CA2367105C - A thrombin blood fraction for use in a medical procedure - Google Patents

Abstract

The subject invention relates to the use of thrombin in a medical procedure in an animal.
More specifically, the subject invention relates to such use of thrombin wherein the thrombin is a thrombin blood fraction, as defined hereinbelow.

Description

s A THROMBIN BLOOD FRACTION FOR USE IN A MEDICAL PROCEDURE.
1. FIELb OF TAE xNVEN,~,~ON
The subject invention relates to the use of thrombin in a medical procedure in an animal. More srecif ically, the subject invention relates to such utie of thrombin wherein the thrombin is a thrombin blood fraction, as defined hereinbelow.

2. B_ACICGROUND OF THE INVENTION
One mechar. ~m for hemostasis, i.e., prevention of blood loss, of an aniatal is the formation of a blood clot. Clot formation, i.e., blood coagulation, occurs by means of a complex cascade of reactions with the final steps being the conversion of fibrinogen by throabin, calcium ions and activated factor XIII to form the fibrin clot. For a review of the mechanisms of blood coagulation and the 2o structure of fibrinogen, see C.M. Jackson, Arin. Rev.
Biochem., 49:765-811 (1980) and. B. Furie and B.C.
Furie, Cell, 53:505-518 (1988).
Thrombin, which is a proteolytic enzyme, is derived from prothrombin. Prothrambin is converted to thrombin by calcium arid prothrombinase.
Prathrombinase is formed through a cascade of reactions that begins with the proteins factor XI and factor XII.
A fibrin sealant is a biological adhesive 80 whose effect imitates the final stages of coagulation, thereby resulting in a fibrin clot. Conventional fibrin sealants generally consist of concentrated human fibrinogen, bovine aprotinin and factor XIII, as the first component and bovine thrombin and calcium s5 chloride as the second component. Application is generally carried out with a double-barrelled syringe, x. s WO 94/00566 PCT/GB93/01323.

which permits simultaneous application of both components to the site where one wants to form the fibrin clot. Aprotinin is a t:ibrinolytic inhibitor added to promote stability of fibrin sealants.
The fibrinogen component of the Fibrin sealant is prepared from pooled human plasma. The ' fibrinogen can be concentrated from the human plasma ~by cryaprecipitation and precipitation using various reagents, a.g., polyethylene glycol, ether, ethanol, io ammonium sulfate or glycine. For an excellent review.
of ffibrin sealants, sae M. Brennan, Blood Reviews, 5:240-244 (1991); J.W. Gibble and P.N. Ness, Transfusion, 30:741-?4? (1990); H. Matras, J. Oral Maxillofac Surg., 43:605-611 (1985) and R. Lerner and N. $inur, J. of Surgical Rese3,rCh, 48:165-181 (1990).
Recently, there has also been an interest in the preparation of fibrin sealants that utilize autologous fibrin. An autologous fibrin sealant is a fibrin sealant wherein the fibrinogen component of the 2o fibrin sealant is extracted from the patients own blood. The use of an autologous fibrin sealant is preferred because it eliminates the risk of transmission of blood-transmitted infections, e.g., hepatitis B, non A, non B hepatitis and acquired 2S immune deficiency syndrome (AIDS), that could otherwise be present in the fibrinogen component extracted from pooled human plasma. See L.E..
Silberstein et al., Transfusion, 28:319-321 (1988); K.
Laitakari and J. Luotonen, Laryngoscope, 99:974-976 30 (1989) and A. Dresdale et al., The Annals of Thoracic Surgery, 40:385-387 (1985).
An infection can be transmitted by a fibrin sealant not only by oceans of the fibrinogen but also by means of the bovine aprotini.n and the bovine 35 thrombin component. Bovine thrombin has been known to .. _. ~ . w u.- ~ a v 1. V V y carry the infectious agent bovine spongiform encephalitis (BSFs) and other viruses pathogenic to mammals.
F~rthertnore, bovine thrombin is a potential antigen, which can cause immunvlogical reactions in humans. Thus, the use of bovine thrombin could reswlt in the recipient of the bovine thrombin being adversely affected. See D_M. Taylor, J. of Hospital Infection, 18(Supplement A):141-146 (1991), S.B. Prusiner et al., Cornell Vet, 81 No. z: 85-96 (1991) and D. Matthews, J. Roy. Soc. Health, CIitGI)~
3 - 5 ( February 19 91 ) .
Accordingly, there is the need for a sealant that utilizes thrombin that can be delivered to a patient without the risk of viral contaminatiozi yr other adverse affects.

3. SUN>rlARY OF THE INVENTION
The subject invention relates to a composition for use in a medical procedure in an animal, which composition is a thrombin containing blood fraction which comprises:
(a) a thrombin concentration of frcm about 1 NIH unit/ml to about 2;, 000 NIFi units/ml, and (b) a specific activity of thrombin of from ~''~ 25 about 1 NIH unit/mg of blood protein to about 200 NIH units/mg of blood protein, wherein said thrombin blood fraction is substantially free of active antithrombin III.
The subject invention also relates to a method 30 for preparing a prothrombin blood fraction from whole blood comprising:

(a) diluting whole blood to an ionic strength of less than about 100 millimolar;
(b) separating plasma from said whale blood;
(c) lowering the pZi of said plasma to precipitate a prothrombin blood fraction; and (d) separating said prothrombin blood l0 fraction from said plasma.
The prothrombin bland fraction is then redissolved and converted to thrombin, i.e., the thrombin blood fraction is farmed, which can then be utilized in a medical procedure in an animal, e.g., as a component of a fibrin sealant.
4. DETAILED DESCRI TION OF THE INVENTION
The subject invention relates to the use of a thrombin blood fraction, as defined hereinbelow, in 20 a medical procedure, e.g., as a component of a fibrin sealant, in an animal, preferably a mammal. Suitable mammals include a human, a cow, a pig, a dog and a rabbit, or other mammals that have an adequate blood volume to prepa=e the thrombin. blood fraction. The 25 thrombin blood fraction can be prepared from whole blood and is impure in that it contains blood proteins .. other than thrombin. However, the thrombin blood fraction can be prepared very simply and rapidly, e.g., in less than about one or two hours, and is 30 believed to be as efficacious as a highly pure thrombin preparation.
The thrombin blood fraction can be prepared from whole blood. It is preferred that the whole blood be obtained from a single individual animal.
'35 Also, it is pref erred that the thrombin blood fraction r.
WO 94/00566 PCTlGB93/OI323 _ S
be administered to the same individual animal from which the whole blood was taken. thus, one aspect of the invention is the use of an autologous thrombin blood fraction in a medical procedure. rn this embodiment, there is also no risk of transmission of blood~transmitted infections because the thrombin blood fraction is to be administered to the same individual animal that donated the whole blood. Also, for the same reason, the blood proteins other than 1o thrombin that are present in the thrombin blood fraction would not be antigenic, Furthermore, since the thrombin blood fraction is preferred to be prepared from a single individual animal and used in the same, generally is small volumes of whole blood are required, especially since it is also preferred to prepare a thrombin blood fraction for a single use. Also, it is preferred to prepare the fraction within several hours of the time of use. It is preferred that ~:rom about 10 ml to 2o about SO ml, more preferably from about 10 ml to about 30 ml and most preferably from about l0 ml to about 20 ml of whole blood be utilized to prepare the thrombin blood fraction of the subject invention.
The thrombin blood fraction of the subject 25 invention has a thrombin concentration of from about 1 NIH unit to about 2,000 NIIi units, preferably from .. about 100 NIH units to about 800 NIH units and most preferably from about 100 NIH units to about 500 NIH
units per ml of the thrombin blood fraction.
It is believed that at such concentrations the thrombin blood fraction possesses a sufficient thrombin concentration for the desired medical use.
of course, the preferred thrombin concentration depends on the medical use of the thrombin blood 35 fraction.

