WO2004045572A1 - Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil - Google Patents
Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil Download PDFInfo
- Publication number
- WO2004045572A1 WO2004045572A1 PCT/IL2003/000980 IL0300980W WO2004045572A1 WO 2004045572 A1 WO2004045572 A1 WO 2004045572A1 IL 0300980 W IL0300980 W IL 0300980W WO 2004045572 A1 WO2004045572 A1 WO 2004045572A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- carrier
- composition according
- composition
- stabilized
- essential oil
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0046—Ear
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0031—Rectum, anus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0034—Urogenital system, e.g. vagina, uterus, cervix, penis, scrotum, urethra, bladder; Personal lubricants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
Definitions
- the present invention relates to a composition for treating infected skin and mucousal membranes. More particularly, the present invention relates to a composition for treating microbially infected skin and mucousal membranes including the treatment of wounds and skin ulcers, comprising a mixture of at least one anti-microbial drug and at least one essential oil, in a liquid or semi-solid carrier delivery system. Preferably said compositions are stabilized with at least one inactive ingredient or excipient which is non-cytotoxic at the concentration used and which does not inhibit wound-healing, and which is isotonic or moderately hypertonic. BACKGROUND OF THE INVENTION
- Mucous and skin infections are in many cases hard to treat since they often involve multi bacterial, yeast and fungal infections. Mucous and skin infections are also commonly associated with inflammation, ulceration and bleeding. There is a need for a more complex product to provide a solution to the many factors encompassing the infected mucous or skin status and clinical manifestations.
- Mucositis, Vaginitis, Anal fissure, Pressure sores, Dermatitis, Otitis, Gingivitis and Periodontitis and skin ulcers, are all prone to multi-microbial infection and inflammation, and involve difficult to cure conditions, because of the enormous number of germs in the affected area.
- Mucositis is an inflammation and ulceration of the lining of the mouth, throat or gastrointestinal tract most commonly associated with chemotherapy or radiotherapy for cancer. .Common manifestations of mucositis include ulcerations, redness, and swelling in the mouth as well as cramping, diarrhea and bleeding. In more severe cases, mucositis can be extremely painful, preventing the patient from eating and necessitating hospitalization for hydration, narcotic pain medication, and/or total parenteral nutrition. The destruction of the protective mucous membrane can also place the patient at a serious risk of infection.
- Mucositis is often a dose- limiting toxicity of chemotherapy and radiation therapy, leading to reductions or delays in chemotherapy .or irradiation doses.
- Dose-limiting toxicities such as mucositis are a major concern for oncologists because they adversely impact the curative potential of the patient's primary therapy.
- mucositis may lead to dehydration, malnutrition, or infection, all of which compromise the desired treatment plan.
- vaginal infections Bacterial vaginosis, Candidiasis, or "yeast infection” and Trichomoniasis. It is common that more than one infection is present.
- Anal fissure tends to become ulcerated or infected because of the enormous number of germs in this area; an anal fissure will always get infected, so there is local inflammation.
- An anal fissure is a superficial linear tear in the anoderm most commonly caused by passage of a large, hard stool. This tear is distal to the dentate line. Anal fissures are among the most common anorectal disorders in the pediatric population; however, adults also are affected.
- a contaminated wound will heal, an infected wound will not.
- Stage 2, 3 and 4 pressure ulcers should all be considered as colonized with bacteria.
- Infected skin ulcer may result from pressure, arterial insufficiency, venous stasis, diabetic, traumatic or burns.
- the antibiotic for pressure sores should be effective against gram-negative, gram-positive, and anaerobic organisms (e.g., silver sulfadiazine, triple antibiotic). Monitoring allergic sensitization and other adverse reactions is necessary due to many non-curing situations.
- Acyclovir an antiviral agent effective in treatment of certain forms of herpes.
- Acyclovir is available from Glaxo Wellcome under the tradename Zovirax.
- Zovirax consists essentially of acyclovir in a polyethylene glycol base and is available as an ointment or rinse. This product approaches the problem of ulcers based on the hypothesis that such ulcers or lesions are viral in nature.
- Aphthasol available from the Block Drug Company. Aphtasol consists of amlexanox, an antihistamine, in an adhesive paste.
- Gingivitis is a disorder involving inflammation of the gums. Gingivitis is caused by the long-term effects of plaque deposits. Plaque is the sticky material that develops on the exposed portions of the teeth, consisting of material such as bacteria, mucus, and food debris. It is a major cause of dental caries. Un-removed plaque mineralizes into a hard deposit called calculus (tartar) that becomes trapped at the base of the tooth. Plaque and calculus cause mechanical irritation and inflammation of the gingiva. Bacteria, and the toxins produced by the bacteria, cause the gums to become infected, swollen, and tender.
- the goal of treatment is reduction of gingival inflammation.
- Daily oral hygiene may include tooth brushing and oral rinse.
- Common toothpastes and mouth rinses comprise antiseptic agents such as Chlohexidine, Cetyl pyridinium chloride, Essential oils such as Menthol, Thymol, Methylsalycilate and Eucaliptol, usually in a hydro-alcoholic solvent carrier.
- Commercial mouth rinses are hypertonic or contain significant concentration of gingivitis inhibiting agents or compositions.
