The present invention relates to apparatus and methods for separating blood components. More particularly, the present invention relates to apparatus and methods for effectively separating and removing specific components from blood.
Blood may be fractionated and the different fractions of the blood used for different medical needs. For instance, anemia (low erythrocyte levels) may be treated with infusions of erythrocytes. Thrombocytopenia (low thrombocyte (platelet) levels) may be treated with infusions of platelet concentrate.
The sedimentation of the various blood cells and plasma is based on the different specific gravity of the cells and the viscosity of the medium. When sedimented to equilibrium, the component with the highest specific gravity (density) eventually sediments to the bottom, and the lightest rises to the top. Under the influence of gravity or centrifugal force, blood spontaneously sediments into three layers. At equilibrium the top, low-density layer is a straw-colored clear fluid called plasma. Plasma is a water solution of salts, metabolites, peptides, and many proteins ranging from small (insulin) to very large (complement components). Plasma per se has limited use in medicine but may be further fractionated to yield proteins used, for instance, to treat hemophilia (factor VIII) or as a hemostatic agent (fibrinogen). The term platelet rich plasma (PRP) is used for this component because most of the plasma proteins and platelets in the whole blood are in the plasma following slow centrifugation so the concentration of platelets in the plasma has increased while suspended in supernatant plasma. The uppermost layer after centrifugation typically contains plasma proteins only and is typically called platelet-poor plasma (PPP) due to the absence or low number of platelets as a result of a “hard spin”.
The bottom, high-density layer is a deep red viscous fluid comprising nuclear red blood cells (RBC) specialized for oxygen transport. The red color is imparted by a high concentration of chelated iron or heme that is responsible for the erythrocytes high specific gravity. Packed erythrocytes, matched for blood type, are useful for treatment of anemia caused by, e.g., bleeding. The relative volume of whole blood that consists of erythrocytes is called the hematocrit, and in normal human beings can range from about 38% to about 54%.
The intermediate layer is the smallest layer, appearing as a thin white band on top the erythrocyte layer and below the plasma, and is called the buffy coat. The buffy coat itself has two major components, nucleated leukocytes (white blood cells) and a nuclear smaller bodies called platelets (or thrombocytes). Leukocytes confer immunity and contribute to debris scavenging. Platelets seal ruptures in the blood vessels to stop bleeding and deliver growth and wound healing factors to the wound site. The buffy coat may be separated from whole blood when the blood is subjected to a “hard spin” in which the whole blood is spun hard enough and long enough so that platelets sediment from plasma onto packed red cells and white cells percolate up through red cell pack to the interface between red cells and plasma.
When whole blood is centrifuged at a low speed (e.g., up to 1,000 g) for a short time (e.g., two to four minutes) white cells sediment faster than red cells and both sediment much faster than platelets. At higher speeds the same distribution is obtained in a shorter time. The method of harvesting PRP from whole blood is based on this principle. Centrifugal sedimentation that takes the fractionation only as far as separation into packed erythrocytes and PRP is called a “soft spin” which is typically used to describe centrifugation conditions under which erythrocytes are sedimented but platelets remain in suspension. “Hard spin” is typically used to describe centrifugation conditions under which erythrocytes sediment and platelets sediment in a layer immediately above the layer of erythrocytes.
The auto-transfusion equipment used to make autologous platelet concentrates requires a skilled operator and considerable time and expense and these devices require a large prime volume of blood. While many of these devices have somewhat reduced the cost and the time required, skilled operators and time are still required. Accordingly, there remains a need for simple and effective methods and devices for separating and removing components from whole blood. Embodiments of the present invention are designed to meet these and other needs.
Some embodiments of the present invention relate to apparatus and methods for rapid fractionation of blood into its different components, e.g., erythrocyte, plasma, and platelet fractions. The devices and methods described have particular value for rapid preparation of autologous concentrated platelet fractions, e.g., to help or speed healing.
Whole blood may be spun in a vented tube with a density-adjusted float mechanism which can float freely and unanchored within the tube along with the whole blood. The density of the float mechanism may be adjusted so that when the whole blood has been separated, the float at equilibrium may rest above the sedimented red blood cell (RBC) pack, isolating the PRP supernatant. The float may serve as a barrier to prevent contamination with RBC when the PRP is withdrawn from the tube.
