CA2121028A1 - Hemostatic composition for local hemostasis - Google Patents
Hemostatic composition for local hemostasisInfo
- Publication number
- CA2121028A1 CA2121028A1 CA002121028A CA2121028A CA2121028A1 CA 2121028 A1 CA2121028 A1 CA 2121028A1 CA 002121028 A CA002121028 A CA 002121028A CA 2121028 A CA2121028 A CA 2121028A CA 2121028 A1 CA2121028 A1 CA 2121028A1
- Authority
- CA
- Canada
- Prior art keywords
- biologically compatible
- fviia
- compatible carrier
- hemostatic composition
- composition according
- 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.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/32—Proteins, polypeptides; Degradation products or derivatives thereof, e.g. albumin, collagen, fibrin, gelatin
-
- 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)
- A61K38/4846—Factor VII (3.4.21.21); Factor IX (3.4.21.22); Factor Xa (3.4.21.6); Factor XI (3.4.21.27); Factor XII (3.4.21.38)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L24/00—Surgical adhesives or cements; Adhesives for colostomy devices
- A61L24/04—Surgical adhesives or cements; Adhesives for colostomy devices containing macromolecular materials
- A61L24/10—Polypeptides; Proteins
- A61L24/108—Specific proteins or polypeptides not covered by groups A61L24/102 - A61L24/106
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
- A61L26/0009—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials
- A61L26/0028—Polypeptides; Proteins; Degradation products thereof
- A61L26/0047—Specific proteins or polypeptides not covered by groups A61L26/0033 - A61L26/0042
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/04—Materials for stopping bleeding
Abstract
Method for arresting local bleedings by topical use of FVIIa and a hemostatic composition containing FVIIa together with a biologically compatible carrier which permits said FVIIa to remain in contact with said bleeding wound.
Description
wo s3/06sss 2 1 2 10 2 8 Pcr/DKs2/002s6 HEMt:)STATIC COMPOSlTiON FOR LOCAL HEMOSTASIS
FIELD OF INVENTION
The present invention relates to a method for arresting local bleedings by topical use of FVlla and a hemostatic composition containing FVlla.
5 B~CKGROUND OF THE INVENTION
When blood vessels are injured by physical traumas including surgical interventions bleeding will occur. If bleedings are left alone they will ev~ntually be arrested by a normally occurring physiolo~ical process characterized by a chain of events involving the combined activity of vascular, platelet, and plasma factors, leading to 10 the formation of a blood clot. This process is referred to as physiological hemostasis (blood coagulation3, which is describ~d in details below. In the case of a minor superficial bleeding this physiological hemostasis is adequate for the arrest.
There are two separate systsms which can promote blood coagulation. These systems are referred to as the intrinsic and the extrinsic coagulation pathways.
15 In the intrinsic pathway, only blood clotting factors present in piasma are u~ilized.
An intermediate event in the intrinsic pathway is the activation of Factor IX to Factor IXa, a reaction catalyzed by Fa~tor Xla and calcium ions. Factor IXa then participates in the activation of Factor X to Factor Xa in the presence of Factor Vllla, phospholipid and calcium ions~
20 The extrinsic pathway involves plasma factors as well as components present in tissue extracts. Factor Vll, a proenzyme present in plasma, participates also in the WO 93/06855 PCl /DK92/00296 212~ 02Ç~ 2 extrinsic pathway of blood coagulation by converting (upon its activation to Vlla) Factor X to Xa in the presence of tissue factor and calcium ions.
Factor Xa in turn then converts prothrombin to thrombin in ths pres~nce of Factor Va, calcium ions and phospholipid. Finally, thrombin converts the plasma fibrinogen into fibrin, which in the presence of Factor Xllla and calcium ions is cross-linked and thus forming the blood clot.
Blood factors such as Factor Vlll:C (see US Patents 4,831,119; 4,868,112; 4,886,876;
4,657l894; Re. 32,011 and 4,649,132) and Factor Vlla (see US Patents 4,784,950;
4,382,083; 4,479,938 and 4,357,321) purified from natural sources or made via 10 recombinant techniques have been used for treating patients, such as hemophiliacs, having blood-clotting deficiencies or inhibi`tors to blood-clotting factors. These blood-clotting factors have been delivered to the patient needing treatme~t as an aqueous solution by infusion or bolus injection depending on the blood factor to be dslivered and the condition of the patient. Cessation of the bleeding is expected to 15 occur typically between 15 minutes to 3 hours or more after the delivery of the blood-clotting factor.
However, faster arresting of the bleeding is necessary in th~ case of severe bleedings emerging from more extensive injuries involving larger arteries or when seeping bleedings occur from larger mucosal surfaces or on cavities without 20 drainage. If the bleeding continues in even a shorter period it may result inextensive losses of blood which may have an adverse effect on the normal function of the body. Also, in the case of bleeding occurring in osseous non-expandable cavities, the accumulation of extravasated blood may cause local damages of softtissues due to increased pressure. The usual treatment of such conditions involve 25 the adaption of surgical and/or medical hemostatic measures.
Surgical arrest of bleeding comprises ligation or suture of disrupted blood vessels, plugging by using tampons in cavities, coagulating tissue surfaces inclu~ing their wo s3/068ss 2 1 2 1 0 2 8 Pcr/DKg2/002g6 exposed disrupted blood vessels by heated instruments or by the application of cauterizing agents or heated air.
Surgical hemostasis may also be aided by the appliGation at the injured site of appropriately sized blocks, plates, or films of biologically absorbable hemostatic 5 sponges. ~:
Pharmaceutical preparations containing bovine thrombin or other blood clotting factors such as Factor Vlll, Factor Xlll or calcium i~ns are currently used in some places as hemostatic adjuncts in surgery, said adjuncts being administered e.g. by spraying a suitable solution thereof onto the site of bleeding such as in US
10 4,298,598. Also textile materials such as gauze or cotton wool fabrics or biologically absorbable sponges, which prior to the application have been soaked in a solution of one or more of said hemostatic compounds, are used such as in US 4,363,319.
US patent 2,558,395 discloses a ready-to-use undenatured gelatine hemostatic sponge containing thrombin. US 4,265,233 discloses wound healing material 15 comprising a structure made from compounds such as gelatine, collagen, polyglycolic and polylactic acid to which FXIII has been fixed by covalent bir~ding.
EP 277096 A discloses a wound dressing comprising a stable thrombin composition and a substrate such as hemostaticl porous sponges of collagen or denatured gelatine and WO 90/13320 discloses a porous sponge containing a hemostatically 20 effective amount of thrombin, and hemostatically effective amounts of one or more blood coagulation factors other than thrombin. US patent 4,563,387 and US patent4,642,111 relate to, respectively, a methvd and device for tr~ating cancer and which disclose an anti-cancer drug and a blood coagulation factor being fixed to a structure, such as a polymer, capable of being delivered by injection to the site of 25 bleeding directly causecl by the cancer treatment.
Japanese published patent application No. 59-116213 discloses an aerosol containing FXIII and thrombin and Japanese published patent application No.
WO 93/06855 PCr/DK92/00296 212~02~
02-167234 discloses adhesive for living tissues containing fibrinogen, prothrombin, FVII, FIX, FX, FXIII, antithrombin, protease inhibitor and calcium ions.
In the recent years increasing concern has however arisen regarding the safe useof bovine derived products e.g. thrombin or prothrombin in pharrnaceutical products 5 for human use. Several reports describe th~ possible risk of transmitting an infectious agent causing Bovine Spongiform Encephalopathy (BSE) in cattle into humans, where the virus-like agent may be the reason for one or more well known diseases characterized by degenerative encephalopathy e.g. Creutzfeldt-Jacob disease and Kuru. Furthermore, clinical investigators have obs~lved thc~ the topical 10 IJse of bovine thrombin in humans may cause the development of an~ibodies cross-reacting to human thrombin and causing bleeding problems.
It is, therefore) an object of the present invention to provide a safe and,effective means to topically arrest bleedings at the site of an injury.
