BUCKWHEAT HONEY AND BACITRACIN WOUND-HEALING DRESSING
20180236009 ยท 2018-08-23
Inventors
Cpc classification
A61L26/0057
HUMAN NECESSITIES
A61L2300/412
HUMAN NECESSITIES
A61K45/06
HUMAN NECESSITIES
A61K38/12
HUMAN NECESSITIES
A61L2300/404
HUMAN NECESSITIES
A61L15/60
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K2300/00
HUMAN NECESSITIES
A61K38/12
HUMAN NECESSITIES
A61K9/14
HUMAN NECESSITIES
A61L15/46
HUMAN NECESSITIES
International classification
A61K45/06
HUMAN NECESSITIES
A61K9/70
HUMAN NECESSITIES
A61K38/12
HUMAN NECESSITIES
Abstract
The present invention is a method of treating acute and chronic wounds and skin conditions. The product comprises a composition or formulation comprising a mixture of buckwheat honey and bacitracin. In one unique embodiment the composition is gelled. The composition is applied directly to a wound or a patient's skin or is impregnated on gauze or other similar material on a bandage or dressing for application to an exuding or non-exuding acute or chronic wound or skin condition.
Claims
1. A therapeutic wound-healing or skin condition treatment composition comprising a wound-healing or skin condition treatment effective amount of buckwheat honey and bacitracin
2. The therapeutic wound-healing or skin condition treatment composition of claim 1, wherein the buckwheat honey is 100% pure and strained.
3. The therapeutic wound-healing or skin condition treatment composition of claim 1 which comprises one or more additional antibacterial agents.
4. The therapeutic wound-healing or skin condition treatment composition of claim 1, wherein the bacitracin comprises a dilution in sterile water.
5. The therapeutic wound-healing or skin condition treatment composition of claim 4, wherein the bacitracin solution is diluted to about 5000 units per ml.
6. The therapeutic wound-healing or skin condition treatment composition of claim 1, wherein the bacitracin is in the form of a white powder.
7. The therapeutic wound-healing or skin condition treatment composition of claim 1 which can be provided in a tube or spray.
8. The therapeutic wound-healing or skin condition treatment composition of claim 1 which includes a gelling agent.
9. The therapeutic wound-healing or skin condition treatment composition of claim 8, wherein the gelling agent is sufficient to thicken the mixture and to substantially prevent the composition from running and to release a desired amount of the dressing to the wound.
10. The therapeutic wound-healing or skin condition treatment composition of claim 1 which comprises from about 5 units to about 500 units of bacitracin per gram of honey.
11. The therapeutic wound-healing or skin condition treatment composition of claim 10 which comprises from about 7.5 units to about 15 units of bacitracin per gram of honey.
12. A therapeutic wound-healing or skin condition treatment bandage or dressing comprising substrate material and a therapeutic wound-healing or skin treatment condition composition of claim 1.
13. The therapeutic wound-healing or skin condition treatment bandage or dressing of claim 12 which comprises an effective amount of the therapeutic wound-healing or skin treatment condition composition.
14. The therapeutic wound-healing or skin condition treatment bandage or dressing of claim 12, wherein the substrate material comprises acetate, cotton (medical gauze), or alginate.
15. The therapeutic wound-healing or skin condition treatment bandage or dressing of claim 14 which comprises a 54 adhesive and non-adhesive bandage with from about 2 to 6 grams of wound healing composition.
16. The therapeutic wound-healing or skin condition treatment bandage or dressing of claim 15 which comprises about 4 grams of wound-healing or skin treatment condition composition.
17. The therapeutic wound-healing or skin condition treatment bandage or dressing of claim 12, wherein the wound-healing or skin treatment condition composition is impregnated into a reinforcing fiber substrate for application to a wound and is released therefrom.
18. A method of therapeutically treating a wound on or in a patient which comprises directly applying an effective amount of a wound-healing composition of claim 1 to the wound.
19. A method of therapeutically treating a skin condition on a patient which comprises directly applying an effective amount of a skin condition treatment composition of claim 1 to the wound.
20. A method of therapeutically treating a wound on a patient which comprises contacting the wound with a therapeutic wound-healing bandage or dressing of claim 12.
21. A method of therapeutically treating a skin condition on a patient which comprises contacting the skin condition with a therapeutic skin condition treatment bandage or dressing of claim 12.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0053]
[0054]
[0055]
[0056]
DETAILED DESCRIPTION OF THE INVENTION
[0057] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood to one of ordinary skill in the art to which this invention belongs. Although any methods, devices or materials similar or equivalent to those described herein can be used in the practice or testing of the invention, the preferred methods, devices, and materials are now described.
[0058] The term wound-healing or skin condition treatment formulation or composition as used herein refers to a formulation or composition designed to treat wounds, lesions, skin conditions, or injuries caused by physical, metabolic, or chemical means. The wound-healing or skin condition treatment process comprises a series of steps where injured tissue is repaired or regenerated. This usually involves three steps: (a) an inflammation stage (0-3 days), (b) a cellular proliferation phase (3-12 days), and (c) a remodeling phase (3-6 months).