One variation may generally comprise a separator assembly which may include a syringe or centrifuge container tube which defines a channel for collecting, e.g., a whole blood sample. The separator float may have an atraumatic and arcuate shape, e.g., spherical, ellipsoidal, cylindrical, etc. and having a diameter which corresponds to the inner diameter of the channel so that the float may move freely within the length of the channel uninhibited and which allows for blood components to pass through the annular space defined between the outer diameter of the float and the inner surface of the channel. However, this annular space may also be small enough so as to discourage the free and uninhibited passage of blood components through.
A float having a spherical shape not only can be used to isolate the upper and lower fluid fractions, but may also decrease the likelihood of the float cocking or jamming during centrifugation. Additionally and/or optionally, select surfaces or all of the surfaces of the float may also be optionally treated as well. For instance, overmold skins, silicone coatings, wetting agents such as latherin, surfactant proteins, etc., may be applied to the select surfaces of the float or over the entirety of the float. In one variation, the upper surface of the float may be treated to trap or retain a thin layer of red blood cells upon which platelets in the PRP layer may sediment upon. The presence of the red blood cells may cushion and minimize any platelets from directly contacting the surface of the float which may potential evert and damage the contacting platelets.
In one variation, the density of the float can be set so that the RBC layer is entirely below the upper surface of the float, e.g., after a “soft spin”. Alternatively, the density of the float may be set to capture a small amount of the RBC layer above the float. If the buffy coat is desired, the density of the float can be set so that after a “hard spin” the buffy coat and a small amount of the RBC layers are above the float. The same float may have its density set so that the float resides between the RBC layer and the PRP layer, e.g., at its midline or anywhere along the float, after a soft spin and then resides with, e.g., its midline or anywhere along the float, below the buffy coat after a “hard spin”. Some plasma can be withdrawn separately before the buffy coat is harvested to produce a more concentrated final product.
As previously mentioned, the float at equilibrium may rest above the sedimented red blood cell (RBC) pack, isolating the PRP supernatant such as after a “soft spin”. The float at equilibrium may accordingly separate the channel between an upper channel in which the PRP layer and/or buffy coat resides above the float (e.g., above the outer diameter of the float) towards a proximal or proximal or upper end of the tube, and a lower channel in which the RBC layer resides below the float (e.g., below the outer diameter of the float) towards a distal or lower end of the tube. In other variations, the density of the float may be tuned so that the buffy coat forms around the periphery of the float, e.g., above the midline of the float or anywhere along the float after a “hard spin”. Separating the PRP layer from the RBC layer helps to ensure that the any red blood cells from the RBC layer are entirely isolated from the supernatant PRP layer contained above the float.
In another variation the tube may optionally include a seal to maintain sterility. The seal may also incorporate a withdrawal tube connected to a withdrawal tube channel defined through the seal. The position of the seal relative to the tube may be optionally adjusted so that once processing has been completed and the float is positioned at equilibrium relative to the upper and lower fluid fractions, the seal may be pushed, screwed, or otherwise urged down upon the tube so as to position the opening of the withdrawal tube into contact against or in proximity to the float so that the PRP layer can be withdrawn through the tube.
In another alternative, the float may optionally incorporate a tether attached to the float to facilitate its removal, if needed, while in other variations the tether may be configured from a length of tubing, e.g., silicone tubing, connected or connectable to an opening for removal of the PRP layer. In yet another variation, the relatively high viscosity of the RBC layer may be utilized to maintain separation when the tube is inverted so that the supernatant PRP layer can be withdrawn from a cap or septum Luer on the top cap of the inverted tube. The tube could also be configured to expand radially relative to its longitudinal axis during centrifugation to allow the float to migrate freely within the tube to its equilibrium position relative to the centrifuged fractional layers. However, when the centrifugation is stopped, the inner diameter of the tube may contract to trap the float in place at its equilibrium position. The float itself could alternatively be compressible under centrifugally generated pressure but re-expand after centrifugation has stopped so as to lock a position of the float against the inner surface of the tube at its equilibrium position.
As previously discussed, the float itself may also be in an alternative shape. Another particular variation of the float may comprise a tapered interface surface formed in a conical configuration which terminates in an apex that may be atraumatically shaped, e.g., blunted, so as to minimize damage to the blood components. The tapered interface surface may be optionally shaped so as to mirror the tapered shape of the tube interior. The tapered interface surface may also prevent red blood cells from accumulating upon the upper surface of the float during centrifugation. The tapered interface surface may present a slanted or non-orthogonal surface relative to a normal surface of the float which may facilitate the platelets to move or slide down upon the slanted interface surface. The degree of the slant may range anywhere from, e.g., about 2 to about 45 degrees, although the degree of the non-orthogonal surface may vary depending on factors such as the volume of fluid present. Moreover, the surfaces may be smoothed from a relatively rough polymer to a polished surface, e.g., utilizing polymer coatings, nanoparticles, etc. Additionally and/or alternatively, a bottom surface of the float may also be tapered as well so as to prevent platelets from depositing upon the lower surface as the red blood cells pack out, squeezing platelets out of the burgeoning pack.