The thrombin concentration of the thrombin blood fraction can be determined by measuring the coagulation time of a standard fibrinogen solution of ter addition of the thrombin blood fraction in a 5 suitable diluted form. As a reference, standard thrombin solutions, containing from 2 to 15 NIH
units/ml, can be utilised.
The thrombin blood fraction of the subject invention has a specific activity of thrombin 4f from 1D about 1 NIH unit to about 200 NIH units, preferably from about 5 NIH units to about 100 NIH units and most preferably from about 5 NIH units to about 50 NIH
units per mg. of total blood protein. Sucb lower specific activities of the thrombin blood fraction are ~5 believed to be as effective in a medical procedure as the more pure thrombin blood fractions. However, such lower specific activity of the thrombin blood fractions can be prepared more readily.
The specific'activity of the thrombin blood 20 fraction is, in essence, a measurement of the amount of thrombin per amount of blood protein in the thrombin blood fraction. Thus, the specific activity of the thrombin blood fraction of the subject invention is quite low relative to thrombin 25 preparations that have been prepared heretofore. For example, United States Patent No. 5,143,838 discloses a thrombin preparation with a specific activity of at least 800 NIH units per mg. of total protein. Also, United States Patent Na. 5,15x.,355 discloses a 30 thrombin preparation with a specific activity of greater than 1,000 NIH units/mg. of total protein.
Although the specific aCtivit~~ of the thrombin blood fraction of the subject is low, never the less it is believed that the blood fraction is efficacious for 35 use in medical procedures.

The specific activity of the thrombin blood fraction of the subject invention can be calculated by measuring the thrombin concentration (NIH units/ml) and by dividing that number by the protein concentration (mgjml) measured by any standard protein assay, e.g., W absorbance.
The thrombin blood fraction is also substantially free of active antithrombin ILI. For the purpose of the subject invention, "substantially 1o free of active antithrombin III" means that the thrombin blood fraction per unit volume contains an amount of active antithrombin III that is less than about SO% by activity of antithrombin III in normal plasma per unit volume. It is preferred that such percentage be less than about 30%, more preferably less than about 10% and most preferably less than about 5%. It is essential that the antithromhin III
either be removed from or in-~tivatad in the thrombin blood fraction. Otherwise, antithrombin III will prevent the conversion of the ps:athrombin in the blood fraction to thrombin and/or inactivate the thrombin that is farmed.
It is preferred that t:he thrombin blood fraction also be substantially free of fibrinogen and fibrin. For the purpose of the subject invention, substantially free of fibrinogen and fibrin means that -. the thrombin blood fraction per unit volume contains an amount of fibrinogen plus fibrin that is less than about 1% by weight of fibrinogen in normal plasma per 3o unit volume. It is preferred that fibrinogen not be present in the thrombin blood fraction because the thrombin will Convert "he fibrinogen to fibrin, which will polymerize to fo: a clot, thereby rendering the thrombin biaod fraction impracticable. The fibrinogen itself pan be removed from the thrombin blood fraction or the fibrinogen can be removed as the fibrin clot, thereby, of course, also removing the fibrin.
However, the fibrinogen need not be removed if, for example, the thrombin is inactivated as described in PCT publication No. W091j09641.
The thrombin blood Fraction can be utilized immediately after it is prepared. If the fraction is not utilized iiamediately after its preparation, the fraction can be stored. Storage of the fraction io requires that the fraction be preserved by, for example, freezing or lyophilizing the fraction or holding the composition at 4°C. The fraction in frozen or lyophilized farm will be stable f or a period of months. When the fraction is held at 4°C, it is ~5 stable for at least a period of days.
If the fraction is frozen, the fraction must be thawed at the time of use. tf the fraction is lyophilized, at time of use, it is preferred that the fraction be reconstituted by addition of distilled 20 water.
The thrombin blood fraction can be in virtually any form, far example, a solution, suspension, emulsion or solid, with a solution being preferred. Thus, for example, such fraction can be a 25 liquid, gel, paste or salve. Also, of course, the fraction can be in the form of a. granule.
If the thrombin blood ;raction is in a solid form, then the concentration of the thrombir. blood fraction can be deterained by dissolving it in a 30 solution and then measuring the thrombin concentration. If the res~:lting thro:~bi~
concentration is from about 1 NIH unitJ:~l to about 2,000 NIH units/ml, then the thrombin blood fraction is within the scope of the subject invention.

WO 94/00566 PCT/GB93/pI3Z3 -~ 9 4.1. METHOD FOR PREPA,R.ATION OF THE
T~iROMHIN.BLOOD FRACTION
The thrombin blood fraction of the subject invention can be prepared by any method known or to be developed. Also, the thrombin blood fraction can be prepared in a device as described in the PCT publication No. W091/17778.
4.1.1. METHOD FOR PREPARATION OF THE THROMBIN
BLOOD FRACTION BY FORMATION OF THE
EUGLOB IN FRACTION FROM PLASMA
Whale blood can be withdrawn from an individual animal, e.g.,.a hunan, and preferably in the presence of an anticoagulant. Any anticoagulant :5 can be utili2ed so long as it does not act by directly inactivating thrombin. Suitable anticoagulants are heparin, EDTA, citrate or any other agent that can, directly or indirectly, prevent the formatian~of thrombin, with citrate being preferred.
=o The plasma, which contains the prothrombin, is then separated from the whole blood. Any separation technique can be utilized, for example, sedimentation, centrifugation or filtration.
Centrifugation can be carried out at about 1,500 to 25 about 3,000 g. far about 10 r~inutas. The supernatant, which contains the plasma, can be re~aoved by standard techniques. If it is desired to obtain a thrombin blood fraction that contains growth factors, then such centrifugation should be at about '25 g. for about 20 30 minutes er l,OdO g. for about.2 to 3 ainutes. The thrombin blood traction of the subject invention will then contain groc.2h Factors, which are released from the platelets during the conversion o~ prothrombin to thrombin.

