EP1635849A1 - Medicament for internal application, in particular against cancerous diseases - Google Patents
Medicament for internal application, in particular against cancerous diseasesInfo
- Publication number
- EP1635849A1 EP1635849A1 EP04733761A EP04733761A EP1635849A1 EP 1635849 A1 EP1635849 A1 EP 1635849A1 EP 04733761 A EP04733761 A EP 04733761A EP 04733761 A EP04733761 A EP 04733761A EP 1635849 A1 EP1635849 A1 EP 1635849A1
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- EP
- European Patent Office
- Prior art keywords
- surfactants
- polydimethylsiloxane
- weight
- proportion
- medicinal product
- 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.)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/80—Polymers containing hetero atoms not provided for in groups A61K31/755 - A61K31/795
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Definitions
- the present invention relates to a remedy for internal use, especially against cancer.
- This object is achieved by a remedy which has polydimethylsiloxane and surfactants, the proportion of polydimethylsiloxane exceeding the proportion of surfactants.
- the special feature of the invention is that the effect according to the invention is achieved only by adding surfactants.
- Mixing the polydimethylsiloxane with surfactants means that the body is given the opportunity to emulsify the siloxane and make it usable. This is achieved by the surfactants breaking up the molecular structure of the polydimethylsiloxane.
- the proportion of surfactants, based on the weight of the solution, can be significantly lower than the proportion of polydimethylsiloxane.
- Anionic, amphoteric and nonionic surfactants can be used, the proportion by weight of the anionic surfactants exceeding the proportion by weight of the amphoteric and nonionic.
- Polydimethylsiloxane is made from raw silicon.
- Raw silicon is obtained from sand and coal, which is further processed into the desired silicones in a continuous process.
- Natural gas or crude oil are used to produce methanol (synthesis gas), another starting material for silicone synthesis.
- Chlorine is obtained by electrolysis of rock salt solutions and is added to the process in the form of HC1.
- methanol is converted to chloromethane with HC1 (chloromethane synthesis).
- a mixture of crude silanes (chlorosilane synthesis) is then obtained by reacting chloromethane with silicon. These are separated by distillation, dichlorodimethylsilane (CH3) 2SiC12 then being converted into polydimethylsiloxane by hydrolysis.
- the remedy is nebulized using suitable nebulization techniques.
- suitable nebulization techniques Various devices are available for this:
- Compressed air operated Venturi nozzle nebulizer a) direct nebulization b) with aerosol reservoir c) with positive pressure inhalation 2.
- Mechanical single-component jet nebulizer a) direct nebulization b) with aerosol reservoir c) with positive pressure inhalation 2.
- aluminum silicate in particular natural zeolite with a grain size of 10 ⁇ m to 70 ⁇ m, in particular 40 ⁇ m and dolomite powder with a grain size of 2 ⁇ m to 30 ⁇ m, in particular 10 ⁇ m, can also be added. This results in powder that can be administered in capsules.
- the basic skeleton of the crystal lattice of the zeolite consists primarily of SiÜ4 tetrahedra. It has cavities in which ions, e.g. B. are sodium, potassium and calcium, which can be easily exchanged with themselves and with their substrate environment.
- This mineral-specific crystal structure (cage structure) of zeolite has the excellent property in living organisms, toxic substances, such as. B. ammonia and other nitrogen compounds, but also heavy metals, to bind (absorb) and excrete via the intestinal metabolism. The extracted toxic substances are exchanged for minerals that the body urgently needs. In this way, the homeostasis of the organism, in particular that of the mineral metabolism, is maintained or restored.
- the zeolite also has a positive stimulating effect on the entire metabolism and in the growth and healing processes of the organism.
- zeolite Because of its open molecular structure, zeolite also has the ability to absorb large quantities of liquids. This is advantageous since, despite mixing with the additional components mentioned above, a flowable powder can be formed.
- the additional components may have the proportions in the end product:
- Aluminum silicate 50 to 90, in particular 70% by weight,
- the resulting mixture is a flowable powder and can be processed into a remedy in a variety of ways. It is thus possible to encapsulate the powdery mixture, for example in the form of the widely used gelatin capsules, which dissolve in the digestive tract. In addition, it is readily possible to press tablets from the powdered mixture, which can be taken with or without liquid.
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- Health & Medical Sciences (AREA)
- Veterinary Medicine (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)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
The invention relates to a medicament for internal application, in particular against cancerous diseases. The medicament comprises polydimethylsiloxane and surfactants, whereby the proportion of polydimethylsiloxane is greater than the proportion of surfactants.