In yet another variation, a syringe or container tube may be used in a vacuum-drawn system for separating and then collecting the supernatant fraction. A translatable plunger may be slidably positioned within the channel and a pull rod may be coupled to the plunger via a plunger lock attached to the plunger on a side of the plunger opposite to the float. A pull rod lock may be integrated with the tube at a distal surface of the tube around a pull rod opening through which the pull rod may be translated. A Luer assembly may be integrated with at a proximal end of the tube along with a valve and a cap or septum Luer which may be used to seal the Luer.
The proximal end of the tube just below the Luer assembly may also define an interface surface which may be tapered or shaped to receive the float in a corresponding manner to optimize the amount of the PRP layer which may be withdrawn from the tube.
One variation for utilizing the container tube may utilize the pull rod which may be pushed to move the plunger and float into an initial position where the float is pushed into contact against the interface surface of tube prior to receiving whole blood. The tube may be supplied preloaded with, e.g., anticoagulant or any other agent, contained within the channel. Having the tube preloaded with anticoagulant would enable the blood to be drawn directly into the tube without the need for additional processing. With the valve closed, the pull rod may be pulled or pushed to move the plunger into a distal position within the tube. Because the valve is closed, a vacuum may be formed within the tube. The pull rod may be rotated partially about its longitudinal axis relative to the tube and plunger so as to lock a position of the pull rod to the tube and to prevent the plunger from being moved back proximally in position due to the vacuum.
A syringe or blood line may be attached to the Luer and the valve may then be opened allowing (whole) blood to be drawn through the Luer and into the channel by the vacuum formed within the tube. Once the blood has filled the channel of tube, the valve may then be closed again and the blood line disconnected and removed. The pull rod may be decoupled or detached from the plunger lock as well as from the pull rod lock such that the pull rod is fully removed so that the tube, float, and whole blood may be centrifuged. With the whole blood introduced within the channel or tube, the float may remain settled at its distal position prior to centrifuging the assembly.
Once the tube and its contents have been sufficiently centrifuged, the whole blood may separate into its fractional components and the float may alter its position within the channel accordingly due to the differing densities of the individual fractional layers. To effect removal of the PRP layer, a syringe or line may be coupled to the Luer and the valve may then be opened to allow withdrawal of the PRP layer through line. The RBC layer may remain between the plunger and float and the float may remain at the interface of the PRP layer and RBC layer as the PRP layer is withdrawn through Luer. As the PRP layer is fully withdrawn the upper surface of the float may come into contact against the interface surface of the tube so that the float and interface surface form a float interface which may seal the tube and prevent any further withdrawal through Luer. The RBC layer may accordingly remain trapped between the lower surface of the float and the plunger.
For shipment and storage of the tube, the float may incorporate an attractive element such as a magnet embedded entirely or partially within the float. An externally positioned attractive element may be located externally of the tube, such as near the bottom of the tube, to attract the embedded element within the float to prevent the float from movement during shipment or handling of the tube. Prior to use of the tube, the external attractive element may be removed to release a position of the float within the tube.
In yet another variation, an external clamp on the tube may be used to trap the position of the float at the bottom of the tube to ensure that the float remains secured in its position particularly if any preloaded anticoagulant is present within the tube. The clamp may be removed before or after blood introduction or before centrifugation.
In one variation, an apparatus for separating blood may generally comprise a tube defining a channel and configured for receiving a quantity of blood, and a float contained within the tube and having a density which is predefined so that the float is maintained at equilibrium between a first layer formed from a first fractional component of the blood and a second layer formed from a second fractional component of the blood.
In another variation, a method for separating blood may generally comprise introducing a volume of blood into a channel of a tube which encloses a float having a density which is predefined, and subjecting the tube to a centrifugation such that the blood separates into at least a first layer formed from a first fractional component of the blood and a second layer formed from a second fractional component of the blood, wherein the float is maintained at equilibrium between the first layer and the second layer.
Throughout the description, terms such as “top”, “above, “bottom”, “below” are used to provide context with respect to the relative positioning of components when, e.g., a container tube with fractional components of blood are positioned when the longitudinal axis of a container tube is positioned upright or non-horizontally. Such description is used for illustrative purposes only.
