EP1628671A1 - Steinmehl, insbesondere dolomitsteinmehlheilmittel , zur behandlung von krebserkrankungen - Google Patents

Steinmehl, insbesondere dolomitsteinmehlheilmittel , zur behandlung von krebserkrankungen

Info

Publication number
EP1628671A1
EP1628671A1 EP04733527A EP04733527A EP1628671A1 EP 1628671 A1 EP1628671 A1 EP 1628671A1 EP 04733527 A EP04733527 A EP 04733527A EP 04733527 A EP04733527 A EP 04733527A EP 1628671 A1 EP1628671 A1 EP 1628671A1
Authority
EP
European Patent Office
Prior art keywords
minerals
weight
added
powder
grain size
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.)
Withdrawn
Application number
EP04733527A
Other languages
German (de)
English (en)
French (fr)
Inventor
Gerd THÖNE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bauer Wulf Dr
Original Assignee
Bauer Wulf Dr
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bauer Wulf Dr filed Critical Bauer Wulf Dr
Publication of EP1628671A1 publication Critical patent/EP1628671A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/075Ethers or acetals
    • A61K31/08Ethers or acetals acyclic, e.g. paraformaldehyde
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/06Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/06Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
    • A61K33/10Carbonates; Bicarbonates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/06Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
    • A61K33/12Magnesium silicate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Definitions

  • the present invention relates to a remedy for internal use, in particular against cancer.
  • This problem is solved by a remedy with a proportion of minerals with a grain size of 1 to 150, in particular 1 to 20 nanometers.
  • the special feature of the invention is that the extremely finely divided minerals have an extremely small diameter. They are so finely divided that they do not remain superficially on a tumor and are therefore filtered off, but can penetrate into it.
  • the diameter of the minerals is smaller than the diameter of a skin pore.
  • the effect of silicon according to the invention only results if it is in finely divided bioactive form, that is to say as nanoparticles. This is achieved by grinding the previously chemophysically processed silicon acid into a liquid substance in which the particles do not settle and therefore no molecular accumulation can take place.
  • This colloidal silicon is similar to the albinoid arrangement of raw protein (without being sticky). It is similar to blood plasma.
  • the colloidal distribution of the silicon considerably facilitates the penetration into the tissue and the bioactive interaction between the human metabolism and the individual silicon particles because of the large absorbent surface.
  • the colloidal distribution and arrangement ensures not only outer boundary surfaces between liquid and air, but also between silicon and the water molecules. In this way, the silicon has surface activity and internal stress energies that have a unique activating effect in the biological processes. It is suitable for internal and external application.
  • 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.
  • the remedy according to the invention can advantageously be supplemented by water, oil (mineral oil or vegetable oil) or alcohol.
  • oil mineral oil or vegetable oil
  • alcohol in the case of an aqueous solution, about 60% by weight of water in the end product has been found to be proven suitable.
  • Vegetable oil is particularly advantageous as an oil, for example safflower oil, since it has no laxative effect when taken.
  • An emulsion of polydimethylsiloxane and water is also possible.
  • the mineral remedy according to the invention is advantageously produced by mixing the starting materials together in a first step. It has proven to be advantageous if the grain size of the rock powder used is already in the range of 10 micrometers or less. In a subsequent process step, the mixed components are ground using a colloid mill, the grinding duration being selected to match the desired grain size of the end product. It has proven to be advantageous if the grinding process is maintained over a period of at least 10 minutes, the use of rotor cooling of the colloid mill being indicated in order to avoid symptoms of overheating.