[0059] Typically a wound-healing or skin condition treatment formulation or composition has at least one active ingredient that helps to repair a wound or treat a skin condition. Examples of active ingredients include, but are not limited to, bacitracin, methylglyoxal, bacitracin, neomycin, and polymyxin (e.g., polymyxin B sulfate). A wound-healing or skin condition treatment formulation or composition may also contain inactive ingredients that are typically required for formulation. (See, e.g., U.S. Pat. No. 5,652,274 and U.S. Published Patent Application No. 2005/0043253, each of which is incorporated herein by reference.)
[0060] Healing time related to wounds or skin conditions, whether acute or chronic, depends on multiple factors. These factors include, but are not limited to, patient medical history, etiology, location, size, depth, length of time present, previous treatment, and drainage (purulent, synovial, serous, and serosanguinous).
[0061] As discussed above, wound-healing or skin condition treatment normally progresses through different phases. Wounds and skin conditions will heal in days to months. Healing may be delayed for any number of reasons. Some of these reasons include, but are not limited to, poor circulation, infection, elevated protease levels, pressure (weight-bearing), increased motion, patient non-compliance, and the like.
[0062] A chronic wound, non-healing wound, slow-to-heal wound, or stalled wound, as used herein, refers to a wound that fails to heal over a 4 to 12 week timeframe from inception of the wound to complete closure of the skin at the wound site. Such wounds commonly include external dermal wounds.
[0063] Skin wounds designated as chronic, non-healing, slow-to-heal, or stalled are commonly observed in clinical settings as venous leg ulcers, diabetic foot ulcers, pressure ulcers, arterial ulcers, ulcers of mixed etiology, burns, or non-healing surgical wounds. Other types of non-healing wounds or conditions are observed in less frequent conditions, such as, fistulae, dermatitis or vasculitis wounds, skin cancers, and radiation burns. This list is not exhaustive and is provided to show examples of such non-healing wounds or skin conditions. These wounds or skin conditions are differentiated from acute wounds or skin conditions that spontaneously heal without complications in a matter of days or weeks through the four normal phases of the wound-healing curve (hemostasis, inflammation, proliferation, and remodeling). Chronic wounds or skin conditions may persist for months or years and occasionally can last a lifetime and are therefore commonly referred to as non-healing wounds. There is a need for treatment of any of these types of non-healing wounds or skin conditions since spontaneous healing has failed to occur. In chronic wounds or skin conditions, at the cellular biological level, there is commonly a prolonged inflammatory phase often caused by elevated proteases or active infection.
[0064] Since it was developed, bacitracin has been used for the treatment of all types of wounds. Wounds such as vascular (arterial and venous), neuropathic, pressure, traumatic, post-operative, and infected wounds responded to treatment with bacitracin. In addition, treatment with bacitracin included wounds of varying depths ranging from pre-ulceration, superficial, and deep to ulcerations that extend to the tendons, joints, and bones.
[0065] During clinical treatment of all types and depths of wounds, treatment protocol was developed using a dilution of bacitracin. Various dilutions of bacitracin have been clinically tested. A typical useful dilution is 50,000 units of bacitracin in 9.8 ml of sterile water, which seemed to have the best reproducible effects on wound healing. There is no decrease in the antimicrobial properties of bacitracin at this dilution. In addition, there has been no bacterial resistance found or developed to bacitracin.
[0066] Further research and clinical case studies conducted on preventing and treating wounds, preventing chronicity of wounds, promoting antioxidation of healthy cells and tissue, and facilitating faster healing led to investigation of the combination of honey with bacitracin. Earlier studies used generic honey (sugar) and bacitracin in no specific combination or dilution. Buckwheat honey (fagopyrum esculentum) showed increased antioxidant, anti-inflammatory, and at least equal antibacterial properties as compared to other mono-floral honeys. The unique combination of buckwheat honey and bacitracin creates specific and unique benefits to wound healing. The buckwheat honey/bacitracin formulation or composition is for use in direct application or as part of a wound dressing for treatment of all types and depths of wounds and acute or chronic skin conditions or skin ulcerations regardless of vascular and neurologic status.
[0067] An embodiment of a buckwheat honey/bacitracin formulation or composition according to the invention comprises a medicinal honey with concentrations of hydrogen peroxide and polyphenols that are all in the upper concentration range of what are naturally found in various native honeys. In this first formulation, buckwheat honey provides a composition containing buckwheat honey with high natural concentrations of hydrogen peroxide and polyphenols to which bacitracin is added in a concentration of from about 5 to about 500 units per gram of honey. The phrase high natural concentrations of hydrogen peroxide and polyphenols is defined as concentrations that naturally exist in buckwheat honey where the concentration of hydrogen peroxide is in the range of about 2-4 mM and where the polyphenol concentration is in the range of about 275-575 gallic acid equivalents per gram of honey.