In one variation of a separator assembly, whole blood may be spun in a vented tube with a density-adjusted float mechanism which can float freely and unanchored within the tube along with the whole blood. The density of the float mechanism may be defined or predefined using various methodologies, e.g., combining differing polymers in differing ratios, integrating weights, removing mass, etc., so that when the whole blood has been separated, the float at equilibrium may rest above the sedimented red blood cell (RBC) pack, isolating the PRP supernatant. The float may serve as a barrier to prevent contamination with RBC when the PRP is withdrawn from the tube.
One variation is shown in the perspective view of
For floats 20 having an outer diameter which equals or exceeds the inner diameter of the channel 18 in which the float 20 is contained when at rest, such floats 20 may be used with container tubes 12 made from flexible materials such as plastics or polymers rather than glass. The inner diameter of the channel 18 may reconfigure itself to radially expand to result in a relatively larger inner diameter, for instance, when spun in a separation procedure. During this spinning process, the float 20 may freely move within the channel 18 to a position of equilibrium relative to the blood components contained within. When the container tube 12 has stopped spinning or has slowed down, the inner diameter of the channel 18 may reconfigure itself to radially retract to a relatively narrower diameter which may then clamp down or compress against the outer diameter of the float 20.
In other variations, the float 20 may have an outer diameter relative to the inner surface of the channel 18 ranging from tens or hundreds of microns of clearance (or interference), depending on the particular application.
The variation shown in
Additionally and/or optionally, select surfaces or all of the surfaces of the float 20 may also be optionally treated as well. For instance, overmold skins, silicone coatings, wetting agents such as latherin, surfactant proteins, etc., may be applied to the select surfaces of the float or over the entirety of the float. In one variation, the upper surface of the float 20 may be treated to trap or retain a thin layer of red blood cells upon which platelets in the PRP layer may sediment upon. The presence of the red blood cells may cushion and isolate any platelets from directly contacting the surface of the float 20 which may potentially evert and damage the contacting platelets. In this instance, at least one layer of the red blood cells upon the surface of the float 20 may be sufficient to provide the cushioning to the platelets.
Although the float 20 is shown as having a spherical shape, the float may be shaped to have various configurations. For example, in other embodiments, the float may be shaped to have a cylindrical body having a length and a curved, domed, or otherwise convex shape along the bottom or distal portion of the float. The upper or proximal portion of the float may also be curved, domed, convex, concave, or angled relative to a longitudinal axis of the float.
In one variation, the density of the float 20 can be set so that the RBC layer is entirely below the upper surface of the float 20, e.g., after a “soft spin”. Alternatively, the density of the float 20 may be set to capture a small amount of the RBC layer above the float 20. If the buffy coat is desired, the density of the float 20 can be set so that after a “hard spin” the buffy coat and a small amount of the RBC layers are above the float 20. The same float 20 may have its density set so that the float 20 resides between the RBC layer and the PRP layer, e.g., at its midline or anywhere along the float, after a soft spin and then resides with, e.g., its midline or anywhere along the float, below the buffy coat after a “hard spin”. Some plasma can be withdrawn separately before the buffy coat is harvested to produce a more concentrated final product.
For discussion purposes, a “hard spin” may range, e.g., between 2000 to 4000×g over 2 to 20 minutes, while a “soft spin” may range, e.g., between 500 to 1000×g over 5 to 20 minutes.
As previously mentioned, the float 20 at equilibrium may rest above the sedimented red blood cell (RBC) pack, isolating the PRP supernatant such as after a “soft spin”. The float 20 at equilibrium may accordingly separate the channel 18 between an upper channel 22 in which the PRP layer and/or buffy coat resides above the float 20 (e.g., above the outer diameter of the float 20) towards a proximal or proximal or upper end 14 of the tube 12, and a lower channel 24 in which the RBC layer resides below the float 20 (e.g., below the outer diameter of the float 20) towards a distal or lower end 16 of the tube 12. In other variations, the density of the float 20 may be tuned so that the buffy coat forms around the periphery of the float 20, e.g., above the midline 34 of the float 20 after a “hard spin” or anywhere along the float. Separating the PRP layer from the RBC layer helps to ensure that the any red blood cells from the RBC layer are entirely isolated from the supernatant PRP layer contained above the float 20. The tube 12 may also have a cover or seal and a removable cap or septum Luer 26 through which the PRP layer and/or buffy coat may be accessed for removal. While a cap may be removable to provide access for withdrawal, the use of a septum Luer 26 may enable the septum Luer 26 to remain in place, e.g., for introducing blood into the tube 50.