Description
Bezeichnung: Heilmittel zur inneren Anwendung, insbesondere gegen KrebserkrankungenName: Remedy for internal use, especially against cancer
Die vorliegende Erfindung betrifft ein Heilmittel für eine innere Anwendung, insbesondere gegen Krebserkrankungen.The present invention relates to a remedy for internal use, especially against cancer.
Seit langem besteht ein Bedarf an Heilmitteln gegen Krebserkrankungen. Zwar sind Heilmittel bekannt und werden auch eingesetzt, jedoch sind diese oftmals mit erheblichen Nebenwirkungen verbunden. Auch sind die derzeit eingesetzten Heilmittel nicht zuletzt wegen ihrer aufwendigen Herstellung sehr teuer. Es besteht deshalb weiterhin der Wunsch nach verträglichen und kostengünstigen Heilmitteln für diesen Bereich.There has long been a need for cures for cancer. Although remedies are known and are also used, they are often associated with considerable side effects. The remedies currently used are also very expensive, not least because of their complex production. There is therefore still a desire for compatible and inexpensive remedies for this area.
Hier setzt nun die Erfindung ein. Sie hat es sich zur Aufgabe gemacht, ein Heilmittel zur inneren Anwendung, insbesondere gegen Krebskrankungen, anzugeben, mit dem ein möglichst wirkungsvolles Bekämpfen von Krebstumoren möglich ist. Die Nebenwirkungen sollen dabei möglichst gering und das Heilmittel möglichst kostengünstig sein.This is where the invention begins. It has set itself the task of specifying a cure for internal use, in particular against cancer, with which the most effective fight against cancerous tumors is possible. The side effects should be as low as possible and the remedy should be as inexpensive as possible.
Gelöst wird diese Aufgabe durch ein Heilmittel, das Polydimethylsiloxan und Tenside aufweist, wobei der Anteil an Polydimethylsiloxan den Anteil an Tensiden übersteigt.This object is achieved by a remedy which has polydimethylsiloxane and surfactants, the proportion of polydimethylsiloxane exceeding the proportion of surfactants.
Die Besonderheit der Erfindung besteht darin, dass nur durch die Zugabe von Tensiden die erfindungsgemäße Wirkung erzielt wird. Die Vermischung des Polydimethylsiloxane mit Tensiden bewirkt nämlich, dass dem Körper die Möglichkeit gegeben wird, das Siloxan zu emulgieren und nutzbar zu machen. Dies wird dadurch erreicht, dass die Tenside die Molekülstruktur des Polydimethylsiloxans aufbrechen. Der Anteil an Tensiden kann bezogen auf das Gewicht der Lösung deutlich geringer sein als der Anteil an Polydimethylsiloxan.
Es können anionische, amphotere und nichtionische Tenside verwendet werden, wobei der Gewichtsanteil der anionischen Tenside den Gewichtsanteil der amphoteren und nichtionischen übersteigt.The special feature of the invention is that the effect according to the invention is achieved only by adding surfactants. Mixing the polydimethylsiloxane with surfactants means that the body is given the opportunity to emulsify the siloxane and make it usable. This is achieved by the surfactants breaking up the molecular structure of the polydimethylsiloxane. The proportion of surfactants, based on the weight of the solution, can be significantly lower than the proportion of polydimethylsiloxane. Anionic, amphoteric and nonionic surfactants can be used, the proportion by weight of the anionic surfactants exceeding the proportion by weight of the amphoteric and nonionic.
In diesem Zusammenhang ist zu erwähnen, dass die meisten Vorkommen von Silizium, selbst das Bergkristall, welches aus purem Silizium besteht, keine bioaktive Wirkung besitzen. Diese Eigenschaft wird, wie bereits ausgeführt, erst durch die Zugabe von Tensiden erreicht.In this context it should be mentioned that most deposits of silicon, even the rock crystal, which consists of pure silicon, have no bioactive effect. As already stated, this property is only achieved by adding surfactants.
