BACKGROUND OF THE INVENTION

I have believed that there had to be a product that would create, within a traumatized (wound) area, conditions as close to fetal surroundings, as possible, so that the individual cells within this area could have the optimum chance for regeneration. Since rapidly dividing cells, in the embryo fetal complex, originate from a single fertilized cell, and then divide into specialized tissues, whether they be muscle, nerve, skin, etc., I have sought a protein source material which is readily available and inexpensive, being from immature poultry feet in which the antibodies were not well developed. Since poultry by-products were readily available, I felt this to be an ideal source.

My protein hydrolysate, described hereinafter, is believed to possess the properties which I have described above.

SUMMARY OF THE INVENTION

Briefly described, my medical protein hydrolysate comprises the soluble polypeptides and soluble amino acid constituents of immature animal protein such as chicken feet and its mineral content, resulting from the hydrolyzing of t animal protein with a dilute acid, preferably a weak organic acid such as acetic acid, and the subsequent drying, or con centrating, of the resulting solution.

The process comprises first cleansing the raw material, such as the feet of eight or nine week old broiler then comminuting this raw material and subjecting it to a dilute acid, under controlled pH and temperature conditions. The resulting solution is decanted, strained or filtered and then spray dried or otherwise dewatered or concentrated to a dry powder or dried gel.

In use, the powder is topically applied to a moist open wound, or is reconstituted with water and injected, wit a syringe, into the area to be treated. The gel is used for the treatment of relatively dry areas and can be reconstitut from the dry powder or from partially dried gel.

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DETAILED DESCRIPTION

I preferably used the feet of freshly killed im¬ mature broilers as my raw material and extract therefrom, polypeptides and amino acids that are lacking in antigenic properties.

In so doing, I wash and comminute the raw material, then selectively dissolve the proteins therefrom, with as little biological disruption as possible, using a dilute weak organic acid, such as acetic acid or lactic acid, as my hydrolyzing agent, supplemented by controlled extraction temperatures. Hydrochloric and phosphoric acid have also been tried with less success. By far the best acid to employ is acetic acid. The solution thus formed is a liquid product which is then dried, either by spray drying or dewatering into a dried product, which can be reconstituted into a gel.

In more detail, I use young "broiler" chicken feet as they have sufficient immature protein and are cheap and abundant. After thoroughly washing the feet in water to rid them of dirt, debris and blood, I grind the feet through a 1/4 inch plate of a Hobart grinder. From 1/8 to 1/2 inch plates can be used; however, a 1/4 inch plate appears to pro¬ vide the most efficient size grind for rapid and- uniform ex¬ traction of the soluble proteins.

In a separate container, I make up a water solution of glacial acetic acid by adding the glacial acetic acid to the water to produce a first dilute acetic acid solution con¬ taining from about 1% to about 1-1/2% by weight, glacial acetic acid. Into this dilute acetic acid solution, on a one to one weight basis, I dump the ground feet so that the acid can break down or hydrolize the blood and other extraneous matter, this at room temperature, i.e., from about 70°F to about 90°F. I allow the comminuted feet and dilute acetic acid solution to work overnight, i.e., eight to ^* twelve hours, stirring it periodically so that it is well mixed. I then wash or flush the mixture with fresh water until the commi¬ nuted feet mix is clear of debris. This initial treatment or pretreatment with acetic acid solution is to remove blood, free fats and serum.

I then make up another mixture of glacial acetic acid and water so as to provide a second solution having a pH 4.6. The pH may run from pH 6.5 to pH 3.6 if desired. However, I have found that, where I have used these extreme ranges, resulting protein material is not as effective. The washed comminuted feet mix is then added to this second solution in a one to one ratio by weight and the resulting mix is heated to a temperature of between 130°F and 140°F an constantly stirred for about 30-40 minutes, but it can be comingled and heated for a shorter period of time, with a de¬ crease in yield.

This solubilized mixture is then decanted or drawn off and sent through a centrifuge to remove most of the fat and particulate matter. The defatted centrifuged solution is then passed through a filter. So far, I have found that the best filter bed to use is "Speed Flow" diatomaceous earth, though I am sure there are other filters that would be equall effective.

I next allow the dissolved protein solution to solidify. I then ^' skim off the remaining fats. To again solubilize this gelled protein, I once again heat it to 1G0° 120°F so that it can be pumped. This mixture (solution) of amino acids and polypeptides generally runs from 4%-9% solids If I want to make a gel of it, I dry the solidified (gelled solution) by low temperature air drying and reconstitute it when I need it by again bringing the solubilizing water up to 100°F-130°F.