SUMMARY OF THE INVENTION
15 The present invention is based on the surprising recognition that FVlla is capable of momentarily arrest of bleedings when appiied topicaily to the site of injury without the presence of thrombin or other coaguiation factors and when FVlla is in association, together with or incorporated into a biologically compatible carrier (which, as used herein, is intended to include a composition or material) capable of 20 preventing FVlla from being washed away from the site of injury.
According to the present invention, FVlla is incorporated into a biologically compatible carrier which does not contain thrombin and is unaccornpanied or uncontaminated by any other blood clotting factors.
wo 93/068~5 2 1 2 1 0 ~ ~ PCI'/DK92/00296 The present invention is thus related to a hemostatic composition comprising a hemostatically effective amount of FVlla incorporated into biologically compatible carrier said composition containing no thrombin.
More specifically, this invention provides a hemostatic composition for inducing5 hemostasis at a bleeding wound comprising a hemostatically effective amount ofFVlla which is uncontaminated or unaccompanied by other blood cl~tting factors and which has sufficient activity alone to produce a hemostatic effect, together with a biologically compatible carrier which permits said factor Vlla to remain affixed to, in association with or contacting said wound site.
Prior to setting forth the invention, it may be helpful to an understanding thereof to set forth definition of certain terms to be used hereinafter.
Hemostat or Hemostatic Agent: An agent that arr~sts hemorrhage.
Hemos~atic Composition: A composition that contains a Hemostat or Hemostatic 15 Agent.
Blood clot: The final uutcome of the blood coagulation cascade, formed by conversion of soluble plasma fibrinogen into insoluble fibrin, which physically stops the bleeding. The blood clot covers the surface, keeps the wound edges together and forms the matrix for the following cell proliferation and wound healing 20 Blood clotting factors: Plasma proteins which participate in the blood coagulation cascade.
WO 93/06855 PCI`/DK~2/00296 212102~ 6 Activated blood ctotting factors: Blood clotting factors converted to active enzymes by the action of an activator, often itseif being an activated blood clotting factor.
They are generally designated by the addition of a lower case postscript "a" (e.g.
Factor Vlla).
5 Proenzymes: An enzyme precursor that in general has reduced or no activity as compared to the mature enzyme.
Biologically absorbable: Material which can be degraded in the body to smaller molecules having a size which allows transport into the blood stream and gradualremoval from the site of application.
10 S~onge: A porous structure being reticulate and having an inner surface considerably larger than the outer surface. The porous structure will contain hollow spaces within the reticulate structure and can absorb many times its own weight in liquids. -Covalent binding: A bond between two atoms in which both of the atoms concerned 1~ contribute the elec~ron or electrons.
Dressing: Material apptied to a wound and fastened in place to provide protection and to promote healing.
Topical: Local.
Biologically Compatible: The ability to be accepted in the body and remain functional 20 for a period without rejection.
Gel: A colloidal system comprising a solid and a liquid phase which exists as a solid or semisolid mass.
wo 93~068~ 2 1 2 ~ 0 2 ~ pcr/DK92/oo296 Paste: An ointment-like preparation of one or more substances in a hydrogel or fatty base. It is less greasy and better absorbed than an aintment.
Granule: A minute particle or mass.
Film: Any thin coYering, coating, or layer.
5 Plaster: A substance intended for external application, made of such material and of such consistency as to adhere to the skin.
Bandage: A strip of gauze, muslin, flannel, or other material used to hold dr~ssings in place, or to check hemorrhage.
DETAILED DESCRIPTION
10 FVlla is to be used in a hemostatically effective amount. By hemostatically sffective arnount is mean~ an amount which will preferably cause arrest of the bleeding if kept in association with or contacting the site of the injury for a sufficient amount of ~ime, preferably from about 60 seconds in patients not having an impaired hemostatic mechanism to less than about 10 minutes in patients having an irnpaired hemostatic 15 mechanism. FVlla should be used in an amount ranging from about û.2 to about 2.0 mg, preferably from about 0.5 to about 1.5 mg and more preferably from about0~9 to about 1.1 mg per application.
FVlla may be derived from plasrna as described in EP 00821 82B or by recombinantDNA-technology as described in EP 0200421A. Human purified factor Vlla is 20 preferably made by the methods described by Broze and Majerus, J. Bio. Chem.
255, 4: 1242-1247, 1980, and Hedner and Kisiel, J. Clin. Invest. 71: 1836-1841, 1983.
These methods yield factor Vll without detectable amounts of other blood coagulation factors.
wo 93/06855 pcr/DKs2/oois6 212~02'~ 8 An even further purified factor Vll preparation may be obtained by including an additional gel filtration as the final purification step. Factor Vll is then converted into activated factor Vlla by known means, e.g. by several different plasma proteins, such as factor X~IA, IXA OR XA. Alternatively, as described by Bjoern et al., ~"Activation S of Coagulation Factor Vll to Vlla", Research Disclosure 269:564-565, 1986) factor Vll may be activated by passing it through an ion-exchange chromatography column, such as MonoQ (Pharmacia Fine Chemicals, Uppsala, Sweden) or the like.
It will be appreciated by those skilled in the art that a suitable factor Vlla for use in the present invention may also be produced by recombinant DNA technology, e.g., 10 by insertion of the cDNA or gene encoding factor Vll (Hagen et al., Proc. Natl. Acad.
Sci. USA 83: 2412-2416, 1986) in a suitable vector, transformir~g of suitable cell lines with the vector and growing the transformed cells in an appropriate medium whereupon the expressed product is isolated and activated into factor Vlla.
Production of FVII by recombinant DNA technology is also described in US Patent 15 4,784,950 which is incorporated herein by reference in its entirety. Factor Vlla produced by recombinant DNA technology may be authentic factor Vlla or a more or less modified factor Vlla, provided that such mod-~ied factor Vlla has substantially the same biological activity for blood coagulation as authentic factor Vlla. Such modified factor Vlla may be prepared by modifying the DNA sequence encoding 20 factor Vil sither by altering the amino acid codons or by removal of some of the amino acid codons in the natural gene by known means, e.g., by site-specific mutagenesis.
It is evident that the practice of the methods described herein is independent of how the factor Vlla is derived and, therefore, the present invention is contemplated to 25 cover the use of any factor Vlla preparation suitable for use herein.
The carrier material may be a gel, a paste, a solid or other suitable biologically compatible/acceptable carrier for topical application of pharmaceuticals or other biologically active compositions.
W093/0685~ 21 21 0 2 8 PCI'/DK92/00296 The viscosity of the gel or paste will preferably be from about 200 cps to about30,000 cps.
The biologically compatible carrier will typically be made of natural macromolecules such as gelatine, collagen, alginic acid, cellulose, chitin, fibrinogen, fibrin, fibrin split 5 products, fibronectin, fibronectin fragments, globulin, myoglobulin, casein, keratin, albumin, polysaccharides e.g. dextrans, glycosaminglycans, agar, pectin, starch or from chemical modified natural molecules such as denatured gelatine, alginicacid-alginates e.g. calcium alginate, oxidized cellulose, substituted cellulose ethers e.g. glycol cellulose, methyl cellulose, ethyl cellulose, hydroxymethyl cellulose, 10 hydroxyethyl cellulose, hydroxypropylmethyl cellulose, substituted cellulose esters e.g. acetylated cellulose, substituted cellulose ether-esters e.g. acetylated ethyl cellulose, chit~osan or from synthetic polymers such as vinyl polymers, e.g.
polyacrylic acid, polymethacrylic acid, polyvinyl pyrrolidone and polyviny~alcohol, polyglycolic acid, polylactic acid, polydextroses or copolymers such as 15 polyo~yethylene-polyoxypropylene copolymers orfrom naturalfibers, syntheticfibers or mixtures of any of the above materials/compounds.
A solid biologically compatible carrier will preferably be a granule, powder, spo~ge, tilm~ plaster, surgical dressing or a bandage.