Polydimethylsiloxan wird Rohsilizium hergestellt. Aus Sand und Kohle wird Rohsilizium gewonnen, das in einem kontinuierlichen Prozess zu den gewünschten Siliconen weiterverarbeitet wird. Erdgas oder Erdöl dienen dazu, Methanol herzustellen (Synthesegas), ein weiterer Ausgangs stoff zur Siliconsynthese. Durch Elektrolyse von Steinsalzlösungen wird Chlor gewonnen, das in Form von HC1 dem Prozess zugeführt wird.Polydimethylsiloxane is made from raw silicon. Raw silicon is obtained from sand and coal, which is further processed into the desired silicones in a continuous process. Natural gas or crude oil are used to produce methanol (synthesis gas), another starting material for silicone synthesis. Chlorine is obtained by electrolysis of rock salt solutions and is added to the process in the form of HC1.
Im ersten Schritt wird Methanol mit HC1 zu Chlormethan umgesetzt (Chlormethansynthese) . Anschließend gewinnt man durch Reaktion von Chlormethan mit Silizium ein Gemisch von Rohsilanen (Chlorsilansynthese) . Diese werden durch Destillation getrennt, wobei Dichlordimethylsilan (CH3)2SiC12 dann durch Hydrolyse in Polydimethylsiloxan überführt wird.In the first step, methanol is converted to chloromethane with HC1 (chloromethane synthesis). A mixture of crude silanes (chlorosilane synthesis) is then obtained by reacting chloromethane with silicon. These are separated by distillation, dichlorodimethylsilane (CH3) 2SiC12 then being converted into polydimethylsiloxane by hydrolysis.
Es ist grundsätzlich möglich, das erfindungsgemäße Heilmittel zu inhalieren. Zur Inhalation wird das Heilmittel mittels geeigneter Vernebelungstechniken apparativ vernebelt. Hierzu werden verschiedene Apparaturen angeboten:In principle, it is possible to inhale the medicinal product according to the invention. For inhalation, the remedy is nebulized using suitable nebulization techniques. Various devices are available for this:
1. Pressluft betriebener Venturi-Düsenvernebler: a) direkte Vernebelung b) mit Aerosolreservoir c) mit Überdruckinhalat
2. Mechanischer Einstoff-Düsenvernebler1. Compressed air operated Venturi nozzle nebulizer: a) direct nebulization b) with aerosol reservoir c) with positive pressure inhalation 2. Mechanical single-component jet nebulizer
3. Ultraschallvernebelung3. Ultrasonic nebulization
4. Ultraschalldruck über perforiertes Sieb4. Ultrasonic printing over perforated screen
5. Ultraschallgetriebene perforierte Membran5. Ultrasound-driven perforated membrane
6. Elektromechanischer Druck durch perforierte Membran6. Electromechanical pressure through perforated membrane
Die Inhalation mit einer Atemmaske sowie mit einem mit Mundstück oder einem Nasenstück haben sich als gut geeignet erwiesen.Inhalation with a breathing mask as well as with a mouthpiece or a nose piece has proven to be well suited.
Neben den genannten Bestandteilen kann zusätzlich Aluminiumsilikat, insbesondere Naturzeolith mit einer Korngröße von 10 μm bis 70 μm, insbesondere 40 μm und Dolomitpulver mit einer Korngröße von 2 μm bis 30 μm, insbesondere 10 μm zugesetzt werden. Somit ergibt sich Pulver, das in Kapseln verabreicht werden kann.In addition to the components mentioned, aluminum silicate, in particular natural zeolite with a grain size of 10 μm to 70 μm, in particular 40 μm and dolomite powder with a grain size of 2 μm to 30 μm, in particular 10 μm, can also be added. This results in powder that can be administered in capsules.
Das Grundskelett des Kristallgitters des Zeoliths besteht in erster Linie aus SiÜ4 Tetraedern. Es weist Hohlräume auf, in denen sich Ionen, z. B. Natrium, Kalium und Calcium befinden, die sich mit sich und mit ihrer Substratumgebung leicht austauschen lassen. Diese mineralstoffspezifische Kristallstruktur (Käfigstruktur) von Zeolith hat in lebenden Organismen die vorzügliche Eigenschaft, toxische Stoffe, wie z. B. Ammoniak und andere Stickstoffverbindungen, aber auch Schwermetalle, an sich zu binden (absorbieren) und über den Darmstoffwechsel auszuscheiden. Die entzogenen toxischen Stoffe werden gegen Mineralien ausgetauscht, die der Körper dringend benötigt. Auf diese Weise wird die Homöostase des Organismus, insbesondere die des Mineralstoffwechsels, aufrechterhalten bzw. wieder hergestellt.The basic skeleton of the crystal lattice of the zeolite consists primarily of SiÜ4 tetrahedra. It has cavities in which ions, e.g. B. are sodium, potassium and calcium, which can be easily exchanged with themselves and with their substrate environment. This mineral-specific crystal structure (cage structure) of zeolite has the excellent property in living organisms, toxic substances, such as. B. ammonia and other nitrogen compounds, but also heavy metals, to bind (absorb) and excrete via the intestinal metabolism. The extracted toxic substances are exchanged for minerals that the body urgently needs. In this way, the homeostasis of the organism, in particular that of the mineral metabolism, is maintained or restored.