- Periodontitis is a dental disorder that results from progression of gingivitis, involving inflammation and infection of the ligaments and bones that support the teeth. Besides dentist intervention, periodontitis is treated by application of antibacterial agents such as Chlohexidine and Metronidazole, directly into periodontal pockets. Otitis
- Acute otitis media is a middle ear infection that may cause a change in the normal eardrum, which is located at the inner end of the ear canal.
- Otitis externa is an infection of the outside ear canal and/or opening to the ear and is commonly called "swimmer's ear.”
- the infection can be caused by a virus or by bacteria. It may also be accompanied by allergies, enlarged adenoids, or a cold that causes blockage of the eustachian tube (the connection between the throat and middle ear that equalizes pressure).
- OE In OE, the infection is often caused by scratching, inserting objects into the ear canal, or moisture, such as pool water. OE may also be caused by bacteria or fungi.
- Dermatitis is an inflammation of the dermis and epidermis (the skin). Symptoms include a rash, blisters, sores, lesions, itching or cracked skin. The term eczema is also used for this condition.
- US patent 5,213,615 discloses a dental material for the control of caries and paradentitis, which contains an active agent combination of thymol and/or carvacrol and chlorhexidine and/or the physiologically compatible salts thereof.
- the dental material can be a dental varnish or a material such as a dental cement and the like, which remains in the oral cavity for a long period and from which the active combination can diffuse out.
- a caries-preventive composition comprises an antibody obtained by immunizing a mammal with at least one antigen selected from the group consisting of Streptococcus mutans, its cell-wall fraction, fibrous substance fraction, glucosyltransferase fraction and protein antigen fraction, and a synergist selected from the group consisting of fluorine compounds, chlorhexidine and its salts, lytic enzymes, bacteriocins, glucosyltransferase inhibitors, proteases and dextranases.
- US patent 6,352,711 discloses pharmaceutical compositions which comprise of an effective amounts of antimicrobials, anti-inflammatories, and antihistamines, to provide an ulcer medication which prevents secondary infections and promotes healing while providing immediate relief from pain.
- the composition may be used to treat a variety of ulcers including but not limited to intraoral aphthous ulcers and non-oral lesions.
- US patent 6,458,777 discloses administration of anti-microbial agents in combination with "inflammatory cytokine inhibitor” which "result in an even more effective method for treating and preventing mucositis".
- Alcohol may. play .a role in toxic and genotoxic biological effects. Consumers are therefore refraining from using products containing alcohol, especially for sensitive body organs such as for the oral cavity and babies' skin. Alcohol is an irritant to the skin, scalp, mucous membrane and gastrointestine. In the oral cavity alcohol has a foul taste, which is especially unpleasant for young and elderly people. Alcohol burns tissues in a way that delays tissue healing after skin traumas. Alcohol dehydrates the skin, mucous membrane and tissues, which in turn causes discomfort and pain. Therefore medical research is investing in finding alcohol free medicaments.
- Chlorhexidine an antimicrobial mouth rinse, has also been used extensively in the treatment and prevention of oral mucositis (Ferretti et al., 1990, Bone Marrow Transplan. 3:483-493; Weisdorf et al., 1989, Bone Marrow Transplan. 4:89-95). It has been noted however that the efficacy of chlorhexidine is significantly decreased in saliva, and that this compound is relatively ineffective against the Gram negative bacteria that tend to colonize the oral cavity in patients undergoing radiation therapy (Spijkervet et al., 1990, Oral Surg. Oral Med. Oral Pathol. 69:444-449). In addition, at least one study has shown that the use of chlorhexidine may be detrimental and result in a higher incidence of mucositis (Foote et al., 1994, J. Clin Oncol. 12:2630- 2633).
- the present invention is based on the discovery that combinations of at least one anti-microbial agent and at least one essential oil, formulated in a liquid or semi- solid delivery system that comprises only such ingredients that are non-toxic and are not wound healing inhibitors, at the concentration used, provide unexpected and highly effective Mucositis and Ulcers medications.
- the present invention provides a medication, which prevents and treats infection,, inflammation, and bleeding and promotes healing while simultaneously providing relief from pain for infected skin and mucousal membranes.
- compositions of matter for treating infected skin and mucousal membranes comprising at least one anti-microbial drug; and at least one essential oil, in combination with a substantially, alcohol-free carrier system, said carrier being selected from a liquid carrier or a semi-solid carrier, said carrier system being selected from isotonic system and a moderately hypertonic system.
- said carrier is made of pharmaceutical or cosmetic ingredients, known to persons skilled in the art, which are selected from stabilizing, suspending or gelling agents, that are devoid of the unwanted effects of fibroblasts and keratocytes toxicity and wound healing inhibition and irritation at the concentrations used at the application.
- stabilizing agents are hydrocolloids and mild non-ionic surfactants, which cause at most only minimal hemolysis.
- Hydrocolloids are hydrophilic polymers, of vegetable, animal, microbial or synthetic origin, that generally contain many hydroxy! groups and may be polyelectrolytes. They are naturally present or added to control the functional properties of aqueous pharmaceutical and cosmetics. Most important amongst these properties are viscosity (including thickening and gelling) and water binding but also significant are many other properties, including emulsion stabilization, prevention of ice re-crystallization and organoleptic properties.