Alternatively, the tube 12 may be sealed with a conventional septum which omits any Luer fittings. By utilizing a septum to seal the tube 12, the tube 12 may be vacuum sealed until used.
While the density may be tuned to have the float 20 positioned at equilibrium at specified positions between the fractional layers, there is relatively greater latitude on the tolerance for the density as the float 20. For example, if the float 20 were used to separate the intermediate buffy coat layer after a “hard spin”, the density tolerance on the float 20 would be much tighter given the relatively thin layer of the buffy coat compared to the PRP or RBC layers. On the other hand, if the float 20 were used to separate the PRP layer from the RBC layer after a “soft spin”, the latitude on the density range for the float 20 would be relatively greater.
Another variation is shown in the partial cross-sectional side view of
In another alternative, the float 20 may optionally incorporate a tether (not shown) attached to the float 20 to facilitate its removal, if needed, while in other variations the tether may be configured from a length of tubing, e.g., silicone tubing, connected or connectable to an opening for removal of the PRP layer. In yet another variation, the relatively high viscosity of the RBC layer may be utilized to maintain separation when the tube 12 is inverted so that the supernatant PRP layer can be withdrawn from a cap or septum Luer 26 on the top cap of the inverted tube 12. If the viscosity of the RBC layer is insufficient to reliably maintain separation when the tube is inverted, the tube 12 could be configured to expand radially relative to its longitudinal axis during centrifugation to allow the float 20 to migrate freely within the tube 12 to its equilibrium position relative to the centrifuged fractional layers, as illustrated in
As previously discussed, the float itself may also be in an alternative shape. Another particular variation of the float may be seen in the perspective view of
In some embodiments, the degree of the slant may range anywhere from, e.g., about 2 to about 45 degrees, optionally from about 2 to about 40 degrees, from about 2 to about 35 degrees, from about 2 to about 30 degrees, from about 2 to about 25 degrees, from about 2 to about 20 degrees, from about 2 to about 15 degrees, from about 2 to about 10 degrees or from about 2 to about 5 degrees, relative to a normal surface of the float. In some embodiments, the degree of slant may range anywhere from, e.g., from about 2 to about 45 degrees, optionally from about 5 to about 40 degrees, from about 7.5 to about 35 degrees, from about 10 to about 30 degrees, from about 12.5 to about 25 degrees, or from about 15 to about 20 degrees, relative to a normal surface of the float. In other embodiments, the degree of the slant may be about 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44 or 45 degrees, relative to a normal surface of the float.
In some embodiments, the float has a surface topography configured to substantially prevent platelet adhesion. In other embodiments, the float is configured to have a surface topography and surface tapered at an angle to substantially prevent platelet adhesion. The present inventors have discovered the optimal relationship between surface topography and taper angle.
In yet another variation, a syringe or container tube 50, as shown in the perspective view of
As discussed previously, a cap may be removable to provide access for withdrawal while the use of a septum Luer 68 may enable the septum Luer 68 to remain in place, e.g., for introducing blood into the tube 50. After centrifugation, the septum Luer 68 may be optionally removed to allow for connection to a withdrawal syringe. Additionally, use of a septum Luer 68 may also obviate the use or need of a separate valve 66.
The proximal end of the tube 50 just below the Luer assembly 64 may also define an interface surface 70 which may be tapered or shaped to receive the float 72 in a corresponding manner to optimize the amount of the PRP layer which may be withdrawn from the tube 50.
A syringe or blood line may be attached to the Luer 64 and the valve 66 may then be opened, as shown in
Once the tube 50 and its contents have been sufficiently centrifuged, the whole blood 76 may separate into its fractional components and the float 72 may alter its position within the channel 74 accordingly due to the differing densities of the individual fractional layers. The variation shown in
Due to the float 72 sealing against the RBC layer 76″, even if the withdrawn PRP layer 76′ were reintroduced back into the tube 50, the RBC layer 76″ will remain contained beneath the float 72 and its volume unchanged.
As discussed herein, the whole blood 76 may be subjected to a “hard spin” to obtain a buffy coat above the midline 34 of the float or anywhere along the float. A volume of the resulting platelet-poor plasma (PPP) which may form above the PRP layer 76′ may be withdrawn from the tube 50. The buffy coat contained within the tube 50 may be resuspended in the smaller remaining volume by pulling the remaining supernatant fluid back-and-forth within the syringe 78 several times with minimal shearing or frothing. A stop may be removably affixed to the tube 50 so that a distance between the float and the interface surface 70 of the tube 50 is fixed in order to define the volume of the supernatant fluid in which the buffy coat is resuspended to a preset amount. The buffy coat may then be resuspended and withdrawn by removing the stop.