[0068] The buckwheat honey useful according to the invention is pure and strained, preferably seasonally harvested raw, monofloral buckwheat honey naturally rich in hydrogen peroxide (containing and/or capable of generating about 2-4 mM concentration of hydrogen peroxide), polyphenols (275-575 gallic acid equivalents of polyphenol compounds per gram of honey). Buckwheat honey, which is derived from the buckwheat flower, is dark brown with a red tint and typically has a pH of from about 3.0 to about 7.5. It has a shelf-life of two or more years if stored in a sealed container at from about 0 to 10 C. Useful buckwheat honey comprises medicinal grade, pure, unheated, microfiltered buckwheat honey such as is commercially available from, for example, Hackenberg Apiaries, Lewisburg, Pa., and other commercial apiaries.
[0069] In another aspect of the invention, a wound-healing or skin condition treatment composition or formulation is applied directly to a wound or skin condition.
[0070] In another aspect of the invention, in a wound-healing or skin condition treatment composition or formulation, bacitracin is present in an amount of from about 5 units to about 500 units per gram of buckwheat honey.
[0071] In another aspect of the invention, in a wound-healing or skin condition treatment composition or formulation, bacitracin is present in an amount of from about 7.5 units to about 150 units per gram of buckwheat honey.
[0072] In another aspect of the invention, in a wound-healing or skin condition treatment composition or formulation, 50,000 units of bacitracin in 9.8 ml of sterile water are mixed with three liters of buckwheat honey.
[0073] In another aspect of the invention, a wound-healing or skin condition treatment composition or formulation includes a gelling agent.
[0074] In another aspect of the invention, a wound-healing or skin condition treatment composition or formulation can be provided in a tube or spray.
[0075] In another aspect of the invention, in a wound-healing or skin condition treatment composition or formulation, the gelling agent is sufficient to thicken the mixture and to substantially prevent the composition from running and to release a desired amount of the dressing to the wound or skin condition.
[0076] In another aspect of the invention, a wound-healing or skin condition treatment bandage or dressing comprises a reinforcing fiber substrate material and a wound-healing or skin condition treatment composition or formulation comprised of buckwheat honey and bacitracin.
[0077] In another aspect of the invention, a wound-healing or skin condition treatment bandage or dressing comprises an effective amount of the wound-healing or skin condition treatment composition or formulation.
[0078] In another aspect of the invention, in a wound-healing or skin condition treatment dressing, the substrate material comprises acetate, cotton (medical gauze), or alginate.
[0079] In another aspect of the invention, a wound-healing or skin condition treatment bandage or dressing comprises a 22 adhesive bandage with from about 2 to about 6 grams of wound treatment dressing.
[0080] In another aspect of the invention, a wound-healing or skin condition treatment bandage or dressing comprises about four grams of wound treatment dressing.
[0081] In another aspect of the invention, in a wound-healing or skin condition treatment dressing, the wound-healing or skin condition treatment composition or formulation is impregnated into a bandage or reinforcing fiber substrate for application to a wound or skin condition and is released therefrom.
[0082] In another aspect of the invention, a method of treating a wound on or in a patient or a skin condition on a patient comprises directly applying an effective amount of a wound-healing or skin condition treatment composition or formulation comprised of buckwheat honey and bacitracin.
[0083] In another aspect of the invention, a method of treating a wound on a patient comprises contacting the wound with a wound treatment substrate comprising a bandage or reinforcing fiber substrate material and a wound treatment composition or formulation comprised of buckwheat honey and bacitracin.
[0084] Bacitracin is a natural antibacterial compound. It typically is a white powder with a pH of from about 1.5 to about 5.0, ideally about 4.5, when diluted in sterile water. Bacitracin has a shelf-life of about 12 months if stored in a light-resistant container at a temperature not to exceed about 35 C. Bacitracin is commercially available, for example, as EVOPURE, from TOKU-E.
[0085] A useful preparation comprising buckwheat honey and bacitracin comprises bacitracin in a concentration of from about 5 units to about 500 units, preferably about 7.5 units to about 150 units, per gram of honey in the final honey product. This buckwheat honey/bacitracin composition has broad-spectrum antimicrobial activity effective to reduce the number of viable microorganisms at a wound site.
[0086] The buckwheat honey/bacitracin formulations or compositions are used in aqueous, ointment, or wound-dressing compositions or formulations to modulate biochemical mechanisms associated with wound healing, including decreasing both wound protease activities and active infection.