- Preferred hydrocolloids are selected from the group consisting of Alginate, Cellulose and cellulose derivatives such as hydroxy methyl ethyl and propyl derivatives, Xanthan gum, Gum arabica, Carrageenan, Guar gum, Gelatin, Pectin, Starch, Carboxy-methylcellulose, Hyaluronic acid and Chitosan, Alginate, pullulan, polyvinyl pyrrolidone, polyvinyl alcohol, dextrin, pectin, chitin, collagen, gelatin, zein, gluten, starch and starch derivatives.
- Preferred mild non-ionic surfactants are Sucrose esters and Sorbitan esters such as spans.
- Example of unwanted ingredients that are irritating and wound healing inhibitors are pharmaceutical solvents such as ethyl-alcohol and stabilizers such as sodium lauryl sulphate or polyoxyethylene polymers derivatives, used extensively in medicine and cosmetics, but are avoided in the formulations and products of the present invention.
- pharmaceutical solvents such as ethyl-alcohol and stabilizers such as sodium lauryl sulphate or polyoxyethylene polymers derivatives, used extensively in medicine and cosmetics, but are avoided in the formulations and products of the present invention.
- Ethanol, propylene glycol, dimethylsulfoxide, dimethylformamide, and Brij 96 have been shown to be cytotoxic to human keratinocyte and fibroblast cultures (Ponec et al. J Pharm Sci 1990 Apr; 79(4): 312-6) and are all inappropriate for use in the invented composition.
- anti-microbial drugs contemplated for use in the present invention are selected from the group consisting of antibiotics, anti-fungafs, anti-protozoals and anti-virals.
- Antibiotics include but are not limited to: beta-lactams penicillins and cephalosporines, Macrolides, Licosamides, Aminoglicosides such as Gentamycin, Tetracyclines, Polyp ' epetides such as Vancomycin, Sulfonamides, Flioroquinolones, chloramphenicol, nitrofurantoin and chlorhexidine.
- Anti-fulgals including but not limited to: Nystatine, Amphotericine B, Griseofulvine, Miconazole, Itraconazole, Fluconazole, Ketoconazole, Terbinafine, Silver Sulfadiazine, Flucytosine and Clotrimazole.
- Anti-protozoals include but arenot limited to: metronidazole, eflornithine, furazolidone, hydroxychloroquine, iodoquinol and pentamidine.
- Anti- virals include but are not limited to acyclovir, amantadine, famciclovir, ganciclovir, rimantadine and valacyclovir.
- Antimicrobial agents are defined as organic chemicals that derive their antimicrobial activity through a chemical or physiochemical interaction with the microbial organisms.
- Cetyl pyridinium chloride, triclosan, biguanides include the free bases or salts of alexidine, chlorhexidine, hexamethylene biguanides and their polymers, and combinations of the foregoing.
- the salts of alexidine and chlorbexidine can be either organic or inorganic and are typically gluconates, nitrates, acetates, phosphates, sulfates, halides and the like.
- the preferred biguanide is the hexamethylene biguanide commercially available from Zeneca, Wilmington, DE under the trademark Cosmocil.TM. CQ.
- the hexamethylene biguanide polymers also referred to as polyaminopropyl biguanide (PAPB) have molecular weights of up to about 100,000.
- An essential oil or volatile oil is a volatile mixture of esters, aldehydes, alcohols, ketones and terpenes, which is prepared from botanical materials or plant cell bio-mass from cell culture.
- essential oils include, but are not limited to, oil of cinnamon, prepared from the dried bark of the roots of Cinnamomum zeyloriaceae; cajeput oil, eucalyptus oil, prepared from the fresh leaves and branches of various species of Eucalyptus, such as E.
- globulus fennel oil, prepared from dried ripe fruit of Foeniculum vulgare; geranium oil, prepared from the aerial parts of Pelargonium species; girofle oil, lavander oil, prepared from fresh flowering tops of Lavandula species such as Lavandula officinalis; lemon oil, obtained from the fresh peel of Citrus lemon; spearmint oil, prepared from the aboveground parts of fresh flowering Mentha species, such as M.
- spicata myrte oil, origano oil, pine oil, rosemary oil, prepared from tops or leafy twigs of Rosmarinus officinalis] sarriette oil, thyme oil, prepared from the leaves and flowering tops of Thymus vulga ⁇ s; and tea-tree oil, obtained from the leaves of Melaleuca olternifolia.
- Also included in this class of essential oils are the key chemical components of the plant oils, which have been found to .be the major constituents of the natural oil and which have in many cases identical activity and typical physical and chemical properties.
- These chemicals include, but are not limited to anethol, catechole, camphene, thymol, eugenol, eucalyptol, ferulic acid, farnesol, hinokitiol, tropolone, limonene, menthol, methyl salicylate, carvacol, terpineol, verbenone, berberine, ratanhiae extract, caryophellene oxide, citronella acid, curcumin, . nerolidol and geraniol.
- composition of the present invention may further include a wound healing agent such as but not limited to Aloe vera dry extract, Herbals tannins, Echinacea extract, Comfrey extract, Allantoin, Turmeric dry extract, and recombinant growth factors.
- a wound healing agent such as but not limited to Aloe vera dry extract, Herbals tannins, Echinacea extract, Comfrey extract, Allantoin, Turmeric dry extract, and recombinant growth factors.
