US3476855A - Sterilizing and enhancing activity of a finely divided cartilage powder - Google Patents

Sterilizing and enhancing activity of a finely divided cartilage powder Download PDF

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US3476855A
US3476855A US698426A US3476855DA US3476855A US 3476855 A US3476855 A US 3476855A US 698426 A US698426 A US 698426A US 3476855D A US3476855D A US 3476855DA US 3476855 A US3476855 A US 3476855A
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cartilage
powder
wound
healing
wounds
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Leslie L Balassa
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/12Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
    • A61K35/32Bones; Osteocytes; Osteoblasts; Tendons; Tenocytes; Teeth; Odontoblasts; Cartilage; Chondrocytes; Synovial membrane

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  • the particle size of the cartilage used has a surprisingly profound effect on the rate of healing'gand on the strength of the healed tissues. Not only is the ,rate of healing increased as the particle size of the cartilage is decreased, but also the manner or the process by which the cartilage is pulverized and the conditions prevailing during the pulverizing have a profound bearing on the results obtained with the cartilage powder.
  • the effectiveness of the present invention has been demonstrated in comparative tests to be highly superior to results obtained on animals treated with either collagen, car ragbeenan, chondroitin sulfate, chondromucoprotein, fibrinogen, gelatin, talc, bone flour or systemic d methionine.
  • cartilage taken from the partly calcified skeletons (including foetal skeletons) of very young or newly born animals is much more effective in accelerating the healing of wounds than was the case with the bovine tracheal cartilage powder on which previous observations were based, which included substantial quantities of coarse adult cartilage powder.
  • the young animal is not over six months old.
  • the present invention relates preferably to young cartilage, i.e. from young animals or young or newly regenerated cartilage from older animals as reptiles, whether finely divided or not, and cartilage from mature animals in finely divided (average particle size 40 microns or less) particle form, it is to be understood that the invention encompasses such cartilage in either the form which would in maturity retain the cartilaginous form or which would in maturity ossify to bone.
  • the cartilage may be prepared by any suitable means to result in a product which is essentially pure cartilage substance free from adhering tissue, which may have been removed by acid-pepsin or other suitable enzyme treatment, with or without mechanical assistance, or otherwise.
  • extraction aids those which are either volatile and therefore can be readily removed from the extract by volatilization such as for example ammonia or ammonium carbonate, or such materials which it remaining in the extract would cause no harm is applied either topically or introduced parenterally.
  • Dialysis may be employed to remove undesired salts or other dialyzable material which may be present.
  • Other extraction aids are urea, sodium citrate, disodium phosphate, trisodium phosphate, sodium formate, sodium chloride, and similar compounds or mixtures of them.
  • the present invention provide dosage units of effective wound-helaing quantity of cartilage powder from a young animal, or from a mature animal, having average particle size between about 1 micron and about 40 microns, or a substantial maximum particle size of about 70 microns, incorporated into a clinically acceptable wound-healing carrier vehicle such as unguent, oil, salve, solution, extract, powder, etc.
  • a clinically acceptable wound-healing carrier vehicle such as unguent, oil, salve, solution, extract, powder, etc.
  • the invention also contemplates methods of enhancing the wound-healing activity of a cartilage powder and of restoring wound-healing activity in substantially inactivated cartilage powder including partially deactivated cartilage powder. Novel methods are also provided whereby finely divided cartilage powder may be stabilized before, during or after the final comminution stage of production thereof.
  • Various techniques for the extraction of active wound-healing components, agents, and compositions from cartilage powder are included within the present invention.
  • the cartilage powder as well as the extract were effective when they were absorbed or incorporated with surgical gauze which then was applied to the wound and when the same materials were applied by spraying onto the wound.
  • clinically acceptable carrier vehicles for the effective cartilage powder or extract such as salves based on aqueous gels such as those from alginates, gum tragacanth, gelatin, gluten, casein, polyvinylpyrrolidone, textran and many others are effective in many applications. They are also convenient to apply especially over large areas such as is the case with burns.
  • the effective cartilage powder or cartilage extracts suspended in oils such as tung oil, corn oil, olive oil, or linseed oil, may be applied directly to wounds.
  • oils such as tung oil, corn oil, olive oil, or linseed oil
  • the oil dispersions may be emulsified in water, forming oil-in-water type emulsions, or conversely, water may be emulsified in the oil dispersions forming water-in-oil type emulsions.
  • the cartilage and cartilage extracts dispersed in aqueous or oil carriers may be applied directly to the wounds by spraying, brushing, by impregnating in bandaging materials or by any other means which makes it possible to bring the cartilage or its extract into intimate contact with the tissues.
  • cartilage or cartilage extract preparations may be introduced subcutaneously, intra-muscularly, intravenously, or through suppositories introduced into rectal or other cavities.
  • Cartilage powders dispersed in suitable oils have been successfully administered orally.
  • Cartilage powder may be administered, as orally, in the form of pellets such as tablets or capsules.
  • the cartilage powder by incorporating the cartilage powder onto silica gel or other gel forming materials which are capable of coating the stomach walls, the rate of healing of stomach ulcers may be noticeably increased.
  • the invention has been used with humans in treatment of keloids (hardened scar tissue).
  • the keloid was initially cut out, and resutured in the presence of the calf cartilage powder of the invention. After more than six months periodic observation, the keloid did not reappear and apparently the invention prevented the re-formation of the keloid scar tissue, contrary to the usual experience of frequent recurrence of keloid formation.
  • the cartilage saline extract of this invention has also demonstrated a marked anti-inflammatory effect. For example, as when introduced parenterally in the areas affected by psoriasis, almost immediate reduction of the inflammation was observed.
  • the statistical average of scores of tests involving the application of the cartilage of the present invention shows that there were produced increases of over 50% in the tensile strengths of seven-day old midline abdominal wounds in rats.
  • the increase in wound-healing rate was even further enhanced when a combination of optimal size (between about 10 and about 30 microns average diameter) and optimal age of the cartilage source (calf) were combined, in an average of which cases maximal increase in wound tensile strength substantially higher than 50% was achieved.
  • Wound strength increase averaging 5 0% results in less likelihood of wound disaster, less likelihood of wound infection, the capability of removing sutures earlier with attendant further lessening the likelihood of infection as well as further acceleration in final wound-healing rate, thereby resulting in earlier discharge of the patient from care and safer post-care experience.
  • the cartilage treated wound ages in accordance with the present invention, it does not become a mass of essentially acellular collagen as does the cicatrix of the untreated wound. Instead, it continues to proliferate in humans actively up to 40 days after wound and frequently longer. It does not however, become hypertrophic or keloidal, and, in fact, appears less bulky than the corresponding control wounds.
  • the local use of the finely ground calf cartilage powder is of great clinical value in the treatment of non-granulating wounds of 50 different kinds, without untoward effects, either locally or systemically, as demonstrated in application to the primarily closed wounds of 87 human surgical incisions in a wide variety of procedures. There was no immediate or late evidence of antigenicity.
  • the cartilage preparations of the present invention have been successfully utilized to accelerate and to improve the healing of the following types of wounds, either by topical application or by injection of saline extract: chemical burns, third degree skin burns, radioactive injury, chest wall, abdominal and other wounds, operative and post-operative wounds, penetrating wounds such as those of thorax and abdomen, ulcers due to arteriosclerosis and to trophic disturbance, ulcers of skin, gangrene of skin due to trauma or physical agent or to undetermined cause, dermatitis, lupus erythematosus with ulcer, keloids, atopic eczema, parapsoriasis and psoriasis.
  • Other types of wounds also have responded successfully to the cartilage preparations of this invention with improved results.
  • the invention is especially useful in cases involving cortisone or other steroid treatment (known to retard healing) or involving diabetes.
  • the wound tensile strength at seven days is determined in millimeters of mercury by a modification of the technique of the method illustrated in the publication cited above.
  • the rat to be tested is killed by an intracardiac injection of paraldehyde or by exposure to toxic fumes such as to diethyl ether.
  • the test is made prior to the onset of rigor mortis.
  • a rubber latex prophylactic pouch is inserted into the peritoneal cavity through a defect made with a Kelly clamp in the apex of the vagina.
  • the rotary air pump connected to the pouch is turned on regulating it in such a manner that the air pressure will increase at a rate of millimeters of mercury every five seconds.
  • the pressure at which the wound splits and the pouch extrudes itself (wholly or in part) through the defect is recorded as the tensile strength of the wound. This is also a quantitive measure of the degree of healing or rate of healing achieved in the experiments.
  • Example 1 Cartilage pebble mill-ground
  • the tracheas of healthy adult beef cattle were removed within 30 to 60 minutes after the animals were slaughtered.
  • the tracheas were then either processed immediately with an acid-pepsin solution or they were frozen to preserve them, in which case the acid-pepsin digestion may be deferred.