[0087] The buckwheat honey/bacitracin formulations or compositions can be applied directly to a wound or skin condition. In another aspect, the present invention provides a bandage or dressing for wound healing or treatment of a skin condition. The bandage or dressing comprises one or more of the buckwheat honey/bacitracin formulations or compositions described herein and a support or substrate. In any embodiment of the dressing, the support or substrate includes, but is not limited to, a fibrous gauze material, a hydrogel, a foam, a film, a hydrocolloid, an alginate, a collagen, or a combination of any two or more of the aforementioned. Useful bandages or dressings include BAND-AID or similar bandages that comprise adhesive backings with cotton or other material that adheres to the adhesive backings and absorbs the buckwheat honey/bacitracin formulations or compositions.
[0088] In another aspect of the invention, a wound or skin condition is treated with a buckwheat honey/bacitracin formulation or composition described herein.
[0089] In another embodiment of the buckwheat honey/bacitracin formulation or composition, the various compositions are used prophylactically to prevent surgical wounds in high-risk patients from post-operative wound dehiscence and non-healing. More than 53 million people undergo surgical procedures annually in the United States, with about half of these occurring under general anesthesia. Post-operative wound dehiscence has been investigated in several studies, and a small incidence has shown to be an issue of concern in all age groups, including the pediatric population, but with a higher incidence in the older population. The failure of these surgical wounds to heal in a normal time frame pushes them into the category of chronic wounds. Diabetes, obesity, cancer therapy, and vascular abnormalities, which are all increasing in incidence in the Western population, contribute to delayed healing and are considered risk factors. The prophylactic application of one or more of the buckwheat honey/bacitracin formulations herein to surgical incisions post-operatively in high-risk patients will aid in reducing the incidence of non-healing surgical wounds.
[0090] The components of the buckwheat honey/bacitracin formulation or composition surprisingly provide a synergistic effect that results in the suppression of the accumulation of a biochemical marker (e.g., proteases, and pro-inflammatory cytokines) associated with inflammation, and the up-regulation of other biochemical markers (e.g. growth factors and protease inhibitors) associated with wound healing. In addition, the components of the buckwheat honey/bacitracin formulations or compositions provide antibacterial activity that acts concomitantly with the anti-inflammatory activity to also provide suppression of active infections.
[0091] In some aspects of the invention pH adjusters may be needed and used in an amount which produces the desired function provided the amount of the pH adjuster does not affect the stability of composition. These pH adjusters are acids or bases that can be used to adjust the pH of the finished composition or formulation to a desired level. Examples of useful pH adjusters include, but are not limited to, acetic acid, ammonia, citric acid, ethanolamine, formic acid, oxalic acid, potassium hydroxide, sodium hydroxide, and triethanolamine. The pH adjusters are used in an effective, pH-adjusting amount of, for example, from about 0.01 to about 2.0% by weight, preferably from about 0.05 to about 1.0% by weight, based upon the desired effect. If buffering agents are required, the compounds can be used to maintain a desired pH in an aqueous environment. Examples of such buffers include, but are not limited to, boric acid, citric acid, lactic acid, fumaric acid, phosphoric acid, and salts thereof. The buffering agents are used in an effective, buffering amount of, for example, from about 0.01 to about 2.0% by weight, preferably from about 0.05 to about 1.0% by weight, based upon the desired effect.
[0092] In another aspect of the invention, the buckwheat honey/bacitracin formulation or composition may additionally compromise one or more hemostatic agents. Examples of such hemostatic agents include, for example, extracellular matrix protein, kaolin, zeolite, chitosan, anhydrous aluminum sulfate, and aluminum chloride hexahydrate. The hemostatic agents are used in an effective, hemostatic amount of, for example, from about 0.01 to about 2.0% by weight, preferably from about 0.05 to about 1.0% by weight, based upon the desired effect.
[0093] In another aspect of the invention addition, the buckwheat honey/bacitracin formulation or composition may additionally compromise one or more anesthetic agents. Examples of such anesthetic agents include, but are not limited to, lidocaine 1% and 2%, with and without epinephrine, and bupivacaine 0.25% and 0.5%, with and without epinephrine. The anesthetic agents are used in an effective, anesthetic amount, for example, from about 0.01 to about 2.0% by weight, preferably from about 0.05 to about 1.0% by weight, based upon the desired effect.
[0094] In another aspect of the invention, the buckwheat honey/bacitracin composition may additionally comprise one or more anesthetic agents and one or more hemostatic agents.
[0095] In another aspect of the invention, a wound-healing or skin condition treatment dressing includes a gelling agent to thicken the mixture and to substantially prevent the composition from running and to release a desired amount of the dressing to the wound. Examples of useful gelling agents include, but are not limited to, natural polymers-proteins like gelatin, casein, collagen, egg whites, polysaccharides and semi synthetic polymers-cellulose subordinates such as carboxylmethyl cellulose, ethylcellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, magnesium aluminum silicate, methylcellulose, sodium alginate, etc. The gelling agents are used in an effective, gelling amount of, for example, from about 0.01 to about 2.0% by weight, preferably from about 0.05 to about 1.0% by weight, based upon the desired effect.
