WO1993005822A1

WO1993005822A1 - Tissue glue prepared by using cryoprecipitate

Info

Publication number: WO1993005822A1
Application number: PCT/EP1991/001850
Authority: WO
Inventors: Uri Martinowitz; Frederic Bal
Original assignee: Octapharma Ag
Priority date: 1991-09-27
Filing date: 1991-09-27
Publication date: 1993-04-01
Also published as: CZ294292A3; AU2528892A; DE69231791T2; NO316155B1; CZ280540B6; BR9203763A; NO923737D0; SK294292A3; HU211631A9; FI924306A0; HUT67051A; IL103118A0; ES2155437T3; ZA927360B; DE69231791D1; FI924306A; IL103118A; ATE200631T1; CA2079077A1; JP2668762B2

Abstract

A tissue glue is described comprising a component A which comprises a cryoprecipitate of whole blood and a component B comprising a proteolytic enzyme being capable of cleaving specifically fibrinogen present in component A, and causing the formation of a fibrine polymer, in a preferred embodiment component A of the tissue glue comprises 3,000 to 5,000 KIU/ml of aprotinin. In another preferred embodiment component B of the tissue glue is a protease derived from the venom of the South American pit viper. This protease is known under the name batroxobin.

Description

"Tissue glue prepared by using cryoprecipitate"

This invention relates to a tissue glue comprising two components A and B, a process for preparing the tissue glue and the use of cryoprecipitate of whole blood for preparing a tissue glue, the use of a high amount of aprotinin and the use of a snake venom proteolytic enzyme for preparing a tissue glue.

Improvement of local hemostaεiε at the site of a surgical wound by application of plasma proteins is a well-known concept. Thus, fibrin patches for hemostasis in cerebral surgery have been used. Blood plasma and thrombin were used to produce a fibrin film over the surgical wound. In the last 20 ..years there are a lot of^' publications describing applications of "fibrin glue" or "fibrin ad¬ hesive" or "fibrin sealant" for most surgical disciplines. In the last 10- years commercial preparations of "glue" are used widly in Europe. The "glue" is composed of two components, whereas a mixture of these components produce a clot. The first component is a fibrinogen concentrate. This concentrate also contains ^■ fibronectin and factor XIII which are important for clot stabilization and strength.. The second component is thrombin, an active enzyme that converts fibrinogen, the last component of the normal coagulation system into a fibrin clot. This process bypasses most of the steps of normal coagulation and mimicks its last phase. Some manufacturers add plasminogen which is an enzyme that will .- induce clot lysis after some time whereas others add aprotinin which is an inhibitor of proteases for preventing .clot lysis. Although, these products give satisfactory results in patients although with mild bleeding disorders, but patients suffering severe bleeding disorders such as hemophilia A or B, still have a very high risk of post¬ operative bleeding. Sometimes a delayed bleeding com¬ plications after . an average of days from the surgery occur. Also patients who are treated with anticoagulation factors cannot be treated with the tissue glue of the prior art. Another severe disadvantage of the commerical concentrates are the high producing costs.

One object of the invention is to provide a tissue glue which can be prepared in an easier and cheaper way. Another object of the present invention is to provide a tissue glue which is also suitable for patients with severe blood coagulation disorders like hemophilia A^' or B. A further object of the present invention is to pro¬ vide a tissue glue which can also be used for patients which have already developed antibodies against bovine thrombin which is the active factor of the component B. Still another object of the present invention is to provide a tissue glue for patients who are treated with anticoagulation factors like heparin. Because of the risk of transferring viral diseases with the components of the tissue glue it must be ensured that fractions of the tissue glue are virus inactivated.

The tissue glue according to the invention, comprises a component A which comprises cryoprecipitate of whole blood and a component B which comprises a proteolytic enzyme capable of cleaving specifically fibrinogen and causing the formation of fibrin by clotting of the activated fibrinogen.

Commercially available cryoprecipitate can be used for preparation of the tissue glue of the invention. However, it can be advantageous to concentrate the cyroprecipitate between a factor 2 and 5, preferably factor 3.

The addition of a protease inhibitor in sufficient con¬ centration to the cryoprecipitate makes the tissue glue of the invention suitable for use in patients with severe bleeding disorders. Preferably the protease inhibitor aprotinin is used in amounts of 3,000 bis 5,000 KIU. Aprotinin is commerically available under the trademark Trasylol or Antagosan . The cryoprecipitate can be obtained from the patient himself by donating an auto- logous blood unit prior to the operation. This approach prevents the risk of transmission of viral infections by blood derivatives. However, in order to have a proper commercial product, the cryoprecipitate has to become virus-inactivated. A procedure for virus-inactivation is described in PCT/EP 91/00503. The basic principle is treatment• of the cryoprecipitate with special detergents and removing the detergent lateron from the cryopre¬ cipitate.