  • the tracheas either fresh or previously frozen were then digested for about six hours at 50 C. in an loaded with one-inch size (average) flint pebbles in a weight ratio of 1 cartilage to 2 pebbles. Dry Ice (CO was then put on top of the mill charge and the mill was kept open for five minutes to allow the CO to displace the air in the mill.
  • CO Dry Ice
  • the lid of the mill was then clamped on tight and the mill rotated as is customary in the performance of the grinding operation, The grinding was carried out at about 20 C. for 96 hours.
  • the ground cartilage was screened through a 325 mesh nylon screen, thereby confining the active cartilage powder to particles less than about 40 microns in side, and having average or majority particle size between about 5 and 10 microns.
  • the cartilage was acid-pepsin digested as in Example 1, granulated, and then without drying was suspended in the extracting liquid and then transferred into a pebble mill which was charged to of its volume with flint pebbles of average size, one inch diameter.
  • the ratio of the cartilage to extracting liquid was kept to 25:75.
  • the liquid suspension was charged into the mill in a quantity just sufficient to fill the voids of the pebbles with the top of the pebbles barely covered by the liquid.
  • the air was then purged from the mill with nitrogen and the mill closed.
  • the mill was allowed to run for six hours at between 3 C. and 4 C. which resulted in a medium fine grinding of the cartilage and in the simultaneous extraction of the active wound-healing agent from the cartilage.
  • the mill was emptied, the fluid paste strained free of the pebbles, the fluid transferred into a centrifuge operated at 6000 r.p.rn. and at a temperature of between 3 C. and 4 C. After one-half hour the centrifuge was stopped and the supernatant liquid strained through a 400 mesh nylon screen. If the strained extract was cloudy, it was returned to the centrifuge and the centrifuging repeated until a clear slightly opalescent extract was obtained.
  • the extracts were stored at 4 C, preserved with 1: 10,- 000 sodium ethyl mercuri thiosalicylate.
  • Norm-The isotonic saline solution was prepared with distilled water and contained 0.9% NaOl.
  • acetic acid U.S.l glacial
  • pepsin NF. IX grade, 3500 activity
  • the cartilage was dried in vacuum 20 mm. mercury at 80 C. The dried cartilage was defatted by extracting it with a solvent, such as hexane. It was then granulated.
  • the granulated purified cartilage was ground to a fine
  • satisfactory powders may be obtained by ball milling, hammer milling in inert atmosphere. While ball or pebble milling the cartilage with the extracting liquid gives satisfactory results, other methods, such as mixing the cartilage powders in the liquids with a high speed, high shear, closed turbine mixer or passing the extraction mixture through a pressure homogenizer, preferably at pressures in excess of 4000 p.s.i., will also give extracts of high powder in a laboratory four-quart size porcelain jar mill, activity.
  • Example lApray-drying cartilage extracts Dry concentrates were prepared from cartilage extracts as follows:
  • a laboratory Bowen type spray-dryer was used with the following modifications. In place of the oil furnace, electric heating coils were used to supply the heat energy necessary for the evaporation of the volatile portions of the extracts. Instead of air, nitrogen was used for the hot gas. A vaned disc, rotating at about 20,000 r.p.m. was used to atomize the extracts. The inlet gas temperature was held to about 280 F., the outlet temperature was between 140 F. and 160 F. The dryer was used as a closed system dryer with the exclusion of oxygen to avoid degrading the active material during the evaporation of the water.
  • the solids percen means percent of solids in the extracting liquid as determined by drying at 100 C. for two hours.
  • Yield percent means the dry solids percent obtained from the liquid by the drying process.
  • the spray-dried powders were stored in tightly closed glass jars in a refrigerator at 4 C.
  • Example 4 Cartilage extracts applied to wound by swabbing to 5.75 cm. longitudinal midline abdominal incision of the female rat.
  • Thyreotrophic hormone 0.008 U.S.P. unit/mgm.
  • Example 7 This example demonstrates the value of reconstituted spray-dried and freeze-dried extracts in the healing of wounds.
  • the dried extracts were dissolved either in water or in isotonic saline solution, depending on the salt content of the original preparation. The solutions were adjusted to correspond with the solids content of the extracts from which the dried materials were prepared. The solutions were applied by parenteral injections into rats as in Example 5.
  • Example 8 This example demonstrates the value of intravenous injections of cartilage extracts or solutions of dried extracts in the healing of wounds. These were made on dogs with circular incisions. Wounds were not sutured but protected only with sterile dressing. The rate of healing was measured by observing the degree of granulation as compared with the control.
  • Rate of Extract wound healing (percent) 1. None-Isotonic saline-control 100 Example No.
  • Example '9 This example demonstrates the effect of applying liquid cartilage extracts on open wounds.
  • Porous fabric i.e. surgical gauze was saturated with the extracts and applied to the open and unsutured wounds while still wet. Tests were made on dogs. The rate of healing was measured by the observed degree of granulation.
  • Example 10 This example demonstrates the effect of applying dried cartilage extract on open wounds.
  • Porous fabric i.e. surgical gauze, was saturated with the extracts, dried to a moisture content of about at 30 C. and at a pressure of 50 mm. mercury. The dried gauze was applied to the open and unsutured wounds. Tests and observations were as in Example 9.
  • Rate of Cartilage extract wound healing (percent) 1. Noneisotonic saline-control Example No.
  • Example 11 These tests involved the intravenous injection of cartilage extracts combined with one or more blood extenders, such as whole blood, blood plasma, and a plasma substitute, namely polyvinylpyrrolidone or dextran. Tests were made on dogs. In carrying out these tests 100 cc. blood was taken from the animal and treated as follows:
  • the blood was mixed with 10 cc. cartilage extract and reinjected into the same animal.
  • the plasma was obtained from the blood mixed with 10 cc. cartilage extract and reinjected into the same animal from which the blood was obtained.
  • control animals were treated as follows:
  • Control -2 The blood taken as in case of Control 1, the plasma separated and reinjected into the same animal;
  • Control 3 The blood was taken from the animal as above in case of Control 1, and replaced with a saline solution of 3.5% polyvinylpyrrolidone viscosity type K-30.
  • Example 2- III 120 Example 21- 150 xample 21 145 Example 2]
  • Example 2p 150 Example 2p II
  • Example 2-p III 136 The animals used in these experiments weighed not less than 30 lbs. each.
  • Example 12.-Sterilization with an antiseptic alcohol 70% Mix the calf cartilage powder of the invention with an excess of about 70% (volume) ethyl alcohol. A sufiicient excess of alcohol is present when the cartilage powder forms a mobile slurry with the powder. The particle size of the powder controls the volume of alcohol required to form the mobile slurry. The smaller the particle size the larger the volume of alcohol is required.
  • the alcohol slurry of the cartilage powder is best mixed at a rate to keep the powder suspended in the liquid.
  • the cartilage swells somewhat and becomes gummy under the influence of the 70% alcohol.
  • the cartilage sediment mixed with the anhydrous alcohol, is dehydrated regaining substantially its original particle size and losing its gumminess. This dehydrated cartilage can be readily filtered and dries to a free flowing powder.
  • Example 13 Sterilization with isopropyl alcohol Anhydrous isopropyl alcohol sterilizes the cartilage as well as 70% ethyl alcohol and in about the same time, i.e., about 30 minutes, without swelling the cartilage particles or causing gumminess.
  • the cartilage slurry prepared with isopropyl alcohol can be readily filtered and the filter cake so obtained can be dried to a free flowing powder.
  • the sterilization either with ethyl alcohol or with isopropyl alcohol can be carried out satisfactorily at ambient room temperatures, although sterilization at elevated temperatures may reduce the time required.
  • Example 14 Stemilization of the cartilage powder by heat Cartilage powder of the invention, surprisingly, is
  • sterilized without loss of wound healing activity, by heating it to about 125-132 C. for 3-4 hours, substantially in the absence of air or oxygen.
  • Other temperatures as low as 110 C., may be utilized, but for longer periods of time to achieve sterilization.
  • the preferred procedure is to place the cartilage powder in a vessel with some Dry Ice over it and then covering the vessel loosely with a metal foil.
  • the vessel is placed in a vacuum oven, then oven is connected with a vacuum pump and the air is evacuated to a vacuum of about 10 mm. of mercury.
  • the oven is then heated to about 127 C. and held there for about four hours.
  • the heat sterilized powder is ready for clinical use.
  • Example 15 Reactivation and enhancement of cartilage by heat in the absence of oxygen This example illustrates lowering of the activity of calf cartilage powder when milled in the presence of air, and air together with heat, respectively, followed by the restoration and further enhancement of the wound-healing activity when the partially or totally inactivated material is exposed to heat of about 127 C. for between 5 hours to 50 hours and in the virtual absence of air or oxygen (Tests 6 and 8).
  • the cartilage powder was inactivated by hammer milling it under conditions of excessive aeration and some generation of heat (Test 5).
