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New Cancer Treatment Center Features Proton Beam Therapy Program

  
  
  
  

proton beam therapy bldg mn

ARCHITECT'S RENDERING OF NEW PROTON BEAM THERAPY FACILITY IN ROCHESTER, MINN.(Courtesy of mayoclinic.org)

A new cancer treatment center in Rochester, Minnesota is well underway thanks to a very generous 100 million dollar donation by Richard Jacobson, among others. This recent project by Mayo Clinic is seen as revolutionary, mainly due to their featuring of the new Proton Beam Therapy Program. Mayo Clinic announced their plans for this center back in 2010 with high hopes for a revolutionary new way of combating cancer (see our previous article Cancer Research and Therapy Gift of $100M to Mayo Clinic from 2011). The uniqueness of this program stems from its commitment to solely using intensity-modulated proton beam therapy instead of generic and far more risky radiotherapy treatments, which can harm healthy tissue unlike proton beams that are specially designed to only target the tumor.

Proton Beam courtesy of protoncancercenters.com

Proton Beam Gantry courtesy of protoncancercenters.com

Other benefits to this new treatment include:

  • better control over the amount of radiation exposed to the patient's body
  • a more precise tumor targeting ability
  • shorter treatment times
  • fewer and less intense side effects
Many have full confidence in this project, especially Mayo Clinic's own president and CEO John Noseworthy, M.D."We are enthusiastically moving forward with this program because we believe it offers additional, innovative options for cancer patients." 

Once this facility is up and running in 2015, an estimated 1,240 patients will be treated there annually, with an astounding average of 138 patients a day! There will also be many new job opportunities opened up to doctors, physicists, and construction workers, around 750 in total, and more than 250 staff employed once the program is fully operational.

Over 400 million dollars have been invested in this project in order to ensure the highest quality care for cancer patients, and because of Mayo Clinic's revolutionary plans with this technology, patients can look forward to state-of-the-art treatment that has never been seen before.

If you are a Rochester, Minnesota researcher looking for new research equipment, or a research supplier who is interested in networking with researchers like these and supplying new science programs like this cancer treatment center at the Mayo Clinic, plan on attending Biotechnology Calendar, Inc.'s BioResearch Product Faire™ in Rochester on July 25 of this year. For more information about our upcoming vendor show, click the button below.


