WO2004096248A2 - Composition et utilisation de l’iode pur dissout dans l’huile essentielle de malaleuca alternifolia et/ou de malaleuca quinquinervia - Google Patents
Composition et utilisation de l’iode pur dissout dans l’huile essentielle de malaleuca alternifolia et/ou de malaleuca quinquinervia Download PDFInfo
- Publication number
- WO2004096248A2 WO2004096248A2 PCT/BE2004/000059 BE2004000059W WO2004096248A2 WO 2004096248 A2 WO2004096248 A2 WO 2004096248A2 BE 2004000059 W BE2004000059 W BE 2004000059W WO 2004096248 A2 WO2004096248 A2 WO 2004096248A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- grams
- melaleuca
- composition
- iodine
- pure
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/73—Rosaceae (Rose family), e.g. strawberry, chokeberry, blackberry, pear or firethorn
- A61K36/736—Prunus, e.g. plum, cherry, peach, apricot or almond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/18—Iodine; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/61—Myrtaceae (Myrtle family), e.g. teatree or eucalyptus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/899—Poaceae or Gramineae (Grass family), e.g. bamboo, corn or sugar cane
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
Definitions
- the original feature of the present invention lies, on the one hand, in the use of 1 PURE IODE, in the solid state, which dissolves instantly in the essential oil of Melaleuca Altemifolia (tea tree) and / or Quinquinervia (Niaouli) and, on the other hand, to allow the pure iodine to be contained in a stable and durable emulsion in a strictly dosed formula described below.
- the invention is characterized precisely in that the iodine in its pure and solid state dissolves instantaneously while retaining its effectiveness and its stability allowing the optimal use of the properties of iodine in the pure state.
- the present invention relates more particularly to the use of this "IODE PUR-MELALEUCA" solution in a formulation whose product is indicated for a general therapeutic treatment for external use and specially indicated in the treatment of labial and genital herpes.
- This composition is in the form of gel, lotion, or cream. This new formulation radically treats labial and genital herpes.
- the iodine presented in the form of iodine alcohol is very well known for its attributes of bactericide, virucide, fungicide.
- the research and experiments carried out by the applicant have resulted in discovering that pure iodine (and not iodine alcohol) dissolves in essential oil of MELALEUCA ALTERNIFOLIA and / or standardized QUINQUINERVIA (following the attached tables) while allowing the iodine to keep its effective attributes by containing it in a stable emulsion.
- MELALEUCA (ALTERNIFOLIA and QUINQUINERVIA) comes from the Australian tea tree. Its substance, called Titrol in its raw form and Melasol in aqueous solution, comes from a species of papery bark tree: LE MELALEUCA ALTERNIFOLIA.
- Simple herpes type 2 corresponds to genital herpes.
- Genital herpes is a sexually transmitted disease characterized by the appearance of bouquet vesicles at the site of inoculation associated with regional lymphadenopathy during primary infection. The hallmark of the infection is the recurrence of vesicles in the same place.
- the usual local treatments for herpes are generally carried out using a pharmaceutical composition containing acyclovir or sodium phosphate vidarabine.
- This new active substance is mainly intended for the treatment of cold and genital herpes (external use).
- the original feature of the present invention lies in the use of pure and therefore solid iodine (and not iodine alcohol) which dissolves in the essential oil of Melaleuca Altemifolia and / or Quinquinervia.
- the composition according to the invention is presented in the form of a cream or a transparent gel on the skin.
- the pH of the compound is between 3% and 8% and preferably between 3.5% and 7%.
- the content of pure iodine is between 1% and 10% and Melaleuca oil between 1% and 30%.
- composition may contain, in addition to the "pure iodine-Melaleuca” solution, liquid glycerin, boric acid, wheat germ standardized according to the formulation, explants adapted according to the intended use such as moisturizing agents, propylene glycol, sweet almond oil, neutralizing agents intended to adjust the PH as an example of sodium hydroxide.
- "pure iodine-Melaleuca” solution liquid glycerin, boric acid, wheat germ standardized according to the formulation, explants adapted according to the intended use such as moisturizing agents, propylene glycol, sweet almond oil, neutralizing agents intended to adjust the PH as an example of sodium hydroxide.
- PURE-MELALEUCA IODE solution - Pure iodine igram dissolved in 2.5 milliliters of Melaleuca Altemifolia (tea tree)
- Carbomer in gel form e.g. carbopol gel
- the new active substance (according to the above formula) has been tested on cases of acute cold sores: - On cold sores: the product is applied three to four times a day to the area of the skin affected by a patient suffering from an outbreak of HSV-1 and HSV-2 (herpes simplex virus) herpes during the primary infection phase. On the treated lesion of more than 4 cm, we found that from the first application the wound stopped causing pain and the patient stopped scratching. The affected areas are no longer painful or numb. They were no longer hot and itchy. From the first evening, the wound stopped flowing and after 36 hours of treatment (3 to 4 times a day) the wound was dry.
- HSV-1 and HSV-2 herpes simplex virus
- the invention provides a process for the solubilization of pure Iodine in the essential oil of Melaleuca Altemifolia (tea-tree) / Quinquinervia (niaouli) in any minimum proportion of the Iodine and maximum thereof. .
- the invention allows, according to the invented formula, pure iodine to contain itself as a stable emulsion , and to retain its attributes of bactericide, virucide, fungicide, extremely useful in compositions indicated for a therapeutic treatment with external use
- the invention relates to a composition intended for treating labial and genital herpes comprising the following components (or the functionally equivalent components) in the ranges of relative ratios indicated below:
- Propylene glycol l to 60 milliliters
- Glycerin l to 95 grams Wheat germ (*): l to 99 grams
- Sweet almond oil 1 to 99 milliliters
- Carbomer l to 5 grams
- Sx lanette wax l to 50 grams
- Boric acid l to 30 grams
- the invention relates to a composition intended for treating labial and genital herpes comprising the following components (or the functionally equivalent components) in the range of relative ratios indicated below:
- the invention relates to a product specially characterized in that it is obtained by such process described above for a therapeutic treatment for general external use other than the treatment of herpes.