  • the activity of the cartilage was lowered to about one-third of its activity by ball milling it in the presence of air (Test 7), as compared with the same material ball milled in a C atmosphere (Test 4).
  • the heating of the cartilage was done in the following manner: A vacuum oven (Freas, Size No. 504, Fisher Scientific Co.) was loaded with the cartilage powder and with a small quantity of Dry Ice (solid CO About 15 to 25 grams of the Dry Ice were placed in an open dish in the oven. The door of the oven was closed, the air evacuated to about 10 mm. pressure, the vacuum pump was disconnected, and the heating cycle started. During heating there was some pressure build-up in the oven caused by the expansion of the Dry Ice as it becomes gaseous carbon dioxide.
  • Rate of wound (7) Calf cartilage, Lot 2AX, ball milled in air (8) #7, heated in CO for /2 hrs., 127
  • test results were based on 20 to over 40 pairs of animals (Sherman strain albino rats) for each of the eight tests enumerated above and the percent figure represents the statistical average of all such tests.
  • Comparison of Test 3 with Test 2 shows that heat sterilization of the powder of this invention may be accomplished together with enhancement (130.5 vs. 127.7%) of wound healing rate.
  • Comparison of Test 5 with Test 4 shows that highly effective powder of this invention may be completely deactivated by hammer-milling air with heat generation.
  • Comparison of Test 8 with Test 7 shows that heating of the degraded powder of Test 7 in CO at elevated temperature reactivates the material to a highly effective rate of wound healing.
  • Example 16 Forty wounds involving a wide spectrum of human chronic non-healing types of ulcers were treated according to the present invention.
  • the wound was thoroughly cleansed with hydrogen peroxide, and washed with alcohol. It was dried with gauze.
  • the cartilage preparation was applied by atomizing the powder onto the surface and into the wound. In 38 of the 40 cases this treatment resulted in the transformation of the wound surface from a non-granulating, sluggish, dirty grey surface to a typical pink, healthy granulating bed within ten days. In the other two cases a somewhat longer time was required.
  • Example 17 The cartilage powder of the invention was atomized into 83 surgical wounds in 39 human patients with 47 operations, as follows:
  • Example 18 Calf tracheal cartilage powder having maximum particle size of 40 microns was mixed with about an equal part of anhydrous propylene glycol. This premix was 13 then added to Neobase (an ointment base made by Burroughs -Wellcome & Co. of Tuckahoe, N.Y.) which contains the following ingredients:
  • Example 19 An ointment particularly useful with surgical gauze was formulated by mixing the following:
  • This ointment is useful in certain dermatological applications and the physical properties may be further adjusted and controlled by varying the ratios of the polyethylene glycols or adding required amounts of propylene glycol and/or glycerol.
  • cartilage with substantially greater potency is obtained from the skeletons of very young animals.
  • the highest potency material is generally obtained from animals less than one month old, although cartilage from adolescent animals taken before maturity may be used in this invention without excessively fine grinding. Young animals are intended to mean those which are still adolescent and have not yet reached maturity. Cartilage from foetal skeletons is often effective.
  • Finely divided cartilage from other mammals, in addition to bovine and porcine and canine, is effective in healing wounds in accordance with the present invention: for example, finely divided cartilage powder from rat trachea and the human knee have been successfully utilized in accordance with the invention; so also with other animals such as the finely divided cartilage of birds, fish, jaw-bone of shark, rib cage of a crocodile (South American caiman known to be one year old, as obtained from the New York City Zoological Gardens, in early adolescence). Finely divided reptile cartilage is particularly elfective in view of the extraordinary ability of the reptiles to regenerate their tissues and even their limbs.
  • the cartilage powder may be dusted on the wound or atomized on it. It may also be applied in the form of ointment on the wound, as exemplified above.
  • the extract may also be applied directly to the wound by spraying it on the wound, swabbing it on, or brushing it on. Both the powder and the extract may be applied first to an absorbent medium which is then applied to the wound and held on by a bandage or adhesive tape, or other suitable means.
  • the cartilage or the extract may be incorporated into tablets, capsules or suppositories and applied orally, rectally or in the vaginal or uteral passages. Implantation as pellets and injection of solution of the extract of the invention has been effective.
  • Cartilage extracts may be injected subcutaneously, intramuscularly or intravenously.
  • the dried extracts may be used as powders or they may be reconstituted and used as the original extracts.
  • the wounds to which the active materials are applied may be sutured or may be left open without materially affecting the rate of healing.
  • the active materials may be administered once, preferably within the first 24 hours of the incision; or they may be applied before the incision or they may be applied in several applications in succession. Irradiating the cartilage powder with ultraviolet radiation in the absence of oxygen increases its activity.
  • the improvement which consists of the steps of (1) mixing, at a rate to keep the powder suspended in the liquid, such dried ground extracted cartilage powder, with a sufiicient excess of ethyl alcohol to form a mobile slurry, in which the cartilage swells and becomes somewhat gummy and is difficult to filter and forms a hard crust when dried, which has then to be ground to the original particle size; (2) centrifuging the slurry to form a firm cartilage sediment; (3) decanting the supernatant liquid and replacing References Cited UNITED STATES PA

Description

United States Patent M 3,476,855 STERILIZING AND ENHANCING ACTIVITY OF A FINELY DIVIDED CARTILAGE POWDER Leslie L. Balassa, Blooming Grove, N.Y. 10914 No Drawing. Original application Feb. 26, 1965, Ser. No. 435,693, now Patent No. 3,400,199, dated Sept. 3, 1968. Divided and this application Jan. 17, 1968, Ser. No. 698,426
Int. Cl. A61k 1 7/ 00, 27/00 U.S. Cl. 424-95 3 Claims ABSTRACT OF THE DISCLOSURE This application is a division of my copending application Ser. No. 435,693 filed Feb. 26, 1965, now U.S. Patent No. 3,400,199 issued Sept. 3, 1968.
It was observed some time ago that the healing of wounds of human patients is inhibited or retarded if the patients were at the same time undergoing cortisone treatment. It was found further that this inhibition of the healing of the wounds could be overcome in some instances by the use of cartilage powder applied locally.
It has also been shown that the healing of wounds has sometimes been accelerated by the use of rather coarse, hand-ground powder of acid-pepsin digested adult bovine tracheal cartilage having maximum particle size of about 400-450 microns. Experiments were carried out on albino Sherman strain female rats. There was observed a maximum average increase in the rate of healing and in the strength of the healed tissues of about 20% over that of the control animals, the control animals being those with wounds untreated.
One of the problems involved in healing wounds has long been recognized as occurring in a primarily closed incision. When a composition is applied to such a wound, any excess in amount of such application at least initially produces a negative effect, which has sometimes been called the interposition effect. This is the reduction in tensile strength observed when any substance is placed into a primarily closed Wound, even in very small amounts. In the test data reported in this specification where the negative results are reported for prior art compositions such as gelatin, talc, collagen, etc., as well as when the compositions of this invention had been deactivated or degraded by one process or another, it appears that a major contributing factor to the negative results has been the interposition effect. Thus, when the active composition of the invention demonstrates any improvement in the rate of wound-healing, it should be remembered that the improvement has occurred in spite of the initial handicap of the interposition effect which must be overcome. Similarly, care must be exercised to avoid the use of excess quantities of the material of the present invention, to reduce the initial interposition effect in topical applications.
Investigation has been made of many compositions in the past, among them chondroitin sulfate, chondromucoprotein, carregheenan and collagen, and in every instance 3,476,855 Patented Nov. 4, 1969 these have yielded no wound-healing effect whatever. Most have given small negative results, probably as a result of the interposition effect. Other compounds tested including local hyaluronic acid, glucuronic acid, n-acetylglucosamine, and lysozyme were tested for wound-healing activity without significanteffect. For example, parenteral injections on rats of the last three named substances were given on the first post-operative day. This time was chosen since it is on this day that injections of a saline extract of the cartilage of this invention have been shown to be effective. The local applications were at the same density as has been employed for such cartilage preparations (2 4 mg./cm. of wound surface), while the parenteral injections were made from 5% solutions and were 2 cc. and 5 cc. in volume. All these tests were without any significant positive result.
I have now found that the particle size of the cartilage used has a surprisingly profound effect on the rate of healing'gand on the strength of the healed tissues. Not only is the ,rate of healing increased as the particle size of the cartilage is decreased, but also the manner or the process by which the cartilage is pulverized and the conditions prevailing during the pulverizing have a profound bearing on the results obtained with the cartilage powder. The effectiveness of the present invention has been demonstrated in comparative tests to be highly superior to results obtained on animals treated with either collagen, car ragbeenan, chondroitin sulfate, chondromucoprotein, fibrinogen, gelatin, talc, bone flour or systemic d methionine. I have also found methods of further increasing the wound-healing activity of the effective powders of this invention and methods of reactivating such powders after they have been inadvertently deactivated or otherwise reduced in activity.
