hello i have bought uralyt-u in china for kidney stone but now i dont know about its use..i mean its dose of using..and other thing i wana know that can we use it for every kind of kidney stone or only stone of uric acid..waiting for reply thanks

Hello habibulhaq,
here is leaflet for Uralyt-U registered in Israel: health.gov.il/units/pharmacy/trufot/alonim/606.pdf

Hi i am currently taking Uralyt-U and it says during the Cytostatic therapy the pH should be kept at pH 7 . How do i know when to start the Cytostatic therapy?

Dear Ms/Mr,
In connection with my research proposal, to prove that the final biological oxidation, in addition to an oxidation-reduction process takes place and a photo-chemical process, the first in the electron transfer, the second in the energy transfer.

Please review the possibility of involvement in this project, and prove that the final biological oxidation, beside reducing-oxidation process, takes place and a photo-chemical process based on complementary colors.

In this view, I believe that the final biological oxidation, it is a reverse process of photosynthesis. If in photosynthesis, the process takes place to reduce carbon oxide and hydrogen oxide, complementary color by absorbing, two protons in the nucleus, increasing their electronegativity and electrons from the oxygen recovery ,will be his freedom, the final biological oxidation is a process of oxidation of C and H atoms coming from carbohydrates, energy release and formation of CO2 and H2O.
This research project, beyond the issue of malignant cell transformation. If we can control cell proliferation and differentiation, we think we can control body growth and maturation. The same theory may reconsider capture sunlight, which would be captured in color and will be reconstructed complementarity on the same principle.
If exogenous monochromatic radiation on photosynthesis, is identical to endogenous monochromatic irradiation, in the final biological oxidation, exogenous monochromatic irradiation,will induce endogenous complementary monochromatic irradiation.
This research project should be addressed to specialists in biochemistry and biophysics and then medical centers. So I do understand the need to explain how I came to these conclusions. First we must accept that there are colors "positive" (hot) and "negative" (cold). The C atom will absorb the positive energy in the four protons in the nucleus
will attract more than four electrons, making ion negative.Thus negative ions are charged with positive energy stored in protons in the nucleus is thus more electronegative. So electronegativity of an atom increases proportionally with the number of protons in the nucleus but also their energy load. In terms of positive ions, they will absorb the negative energy in the electronic shell and fix in the form of H + protons. In conclusion, negative ions will be charged with positive energy, and positive ions with negative energy (law of opposites and the principle of complementarity).
These forms of energy (negative ions with positive energy and positive ions with negative energy) will represent the combinations are chemically stable in various biological structures. The fact that they have positive energy (red) or negative (blue) does not mean it will be colored red or blue as I hinted in the article, to be more suggestive.It should be noted that in my view, the final biological oxidation, represents a reverse process of photosynthesis. If photosynthesis is a process of reducing carbon oxide and hydrogen oxide, by increasing electronegativity of C and H atoms, with the electrons back to oxygen, which will be released in the mitochondria is a process of oxidation of atoms C and H, derived from carbohydrates, with energy release and absorption of its selection (the color), by the structures involved, which is the nature of porphyrins, are photosensitive and colorful.