The second component, component B, of the tissue glue of the present invention is prepared by a solution of a pro¬ teolytic enzyme being capable of cleaving specifically fibrinogen. Usually thrombin has been used which was isolated from plasma of human beings or mamals such as bovine. This thrombin can be delivered in a lyophilized form. The reconstitution of thrombin occurs with a 40 mmol solution of calcium chloride. The preferred concen¬ tration of thrombin is 50 to 200 u/ml.

For preparing a fast tissue glue the thrombin solution of roughly 100 u/ml of calcium chloride will be prepared. For preparing a slow glue ^■ for example by filing of cavities, i. e. tooth extraction or sealing the cavity of transphenoided hypophisectomy the thrombin will be further dissolved to a concentration of 25 u/ml with the appropiate calcium chloride solution.

Another preferred embodiment of the present tissue glue comprises as component B a proteolytic enzyme which is isolated from snake venom. This embodiment is advantageous because also patients having developed antibodies against thrombin can be treated. Moreover, patients which are pretreated with heparin can be treated with the tissue glue according to the invention, because heparin does not influence the reaction of the snake venom enzyme. In a very preferred embodiment of the present invention there is used the snake venom enzyme batroxobin which can be isolated from the South American pit viper Bothrpos mou eni. Preferably component B contains 0.5 to 10 u/ml of the respective proteolytic enzyme of snake venom.

Chemically it is a single chain glycopeptide with a mole- cular weight of approximately 36,000. Defibrase causes cleavage of 16 Arg/17 Gly bound in fibrinogen which causes the release of fibrinopeptide A and the formation, of monomeric fibrin I. .

When aprotinin is used in the amounts of the invention, also the ^• tissue glues comprising purified fibrinogen, fibronectin and factor XIII can be used as component A. The risk of after-bleeding is then dramatically reduced.

When proteolytic proteases from snake venom .are used for the preparation of component B, also "conventional" com¬ ponents A having fibrinogen, fibronectin and factor XIII can be used. The use of high amounts of aprotinin according to the invention is preferred. A very preferred embodiment is the combination of the component A of the invention derived from cryoprecipitate with or without high amounts of aprotinin- and the component B of the invention having the proteolytic enzyme isolated from snake venom.

The process for preparing the fibrin glue of the invention comprises the ^■ steps of manufacturing component A com¬ prising the steps of preparing a cryosolution from cryo¬ precipitate,

a virus inactivation, the removal of virucidal agent, the addition of the protease inhibitor and preparing a appropiate protease-solution..

Preferably a cryopaste is prethawed over night at 4 to 10 °C. The cryopaste is dissolved in a buffer containing sodiumchlorid trisodiumcitrate and glycin and having a pH of 7.0 to 7.2 and than heated to 30 to 35°C. The cryopaste should dissolve readily otherwise it is not suitable for the preparation. The dissolution can be speeded up by cutting.^' the cryopaste in small pieces after thawing. After cooling the solution to almost room temperature and adjusting the pH to a value of 7..0 to 7.2 aluminium- hydroxid is added under stirring. The precipitate- is centrifuged and discarded. Optionally a filtration step is carried out. Than calcium chloride is added up to the desired final concentration of calcium chloride.

For the virus inactivation the solution is heated up to 30^eC. Than the detergents are added. Other stirring for some time the solution is transferred into a virus free container -and left at slightly elevated temperatures for several hours without stirring.

The virucidal agents are removed by adding an amount of ricine oil and gently stirring for several ^' inutes. When the oil-/water-phases have been seperated the solution is cooled to room temperature. The aqueous layer is withdrawn in a virussafe container and the oillayer is discarded. The aqueous layer is clarified by filtration. The pH must be checked to be 7.0 to 7.2. Then the protein solution is pumped through a reversed phase column at ambient tem¬ perature. After having measured the protein content (in the range of 10 to 60 mm/ml the eluate is concentrated by diafiltration to a protein content of 60 to 100 g/ml and dialysed against a buffer which is identical to the buffer mentioned above but having additionally a relatively high concentration of calcium chloride. Then the protease in¬ hibitor is added. A sterile filtration is carried out and the sample is filled and deep frozen in suitable con¬ tainers.

Component B is preferably a freeze dried protease. Parti¬ cularly preferred is lyophilized thrombin or lyophilized fraction of the South American pip viper Bothrpos moujeni. The proteolyic enzyme is known under the tradename Repti- lase and is the enzyme batroxobin.

