WO2000074713A1 - Autologous thrombin - Google Patents

Autologous thrombin Download PDF

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Publication number
WO2000074713A1
WO2000074713A1 PCT/US2000/011865 US0011865W WO0074713A1 WO 2000074713 A1 WO2000074713 A1 WO 2000074713A1 US 0011865 W US0011865 W US 0011865W WO 0074713 A1 WO0074713 A1 WO 0074713A1
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WO
WIPO (PCT)
Prior art keywords
thrombin
plasma
clotting
composition
etoh
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2000/011865
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English (en)
French (fr)
Inventor
Philip H. Coelho
Phil Kingsley
Jim Brausch
James H. Godsey
Gail Rock
Trista K. Madsen
Sona B. Frausto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Thermogenesis Holdings Inc
Original Assignee
Thermogenesis Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Thermogenesis Corp filed Critical Thermogenesis Corp
Priority to HK02107715.7A priority Critical patent/HK1046241B/en
Priority to DE60038884T priority patent/DE60038884D1/de
Priority to JP2001501247A priority patent/JP4860857B2/ja
Priority to AU54394/00A priority patent/AU5439400A/en
Priority to EP00939285A priority patent/EP1198242B9/en
Publication of WO2000074713A1 publication Critical patent/WO2000074713A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6424—Serine endopeptidases (3.4.21)
    • C12N9/6429—Thrombin (3.4.21.5)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
    • A61K38/46—Hydrolases (3)
    • A61K38/48—Hydrolases (3) acting on peptide bonds (3.4)
    • A61K38/482—Serine endopeptidases (3.4.21)
    • A61K38/4833—Thrombin (3.4.21.5)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
    • C12Y304/21—Serine endopeptidases (3.4.21)
    • C12Y304/21005—Thrombin (3.4.21.5)

Definitions

  • the following invention relates generally to the preparation of a high specific activity thrombin enzyme from a given unit of plasma, which is sufficiently stable that it provides rapid clotting of a fibrinogen-rich solution of clotting and adhesive proteins for more than six hours when held at room temperature or lower.
  • Formulation of a fibrin sealant mimics the last step of the coagulation cascade wherein the enzyme thrombin cleaves fibrinogen which is then cross-linked into a semi-rigid or flexible fibrin clot.
  • This fibrin clot adheres to wound sites, forming a barrier to fluid leaks and generates adhesion between tissues, while providing hemostatic and healing properties to the treated site.
  • CryoSealTM system is a device which harvests cryoprecipitated, concentrated clotting and adhesive proteins, including fibrinogen and Factor XIII from a donor's plasma in approximately one hour.
  • the one hour cryoprecipitation harvesting provided by the CryoSealTM system, compared to the 1 to 2 day cryoprecipitation process routinely practiced in Blood Banks, means that CryoSealTM harvesting of clotting and adhesive proteins can occur right in the perioperative theater with the patient close by, thereby avoiding the need to initiate the process days in advance.
  • CryoSealTM harvested clotting and adhesive proteins when combined with bovine or human thrombin, forms a biological glue useful for surgical hemostasis and tissue adhesion.
  • Commercially available thrombin is generally sourced from bovine or human plasma pools, so the patient would still be at risk of negative immune reactions or contamination by infectious blood born viruses and, possibly Crutzfeld-Jacobs Disease (CJD) or new variants of QD (NVCJD).
  • CJD Crutzfeld-Jacobs Disease
  • NVCJD new variants of QD
  • Cederholm-Williams PCT Patent (W094/ 00566 - 6 January 1994) describes an improved fibrin glue in which the thrombin component, which required thirteen steps, including centrifugation, and separation of intermediate precipitates and adjusting the ionic strength of the blood and pH of the plasma to prepare, would be combined with a fibrinogen component also sourced from the plasma of the same donor.
  • these many preparation steps are so time consuming they become impractical for use in the perioperative theater where processing times should be less than one hour.
  • Hirsh, et al. (U.S. Patent No. 5,643,192) follows Cederholm-Williams by teaching another method of preparing fibrin glue in which both the fibrinogen and thrombin components of a fibrin glue are sourced from the same donor's plasma.