In yet another variation of a system that may be used to maintain the float 96 in a secured configuration particularly during shipping and handling,
As shown, the float 96 may be enclosed within the tube 92 along with the volume of anticoagulant. However, the float 96 may potentially rise within the tube 92 due to density differences with the anticoagulant and the float 96 is desirably secured into an immobile position for shipping and handling. In this variation, the float 96 may be fabricated from any number of biocompatible materials, such as HDPE, and may have a density of, e.g., 1.03 to 1.07 or just under 1.04 in this variation. Because of the hardness of a glass tube 92, an external clamp may be inappropriate for securing a position of the float 96 within the tube 92. If the tube 92 were made from a plastic material, a clamp may be simply positioned over the external surface of the tube 92 in proximity to the float 96 such that the walls of the tube 92 deform slightly and compress upon the float 96 to maintain it in position and prevent its movement (as described in further detail below); however, applying a compressive force may not be feasible with a tube 92 made from a relatively harder material such as glass. The float 96 may accordingly have an attractive element 98, such as a magnet, integrated within the float 96 such as a distal end or portion of the float 96 in proximity to the distal end or bottom of the tube 92 interior. The attractive element 98 may be varied in dimension (e.g., 3.175 mm length and 3.175 mm diameter) and magnetic strength depending on the desired attractive force to retain the float 96 position.
The attractive element 98 may be embedded entirely within the float 96 to prevent direct contact with any fluids within the tube 92 or it may be configured to project beyond the surface of the float 96. A corresponding external attractive element 102 (described below) may be positioned along or against the exterior of the tube 92 in apposition to the attractive element 98 contained within or along the float 96, e.g., a removable external magnet positioned over the tube 92 or within or along packaging containing the tube 92. Because the external attractive element 102 is positioned externally of the tube 92, the external element 102 may be simply removed a distance from the tube 92 to sever the magnetic attraction between the elements and thereby release the position of the float 96 prior to or after receiving blood within the tube 92 so that the float 96 may be free to reposition itself accordingly within the tube 92.
In use, the external attractive element 102 may be removed to allow for the float 96 to reposition itself during layer separation, as described herein.
In yet another variation which may be used with or without the attractive elements embedded within the float, a removable packaging post 120 may be incorporated within a cap 124, e.g., Luer cap, which may be removably attached to the opening of the tube, as shown in the side view of
In yet another variation for maintaining a position of the float 130 during shipping and handling, the tube 92 may be fabricated from a plastic material and a clamp or other compressive mechanism having one or more compressive members 132A, 132B may be simply positioned over the external surface of the tube 92 in proximity to the float 130, as shown in the perspective view of
Statements of the Disclosure include:
In one example utilizing the devices and methods described, samples of human blood were collected into tubes filled with an anticoagulant (ACD-A). Each of the tubes were spun at 3200 rpm (1500×g) for a period of 5 minutes in a swinging bucket centrifuge. The float contained within the collection tubes had a predefined density of 1.04 g/ml.
After spinning the blood samples into their constituent components, the collection tubes were inverted several times to resuspend the platelets and the harvested upper fractional layers. The volume of the whole blood introduced into the tubes, the volume of the PRP harvested, the relative baseline counts, and the fold increase and percentage recovered were recorded and calculated, as presented in the following TABLE 1.
As shown in TABLE 1 above, the use of the float having the predefined density of 1.04 g/ml proved to be effective in separating the component layers from whole blood for harvesting from the collection tubes.
The apparatus and methods disclosed above are not limited to the individual embodiments which are shown or described but may include combinations which incorporate individual features between the different variations. Modification of the above-described assemblies and methods for carrying out the invention, combinations between different variations as practicable, and variations of aspects of the invention that are obvious to those of skill in the art are intended to be within the scope of the claims.