Somit werden empfindliche Organsysteme, z. B. Gehirn, Nervensystem, Hormonsystem, Immunsystem, Leber, Nieren u. a. nicht nur von toxischen Schäden geschützt, sondern auch ihre Widerstandsfähigkeit gegenüber schädlichen pathogenen Einflüssen erhöht
Das Zeolith greift außerdem, wie das Silizium, positiv stimulierend in den gesamten Stoffwechsel und in die Wachstums- und Heilungsprozesse des Organismus ein.Thus sensitive organ systems, e.g. B. brain, nervous system, hormone system, immune system, liver, kidneys, among other things, not only protected from toxic damage, but also increases their resistance to harmful pathogenic influences Like the silicon, the zeolite also has a positive stimulating effect on the entire metabolism and in the growth and healing processes of the organism.
Zeolith hat zudem wegen seiner offenen Molekülstruktur die Fähigkeit, größere Mengen Flüssigkeiten aufzunehmen. Dies ist vorteilhaft, da dadurch trotz Vermischung mit den oben genannten zusätzlichen Bestandteilen ein fließfähiges Pulver gebildet werden kann.Because of its open molecular structure, zeolite also has the ability to absorb large quantities of liquids. This is advantageous since, despite mixing with the additional components mentioned above, a flowable powder can be formed.
Beispielsweise können die zusätzlichen Bestandteile die Anteile im Endprodukt aufweisen:For example, the additional components may have the proportions in the end product:
- Aluminiumsilikat: 50 bis 90, insbesondere 70 Gew.%,Aluminum silicate: 50 to 90, in particular 70% by weight,
- Dolomitpulver: 5 bis 45, insbesondere 25 Gew.%.- Dolomite powder: 5 to 45, in particular 25% by weight.
Die so entstehende Mischung ist ein fließfähiges Pulver und kann auf vielfältige Weise zu einem Heilmittel verarbeitet werden. So ist es möglich, die pul- verförmige Mischung zu verkapseln, beispielsweise in Form der weit verbreiteten Gelatinekapseln, die sich im Verdauungstrakt auflösen. Darüber hinaus ist es ohne weiteres möglich, aus der pulverförmigen Mischung Tabletten zu pressen, die mit oder ohne Flüssigkeit eingenommen werden können.The resulting mixture is a flowable powder and can be processed into a remedy in a variety of ways. It is thus possible to encapsulate the powdery mixture, for example in the form of the widely used gelatin capsules, which dissolve in the digestive tract. In addition, it is readily possible to press tablets from the powdered mixture, which can be taken with or without liquid.
Es hat sich gezeigt, dass die Lösungen gegen Krebszellen wirksam sind, jedoch keinen Einfluss auf gesunde Zellen haben.The solutions against cancer cells have been shown to be effective, but have no effect on healthy cells.
Es hat sich in klinischen Versuchen gezeigt, dass das erfindungsgemäße Heilmittel folgende Wirkungen aufweist:Clinical trials have shown that the medicinal product according to the invention has the following effects:
- bessere Verträglichkeit von Chemo- und Strahlentherapien,- better tolerance of chemotherapy and radiation therapies,
- Stornieren des Tumorwachstums,- Canceling tumor growth,
- Verhärten (Mineralisieren des Tumors),Hardening (mineralization of the tumor),
- Teilweise Einkapseln und Reduzierung des Tumors,
- Verbesserung des Allgemeinzustandes,- partial encapsulation and reduction of the tumor, - improvement of general condition,
- Beseitigung von entzündlichen Prozessen als Nebenwirkung der Strahlen und Chemotherapie, z.B. der Mundschleimhaut.- Eliminate inflammatory processes as a side effect of radiation and chemotherapy, e.g. the oral mucosa.
Außerdem hat sich in ersten Tests erwiesen, dass das erfindungsgemäße Heilmittel virenhemmend wirkt. Es haben sich erste Erfolge bezüglich der Behandlung von AIDS (HIV) und SARS gezeigt. Diesbezüglich behält sich der Anmelder eine Teilanmeldung vor.