WO 94!00566 PCTIGB93/OI323 - is -The plasma in then treated, for example, by dilution with distilled water., followed by the addition of acid, e.g., citric acid, to lower the ionic strength to less than about 100 millimolar, 5 preferably less than about 50 millimolar and :host preferably from about 20 to about 40 millimolar and lower the pH to about 4.5 to about 6 and preferably to from about 5 to about 5.5. Lactic acid or acetic acid are also suitable acids. Generally, a weight ratio of 10 the plasma: distilled water or acid of from about 1:5 to about 1:50, with 1:10 being pref erred.
This treatment, i.e., the lowering of the ionic strength and pH of the plasma, results in the formation of a precipitate that is generally referred L5 to as the °euglobulin fraction." The euglobulin fraction captains the prothron~bin, fibrinogen and many other blood proteins, but is substantially free of antithrombin III.
Rather than diluting the plasma to lower the 2o ionic strength, and before acidifying the plasma, the ionic strength can be lowered by dialyzing the plasma by placing the plasma in a dialysis bag, Which is then placed in distilled water. The dialysis permits the ions to diffuse out of the plasma, thereby lowering 25 the ionic strength. A suitable dialysis bag is composed of cellulose nitrate. Also, the ionic - strength can be lowered by diafiltration or occlusion chromatography.
The euglobulin fraction can be prepared as 3o described in A. Quick, Production of Thrombin From Precipitate Obtained by Acidification of Diluted Plasma, Am. J. Phys3.ol., ,~,:i14-118 (1955) and R.
Biggs and R.G. Macfarlane, Human Blood Coagulation, pages 3?5-376, Blackwells Scientif is Publications, w0 94!00566 PCT/GB93/013Z3 -- i~ _ Oxford, 3rd Edition (1962).
The excess fluid can then be separated from the euglobulin fraction by, for example, centrifugation, filtration or sedimentation.
Centrifugation can be carried at about 1,500 g. for about 2 to about 5 minutes.
The prothrombin of the euglobulin fraction is then redissolved and converted to thrombin, thereby to forming a thrombin blood fraction of the subject invention. This can be carried out by solubilizing the euglobulin fraction in a physiologically acceptable solution, e.g., saline, in an amount equal to or pref erably less than ( about 10% ) the original amount of plasma. An alkaline buffer can be added in an amount to raise the pH of the solution to about 6 to about 8 and preferably to about 6.5 to about 7.5.
Nonlimiting examples of suitable alkaline buffers include sodium hydroxide, potassium hydroxide, calcium 2o hydroxide, bicarbonate buff ers such as sodium bicarbonate and potassium bicarbonate, salts of acetic acid and salts of sulfuric acid. Preferred alkaline buffers include: Sodium carbonatejbicarbonate pH 7.0, Sodium bicarbonate/NaOH pH 7.0, 1.5M Glycine/NaOH pH
6.5-?.5, Bis hydroxyethylaminaethane sulphonic acid fBES) pH 7.5, Hydroxyethylpiperazine propane sulphonic acid (EPPS) pH 7.5, Tricine pH 7.5, Morpholino propane sulphonic acid (MOPS) pH 7.0, Trishydroxymethyl aminoethane sulphonic acid (TES) pH 7.o and 3o Cyclohexylaminoethane sulphonic acid (CHES) pH ~.0;
with Sodium carbonate/bicarbonate pH 6.5 - 7.5 Bis hydroxethylaminoethane sulphonic acid (BES) pH ~.5, Fiydroxyethylpigerazine propane sulphonic acid fEPPS) pH 7.5 and Trishydroxymethyl aminoethane sulphonic acid (TES) pH 7.5 being most preferred.

CVO 94/00566 PCTlGB93l0I323 Calcium is added to the neutral solution in order to convert the prothrombin to thrombin. Of course, the calcium can be part of the alkaline buffer. Calcium can be added in the form of, far S example, calcium chloride. The amount of calcium added should be sufficient to convert an amount of ' prothrombin to thrombin that .is sufficient for theca intended medical use. Furthermore, the reaction should be permitted to occur .for a period of time sufficient to convert enough of the prothrombin to thrombin that is sufficient for the intended medical use. Generally, from about 5 millimolar to about 5O
millimolar calcium chloride ib sufficient.
Also, rather than adding a source of calcium ions, prothrombin activating enzymes from snake venams can be utilized. For example, snake venom-grom Eccis carinatus or the Australian Tiger snake can be utilized.
As the thrombin forms, it converts the 2o fibrinogen to fibrin, which farms a fibrin clot. It is preferred to remove the fibrin clot, Which can be carried out by, for example, wrapping the fibrin clot around a stirring rod or collecting the fibrin onto glass beads.
4.1.2. METHOD FOR PREPARATION OF THROMBIN BLOOD
FR~C'~,ION BY DILUTIhIG WHOLE BLOOD
In a preferred embodiment, the thrombin blood fraction can be prepared by initially preparing 3o a Prothrombin blood fraction from whole blood comprising:
(a) diluting whole bland to an ionic strength of less than about iQQ
millimolar;
3s (b) separating plasma from said whole blood;