  • the Hirsh patent describes a method of preparing thrombin in which most of the fibrinogen in the plasma is first precipitated and removed to prepare a supernatant and then clotting the residual fibrinogen in the supernatant which is different and simpler than the method taught by Cederholm-Williams, but does not result in a commercially useful thrombin in that (see figure 1 of Hirsh, et al.) the thrombin provides clotting speeds of five seconds or less for only 4 minutes, and less than 10 seconds for only 47 minutes.
  • Coated Glass Capillaries Role Of Adhesive Platelet -Granule Proteins", Thrombosis and Haemostasis, Vol. 62(3), pp. 989-995, 1989.
  • the instant invention addresses the long felt need for a simple, practical, fast method of preparing stable human thrombin from a donor's blood, which will provide fast clots ( ⁇ 5 seconds) throughout a lengthy surgery (e.g. six hours) to combine with the clotting and adhesive proteins harvested and concentrated from the same unit of blood to form a biological sealant with no patient exposure to microbial or possible CJD or NVCJD contaminations.
  • the present invention provides a stable thrombin enzyme which can cause precise, repeatable fast or slow polymerization of clotting and adhesive proteins over a duration of up to six hours - throughout even a long surgery. Further, the use of clotting and adhesive proteins and thrombin all sourced from a single donor will eliminate various disease risks posed from the use of commercial fibrin glues where the fibrinogen is sourced from plasma pooled from thousands of donors and the thrombin is either sourced from a similar pool of human plasma or of bovine origin. The speed and simplicity of the production of stable thrombin by use of this invention allows it to be prepared just prior to or during operative procedures and it will provide fast clotting throughout even the longest surgeries.
  • the thrombin produced by this invention can be diluted in saline, water and a dilute CaCT ⁇ solution (e.g. 125 mM CaCL2) to provide precise, slower clotting times thereby allowing any preferred time from less than five seconds to longer than 2 minutes.
  • a dilute CaCT ⁇ solution e.g. 125 mM CaCL2
  • the procedure of the invention is preferably comprised of three steps, the first two of which should preferably occur at the same time: 1. Preparing a fraction enriched in prothrombin by use of Ethanol to substantially enhance the concentration of prothrombin and at the same time remove or denature naturally occurring ingredients within plasma, such as Fibrinogen and Antithrombin III which can bind to, block, interfere with or inhibit prothrombin or its subsequent activation to long-term functional thrombin. 2. Adding calcium ions to the enriched prothrombin solution and briefly agitating the solution to convert the pro-thrombin to stable, long term thrombin.
  • the object of the present invention to provide a novel and practical method for producing stable human thrombin from a prothrombin fraction which has been substantially enriched by ethanol fractionation to increase the prothrombin concentration and at the same time remove contaminating proteins.
  • the addition of calcium chloride (CaCl 2 ) to the enriched prothrombin converts prothrombin to thrombin.
  • CaCl 2 calcium chloride
  • an object of the present invention to provide an autologous thrombin which provides fast clotting in less than five seconds for more than fifteen minutes.
  • composition for extracting thrombin from plasma consisting essentially of: Plasma; Ethanol (ETOH); CaCL2.
  • ETOH and CaCL2 to the plasma, forming a composition: agitating the composition; incubating the composition in a static or rocking mode; filtering the composition of particulate, thereby passing the thrombin through the filter.
  • a device for preparing thrombin from plasma comprising: a reaction chamber having a solution of CaCL_2 and ETOH therein; means for admitting plasma into the reaction chamber; thrombin receiving syringe coupled to the reaction chamber to receive the thrombin; and a filter located between the reaction chamber and the thrombin receiving syringe.
  • an autologous biological glue processing device comprising, in combination: a thrombin processing means, a clotting and adhesive proteins processing means operatively coupled to the thrombin processing means, means for receiving plasma via the operative coupling for subsequent conversion of the plasma to, respectively thrombin and clotting and adhesive proteins.
  • the present invention provides a method and apparatus that produces thrombin which is sufficiently stable that it can provide less-than-5-second clots for up to six hours, substantially more stable than demonstrated in all prior art. Further, the clot time can be modified at will through dilution with saline. The present invention further provides an efficient method of preparation.