This application is a divisional of U.S. patent application Ser. No. 16/454,525 filed Jun. 27, 2019 which claims the benefit of priority to U.S. Prov. 62/695,631 filed Jul. 9, 2018, each of which is incorporated herein by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
2889848 | Redmer | Jun 1959 | A |
3647070 | Adler | Mar 1972 | A |
3774454 | Shaw | Nov 1973 | A |
3814248 | Lawhead | Jun 1974 | A |
3897343 | Ayres | Jul 1975 | A |
3909419 | Ayres | Sep 1975 | A |
3919085 | Ayres | Nov 1975 | A |
3931018 | North | Jan 1976 | A |
3957654 | Ayres | May 1976 | A |
4088582 | Murty et al. | May 1978 | A |
4477574 | Silander | Oct 1984 | A |
4877520 | Burns | Oct 1989 | A |
5251474 | Wardlaw et al. | Oct 1993 | A |
5393674 | Levine et al. | Feb 1995 | A |
5560830 | Coleman et al. | Oct 1996 | A |
5707876 | Levine | Jan 1998 | A |
6123655 | Fell | Sep 2000 | A |
6465256 | Iskra | Oct 2002 | B1 |
7074577 | Haubert et al. | Jul 2006 | B2 |
7077273 | Ellsworth et al. | Jul 2006 | B2 |
7153477 | DiCesare et al. | Dec 2006 | B2 |
7179391 | Leach et al. | Feb 2007 | B2 |
7223346 | Dorian et al. | May 2007 | B2 |
7329534 | Haubert et al. | Feb 2008 | B2 |
7358095 | Haubert et al. | Apr 2008 | B2 |
7374678 | Leach et al. | May 2008 | B2 |
7445125 | Ellsworth et al. | Nov 2008 | B2 |
7470371 | Dorian et al. | Dec 2008 | B2 |
7524641 | Jurgensen | Apr 2009 | B2 |
7771590 | Leach et al. | Aug 2010 | B2 |
7780860 | Higgins et al. | Aug 2010 | B2 |
7837884 | Dorian et al. | Nov 2010 | B2 |
7845499 | Higgins et al. | Dec 2010 | B2 |
7947236 | Losada et al. | May 2011 | B2 |
7992725 | Leach et al. | Aug 2011 | B2 |
8012742 | Haubert et al. | Sep 2011 | B2 |
8048297 | Leach et al. | Nov 2011 | B2 |
8048321 | Leach et al. | Nov 2011 | B2 |
8119013 | Leach et al. | Feb 2012 | B2 |
8177072 | Chapman et al. | May 2012 | B2 |
8187477 | Dorian et al. | May 2012 | B2 |
8236258 | Leach et al. | Aug 2012 | B2 |
8328024 | Leach et al. | Dec 2012 | B2 |
8348066 | Ellsworth | Jan 2013 | B2 |
8377395 | Coleman | Feb 2013 | B2 |
8394342 | Felix et al. | Mar 2013 | B2 |
8445264 | Seubert et al. | May 2013 | B2 |
8474630 | Dorian et al. | Jul 2013 | B2 |
8506823 | Chapman et al. | Aug 2013 | B2 |
8511479 | Chapman et al. | Aug 2013 | B2 |
8511480 | Chapman et al. | Aug 2013 | B2 |
8518272 | Hoeppner | Aug 2013 | B2 |
8596470 | Leach et al. | Dec 2013 | B2 |
8603345 | Ross et al. | Dec 2013 | B2 |
8603346 | Leach et al. | Dec 2013 | B2 |
8632736 | Spatafore et al. | Jan 2014 | B2 |
8632740 | Dastane et al. | Jan 2014 | B2 |
8747781 | Bartfield et al. | Jun 2014 | B2 |
8794452 | Crawford et al. | Aug 2014 | B2 |
8808551 | Leach et al. | Aug 2014 | B2 |
8950586 | Dorian et al. | Feb 2015 | B2 |
8992862 | Leach et al. | Mar 2015 | B2 |
8998000 | Crawford et al. | Apr 2015 | B2 |
9011800 | Leach et al. | Apr 2015 | B2 |
9079123 | Crawford et al. | Jul 2015 | B2 |
9114334 | Leach et al. | Aug 2015 | B2 |
9120095 | O'Connel, Jr. | Sep 2015 | B2 |
9138664 | Leach et al. | Sep 2015 | B2 |
9162232 | Ellsworth | Oct 2015 | B2 |
9239276 | Landrigan et al. | Jan 2016 | B2 |
9272083 | Duffy et al. | Mar 2016 | B2 |
9333445 | Battles et al. | May 2016 | B2 |
9339741 | Newby et al. | May 2016 | B2 |
9364828 | Crawford et al. | Jun 2016 | B2 |