- Hyaluronic acid, alginates and chitosans which are also known to be a wound-healing agent may serve double functions, wound healing and major vehicle stabilizing excipient.
- the liquid and/or semi-solid delivery system of the present invention may be used as is for application on the affected disease location, or can be provided as a concentrated formula to be diluted before use to obtain proper concentration of the bio-actives: the anti-microbial drug and the essential oil. Concentrated formulas are simpler to stabilize and achieve long shelf life and microbiological preservation, while producing a non-cytotoxic and wound healing formulation upon dilution before use.
- Bactericidal ointments for the treatment of wounds are well known. Such ointments typically contain an antibiotic or an anti-bacterial agent in an inert vehicle or carrier, such as a paraffin base ointment or an oil-in-water emulsion.
- Antibiotics which are used, include gentamycin sulphate and neomycin sulphate, while antibacterial agents include cetrimide, chlorhexidine gluconate and silver sulphadiazine.
- An inactive ingredient which is non-cytotoxic and which does not inhibit wound-healing is known per se and is selected from those chemical or pharmaceutical non-active ingredients used for stabilizing the formulation which do not show toxicity or killing effect to fibroblats and keratinocytes in in-vitro culture.
- Non-irritating chemicals are those that do not cause local inflammatory reaction and which do not produce tissue destruction or irreversible change at the site of contact; the macroscopic manifestations of irritation are edema and erythema. Alcohol causes moderate skin irritation.
- Other common irritating ingredients are ionic surfactants, microbial preservatives and non-ionic PEO. surfactants.
- Essential oils are potent anti-microbials with no reported major bacterial resistance. Combining anti-microbial drug and essential oil enables application of reduced drug concentration while keeping anti-microbial activity, hence improving therapeutic index and overcoming the multiple resistance problems.
- Anhydrous bases are made of olefins, silicon or polyols and may be liquid or semi-solid.
- polyols include, but are not restricted to polyethylene glycol, propylene glycol, polypropylene glycol, diethylene glycol, glycerine and ethylene glycol.
- Liquid or semi-solid aqueous formulas at the final application concentration may include polyols only in limited quantities that should not produce cytotoxic product.
- High polyols concentration is possible according to the current invention, in cases of products that are diluted before use, in a way that the final application product is so much diluted as to not have cytotoxic or wound-healing inhibition effects.
- Liquid or semi-solid compositions of the present invention may be further packaged in plastic bottles, tubes, aluminum tubes pressurized aerosol or foam or non pressurized aerosol or drops or glass bottles, as well as in any other conventional packaging and closure materials.
- Solid dosage forms may be shaped into small unit chips for periodontal pocket insertion or into confectionary or strips for oral mastication.
- a preferred composition of the present invention is formulated in concentrate form for subsequent dilution before use. Precise dilution is obtained by using a dosing pump or any other dosing device such as droppers or measuring cups.
- a preferred method is a dual chamber packaging wherein the concentrate is placed in one compartment and the dilution aqueous medium is placed in the second compartment and two compartments or chambers are mixed together before use to obtain the desired composition and concentrations of the anti-microbial drug and .
- the essential oil or oils composition in an isotonic or moderately hypertonic product that do not comprise ingredients in concentrations that inhibit tissue healing.
- the anti-microbial and essential oil mixture for treating mucous, wound infections and ulcers may also contain common pharmaceutical additives, such as but not limited to; flavors or sweeteners in oral use, anti-oxidants such as vitamin E or CoenzymeQI O or colorant or emollients, as common in the- pharmaceutical art, in such concentration that no cytotoxic effect is present in the method of application.
- common pharmaceutical additives such as but not limited to; flavors or sweeteners in oral use, anti-oxidants such as vitamin E or CoenzymeQI O or colorant or emollients, as common in the- pharmaceutical art, in such concentration that no cytotoxic effect is present in the method of application.
- the preferred anti-microbial drug concentration is dictated from its USP-NF monograph, the PDR or instruction for use as approved by the regulatory agencies. Concentrated formulas may have for example 10 times the recommended use concentration, and are diluted accordingly, 10 times before use by medical team or patient, to obtain the desired drug concentration for application.
- finally diluted composition which is directly applied onto affected area should be isotonic or of low or moderate hyper- tonicity and not hypertonic.
- unwanted hypertonic compositions are: 70% Sorbitol or 10% Glycerin in final formulation.
- An isotonic solution in medicine is one that can be mixed with body fluids without causing any disturbance that is about 280 to 320 milliosmolar.
- Moderate hypertonic is a solution with osmotic pressure of less than twice the isotonic pressure and preferably not higher than 50% of isotonic solution.
- Essential oils such as Thyme, Eucalyptus and Cinnamon oils are most preferably used at concentrations of 0.05% to 0.5%, whereas 10 times concentrated formula may contain 0.5% to 5% to be diluted 10 times before use to obtain desired final concentration for application.
- Mucositis treatment requires low essential oils concentration while aphtouse or mouth ulcers are treated with much higher concentration.
- Preferred stabilizing agents include alginate, hyaluronic acid, chitosan, acacia, xanthan gum, locust bean gum, guar gum, cellulose derivatives and gelatin and the like, in amounts ranging from about 0.01 to about 10.0 wt. %, preferably about 0.2 to about 4 wt. %.