[0096] Buckwheat honey/bacitracin formulations or compositions according to the present invention are useful for treating common chronic wounds, such as venous leg ulcers, diabetic foot ulcers, pressure ulcers, arterial ulcers, burns, non-healing surgical wounds, chronic rhinosinusitis and metritis. In addition, such formulations or compositions are also useful for treating abrasions, lacerations, minor cuts, scalds and burns, and other partial thickness wounds. The formulations or compositions are advantageously applied in a cream or ointment base for a period of time (e.g., several hours to several days) that are optionally impregnated into or associated with carrier dressing supports (e.g., fibrous gauze, hydrogel, foam, film, hydrocolloid, collagen, or alginate).
[0097] The buckwheat honey/bacitracin formulations or compositions can be applied directly to a wound as a cream or spray or administered on a bandage or dressing comprising a substrate. For example, a 54 dressing containing the buckwheat honey/bacitracin formulation or composition could contain approximately four grams of pure strained buckwheat honey and from about 1 to about 20 to about 2000 units of bacitracin.
[0098] This standard formulation is useful applied to a substrate in variously sized bandages or dressings or in an ointment or cream from a tube or spray. This formulation will preferably be sterilized by gamma radiation. This sterilization process was chosen because gamma radiation (25 kGy) did not affect the properties of the buckwheat honey.
[0099] The present disclosure further provides a method for treating wounds or skin conditions. In some embodiments, the method includes contacting a wound or skin condition with any buckwheat honey/bacitracin formulation or composition disclosed herein wherein the composition includes a medicinal honey fortified with the natural non-peroxide antibacterial compound, bacitracin; a pharmaceutically acceptable carrier; 1-5% w/v and the natural non-peroxide antibacterial compound effective to reduce the number of viable microorganisms at a wound site. The buckwheat honey/bacitracin formulations or compositions are applied to a wound or skin condition, for example, in a liquid (e.g., by irrigating or lavaging the wound or skin condition with the liquid) or in a gel or an ointment. Liquid compositions provide immediate availability of the ions and bacitracin to the healing tissue. In contrast, gels or ointments provide regulated delivery of the ions, medicinal honey, and bacitracin to the healing tissue over a sustained period of time. In some embodiments, the buckwheat honey/bacitracin formulation or composition is applied to a wound dressing substrate, which is subsequently applied to the wound. Advantageously, a wound dressing including any of the compositions is contacted with the wound until it is healed (3-8 months) with wound dressing changes every 24-96 hours, thereby providing a moist environment enriched with fortified medicinal honey to facilitate healing of the skin. Similarly, a dressing comprising any of the formulations described herein can be contacted with a skin condition over a period of time with periodic changes.
[0100] In another aspect of the invention, a buckwheat honey/bacitracin formulation or composition can be provided in a tube or spray.
[0101] In another aspect of the invention, a wound-healing or skin condition treatment bandage or dressing comprises a substrate comprising a reinforcing fiber substrate material and a wound-healing or skin condition treatment formulation comprised of buckwheat honey and bacitracin.
[0102] In another aspect of the invention, a wound-healing or skin condition treatment substrate comprises an effective amount of the wound-healing or skin condition treatment formulation.
[0103] In another aspect of the invention, in a wound-healing or skin condition treatment substrate, the substrate material comprises acetate, cotton (medical gauze), or alginate.
[0104] In another aspect of the invention, a wound-healing or skin condition treatment substrate comprises a 54 adhesive or non-adhesive bandage with from about 2 to about 8 grams of wound treatment dressing.
[0105] In another aspect of the invention, a wound-healing or skin condition treatment substrate comprises about four grams of buckwheat honey/bacitracin formulation or composition.
[0106] In another aspect of the invention, in a wound-healing or skin condition treatment substrate, the buckwheat honey/bacitracin formulation or composition is impregnated into a reinforcing fiber substrate for application to a wound or skin condition and is released therefrom.
[0107] In another aspect of the invention, a method of treating a wound on or in a patient comprises directly applying an effective amount of a wound treatment formulation comprised of buckwheat honey and bacitracin.
[0108] In another aspect of the invention, a method of treating a skin condition on a patient comprises directly applying an effective amount of a skin condition treatment formulation comprised of buckwheat honey and bacitracin.