Solid biologically compatible carriers will typically be selected frorn those-already 20 used as hemostats such as modified cellulose, collagen, gelatine, alginate orsynthetic polymers.
The biologically compatible carrier may furthermore contain a fibrinolysis inhibitor, such as aprotinin, epsilon-aminocaproic acid or tranexamic acid. It may also contain a stabi!izer, such as naturally occurring amino acids, mono- or disaccharides, 2~ polyglycols, glycerol, proteins or a metal salt, such as calcium salts, and mixtures thereof. Also buffering salts may be added, such as alkaline metal acetates, alkaiine metal carbonates or hydrogen carbonates, alkaline metal citrates, alkaline metal WO 93/06855 PCr/DK92/00296 2~2~0?.8 phosphates or hydrogen phosphates, alkaline metal succinates, imidazole, TRIS, and zwitteranionic buffering systems, and mixtures thereof. Furthermore, antimicrobial or bacteriostatic agents, such as antibiotics, sulphonamides, antimycotic agents, antiviral compounds, and preservatives may be added.
5 The present method and hemostatic composition will be useful for enhancing thearrest of bleedings in several instances of surgical interventions or other injuries such as in the accidental injury of the skin and/or adjacent tissues or of larger abdominal organs (liver, spleen, or intestines); in lung surgery; in neurosurgery to prevent pressure damages of the cerebral or nerve tissues; in orthopedic surgcry during 10 which extensive hemorrhages frequently occur which are difficult to arrest by other means; in vascular surgery to arrest seepage of blood from the sites of suturing; in oral or dental surgery such as extraction of teeth; and in nose-bleeding (epistaxis).
- In a ready-to-use product incorporation of FVlla into the carrier material may be done by various known methods, such as co-precipitation, swelling, dispersion, 15 mixing, soaking, spraying, embedding, injection or a combination thereof.
If the carrier is a gel or a paste, FVlla is preferably incorporated into the c~rrier material under aseptical conditions. This may be carried out by adding a suitable solution of FVlla to the carrier material whiCh is then stirre~ gently by suitable means to obtain a uniform distribution of FVlla within the gei or paste. The FVlla Ioaded 20 carrier material is then transferred to a suitable package form e.g. a tube, a plastic container or a syringe. Terminal sterilization may be carried out by means of, for instance, heat or ionizing irradiation.
If the carrier is solid it may be loaded with FVlla by placing the material in a suitable solution of FVlla for a period sufficient to ensure that the carrier material is25 adequately soaked with the FVlla solution. FVlla may also be incorporated into the solid carrier by means of spraying, embedding or multiple injections. After vacuum drying or freeze drying to evaporate excess of water the FVlla impregnated carrier W093J06855 212 1 0 2 8 PCI`/DK92/00296 is transferred to a suitable package, such as paper bags or a blister paGkage and terminally sterilized by means of, for instance, heat, ethyleneoxide or ionizingirradiation.
FVlla may be fixed to the carrier by electrostatic interaction between FVlla and the 5 carrier material.
FVlla may also be covalently bound to the carrier by means of chemical crosslinking reagents, such as bifunctional N-hydroxy succinimide esters or other bifunctional chemical crosslinking reagents.
Finally, FVlla may be fixed to the carrier by physical means such as absorption,10 dispersion or adsorption.
FVlla may also be added to the carrier just before use, e.g. by spraying a suitable solution of FVlla onto the carrier material or by embedding the carrier into a FVlla solution. Alternatively, ths FVlla solution may be injected into the carrier.
A preferred carrier is a biodegradable sponge material known in the prior art ~s15 hemostatic sponges.
Materials for the preparation of hemostatic sponges are conventionally selected from biodegradable or biologicaJly absorbable compounds such as collagenl gelatine, chitin, cellulose, polyglycolic acid and polyacetic acid. Such absorbable hemostats can be left at the site of bleeding even after suturing of internal injuries and will exert ~0 their effect over a period of time, dependent on their water solubility, degradability, and size.
The characteristics of the above materials may be conditioned by various chemical or physical treatments resulting in e.g. a preferred improved mechanical strength of WO 93/0685~ PCr/DK92/00296 21210~.8 12 the structure or in rendering the material less water soluble thereby retarding the rate of absorption which may extend the period of hemostatic activity.
As an example, gelatine may be denatured by treatment at temperatures in the range of 100 - 160C for several hours. After such treatment the originally water 5 soluble gelatine will become substantially water insoluble but can still be degraded to absorbable molecules by proteolytic enzymes present in the body.
In contrast, hemostatic sponges prepared from undenatured gelatine will dissolverather rapidly and turn into a soft gel when brought into contact with aqueous solutions or bleeding wounds.
10 The FVlla containing dry hemostatic sponge may be prepared either by forming a foam of undenatured gelatine and FVlla which is thereafter freeze-dried or by saturating a preformed dried sponge with a solution of FVlla, the wet sponge thereafter being freeze-dried.
The latter technique implies the possibility to apply water insoluble sponge material 15 which may be advantageQus because Such sponges ret~in their physical.structure - after application to the site of bleeding for considerably longer tirne than undenatured sponges.
In a preferred embodiment of the present invention the carrier is a ready-to-usehemostatic sponge to which FVlla has been added prior to packaging and terminal 20 sterilization.
WO 93/06$~iS 2 1 2 1 0 2 8 PCI/DK92/00296 EXAMPLES
Example 1:
Four 5 mrn cores of a gelatine sponge (Spongostan commercially available from Novo Nordisk A/S~ were cut using a punch. Two of these were soaked in sterile 5 water and the other two were soaked in two ml of sterile water in which was dissolved 1.13 mg of Factor Vlla. The soaking time was approxim~tely five minutes before application to bleeding sites which were made as described below.
A 450 gram Spraque-Dawley rat was anesthetized with halothane, followed by 0.2 ml/kg of a stock anesthetic solution, which was given intraperitoneally.
10 The rat was placed on a warrning pad and the abdomen was opened udth a long, mid-line incision to expose the liver. Gut contents were packed with warm salineswabs.
A piece of steel was placed behind the liver to provide a firm bed. Four 5 mm biopsies were cored through the full thickness of the liver and removed and the four 15 prepared pieces of gelatine spon~ were placed into the holes.
These four sites were observed for 20 minutes and at the end of the time the iiver was excised and an attempt was made to remove the gelatine plugs by grasping with fine toothed forceps and pulling gently.
The two sites which were plugged with geiatine sponge plugs impregnated with 20 Factor Vlla stopped bleeding, while the two other sites continued to ooze~ It was not difficult to remove any of the four plugs from the liver biopsy sites, but it appeared more difficult to remove those soaked in Factor Vlla.
WO 93/068~5 PCr/DK92/00296 Example 2:
Prior to the surgical intervention, a small piece (45 x 20 x 10 mm) was cut out of a dry, gelatine sponge (Spongostan Standard~. The size stated was chosen to ensurethat the sponge would exactly cover an incision 25 mm in length with an overlap of 5 10mm.
Also an aqueous solution (1.0 mg/ml) of freeze dried Factor Vlla, containing calcium ions (concentration of 10.0 mMol~, was made and kept at room temperature prior to the operation.
In an anaesthetized pig, laparotomy was performed through a midline incision and10 the spleen was delivered into the wound. Incisions were made 3.0 mm deep and 25 mm in length ~sing a special device made from a scalpel mounted with a stop block and a pattern with a linear groove. The first incision was a control incision left for free bieeding for 12 minutes to ensure that coagulation did not occur spontaneously.
Another incision was then made 30 mm apart from the first incision and allowed ~o 15 bleed freely ~or 60 seconds. A pieee of gelatin~ sponge was then carefully piace upon ~he incision and 1.0 ml of Fa~:tor Vlla solution was dropped onto and gently massaged into the sponge under light finger pressure for 30 seconds. Complete hemostasis was obtained momentarily.