ARTICLE: CHROMOTHERAPY AND THE IMPLICATIONS IN THE METABOLISM OF THE NORMAL AND NEOPLAZIC CELL
"Green chlorophyll and red hemoglobin, the main difference between the two pigments of life, is proof of a common origin of the two kingdoms".HEILMEYER.
In my opinion, at the basis of malign transformation is a disturbance of energetical metabolism, which reached a level that cell can not correct (after having succeeded before, many times), disturbance that affects the whole body in different degrees and requires corection from outside starting from the ideea that the final biological oxidizing takes place through photochemical process with releasing and receieving energy.
The final biological oxidation is achieved through a process of oxidation-reduction, while a photochemical process, based on the principle of complementary colors, if we accept as coenzymes involved, containing a metal atom gives them a certain color, depending on the state of oxidation or reduction (red ferment of Warburg with copper, all copper cerloplasmin blue, green chlorophyll magnesium, red iron hemoglobin,etc.) I SUGGEST TO YOU AN EXPERIMENT: CULTURE OF NEOPLASTIC TISSUE IN A GREEN CONTAINER OR IN A COLOURLESS CONTAINER, IRRADIATED WITH MONOCHROMATIC GREEN LIGHT, IN AN ALKALINE MEDIUM, WILL IN REGRESSION OF THE TISSUE CULTURE; CULTURE OF NEOPLASTIC TISSUE IN A RED CONTAINER, OR SINGLE IRRADIATED WITH RED LIGHT, IN AN ACID MEDIUM, WILL LEAD TO EXAGERATED AND ANARCHICAL MULTIPLICATION.
If satisfied, the final biological oxidation is achieved by a photochemical mechanism (besides the oxidation-reduction), that energy is released based on complementary colors, means that we can control the final biological oxidation mechanism, irreversibly disrupted in cancer, by chromotherapie and correction of acid-base imbalance that underlies this disorder.We reached this conclusions studying the final biological oxidation, for understanding the biochemical mechanism of aerobic glycolysis in cancer. We found that cancer cell, energy metabolism is almost exclusively on hydrogen by oxidative dehydrogenation, due to excessive acidosis , coenzymes which makes carbon oxidation, as dormant (these coenzymes have become inactive). If we accept the nature of these coenzymes chloride (see Warburg ferment red), could be rectivate, by correcting acidosis (because that became leucoderivat), and by chromoterapie, on the basis of complementary colors.
According to the principle electronegativity metals, under certain conditions the acid-base imbalance (acidosis), iron will replace copper in combination , cytocromoxidase became inactive (it contains two copper atoms) leading to changing oxidation-reduction potential, BUT THE COLOR, FROM BLUE-GREEN TO REED, to block the final biological oxidation and the appearance of aerobic glycolysis.
In conclusion, malignant transformation occurs by energy metabolism imbalance in power generation purposes in the predominantly (exclusively) of the hydrogen atom of carbon oxidation is impossible. Thus at the cellular level will produce a multiplication (growth) exaggerated (exclusive), energy from hydrogen favoring growth, multiplication, at the expense of differentiation (maturation). Differentiation is achieved by energy obtained by oxidation of the carbon atom can not take, leading to carcinogenesis .
The energy metabolism of the cell, an energy source is carbohydrate degradation, which is done by OXIDATIVE DEHYDROGENATION AND OXIDATIVE DECARBOXYLATION , to obtain energy and CO2 and H2O. In normal cells there is a balance between the two energy sources. If cancer cells, oxidation of the carbon atom is not possible, the cell being forced to summarize the only energy source available, of hydrogen. This disorder underlying malignant transformation of cells and affect the whole body, in various degrees, often managing to rebalance process, until at some point it becomes irreversible.
The exclusive production of hydrogen energy will cause excessive multiplication, of immature cells, without functional differentiation. Exclusive carbon energy production will lead to hyperdifferentiation, hyperfunctional, multiplication is impossible. Normal cell is between two extremes, between some limits depending on the adjustment factors of homeostasis. Energy from energy metabolism is vital for cell (body). If the energy comes predominantly (or exclusively) by oxidation of the hydrogen atom, green energy, will occur at the structural level (biochemical), acidification of the cellular structures that will turn red, so WE HAVE MORPHOLOGICAL AND CHEMICAL STRUCTURES "RED", WITH "GREEN" ENERGY. This background predisposes to accelerated growth, without differentiation, reaching up uncontrolled, anarchical. ENERGY STRUCTURE OF THE CELL BODY WOULD BE INN. If necessary energy cell derived mainly by oxidation of the carbon atom, red energy,cell
structures will be colored green, will be alkaline(basic), so WE HAVE MORPHOLOGICAL AND CHEMICAL STRUCTURES "GREEN", WITH "RED" ENERGY, on the same principle of complementarity. This context will lead hyperdifferentiation, hyperfunctional ,maturation, and grouth stops. ENERGY STRUCTURE OF THE CELL BODY WOULD BE YANG.