Furthermore, I found most unexpectedly that cartilage taken from the partly calcified skeletons (including foetal skeletons) of very young or newly born animals is much more effective in accelerating the healing of wounds than was the case with the bovine tracheal cartilage powder on which previous observations were based, which included substantial quantities of coarse adult cartilage powder. Preferably the young animal is not over six months old.
While the present invention relates preferably to young cartilage, i.e. from young animals or young or newly regenerated cartilage from older animals as reptiles, whether finely divided or not, and cartilage from mature animals in finely divided (average particle size 40 microns or less) particle form, it is to be understood that the invention encompasses such cartilage in either the form which would in maturity retain the cartilaginous form or which would in maturity ossify to bone.
The cartilage may be prepared by any suitable means to result in a product which is essentially pure cartilage substance free from adhering tissue, which may have been removed by acid-pepsin or other suitable enzyme treatment, with or without mechanical assistance, or otherwise.
I have succeeded in preparing highly effective extracts by the use of aqueous solutions of materials which are in the pH range of about 6.5 to 10, and preferably between 5 and 8, at the concentrations employed in preparing the extracts. I prefer to use as extraction aids those which are either volatile and therefore can be readily removed from the extract by volatilization such as for example ammonia or ammonium carbonate, or such materials which it remaining in the extract would cause no harm is applied either topically or introduced parenterally. Dialysis may be employed to remove undesired salts or other dialyzable material which may be present. Other extraction aids are urea, sodium citrate, disodium phosphate, trisodium phosphate, sodium formate, sodium chloride, and similar compounds or mixtures of them.
I succeeded in concentrating the extracts and even obtained dry extracts of substantially unimpaired activity and which could be redissolved or diluted back to the original strength with saline solution by concentrating the extracts in vacuum at low temperature or by freeze-drying them. subjecting the cartilage or the cartilage powder or the extracts of the invention to irradiation by ultraviolet light for a short period of time may increase the activity of the material to a noticeable degree. Irradiation with ionizing radiation such as gamma rays may also increase the activity of the cartilage.
I have found a surprising synergistic effect in the combination of cartilage powder or cartilage extract of the invention with growth hormone. This effect can be ob served both in topical and in parenteral applications.
I succeeded in obtaining satisfactory effects through oral administration of suitably pelletized or encapsulated cartilage powder or cartilage extracts of the invention.
The present invention provide dosage units of effective wound-helaing quantity of cartilage powder from a young animal, or from a mature animal, having average particle size between about 1 micron and about 40 microns, or a substantial maximum particle size of about 70 microns, incorporated into a clinically acceptable wound-healing carrier vehicle such as unguent, oil, salve, solution, extract, powder, etc. The invention also contemplates methods of enhancing the wound-healing activity of a cartilage powder and of restoring wound-healing activity in substantially inactivated cartilage powder including partially deactivated cartilage powder. Novel methods are also provided whereby finely divided cartilage powder may be stabilized before, during or after the final comminution stage of production thereof. Various techniques for the extraction of active wound-healing components, agents, and compositions from cartilage powder are included within the present invention.
I found that there were very great differences in the activity of the preparations, depending on the method used in their preparation, the auxiliaries or carrier employed, and in the technique of application. For example, the cartilage powder as well as the extract were effective when they were absorbed or incorporated with surgical gauze which then was applied to the wound and when the same materials were applied by spraying onto the wound. Also, clinically acceptable carrier vehicles for the effective cartilage powder or extract, such as salves based on aqueous gels such as those from alginates, gum tragacanth, gelatin, gluten, casein, polyvinylpyrrolidone, textran and many others are effective in many applications. They are also convenient to apply especially over large areas such as is the case with burns.
The effective cartilage powder or cartilage extracts suspended in oils such as tung oil, corn oil, olive oil, or linseed oil, may be applied directly to wounds. The oil dispersions may be emulsified in water, forming oil-in-water type emulsions, or conversely, water may be emulsified in the oil dispersions forming water-in-oil type emulsions. The cartilage and cartilage extracts dispersed in aqueous or oil carriers may be applied directly to the wounds by spraying, brushing, by impregnating in bandaging materials or by any other means which makes it possible to bring the cartilage or its extract into intimate contact with the tissues. In the case of parenteral applications the cartilage or cartilage extract preparations may be introduced subcutaneously, intra-muscularly, intravenously, or through suppositories introduced into rectal or other cavities. Cartilage powders dispersed in suitable oils have been successfully administered orally. Cartilage powder may be administered, as orally, in the form of pellets such as tablets or capsules. n the other hand, by incorporating the cartilage powder onto silica gel or other gel forming materials which are capable of coating the stomach walls, the rate of healing of stomach ulcers may be noticeably increased.
The invention has been used with humans in treatment of keloids (hardened scar tissue). The keloid was initially cut out, and resutured in the presence of the calf cartilage powder of the invention. After more than six months periodic observation, the keloid did not reappear and apparently the invention prevented the re-formation of the keloid scar tissue, contrary to the usual experience of frequent recurrence of keloid formation.
The cartilage saline extract of this invention has also demonstrated a marked anti-inflammatory effect. For example, as when introduced parenterally in the areas affected by psoriasis, almost immediate reduction of the inflammation was observed.
The statistical average of scores of tests involving the application of the cartilage of the present invention shows that there were produced increases of over 50% in the tensile strengths of seven-day old midline abdominal wounds in rats. The increase in wound-healing rate was even further enhanced when a combination of optimal size (between about 10 and about 30 microns average diameter) and optimal age of the cartilage source (calf) were combined, in an average of which cases maximal increase in wound tensile strength substantially higher than 50% was achieved. Wound strength increase averaging 5 0% results in less likelihood of wound disaster, less likelihood of wound infection, the capability of removing sutures earlier with attendant further lessening the likelihood of infection as well as further acceleration in final wound-healing rate, thereby resulting in earlier discharge of the patient from care and safer post-care experience.
Furthermore, as the cartilage treated wound ages in accordance with the present invention, it does not become a mass of essentially acellular collagen as does the cicatrix of the untreated wound. Instead, it continues to proliferate in humans actively up to 40 days after wound and frequently longer. It does not however, become hypertrophic or keloidal, and, in fact, appears less bulky than the corresponding control wounds. These observations point to the presence of inhibitory activity in the cartilage of the invention, in addition to the acceleratory factor.
The local use of the finely ground calf cartilage powder is of great clinical value in the treatment of non-granulating wounds of 50 different kinds, without untoward effects, either locally or systemically, as demonstrated in application to the primarily closed wounds of 87 human surgical incisions in a wide variety of procedures. There was no immediate or late evidence of antigenicity.
Controlled tensiometric observations in 15 human volunteers utilizing in each instance paired incisions in the same individual with tensiometry from 7 to 14 days after wounding have shown that the wound treated therein locally with the cartilage preparation of the present invention has been so much stronger than the untreated wounds as to exhibit a measured mean positive differential of approximately 50% over the control value.
The cartilage preparations of the present invention have been successfully utilized to accelerate and to improve the healing of the following types of wounds, either by topical application or by injection of saline extract: chemical burns, third degree skin burns, radioactive injury, chest wall, abdominal and other wounds, operative and post-operative wounds, penetrating wounds such as those of thorax and abdomen, ulcers due to arteriosclerosis and to trophic disturbance, ulcers of skin, gangrene of skin due to trauma or physical agent or to undetermined cause, dermatitis, lupus erythematosus with ulcer, keloids, atopic eczema, parapsoriasis and psoriasis. Other types of wounds also have responded successfully to the cartilage preparations of this invention with improved results. For example, the invention is especially useful in cases involving cortisone or other steroid treatment (known to retard healing) or involving diabetes.
Test methods: Unless otherwise stated, the effectiveness of the preparations of the examples herein was established in animal tests as described by J. Prudden, G. Nishihara and L. Baker in The Acceleration of Wound Healing with Cartilage-I, Surgery, Gynecology & Obstetrics, 105: 283 (1957).
Sherman strain albino female rats were employed in the tests. The preparation consisted of 5.5 centimeter midline abdominal incision under controlled conditions and closed with interrupted through-and-through sutures of No. 000 silk.
The wound tensile strength at seven days is determined in millimeters of mercury by a modification of the technique of the method illustrated in the publication cited above.
The rat to be tested is killed by an intracardiac injection of paraldehyde or by exposure to toxic fumes such as to diethyl ether. The test is made prior to the onset of rigor mortis. After the sutures have been removed from the wound, a rubber latex prophylactic pouch is inserted into the peritoneal cavity through a defect made with a Kelly clamp in the apex of the vagina. After the rubber pouch is in place, and the introitus has been snugged firmly (with a hemostat) around the tube leading to theperitoneal cavity, the rotary air pump connected to the pouch is turned on regulating it in such a manner that the air pressure will increase at a rate of millimeters of mercury every five seconds. The pressure at which the wound splits and the pouch extrudes itself (wholly or in part) through the defect is recorded as the tensile strength of the wound. This is also a quantitive measure of the degree of healing or rate of healing achieved in the experiments.