  • cryoprecipitation of clotting and adhesive proteins through the CryoSealTM invention requires less than one hour.
  • the autologous human thrombin component can be manufactured with minimal materials and methods from the same source plasma. Both of the biological components of the biological glue are easily combined in a surgical setting, administered to the very same donor patient, and the resultant clotting provides hemostasis or tissue adhesion at the wound site.
  • the present invention additionally provides a method for sterile production of both components of the biological glue.
  • the improved sterile manufacturing described herein provides a final product that is essentially free of contamination by non autologous microbes.
  • Figures 1A and IB are perspective views of apparatuses for sequestering prothrombin from plasma, processing the prothrombin into thrombin and taking - li ⁇
  • Figures 2A and 2B are plan views of the thrombin processing sets removed from the processing sets that extracts clotting and adhesive proteins.
  • Figures 3A and 3B are perspective views of the interior of the thrombin processing cases with the thrombin syringe shown in figures 2A and 2B removed therefrom.
  • Figures 4A and 4B are perspective views of the thrombin cases upper halves.
  • Figures 5A and 5B are perspective views of the thrombin cases lower halves.
  • Figures 6A and 6B are exploded parts views of the reaction chamber 26 shown in figures 3A and 3B along with the valving structure at opposed ends thereof.
  • Figures 7A and 7B are sectional views of the reaction chambers and valving structures depicted in figures 6 A and 6B.
  • Figures 8A and 8B are detail of construction of that which is shown in figures
  • Figures 9 A and 9B are exploded parts view of filter alternatives used in figures 3A and 3B.
  • Figure 10 is a perspective view of that which is shown in figure 9.
  • Figure 11 graphs clot time versus lifespan of thrombin fractionated at different ETOH concentrations.
  • Figure 12 graphs clot time versus lifespan of thrombin fractionated at different ETOH concentrations at different CaCL 2 concentrations.
  • Figure 13 graphs clot time versus lifespan of thrombin showing reagent volume sensitivity when the thrombin is stored on ice.
  • Figure 14 graphs clot time versus lifespan of thrombin showing reagent volume sensitivity when the thrombin is stored at room temperature.
  • Figure 15 graphs clot time versus lifespan of thrombin showing plasma volume sensitivity when the thrombin is stored on ice.
  • Figure 16 graphs clot time versus lifespan of thrombin showing plasma volume sensitivity when the thrombin is stored at room temperature.
  • reference numeral 10 is directed to the processing set according to the present invention and shown in figures 1A and IB.
  • the processing set 10 includes a fluid receiving system 20 which communicates with both a thrombin processing unit 40 and a clotting and adhesive proteins processing unit 60. More particularly, viewing both figures 1A and IB, the fluid receiving system
  • the 20 includes an inlet 2 communicating with tubing 4 through which plasma will enter the processing units 40, 60.
  • the conduit 4 has plural positions for stop valves 6 which can occlude the tubing 4 preventing fluids through passage.
  • the tubing 4 communicates through a T fitting 8 to divide plasma into two branches, a first branch 12 which leads to the thrombin processing unit 40 and a second branch 14 leading to the clotting and adhesive proteins processing unit 60.
  • the first valve branch 12 also includes a stop valve 6.
  • reagent from preloaded syringe 95 is injected pushing plunger mechanism 94 in the direction of A', into receiving system 20 through sterile barrier filter 92.
  • the reagent passes through one way valve 91; Y connector 90, that merge coupling 18 and valve 91, through branch tubing 93; and finally into the interior of casing 22.
  • a valve 24 initially directs the reagent to a reaction chamber 26.
  • the whole blood is first processed either by filtering, centrifugation, or another means of settling to remove the heavier red blood cells from the blood products, leaving plasma therebeyond for use in the figure 1 device.
  • the plasma required for the thrombin processing unit will typically be 9-10 ml so that the final volume of concentrated thrombin matches a typical yield of cryoprecipitated clotting and adhesive proteins from the clotting and adhesive proteins processing unit 60.