- Preferred emulsifying agents include sucrose esters, sorbitan esters, polyglyceryl esters, lecithin, bentonite, veegum, and the like, in amounts ranging from about 0.01 to about 4 wt. %, preferably about 0.1 to about 1.0 wt. %.
- Preferred thickening agents include methylcellulose, hydroxypropylmethyl cellulose, carboxy-methylcellulose, and the like, in amounts ranging from about 0.01 to about 10 wt. %, preferably about 0.1 to about 4 wt. %.
- This Mucositis mouthwash is a concentrated formula to be diluted with water before use by the patient. Precise twenty times dilution with water is enabled by using dosing pump or dual chamber device to obtain final Chlorhexidine gluconate concentration of 0.2%.
- This aphtouse formula was effective in treating recurrent aphtouse (mouth ulcers) conditions, reducing pain, shortening healing period and enabling comfortable eating including acidic orange juice, within 24 hour of aphtouse eruption and treatment.
- This Anal fissure formula was effective in reducing pain, shortening healing period and treating anal fissures without use of steroids.
- This anti gingivitis mouth rinse formula is diluted 20 times with water before d is stable after reconstitution for couple of months and has been proved to ctive anti-gingivitis treatment in kids, diabetics and other conditions where alcohol prohibited or not recommended.
- This anti gingivitis mouth rinse formula is diluted 20 times with water before d is stable after reconstitution for couple of months.
- This anti gingivitis mouth rinse formula is diluted 20 times with water before use and is stable after reconstitution for couple of months.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Reproductive Health (AREA)
- Gynecology & Obstetrics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003282358A AU2003282358A1 (en) | 2002-11-21 | 2003-11-19 | Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil |
EP03773971A EP1562543A1 (en) | 2002-11-21 | 2003-11-19 | Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil |
US10/535,961 US20060105000A1 (en) | 2002-11-21 | 2003-11-19 | Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil |
US11/807,901 US20080064711A1 (en) | 2002-11-21 | 2007-05-29 | Composition for treating oral cavity and Mucousal infections |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL152,993 | 2002-11-21 | ||
IL15299302A IL152993A0 (en) | 2002-11-21 | 2002-11-21 | Composition and method of treating infected mucous and skin wounds |
IL158,901 | 2003-11-17 | ||
IL15890103A IL158901A0 (en) | 2003-11-17 | 2003-11-17 | Compositions for treating infected skin and mucous membrane |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/807,901 Continuation-In-Part US20080064711A1 (en) | 2002-11-21 | 2007-05-29 | Composition for treating oral cavity and Mucousal infections |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2004045572A1 true WO2004045572A1 (en) | 2004-06-03 |
WO2004045572A8 WO2004045572A8 (en) | 2004-07-08 |
Family
ID=32328183
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IL2003/000980 WO2004045572A1 (en) | 2002-11-21 | 2003-11-19 | Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil |
Country Status (4)
Country | Link |
---|---|
US (2) | US20060105000A1 (en) |
EP (1) | EP1562543A1 (en) |
AU (1) | AU2003282358A1 (en) |
WO (1) | WO2004045572A1 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005084627A1 (en) * | 2004-03-01 | 2005-09-15 | University Of Iowa Research Foundation | Alcohol-free chlorhexidine compositions |
WO2006029893A2 (en) * | 2004-09-17 | 2006-03-23 | Oystershell Nv | Composition for inhibiting or preventing the formation of a biofilm |
WO2007096924A2 (en) * | 2006-02-20 | 2007-08-30 | Maiello, Adolfo | Extraction, preparation and use of active principles of the aloe plant for producing self-meditaion devices such as controlled-release gauzes, bandages, stockings, elastic bands and arch supports |
JP2008540507A (en) * | 2005-05-13 | 2008-11-20 | アドヴァンスト・サイエンティフィック・ディヴェロップメンツ | Pharmaceutical composition comprising an antibacterial agent and an active ingredient selected from carveol, thymol, eugenol, borneol and carvacrol |
FR2918571A1 (en) * | 2007-07-10 | 2009-01-16 | Aroma Technologies Soc Par Act | ANTIBIOTIC COMPOSITIONS BASED ON ESSENTIAL OILS PROPHYLAXIS AND TREATMENT OF NOSOCOMIAL INFECTIONS |
JP2010536836A (en) * | 2007-08-24 | 2010-12-02 | インサイト ヘルス リミテッド | Fungicide |
DE102010013081A1 (en) * | 2010-03-26 | 2011-09-29 | B. Braun Melsungen Ag | Antimicrobial oil in water emulsion |
WO2012145307A1 (en) | 2011-04-19 | 2012-10-26 | Brian Sokol | Method of inhibiting harmful microorganisms and barrier-forming composition therefor |