In addition, it has been shown in initial tests that the medicinal product according to the invention has an antiviral effect. The first successes with the treatment of AIDS (HIV) and SARS have been shown. In this regard, the applicant reserves a divisional application.
Claims
1. Heilmittel zur inneren Anwendung, insbesondere gegen Krebserkrankungen, gekennzeichnet durch die Bestandteile Polydimethylsiloxan und Tenside, wobei der Anteil an Polydimethylsiloxan den Anteil an Tensiden übersteigt.1. Remedies for internal use, in particular against cancer, characterized by the components polydimethylsiloxane and surfactants, the proportion of polydimethylsiloxane exceeding the proportion of surfactants.
2. Heilmittel nach Anspruch 1, dadurch gekennzeichnet, dass in der Mischung der beiden Bestandteile der Anteil an Polydimethylsiloxan etwa 90-99,9, insbesondere 99 Gew.% und der Anteil an Tensiden von 0, 1- 10, insbesondere 1 Gew.% beträgt.2. Medicament according to claim 1, characterized in that in the mixture of the two constituents the proportion of polydimethylsiloxane is approximately 90-99.9, in particular 99% by weight and the proportion of surfactants is 0.1-1, in particular 1% by weight. is.
3. Heilmittel nach Anspruch 1 oder Anspruch 2, dadurch gekennzeichnet, dass zusätzlich Aluminiumsilikat, insbesondere Naturzeolith mit einer Korngröße von 10 μm bis 70 μm, insbesondere 40 μm und Dolomitpulver mit einer Korngröße von 2 μm bis 30 μm, insbesondere 10 μm zugesetzt ist.3. Medicinal product according to claim 1 or claim 2, characterized in that aluminum silicate, in particular natural zeolite with a grain size of 10 μm to 70 μm, in particular 40 μm and dolomite powder with a grain size of 2 μm to 30 μm, in particular 10 μm, is additionally added.
4. Heilmittel nach Anspruch 3, dadurch gekennzeichnet, dass die zusätzlichen Bestandteile folgende Anteile im Endprodukt aufweisen:4. Medicinal product according to claim 3, characterized in that the additional components have the following proportions in the end product:
- Aluminiumsilikat: 50 bis 90, insbesondere 70 Gew.%,Aluminum silicate: 50 to 90, in particular 70% by weight,
- Dolomitpulver: 5 bis 45, insbesondere 25 Gew.%.- Dolomite powder: 5 to 45, in particular 25% by weight.
5. Heilmittel nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass anionische, amphotere und nichtionische Tenside enthalten sind, wobei der Gewichtsanteil der anionischen Tenside den Gewichtsanteil der amphoteren und nichtionischen Tenside überwiegt. 5. Medicinal product according to one of claims 1 to 4, characterized in that it contains anionic, amphoteric and nonionic surfactants, the weight fraction of the anionic surfactants outweighing the weight fraction of the amphoteric and nonionic surfactants.
6. Verwendung von Polydimethylsiloxan und Tensiden zur Herstellung eines Heilmittels zur inneren Anwendung, insbesondere gegen Krebserkrankungen.6. Use of polydimethylsiloxane and surfactants for the manufacture of a medicinal product for internal use, in particular against cancer.
7. Verwendung von Polydimethylsiloxan und Tensiden zur Herstellung eines Heilmittels nach Anspruch 7, dadurch gekennzeichnet, dass in der Mischung der beiden Bestandteile der Anteil an Polydimethylsiloxan etwa 90 - 99,9, insbesondere 99 Gew.% und der Anteil an Tensiden von 0, 1°- 10, insbesondere 1 Gew.% beträgt.7. Use of polydimethylsiloxane and surfactants for the production of a medicinal product according to claim 7, characterized in that in the mixture of the two constituents the proportion of polydimethylsiloxane is approximately 90-99.9, in particular 99% by weight and the proportion of surfactants is 0.1 ° - 10, in particular 1% by weight.
8. Verwendung von Polydimethylsiloxan und Tensiden zur Herstellung eines Heilmittels nach Anspruch 6 oder Anspruch 7, dadurch gekennzeichnet, dass zusätzlich Aluminiumsilikat, insbesondere Naturzeolith mit einer Korngröße von 10 bis 70, insbesondere 40 μm und Dolomitpulver mit einer Korngröße von 2 bis 30, insbesondere 10 μm zugesetzt ist.8. Use of polydimethylsiloxane and surfactants for the preparation of a medicament according to claim 6 or claim 7, characterized in that in addition aluminum silicate, in particular natural zeolite with a grain size of 10 to 70, in particular 40 μm and dolomite powder with a grain size of 2 to 30, in particular 10 μm is added.