The proteolytic enzymes are dissolved in a calcium chloride buffer.

The application of the two components A and B is performed using a double syringe technique for example through a plastic connector. Upon mixing of the two components a clot will be formed. The application can occur via a canula or may be sprayed to a three lumen catheter. Each one of the two components is injected into a separate lumen and an air pressure source in the range of some atmospheres is connected to the third lumen in order to spray the mixture.

The tissue glue of the invention is advantageous because it can be used with patients having severe blood coagu- lation disorders and being still cheaper than the known tissue glues. Patients with severe hemophilia can sub-, sequently, for example undergo tooth extractions without preventive infusions of factor VIII concentrates with a success rate of over 80%. This means only about one fifth of the patients need infusions due to post extraction bleeding. Moreover, such patients who are pretreated with heparin can be treated with the tissue glue of the in¬ vention. Another advantage is that people who raised antibodies against thrombin the second component of the tissue glue can be treated with a tissue glue according to the invention wherein thrombin is substituted by a protease from snake venom especially Defibrase which is the εerine protease batroxobin isolated from the venum of the South American pit viper Bothrpos moujeni.

The invention is further disclosed in the following examples which are non limiting.

Human fibrinogen (grade L) was from Kabi (Stockholm), bovine thrombin from Merz-Dade. Chromogenic substrate N-a-benzoyl-DL-arginine-p-nitroanilide (BAPNA) and analy¬ tic grade reagents were from Sigma (St. Louis, MO). Reagents and salts were diluted with 0.015 M Tris, 0.15 M NaCl, with pH 7.4. Fibrinogen was dialyzed in Tris buffer with concentration determined from Abs__Dπ using a con- version factor of E "280 = 15.

Bovine thrombin was from commercial sources (Merz-Dade or

Parke Davis) with activity rating by the manufacturer.

Reptilase , a snake venom which only releases FPA, was from Pentapharm (Basel) . The proteolytic activity of

ReptilaseR was normalized to that of thrombin by com¬ paring their rates of prpteolysis of a non-specific chromogenic- substrate BAPNA (0.25 mM) at 37'C, in Tris/saline, pH 8.0, monitored at 405 nm for 15 minutes. On the basis of their esterolytic activity, the unit- activity of the reptilase was normalized to that of thrombin.

Fibrin glue was essentially generated by a dual syringe method with pure or cryoprecipitate fibrinogen substrate in one syringe, and reptilase (20 U/ml) or thrombin with CaCl„ (20 mM) in the other.

Clotting time (CT) was determined with a Research Model 300-R ACL Coagulation Analyzer (IL, Milan) . Viscoelasti- city (TEG) was determined on a 3-channel Heiliger Thrombo- elastograph at 37°C. Breaking strength (BS) of glues (in gra. Ξ) was determined by mixing the glue components between two pieces of coarse weaved, synthetic fiber (0.5 x 1 cm) , allowing the formation of gel totally interweaved between the two pieces of coarse mesh and after 2 hours at 2 °C the ensemble of mesh-glue-mesh pulled apart using an Accuforce Cadet Tenεionometer (AMATEK, Mansfield & Greene, USA) .

Sterile cryoprecipitate (cryo) was prepared from frozen (-30^βC) human plasma which was thawed at ^βC and the supernatant plasma removed. Five such units were pooled to determine protein and fibrinogen concentrations was determined by.the Buiret method before and after clotting the cryoprecipitate (diluted 1 : 5) with 2 U/mL thrombin. Factor XIII was determined by measuring [ 3H]-putrescine incorporation into dimethylated casein after activation of the samples with 4 U/mL bovine thrombin, 10 min, 22^βC.

A notable f ature of the CT-fibrinogen curve is. that it is biphasic for a fixed level of thrombin or reptilase (i.e. 1 U/ml, figure 1A) and reaches a minimum in the 1 - 8 mM fibrinogen range. This differs somewhat from the maximal turbidity (after 10 min) which peaks in the range 20 to 40 mM fibrinogen. A converse experiment shows the dependency of CT on either thrombin or reptilase levels. This curve shows a near linear inverse dependency of gelling rate at low enzyme levels (lesε than 2 U/mL) , which plateaus above at higher levels..

The development of viscoelasticity of pure fibrin is some¬ what slower than its turbidity. Ca(II) is a major cofactor in gel reinforcement through factor Xllla-induced covalent interlocking of protein chains. Such gel crosslinking is a major source of mechanical strength of the gel, which plateaus after 20 min.