  • the resulting mixture is a flowable gel-like liquid and can be processed into a remedy in a variety of ways. It is possible to prepare a powdery mixture by mixing the above liquid with zeolite and dolomite powder. This powder can then be supplied, for example, in the form of the widespread gelatin capsules that 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.
  • 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 inhalate
  • quartz flour, dolomite stone flour and magnesium powder has proven to be particularly advantageous.
  • the proportions of zeolite and dolomite can add up to 100% by weight of the weight fraction of the rock powder.
  • aluminum silicate in particular natural zeolite with a grain size of 10 to 70 ⁇ m, in particular 40 ⁇ m and dolomite powder with a grain size of 2 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 SiO 4 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. Untitled. In this way, the homeostasis of the organism, in particular that of the mineral metabolism, is maintained or restored.
  • sensitive organ systems e.g. B. brain, nervous system, hormonal system, immune system, liver, kidneys and. a. not only protected from toxic damage, but also increased their resistance to harmful pathogenic influences
  • the zeolite 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.
  • zeolite Because of its open molecular structure, zeolite also has the ability to absorb large quantities of liquids. This is advantageous because, despite mixing with the above-mentioned components, a flowable powder can be formed.
  • final grain size of the minerals in the range 1 to 100 nanometers, preferably 1 to 10 nanometers.
  • the product is called Liquidum Th (with castor oil instead of vegetable oil) and is approved as a dietary supplement.
  • the advantage of using vegetable oil is that the slightly laxative effect of castor oil is avoided.
  • composition of an oil emulsion according to the invention with minerals and precipitated silica
  • final grain size of the minerals in the range 1 to 100 nanometers, preferably 1 to 10 nanometers.
  • composition of a medicinal product according to the invention as an aqueous solution with quartz powder or precipitated silica as an aqueous solution with quartz powder or precipitated silica:
  • 40 - 80 60 wt% water.
  • composition of a medicinal product according to the invention as an alcoholic solution with quartz powder or precipitated silica is an alcoholic solution with quartz powder or precipitated silica:
  • final grain size of the minerals in the range 1 to 100 nanometers, preferably 1 to 10 nanometers.
  • the mixtures from Examples 1 to 4 are first kneaded intensively in a kneader at a temperature of approximately 50 ° C. and then fed inline to a colloid mill.
  • the colloid mill has cross toothing with pumping device and rotor cooling.
  • the minerals are ground to a size of 10 " 9 m.
  • the vegetable oil emulsifies in warm water and is stabilized by the methyl cellulose.
  • cooling of the grinding head is necessary in the grinding stage.
  • the emulsion obtained in this way is stable and can be further diluted with water and incorporated. It has been shown that the solutions from Examples 1 to 4 are effective against cancer cells, but a coarser grinding of the minerals of 10 ⁇ m has no effect. It has also been shown that the solutions only have an effect on cancer cells, but not on healthy cells.
  • composition of a powder according to the invention based on the liquid products described in Examples 2 and 3:
  • aluminum silicate in particular natural zeolite with a grain size of 10 to 70, in particular 40 ⁇ m,
  • dolomite powder with a grain size of 2 to 30, in particular 10 ⁇ m.