The following examples illustrate certain present preferred embodiments of the invention, and it isunderstood that other methods and embodiments within the spirit of the invention may be made without departing from the scope of the appended claims. Parts and ratios are bv weight except as otherwise stated.
Example 1.-Cartilage pebble mill-ground The tracheas of healthy adult beef cattle were removed within 30 to 60 minutes after the animals were slaughtered. The tracheas were then either processed immediately with an acid-pepsin solution or they were frozen to preserve them, in which case the acid-pepsin digestion may be deferred. The tracheas either fresh or previously frozen were then digested for about six hours at 50 C. in an loaded with one-inch size (average) flint pebbles in a weight ratio of 1 cartilage to 2 pebbles. Dry Ice (CO was then put on top of the mill charge and the mill was kept open for five minutes to allow the CO to displace the air in the mill. The lid of the mill was then clamped on tight and the mill rotated as is customary in the performance of the grinding operation, The grinding was carried out at about 20 C. for 96 hours. The ground cartilage was screened through a 325 mesh nylon screen, thereby confining the active cartilage powder to particles less than about 40 microns in side, and having average or majority particle size between about 5 and 10 microns.
Example 2.Preparation of cartilage extracts in the pebble mill Extracts of cartilage having high wound-healing activity were produced as follows:
The cartilage was acid-pepsin digested as in Example 1, granulated, and then without drying was suspended in the extracting liquid and then transferred into a pebble mill which was charged to of its volume with flint pebbles of average size, one inch diameter. The ratio of the cartilage to extracting liquid was kept to 25:75. The liquid suspension was charged into the mill in a quantity just sufficient to fill the voids of the pebbles with the top of the pebbles barely covered by the liquid. The air was then purged from the mill with nitrogen and the mill closed. The mill was allowed to run for six hours at between 3 C. and 4 C. which resulted in a medium fine grinding of the cartilage and in the simultaneous extraction of the active wound-healing agent from the cartilage.
At the end of the six-hour cycle, the mill was emptied, the fluid paste strained free of the pebbles, the fluid transferred into a centrifuge operated at 6000 r.p.rn. and at a temperature of between 3 C. and 4 C. After one-half hour the centrifuge was stopped and the supernatant liquid strained through a 400 mesh nylon screen. If the strained extract was cloudy, it was returned to the centrifuge and the centrifuging repeated until a clear slightly opalescent extract was obtained.
The extracts were stored at 4 C, preserved with 1: 10,- 000 sodium ethyl mercuri thiosalicylate.
The following extracts were thus prepared:
Total Solids of Clear Extrapt lily ei t Cartilage Source Extracting Liquid pmfint (2.) Bovine tracheal Distilled water 1,3 (b) Bovine tracheal Isotonic saline sol 5, 2 (0) Bovine tracheal Ammonia (28%) 1% in water 6, 5 (d) Bovine tracheal. 2% Urea in water. 9, 6 (e) Bovine tracheal. 1% Ammonium carbonate in water. 6, 4 (i) Bovine tracheal. 1% Disodium phosphate in water 6, 3 (g) Bovine tracheal- 3% Ammonium carbonate in water 7, 2 (h) Bovine tracheal. 1% Trisodium phosphate in water. 7, 6 (i) Bovine tracheal 1% Sodium citrate in water 7, 0 (j) Bovine tracheal 3% Sodium citrate in water. 9, 2 (k) Bovine tracheal 1% Sodium formate in water. 8. 2 (l) Piglet 1 day old. Isotonie saline solution 6, 4 (m) Piglet 1 day old-- 1% Ammonia (28%) in water 7, 1 (n) P glet 1 day old-.- 3% Ammonium carbonate in water 8, 1 (o) Piglet 1 day old. 3% Sodium citrate in water 10.0 (p) Cali 1 day old Isotonic saline solution 6, 2 (q) Call 1 day old 1% Ammonia (28%) in water 7. 3 (r) Cali 1 day old Isotonic saline solution plus ammonia to pH 8... 8. 2
Norm-The isotonic saline solution was prepared with distilled water and contained 0.9% NaOl.
aqueous solution containing 0.6% acetic acid (U.S.l glacial) and 0.3% pepsin (NF. IX grade, 3500 activity). After digestion the tracheal cartilage was removed from the acid-pepsin solution, washed first with water of about C. and then with water of about 25 C. until the effluent wash water showed no trace of pepsin or acetic acid. The cartilage was dried in vacuum 20 mm. mercury at 80 C. The dried cartilage was defatted by extracting it with a solvent, such as hexane. It was then granulated.
The granulated purified cartilage was ground to a fine In addition to pebble mill and fluid energy mill grinding, satisfactory powders may be obtained by ball milling, hammer milling in inert atmosphere. While ball or pebble milling the cartilage with the extracting liquid gives satisfactory results, other methods, such as mixing the cartilage powders in the liquids with a high speed, high shear, closed turbine mixer or passing the extraction mixture through a pressure homogenizer, preferably at pressures in excess of 4000 p.s.i., will also give extracts of high powder in a laboratory four-quart size porcelain jar mill, activity.
Example lApray-drying cartilage extracts Dry concentrates were prepared from cartilage extracts as follows:
A laboratory Bowen type spray-dryer was used with the following modifications. In place of the oil furnace, electric heating coils were used to supply the heat energy necessary for the evaporation of the volatile portions of the extracts. Instead of air, nitrogen was used for the hot gas. A vaned disc, rotating at about 20,000 r.p.m. was used to atomize the extracts. The inlet gas temperature was held to about 280 F., the outlet temperature was between 140 F. and 160 F. The dryer was used as a closed system dryer with the exclusion of oxygen to avoid degrading the active material during the evaporation of the water.
The following dry extracts were thus produced.
Appearance Solids Yield of ried Extract Used percent percent Powder a Example 2b- 5. 2 4. 8 S1. yellow. (10 Example 2c 6.5 6.2 D0. Example 2h 7. 6 7. 3 Do (d) Example 2-j 9. 2 8. 9 Ofi white. (e). Example 2-1. 6. 4 6. 2 S1. yellow. (f) Example 2-m. 7. 1 6.8 Do. (g) Example 2o 10. 0 9. 8 Ofi white. (h). Example 2p 6. 2 6.0 $1. yellow. (i) Example 2q 7.3 7. 1 D0. (j) Example 2-1'. 8. 2 8.0 Do.
The solids percen means percent of solids in the extracting liquid as determined by drying at 100 C. for two hours.
Yield percent means the dry solids percent obtained from the liquid by the drying process.
The spray-dried powders were stored in tightly closed glass jars in a refrigerator at 4 C.
Example 4 Cartilage extracts applied to wound by swabbing to 5.75 cm. longitudinal midline abdominal incision of the female rat.
Rate of wound Cartilage extract (liquid): healing (percent) 1. None-isotonic sa1inecontr0l 100 Example No.- 2 2 a 100 3 2.1) 125 4. 2-c 125 5. 2-d 125 6 2-e 125 7 2-f 130 8 2-g 115 9. 2-h 130 10. Z-i 130 11. 2-j 130 12. 2-k 135 13. 2-1 140 14. 2-m 140 15. 2-n 130 16. 20 135 17. 2-p 140 18. 2-q 145 19. 2-r 150 Example The effect of parenterally injected cartilage extracts on the healing of wounds. In each case 5 cc. of the extract was injected into the subcutaneous tissue on the rats back within 24 hours after the abdominal incision.
injected cartilage extracts combined with a bovine growth hormone. In each case 5 cc. of the extract was mixed with 10 mgm. of a bovine growth hormone, distributed by the Endocrinology Study Section of the National Institutes of Health through the pituitary hormone distribution program. Approximately assay of the growth hormone:
Adenocorticotrophic hormone-0.06 U.S.P. milliunit/ mgm.;
Prol-actin-O.l International unit/mgm.;
Vasopressin0.01 U.S.P. unit/mgm.;
Thyreotrophic hormone-0.008 U.S.P. unit/mgm.;
Oxytocin0.008 U.S.P. unit/mgm.;
Test animals and wounds are as stated in Example 5.
Rate of wound Cartilage extract (liquid): healing (percent) 1. None-isotonic saline-control 2. None-isotonic saline with growth hormone control 108 Example No. (with growth hormone) 3. 2-a 110 4. 2-b 130 5. 2-f 135 6. 2-i 135 7. 2-1 145 8. 2-p 145 9. 2*! Example 7 This example demonstrates the value of reconstituted spray-dried and freeze-dried extracts in the healing of wounds. The dried extracts were dissolved either in water or in isotonic saline solution, depending on the salt content of the original preparation. The solutions were adjusted to correspond with the solids content of the extracts from which the dried materials were prepared. The solutions were applied by parenteral injections into rats as in Example 5.
