||Mar 25, 2011||Apr 24, 2012||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US8187475||Mar 6, 2009||May 29, 2012||Biomet Biologics, Llc||Method and apparatus for producing autologous thrombin|
|US8187477||Nov 22, 2010||May 29, 2012||Hanuman, Llc||Methods and apparatus for isolating platelets from blood|
|US8313954||Apr 3, 2009||Nov 20, 2012||Biomet Biologics, Llc||All-in-one means of separating blood components|
|US8328024||Aug 4, 2011||Dec 11, 2012||Hanuman, Llc||Buoy suspension fractionation system|
|US8337711||Feb 27, 2009||Dec 25, 2012||Biomet Biologics, Llc||System and process for separating a material|
|US8567609||Apr 19, 2011||Oct 29, 2013||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US8591391||Apr 12, 2010||Nov 26, 2013||Biomet Biologics, Llc||Method and apparatus for separating a material|
|US8596470||Feb 20, 2012||Dec 3, 2013||Hanuman, Llc||Buoy fractionation system|
|US8603346||Sep 22, 2011||Dec 10, 2013||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US8728315||Mar 9, 2012||May 20, 2014||Spf Innovations, Llc||Method and apparatus for the filtration of biological solutions|
|US8783470||May 25, 2012||Jul 22, 2014||Biomet Biologics, Llc||Method and apparatus for producing autologous thrombin|
|US8801586 *||Dec 20, 2012||Aug 12, 2014||Biomet Biologics, Llc||System and process for separating a material|
|US8808551||Nov 15, 2010||Aug 19, 2014||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US8905960 *||May 14, 2009||Dec 9, 2014||Direction Et Priorites||Device for the filtering a complex liquid such as blood, in particularly applicable to an autotransfuser|
|US8950586||Jul 1, 2013||Feb 10, 2015||Hanuman Llc||Methods and apparatus for isolating platelets from blood|
|US8992862||Nov 15, 2012||Mar 31, 2015||Biomet Biologics, Llc||All-in-one means of separating blood components|
|US9011800||Jul 16, 2009||Apr 21, 2015||Biomet Biologics, Llc||Method and apparatus for separating biological materials|
|US9114334||Dec 9, 2013||Aug 25, 2015||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US9138664||Dec 2, 2013||Sep 22, 2015||Biomet Biologics, Llc||Buoy fractionation system|
|US9239276||Oct 28, 2013||Jan 19, 2016||Biomet Biologics, Llc||Apparatus and method for separating and concentrating fluids containing multiple components|
|US9533090||Nov 21, 2013||Jan 3, 2017||Biomet Biologics, Llc||Method and apparatus for separating a material|
|US9556243||Oct 10, 2013||Jan 31, 2017||Biomet Biologies, LLC||Methods for making cytokine compositions from tissues using non-centrifugal methods|
|US20050109716 *||Sep 2, 2004||May 26, 2005||Michael Leach||Apparatus and method for separating and concentrating fluids containing multiple components|
|US20050143565 *||Mar 3, 2005||Jun 30, 2005||Biopure Corporation||Method for separating unmodified hemoglobin from cross-linked hemoglobin|
|US20060175242 *||Jan 30, 2006||Aug 10, 2006||Hanuman Llc||Method and apparatus for preparing platelet rich plasma and concentrates thereof|
|US20060175244 *||Jan 30, 2006||Aug 10, 2006||Hanuman Llc||Apparatus and method for preparing platelet rich plasma and concentrates thereof|
|US20060273050 *||May 25, 2006||Dec 7, 2006||Higgins Joel C||Apparatus and method for separating and concentrating fluids containing multiple components|
|US20070221570 *||Mar 15, 2007||Sep 27, 2007||Beat Aregger||Water filter|
|US20070276191 *||May 26, 2006||Nov 29, 2007||Sean Selover||Illuminated surgical access system including a surgical access device and integrated light emitter|
|US20080017577 *||Jul 21, 2006||Jan 24, 2008||Becton, Dickinson And Company||Membrane-based Double-layer Tube for Sample Collections|
|US20080217264 *||May 19, 2008||Sep 11, 2008||Biomet Manufacturing Corp.||Apparatus And Method For Separating And Concentrating Fluids Containing Multiple Components|
|US20080217265 *||May 19, 2008||Sep 11, 2008||Biomet Manufacturing Corp.||Apparatus And Method for Separating And Concentrating Fluids Containing Multiple Components|
|US20080283474 *||Apr 11, 2008||Nov 20, 2008||Biomet Biologics, Llc||Buoy suspension fractionation system|
|US20090101599 *||Dec 29, 2008||Apr 23, 2009||Hanuman, L.L.C.||Methods And Apparatus For Isolating Platelets From Blood|
|US20090221075 *||Feb 27, 2009||Sep 3, 2009||Biomet Manufacturing Corp.||System And Process For Separating A Material|
|US20090289014 *||May 23, 2008||Nov 26, 2009||Biomet Biologics, Llc||Blood Separating Device|
|US20100206798 *||May 3, 2010||Aug 19, 2010||Hanuman Llc||Method And Apparatus For Preparing Platelet Rich Plasma And Concentrates Thereof|
|US20100256595 *||Apr 3, 2009||Oct 7, 2010||Biomet Biologics, Llc||All-In-One Means Of Separating Blood Components|
|US20110014705 *||Jul 16, 2009||Jan 20, 2011||Biomet Biologics, Llc||Method and apparatus for separating biological materials|
|US20110042296 *||Nov 1, 2010||Feb 24, 2011||Hanuman Llc||Apparatus and method for preparing platelet rich plasma and concentrates thereof|
|US20110056893 *||Nov 15, 2010||Mar 10, 2011||Biomet Biologics, LLC.||Apparatus and Method for Separating and Concentrating Fluids Containing Multiple Components|
|US20110058983 *||May 14, 2009||Mar 10, 2011||Direction Et Priorites||Device for the filtering a complex liquid such as blood, in particularly applicable to an autotransfuser|
|US20110168193 *||Mar 25, 2011||Jul 14, 2011||Biomet Biologics, Llc||Apparatus and Method for Separating and Concentrating Fluids Containing Multiple Components|
|US20110215051 *||May 15, 2011||Sep 8, 2011||Spf Innovations, Llc||Method and apparatus for the filtration of biological solutions|
|US20130196425 *||Dec 20, 2012||Aug 1, 2013||Biomet Biologics, Llc||System and Process for Separating a Material|
|U.S. Classification||210/651, 210/456, 210/321.85|
|International Classification||A61M1/34, B01D61/18, B01D61/14, A61M1/36, B01D63/08|
|Cooperative Classification||B01D63/087, A61M1/3496, B01D61/18, A61M1/3603, A61M2206/12, B01D61/145|
|European Classification||B01D61/14D, B01D63/08F, A61M1/34P, B01D61/18|
|Nov 22, 1985||AS||Assignment|
Owner name: W. R. GRACE & CO., 1114 AVENUE OF THE AMERICAS, NE
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:AMICON CORPORATION;REEL/FRAME:004480/0419
Effective date: 19850930