The test series did also include four different, commercially available hemostatic 20 sponges moistened with an isotonic Sodium chloride solution. The individual time for hemostasis ranged from 1.8 minutes to 7.5 minutes.
Using the same test procedure bovine thrombin, applied in a watery solution (50 NIH
Units/ml), also provoked momentary hemostasis.
wo 93/06ss~ 2 :1 2 1 0 2 8 pcr/DKs2~oo296 Example 3:
Without being incorporated into a matrix, an aqueous solution of Factor Vlla wasapplied topically as a spray to control venous bleeding from the gallbladder bed and from abdominal surgical incisions. The investigation was divided into two parts 5 involYing a total of 8 patients. The study was designed as a doubls-blind randomized placebo controlled study.
Vials containing 562.5 ,I~g of Iyophilized Factor Vlla or placebo preparations resembling Factor Vlla were reconstituted with 3.7 ml of sterile water immediately before use and transferred into syringes with sprinkler needles. All 3.7 ml were10 syringed at each administration.
Four patients undergoing cholecystectomy were investigatecl, two receiving Factor Vlla and two matchlng placebo. After removal of the gallbladder, Fac~or Vlla or placebo was syringed on to the ~allbladder bed. Efficacy was assessed 2 minutes later. In each case the efficacy of the pr~paration was rated comparing ooze before 15 and after application.
Four other patients undergoing general elective abdominal surgery were investigated. Each incision was extended down to but not through the peritoneum with arterial "spurters" being controlled using the surgeon~s usual technique.
Immediately after the surgical incision the middle of the wound was cover~d with a 20 thick swab and Factor Vlla was syringed on to tne one end of the wound and matching placebo to the other. Efficacy was assessed 3 minutes after the wound was syringed. The surgeon judged blindly which half of the wound was bleeding less.
In these studies, Factor Vlla had no effect in the control of venous bleeding. The 25 likely reason was considered to be that Factor Vlla was washed away from the wound when applied only in an aqueous solution and not incorporated into a rnatrix 2 l 21028 16 or a biologically compatible carrier which would have allowed factor Vlla to remain in contact with the bleeding wound.
The present invention is not to be limited in scope by the above examples since they are intended as single illustrations of the invention. Indeed, various modifications of 5 the invention in addition to those shown and described herein will become apparent to those skilted in the art from the foregoing description. Such modifications are intended to fall within the scope of the appended claims.
FIELD OF INVENTION
The present invention relates to a method for arresting local bleedings by topical use of FVlla and a hemostatic composition containing FVlla.
5 B~CKGROUND OF THE INVENTION
When blood vessels are injured by physical traumas including surgical interventions bleeding will occur. If bleedings are left alone they will ev~ntually be arrested by a normally occurring physiolo~ical process characterized by a chain of events involving the combined activity of vascular, platelet, and plasma factors, leading to 10 the formation of a blood clot. This process is referred to as physiological hemostasis (blood coagulation3, which is describ~d in details below. In the case of a minor superficial bleeding this physiological hemostasis is adequate for the arrest.
There are two separate systsms which can promote blood coagulation. These systems are referred to as the intrinsic and the extrinsic coagulation pathways.
15 In the intrinsic pathway, only blood clotting factors present in piasma are u~ilized.
An intermediate event in the intrinsic pathway is the activation of Factor IX to Factor IXa, a reaction catalyzed by Fa~tor Xla and calcium ions. Factor IXa then participates in the activation of Factor X to Factor Xa in the presence of Factor Vllla, phospholipid and calcium ions~
20 The extrinsic pathway involves plasma factors as well as components present in tissue extracts. Factor Vll, a proenzyme present in plasma, participates also in the WO 93/06855 PCl /DK92/00296 212~ 02Ç~ 2 extrinsic pathway of blood coagulation by converting (upon its activation to Vlla) Factor X to Xa in the presence of tissue factor and calcium ions.
Factor Xa in turn then converts prothrombin to thrombin in ths pres~nce of Factor Va, calcium ions and phospholipid. Finally, thrombin converts the plasma fibrinogen into fibrin, which in the presence of Factor Xllla and calcium ions is cross-linked and thus forming the blood clot.
Blood factors such as Factor Vlll:C (see US Patents 4,831,119; 4,868,112; 4,886,876;
4,657l894; Re. 32,011 and 4,649,132) and Factor Vlla (see US Patents 4,784,950;
4,382,083; 4,479,938 and 4,357,321) purified from natural sources or made via 10 recombinant techniques have been used for treating patients, such as hemophiliacs, having blood-clotting deficiencies or inhibi`tors to blood-clotting factors. These blood-clotting factors have been delivered to the patient needing treatme~t as an aqueous solution by infusion or bolus injection depending on the blood factor to be dslivered and the condition of the patient. Cessation of the bleeding is expected to 15 occur typically between 15 minutes to 3 hours or more after the delivery of the blood-clotting factor.
However, faster arresting of the bleeding is necessary in th~ case of severe bleedings emerging from more extensive injuries involving larger arteries or when seeping bleedings occur from larger mucosal surfaces or on cavities without 20 drainage. If the bleeding continues in even a shorter period it may result inextensive losses of blood which may have an adverse effect on the normal function of the body. Also, in the case of bleeding occurring in osseous non-expandable cavities, the accumulation of extravasated blood may cause local damages of softtissues due to increased pressure. The usual treatment of such conditions involve 25 the adaption of surgical and/or medical hemostatic measures.
Surgical arrest of bleeding comprises ligation or suture of disrupted blood vessels, plugging by using tampons in cavities, coagulating tissue surfaces inclu~ing their wo s3/068ss 2 1 2 1 0 2 8 Pcr/DKg2/002g6 exposed disrupted blood vessels by heated instruments or by the application of cauterizing agents or heated air.
Surgical hemostasis may also be aided by the appliGation at the injured site of appropriately sized blocks, plates, or films of biologically absorbable hemostatic 5 sponges. ~:
Pharmaceutical preparations containing bovine thrombin or other blood clotting factors such as Factor Vlll, Factor Xlll or calcium i~ns are currently used in some places as hemostatic adjuncts in surgery, said adjuncts being administered e.g. by spraying a suitable solution thereof onto the site of bleeding such as in US
10 4,298,598. Also textile materials such as gauze or cotton wool fabrics or biologically absorbable sponges, which prior to the application have been soaked in a solution of one or more of said hemostatic compounds, are used such as in US 4,363,319.
US patent 2,558,395 discloses a ready-to-use undenatured gelatine hemostatic sponge containing thrombin. US 4,265,233 discloses wound healing material 15 comprising a structure made from compounds such as gelatine, collagen, polyglycolic and polylactic acid to which FXIII has been fixed by covalent bir~ding.
EP 277096 A discloses a wound dressing comprising a stable thrombin composition and a substrate such as hemostaticl porous sponges of collagen or denatured gelatine and WO 90/13320 discloses a porous sponge containing a hemostatically 20 effective amount of thrombin, and hemostatically effective amounts of one or more blood coagulation factors other than thrombin. US patent 4,563,387 and US patent4,642,111 relate to, respectively, a methvd and device for tr~ating cancer and which disclose an anti-cancer drug and a blood coagulation factor being fixed to a structure, such as a polymer, capable of being delivered by injection to the site of 25 bleeding directly causecl by the cancer treatment.
Japanese published patent application No. 59-116213 discloses an aerosol containing FXIII and thrombin and Japanese published patent application No.
WO 93/06855 PCr/DK92/00296 212~02~
02-167234 discloses adhesive for living tissues containing fibrinogen, prothrombin, FVII, FIX, FX, FXIII, antithrombin, protease inhibitor and calcium ions.
In the recent years increasing concern has however arisen regarding the safe useof bovine derived products e.g. thrombin or prothrombin in pharrnaceutical products 5 for human use. Several reports describe th~ possible risk of transmitting an infectious agent causing Bovine Spongiform Encephalopathy (BSE) in cattle into humans, where the virus-like agent may be the reason for one or more well known diseases characterized by degenerative encephalopathy e.g. Creutzfeldt-Jacob disease and Kuru. Furthermore, clinical investigators have obs~lved thc~ the topical 10 IJse of bovine thrombin in humans may cause the development of an~ibodies cross-reacting to human thrombin and causing bleeding problems.