Rate of Wound Healing Dried Extract Solvent Percent (1). None Isotonlc saline-control. 100 g; Example 3a Wate (4) Example 3-e (5) Example 3-h .d0 (6) Example 3-] -do 140 Example 8 This example demonstrates the value of intravenous injections of cartilage extracts or solutions of dried extracts in the healing of wounds. These were made on dogs with circular incisions. Wounds were not sutured but protected only with sterile dressing. The rate of healing was measured by observing the degree of granulation as compared with the control.
Rate of Extract: wound healing (percent) 1. None-Isotonic saline-control 100 Example No.
Example '9 This example demonstrates the effect of applying liquid cartilage extracts on open wounds. Porous fabric, i.e. surgical gauze was saturated with the extracts and applied to the open and unsutured wounds while still wet. Tests were made on dogs. The rate of healing was measured by the observed degree of granulation.
Example 10 This example demonstrates the effect of applying dried cartilage extract on open wounds. Porous fabric, i.e. surgical gauze, was saturated with the extracts, dried to a moisture content of about at 30 C. and at a pressure of 50 mm. mercury. The dried gauze was applied to the open and unsutured wounds. Tests and observations were as in Example 9.
Rate of Cartilage extract: wound healing (percent) 1. Noneisotonic saline-control Example No.
Example 11 These tests involved the intravenous injection of cartilage extracts combined with one or more blood extenders, such as whole blood, blood plasma, and a plasma substitute, namely polyvinylpyrrolidone or dextran. Tests were made on dogs. In carrying out these tests 100 cc. blood was taken from the animal and treated as follows:
I. The blood was mixed with 10 cc. cartilage extract and reinjected into the same animal.
II. The plasma was obtained from the blood mixed with 10 cc. cartilage extract and reinjected into the same animal from which the blood was obtained.
III. The blood was replaced by an equal volume of an isotonic aqueous saline solution of polyvinylpyrrolidone 3.5%, viscosity grade K-30 and 10 cc. of a cartilage extract.
The control animals were treated as follows:
Control 1.100 cc. blood taken and then reinjected into the same animal;
Control -2.-The blood taken as in case of Control 1, the plasma separated and reinjected into the same animal;
Control 3.-The blood was taken from the animal as above in case of Control 1, and replaced with a saline solution of 3.5% polyvinylpyrrolidone viscosity type K-30.
Note: All blood samples taken were citrated to prevent coagulation. The rate of heating was measured by the observed degree of granulation.
Rate of Healing,
Cartilage Extract Test as per Percent (1). None, Control 1 2 one, Control 2 90 None, Control 3 85 Example 2b.. 130
Example 2b..
Example 2- III 120 Example 21- 150 xample 21 145 Example 2] Example 2p 150 Example 2p II Example 2-p III 136 The animals used in these experiments weighed not less than 30 lbs. each.
Example 12.-Sterilization with an antiseptic alcohol 70% Mix the calf cartilage powder of the invention with an excess of about 70% (volume) ethyl alcohol. A sufiicient excess of alcohol is present when the cartilage powder forms a mobile slurry with the powder. The particle size of the powder controls the volume of alcohol required to form the mobile slurry. The smaller the particle size the larger the volume of alcohol is required.
In general, 2 ml. alcohol mixed with each gram of a 30-micron average particle size cartilage powder is well in excess of the minimum required to form the slurry.
The alcohol slurry of the cartilage powder is best mixed at a rate to keep the powder suspended in the liquid. The cartilage swells somewhat and becomes gummy under the influence of the 70% alcohol.
In about 30 minutes the cartilage is sterilized by the alcohol. However, this sterilized cartilage, due to its swollen condition and gummy character, is difficult to filter and forms a hard crust when dried. This hard crust has then to be re-ground to the original particle size.
The difficulties caused by the swelling and gummy nature of the sterilized cartilage can be overcome by centrifuging the slurry to form a firm cartilage sediment, decanting the supernatant liquid and replacing it with anhydrous alcohol.
The cartilage sediment, mixed with the anhydrous alcohol, is dehydrated regaining substantially its original particle size and losing its gumminess. This dehydrated cartilage can be readily filtered and dries to a free flowing powder.
Example 13.Sterilization with isopropyl alcohol Anhydrous isopropyl alcohol sterilizes the cartilage as well as 70% ethyl alcohol and in about the same time, i.e., about 30 minutes, without swelling the cartilage particles or causing gumminess.
The cartilage slurry prepared with isopropyl alcohol can be readily filtered and the filter cake so obtained can be dried to a free flowing powder.
The sterilization either with ethyl alcohol or with isopropyl alcohol can be carried out satisfactorily at ambient room temperatures, although sterilization at elevated temperatures may reduce the time required.
Example 14.-Sterilization of the cartilage powder by heat Cartilage powder of the invention, surprisingly, is
sterilized, without loss of wound healing activity, by heating it to about 125-132 C. for 3-4 hours, substantially in the absence of air or oxygen. Other temperatures, as low as 110 C., may be utilized, but for longer periods of time to achieve sterilization.
The preferred procedure is to place the cartilage powder in a vessel with some Dry Ice over it and then covering the vessel loosely with a metal foil. The vessel is placed in a vacuum oven, then oven is connected with a vacuum pump and the air is evacuated to a vacuum of about 10 mm. of mercury. The oven is then heated to about 127 C. and held there for about four hours.
It is important that the entire mass of material in the vessel be heated through and maintained at about 125 to 132 C. for about three to four hours.
The heat sterilized powder is ready for clinical use.
Example 15.Reactivation and enhancement of cartilage by heat in the absence of oxygen This example illustrates lowering of the activity of calf cartilage powder when milled in the presence of air, and air together with heat, respectively, followed by the restoration and further enhancement of the wound-healing activity when the partially or totally inactivated material is exposed to heat of about 127 C. for between 5 hours to 50 hours and in the virtual absence of air or oxygen (Tests 6 and 8).
The cartilage powder was inactivated by hammer milling it under conditions of excessive aeration and some generation of heat (Test 5 The activity of the cartilage was lowered to about one-third of its activity by ball milling it in the presence of air (Test 7), as compared with the same material ball milled in a C atmosphere (Test 4).
The heating of the cartilage was done in the following manner: A vacuum oven (Freas, Size No. 504, Fisher Scientific Co.) was loaded with the cartilage powder and with a small quantity of Dry Ice (solid CO About 15 to 25 grams of the Dry Ice were placed in an open dish in the oven. The door of the oven was closed, the air evacuated to about 10 mm. pressure, the vacuum pump was disconnected, and the heating cycle started. During heating there was some pressure build-up in the oven caused by the expansion of the Dry Ice as it becomes gaseous carbon dioxide.
Rate of wound (7) Calf cartilage, Lot 2AX, ball milled in air (8) #7, heated in CO for /2 hrs., 127
The above test results were based on 20 to over 40 pairs of animals (Sherman strain albino rats) for each of the eight tests enumerated above and the percent figure represents the statistical average of all such tests.
Comparison of Test 3 with Test 2 shows that heat sterilization of the powder of this invention may be accomplished together with enhancement (130.5 vs. 127.7%) of wound healing rate.
Comparison of Test 5 with Test 4 shows that highly effective powder of this invention may be completely deactivated by hammer-milling air with heat generation.
Comparison of Test 6 with Test 5 shows that the thus deactivated hammer-milled powder may be reactivated by prolonged heating as stated.
Comparison of Test 7 with Test 4 shows that ballmilling highly effective powder of the invention in air seriously lowers (from 137.2% to 110.9%) the rate of wound healing.
Comparison of Test 8 with Test 7 shows that heating of the degraded powder of Test 7 in CO at elevated temperature reactivates the material to a highly effective rate of wound healing.
Example 16 Forty wounds involving a wide spectrum of human chronic non-healing types of ulcers were treated according to the present invention.
The types of wounds treated were as follows:
No. of wounds (1) Chronic varicose ulcer on bedrest or after surgical correction of venous incompetency 16 (2) Chronic non-healing ulcers of the abdomen following wound disruption in cachectic patients with inoperable carcinoma 6 (3) Radiation ulcer l (4) Ulcers of the extremities in chronic ulcerative 'colitis (gangreneous pyoderma) 2 There was no particular sex or age distribution except that all were adults and none was older than 60 or younger than 25 years of age.
In each instance the local therapy was:
At the time of the dressing, the wound was thoroughly cleansed with hydrogen peroxide, and washed with alcohol. It was dried with gauze. The cartilage preparation was applied by atomizing the powder onto the surface and into the wound. In 38 of the 40 cases this treatment resulted in the transformation of the wound surface from a non-granulating, sluggish, dirty grey surface to a typical pink, healthy granulating bed within ten days. In the other two cases a somewhat longer time was required.