EP2531167A1 (en) * | 2010-02-07 | 2012-12-12 | J.P.M.E.D. Ltd | Hair follicle targeting compositions |
WO2013070198A1 (en) * | 2011-11-09 | 2013-05-16 | Colgate-Palmolive Company | Alcohol-free mouthwash |
WO2014117265A1 (en) * | 2013-02-01 | 2014-08-07 | Ddrops Company | Liquid menthol compositions |
EP2974725A1 (en) * | 2014-07-16 | 2016-01-20 | Luca D'Alfonso | Pharmaceutical composition |
US10426761B2 (en) | 2011-04-19 | 2019-10-01 | Arms Pharmaceutical, Llc | Method for treatment of disease caused or aggravated by microorganisms or relieving symptoms thereof |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0502046D0 (en) * | 2005-02-01 | 2005-03-09 | Sinclair Pharmaceuticals Ltd | Method |
US20090076132A1 (en) * | 2005-03-11 | 2009-03-19 | Gary Pekoe | Antiviral compositions and methods of treatment |
WO2007149868A2 (en) * | 2006-06-20 | 2007-12-27 | The Regents Of The University Of California | Controlled release encapsulated anti-bacterial and anti-inflammatory nanoparticles |
GB0714338D0 (en) * | 2007-07-23 | 2007-09-05 | Sinclair Pharmaceuticals Ltd | method |
WO2009024964A2 (en) * | 2007-08-22 | 2009-02-26 | Nitsan Primor | Composition and method for the treatment of otitis externa |
WO2009099405A2 (en) * | 2008-01-30 | 2009-08-13 | Dalos, Llc | Antibacterial compositions and methods of treatment |
US8636988B2 (en) * | 2008-01-31 | 2014-01-28 | Doctor Essentials | Composition for treatment of sunburned skin |
US20100051051A1 (en) * | 2008-09-03 | 2010-03-04 | Han-Chung Hsu | Dental floss Combined with Powders |
CN102186341B (en) * | 2008-10-20 | 2013-12-25 | 荷兰联合利华有限公司 | Antimicrobial composition |
RU2553363C2 (en) | 2009-02-11 | 2015-06-10 | Рамот Ат Тель-Авив Юниверсити Лтд. | Antiseptic compositions and applications thereof |
US9132103B2 (en) | 2009-09-24 | 2015-09-15 | Conopco, Inc. | Disinfecting agent comprising eugenol, terpineol and thymol |
US20120003162A1 (en) | 2010-06-30 | 2012-01-05 | Mcneil-Ppc, Inc. | Methods of Preparing Non-Alcohol Bioactive Esential Oil Mouth Rinses |
US9084902B2 (en) | 2010-06-30 | 2015-07-21 | Mcneil-Ppc, Inc. | Non-alchohol bioactive essential oil mouth rinses |
CN103354741B (en) | 2010-12-07 | 2016-01-13 | 荷兰联合利华有限公司 | Oral care composition |
CN103998011B (en) | 2011-11-03 | 2016-11-23 | 荷兰联合利华有限公司 | Personal cleaning compositions |
EP2782550A2 (en) * | 2011-11-25 | 2014-10-01 | Unilever N.V. | An oral care composition comprising polyphenol |
IL217807A (en) * | 2012-01-29 | 2017-01-31 | Tel-Ari Ruben | Tea tree oil (tto)- based topical therapeutic compositions |
MX354749B (en) | 2012-08-28 | 2018-03-20 | 3M Innovative Properties Co | Chlorhexidine gluconate compositions, resin systems and articles. |
US20150238444A1 (en) * | 2012-08-28 | 2015-08-27 | 3M Innovative Properties Company | Chlorhexidine gluconate solubilized in a hydrophobic monoacylglyceride |
CZ308891B6 (en) * | 2014-10-01 | 2021-08-11 | Wald Pharmaceuticals s.r.o | Application composition for increasing the effectiveness of antiseptics and / or disinfectants, application composition containing the application composition, and using this composition |
WO2016168179A1 (en) * | 2015-04-13 | 2016-10-20 | Capsulent | Succulent extract and alginate combined solutions and products incorporating them |
CN110621286A (en) * | 2017-02-23 | 2019-12-27 | 阿里拉健康波士顿有限责任公司 | Eco-friendly biofilm-disrupting antimicrobial formulations, development and use thereof |
CN110141567B (en) * | 2018-02-12 | 2023-07-07 | 四川好医生攀西药业有限责任公司 | Application of berberine in preparation of medicine for treating radiation stomatitis |
US10463590B1 (en) * | 2018-12-20 | 2019-11-05 | Matthias W. Rath | Antiplaque and dental health oral formulation |
US20210299203A1 (en) * | 2020-03-26 | 2021-09-30 | Johnson & Johnson Consumer Inc. | Compositions comprising carum carvi and rosmarinus officinalis extracts and methods of using same |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3097135A (en) * | 1960-02-04 | 1963-07-09 | Abbott Lab | Erythromycin suspensions and method of stabilizing the same |
US3183230A (en) * | 1961-01-13 | 1965-05-11 | Us Vitamin Pharm Corp | Haloaralkyl biguanides |
US5322689A (en) * | 1992-03-10 | 1994-06-21 | The Procter & Gamble Company | Topical aromatic releasing compositions |
US5328682A (en) * | 1990-10-25 | 1994-07-12 | Boots Company Plc | Mouthwash |
WO1994018939A1 (en) * | 1993-02-19 | 1994-09-01 | Warner-Lambert Company | Pre-brushing rinse composition |
US6117415A (en) * | 1999-06-17 | 2000-09-12 | Alpharx Inc. | Toothpaste comprising bioadhesive submicron emulsion for improved delivery of antibacterial and anticaries agents |