[0109] In another aspect of the invention, a method of treating a wound or a skin condition on a patient comprises contacting the wound or skin condition with a wound-healing or skin condition treatment dressing comprising a reinforcing fiber substrate material and a wound-healing or skin condition treatment formulation or composition comprised of buckwheat honey and bacitracin. The formulation could be, for example, as follows:
TABLE-US-00001 (a) Buckwheat Honey 2-8 grams, preferably 4 grams (b) Bacitracin 10-4000 units (preferably 20-2000 units) (c) H.sub.2O (sterile) Dependent on dilution
[0110] The buckwheat honey/bacitracin formulation is preferably applied to an entire wound or skin condition. The treatment protocol includes complete evaluation of the wound or skin condition and clinical preparation of the wound or skin condition. For example:
Dressing Preparation:
[0111] An amount of 0.10 grams of bacitracin powder is dissolved in 1.0 cc sterile water, and the resulting solution is mixed with 4 grams buckwheat honey pure, strained. The mixture is impregnated into a 54 acetate, non-woven medical grade substrate. Multiples of the buckwheat/bacitracin solution are made for multiple dressings. Each such substrate is protected with polyethylene liners applied to both sides, and each impregnated substrate is sealed individually in a foil pouch constructed of white polyester film fused to aluminum foil that constitutes the entire dressing package. The dressings are sterilized using a gamma radiation (minimum 25 kGy) and verified as sterile before use.
Clinical Procedure:
[0112] 1. Clinical examination of patient's skin and condition of wound, including location, etiology, size, depth, viability of all tissues, odor, infection, culture, neurovascular status, and nutrition. [0113] 2. Debridement of all devitalize/necrotic, purulent tissue from the wound, using clinical judgment. [0114] 3. Wound irrigation. [0115] 4. Application of buckwheat honey/bacitracin dressing for complete coverage of wound, daily dressing, and appropriate and timely debridement/irrigation of wound (no soaking).
EXAMPLES
[0116] Objects and advantages of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention.
Example 1
[0117] A composition comprises a buckwheat honey with high peroxide-induced and polyphenol-facilitated antimicrobial activity and an effective amount of bacitracin (100 units per gram of honey) to add non-peroxide antimicrobial activity, wherein each of the antimicrobial activities provides a different mechanism of antibacterial inhibition. This provides a broad spectrum antimicrobial activity effective to reduce the number of viable microorganisms at a wound site.
Example 2
[0118] In a composition similar to the composition described in Example 1, the honey is monofloral buckwheat honey that naturally generates 2-4 mM hydrogen peroxide and which naturally contains 275-575 gallic acid equivalents of polyphenol compounds per gram of honey, and wherein the amount of bacitracin is 100 units per gram of honey.
Example 3
[0119] A wound dressing comprises a composition of Example 1 or 2 and a support. The support is, for example, a hydrogel, a foam, a film, a hydrocolloid, an alginate, collagen, or a combination of any two or more thereof.
Example 4
[0120] Prior to treatment, a patient should be thoroughly informed of the nature of the treatment and any risks, and the patient should sign appropriate consent forms. In addition, a complete medical history and physical examination should be carried out prior to the initiation of treatment, medical or surgical. Understanding the etiology of the wound and the factors that are affecting the wound healing process (i.e., weight bearing, vascular status, neuropathy, osteomyelitis, etc.) are important. Obviously, addressing such factors as these is extremely important in the successful treatment with all types of skin conditions and wounds. Multiple surgical procedures may be necessary to remove the devitalized, necrotic tissue and the surface exudate (biofilm) that may be present. Also, irrigation of the wounds can be performed at the same time the wounds are surgically debrided during hospitalization.
[0121] A combined buckwheat honey and bacitracin sterile dressing can be used as an outpatient dressing. This dressing should be changed daily, and each patient should be seen in the office at least once a week. At each visit the patient would be examined, wounds would be measured, photographs would be taken, and wounds would be debrided, as necessary, with sharp non-excisional technique.
[0122] The sterile buckwheat honey (4 grams) and bacitracin dressing (2.5% w/v) would be cut to the size and shape to completely cover a wound at each dressing change. The dressing would be applied directly to the surface of a wound entirely covering the wound. The dressing or bandage would be covered with at least one or more 44 fibrous (cotton) gauze and wrapped with 4 fibrous (cotton) KLING gauze dressings. Preferably the entire wound is covered at every dressing or bandage change in this manner whether in the office or at home. The patient's spouse or home health care provider should be educated on the proper technique for the dressing or bandage changes. The dressings or bandages should be kept clean and dry. No soaking or irrigation should be performed to the wound on an out-patient basis.
[0123] There could be indications where twice daily dressing or bandage changes are required. These indications could include increased wound drainage or increased wound desiccation.
[0124] While the present invention is described with respect to what is presently considered to be the preferred aspects, it is to be understood that the invention as claimed is not limited to the disclosed aspects.
[0125] Furthermore, it is understood that this invention is not limited to the particular methodology, materials and modifications described and as such may, of course, vary. It is also understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to limit the scope of the present invention, which is limited only by the appended claims.