  • sealed bags 16 and 78 overlie both the thrombin dispensing syringe 42 (and a lead in of conduit 64) and cryoprecipitate storage tube 76 to provide sterility until both storage containers are introduced into a sterile surgical field (e.g., operatory).
  • a sterile surgical field e.g., operatory
  • the thrombin processing unit 40 operates as shown and described with reference to figures 2A through 10.
  • FIG. IB after reagent is added, plasma enters the first branch 12 and passes beyond a coupling 18, through tubing branch 93, and into an interior of the casing 22.
  • the thrombin processing unit 40 operates as shown and described with reference to figures 2A, 3A, 4A, 5A, 6A, 7A, 8A, 9A and 10.
  • fluid enters the first branch 12 and (figure 1A) passes beyond a coupling 18 and into an interior of a casing 22.
  • Coupling 18 is preferably frictionally and /or adhesively attached to the first branch 12 yet the thrombin processing unit 40 can still be removed (e.g. figure 2A) from the processing set 10 (e.g., by merely detaching or severing branch 12 followed perhaps with heat sealing) after receiving the plasma as shown in figure 2.
  • adhesive is used, it is a sterile grade for use in an operatory.
  • a valve 24 initially directs the plasma to a reaction chamber 26 having an interior tube 28a (figure 6A) preferably formed from glass and capable of receiving a volume, for example 15 ml.
  • Glass tube 28a is preferably shorter than and circumscribed by an overlying barrel 32 preferably formed from PVC.
  • a window 31a in the PVC barrel 32 can be used to gauge and/or verify the contents within the glass tube 28a. Gauging may also include gradations 29, indicating a volume on the glass tube.
  • the glass tube 28a of the reaction chamber 26 receives the plasma from the first branch 12 and into its interior for mixing with reagents preloaded in the glass tube 28a and described hereinafter.
  • the interior of the glass tube is preferably prefilled only partially with beads 25 preferably formed from borosilicate, glass or ceramic to enhance the reaction and agitation.
  • a valve 24 initially directs the plasma to a reaction chamber 26 having tube 28b (figure 6B) preferably formed from clear polycarbonate and capable of receiving a volume, for example, 15 ml.
  • Tube 28b (figure 6B) preferably formed from clear polycarbonate and capable of receiving a volume, for example, 15 ml.
  • Graduated lines 31b on the polycarbonate tube 28b can be used to gauge the contents within the tube 28b.
  • the polycarbonate tube 28b of the reaction chamber 26 receives the plasma from the first branch 12 and into the interior for mixing with reagents previously added into the polycarbonate tube 28b and described hereinafter.
  • the interior of the tube 28b is preferably prefilled only partially with beads 25 preferably formed from borosilicate or ceramic to enhance the reaction and agitation.
  • the reaction chamber 26 of the embodiment shown in figures 1A and 3A is formed with first and second end caps 34 detailed in figures 6 A, 7A and 8 A.
  • Each end cap includes a central outwardly conically tapering spout 36 which communicates with the valve 24 at one end and a further valve 44 at an opposite end.
  • Each spout 36 is isolated from the beads 25 by a screen 23 nested within necked- down portion 48.
  • Valve 24 has three branches as does valve 44, but valve 44 has one branch capped off with a cap 45 thereby defining a two branch valve.
  • One branch of each valve 24, 44 communicates with a respective one spout 36 projecting out from each cap 34.
  • the cap 34 includes an annular necked-down portion 48 which frictionally and /or adhesively resides within an interior hollow of the PVC barrel 32. In this way, the necked-down portion 48 rests upon ends of the glass tube 28a in sealing engagement therewith, isolating the interior of the reaction chamber from the PVC barrel 32.
  • each end cap includes a central outwardly conically tapering spout 36 which communicates with the valve 24 at one end and a further valve 44 at an opposite end.
  • Each spout 36 has interior obstructions preventing passage of beads 25 while allowing passage of fluid.
  • Valve 24 has three branches as does valve 44, but valve 44 has one branch capped off with a cap 45 thereby defining a two branch valve.
  • One branch of each valve 24, 44 communicates with a respective one spout 36 projecting out from each cap 34.
  • the cap 34 includes an annular interior recess portion 48 which adhesively resides on the interior surface of the polycarbonate tube 28b.