Example 17 The cartilage powder of the invention was atomized into 83 surgical wounds in 39 human patients with 47 operations, as follows:
CARTILAGE POWDER INSTILLA'IION IN CLOSED SURGICAL WOUNDS o. No. Type of operation Operations Wounds (1) Bilateral phlebectomies 7 43 (2) Cholecystectomy (with and without common duct drainage); right subeostal incision l5 5 (3) Gastrectomy linea alba incision 1 1 (4) Exploratory laparotomy for regional enteritis with emaciation and partial mechanical obstruction, midline incisionl 1 (5) Hysterectomy; midline incision 1 1 (6) Breast biopsy (circum-areolar). l 1 (7) Inguinal herniorrhaphy 22 22 (8) Cecotomy for excision villous adenoma (right lower abdominal oblique) l 1 (9) Lipomectomy 1 1 (10) Pilonidal cystectomy 1 1 (11) Small bowel resection for obstructing mesenterlc tumor metastic from pancreas (midline incision) 1 1 (12) Abdominoperineal resection for squamous cell carcinoma of anus (midline incision) 1 1 (13) Ventral herniorraphy 1 1 (14) Anterior resection of rectosigmoid (midline incision) r 1 1 (15) Resection terminal 30 in. of ileum proximal to ileostomy for regional ileitis; (reopening midline incision used for previous tote colectomy) 1 1 (16) Lysis of adhesions and vagectomy (midline) 1 1 Total Operations 47 Total Wounds 83 In all 83 cases there was primary healing of all wounds except for intermediate suture abscess formation which wsa followed by healing without event. In none of these cases was there any abnormal liver chemistry, disturbed renal function, or evidence of sensitivity to the material of the invention. In no case was the wound non-flexible, thick or keloidal and all wounds appeared to be more flexible and less bulky than normally expected.
Example 18 Calf tracheal cartilage powder having maximum particle size of 40 microns was mixed with about an equal part of anhydrous propylene glycol. This premix was 13 then added to Neobase (an ointment base made by Burroughs -Wellcome & Co. of Tuckahoe, N.Y.) which contains the following ingredients:
diluted with about 50% additional water in an amount to yield a composition having about 10% of said powder.
Thus, a useful wound healing or dermatological salve was formed, although it is to be understood that other ointments and salves and salve bases may incorporate the powder or extract of the present invention.
Example 19 An ointment particularly useful with surgical gauze was formulated by mixing the following:
Parts by Weight Ex. 19-A Ex. 19-B Polyethylene glycol, mol. wt. 4,000 5 Polyethylene glycol, mol. wt. 1,540 30 25 Polyethylene glycol, mol. wt. 300 60 60 Cartilage powder, maximum particle size 40p. 50
This ointment is useful in certain dermatological applications and the physical properties may be further adjusted and controlled by varying the ratios of the polyethylene glycols or adding required amounts of propylene glycol and/or glycerol.
While isotonic saline is an effective extraction medium, more complete extraction with higher healing activity is obtained when the pH is raised slightly with ammonia. Salts other than NaCl provide more elfective extraction, as shown in Example 2. An inert atmosphere during the extraction results in extracts of greater potency than when the extraction is carried out in the presence of oxygen. Since the presence of oxygen during processing has completely inactivated extracts of the cartilages herein shown otherwise to be vastly superior, the use of suitable known non-toxic anti-oxidants such as ascorbic acid or its salts or vitamin A may permit carrying out the extraction in the presence of some air without serious loss of potency.
Though bovine tracheal cartilage from mature animals, i.e., a year old or older, is for some purposes a satisfactory source, cartilage with substantially greater potency is obtained from the skeletons of very young animals. The highest potency material is generally obtained from animals less than one month old, although cartilage from adolescent animals taken before maturity may be used in this invention without excessively fine grinding. Young animals are intended to mean those which are still adolescent and have not yet reached maturity. Cartilage from foetal skeletons is often effective. Finely divided cartilage from other mammals, in addition to bovine and porcine and canine, is effective in healing wounds in accordance with the present invention: for example, finely divided cartilage powder from rat trachea and the human knee have been successfully utilized in accordance with the invention; so also with other animals such as the finely divided cartilage of birds, fish, jaw-bone of shark, rib cage of a crocodile (South American caiman known to be one year old, as obtained from the New York City Zoological Gardens, in early adolescence). Finely divided reptile cartilage is particularly elfective in view of the extraordinary ability of the reptiles to regenerate their tissues and even their limbs.
For example, young cartilage from the tail of a tegu salamander, which tail had regenerated for three months, obtained from the same zoo was used without excessively fine grinding in effective wound-healing experiments. Cartilage from the rib cage of young lambs taken prior to ossification was successfully utilized.
When dry cartilage extract is desired, freeze-drying is preferred, but spray-drying is satisfactory in inert atmosphere. Vacuum drying is satisfactory when oxygen is excluded and temperature of the liquid is held below 40 C.
The cartilage powder may be dusted on the wound or atomized on it. It may also be applied in the form of ointment on the wound, as exemplified above. The extract may also be applied directly to the wound by spraying it on the wound, swabbing it on, or brushing it on. Both the powder and the extract may be applied first to an absorbent medium which is then applied to the wound and held on by a bandage or adhesive tape, or other suitable means. The cartilage or the extract may be incorporated into tablets, capsules or suppositories and applied orally, rectally or in the vaginal or uteral passages. Implantation as pellets and injection of solution of the extract of the invention has been effective.
Cartilage extracts may be injected subcutaneously, intramuscularly or intravenously. The dried extracts may be used as powders or they may be reconstituted and used as the original extracts. The wounds to which the active materials are applied may be sutured or may be left open without materially affecting the rate of healing. The active materials may be administered once, preferably within the first 24 hours of the incision; or they may be applied before the incision or they may be applied in several applications in succession. Irradiating the cartilage powder with ultraviolet radiation in the absence of oxygen increases its activity.
While certain present preferred embodiments of the invention have been described and exemplified herein, it is to be understood that the invention may be otherwise embodied within the spirit thereof and within the scope of the appended claims.
What is claimed is:
1. In the method of sterilizing and enhancing activity of a finely divided cartilage powder having an average particle between about 1 micron and about 40 microns, and a substantial maximum particle size of about 70 microns, which has been aqueous-extracted from granulated defatted acid-pepsin digested essentially pure cartilage freed from adhering tissue, ground, and dried, in the virtual absence of oxygen, in closed-system extraction, grinding and drying means, the improvement which consists of the step of heat-sterilizing such dried ground extracted cartilage powder by heating thoroughly in the virtual absence of oxygen the entire mass of material in a closed-system heating means to about to about- 132 C., for three to four hours.
2. In the method of sterilizing and enhancing activity of a finely divided cartilage powder having an average particle size between about 1 micron and about 40 microns, and a substantial maximum particle size of about 70 microns, which has been aqueous-extracted from granulated defatted acid-pepsin digested essentially pure cartilage freed from adhering tissue, ground, and dried, in the virtual absence of oxygen, in close-system extraction, grinding and drying means, the improvement which consists of the step of sterilizing such dried ground extracted cartilage powder as a slurry with anhydrous isopropyl alcohol without substantially swelling the cartilage powders or causing gumminess.
3. In the method of sterilizing and enhancing activity of a finely divided cartilage powder having an average particle size between about 1 micron and about 40 microns, and a substantial maximum particle size of about 70 microns, which has been aqueous-extracted from granulated defatted acid-pepsin digested essentially pure 15 cartilage freed from adhering tissue, ground, and dried, in the virtual absence of oxygen, in closed-system extraction, grinding and drying means, the improvement which consists of the steps of (1) mixing, at a rate to keep the powder suspended in the liquid, such dried ground extracted cartilage powder, with a sufiicient excess of ethyl alcohol to form a mobile slurry, in which the cartilage swells and becomes somewhat gummy and is difficult to filter and forms a hard crust when dried, which has then to be ground to the original particle size; (2) centrifuging the slurry to form a firm cartilage sediment; (3) decanting the supernatant liquid and replacing References Cited UNITED STATES PATENTS 5/1967 Dingwall et al. 424-95 9/1968 Balassa 424-95 S. K. ROSE, Primary Examiner US. Cl. X.R. 2l2, 58, 93
*zggg UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION 3,476,855 November 4, 1969 Patent No. Dated Inventor-(s) LESLIE L. BALASSA It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 2, line 67, after "harm" for "is" read -if--. Col. 3, line 19, for "provide" read --provides--; line 20, for "helaing" read -healing. Column 8, line 21, for "Approximatel read -Approximate-. Column 10, line 72, for "then" read -the- Column 12, line 65, change "wsa" to -was-. Column 14, line 44 (claim 1) after "particle" insert --size--; line 64 (claim 2) f0. "close-system" read -closedsystem-.