If in photosynthesis, porphyrins chemicals group, whic be photosensitivity(their first feature), shows and a great affinity for metals with chelate forming and becoming colored (pigments of life), can absorb monochromatic light complementary, so if these pigments, which constitutes the group of chromoprotheine, in photosynthesis will achieve CO2 and H2O reduction the recovery of C, H respectively, and the issuance of and release of O, atoms as H and C that reduced the energy load, representing carbohydrates, is in the form of solar energy storage, in cellular energy metabolism, processes necessary life, energy will come from the degradation of substances produced in photosynthesis, the carbohydrates, by oxidative dehydrogenation and oxidative decarboxylation, through like substances, which form chelates with the metals, are colored, metals contained in the form of oxides of various colors(green Mg, red Fe, blue Cu,etc.),suffering from
complementary color absorption process of reduction with H in case,if the oxidative dehydrogenation, when chelated metal pigment is red, becoming leucoderivat (colorless) by absorbing complementary color (green) of hydrogen, formation of H2O, or C, if the oxidative decarboxylation when chelated metallic pigment is green, energy absorbing additional, red energy of atom C, CO2 production, the process is identical.
The process that lies at base cellular energy metabolism, takes place in the final biological oxidation, reducing the O atom in the form of metal oxide, in combination with photosensitive substance, porohyrin, colorful,absorbing complementary color, will reduce the O atom, with H and C, with the production of H2O and CO2.
Green energy release of H atom in the oxidative dehydrogenation process, it is a process of"IRADIATION MONOCHROMATIC ENDOGENOUS WITH GREEN", and red energy release of C atom in the oxidative decarboxylation process, consists in an "IRADIATION MONOCHROMATIV ENDOGENOUS WITH RED". Porphyrin-metal combination in photosynthesis, the chelated form, by absorbing light in the visible spectrum, will be able to reduce to low and turn, C and H respectively, the state of oxide (CO2 and H2O),release of O. The final biological oxidation, the combination of metal-porphyrins in aerobically in the absence of light, will find in the oxidized state, so in the form of porphyrins and metal-oxide, will oxidize to C and H ato hydrocarbonates, with formation of CO2 and H2O, or rather, will be reduced by C and H atom of hydrocarbonates,formation of CO2 and H2O, by absorbing energy produced by photosynthesis.
If we can control the final biological oxidation, we can control cellular growth, thus multiplying, and on the other hand, maturation, so differentiation. The names as green energy (tourquoise) and somatic red (corail) and vice versa, are generic for relevance, there is the additional energy in different proportions. Green energy(tourquoise) will prevail if the cell (body) which multiplies (during growth), will in case of adult cell (functional) will prevail red energy (corail). I put on a scientific basis (biochemical and biophysics) chromotherapy, and light therapy generally through tie the two types of energy, that obtained by oxidative dehydrogenation (tourquoise), which will cause cell multiplication without differentiation , and that obtained by oxidative decarboxylation (corail), which will be to stop proliferation, and will determine the differentiation (maturity, functionality). This process is carried out
based on complementary colors, which are coenzymes oxidative dehydrogenation and oxidative decarboxylation is colored . It reveals the importance of acid-base balance, the predominance of the acidic or basic, as an acid structure (red), not only can gain energy from the carbon atom red (the principle of complementarity), but can not assimilate ( under the same principle). It must therefore acid-base balance of internal environment, and alkalinization his intake of organic substances by the electron donor. By alkalinization (addition of electrons) will occur neutralize acid structures, the red, they become leucoderivat, colorless, and inactive, while the basic, which because of acidosis became neutral, colorless and inactive, will be alkaline in electron contribution, will be in green, and will absorb red energy from the carbon atom. So, on two kinds of vital energy, it is clear correlation between the chemicalstructure of the cell(body),and type of
energy that can produce and use. Thus a cell with acidic chemical structure, can produce only energy by oxidative dehydrogenation (green energy), because the acid can only be active coenzymes with acid chemical structure, red, will absorb the complementarity only green energy of hydrogen. Basic structures which should absorb red energy from carbon , are inactive due to acid environment, which in turn chemically in leucoderivat, so colorless structures, inactive. Conversion of these structures to normal, operation by alkalinization could be a long lasting process, therefore, we use parallel chromotherapy, based on the fact that these COENZYMES INVOLVED IN BIOLOGICAL OXIDATION FINALS ARE COLORED AND PHOTOSENSITIVE. Thus, exogenous irradiation with monochromatic green will neutralize, by complementarity, coenzymes red, acidic. In will reactivate alkaline coenzymes, which have become due acidosis leucoderivat, so colorless and inactictive.
Without producing CO2, carbonic anhydrase can not form H2CO3, severable and thus transferred through mitochondrial membrane. Will accumulate in the respiratory Flavin, OH groups, leading to excessive hydroxylation, followed by consecutive inclusion of amino (NH2). It is thus an imbalance between the hydrogenation-carboxylation and hydroxylation-amination, in favor of the latter.This will predominate AMINATION and HYDROXYLATION at the expense CARBOXYLATION and HYDROGENATION, leading to CONVERSION OF STRUCTURAL PROTEINS IN NUCLEIC ACIDS. Meanwhile, after chemical criteria not genetic, it synthesizes the remaining unoxidized carbon atoms, nucleic bases "de novo" by the same process of hydroxylation-amination, leading to THE SYNTHESIS OF NUCLEIC ACIDS "DE NOVO".
To put into practice the idea of this research proposal,(in parallel with chromotherapy) there is a need of environmental alkalifying internal electron donor, such as tricarboxylic acids, alkaline form (COO-)(URALYT),and captors acid form of H + (THAM), a combination of the two forms, a new alkalizing formula, starting from the two categories. I might call BIOALCALINIZANT, and I could experiment with, the Fam Med Cab Dr Viorel & Daniel Bungau, under the "MADAUS" , or any other form of
cooperation.
Sincerely yours,
Dr Viorel Bungau