Comments

Dear Mrs./Mr., We designed an experiment to prove that the final biological oxidation, in addition to its oxidation-reduction, with formation of H2O and CO2, there is a photochemical effect, by which energy is transferred from the H atom, or C, process is done selct, the colors, complementary colors on the basis of the structures involved are colored (red hemoglobin Fe, Mg chlorophyll green, blue ceruloplasmin Cu, Fe cytochrome oxidase red, green and blue with Cu). What is your opinion about this hypothesis. Thank you very much, Sincerely, Dr. Viorel Bungau "Duality of cytochrome-oxidase. Proliferation (growth) and Differentiation (maturation) cell" Cytochrome-oxidase is present in two forms, depending on the context of acid-base internal environment : 1.- Form acidic (acidosis), which contains two Iron atoms, will be red, will absorb the additional green energy of the hydrogen atom, derived from carbohydrates, with formation of H2O, metabolic context that will promote cell proliferation. 2.-Form alkaline (alkalosis), containing two copper atoms, will be green, will absorb the additional red energy of the carbon atom, derived from carbohydrates, with formation of CO2, metabolic context that will promote cell differentiation. " Chlorophyll and hemoglobin, pigments life, porphyrin structure, differ only by the green chlorophyll, due to the atom of magnesium, and red hemoglobin, due to iron atoms in the structure - PROOF OF ORIGIN COMMON LIFE." (HEILMEYER) Please make possible this experiment , under your auspices, because they are one and exceeds my abilities. Please get involved in identifying the green form of ferment of Warburg. Red form has identified himself. "Copper role in metabolism." Cytochrome-oxidase structure has two atoms of copper. It is known that in conditions of acidosis (oxidative potential), the principle electronegativity metals, copper is removed from combinations of the Iron. So cytochrome oxidase will contain two atoms of iron instead of copper atoms, which changes its oxidation-reduction potential, but (most important), and color. If the copper was green, the iron is red, which radically change its absorption spectrum, based on the principle of complementary colors. Normality consists of alternating the two forms of cytochrome oxidase by successive passage of acid in the alkaline form, in terms of acid-basic balance maintained within normal limits. If neoplastic cell is dark continuously, in schizophrenic neuron is continuous light. Sincerely , Dr. Viorel Bungau 
"Inner Light- Light of Life. Endogenous monochromatic irradiation. Red ferment of Warburg - Green ferment of Warburg". 
I was involved in a research project of passion, and I reached some conclusions should be confirmed experimentally. No one wants to do the experiment that I proposed, that has no academic opinion (I am a medical practitioner and no access to a research center). Please make known the research project, and to communicate how I could be experienced. I'm very hard for that I'm alone and outside the system. Please get involved in this project, with all rights involving this. I can not do alone. Thank you very much, Yours sincerely, Dr. Viorel Bungau "INNER LIGHT - LIGHT OF LIFE" 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. If the structures involved in biological oxidation finals are colored, then their energy absorption is made based on the principle of complementary colors. If we can determine the absorption spectrum at different levels, we can control energy metabolism by chromotherapy - EXOGENOUS MONOCHROMATIC IRRADIATION . Energy absorption in biological oxidation process itself, based on complementary colors, the structures involved (cytochromes), is the nature of porphyrins, in combination with a metal becomes colored, will absorb the complementary color, corresponding to a specific absorption spectrum, it will be in - ENDOGENOUS MONOCHROMATIC IRRADIATION. They demonstrated that : Blue-green algae irradiated with monochromatic light green-blue, color will change to red in color that is complementary. 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. 
Krebs cycle and the final biological oxidation does not occur in darkness. The cell is illuminated from within, so that the cytochrome oxidase (red ferment of Warburg), along with the redox electron transfer, photochemical process occurs energy transfer based on complementary colors. A electrophotography the living cell, the mitochondria alive and functional, it shows an image with alternate flashes of red and green, depending on successive passes of the acid form of cytochrome oxidase, red, two iron atoms in the structure, when will absorb green energy the H atom with formation of H2O, in basic form, green, with two copper atoms in the structure, they will absorb red energy from the carbon atom with formation of CO2 . If Warburg cytochrome oxidase identified as red, green form will be identified that the analogy to green's call ferment Warburg. The neoplastic cell is dark, condemned to death so multiply uncontrollably, as a means of survival . This entitles us to believe that: In photosynthesis, light absorption and its storage form of carbohydrates, are selected, the colors, as in cellular energy metabolism, absorption of energy by the degradation of carbohydrates, is also done selectively, based on complementary colors. In the final biological oxidation, in addition to an oxidation-reduction process takes place and a photo-chemical process,based on complementary colors, the first in the electron transfer, the second in the energy transfer. So, 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, 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. 
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 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. 
Aerobic glycolysis appearance (in the presence of oxygen so), is key to cell malignant transformation. It means that you can not produce oxidation of carbon and hydrogen atoms with H2O that CO2 production. Why? For the cytochromoxidase, the last phase of the final biological oxidation in conditions of acidosis will be implicit structure acid, will bind two atoms of iron, will be red, and will absorb additional green energy from the hydrogen atom (exclusively), the production of H2O. This disorder is specific to cancer cells. Carbon atom may be oxidized in conditions of acidosis. In order to be oxidized, acid-base imbalance should be corrected, the deficit of electrons, so the alkalizing, cytochromoxidase alkaline will have a structure , will bind two atoms of copper, will be green and will absorb red complementary energy of the atom carbon to CO2 production. This process can occur in neoplastic cells, remaining unoxidized carbon atoms, will serve the anarchic synthesis of nucleic bases, nucleic acids in excess and anarchic proliferation of the cell. 
I imagine that for an experiment that does not make one. 
With your permission I submit to you. I would be very happy if this experiment were done under your leadership. What do you think about this experiment: 
 
TWO PLANTS, A RED LIGHT ONLY(CORAILLE), IN BASIC MEDIUM, WITH ADDED COOPER, WILL GROW, FLOWER AND FRUIT WILL SHORT TIME, AND THE OTHER ONLY LIGHT GREEN (TOURQUOISE), IN AN ACID MEDIUM, WITH ADDED COOPER CHELATOR ( CUPRENIL ), WHICH GROWS THROUGHOUT WILL NOT GROW FLOWERS AND FRUIT WILL DO. 
 