  • ethanol and calcium chloride are the reagents which have been preloaded into the reaction chamber 26 or within reagent syringe 95.
  • both valves 24 and 44 are oriented so that reagents will not pass therebeyond to seal the chamber for the embodiment of figure 1A.
  • valve 24 is oriented so plasma will not enter reaction chamber 26, and valve 44 is oriented to allow passageway between the reaction chamber 26 and the draw plunger 56.
  • valve 44 is turned to allow access to the draw plunger 56 and valve 24 is oriented to allow access between the passageway 21 and the reaction chamber 26.
  • syringe 56 includes a filter 62 located in the flow path. More specifically, the path 43 between valve 44 and syringe 56 includes a filter 62 located in the flow path.
  • the filter 62 provides an aesceptic microbial barrier so that, upon subsequent delivery of the thrombin to the dispensing syringe 42 (figure 1), there is no contamination from around the seal 57 of plunger 58 delivered to syringe 42. Plasma will subsequently enter chamber 26 from conduit 4 to replace air.
  • Valve 24 is oriented to address filter 66. The reagents and plasma are briefly agitated assisted by beads 25 (and allowed to incubate for about 40 to 70 minutes).
  • thrombin processing unit 40 After incubation, thrombin processing unit 40 is agitated to loosen and break up gel formation. For the embodiment of figure IB, the thrombin processing unit 40 is then returned to a motionless horizontal position for no less than 10 minutes. Afterwards the thrombin processing unit 40 is again agitated to loosen and break up gel formation.
  • the plunger of syringe 56 is pushed in the direction opposite arrow A to move thrombin from chamber 26 through filter 66 into syringe 42. Delivery of thrombin to syringe 42 can be enhanced by retracting plunger 43 of syringe 42, defining a push pull system. Filter 66 removes particulate matter from the thrombin, including gel.
  • FIGS 9A, 9B and 10 reveal alternative embodiments of filter 66 which includes an outer cylindrical wall 65 with end caps 34 each having a cylindrical spout 37 circumscribed by an annular recess 39.
  • the alternative embodiment shown in figure 9A shows the centrally disposed cylindrical filter element 67a is perferably formed from polyurethane foam.
  • centrally disposed cylindrical filter element 67b is preferably formed from rolled polyester. Also shown in figure 9B, are circular filters 68 preferably formed from glass fiber or polyester. In each alternative embodiment, filter 67a or 67b filters by weight, size and protein binding.
  • clotting and adhesive protein processing unit 60 All of the plasma not diverted to the thrombin processing unit 40 is admitted to an interior chamber 72 of the clotting and adhesive protein processing unit 60.
  • the clotting and adhesive protein processing unit 60 is manipulated by heat exchange and rotation so that all clotting and adhesive proteins extracted from the plasma will sediment at a nose 74 of the chamber 72 for subsequent extraction by means of a clotting and adhesive protein collection tube or dispensing syringe 76 contained in a sterile pouch 78.
  • Chamber 72 is protected during this process by a filter vent 82 preventing contamination.
  • the two storage containers 42, 76 can be decoupled from the processing set 10 (e.g. sterile disconnect device), and passed near the sterile, surgical arena.
  • the overwrap bags are subsequently opened, and the storage containers 42, 76 are decoupled and transferred into the surgical area where the contents are dispensed into individual sterile 3cc plastic syringes which are subsequently loaded into the fibrin glue applicator for spraying or line and dot application.
  • the processing set 10 e.g. sterile disconnect device
  • Both dispensing syringes 42 and 76 are stored at room temperature, or preferably stored at their optimal conditions: cryoprecipitate 76 being stored at room temperature and thrombin 42, stored in an ice bath at 1°C to 5°C. Please see figures 13 through 16.
  • the thrombin lifespan also extends to at least 360 minutes while maintaining a clot time of 5.98 seconds when thrombin is stored at room temperature. Storing thrombin in optimal 1°C to 5°C ice bath typically maintains lot times of 2 to 3 seconds at 360 minutes. Calcium chloride stock solution concentrations ranging between 50 mM and 250 mM, however, have utility. Please see figure 12. The final concentrations range from 4.5mM to 23 mM.