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
EP04733527A 2003-05-22 2004-05-18 Steinmehl, insbesondere dolomitsteinmehlheilmittel , zur behandlung von krebserkrankungen Withdrawn EP1628671A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10323759A DE10323759A1 (de) 2003-05-22 2003-05-22 Heilmittel zur inneren Anwendung, insbesondere gegen Krebserkrankungen
PCT/DE2004/001047 WO2004105777A1 (de) 2003-05-22 2004-05-18 Steinmehl, insbesondere dolomitsteinmehlheilmittel, zur behandlung von kresbserkrankungen

Publications (1)

Publication Number Publication Date
EP1628671A1 true EP1628671A1 (de) 2006-03-01

Family

ID=33441300

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04733527A Withdrawn EP1628671A1 (de) 2003-05-22 2004-05-18 Steinmehl, insbesondere dolomitsteinmehlheilmittel , zur behandlung von krebserkrankungen

Country Status (9)

Country Link
US (1) US20060251738A1 (enExample)
EP (1) EP1628671A1 (enExample)
JP (1) JP2006528210A (enExample)
CN (1) CN1795002A (enExample)
AU (1) AU2004243523A1 (enExample)
CA (1) CA2525908A1 (enExample)
DE (1) DE10323759A1 (enExample)
RU (1) RU2005140098A (enExample)
WO (1) WO2004105777A1 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE112006002042A5 (de) * 2005-05-18 2008-04-30 Mijo Ljubicic Mikronisierte mineralische Materialien und deren Herstellung
WO2007008711A2 (en) * 2005-07-08 2007-01-18 George Mason University Synthetic nanoparticle soil materials
KR101199897B1 (ko) 2011-11-14 2012-11-09 권태동 천연 광물 및 이의 용해물을 유효성분으로 함유하는 암 예방 및 치료용 조성물
KR101199895B1 (ko) 2011-11-14 2012-11-09 권태동 천연 광물 및 이의 용해물을 유효성분으로 함유하는 당뇨병 예방 및 치료용 조성물
DE102013013029A1 (de) * 2013-08-05 2015-02-05 Ernst Fekete Lobbyist-Zellschutz PNI (Psychoneuroimmunium)
CN104606261B (zh) * 2015-03-05 2018-02-09 潘友长 一种沸石药物组合物及其制备方法和用途
RU2629338C1 (ru) * 2016-08-26 2017-08-28 Алам Джан Фармацевтическая композиция для стабилизации гомеостаза и купирования патологических процессов в организме и инъекционная лекарственная форма этой композиции
KR101996383B1 (ko) 2017-12-01 2019-07-04 (주)카데시인코퍼레이션 퓨리톤을 유효성분으로 포함하는 항암용 조성물
CN108403755A (zh) * 2018-05-03 2018-08-17 北京胜泰生物医药科技有限公司 一种沸石药物的组合、制备及用途
US20230225386A1 (en) * 2021-12-30 2023-07-20 H2 Universe Llc Hydrogen-generating composition for dietary and agricultural applications

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU200933B (en) * 1988-12-22 1990-09-28 Jozsef Markus Process for producing pharmaceutical composition for profilacting and treating osteoporosis
DE19530882A1 (de) * 1995-08-11 1997-02-13 Thomas Dr Ing Loeser Arzneimittel zur Vorbeugung, Begleittherapie und Heilung von Geschwulstkrankheiten
DE19603477A1 (de) * 1996-01-31 1997-08-07 Klaus Dr Med Reuter Tumormittel
DE59707063D1 (de) * 1996-03-25 2002-05-23 Bauer Wulf Heilmittel zur äusserlichen anwendung und verwendung einer wässrigen öl-emulsion für ein derartiges heilmittel
DE19750328A1 (de) * 1997-11-13 1999-05-20 Klaus Dr Med Reuter Tumormittel
US6251439B1 (en) * 1998-12-16 2001-06-26 Trustee Of The Dartmouth College Composition and method for reducing the risk of carcinogenesis
EP1107826A1 (de) * 1999-04-26 2001-06-20 Tihomir Lelas Vorrichtung zum mikronisieren von materialien
EP1129715A1 (de) * 2000-02-25 2001-09-05 Werner Dr. Reichen Anwendung von Magnesium, Kalzium und Silizium zur Heilung verschiedener Krankheiten und zum allgemeinen Wohlbefinden
CA2419434A1 (en) * 2000-09-19 2003-02-07 Daiichi Pharmaceutical Co., Ltd. Medicinal composition
JP2003063951A (ja) * 2001-08-23 2003-03-05 Nonogawa Shoji Kk 錠剤及びその製造方法
DE10323758A1 (de) * 2003-05-22 2004-12-16 Bauer, Wulf, Dr. Heilmittel zur inneren Anwendung, insbesondere gegen Krebserkrankungen

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
"COMPOSITE SAFFLOWER OIL PREPARATION/PHARMACEUTICAL COMPOSITION FOR TREATING CANCER AND CARDIOVASCULAR AND CEREBROVASCULAR DISEASE, AND ITS PREPARATION METHOD", XP002456165 *
"Neosino Wikipedia", Retrieved from the Internet <URL:http://de.wikipedia.org/wiki/Neosino#cite_note-7> *
See also references of WO2004105777A1 *

Also Published As

Publication number Publication date
AU2004243523A1 (en) 2004-12-09
US20060251738A1 (en) 2006-11-09
CA2525908A1 (en) 2004-12-09
DE10323759A1 (de) 2004-12-16
CN1795002A (zh) 2006-06-28
JP2006528210A (ja) 2006-12-14
WO2004105777A1 (de) 2004-12-09
RU2005140098A (ru) 2006-08-10

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