Message contains attachments
1 File (28KB)
* Copy of Document Dr Bungau-7.docCopy of Document Dr Bungau-7.doc
> This research project,
> beyond the issue of malignant cell transformation. If
> we can control cell proliferation and differentiation, we
> think we can control body growth and maturation. The same
> theory may reconsider capture sunlight, which would be
> captured in color and will be reconstructed complementarity on the
> same principle.

> With your
> agreement I will come back with clarifications. Please
> help me solve for this project.
>
Message contains attachments
1 File (27KB)
* Chromotherapy in cancer.pdfChromotherapy in cancer.pdf

My name is Viorel Bungau and I am a general pratictioner (family medicine). I a very passionate about Biochemistry and I reached to someinteresting conclusions regarding the metabolism of the normal cell in generally and particularly of the neoplazic cell. I don't have access to a Research Institute in this field ( in Romania they don't do fundamental research).
So, I thought to bring to your attention, in the text below, some considerations about the malign development, for experimental evaluation. If you consider that i well argumented I can give more details on what I call Chromotherapy and the implications in the Metabolism of the Normal and Neoplazic Cell.

In my opinion, at the basis of malign is a disturbance of energetical metabolism, which reached a level that cell can not correct
(after having succeeded before, many times), disturbance that affects the whole body in different degrees an requires corection from outside starting from the ideea that the final biological oxidizing takes place through photochemical process with releasing and receieving energy.

To put into practice the idea of this research proposal,(in parallel with chromotherapy) there is a need of environmental alkalifying internal electron donor,msuch as tricarboxylic acids, alkaline form (COO-),(URALYT),and captors acid form of H + (THAM), a combination of the two forms, a new alkalizing formula, starting from the two categories. I might call BIOALCALINIZANT-MADAUS.

Sincerely yours, Dr Viorel Bungau

My address is :
Dr. Bungau Viorel
Str. Libertatii 22
com. Cristian 507055
Brasov
Romania
email adress viorel.bungau@yahoo.com

I am near the Baile Felix (Oradea), 6 miles, where we land, that (free) will aim to build a sanatorium-thermal water-MADAUS PREVENTION AND TREATMENT OF CANCER-by CHROMOTHERAPY, and acid-base balance with MADAUSBIOALCALINIZANT. I am sure that this project will be of European interest.
Waiting for your opinion,
Sincerely,
Dr Viorel Bungau

Please confirm my message and an address for the research proposal. Thanks very much, Yours sincerely, Dr Viorel Bungau

dear Doctor Viorel Bungau
I m Suffring kidny pain due to stone in urinals, even though i have made an laser operation in the kingdom of saudi arabia,and one of my friend advise me to use URALYT-U, so plz let me know how to use and is there any side effetcs and it could remove stone from urinals

show patient information leaflet

comment on product

my mother is using uralit u its using for kidney stone this drug how we us how many days using this, this prodecte how available in india