  • Solutions such as saline, dilute CaCL 2 (e.g. 40mM to 125 mM CaCL 2 ) or even sterile water added to the thrombin can alter both the clotting time and life span of the thrombin. Assume an ethanol final concentration of 18.9% and a final calcium chloride concentration of 5.7 mM was used in the reaction chamber 26. When the thrombin has been diluted 1 to 1.5 with water, the clot time has been extended to just less than 30 seconds, and has a life span of up to 150 minutes.

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PCT/US2000/011865 1999-06-04 2000-06-02 Autologous thrombin Ceased WO2000074713A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
HK02107715.7A HK1046241B (en) 1999-06-04 2000-06-02 Autologous thrombin
DE60038884T DE60038884D1 (en) 1999-06-04 2000-06-02 Autologes thrombin
JP2001501247A JP4860857B2 (ja) 1999-06-04 2000-06-02 自己由来トロンビン
AU54394/00A AU5439400A (en) 1999-06-04 2000-06-02 Autologous thrombin
EP00939285A EP1198242B9 (en) 1999-06-04 2000-06-02 Autologous thrombin

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/328,350 1999-06-04
US09/328,350 US6472162B1 (en) 1999-06-04 1999-06-04 Method for preparing thrombin for use in a biological glue

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WO2000074713A1 true WO2000074713A1 (en) 2000-12-14

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EP (1) EP1198242B9 (https=)
JP (1) JP4860857B2 (https=)
AT (1) ATE395074T1 (https=)
AU (1) AU5439400A (https=)
DE (1) DE60038884D1 (https=)
HK (1) HK1046241B (https=)
WO (1) WO2000074713A1 (https=)

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6596180B2 (en) 1996-04-30 2003-07-22 Medtronic, Inc. System and method for the production of autologous platelet gel
US6679300B1 (en) 2002-01-14 2004-01-20 Thermogenesis Corp. Biological adhesive loading station and method
WO2004058943A3 (en) * 2002-12-23 2005-02-10 Cobe Cardiovascular Inc Device and process for the preparation of autologous thrombin serum
US6942880B1 (en) 2001-04-09 2005-09-13 Medtronic, Inc. Autologous platelet gel having beneficial geometric shapes and methods of making the same
JP2006516630A (ja) * 2003-01-27 2006-07-06 ハーベスト テクノロジーズ インコーポレーテッド 抗凝固処理全血から産生される自己又は同種の凝固剤
WO2007127834A3 (en) * 2006-04-26 2011-09-22 Medtronic, Inc. Compositions and methods of preparation thereof
WO2012015785A1 (en) * 2010-07-30 2012-02-02 Biomet Biologics, Llc Method for generating thrombin
CN102766616A (zh) * 2011-05-02 2012-11-07 拜欧米特生物制剂有限责任公司 从血液或血液级分中分离的凝血酶
US8586324B2 (en) 2011-08-15 2013-11-19 Biomet Biologics, Llc Method and apparatus to create autologous clotting serum
WO2014052496A1 (en) * 2012-09-25 2014-04-03 Stem Cell Partners Llc Method and apparatus for preparing single donor thrombin serum
US8801586B2 (en) 2008-02-29 2014-08-12 Biomet Biologics, Llc System and process for separating a material
US8950586B2 (en) 2002-05-03 2015-02-10 Hanuman Llc Methods and apparatus for isolating platelets from blood
US8992862B2 (en) 2009-04-03 2015-03-31 Biomet Biologics, Llc All-in-one means of separating blood components
US9011800B2 (en) 2009-07-16 2015-04-21 Biomet Biologics, Llc Method and apparatus for separating biological materials
US9114334B2 (en) 2002-05-24 2015-08-25 Biomet Biologics, Llc Apparatus and method for separating and concentrating fluids containing multiple components
US9138664B2 (en) 2007-04-12 2015-09-22 Biomet Biologics, Llc Buoy fractionation system
US9239276B2 (en) 2011-04-19 2016-01-19 Biomet Biologics, Llc Apparatus and method for separating and concentrating fluids containing multiple components
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