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, WITH ADDED COOPER, 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, WITH ADDED COOPER CHELATOR (CUPRENIL), WILL LEAD TO EXAGERATED AND ANARCHICAL MULTIPLICATION. 
-In addition- 
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, BASICS 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 BIOALKALIZING. 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 MONOCHROMATIC 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 atom of 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 chemical structure 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 inactive. (Lack of equipment, that determines the alkaline reserve -HCO3-, PCO2, pH, rH, X-ray energy , spectroscopy, and lack of team, cooperation are necessary for completing this proiect). 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". Basically I want to experiment demonstrate that an energy metabolism disorder that could be corrected after several times by means of maintaining acdo-base balance within normal limits, has become irreversible by depleting these resources. Acid-base balance and its adjustment mechanisms underlying this disorder.Basically it involves two comparative cell culture, an acidic (lactic acid), which will grow excessively, and the other in basic medium (URALYT+ THAM), which will not grow at all. To be more eloquent in acidic cell culture should be irradiated with monochromatic red light, in this way the structures performed oxidative decarboxylation, green (base), by absorbing the complementary color (red), will become colorless (leucoderivat) and inactive. At the same time will become hyperactive those achieved oxidative dehydrogenation (red and acid), which is responsible for the accelerated growth of cell culture, immature undifferentiated forms, dysfunctional, anarchic. Cell culture in basic medium, exogenous irradiated with monochromatic green light by neutralizing dehydrogenases (which is red, will become leucoderivat and unworkable, absorbing parts complementary color)while activating decarboxylases ,green, base, so this basic culture medium and irradiated with green light, will not grow at all, will tend to differentiate sharp and will perish. If I have a device that makes ELECTROPHOTOGRAPHY a segment of the body or whole body, I could see it this way : 1.-color image Electrphotography will prevail in, say RED, hyperactivity structures will require a red, acid does not absorb red, leaving it to pass through body tissues examined. That means Irradiation Endogenous Hyperactivity Monochromatic Green. It will be corrected by Exogenous Chromotherapy Monochromatic Irradiation with Green, which will become leucoderivat (colorless) and inactive and in parallel by Alkalinization Internal Environment with Electron Donors and Traps H +, thus neutralizing the acidic chemical structure of these structures . 2.-if the image will prevail ELECTROPHOTOGRAPHY green, that means Monochromatic Hyperactivity Endogenous IRRADIATION WITH RED, resists these structures will absorb the red light beam so that the red color will not find in the image ELECTROPHOTOGRAPHY. It will correct the CHROMOTHERAPY Exogenous Monochromatic Irradiation with red. Also, acid-base balance correction by acidifying the internal environment. 3.-establishing acid-base imbalance and its correction. Also setting the standard proportions of the colors in the image ELECTROPHOTOGRAPHY, by examining a number of normal subjects and necessary equipment. Also CHROMOTHERAPY appliances. Yours sincerely, Dr. Viorel Bungau -Conclusion- "Duality of cytochrome-oxidase. Proliferation (growth) and Differentiation (maturation) cell." Cytochrome-oxidase is present in two forms, depending on the context of acid-base internal environment : 1.- Form acidic (acidosis), which contains two Iron atoms, will be red, will absorb the additional green energy of the hydrogen atom, derived from carbohydrates, with formation of H2O, metabolic context that will promote cell proliferation. 2.-Form alkaline (alkalosis), containing two copper atoms, will be green, will absorb the additional red energy of the carbon atom, derived from carbohydrates, with formation of CO2, metabolic context that will promote cell differentiation. A body with cancer disease will become chemically color "red"-ACID-(pH, Rh, pCO2, buffered), and in terms of energy, green (X-ray). A healthy body will be in terms of "green"-ALKALINE - (as evidenced by laboratory), and in terms of energy, red (visible by X-ray). Please think of an exclusive collaboration. Sincerely, 
Sincerely yours, Dr Viorel Bungau
Posted @ Friday, August 10, 2012 8:17 PM by Viorel Bungau
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