WO2000056346A1 (en) * | 1999-03-22 | 2000-09-28 | J.P.M.E.D. Ltd. | Stable oil-in-glycerin emulsion |
WO2002024152A2 (en) * | 2000-09-21 | 2002-03-28 | J.P.M.E.D. Ltd. | Oil in glycerin emulsion |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2286862T3 (en) * | 1997-11-12 | 2007-12-01 | BAUSCH & LOMB INCORPORATED | CLEANING AND DISINFECTION OF CONTACT LINES WITH BIGUANIDA AND A PHOSPHATE AND BORATE STAMP. |
US6660306B2 (en) * | 2000-10-12 | 2003-12-09 | Mickey L. Peshoff | Wound healing compound |
US20040126430A1 (en) * | 2002-09-05 | 2004-07-01 | Angel Arturo J. | Compositions and kits for the removal of irritating compounds from bodily surfaces |
-
2003
- 2003-11-19 WO PCT/IL2003/000980 patent/WO2004045572A1/en not_active Application Discontinuation
- 2003-11-19 US US10/535,961 patent/US20060105000A1/en not_active Abandoned
- 2003-11-19 AU AU2003282358A patent/AU2003282358A1/en not_active Abandoned
- 2003-11-19 EP EP03773971A patent/EP1562543A1/en not_active Withdrawn
-
2007
- 2007-05-29 US US11/807,901 patent/US20080064711A1/en not_active Abandoned
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3097135A (en) * | 1960-02-04 | 1963-07-09 | Abbott Lab | Erythromycin suspensions and method of stabilizing the same |
US3183230A (en) * | 1961-01-13 | 1965-05-11 | Us Vitamin Pharm Corp | Haloaralkyl biguanides |
US5328682A (en) * | 1990-10-25 | 1994-07-12 | Boots Company Plc | Mouthwash |
US5322689A (en) * | 1992-03-10 | 1994-06-21 | The Procter & Gamble Company | Topical aromatic releasing compositions |
WO1994018939A1 (en) * | 1993-02-19 | 1994-09-01 | Warner-Lambert Company | Pre-brushing rinse composition |
WO2000056346A1 (en) * | 1999-03-22 | 2000-09-28 | J.P.M.E.D. Ltd. | Stable oil-in-glycerin emulsion |
US6117415A (en) * | 1999-06-17 | 2000-09-12 | Alpharx Inc. | Toothpaste comprising bioadhesive submicron emulsion for improved delivery of antibacterial and anticaries agents |
WO2002024152A2 (en) * | 2000-09-21 | 2002-03-28 | J.P.M.E.D. Ltd. | Oil in glycerin emulsion |
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005084627A1 (en) * | 2004-03-01 | 2005-09-15 | University Of Iowa Research Foundation | Alcohol-free chlorhexidine compositions |
US7691418B2 (en) | 2004-09-17 | 2010-04-06 | Oystershell Nv | Composition for inhibiting or preventing the formation of a biofilm |
WO2006029893A2 (en) * | 2004-09-17 | 2006-03-23 | Oystershell Nv | Composition for inhibiting or preventing the formation of a biofilm |
WO2006029893A3 (en) * | 2004-09-17 | 2006-10-19 | Oystershell Nv | Composition for inhibiting or preventing the formation of a biofilm |
JP2008540507A (en) * | 2005-05-13 | 2008-11-20 | アドヴァンスト・サイエンティフィック・ディヴェロップメンツ | Pharmaceutical composition comprising an antibacterial agent and an active ingredient selected from carveol, thymol, eugenol, borneol and carvacrol |
WO2007096924A2 (en) * | 2006-02-20 | 2007-08-30 | Maiello, Adolfo | Extraction, preparation and use of active principles of the aloe plant for producing self-meditaion devices such as controlled-release gauzes, bandages, stockings, elastic bands and arch supports |
WO2007096924A3 (en) * | 2006-02-20 | 2007-11-22 | Maiello Adolfo | Extraction, preparation and use of active principles of the aloe plant for producing self-meditaion devices such as controlled-release gauzes, bandages, stockings, elastic bands and arch supports |
FR2918571A1 (en) * | 2007-07-10 | 2009-01-16 | Aroma Technologies Soc Par Act | ANTIBIOTIC COMPOSITIONS BASED ON ESSENTIAL OILS PROPHYLAXIS AND TREATMENT OF NOSOCOMIAL INFECTIONS |
WO2009043987A1 (en) * | 2007-07-10 | 2009-04-09 | Aroma Technologies | Antibiotic compositions containing essential oils, prophylaxis and treatment of nosocomial diseases |
JP2010536836A (en) * | 2007-08-24 | 2010-12-02 | インサイト ヘルス リミテッド | Fungicide |
EP2531167A4 (en) * | 2010-02-07 | 2014-10-15 | J P M E D Ltd | Hair follicle targeting compositions |
EP2531167A1 (en) * | 2010-02-07 | 2012-12-12 | J.P.M.E.D. Ltd | Hair follicle targeting compositions |
DE102010013081A1 (en) * | 2010-03-26 | 2011-09-29 | B. Braun Melsungen Ag | Antimicrobial oil in water emulsion |
EP2699246A1 (en) * | 2011-04-19 | 2014-02-26 | Arms Pharmaceutical LLC. | Method of inhibiting harmful microorganisms and barrier-forming composition therefor |
JP2017081951A (en) * | 2011-04-19 | 2017-05-18 | アームズ ファーマシューティカル エルエルシーArms Pharmaceutical Llc. | Method of inhibiting harmful microorganisms and barrier-forming composition therefor |