REFERENCES
[0126] 1. Zumla A, Lulat A. Honey-A remedy rediscovered. J R Soc Med 1989; 82:384-5. [0127] 2. Molan P C Potential of Honey in treatment of wounds and burns. Am J Clin Dermatol 2001; 2:13-9. [0128] 3. Brudzynski, Katrina, Kamal Abubaker, Tony Wang Powerful bacterial killing by buckwheat honeys is concentration-dependent, involves complete DNA degradation and requires hydrogen peroxide. Frontiers in MICROBIOLOGY July 2012; Vol 3, Article 242. [0129] 4. Armon P J (1980) The use of honey in the treatment of infected wounds. Trop Doct 10:91PubMed. [0130] 5. Molan P C (2006) The evidence supporting the use of honey as a wound dressing. Int J Low Extrem 5:40 [0131] 6. Effem S E (1988) Clinical observations on the wound healing properties of honey. Br J Surg 75:679-681 [0132] 7. Molan P C, Betts J A (2004) Clinical usage of honey as a wound dressing: an update. J Wound Care 13(9):353-356PubMedCrossRefGoogle Scholar [0133] 8. White J W (1975) Composition of honey. In: Crane E (ed) Honey: a comprehensive survey. Heinemann, London, pp 157-206 [0134] 9. Luciana P, Fernandez S L (2005) Venous ulcer: epidemiology, physiopathology, diagnosis and treatment. Int Soc Dermatol 44:449-456. [0135] 10. Yapucu Gne U, Eer I (2007) Effectiveness of a honey dressing for healing pressure ulcers. J Wound Ostomy Cont Nurs 34(2):184-190 [0136] 11. Okeniyi J A, Olubanjo O O, Ogunlesi T A, Oyelami O A (2005) Comparison of healing of incised abscess wounds with honey and EUSOL dressing. J Alternative Compl Med 11(3):511-513 [0137] 12. Subrahmanyam M (1998) A prospective randomized clinical and histological study of superficial burn wound healing with honey and silver sulfadiazine. Burns 24(2):157-161PubMed [0138] 13. Wood B, Rademaker M, Molan P C (1997) Manuka honey, a low cost leg ulcer dressing. N Z Med J 110(1040):107 [0139] 14. Subrahmanyam M (1994) Honey-impregnated gauze versus amniotic membrane in the treatment of burns. Burns 20(4):331-333PubMedCrossRefGoogle Scholar [0140] 15. Ndayisaba G, Bazira L, Habonimana E, Muteganya D (1993) Clinical and bacteriological results in wounds treated with honey. J Orthop Surg 7(2):202-204Google Scholar [0141] 16. Weheida S M, Nagubi H H, El-Banna H M, Marzouk S (1991) Comparing the effects of two dressing techniques on healing of low grade pressure ulcers. J Med Res Inst 12(2):259-278 [0142] 17. Kramer S A (1999) Effect of bacitracin on wound healing: a review. J Vasc Nurs 17(1):17-23PubMed [0143] 18. Efem S E E (1988) Clinical observations on the wound healing properties of honey. Br J Surg 75:679-681PubMed [0144] 19. Hamdy M H, El Banby M A, Khakifa K I, Gad E M (1988) The antimicrobial effect of honey in the management of septic wounds. Proceedings of the Fourth International Conference on Apiculture in Tropical Climates, Cairo, Egypt 6-10 November London, UK; International Bee Research Association [0145] 20. Mphande A N, Killowe C, Phalira S, Jones H W, Harrison W J (2007) Effects of honey and sugar dressings on wound healing. J Wound Care 16(7):317-319PubMed [0146] 21. Subrahmanyam M (1991) Topical application of honey in treatment of burns. Br J Surg 78(4):497-498PubMed [0147] 22. Medhi B, Puri A, Upadhyay S, Kaman L (2008) Topical application of honey in the treatment of wound healing: a metaanalysis. Alternative Med 10(4):166-169 [0148] 23. U.S. Pat. No. 5,652,274, THERAPEUTIC-WOUND HEALING COMPOSITIONS AND METHODS FOR PREPARING AND USING SAME, Alain Martin, Jul. 29, 1997 [0149] 24. Efem S E. Clinical observations on the wound healing properties of honey. Br J Surg. 1988; 75:679-81. doi: 10.1002/bjs.1800750718. [PubMed] [0150] 25. Postmes T, van den Bogaard A E, Hazen M. Honey for wounds, ulcers, and skin graft preservation. Lancet. 1993; 341:756-7. doi: 10.1016/0140-6736(93)90527-N. [PubMed] [0151] 26. Ranzato E, Martinotti S, Volante A, Mazzucco L, Burlando B. Platelet lysate modulates MMP-2 and MMP-9 expression, matrix deposition and cell-to-matrix adhesion in keratinocytes and fibroblasts. Exp Dermatol. 