WO 9a/oo566 PCT/GB93/01323 (c) lowering the pH of said plasma to precipitate a prothrombin blood fraction; and (d) separating said prathrombin blood fraction from said plasma.
The prathrombin blood fraction is then redissolved and converted to thrombin, i.e., the thrombin blood Fraction of the subject invention is formed, which can then be utilized in a medical lo pracedure in an animal, e.g., as a component of a fibrin sealant. This method provides a thrombin blood fraction of the subject invention, which can be prepared in anly about 45 minutes:
specifically, whole blood is drawn from an individual animal. the whole blood is then immediately (within about five minutes) diluted in order to lower the ionic strength to less than about loo milliaiolar, preferably less than about 50 millimolar and preferably to from about 20 to about 40 2o millimolar. It should be noted that since the whole blood is diluted immediately, there is no need for the use of an anticoagulant. Any physiologically acceptable solution at physiological osmotic pressure can be utilized to lower the ionic strength, e.g., a glucose aqueous solution such as a 5.5% isotonic aqueous glucose solution.
The plasma is then separated from the whole blood. Any separation technique can be utilized, for example, sedimentation, centrifugation or filtration.
Centrifugation can be carried out at about 1,500 to about 3,000 g. for about 5 to about 10 minutes. The supernatant, which contains the plasma, can be removed by standard techniques.
The plasma fractivn~ is then acidif led, 3S thereby resulting in the formation of a prothrombin blood fraction, which is generally referred to as the euglobulin fraction, which is a precipitate. The plasma fraction can be acidified with, for example, citric acid, lactic acid or acetic acid. The pH
5 should be lowered to from about 4.5 to about 6 and preferably to from about 5 to about 5.5.
The excess fluid can then be separated from the prothrombin blood fraction by, for example, centrifugation, filtration or sedimentation.
1o Centrifugation can be carried out at about 1,500 g fvr about 2 to about 5 minutes. This prothrombin blood fraction contains prothrombin, fibrinogen ahd many other blood proteins, but does not contain antithrombin III. The prothrombin blood fraction is 15 then redissolved and the prothrombin is converted to thrombin. Any physiologically acceptable solution, e.g., saline, can be utilized to redissolve the prothrombin fraction. Furthermore, only a small volume of solution is required to redissolve the 2o prathrombin fraction. It is believed that only from about 0.4 ml to about 1 ml of solution is required if about 17 ml of whole blood was initially drawn. An alkaline buffer can be added in an amount to raise the pH of the solution to about 6 to about 8 and ZS preferably to about b.5 to about 7.5. Nonlimiting examples of suitable alkaline buffers include sodium hydroxide, potassium hydroxide, calcium hydroxide, bicarbonate buffers such as sodium bicarbonate and potassium bicarbonate, tri-metal salts of citric acid, 30 salts of acetic acid and salts of sulfuric acid.
Preferred alkaline buffers include: Sodium carbanate/bicarbonate pH 5-8, Sodium bicarbonate/NaOH
pH 6-8, Glycine/NaOH pH 6-8, Bis hydroxyethylaminoethane sulphanic acid (BES) pH 6-8, 35 Hydraxyethylpiperazine propane sulphonic acid (EPPS) WO 94/00566 PCTl~GB93/01323 pH 6-8, Tricine pH 6-e, Morpholino propane sulphonic acid (MAPS) pH 6-8, Trishydroxymethyl aminoethane sulphonic acid (TES) pH 6-8 and Cyclohexylaminoethane sulphonic acid (CHES) pH 6-e; with Sodium 5 carbonatejbicarbonate pH 6-8 B:~s hydroxethylaminoethane sulphonic acid (BES) pH 6-8, Hydroxyethylpiperazine propane sulphonic acid (EPPS) pH 6-8 and Trishydroxymethyl aminoethane sulphonic acid (TES) pH 6-8 being most preferred.
10 Calcium is added to the neutral solution in order to convert the prothrambin to thrombin. Of course the calcium can be part of the alkaline buffer.
Calcium can be added in the form of farm of, for example, calcium chloride. The amount of calcium t5 added should be sufficient to convert an amount of prothrambin to thrombin that is sufficient for the intended medical use. Furthermore, the reaction should be permitted to occur for a period of time sufficient to convert enough of the prothrornbin to 20 thrombin that is sufficient f nr the intended medical use. Generally, from about 5 millimolar to about 50 millimolar calcium chloride is sufficient. It has been observed that at about 25 minutes of react-ion sufficient amounts of thrombin are formed for most 25 medical uses of the thrombin blood fraction of the subject invention.
Also, rather than adding a source of calcium ions, prothrombin activating enzymes from snake venoms can be utilized . For example, snake venom from Eccis 30 carinatus or the Australian Tiger snake can be utilized.
As the thrombin forms, it converts the fibrinogen to fibrin,.which forms a fibrin clot. It is preferred to remove the fibrin clot, which can be 35 carried out by, for example, wrapping the fibrin clot around a stirring rod or collection of the fibrin onto glass beads.
4:1.3. PREPARATION OF THROMBIN BLOOD
FRACTION BY REMOVING OR INACTIVATING
ANTITHROMBIN III FROM hLASMA
In an alternative method, the thrombin blood fraction of the subject invention can be prepared by withdrawing whole blood from an individual animal, e.g., a human, and preferably in the presence of an 10 anticoagulant. Any anticoagulant can be utilized.
Suitable anticoagulants are heparin, EDTA, citrate or any other agent that can, directly or indirectly, prevent the formation of thrombin, with citrate being preferred.
15 The lasma, which contains the p prothrombin, is then separated from the whole blood. Any separation technique can be utilized, for example, sedimentation, centrifugation or filtration.
Centrifugation can be carried out at about 3,000 g.
20 for about 10 minutes. The supernatant, which contains the plasma, can be removed by standard techniques.
Antithrombin III is then removed from the plasma or is inactivated. For example, the pH of the plasma can be lowered to at least to about 5. Such 25 lowering of pH inactivates antithrombin III; otherwise antithromhin III would prevent 'the conversion of prothrombin to thrombin. Antithrombin III can be inactivated by any technique. :for example, by the addition of 0.05 m1 of 5 mol./liter FiCl per l.0 ml 30 plasma. After about 10 to about 20 minutes of incubation, the plasma can be neutralized with 0.05 ml of 5 mol./liter NaOfi per ml of plasma.
Rather than inactivating the antithrombin III, the antithrombin III can be removed from the 3s plasma by passing the plasma through a column that binds antithrombin III, e.g., a heparin column or a column with antibodies to antithrombin III.
The plasma fraction, which contains prothrombin, is then treated to convert prothrombin to thrombin. This can be carried out by, for example, the addition of a source of calcium ions, as described above,. or by the addition of 0.1 ml CaCl= of 0.36 mol.Jliter per ml of plasma. Also, rather than adding a source of calcium ions, prothrombin activating to enzymes froze snake venoms can be utilized. For example, snake venom from Ecci~~ carinatus or the Australian Tiger snake.
As the thrombin f arms, it converts the fibrinogen to fibrin, which forms a fibrin clot. It is preferred to remove the fibrin clot, which can be carried out by, for example, wrapping the fibrin clot around a stirring rod or collection of the fibrin onto glass beads.
The resulting plasma is a thrombin blood 2o fraction of the subject invention.
4.1.4. METHOD FOR THE PREPAFL~1TION OF A
TXROMBIN BLOOD FRACTION BY DILUTING
WITH AN ACID SOLUTION DIRECTLY
8y the known process for preparing thrombin f ram plasma, plasma is diluted in the ratio 1:10 with water, whereafter a pH-reducing acid is added, such as acetic acid, with the result that the pH-value is about 5.0 to 5.3. The mixture is then centrifuged for 20 min. at 2,000 g. The resulting precipitate 3o contains different coagulation factors, such as inter olio prothrombin and fibrinogen. When the excess fluid has been removed, the precipitate is dissolved in a physiological solution, preferably a 0.9% sodium chloride solution, whereagter a pH-value-increasing ss agent, such as sodium carbonate, is added until the pH-value is about 7.9. When the precipitate has been dissolved, calcium chloride is added and pauses the conversion of the prothrombin into thrombin by a conventional, so-called coagulation cascade. The 5 resulting thrombin causes a conversion of fibrinogen into fibrin, whereafter the thrombin is separated by centrifuging and then subjected to a succeeding purification (column purification).
Another aspect of the subject invention is to that the diluting step -is performed directly with a diluted acid solution, e.g., 0.4% acetic acid, by the centrifuging step being performed in a container with a relatively large flat precipitation surface, by the physiological solution, with. the agent far increasing 15 pH, and the calcium chloride being added at the same time to the precipitate as a m:'txture, whereby said precipitate is dissolved and then coagulates while forming fibrin, and by the thrombin then being removed.
2o As a result, it is now possible to prepare thrombin from plasma of autologous blood in a relatively quick way, which is in particular due to the fact that the precipitation is performed in a container with a relatively las:ge flat precipitation 25 surface. A quick and complete dissolution is thereby ensured of the precipitate containing prothrombin and w fibrinogen. The complete dissolution is important before the presence of calcium chloride causes the conversion of prcthrombin to thrombin. A too early 3o thrombin formation leads to fibrin formation and the ffibrin will bind the added f lurid, whereby the dissolution of the precipitate stops and cannot continue until said fluid has again been passed out of the fibrin. The relatively small precipitate with a 35 relatively large surface area relative to the amount WO 94/00566 PC'T/GB93/01323 causes a complete dissolving of said precipitate by addition of the combined mixture of physiological solution, with the agent for increasing pFi, and calcium chloride before the thrombin has been formed through said coagulation cascade and starts the formation of fibrin.
Moreover according to the invention, the mixture may be admixed with a plasminogen catalyst, such as streptokinase, before being added to the precipitate with the effect that the following separation of thrombin from fibrin is promoted.
According to the invention, the mixture added to the precipitate can advantageously be set to increase the pH-value to 6.5, whereby the resulting active thrombin is found to obtain the best keeping qualities as the thrombin has a tendency to become inactive on standing, which is usually the case in connection with enzymes. In addition, the dissolved precipitate can he transferred to a flexible material before the coagulation starts, said flexible material presenting a relatively large surface upon which the fibrin resulting from the coagulation can be deposited, whereafter the thrombin may be pressed out of the fibrin by the flexible material being subjected to a compaction. Exactly the obtained complete dissolving of the precipitate prior to formation of fibrin turned out to allow a quick transfer of the solution to a flexible material prior to said formation of fibrin. The flexible material ensures 3o that the fibrin is deposited across a particularly large surface, the compaction of which facilitates the separation of thrombin from fibrin.
It is particularly preferred when the flexible material is a sponge with open pores.