A note about the ability of reptilase to induce factor Xllla activity seems appropriate.

Protein Levels of pooled cryoprecipitate:

Pooled cryo prepared from 5 units, gave the following mean values:

Protein: 75 mg/mL Fibrinogen: 36 mg/mL Factor XIII: 4.10 U/mL

Coagulation rates:

The clotting time (CT) of cryo is linearly dependent on thrombin or reptilase levels. However, above 3 U/ml, increasing enzyme levels exert little effect on CT. For a fixed level of enzyme, serial dilution of cryo, gives a biphasic CT-curve equivalent to the fibrinogen-dependency noted- in.the pure- fibrin system. Viscoelasticity (TEG) and Breaking Strength (BS) of Cryo Glues.

The development of viscoelasticity of cryo glues was investigated with either thrombin or reptilase. This parameter takes much longer to develop than turbidity. However, cryo glues prepared with excesε of CaCl, and either thrombin or reptilase achieve equivalent TEG values in roughly the same, time frame. It seems that after the initial onset of gelation, factor Xllla-induced cross-linking bolsters the gel fiber structure, so that the TEG values for both glues converge within 1 hour. Similarly with the final BS of both cryo glues formed with an excess of CaCl,. Both cryo glues break at 50 to 60g. These experiments indicate that the gel fibers within the glue become reinforced by factor Xllla-in- duced, covalent cross-linking.

Preparation of a cryo-solution. Commerically cryopaste is prethawed over night at 4 to 10°C. One kilo of the cryo is dissolved in two liters of buffer A (120 mM/1 NaCl, 10. mM/1 trisodiumcitrate, 120 mM/1 glycin and pH 7.0 to 7.2) and preheated to 30 to 35*C. The cryopaste should dissolve readily otherwise it is not suitable for the preparation. In order to speed up the dissolution, cut the cryopaste in small pieces after thawing. Then the solution is cooled to 20"C to 22^βC and the pH is checked. Optionally it must be adjusted to pH 7.0 to 7.2 by adding diluted sodiumhydroxid or acidic acid. 100 ml aluminiu - hydroxid is added and stirred for another 30 minutes. The precipitated is centrifuged and discarded. ^'The supernatant is filtrated using a 1 μm filter. 0.1 M/l CaCl is added to render a final concentration of Ca 2+ of 1 mM/1. Again the pH must be checked. Virus inactivation.

The solution is heated up to 30°C. 1% w/v TNBP and 1% w/v Triton X 100 iε added. The mixture iε gently stirred for 1/2 hour. The- solution is than transferred into a- virus- free container and left at 30^βC for 3 1/2 hours without stirring.

Removal of Virucidal Agents.

150 ml Ricine oil is added to the mixture prepared as described above and stirred gently for 30 minutes._. While waiting for the oil/water separation (30 to 45 minutes) the solution is cooled to 20°C. The aqueous layer is with¬ drawn into a virussafe container whereaε the oillayer is discarded. The aqueous layer iε clarified by filtration on .1 μm/0.45 μm filter cascade. The protein solution is than pumped through a reversed phase column (C-18-Column) at a rate of 3 liter/h at ambient temperature. The throughput is monitored by UV and collected until the absorbance has returned to 50%. The fraction contains roughly 40 mg/ml as measured in a protein, assay.

The eluate is concentrated by diafiltration to a protein content of 70 to 80 mg/ml and ^'dialyse againεt εufficient amount of a buffer B (same ingredients as buffer A but additionally 1 mM/1 calcium chloride) . Then 4 io. KIU aprotinin per liter solution is added. Afterwards a sterile filtration carried out using a 0.45 μm + 0.2 μm cascade. The solution is than filled and deep .frozen in plastic bags, optionally lyophilized.

Preparation of a thrombin solution

Lyophilized thrombin is diεsolved in a solution of 40 mM/L calcium chloride. The.amount of thrombin is 100 U/ml in the glue. For a fast working glue, for example for spraying of the glue to the area of the wound, a thrombin solution of 100 U/ml in calcium chloride will be suffi¬ cient. For a slow glue, for example filling of cavities during a tooth extraction or sealing the cavity of trans¬ phenoided hypophisectomy the thrombin will be further dissolved to a final concentration of 25 U/ml by adding great amounts of CaCl₂.

The preparation of reptilase is similar to that of thrombin. However, the amount of reptilase is roughly 2 U/ml.