It is, therefore) an object of the present invention to provide a safe and,effective means to topically arrest bleedings at the site of an injury.
SUMMARY OF THE INVENTION
15 The present invention is based on the surprising recognition that FVlla is capable of momentarily arrest of bleedings when appiied topicaily to the site of injury without the presence of thrombin or other coaguiation factors and when FVlla is in association, together with or incorporated into a biologically compatible carrier (which, as used herein, is intended to include a composition or material) capable of 20 preventing FVlla from being washed away from the site of injury.
According to the present invention, FVlla is incorporated into a biologically compatible carrier which does not contain thrombin and is unaccornpanied or uncontaminated by any other blood clotting factors.
wo 93/068~5 2 1 2 1 0 ~ ~ PCI'/DK92/00296 The present invention is thus related to a hemostatic composition comprising a hemostatically effective amount of FVlla incorporated into biologically compatible carrier said composition containing no thrombin.
More specifically, this invention provides a hemostatic composition for inducing5 hemostasis at a bleeding wound comprising a hemostatically effective amount ofFVlla which is uncontaminated or unaccompanied by other blood cl~tting factors and which has sufficient activity alone to produce a hemostatic effect, together with a biologically compatible carrier which permits said factor Vlla to remain affixed to, in association with or contacting said wound site.
Prior to setting forth the invention, it may be helpful to an understanding thereof to set forth definition of certain terms to be used hereinafter.
Hemostat or Hemostatic Agent: An agent that arr~sts hemorrhage.
Hemos~atic Composition: A composition that contains a Hemostat or Hemostatic 15 Agent.
Blood clot: The final uutcome of the blood coagulation cascade, formed by conversion of soluble plasma fibrinogen into insoluble fibrin, which physically stops the bleeding. The blood clot covers the surface, keeps the wound edges together and forms the matrix for the following cell proliferation and wound healing 20 Blood clotting factors: Plasma proteins which participate in the blood coagulation cascade.
WO 93/06855 PCI`/DK~2/00296 212102~ 6 Activated blood ctotting factors: Blood clotting factors converted to active enzymes by the action of an activator, often itseif being an activated blood clotting factor.
They are generally designated by the addition of a lower case postscript "a" (e.g.
Factor Vlla).
5 Proenzymes: An enzyme precursor that in general has reduced or no activity as compared to the mature enzyme.
Biologically absorbable: Material which can be degraded in the body to smaller molecules having a size which allows transport into the blood stream and gradualremoval from the site of application.
10 S~onge: A porous structure being reticulate and having an inner surface considerably larger than the outer surface. The porous structure will contain hollow spaces within the reticulate structure and can absorb many times its own weight in liquids. -Covalent binding: A bond between two atoms in which both of the atoms concerned 1~ contribute the elec~ron or electrons.
Dressing: Material apptied to a wound and fastened in place to provide protection and to promote healing.
Topical: Local.
Biologically Compatible: The ability to be accepted in the body and remain functional 20 for a period without rejection.
Gel: A colloidal system comprising a solid and a liquid phase which exists as a solid or semisolid mass.
wo 93~068~ 2 1 2 ~ 0 2 ~ pcr/DK92/oo296 Paste: An ointment-like preparation of one or more substances in a hydrogel or fatty base. It is less greasy and better absorbed than an aintment.
Granule: A minute particle or mass.
Film: Any thin coYering, coating, or layer.
5 Plaster: A substance intended for external application, made of such material and of such consistency as to adhere to the skin.
Bandage: A strip of gauze, muslin, flannel, or other material used to hold dr~ssings in place, or to check hemorrhage.
DETAILED DESCRIPTION
10 FVlla is to be used in a hemostatically effective amount. By hemostatically sffective arnount is mean~ an amount which will preferably cause arrest of the bleeding if kept in association with or contacting the site of the injury for a sufficient amount of ~ime, preferably from about 60 seconds in patients not having an impaired hemostatic mechanism to less than about 10 minutes in patients having an irnpaired hemostatic 15 mechanism. FVlla should be used in an amount ranging from about û.2 to about 2.0 mg, preferably from about 0.5 to about 1.5 mg and more preferably from about0~9 to about 1.1 mg per application.
FVlla may be derived from plasrna as described in EP 00821 82B or by recombinantDNA-technology as described in EP 0200421A. Human purified factor Vlla is 20 preferably made by the methods described by Broze and Majerus, J. Bio. Chem.
255, 4: 1242-1247, 1980, and Hedner and Kisiel, J. Clin. Invest. 71: 1836-1841, 1983.
These methods yield factor Vll without detectable amounts of other blood coagulation factors.
wo 93/06855 pcr/DKs2/oois6 212~02'~ 8 An even further purified factor Vll preparation may be obtained by including an additional gel filtration as the final purification step. Factor Vll is then converted into activated factor Vlla by known means, e.g. by several different plasma proteins, such as factor X~IA, IXA OR XA. Alternatively, as described by Bjoern et al., ~"Activation S of Coagulation Factor Vll to Vlla", Research Disclosure 269:564-565, 1986) factor Vll may be activated by passing it through an ion-exchange chromatography column, such as MonoQ (Pharmacia Fine Chemicals, Uppsala, Sweden) or the like.
It will be appreciated by those skilled in the art that a suitable factor Vlla for use in the present invention may also be produced by recombinant DNA technology, e.g., 10 by insertion of the cDNA or gene encoding factor Vll (Hagen et al., Proc. Natl. Acad.
Sci. USA 83: 2412-2416, 1986) in a suitable vector, transformir~g of suitable cell lines with the vector and growing the transformed cells in an appropriate medium whereupon the expressed product is isolated and activated into factor Vlla.
Production of FVII by recombinant DNA technology is also described in US Patent 15 4,784,950 which is incorporated herein by reference in its entirety. Factor Vlla produced by recombinant DNA technology may be authentic factor Vlla or a more or less modified factor Vlla, provided that such mod-~ied factor Vlla has substantially the same biological activity for blood coagulation as authentic factor Vlla. Such modified factor Vlla may be prepared by modifying the DNA sequence encoding 20 factor Vil sither by altering the amino acid codons or by removal of some of the amino acid codons in the natural gene by known means, e.g., by site-specific mutagenesis.
It is evident that the practice of the methods described herein is independent of how the factor Vlla is derived and, therefore, the present invention is contemplated to 25 cover the use of any factor Vlla preparation suitable for use herein.
The carrier material may be a gel, a paste, a solid or other suitable biologically compatible/acceptable carrier for topical application of pharmaceuticals or other biologically active compositions.
W093/0685~ 21 21 0 2 8 PCI'/DK92/00296 The viscosity of the gel or paste will preferably be from about 200 cps to about30,000 cps.
The biologically compatible carrier will typically be made of natural macromolecules such as gelatine, collagen, alginic acid, cellulose, chitin, fibrinogen, fibrin, fibrin split 5 products, fibronectin, fibronectin fragments, globulin, myoglobulin, casein, keratin, albumin, polysaccharides e.g. dextrans, glycosaminglycans, agar, pectin, starch or from chemical modified natural molecules such as denatured gelatine, alginicacid-alginates e.g. calcium alginate, oxidized cellulose, substituted cellulose ethers e.g. glycol cellulose, methyl cellulose, ethyl cellulose, hydroxymethyl cellulose, 10 hydroxyethyl cellulose, hydroxypropylmethyl cellulose, substituted cellulose esters e.g. acetylated cellulose, substituted cellulose ether-esters e.g. acetylated ethyl cellulose, chit~osan or from synthetic polymers such as vinyl polymers, e.g.
polyacrylic acid, polymethacrylic acid, polyvinyl pyrrolidone and polyviny~alcohol, polyglycolic acid, polylactic acid, polydextroses or copolymers such as 15 polyo~yethylene-polyoxypropylene copolymers orfrom naturalfibers, syntheticfibers or mixtures of any of the above materials/compounds.