WO 94/00566 PCT/G B93/Ot323 The flexible material can be placed in a syringe, into which the dissolved precipitate can be absorbed and from which the thrombin can be squeezed out by an activation of the piston of the syringe. In this manner, a particularly easy separation of the thrombin from the flexible material is ensured:
Moreover, the centrifuging may according tv the invention suitably be performed at about 1,500 g for about 5 min; which also accelerates the preparing to of thrombin.
Thus, the subject invention comprises a process f or preparing thrombin from human blood plasma, whereby the blood plasma is diluted to about 20 to 17%.with water or another ion-intensity-reducing is fluid and an acid to reduce pH to about 5.0 to 5.3, whereafter the iaixture is centrifuged, and whereby the precipitate resulting from the centrifuging is admixed a physiological solution and ca.lciura chloride, said physiological solution increasing pH to about 6 to 8, 20 characterized by the diluting step being performed directly caith a diluted acid solution, by the centrifuging step being performed in a container with a relatively large plane precipitation surface, by the physiological solution, with the agent for increasing 25 pH, and the calcium chloride being added at the same time to the precipitate as a mixture, whereby said precipitate is dissolved and then'coagulates while forming ffibrin, and by the thrombin then being removed from the ffibrin.
3d w0 94i00566 PCT/GB93/01323 4.2. ACCELERATION OF THROMBIN FORMATION
BY CONTACTING BLOOD OR PLASMA WITH
A SU1~FACE THAT ACTIVATES BLOOD
COAGULATION FACTORS XI AND XII
Another aspect of the subject invention is the preparation of a thrombin blood fraction wherein whole blood or plasma is contacted with a surface that activates blood coagulation factors XI and XII. It is believed that a negatively charged surface such as glass or kaolin, with glass being preferred, can 10 provide such activation. Nonlimiting examples of glass surfaces are glass beads, glass wool, glass filters and glass capillary tubes.
The whole blood or plasma should contact the surface fvr a period of time sufficient to activate 15 such blood coagulation factor.., e.g., far about 5 to about 10 minutes. If the whale blood or plasma has not been treated with an a:....ic:oagulan~, then the whole blood or plasma should be in contact with such a surface for not more than about 60 seconds, preferably 20 less than about 30 seconds and more preferably about seconds. Without the anticoagulant, and if the contact of the whole blood ar plasma crith the surface is too long, then fibrin ciats will fore prematurely.
It is preferred that plasma be exposed to a surface of about 4 cm2 to about 60 cm=, preferably from about 10 cm to about 30 cmZ and most preferably about 20 cmz of such surface f or each milliliter of plasma.
Also, it is preferred that whale blood be exposed to a surface of from about 2 cm= to about 3o cm', preferably 3o from about 5 cm= to about 15 ctr~2 and most preferably about 10 cm' of such surface for each milliliter of whole blood.
It is believed that the contacting of the plasma or whale blood with a surface that can activate factors XI and XII,accelerates the conversion time of prothrombin to thrombin. Thus, a thrombin blood fraction can be prepared in an extremely short period of time.
This activation of factors XI and XII can be utilized to accelerate the preparation of any thrombin blood fraction ,regardless of how the fraction is made and regardless of its purity and specific activity, However, it is essential that the thrombin blood fraction be substantially free of active antithrombin III. It is essential that the antithrombin III either be removed from or inactivated in the thrombin blood Fraction prior to converting the prothroiabin to thrombin. Otherwise, antithrombin III will prevent the conversion of the prothrombin to thrombin andjor Z5 inactivate the thrombin. It is also preferred that the thrombin blood fraction be substantially free of fibrinogen and fibrin. Far example, with respect to the activation when the thrombin blood fraction is prepared by means of the euglobulin fraction as described in Section 4.1.1., the contacting of the plasma should be carried out immediately prior to the dilution of the plasma, When a thrombin blood fraction is prepared by diluting whole blood, as described in Section 4.1.2., the contacting of the i5 whole blood should be carried out immediately prior to the dilution of the whole blood. For example, this contacting step can be carried out by withdrawing whole blood into a syringe that contains, for example, glass beads. After not more than about 60 seconds, the whole blood is discharged from the syringe and the thrombin blood fraction of the subject invention is then prepared, as described above.