If desired, another or second extraction, using the second acetic acid solution (pH 4.6) on a pound for pound basis of the previously extracted ground feet and acetic acid solution. I extract for 30 minutes at 140°F-155°F and blend this mixture in with the other filtered and clarified protein solution, after first going through the same defatting and clarifying steps as on the first extraction. I have not foun that this second product is as good as the first extraction a I think there is too much denaturation of the proteins, there in.

To produce the dry powder, the resulting solution i spray dried. The powder has an average particle size of fro

about 1 micron to about 20 microns.

The same procedure was followed with a solution of lactic acid, also diluted until the pH was about 4.6. The resultant powder was effective, but to a lesser extent than that produced with acetic acid. As is conventional, other weak organic acids could be used with similar results. The same occurred when hydrochloric and phosphoric acid were used.

A better understanding of the present invention will be had by reference to the following examples.

EXAMPLE I

100 pounds of frozen poultry feet, obtained from freshly killed commercial broilers, eight to nine weeks old, grown and processed in Maryland, U.S.A., were washed with water to remove coarse debris, dirt and blood. They were then ground using a Hobart Grinder with a 1/4" plate and this com¬ minuted material was immersed in 100 pounds of a II solution of aqueous glacial acetic acid for a period of ten hours at room temperature. The mixture was stirred at least once per hour to maximize the area exposed to the dilute acetic acid.

Next the solution was drained from the comminuted feet by being poured onto a 1/3.2" esTi screen. The material on the screen was then washed with water until the wash water was clear. This resulted in 87 pounds of cleansed comminuted or ground broiler or poultry feet.

A first extraction was made up by.mixing glacial acetic acid and water to produce a resulting solution having about 1% by weight, glacial acetic acid.

To 87 pounds of the first extraction solution was added the 87 pounds of cleansed comminuted poultry feet. The pH of the mix was then adjusted to a pH of 4.6 by the addition of glacial acetic acid. This mixture was then constantly stirred and brought to a temperature of about 130°F and main¬ tained within the range of about 130°F to about 140°F for about 1/2 hour so as to dissolve the soluble protein from the ground material.

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This hot solubilized mixture was then passed throu a milk centrifuge so that the fat was discharged from the so tion and the solids or non-solubilized material removed ther from.

Thence, the centrifuged solution was filtered by being passed through diatomaceous earth (Speed Flow - a Dow Chemical [Grefco] product). At this stage the solution was clear solution containing approximately 5.7 pounds of the polypeptides and amino acids mix.

While still in its liquid state, the clear solutio at a temperature of from about 100°F to about 120°F was pass through a spray dryer. The inlet temperature of the air was about 250°F and the outlet temperature was about 120°F. The resulting non-antigenic protein hydrolysate powder, being hydroscopic, was then immediately placed in an air tight, moisture impervious container so that it would not cake.

The resulting powder assayed as follows: pH 4.6 water 7.9

Total N 15.73 ash 6.10

Amino acid distributio: aspartic acid 5.51 glutamic acid 10.24 histidine 0.81 l sine 3.80 argenine 8.01 hydrox lysine 1.19 hydroxyproline 10.14 threonine 2.26 serine 2.86 tyrosine 0.73 glycine 23.41

1/2 cystine 0.32 proline 11.83 alanine 9.14 valine 2.43 methionine 1.24 leucine 3.00 isoleucine 1.76 phenylalanine 2.23

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EXAMPLE II

The procedure of Example I was repeated but instead of spray drying, the filtered solution was dried in dry air at a temperature of from 65° to 75°F, until it contained about 5%, by weight, moisture.

The resulting protein hydrolysate material weighed 6.1 pounds and was placed in an airtight, moisture impervious container.

The material was later mixed with water to produce various samples of gels containing from about 15% to about 30%, by weight, of the material. The water was preheated to from about 120°F to about 130°F and the material added to the warm water. The gels were kept under refrigeration.

In Examples I and II a Sharpless centrifuge or cream separator with fixed parts was used. A Bowen spray dryer was used in Example I.

In the procedure of the protein hydrolysate described above, i.e., by extracting the polypeptides and amino acids through the use of acetic acid as a solvent for the extracted proteins, the proteins are broken down from their complex pro¬ tein structures to the simpler structures. It is important, for best results, that the solids, i.e., minerals, which pre¬ cipitate out as the filtered hydrolyzed protein is dewatered and cooled be retained in the resulting product. Protein hydrolysate, without such minerals, while causing .excellent repair of a wound, may result in concomitant hyperplasia which should be debrided to bring it in line with adjacent tissue. Thereafter, the wound will slowly continue to repair.