A solid biologically compatible carrier will preferably be a granule, powder, spo~ge, tilm~ plaster, surgical dressing or a bandage.
Solid biologically compatible carriers will typically be selected frorn those-already 20 used as hemostats such as modified cellulose, collagen, gelatine, alginate orsynthetic polymers.
The biologically compatible carrier may furthermore contain a fibrinolysis inhibitor, such as aprotinin, epsilon-aminocaproic acid or tranexamic acid. It may also contain a stabi!izer, such as naturally occurring amino acids, mono- or disaccharides, 2~ polyglycols, glycerol, proteins or a metal salt, such as calcium salts, and mixtures thereof. Also buffering salts may be added, such as alkaline metal acetates, alkaiine metal carbonates or hydrogen carbonates, alkaline metal citrates, alkaline metal WO 93/06855 PCr/DK92/00296 2~2~0?.8 phosphates or hydrogen phosphates, alkaline metal succinates, imidazole, TRIS, and zwitteranionic buffering systems, and mixtures thereof. Furthermore, antimicrobial or bacteriostatic agents, such as antibiotics, sulphonamides, antimycotic agents, antiviral compounds, and preservatives may be added.
5 The present method and hemostatic composition will be useful for enhancing thearrest of bleedings in several instances of surgical interventions or other injuries such as in the accidental injury of the skin and/or adjacent tissues or of larger abdominal organs (liver, spleen, or intestines); in lung surgery; in neurosurgery to prevent pressure damages of the cerebral or nerve tissues; in orthopedic surgcry during 10 which extensive hemorrhages frequently occur which are difficult to arrest by other means; in vascular surgery to arrest seepage of blood from the sites of suturing; in oral or dental surgery such as extraction of teeth; and in nose-bleeding (epistaxis).
- In a ready-to-use product incorporation of FVlla into the carrier material may be done by various known methods, such as co-precipitation, swelling, dispersion, 15 mixing, soaking, spraying, embedding, injection or a combination thereof.
If the carrier is a gel or a paste, FVlla is preferably incorporated into the c~rrier material under aseptical conditions. This may be carried out by adding a suitable solution of FVlla to the carrier material whiCh is then stirre~ gently by suitable means to obtain a uniform distribution of FVlla within the gei or paste. The FVlla Ioaded 20 carrier material is then transferred to a suitable package form e.g. a tube, a plastic container or a syringe. Terminal sterilization may be carried out by means of, for instance, heat or ionizing irradiation.
If the carrier is solid it may be loaded with FVlla by placing the material in a suitable solution of FVlla for a period sufficient to ensure that the carrier material is25 adequately soaked with the FVlla solution. FVlla may also be incorporated into the solid carrier by means of spraying, embedding or multiple injections. After vacuum drying or freeze drying to evaporate excess of water the FVlla impregnated carrier W093J06855 212 1 0 2 8 PCI`/DK92/00296 is transferred to a suitable package, such as paper bags or a blister paGkage and terminally sterilized by means of, for instance, heat, ethyleneoxide or ionizingirradiation.
FVlla may be fixed to the carrier by electrostatic interaction between FVlla and the 5 carrier material.
FVlla may also be covalently bound to the carrier by means of chemical crosslinking reagents, such as bifunctional N-hydroxy succinimide esters or other bifunctional chemical crosslinking reagents.
Finally, FVlla may be fixed to the carrier by physical means such as absorption,10 dispersion or adsorption.
FVlla may also be added to the carrier just before use, e.g. by spraying a suitable solution of FVlla onto the carrier material or by embedding the carrier into a FVlla solution. Alternatively, ths FVlla solution may be injected into the carrier.
A preferred carrier is a biodegradable sponge material known in the prior art ~s15 hemostatic sponges.
Materials for the preparation of hemostatic sponges are conventionally selected from biodegradable or biologicaJly absorbable compounds such as collagenl gelatine, chitin, cellulose, polyglycolic acid and polyacetic acid. Such absorbable hemostats can be left at the site of bleeding even after suturing of internal injuries and will exert ~0 their effect over a period of time, dependent on their water solubility, degradability, and size.
The characteristics of the above materials may be conditioned by various chemical or physical treatments resulting in e.g. a preferred improved mechanical strength of WO 93/0685~ PCr/DK92/00296 21210~.8 12 the structure or in rendering the material less water soluble thereby retarding the rate of absorption which may extend the period of hemostatic activity.
As an example, gelatine may be denatured by treatment at temperatures in the range of 100 - 160C for several hours. After such treatment the originally water 5 soluble gelatine will become substantially water insoluble but can still be degraded to absorbable molecules by proteolytic enzymes present in the body.
In contrast, hemostatic sponges prepared from undenatured gelatine will dissolverather rapidly and turn into a soft gel when brought into contact with aqueous solutions or bleeding wounds.
10 The FVlla containing dry hemostatic sponge may be prepared either by forming a foam of undenatured gelatine and FVlla which is thereafter freeze-dried or by saturating a preformed dried sponge with a solution of FVlla, the wet sponge thereafter being freeze-dried.
The latter technique implies the possibility to apply water insoluble sponge material 15 which may be advantageQus because Such sponges ret~in their physical.structure - after application to the site of bleeding for considerably longer tirne than undenatured sponges.
In a preferred embodiment of the present invention the carrier is a ready-to-usehemostatic sponge to which FVlla has been added prior to packaging and terminal 20 sterilization.
WO 93/06$~iS 2 1 2 1 0 2 8 PCI/DK92/00296 EXAMPLES
Example 1:
Four 5 mrn cores of a gelatine sponge (Spongostan commercially available from Novo Nordisk A/S~ were cut using a punch. Two of these were soaked in sterile 5 water and the other two were soaked in two ml of sterile water in which was dissolved 1.13 mg of Factor Vlla. The soaking time was approxim~tely five minutes before application to bleeding sites which were made as described below.
A 450 gram Spraque-Dawley rat was anesthetized with halothane, followed by 0.2 ml/kg of a stock anesthetic solution, which was given intraperitoneally.
10 The rat was placed on a warrning pad and the abdomen was opened udth a long, mid-line incision to expose the liver. Gut contents were packed with warm salineswabs.
A piece of steel was placed behind the liver to provide a firm bed. Four 5 mm biopsies were cored through the full thickness of the liver and removed and the four 15 prepared pieces of gelatine spon~ were placed into the holes.
These four sites were observed for 20 minutes and at the end of the time the iiver was excised and an attempt was made to remove the gelatine plugs by grasping with fine toothed forceps and pulling gently.
The two sites which were plugged with geiatine sponge plugs impregnated with 20 Factor Vlla stopped bleeding, while the two other sites continued to ooze~ It was not difficult to remove any of the four plugs from the liver biopsy sites, but it appeared more difficult to remove those soaked in Factor Vlla.
WO 93/068~5 PCr/DK92/00296 Example 2:
Prior to the surgical intervention, a small piece (45 x 20 x 10 mm) was cut out of a dry, gelatine sponge (Spongostan Standard~. The size stated was chosen to ensurethat the sponge would exactly cover an incision 25 mm in length with an overlap of 5 10mm.
Also an aqueous solution (1.0 mg/ml) of freeze dried Factor Vlla, containing calcium ions (concentration of 10.0 mMol~, was made and kept at room temperature prior to the operation.
In an anaesthetized pig, laparotomy was performed through a midline incision and10 the spleen was delivered into the wound. Incisions were made 3.0 mm deep and 25 mm in length ~sing a special device made from a scalpel mounted with a stop block and a pattern with a linear groove. The first incision was a control incision left for free bieeding for 12 minutes to ensure that coagulation did not occur spontaneously.