WO 9a/00566 PCT/G 893101323 _ 23 _ 4.3. THE USES OF TfiE THROMBIN BLOOD
FRACTIOft OF TH~ SUBJECT INVE~1TION
The thrombin blood fraction of the subject invention can be utilized in any medical procedure, known or to be developed, in an animal, including vetinary praceduras. Any species of animal is suitable, but, of course, humans are preferzed.
The thrombin blood fraction can be employed as a component of a fibrin sealant or can be employed 1Q alone just as conventional thrombin preparations have been eiaployed. The thrombin blood fraction is utilized by contacting the desired site of the animal with the thrombin blood fraction. Far the purpose of the subject invention, the "desired site" is that location in or an an animal where one desires to form a fibrin clot. What or where the desired site is depends on the use of the thrombin blood fraction of the subject invention.
The use of the thrombin blood fraction as a 2p component of a fibrin sealant, can be utilized for connecting tissues or organs, stopping bleeding, healing wounds, sealing a surgical wound, use in vascular surgery include providing hemostasis for stitch hole bleeding of distal coronary. artery anastomoses; left ventricular suture lines; aortotomy and cannulation sites; diffuse epimyocardial bleeding seen in reoperations; and oozing,from venous bleeding sites, e.g. at atrial, caval, or right ventricular levels. The subject invention is also useful for sealing of dacran artery grafts prior to grafting, sealing tissues outside the body, producing fibrin rafts for cell growth, stopping bleeding from damaged spleens (thereby savinq the organ), livers, and other parenchymatous organs; sealing tracheal and bronchial ss anastamoses and air leaks or lacera-ions of the lung, sealing bronchial stumps, bronchial fistulas and WO 9x/00566 PCTlGB93101323 esophageal fistulas; for sutureless seamless healing ("Zipper~' technique), and embalization in vascular radiology of intracerebral AVM's, liver AVM's, angiadysplasia of colon, esophageal varices, "pumping"
GI bleeders~secondary to peptic ulcers, etc. The subject invention is further useful f or providing hemostasis in corneal transplants, nosebleeds, post tonsillectoaties, teeth extractions and other applications. See G.F. Gestring and R. Leaner, :0 Vascular Surgery, 294-304, Sept./Oct. 1983.
The thrombin blood fraction of the subject invention can be employed alone to staunch oozing hemorrhages or hemorrhages in hollow organs. The thrombin blood fraction can also be utilized in the treatment of damaged live animal tissue by utilizing the fraction to activate the release of the materials, i.e., plated-derived factors, from platelets, wherein such materials can be utilized to heal damaged tissue.
See United States Patent No. 5,155,938. The thrombin 2a blood fraction can also be utilized to assist in the cell culture growth of keratinocytes and to assist in the autologous transplantation of keratinocytes, or any other skin-derived cells, e.g., fibroblasts. See V. Ronfard et al., Burns 17:183-184 (1991); H. Hroly, Canadian Patent No. 2,018,020 and J. Hunyadi et al., J. Dermatol. Surg. Oncol. 1:75-?8.(1988).
Also, the thro~ubin blood Fraction can be placed on a solid support, e.g., bandage, suture, prosthesis., or dressing, that will be in contact with 3o the desired site. Such support is then placed ir, contact with the desired site until, Eor example, ~he fibrin clot corms.

The dosage of the thrombin blood fraction depends an its particular use, but the dosage should be an effective amount for the composition to perform its intended use. Generally, it is believed that from 5 about 0.5 ml to about 5 ml of the thrombin blood fraction is sufficient. However, depending on the use, the dosage can range from about 0.05 ml to about 40 ml.
If the thrombin blood fraction is utilized 1o as a component of a fibrin sealant, then the fibrin sealant can be applied to the desired site with, for example, a double-barrelled syringe. The double-barrelled syringe can be Y-shaped, thereby permitting the mixing of fibrinogen and the thrombin 15 blood fraction immediately prior to the contacting step. Also, rather than a Y-shaped double-barrelled syringe a double-barrelled syringe with two openings can be utilized. This permits the simultaneous contacting of the desired site.. Also, the 2o compositions of the double-barrelled syringe can be sprayed onto the desired site. See H.B. Kram et al., The American Surgeon, 57:381 (1991). Also, if the blood fraction is employed as a component of a fibrin sealant, then autologous fibrinogen caz be utilized, 25 thereby rendering the entire fibrin sealant autologous. Also, if the thrombin blood fraction is .. employed alone, then the fraction can be applied to the desired site with a single-barrelled syringe.
It should also be noted that the thrombin 30 blood fraction of the subject invention can further comprise a source of calcium ions, e.g., calcium chloride. The source of calcium ions assists in the conversion of fibrinogen to the fibrin clot. The amount of calcium ions should be the same as that 35 utilized in conventional fibrin sealants. However, since the thrombin blood fraction may contain a source of calcium ions already due to the conversion of prothrombin to thrombin, an additional source of calcium ions may not be required. But, if more calcium, is needed to form the fibrin clot than to form thrombin, then, as an option, excess calcium from what is requixed to form thrombin can be utilized so that no additional calcium need be added when the thrombin blood fraction is utilized in t:he medical procedure, e.g., as a component of a fibrin sealant.
5. EXA.MP ES
EXAMPLE I
Preparation of a Composition Containing a =5 Thrombin Blood Fraction Obtained Frvm 17 ml of Fresh Blood From a Human Aduit Donor A puncture of the vein of a human was performed by a needle and 17 ml of brood was drawn into an empty 30 ml syringe. Immediately after ZO drawing the blood, it was transferred to a 50 ml test tube containing 34 ml of a so7.ution containing 5.5~
glucose. The 50 ml test tube was placed in a centrifuge and centrifuged for 5 minutes at 1,500 x g at room temperature. After centrifugation, 40 ml of 25 the supernatant plasma/glucose: solution was removed by a syringe, and transferred to a new 50 ml test tube.
By means of 1.07 ml of~a 2.8$ citric acid solution; the pH in the plasma/glucose solution was lowered tQ 5.2 and after a period of 10 minutes at 3a room temperature, the solution was centrifuged at 18°C
at 1,500 x g for 5 minutes. After centrifugation, the supernatant Was drained off and the precipitate was dissolved in 0.424 ml of a solution containing 14 mmole/L of NaHC03 and 8 gram/L of NaCl. This 35 precipitate contains fibrinogen, prothrambin and ether WO 94/00566 PCT/GB93/Ot323 _ 27 blood proteins, but is substantially tree of antithrombin III. The pH of this dissolved prothrombin containing euglobu,lin solution was 7.35.
Activation of the prothrombin was performed by the addition of 0.027 m1 of a solution containing CaCl2, 0.f mole/L. From 12 to 17 minutes after the addition of the CaClz, the fibrinogen in the solution started to coagulate, and the fibrin thus formed~was removed by means of a polystyrene spatula. Small to samples were removed at different intervals and the thrombin concentration was measured. The results from the example are shown in Table I.
Table I