9. Verwendung von Polydimethylsiloxan und Tensiden zur Herstellung eines Heilmittels nach einem der Ansprüche 6 bis 8, dadurch gekennzeichnet, dass die zusätzlichen Bestandteile folgende Anteile im Endprodukt aufweisen:9. Use of polydimethylsiloxane and surfactants for the production of a medicinal product according to one of claims 6 to 8, characterized in that the additional components have the following proportions in the end product:
- Aluminiumsilikat: 50 bis 90, insbesondere 70 Gew.%,Aluminum silicate: 50 to 90, in particular 70% by weight,
- Dolomitpulver: 5 bis 45, insbesondere 25 Gew.%.- Dolomite powder: 5 to 45, in particular 25% by weight.
10. Verwendung von Polydimethylsiloxan und Tensiden zur Herstellung eines Heilmittels nach einem der Ansprüche 6 bis 9, dadurch gekennzeichnet, dass anionische, amphotere und nichtionische Tenside enthalten sind, wobei der Gewichtsanteil der anionischen Tenside den Gewichtsanteil der amphoteren und nichtionischen Tenside überwiegt. 10. Use of polydimethylsiloxane and surfactants for the production of a medicament according to one of claims 6 to 9, characterized in that anionic, amphoteric and nonionic surfactants are contained, the weight fraction of the anionic surfactants outweighing the weight fraction of the amphoteric and nonionic surfactants.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE10323758A DE10323758A1 (en) | 2003-05-22 | 2003-05-22 | Remedies for internal use, especially against cancer |
PCT/DE2004/001048 WO2004105776A1 (en) | 2003-05-22 | 2004-05-19 | Medicament for internal application, in particular against cancerous diseases |
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Publication Number | Publication Date |
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EP1635849A1 true EP1635849A1 (en) | 2006-03-22 |
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EP04733761A Withdrawn EP1635849A1 (en) | 2003-05-22 | 2004-05-19 | Medicament for internal application, in particular against cancerous diseases |
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US (1) | US20070172435A1 (en) |
EP (1) | EP1635849A1 (en) |
JP (1) | JP2006528211A (en) |
CN (1) | CN1795001A (en) |
AU (1) | AU2004243524A1 (en) |
CA (1) | CA2526175A1 (en) |
DE (1) | DE10323758A1 (en) |
RU (1) | RU2005140097A (en) |
WO (1) | WO2004105776A1 (en) |
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DE10323759A1 (en) * | 2003-05-22 | 2004-12-16 | Bauer, Wulf, Dr. | Remedies for internal use, especially against cancer |
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CN104606261B (en) * | 2015-03-05 | 2018-02-09 | 潘友长 | A kind of zeolite pharmaceutical composition and its production and use |
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2003
- 2003-05-22 DE DE10323758A patent/DE10323758A1/en not_active Withdrawn
-
2004
- 2004-05-19 CA CA002526175A patent/CA2526175A1/en not_active Abandoned
- 2004-05-19 CN CNA2004800140406A patent/CN1795001A/en active Pending
- 2004-05-19 US US10/557,317 patent/US20070172435A1/en not_active Abandoned
- 2004-05-19 JP JP2006529603A patent/JP2006528211A/en not_active Withdrawn
- 2004-05-19 EP EP04733761A patent/EP1635849A1/en not_active Withdrawn
- 2004-05-19 AU AU2004243524A patent/AU2004243524A1/en not_active Abandoned
- 2004-05-19 WO PCT/DE2004/001048 patent/WO2004105776A1/en active Application Filing
- 2004-05-19 RU RU2005140097/15A patent/RU2005140097A/en unknown
Non-Patent Citations (1)
Title |
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See references of WO2004105776A1 * |
Also Published As
Publication number | Publication date |
---|---|
CA2526175A1 (en) | 2004-12-09 |
WO2004105776A1 (en) | 2004-12-09 |
JP2006528211A (en) | 2006-12-14 |
DE10323758A1 (en) | 2004-12-16 |
RU2005140097A (en) | 2006-08-10 |
US20070172435A1 (en) | 2007-07-26 |
AU2004243524A1 (en) | 2004-12-09 |
CN1795001A (en) | 2006-06-28 |
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