In other words, I have found that it is not desir¬ able to remove the precipitated minerals which precipitated out as the extracted (solubilized) proteins lose moisture and that it is not desirable to filter the product ^" after it is in concentrated form. When the non-precipitated mixtures of Examples I and II were used, the hyperplasia of regenerating tissue disappeared and remarkable regrowth of not only muscle tissue, but skin and nerve tissue, also, regenerated and re¬ turned to its normal position and contour and function,

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indicating that it restored memory to the tissues.

Treatment Using My Medical Protein Hydrolysate

My protein hydrolysate is particularly useful for the treatment of burns, particularly third degree burns. T dry powder is sprinkled over the affected area and combines with the moisture in the tissue to provide a protective cel stimulating coating. The gel is preferably used for first and second degree burns, where a relatively dry area is in¬ volved. Pain is usually stopped in three to five minutes after application to the affected area. I have found it preferable to apply a sprinkled layer of dry powder or gel to the burned area about every third day.

In the case of third degree burns, the powder all for the fiberblasts or regenerative cells to continue to gro out from the center and edges of the wound so that skin gra ing is materially reduced or entirely eliminated. Further¬ more, the new skin even appears to be formed from normal cel and hair actually grows from the new skin in a normal way.

In most cases of wounds in animals treated with m material, either spray dried or in gel form, bacterial infec tions have generally been eliminated after the first three days, and in all cases, infection appeared to be eliminated at the end of the seventh day (end of second application) . This has been demonstrated with gas gangrene (clinically) , massive disruptive wounds resulting from auto and other tra matic disruptions of the skin and underlying muscle, nerve and vascular tissues.

When using my material topically applied, either i spray dried powder or gel form, the hyperplasia of regenerat tissue disappeared and remarkable regrowth of not only muscl tissue, but skin and nerve tissue, also, regenerated and re¬ turned to its normal position and contour and function, indi cating that it restored memory to the tissues.

Bed sores which have existed for some time have healed quite well after treatment with my material. Indeed, even cells which appeared to have died around a wound were

restored to normal.

COMPARATIVE TEST

To demonstrate the importance of using immature animal tissue and particularly immature poultry feet, the following test was run. Four cats of like weight, maturity and state of health were operated on, and three muscles of the upper right thigh were severed: the Bicepts femoris, the Vastus lateralis and the Semitendinosus. Each cat was treated with an agent topically applied to cover the wound twice a week until all wounds healed.

The first cat was treated with protein hydrolysate prepared according to Example II above. Its wounds healed in 21 days without complications. It walked without a limp in 7 days.

A second cat, treated with a protein hydrolysate prepared in an identical manner from the feet of chicken about one year old. Healing took 33 days and hyperplasia developed on the 8th day. Normal walking occurred only on the 15th day.

A third cat was treated with a prior art protein hydrolysate, hydrolysed casein, a Borden product. It developed hyperplasia on the 7th day and a secondary infection, both of which persisted until final healing at 33 days. This cat limped until final healing.

The fourth cat, treated with the broad spectrum antibiotic 5-Nitro 2-fureldehyde semi-carbazone ("FURACIN", a product of Eaton Laboratories). Healing took 33 days. A lesser amount of hyperplasia was noted and the cat walked with a limp for the entire period.

The third and fourth cats also exhibited progressive atrophy of the muscles posterior to the incision continuing until the femur could be palpitated.

This test demonstrates the effectiveness and advan¬ tages of protein hydrolysate prepared according to the present invention and particularly speed of recovery, lack of infec¬ tion, absence of hyperplasia and full return of muscle function.

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It is thus seen that the therapeutic agent of the present invention, i.e., my medical protein hydrolysate, is hydroscopic mixture of polypeptides and amino acids. It appears to have the fantastic ability to create, around a wound area, conditions that allow true tissue regeneration, this in the total absence of antibodies, even in the most critically infected wounds.

Preferably, the wound is heavily covered with my powder or gel. When powder is used, the area must be moist that the powder can stick. No adverse tissue reaction has been observed in any treatment using my Protein Hydrolysate.

It is desirable to cover the wound with a non- adhering dressing (Telfa) to keep the powder/gel in contact with the wound. The treatment of the wound with my material should be repeated every three or four days.