- the components below can be part of a composition intended for external therapeutic use. They are present in the ranges of relative reports indicated below:
- this formulation can be part of a composition intended especially for treating labial and genital herpes, this composition comprising the following components (or the functionally equivalent components) in the ranges of relative ratios indicated below:
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Medical Informatics (AREA)
- Mycology (AREA)
- Alternative & Traditional Medicine (AREA)
- Botany (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Inorganic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04729797A EP1628672A2 (fr) | 2003-04-28 | 2004-04-28 | Composition et utilisation de l'iode pur dissout dans l'huile essentielle de malaleuca alternifolia et/ou de malaleuca quinquinervia |
| CA002524092A CA2524092A1 (fr) | 2003-04-28 | 2004-04-28 | Composition et utilisation de l'iode pur dissout dans l'huile essentielle de malaleuca alternifolia et/ou de malaleuca quinquinervia |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE2003/0265A BE1015498A5 (fr) | 2003-04-28 | 2003-04-28 | Composition et utilisation de l'iode pur dissout dans l'huile essentielle de melaleuca alternifolia et/ou de melaleuca quinquinervia. |
| BE2003/0265 | 2003-04-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2004096248A2 true WO2004096248A2 (fr) | 2004-11-11 |
| WO2004096248A3 WO2004096248A3 (fr) | 2005-01-13 |
Family
ID=33315071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/BE2004/000059 Ceased WO2004096248A2 (fr) | 2003-04-28 | 2004-04-28 | Composition et utilisation de l’iode pur dissout dans l’huile essentielle de malaleuca alternifolia et/ou de malaleuca quinquinervia |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP1628672A2 (fr) |
| BE (1) | BE1015498A5 (fr) |
| CA (1) | CA2524092A1 (fr) |
| WO (1) | WO2004096248A2 (fr) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006089348A1 (fr) * | 2005-01-20 | 2006-08-31 | Kayban Pty Ltd | Agent antimicrobien |
| WO2009153791A1 (fr) * | 2008-06-19 | 2009-12-23 | Avivi-Easy-Life Ltd. | Composés terpénoïdes antiviraux |
| ITRE20090011A1 (it) * | 2009-02-11 | 2010-08-12 | Gianni Magnanini | Composizione terapeutica per il trattamento dell'herpes labialis |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB589097A (en) * | 1945-02-15 | 1947-06-11 | Parisepsin Ltd | Improvements in or relating to the manufacture of antiseptic preparations |
| DD210384A3 (de) * | 1982-09-24 | 1984-06-06 | Pharmazeutisches Werk Halle Bo | Verfahren zur herstellung eines medizinischen schwefelbades mit komplexer wirkung |
| IT1255450B (it) * | 1992-06-30 | 1995-10-31 | Montefarmaco Spa | Uso di acidi biliari come agenti antivirali |
| US6019941A (en) * | 1996-01-30 | 2000-02-01 | Porcello; Joseph A. | Method for disinfecting dermal surfaces and inanimate surfaces, and particularly air ducts |
| US5972362A (en) * | 1997-12-23 | 1999-10-26 | Wenker; Naamah T. | Therapeutic skin preparation |
| RU2150935C1 (ru) * | 1999-06-22 | 2000-06-20 | Московский государственный медико-стоматологический университет | Защитно-профилактический крем |
| WO2001087247A2 (fr) * | 2000-05-18 | 2001-11-22 | Elena Lurya | Composition a base d'herbes medicinales utiles dans le traitement de la cavite buccale et procede d'administration de cette composition |
| RU2178290C1 (ru) * | 2000-11-22 | 2002-01-20 | Московский государственный медико-стоматологический университет | Защитно-профилактический крем |
| ATE525061T1 (de) * | 2001-02-28 | 2011-10-15 | Axiomedic Ltd | Feste selbst-haftende zusammensetzungen zur topischen behandlung von störungen der mundschleimhaut |
-
2003
- 2003-04-28 BE BE2003/0265A patent/BE1015498A5/fr not_active IP Right Cessation
-
2004
- 2004-04-28 EP EP04729797A patent/EP1628672A2/fr not_active Withdrawn
- 2004-04-28 WO PCT/BE2004/000059 patent/WO2004096248A2/fr not_active Ceased
- 2004-04-28 CA CA002524092A patent/CA2524092A1/fr not_active Abandoned
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006089348A1 (fr) * | 2005-01-20 | 2006-08-31 | Kayban Pty Ltd | Agent antimicrobien |
| EP1883401A4 (fr) * | 2005-01-20 | 2009-06-10 | Kayban Pty Ltd | Agent antimicrobien |
| US9078845B2 (en) | 2005-01-20 | 2015-07-14 | Kayban Pty Ltd | Anti-microbial agent |
| WO2009153791A1 (fr) * | 2008-06-19 | 2009-12-23 | Avivi-Easy-Life Ltd. | Composés terpénoïdes antiviraux |
| ITRE20090011A1 (it) * | 2009-02-11 | 2010-08-12 | Gianni Magnanini | Composizione terapeutica per il trattamento dell'herpes labialis |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004096248A3 (fr) | 2005-01-13 |
| CA2524092A1 (fr) | 2004-11-11 |
| EP1628672A2 (fr) | 2006-03-01 |
| BE1015498A5 (fr) | 2005-05-03 |
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