Another incision was then made 30 mm apart from the first incision and allowed ~o 15 bleed freely ~or 60 seconds. A pieee of gelatin~ sponge was then carefully piace upon ~he incision and 1.0 ml of Fa~:tor Vlla solution was dropped onto and gently massaged into the sponge under light finger pressure for 30 seconds. Complete hemostasis was obtained momentarily.
The test series did also include four different, commercially available hemostatic 20 sponges moistened with an isotonic Sodium chloride solution. The individual time for hemostasis ranged from 1.8 minutes to 7.5 minutes.
Using the same test procedure bovine thrombin, applied in a watery solution (50 NIH
Units/ml), also provoked momentary hemostasis.
wo 93/06ss~ 2 :1 2 1 0 2 8 pcr/DKs2~oo296 Example 3:
Without being incorporated into a matrix, an aqueous solution of Factor Vlla wasapplied topically as a spray to control venous bleeding from the gallbladder bed and from abdominal surgical incisions. The investigation was divided into two parts 5 involYing a total of 8 patients. The study was designed as a doubls-blind randomized placebo controlled study.
Vials containing 562.5 ,I~g of Iyophilized Factor Vlla or placebo preparations resembling Factor Vlla were reconstituted with 3.7 ml of sterile water immediately before use and transferred into syringes with sprinkler needles. All 3.7 ml were10 syringed at each administration.
Four patients undergoing cholecystectomy were investigatecl, two receiving Factor Vlla and two matchlng placebo. After removal of the gallbladder, Fac~or Vlla or placebo was syringed on to the ~allbladder bed. Efficacy was assessed 2 minutes later. In each case the efficacy of the pr~paration was rated comparing ooze before 15 and after application.
Four other patients undergoing general elective abdominal surgery were investigated. Each incision was extended down to but not through the peritoneum with arterial "spurters" being controlled using the surgeon~s usual technique.
Immediately after the surgical incision the middle of the wound was cover~d with a 20 thick swab and Factor Vlla was syringed on to tne one end of the wound and matching placebo to the other. Efficacy was assessed 3 minutes after the wound was syringed. The surgeon judged blindly which half of the wound was bleeding less.
In these studies, Factor Vlla had no effect in the control of venous bleeding. The 25 likely reason was considered to be that Factor Vlla was washed away from the wound when applied only in an aqueous solution and not incorporated into a rnatrix 2 l 21028 16 or a biologically compatible carrier which would have allowed factor Vlla to remain in contact with the bleeding wound.
The present invention is not to be limited in scope by the above examples since they are intended as single illustrations of the invention. Indeed, various modifications of 5 the invention in addition to those shown and described herein will become apparent to those skilted in the art from the foregoing description. Such modifications are intended to fall within the scope of the appended claims.
Claims (27)
1. A hemostatic composition for inducing hemostasis at a bleeding wound comprising a hemostatically effective amount of FVIIa which is unaccompanied by other blood clotting factors and which has sufficient activity alone to produce a hemostatic effect, together with a biologically compatible carrier in the form of a gel, paste or solid, which carrier permits said factor VIIa to remain in contact with said bleeding wound.
2. Hemostatic composition according to claim 1, wherein the gel or paste has a viscosity in the range of about 200 cps to about 30,000 cps.
3. Hemostatic composition according to claim 1, wherein the biologically compatible carrier is selected from the group consisting of natural macromolecules, chemically modified natural molecules, synthetic polymers, natural or synthetic fibers or mixtures thereof.
4. Hemostatic composition according to claim 3, wherein the biologically compatible carrier is selected from the group consisting of polysaccharides or proteins or mixtures thereof.
5. Hemostatic composition according to claim 1, wherein the biologically compatible carrier is a granule, powder, sponge, film, plaster, surgical dressing or a bandage.
6. Hemostatic composition according to claim 1, wherein the biologically compatible carrier is made of modified cellulose, collagen, gelatine or natural or synthetic fibers.
7. Hemostatic composition according to claim 1, wherein FVIIa is fixed to the biologically compatible carrier by electrostatic interaction between FVIIa and the biologically compatible carrier or by covalent binding of FVIIa to the biologically compatible carrier.
8. Hemostatic composition according to claim 7, wherein FVIIa is bound covalently to the biologically compatible carrier by means of chemical crosslinking reagents, such as bifunctional N-hydroxy succinimide esters or other bifunctional chemical crosslinking reagents.
9. Hemostatic composition according to claim 1, wherein FVIIa is fixed to the biologically compatible carrier by physical means, such as absorption, dispersion or adsorption.
10. Hemostatic composition according to claim 1, wherein the amount of FVIIa is in the range of from about 0.2 to about 2.0 mg.
11. Hemostatic composition according to claim 10, wherein the amount of FVIIa is in the range of from about 0.9 to about 1.1 mg.
12. Hemostatic composition according to claim 1, comprising a fibrinolysis inhibitor such as aprotinin, epsilon-aminocaproic acid or tranexamic acid.
13. Hemostatic composition according to claim 1, further comprising a stabilizer.
14. Hemostatic composition according to claim 13, wherein the stabilizer is selected from the group consisting of naturally occurring amino acids, mono- or disaccharides, polyglycols, glycerol, proteins or divalent metal ions and mixtures thereof.
15. Hemostatic composition according to claim 1, comprising one or more buffering salts selected from alkaline metal acetates, alkaline metal carbonates or hydrogen carbonates, alkaline metal succinates, imidazole, TRIS, and zwitteranionic buffering systems, and mixtures thereof.
16. Hemostatic composition according to claim 1, comprising one or more antimicrobial or bacteriostatic agents selected from antibiotics, sulphonamides, antimycotic agents, antiviral compounds, and preservatives.
17. A method for inducing hemostasis at a bleeding wound comprising providing topically to the site of the bleeding wound a hemostatically effective amount of FVIIa which is unaccompanied by other blood clotting factors and which has sufficient activity alone to produce a hemostatic effect, together with a biologically compatible carrier which is a gel, paste or solid, which carrier permits said factor VIIa to remain in contact with said bleeding wound.
18. A method according to claim 17, wherein the gel or paste has a viscosity in the range of about 200 cps to about 30,000 cps.
19. A method according to claim 17, wherein the biologically compatible carrier is selected from the group consisting of natural macromolecules, chemically modified natural molecules, synthetic polymers, natural or synthetic fibers or mixtures thereof.
20. A method according to claim 17, wherein the biologically compatible carrier is selected from the group consisting of polysaccharides or proteins of mixtures thereof.
21. A method according to claim 17, wherein the biologically compatible carrier is a granule, powder, sponge, film, plaster, surgical dressing or a bandage.
22. A method according to claim 21, wherein the biologically compatible carrier is made of modified cellulose, collagen, geletine or natural or synthetic fibers.
23. A method according to claim 17, wherein FVIIa is fixed to the biologically compatible carrier by electrostatic interaction between FVIIa and the biologically compatible carrier or by covalent binding of FVIIa to the biologically compatible carrier.
24. A method according to claim 23, wherein FVIIa is bound covelently to the biologically compatible carrier by means of chemical crosslinking reagents, such as bifunctional N-hydroxy succinimide esters or other bifunctional chemical crosslinking reagents.
25. A method according to claim 17, wherein FVIIa is fixed to the biologically compatible carrier by physical means, such as absorption, dispersion or adsorption.