SIGNED AND SEALED JUN161970 Amt:
Emirmm 1:. .m Atteatmg Offioor Oomissioner of Patents
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* Cited by examiner, † Cited by third party
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US3966908A (en) * 1973-11-29 1976-06-29 Lescarden Ltd. Method of treating degenerative joint afflictions
US4191747A (en) * 1976-12-17 1980-03-04 Hans Scheicher Corrective agent for the covering and/or filling of bone defects, method for the preparation of same and method of using the same
WO1980002501A1 (en) * 1979-05-11 1980-11-27 Lescarden Ltd Cartilage extraction processes and products
US4469676A (en) * 1983-06-21 1984-09-04 Michel Hecmati Method for eliminating wrinkles occurring in the human skin
US4486416A (en) * 1981-03-02 1984-12-04 Soll David B Protection of human and animal cells subject to exposure to trauma
WO1993010712A1 (en) * 1991-12-06 1993-06-10 The General Hospital Corporation Cartilage degradation assay system
US5360593A (en) * 1987-12-29 1994-11-01 Alcon Laboratories, Inc. Heat sterilization of labile antibiotics
US5733884A (en) * 1995-11-07 1998-03-31 Nestec Ltd. Enteral formulation designed for optimized wound healing
US20050288796A1 (en) * 2004-06-23 2005-12-29 Hani Awad Native soft tissue matrix for therapeutic applications
US20100241228A1 (en) * 2006-07-07 2010-09-23 Carina Syring Engineered osteochondral construct for treatment of articular cartilage defects
US20100274362A1 (en) * 2009-01-15 2010-10-28 Avner Yayon Cartilage particle tissue mixtures optionally combined with a cancellous construct
US20100322994A1 (en) * 2003-12-11 2010-12-23 Isto Technologies, Inc. Particulate cartilage system
US20110196508A1 (en) * 2003-04-29 2011-08-11 Katherine Gomes Truncale Cartilage repair mixture containing allograft chondrocytes
US20110224797A1 (en) * 2007-01-24 2011-09-15 Semler Eric J Two piece cancellous construct for cartilage repair
US8221500B2 (en) 2003-05-16 2012-07-17 Musculoskeletal Transplant Foundation Cartilage allograft plug
US8292968B2 (en) 2004-10-12 2012-10-23 Musculoskeletal Transplant Foundation Cancellous constructs, cartilage particles and combinations of cancellous constructs and cartilage particles
US8435551B2 (en) 2007-03-06 2013-05-07 Musculoskeletal Transplant Foundation Cancellous construct with support ring for repair of osteochondral defects
US8480757B2 (en) 2005-08-26 2013-07-09 Zimmer, Inc. Implants and methods for repair, replacement and treatment of disease
US8497121B2 (en) 2006-12-20 2013-07-30 Zimmer Orthobiologics, Inc. Method of obtaining viable small tissue particles and use for tissue repair
US8642061B2 (en) * 2007-06-15 2014-02-04 Warsaw Orthopedic, Inc. Method of treating bone tissue
US9138318B2 (en) 2007-04-12 2015-09-22 Zimmer, Inc. Apparatus for forming an implant
US9675645B2 (en) * 2013-01-22 2017-06-13 Warsaw Orthopedic, Inc. Method of preparing bone material having enhanced osteoinductivity
US9701940B2 (en) 2005-09-19 2017-07-11 Histogenics Corporation Cell-support matrix having narrowly defined uniformly vertically and non-randomly organized porosity and pore density and a method for preparation thereof
US10077420B2 (en) 2014-12-02 2018-09-18 Histogenics Corporation Cell and tissue culture container
US10167447B2 (en) 2012-12-21 2019-01-01 Zimmer, Inc. Supports and methods for promoting integration of cartilage tissue explants

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US3318774A (en) * 1961-03-15 1967-05-09 Squibb & Sons Inc Treatment of osseous and other tissue
US3400199A (en) * 1965-02-26 1968-09-03 Leslie L. Balassa Wound-healing cartilage powder

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3966908A (en) * 1973-11-29 1976-06-29 Lescarden Ltd. Method of treating degenerative joint afflictions
US4191747A (en) * 1976-12-17 1980-03-04 Hans Scheicher Corrective agent for the covering and/or filling of bone defects, method for the preparation of same and method of using the same
WO1980002501A1 (en) * 1979-05-11 1980-11-27 Lescarden Ltd Cartilage extraction processes and products
US4350682A (en) * 1979-05-11 1982-09-21 Lescarden Ltd. Cartilage extraction processes and products
US4486416A (en) * 1981-03-02 1984-12-04 Soll David B Protection of human and animal cells subject to exposure to trauma
US4469676A (en) * 1983-06-21 1984-09-04 Michel Hecmati Method for eliminating wrinkles occurring in the human skin
US5360593A (en) * 1987-12-29 1994-11-01 Alcon Laboratories, Inc. Heat sterilization of labile antibiotics
WO1993010712A1 (en) * 1991-12-06 1993-06-10 The General Hospital Corporation Cartilage degradation assay system
US5284155A (en) * 1991-12-06 1994-02-08 The General Hospital Corporation Cartilage degradation assay system
US5733884A (en) * 1995-11-07 1998-03-31 Nestec Ltd. Enteral formulation designed for optimized wound healing
US20110196508A1 (en) * 2003-04-29 2011-08-11 Katherine Gomes Truncale Cartilage repair mixture containing allograft chondrocytes
USRE43258E1 (en) 2003-04-29 2012-03-20 Musculoskeletal Transplant Foundation Glue for cartilage repair
US8221500B2 (en) 2003-05-16 2012-07-17 Musculoskeletal Transplant Foundation Cartilage allograft plug
US8765165B2 (en) 2003-12-11 2014-07-01 Zimmer, Inc. Particulate cartilage system
US8518433B2 (en) 2003-12-11 2013-08-27 Zimmer, Inc. Method of treating an osteochondral defect
US8834914B2 (en) 2003-12-11 2014-09-16 Zimmer, Inc. Treatment methods using a particulate cadaveric allogenic juvenile cartilage particles
US8652507B2 (en) 2003-12-11 2014-02-18 Zimmer, Inc. Juvenile cartilage composition
US20100322994A1 (en) * 2003-12-11 2010-12-23 Isto Technologies, Inc. Particulate cartilage system
US8784863B2 (en) 2003-12-11 2014-07-22 Zimmer, Inc. Particulate cadaveric allogenic cartilage system
US8524268B2 (en) 2003-12-11 2013-09-03 Zimmer, Inc. Cadaveric allogenic human juvenile cartilage implant
US20050288796A1 (en) * 2004-06-23 2005-12-29 Hani Awad Native soft tissue matrix for therapeutic applications
US8292968B2 (en) 2004-10-12 2012-10-23 Musculoskeletal Transplant Foundation Cancellous constructs, cartilage particles and combinations of cancellous constructs and cartilage particles
US8480757B2 (en) 2005-08-26 2013-07-09 Zimmer, Inc. Implants and methods for repair, replacement and treatment of disease
US9701940B2 (en) 2005-09-19 2017-07-11 Histogenics Corporation Cell-support matrix having narrowly defined uniformly vertically and non-randomly organized porosity and pore density and a method for preparation thereof
US20100241228A1 (en) * 2006-07-07 2010-09-23 Carina Syring Engineered osteochondral construct for treatment of articular cartilage defects
US8497121B2 (en) 2006-12-20 2013-07-30 Zimmer Orthobiologics, Inc. Method of obtaining viable small tissue particles and use for tissue repair
US8906110B2 (en) 2007-01-24 2014-12-09 Musculoskeletal Transplant Foundation Two piece cancellous construct for cartilage repair
US20110224797A1 (en) * 2007-01-24 2011-09-15 Semler Eric J Two piece cancellous construct for cartilage repair
US8435551B2 (en) 2007-03-06 2013-05-07 Musculoskeletal Transplant Foundation Cancellous construct with support ring for repair of osteochondral defects
US9138318B2 (en) 2007-04-12 2015-09-22 Zimmer, Inc. Apparatus for forming an implant
AU2008265852B2 (en) * 2007-06-15 2014-04-17 Warsaw Orthopedic, Inc. Method of treating tissue
US8642061B2 (en) * 2007-06-15 2014-02-04 Warsaw Orthopedic, Inc. Method of treating bone tissue
US20100274362A1 (en) * 2009-01-15 2010-10-28 Avner Yayon Cartilage particle tissue mixtures optionally combined with a cancellous construct
US10167447B2 (en) 2012-12-21 2019-01-01 Zimmer, Inc. Supports and methods for promoting integration of cartilage tissue explants
US9675645B2 (en) * 2013-01-22 2017-06-13 Warsaw Orthopedic, Inc. Method of preparing bone material having enhanced osteoinductivity
US10077420B2 (en) 2014-12-02 2018-09-18 Histogenics Corporation Cell and tissue culture container
US11555172B2 (en) 2014-12-02 2023-01-17 Ocugen, Inc. Cell and tissue culture container

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