2011; 20:308-13. doi: 10.1111/j.1600-0625.2010.01173.x. [PubMed] [0152] 27. Gurtner G C, Werner S, Barrandon Y, Longaker M T. Wound repair and regeneration. Nature. 2008; 453:314-21. doi: 10.1038/nature07039. [PubMed] [0153] 28. Molan P C. Potential of honey in the treatment of wounds and burns. Am J Clin Dermatol. 2001; 2:13-9. doi: 10.2165/00128071-200102010-00003. [PubMed] [0154] 29. Ranzato E, Martinotti S, Burlando B. Epithelial mesenchymal transition traits in honey-driven keratinocyte wound healing: Comparison among different honeys. Wound Repair Regen. 2012; 20:778-85. doi: 10.1111/j.1524-475X.2012.00825.x. [PubMed] [0155] 30. Ranzato E, Mazzucco L, Patrone M, Burlando B. Platelet lysate promotes in vitro wound scratch closure of human dermal fibroblasts: Different roles of cell calcium, P38, ERK and PI3K/AKT. J Cell Mol Med. 2009; 13:2030-8. doi: 10.1111/j.1582-4934.2008.00467.x. [PubMed] [0156] 31. Ranzato E, Patrone M, Pedrazzi M, Burlando B. Hmgb1 promotes wound healing of 3T3 mouse fibroblasts via RAGE-dependent ERK1/2 activation. Cell Biochem Biophys. 2010; 57:9-17. doi: 10.1007/s12013-010-9077-0. [PubMed] [0157] 32. Houghton P J, Hylands P J, Mensah A Y, Hensel A, Deters A M. In vitro tests and ethnopharmacological investigations: Wound healing as an example. J Ethnopharmacol. 2005; 100:100-7. doi: 10.1016/j.jep.2005.07.001. [PubMed] [0158] 33. Iftikhar F, Arshad M, Rasheed F, Amraiz D, Anwar P, Gulfraz M. Effects of acacia honey on wound healing in various rat models. Phytother Res. 2010; 24:583-6. [PubMed] [0159] 34. Lusby P E, Coombes A, Wilkinson J M. Honey: A potent agent for wound healing? J Wound Ostomy Continence Nurs. 2002; 29:295-300. [PubMed] [0160] 35. Gethin G, Cowman S. Case series of use of Manuka honey in leg ulceration. Int Wound J. 2005; 2:10-5. doi: 10.1111/j.1742-4801.2005.00078.x. [PubMed] [0161] 36. Ranzato E, Burlando B. Signaling pathways in wound repair. In: Middleton J E, editor. Wound healing: Process, phases and promotion. Hauppauge, N.Y.: Nova Publishers Inc.; 2011. pp. 123-35. [0162] 37. Cipriani V, Ranzato E, Balbo V, Mazzucco L, Cavaletto M, Patrone M. Long-term effect of platelet lysate on primary fibroblasts highlighted with a proteomic approach. J Tissue Eng Regen Med. 2009; 3:531-8. doi: 10.1002/term.195. [PubMed] [0163] 38. Ranzato E, Balbo V, Boccafoschi F, Mazzucco L, Burlando B. Scratch wound closure of C2C12 mouse myoblasts is enhanced by human platelet lysate. Cell Biol Int. 2009; 33:911-7. doi: 10.1016/j.cellbi.2009.06.017. [PubMed] [0164] 39. Ranzato E, Boccafoschi F, Mazzucco L, Patrone M, Burlando B. Role of ERK1/2 in platelet lysate-driven endothelial cell repair. J Cell Biochem. 2010; 110:783-93. doi: 10.1002/jcb.22591. [PubMed] [0165] 40. Ranzato E, Martinotti S, Magnelli V, Murer B, Biffo S, Mutti L, et al. Epigallocatechin-3-gallate induces mesothelioma cell death via H(2) O(2)-dependent T-type Ca(2+) channel opening. J Cell Mol Med. 2012; 16:2667-78. doi: 10.1111/j.1582-4934.2012.01584.x.[PMC free article] [PubMed] [0166] 41. Ranzato E, Patrone M, Mazzucco L, Burlando B. Platelet lysate stimulates wound repair of HaCaT keratinocytes. Br J Dermatol. 2008; 159:537-45. [PubMed] [0167] 42. Ranzato E, Patrone M, Pedrazzi M, Burlando B. HMGb1 promotes scratch wound closure of HaCaT keratinocytes via ERK1/2 activation. Mol Cell Biochem. 2009; 332:199-205. doi: 10.1007/s11010-009-0192-4. [PubMed] [0168] 43. Ranzato E, Marinotti S, Pedrazzi M, Patrone M. High mobility group box protein-1 in wound repair. Cells. 2012; 1:699-710. doi: 10.3390/cells1040699. [PMC free article] [PubMed] [0169] 44. Li J, Kim Y N, Bertics P J. Platelet-derived growth factor-stimulated migration of murine fibroblasts is associated with epidermal growth factor receptor expression and tyrosine phosphorylation. J Biol Chem. 2000; 275:2951-8. doi: 10.1074/jbc.275.4.2951. [PubMed] [0170] 45. Sabacinski K A, Tillo T H, Giurini J M, Madras T M, Miller L B. J Foot Surgery 28(2):106-11, 1989.