26. A method according to claim 17, wherein the amount of FVIIa is in the range of from about 0.2 to about 2.0 mg.
27. A method according to claim 26, wherein the amount of FVIIa is in the range of from about 0.9 to about 1.1 mg.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US77566491A | 1991-10-11 | 1991-10-11 | |
US775,664 | 1991-10-11 |
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CA002121028A Abandoned CA2121028A1 (en) | 1991-10-11 | 1992-10-09 | Hemostatic composition for local hemostasis |
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JP (1) | JPH07500095A (en) |
AU (1) | AU2793292A (en) |
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CZ (1) | CZ83194A3 (en) |
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CN115605234A (en) * | 2019-12-25 | 2023-01-13 | 广州倍绣生物技术有限公司(Cn) | Hemostatic paste and use thereof |
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EP0726749B1 (en) * | 1993-11-03 | 2004-08-11 | Clarion Pharmaceuticals, Inc. | Hemostatic patch |
DE19903693A1 (en) * | 1998-04-24 | 1999-10-28 | Centeon Pharma Gmbh | Protease for activation of coagulation factor VII |
FR2754183A1 (en) * | 1996-10-08 | 1998-04-10 | Lefebvre Jean Marie | VISCOUS HEMOSTATIC COMPOSITION, IN PARTICULAR IN THE CONDITION OF FROST |
DE19710190A1 (en) * | 1997-03-12 | 1998-09-17 | Immuno Ag | Activated vitamin K-dependent blood factor and method for its production |
AU7907398A (en) * | 1997-06-23 | 1999-01-04 | Novo Nordisk A/S | Use of fviia for the treatment of bleedings in patients with a normal blood clotting cascade and normal platelet function |
KR100821644B1 (en) * | 1999-07-14 | 2008-04-11 | 노보 노르디스크 헬스 케어 악티엔게젤샤프트 | USE OF FVIIa OR A TISSUE FACTOR ANTAGONIST FOR REGULATING GENE EXPRESSION AND CELL MIGRATION OR CHEMOTAXIS |
GB0011053D0 (en) | 2000-05-09 | 2000-06-28 | Hudson John O | Medical device and use thereof |
US7015194B2 (en) | 2000-05-10 | 2006-03-21 | Novo Nordisk A/S | Pharmaceutical composition comprising factor VIIa and anti-TFPI |
JP2004505016A (en) * | 2000-05-10 | 2004-02-19 | ノボ ノルディスク アクティーゼルスカブ | Pharmaceutical composition comprising factor VIIa and factor XIII |
ATE316387T1 (en) * | 2000-09-22 | 2006-02-15 | Perlei Medical Produkte Gmbh | USE OF ANTIFIBRINOLYTICS FOR THE PREPARATION AND MANUFACTURING OF SWABS, COMPRESSES OR PLASTERS |
WO2003039590A1 (en) * | 2001-11-09 | 2003-05-15 | Novo Nordisk Health Care Ag | Pharmaceutical composition comprising factor vii polypeptides and aprotinin polypeptides |
WO2003039581A1 (en) * | 2001-11-09 | 2003-05-15 | Novo Nordisk Health Care Ag | Pharmaceutical composition comprising factor vii polypeptides and tranexamic acid |
EP1446148A1 (en) * | 2001-11-09 | 2004-08-18 | Novo Nordisk A/S | Pharmaceutical composition comprising a factor vii polypeptide and epsilon-aminocapronic acid |
US7125846B2 (en) | 2001-11-09 | 2006-10-24 | Novo Nordisk Healthcare A/G | Pharmaceutical composition comprising factor VII polypeptides and factor V polypeptides |
US7291587B2 (en) | 2001-11-09 | 2007-11-06 | Novo Nordisk Healthcare A/G | Pharmaceutical composition comprising factor VII polypeptides and TAFI polypeptides |
JP2005510513A (en) | 2001-11-09 | 2005-04-21 | ノボ ノルディスク ヘルス ケア アクチェンゲゼルシャフト | Pharmaceutical compositions comprising factor VII polypeptide and TAFI polypeptide |
US7078479B2 (en) | 2001-11-09 | 2006-07-18 | Novo Nordisk Healthcare A/G | Pharmaceutical composition comprising factor VII polypeptides and alpha2-antiplasmin polypeptides |
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FR2894831B1 (en) | 2005-12-16 | 2008-02-15 | Lab Francais Du Fractionnement | THROMBIN FREE BIOLOGICAL GLUE AND USE THEREOF AS MEDICAMENT. |
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RU2545810C2 (en) | 2008-02-29 | 2015-04-10 | Ферросан Медикал Дивайсиз А/С | Device for fastening haemostasis and/or wound healing |
EP2252335B1 (en) | 2008-03-03 | 2013-04-24 | Omrix Biopharmaceuticals Ltd. | A gelatin sponge comprising an active ingredient, its preparation and use |
RU2501556C2 (en) * | 2011-10-06 | 2013-12-20 | Владимир Лазаревич Адамян | Heamostatic match |
JP6241624B2 (en) | 2012-03-06 | 2017-12-06 | フェロサン メディカル デバイシーズ エイ/エス | Pressurized container containing hemostatic paste |
CA2874290C (en) | 2012-06-12 | 2020-02-25 | Ferrosan Medical Devices A/S | Dry haemostatic composition |
CA2912357C (en) | 2013-06-21 | 2019-12-31 | Ferrosan Medical Devices A/S | Vacuum expanded dry composition and syringe for retaining same |
AU2014361291B2 (en) | 2013-12-11 | 2017-11-30 | Ferrosan Medical Devices A/S | Dry composition comprising an extrusion enhancer |
CN106999621B (en) | 2014-10-13 | 2020-07-03 | 弗罗桑医疗设备公司 | Dry composition for hemostasis and wound healing |
AU2015371184B2 (en) | 2014-12-24 | 2020-06-25 | Ferrosan Medical Devices A/S | Syringe for retaining and mixing first and second substances |
WO2017005590A1 (en) | 2015-07-03 | 2017-01-12 | Ferrosan Medical Devices A/S | Syringe for mixing two components and for retaining a vacuum in a storage condition |
WO2017037178A1 (en) * | 2015-09-01 | 2017-03-09 | Trauma Care Consult Traumatologische Forschung Gemeinnützige Gesellschaft Mbh | Hemostatic material |
EP3790600B1 (en) | 2018-05-09 | 2023-12-27 | Ferrosan Medical Devices A/S | Method for preparing a haemostatic composition |
WO2024042148A1 (en) | 2022-08-26 | 2024-02-29 | Stellaris Pharmaceuticals Aps | Haemorrhage inhibiting compositions and methods involving the same |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4382083A (en) * | 1981-06-25 | 1983-05-03 | Baxter Travenol Laboratories, Inc. | Therapeutic method for treating blood-clotting defects with factor VIIa |
JPH0780783B2 (en) * | 1985-11-26 | 1995-08-30 | ノボ ノルディスク アクティーゼルスカブ | Therapeutic composition containing factor VIIa for the treatment of bleeding disorders |
-
1992
- 1992-10-09 CZ CS94831A patent/CZ83194A3/en unknown
- 1992-10-09 EP EP92922509A patent/EP0613377A1/en not_active Withdrawn
- 1992-10-09 HU HU9401008A patent/HUT67693A/en unknown
- 1992-10-09 JP JP5506562A patent/JPH07500095A/en active Pending
- 1992-10-09 WO PCT/DK1992/000296 patent/WO1993006855A1/en not_active Application Discontinuation
- 1992-10-09 CA CA002121028A patent/CA2121028A1/en not_active Abandoned
- 1992-10-09 AU AU27932/92A patent/AU2793292A/en not_active Abandoned
-
1994
- 1994-04-08 NO NO941285A patent/NO941285L/en unknown
- 1994-04-08 FI FI941628A patent/FI941628A/en not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115605234A (en) * | 2019-12-25 | 2023-01-13 | 广州倍绣生物技术有限公司(Cn) | Hemostatic paste and use thereof |
Also Published As
Publication number | Publication date |
---|---|
NO941285L (en) | 1994-06-07 |
NO941285D0 (en) | 1994-04-08 |
WO1993006855A1 (en) | 1993-04-15 |
HU9401008D0 (en) | 1994-07-28 |
FI941628A (en) | 1994-06-08 |
AU2793292A (en) | 1993-05-03 |
HUT67693A (en) | 1995-04-28 |
CZ83194A3 (en) | 1994-11-16 |
EP0613377A1 (en) | 1994-09-07 |
FI941628A0 (en) | 1994-04-08 |
JPH07500095A (en) | 1995-01-05 |
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