Clinical case report

The patient from the age of 21, MY (a 21 year old male) suffered from severe bleeding diathesis due to acquired inhibitor against thrombin. No background disease (i.e. tumor, or autoimmune diseaεe) could explain this problem. Laboratory test, confirmed by two outside laboratories indicated that MY had high levels of anti-thrombin IgG anitbody. In the last year he suffered repeated attacks of renal colic due to a large stone in his left kidney pelvis: Elective lithotripsy by ultrasound was planned. Based on the technique that IgG bindε to protein-A affinity columns, the patient was placed on^' immuno- suppressive therapy combined with extra-corporal immuno-adsorption. After 8 treatments, in which 60 L of the patient's plasma was procesεed through passage on the protein-A column, the inhibitor titer decreased by 98%. this was determined by measuring the thrombin time (TT) of normal pooled plasma, with pre- and post-affinity purified MJ plasma. Nevertheless, the TT as well as PT and APTT values were prolonged. At this time, the kidney stone moved to the urethra, causing complete blockage of the kidney accompanied by hydronephrosis. The patient received 10 more immuno-adsorption treatments (roughly 80 liter plasma) followed by intensive plasmapheresiε (roughly 50 liter) and high doese immunoglobulin infusion (2 g/kg) . At this point, the thrombin-inhibitor level dereased to 0.5 %. PTT was decreased to 47" (vs. 85 - 90" pretreat ent) and the TT was 35" (vs. 90" pre-treatment and 27" normal control) . It was decided to remove the stone by surgery, using biological adhesive (cryo glue) made up from cryoprecipitate and high levels (200 U/mL) of thrombin. With this mix, the cryo gelled immediately upon being sprayed. However, in the patient gelling did not occur and local hemostasiε was achieved by suturing. At the end of surgery the wound looked "dry". Neverthe- leεε, six hours later, the patient was bleeding from surgical drains. Immuno-absorption of 10 liter plasma was carried out, but with no effect on bleeding which actually increased.

The patient was re-operated to find the source of bleeding. Though no surgical bleeding was found. Diffuse bleeding was observed from the entire wound εurface areaε. This time, a mix of cryo and reptilaεe (2 U/mL; Defibraεe) waε sprayed onto the wound. The spray clotted immediately, the wound surface appeared turbid and bleeding stopped. The patient, continued to receive daily immuno-adsorption therapy for another 5 days, with no bleeding. This demonstrates the advantage of using the snake proteasis as component B of the tiεεue glue of the invention.

Claims

C l i m s

^' 1. A tissue glue comprising a component A which com¬ prises a cryoprecipitate of whole blood and a com¬ ponent B comprising a proteolytic enzyme being capable of cleaving specifically fibrinogen present in component A and cauεing the formation of a fibrine polymer..

2. The tissue glue of claim 1 wherein the cryopre¬ cipitate of component A is concentrated.

3. The tissue glue of claims 1 or 2 wherein the com¬ ponent A contains a protease inhibitor.

4. The tissue glue of claim 3 wherein the protease inhibitor is aprotinin in amounts of 3,000 bis 5,000 KIU units.

5. The tissue glue of anyone of the claims 1 to 4 wherein the proteolytic enzyme iε thrombin derived from mamals or human beings.

6. The tissue glue of anyone of the claims 1 to 5 wherein the proteolytic enzyme is an enzyme derived from snake venom.

7. The tissue glue of anyone of the claims l to 6 wherein the snake venom enzyme is batroxobin iso-* lated from the venom of the South American pit viper Bothrpos Moujeni.

8. The tisεue glue of anyone of the claims 1 to 7 wherein the cryoprecipitate is virus inactivated.

9. Process for manufacturing a fibrin glue according to claims 1 to 8 having the steps of

manufacturing component A comprising the εteps of preparing a cryo solution from cryopre¬ cipitate, a virus inactivation, the removal of virucidal agents, addition of the protease inhibitor and preparing an appropiate solution of a suitable protease as component B.

10. A tissue glue comprising as component A fibrinogen, fibronectin and factor XIII and a aprotinin in amounts of from 3,000 to 5,000 KlU/ml.

11. The tissue glue of claim 10 wherein component B is a proteolytic enzyme according to claims 6 to 8 or thrombin.

12. A tissue glue comprising as component A fibrinogen, fibronectin and factor XIII and component B is a proteolytic enzyme according to claimε 6 to 8.

13. Use of cyroprecipitate of whole blood for preparing a tissue glue.

14. Use of a high amount of aprotinin of from 3,000 to 5,000 KlU/ml in combination with cyroprecipitate or a combination of fibrinogen, fibronection and factor XIII for preparing a tissue glue.

15. Use of a snake venom protease for the preparation of a tissue glue.

16. Use of batroxobin isolated from Bothrpos Moujeni for the preparation of a tissue glue.