9375661 | Chapman et al. | Jun 2016 | B2 |
9393575 | Ellsworth et al. | Jul 2016 | B2 |
9393576 | Ellsworth et al. | Jul 2016 | B2 |
9399226 | Ellsworth et al. | Jul 2016 | B2 |
9452427 | Felix et al. | Sep 2016 | B2 |
9642956 | Landrigan et al. | May 2017 | B2 |
9649579 | Leach et al. | May 2017 | B2 |
9656274 | Ellsworth et al. | May 2017 | B2 |
9694359 | Losada et al. | Jul 2017 | B2 |
9700886 | Felix et al. | Jul 2017 | B2 |
9714890 | Newby et al. | Jul 2017 | B2 |
9731290 | Crawford et al. | Aug 2017 | B2 |
9802189 | Crawford et al. | Oct 2017 | B2 |
9897589 | Woodell-May | Feb 2018 | B2 |
9919307 | Crawford et al. | Mar 2018 | B2 |
9919308 | Crawford et al. | Mar 2018 | B2 |
9919309 | Crawford et al. | Mar 2018 | B2 |
9933344 | Newby et al. | Apr 2018 | B2 |
9937445 | King et al. | Apr 2018 | B2 |
10005081 | Duffy et al. | Jun 2018 | B2 |
10183042 | Leach et al. | Jan 2019 | B2 |
10343157 | Crawford et al. | Jul 2019 | B2 |
10350591 | Felix et al. | Jul 2019 | B2 |
10376879 | Crawford et al. | Aug 2019 | B2 |
10393728 | Woodell-May | Aug 2019 | B2 |
10413898 | Crawford et al. | Sep 2019 | B2 |
10456782 | Crawford et al. | Oct 2019 | B2 |
10603665 | Levine et al. | Mar 2020 | B2 |
10618044 | Petrie, Jr. | Apr 2020 | B1 |
11541388 | Dorian et al. | Jan 2023 | B2 |
20030205538 | Dorian et al. | Nov 2003 | A1 |
20070034579 | Dorian et al. | Feb 2007 | A1 |
20120308447 | Abrahamson | Dec 2012 | A1 |
20140219888 | Campton et al. | Aug 2014 | A1 |
20140287487 | Campton | Sep 2014 | A1 |
20150231626 | Shi et al. | Aug 2015 | A1 |
20160008808 | Levine et al. | Jan 2016 | A1 |
20160041077 | U'Ren et al. | Feb 2016 | A1 |
20170304823 | Sparks et al. | Oct 2017 | A1 |
20180304251 | Ellson et al. | Oct 2018 | A1 |
20180353952 | Olson | Dec 2018 | A1 |
20200009304 | Dorian et al. | Jan 2020 | A1 |
20200009551 | Dorian et al. | Jan 2020 | A1 |
20200009552 | Crawford et al. | Jan 2020 | A1 |
20200129560 | Centeno et al. | Apr 2020 | A1 |
20200197929 | Weinstock et al. | Jun 2020 | A1 |
20200215243 | Dorian et al. | Jul 2020 | A1 |
20200246516 | Dorian et al. | Aug 2020 | A1 |
20200289720 | Streit | Sep 2020 | A1 |
20210283600 | Dorian et al. | Sep 2021 | A1 |
Number | Date | Country |
---|---|---|
0744026 | Nov 2001 | EP |
3020481 | May 2016 | EP |
1005909 | Jun 2020 | EP |
2006-502389 | Jan 2006 | JP |
2016-505825 | Aug 2016 | JP |
WO 2018197562 | Nov 2018 | WO |
WO 2018197564 | Nov 2018 | WO |
WO 2018197592 | Nov 2018 | WO |
WO 2020013981 | Jan 2020 | WO |
WO 2020013997 | Jan 2020 | WO |
WO 2020154305 | Jul 2020 | WO |
WO 2020163105 | Aug 2020 | WO |
Entry |
---|
Wardlaw SC, Levine RA. Quantitative Buffy Coat Analysis: A New Laboratory Tool Functioning as a Screening Complete Blood Cell Count. JAMA. 1983;249(5) :617-620. doi: 10.1001 /jama.1983.03330290039026 (Year: 1983). |
Klein, Harvey et al. “Mollison's Blood Transfusion in Clinical Medicine” 12th Edition, Jan. 2014, Wiley-Blackwell, University of Bristol, UK. |
Number | Date | Country | |
---|---|---|---|
20230001408 A1 | Jan 2023 | US |
Number | Date | Country | |
---|---|---|---|
62695631 | Jul 2018 | US |
Number | Date | Country | |
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Parent | 16454525 | Jun 2019 | US |
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