JP2014518555A (en) * | 2011-04-19 | 2014-07-31 | アームズ ファーマシューティカル エルエルシー | Method for inhibiting harmful microorganisms and barrier-forming composition therefor |
US10426761B2 (en) | 2011-04-19 | 2019-10-01 | Arms Pharmaceutical, Llc | Method for treatment of disease caused or aggravated by microorganisms or relieving symptoms thereof |
EP2699246A4 (en) * | 2011-04-19 | 2014-10-08 | ARMS Pharmaceutical LLC | Method of inhibiting harmful microorganisms and barrier-forming composition therefor |
WO2012145307A1 (en) | 2011-04-19 | 2012-10-26 | Brian Sokol | Method of inhibiting harmful microorganisms and barrier-forming composition therefor |
US10398645B2 (en) | 2011-04-19 | 2019-09-03 | Arms Pharmaceutical, Llc | Method of inhibiting harmful microorganisms and barrier-forming composition therefor |
AU2011380951B2 (en) * | 2011-11-09 | 2015-11-26 | Colgate-Palmolive Company | Alcohol-free mouthwash |
AU2016200465B2 (en) * | 2011-11-09 | 2016-10-13 | Colgate-Palmolive Company | Alcohol-free mouthwash |
WO2013070198A1 (en) * | 2011-11-09 | 2013-05-16 | Colgate-Palmolive Company | Alcohol-free mouthwash |
US9192565B2 (en) | 2011-11-09 | 2015-11-24 | Colgate-Palmolive Company | Alcohol-free mouthwash |
US9999602B2 (en) | 2013-02-01 | 2018-06-19 | Ddrops Company | Liquid menthol compositions |
AU2014211953B2 (en) * | 2013-02-01 | 2018-08-02 | Ddrops Company | Liquid menthol compositions |
WO2014117265A1 (en) * | 2013-02-01 | 2014-08-07 | Ddrops Company | Liquid menthol compositions |
EP2974725A1 (en) * | 2014-07-16 | 2016-01-20 | Luca D'Alfonso | Pharmaceutical composition |
Also Published As
Publication number | Publication date |
---|---|
AU2003282358A1 (en) | 2004-06-15 |
WO2004045572A8 (en) | 2004-07-08 |
US20080064711A1 (en) | 2008-03-13 |
US20060105000A1 (en) | 2006-05-18 |
EP1562543A1 (en) | 2005-08-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20060105000A1 (en) | Compositions for treating infected skin and mucous membrane comprising an anti-microbial agent and an essential oil | |
Davis et al. | Wound healing. Oral and topical activity of Aloe vera | |
DE69033994T2 (en) | Liquid polymer composition and method of using it | |
RU2571063C2 (en) | Polysaccharide of tamarind seed for application in treatment of microbial infections | |
EP2896396A1 (en) | Herbal formulation for topical wound treatment | |
CN106794210A (en) | Comprising mangosteen extract or α, γ mangostin as the periodontosis prevention of active ingredient or improvement composition | |
US20210220292A1 (en) | Cannabinoid and anesthetic compositions and methods | |
CN110787078A (en) | Toothpaste containing licoflavone and preparation method and application thereof | |
DE69801820T2 (en) | Use of dichlorobenzyl alcohol to make a composition for topical treatment of inflammation | |
DE202006011920U1 (en) | Pharmaceutical composition for preventive and/or curative topical treatment of e.g. rhinitis, comprises combination of aqueous physiological sodium chloride solution and drug mucus in the form of aqueous extract of Lichen islandicus | |
WO2008150246A1 (en) | Herbal haemostatic composition | |
CN111973656B (en) | Oral ulcer preparation containing antibacterial healing-promoting composition | |
RU2790528C1 (en) | Method of local treatment of erosive and ulcerative form of flat lichen of the mucous membranes of the mouth | |
DE102012000416A1 (en) | Topical composition, useful for treating wounds, preferably open wounds and ulcers, comprises fusafungine and/or one of its derivative and onion extract | |
KR102445058B1 (en) | Roll type ointment improved usability and hygiene | |
Boddu et al. | Excipients and non-medicinal agents as active pharmaceutical ingredients | |
WO2021177936A1 (en) | Cannabinoid and anesthetic compositions and methods | |
YN et al. | PHYTOTHERAPEUTIC HERBAL TREATMENT FOR PERIODONTAL POLYMICROBIAL INFECTION: A REVIEW AND UPDATE | |
RO118929B1 (en) | Preparation for treating burns |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PG PH PL PT RO RU SC SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): BW GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
WR | Later publication of a revised version of an international search report | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2003773971 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2006105000 Country of ref document: US Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 10535961 Country of ref document: US |
|
WWP | Wipo information: published in national office |
Ref document number: 2003773971 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 10535961 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: JP |