time after 10 20 30 60 120 27 n M

Ca-addition min min mA ain min hour NIH u~ml 0 180 3~8 540 600 737 ZO EXAMPLE II
Preparation of a Composition containing a Thrombin Blood Fraction Obtained From 17 ml of Fresh Glass Activated 8load From a Human Adult Donor 25 In this experiment, the donor and the day for the performance was the same as used in Example I.
A puncture of the vein of a human was performed by a needle and 20 ml of blood was dratan into a 30 ml syringe captaining 20 grams of glass beads witr: a 30 diameter of approximately 2 mm: The total surface area of the beads was approximately 230 cmZ and, therefore, the surface area wa:5 about 11.5 cm~ per m2 of whole blood.
Immediately after drawing the blood, the ss syringe was turned gently for 10 to 15 seconds before 17 ml of the blood was transferred to a 50 ml test a - 28 _ tube containing 34 ml of a solution containing 5.5%
glucose. The 50 ml test tube was placed in a centrifuge and centrifuged for 5 minutes at 1,500 x g at room temperature. After centrifugation, 40 ml of s the supernatant plasma/glucose solution was removed by a syringe, and transferred to another 50 ml test tube. "
By means of 1.07 ml of a 2.8% citric acid solution, the pH was lowered to 5.2 and after a period of 10 minutes at room temperature, the solution Was 1o centrifuged at is°C at 1,500 x g for 5 minutes.
After centrifugation the supernatant was drained off and the precipitate was dissolved in 4.424 ml of a solution containing 14 mmole/L of NaIiC~3 and 8 gram/L of NaCl. This precipitate contains 15 prothrombin, fibrinogen and other blood proteins, but is substantially free of antithrombin III. The pH of this dissolved prothrambin containing euglobulin solution was 7.35.
Activation of the prothrombin was performed 20 by the addition of a 0.027 ml of a solution containing CaClz, 0.5 mole/L. From 4 to 9 minutes after the addition of the CaClZ, the fibrinogen in the solution started to coagulate, and the fibrin thus formed was removed by means of a polystyrene spatula. Small 25 samples ware removed at different intervals and the thrombin concentration was measured. The results are shown in Table II.
Table II

time after 10 20 30 60 120 27 Ca-addition min min min min min hour NIH u/ml 130 444 560 720 695 880 as Thus, from Table II it is readily apparent that the glass activation accelerates the time t =

required for the conversion of the prothrombin to thrombin. For example, at only 10 minutes after the addition of a source of calcium ions, 130.NIH unita/ml of thrombin activity was measured. In contrast, without glass activation, as in Example I, at 10 minutes after the addition of a source of calcium ions, there was no detectableythrombin activity.
EXAMPLE III
Preparation of a Composition Containing a Thrombin Fraction Obtained From 17 ml of Fresh Blood From Human Adult Donors, Characterized by Low Specific Thrombin Actiyity In four experiments, performed as described in Example I, the thrombin concentration and the specific activity of thrombin were measured. The results are given in Tables III and IV where the pH
value is the pH in the dissolved euglobulin fractions.
Table III
A thrombin measured from z5 min to 2 hours after dissclution~of the euglobulin fraction.
Nll~i u/ml donor pH -280 15 min 30 min 60 min 2 hr ~

JH 6.96 25.8 142 483 661 779 HJS 6.35 26.7 0 !56 942 1,238 LK 6.98 19.5 30 249 430 562 ICN 6.?1 31.5 0 142 ~ 67.6 725 I

(E-280 is a measurement of the total protein concentration in mg/ml).

a WO 94/00566 PCflGB93/01323 Table IV
8 Specific activity of thrombin measured from 15 min to 2 hours after dissolution of the euglobulin traction.
~IIH u/mg protein donor 15 min 30 min 6o min 2 hr JH 5.5 19 26 30 HJS 0 2 .1 3 5 ~ 4 6 LK 1.5 13 22 29 10 ~ 0 4.5 20 23 Thus, the preparation of a thrombin blood traction as described in Example I results in a thrombin blood fraction of a concentration and 1g specific activity of the subject invention.
EXAMPLE IV
Preparation of Thrombin From Whole Blood Using the Device of w091/I7778 The device described in W091/17?78 was used for the preparation of thrombin. Bef ore the blood was introduced into the de~rice, 40 n1 ef a 5.5~
glucose solution was introduced into the first chamber (14) through the filter (43) mounted on the tubing (39).
Blood, 10 ml, was collected from human donors into a syringe and irunediately 'hereafter transferred through the tubing (=!9) into the glucose solution. The device was placed in a centrifuge and centrifuged f or 5 min at 1,500 x g. after centrifugation, the plasma/glucose solution was transferred into the second chamber ( 3 0 ) c,rit:~ the red cells remaining in the chamber (1.:). Through the sterile filter in tube (0'0) 0.6 ml of 2.8% citric acid solution was introduced into the' plasrra/glucose l >
w0 9a!00566 PCTlGB93lOt323 solution. After 5 to 10 min, the device was placed in a centrifuge and centrifuged rot 5 min at 1,500 x g.
After centrifugation the supernatant was transferred to the first chamber (14) and the precipitate, the euglobulin fraction, remained in the second chamber (30). Through the sterile filter in tube (60) 0,85 ml of a solution containing 7.5 mrR NaIiC03, 52 mM NaCl and 30 mM CaClZ was introduced into the second chamber (30). The euglobulin precipitate was dissolved within 1-2 minutes, and transferred to the syringe (51) connected to the second chamber (30). The syringe contained a polyurethane sponge; facilitating the removal of the formed fibrin. Thrombin concentrations were measured after 30 min to 22 hours. The results ~5 are recited in Table V.
Table V
~ throabin concentration NiH
u/m1 Zo Donor plasma 30 min 1 hour 2 hour 2Z hour dilution RH-A 11.9% I86 1240 231 279 RFi-H 12.3% 54 7.30 130 ~ 132 , RH-C 11.7$ ~ 1?8 , 7.86 180 192 ~

25 ~'D 12.5$ ~ 104 92 123 I ~ 120 I

EXAMPLE v Preparation of Thr o:abin and Fibrinogen arc.;.
whole Blood Using a Device System riade From Two Inter-Connected Devices of 30 W091/17778, and the Use of Thrombin and Fibrinogen in a Fibrin Glue The device system: consists of two devices as described in W091/17778. The two tubings (39) 3s from the too devices wets connected to the sate WO 94/00566 PCT/GB93l01323 - 3 2 ~-cannula (40) by means of a three-way connector. In the device used for the thrombin precipitation 5 glass beads, 3 mm in diameter, were placed in the second chamber (30). The syringe in the thrombin device was s changed from being a 3 ml syringe in the fibrinogen device to a 1 ml syringe. ' Before the blood was collected from the donor, citrate and glucose solutions were filled into the two devices. Citrate, 5 ml of a 3.8% salut~.on, 1.0 was,introduced into the ffirst chamber (14) of the fibrinogen device (hereafter named Device-F) through the filter (43) mounted on the tubing (39). Glucose, 34 ml of a 5.5% solution was introduced into the first chamber (14) of the thrombin device (hereafter named i5 Device-T) through the filter (43) mounted on the tubing (39).
Blood, 45 ml was collected through the cannula into the first chamber (14) in Device-F
containing the citrate solution, and 1.7 ml was 20 collected into the first chamber (14) in the Device-T
containing the glucose solution. After collection of the blood, the separator-system was disconnected from the donor, and the tubing (39) was sealed close~to inlet (38). Both devices Were placed in a centrifuge 25 and centrifuged for 10 min at 1,500 x g.
The separated plasma in Device-F was . transferred to the second chamber,(30) and 2.5 ml of a 96% ethanol solution was introduced into the second chamber (30) through the sterile filter in tube (60).
30 The device was now placed into a ice-water bath f or 20 minutes to reduce the temperature in the plasma/ethanol solution to approximately 0 to 4~C. At this temperature; 85% of the fibrinogen in plasma was precipitated. The device was now placed in a 35 centrifuge and centrifuged for 5 min at 2,500 x g.

a The supernatant serum was transferred to the first chamber (14), and the solid fibrinogen was dissolved by incubation for 5 minutes at 37°C. The dissolved solution was transf erred to the sterile syringe (51).
The concentration of fibrinogen was measured to be 31 mg~ml.
The separated plasma/glucose in Device-T was transferred into the second chamber (30) with the red cells remaining in the first chamber (14). Through io the sterile filter in tube (60) 1.2 ml of a 2.8%
citric acid solution was introduced into the plasma/glucose solution. After 5 to i0 min the device was placed in a centrifuge and centrifuged for 5 min at 1,500 x g. After centrifugation, the supernatant was transferred to the first chamber (14) and the precipitate, the euglohulin fraction, remained in the second chamber (30). Through the sterile filter in the tube (60), 0.85 ml of a solution containing 7.5 mM
NaHC03, 52 mM NaCI and 30 mM Ca~Cl~ was introduced into 2o the second chamber (30). The ~euglobulin precipitate was dissolved within Z-2 minutes, and the fibrin formed during the activation o:f prothrombin to thrombin was collected onto 5 glass beads placed in the second chamber (30). After 15 minutes the thrombin solution was transferred to the syringe (51) connected to the second chamber (30). Thrombin w concentration was measured to be 24a-340-372 NIA u/m1 after 15-30-60 minutes, respectively:
The two syringes containing the fibrinogen and the thrombin were used as a double barrelled syringe. The two solutions ware expelled from the syringes and formed immediately a firm fibrin clot.

_ 34 ..
EXAMPLE VI
54 ml of 0.04% HAc were added to 6 1n1 of plasma. This mixture was placed in a flat-bottomed container of the type known from the above PCT/DK91/00131. The container is of a circular cross section with an inner diameter of 4.5 am. The pli-value was 5.3. The pH-value and the relatively low concentration of ions in the provided mixture ensure the following precipitation of the coagulation factors, inter olio prothrombin, as a precipitate by a centrifuging. The centrifuging was performed at 1,500 g f or 5 min. Thus the centrifuging was relatively quickly terminated, which is due to the relatively short falling height and large precipitation surface.
After removal of excess f laid, an 0.75 ml ac;ueous solution of 0.9% NaCl, 0.03% Na:C03 and 25 mM CaClz was added to the precipitate. After dissolving of the precipitate, the solution was sucked into a 2.5 ml syringe containing a polyurethane sponge. The 2o formation of fibrin did not start until about 1 to 2 min. after the precipitate had become completely dissolved, and accordingly more: than enough time for the sucking procedure. After termination of the formation of fibrin in the syringe, the thrombin solution could be expelled by squeezing the sponge by means of the piston of the syr.i:nge, the fibrin remaining depositing on the large surface of the sponge.
The dissolved precipitate had a pH-value of 6.5. Other amounts of NazCO3 or another base or a buffer system can be used provided the pH-value is between 6.0 and 7.5, but an optimum balance between the keeping qualities of the thrombin and the capacity of the thrombin to accelerate the coagulation process is found at 6.5.

The thrombin was expelled From the syringe after 30 min, and a concentration of 256 NIFi units per ml was obtained. The thrombin concentration increased by time, but after 30 to 60 min a sufficient amount of thrombin was obtained for a conventional use in a Fibrin sealant.
The preparation of thrombin was in the present Example produced from 12 ml os autalogous blood and was terminated over a period of 45 to 60 :0 min, i.e., almost simultaneously with the termination of the preparation of fibrinogen. The produced amount of thrombin was sufficient for being used in combination with fibrinogen produced from 45 ml of autolagous blood in the manner described in t5 W091/I???8.
The fibrin formed during the thrombin preparation has always a tendency to bind the thrombin. The release of this thrombin can, however, be promoted by the addition of a plasminogen catalyst, 2o such as streptokinase, urokinase or t-PA (tissue plasminogen catalyst) optional:ty admixed With a physiological solution.

Claims (2)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. Use of thrombin for cell culture growth of keratinocytes from skin, wherein the thrombin is derived from the same individual animal or human from which said skin is derived.

2. The use of claim 1 wherein said thrombin is a thrombin blood fraction comprising:
(a) a thrombin concentration of from 1 NIH unit/ml to 2,000 NIH units/ml;
and (b) a specific activity of thrombin of from 1 NIH unit,/mg of blood protein to 200 NIH units/mg of blood protein;
wherein said thrombin blood fraction containing less than 50% activity of antithrombin III in normal plasma per unit volume.