Violation of time reversal invariance in living tissue

Surgery: light – thermal – and electrical application – Light – thermal – and electrical application – Light application

Reexamination Certificate

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C606S003000, C606S011000

Reexamination Certificate

active

06592611

ABSTRACT:

CROSS REFERENCES TO CO-PENDING APPLICATIONS
None.
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention is for a violation of time reversal invariance in living tissue, and more particularly, pertains to a violation of time reversal invariance in living tissue by means of exogenously applied electromagnetic radiation with wavenumbers between k=33,333 cm
−1
to k=33,333 cm
−1
.
The present invention is designed for use in non-invasive therapy. This is a non-invasive technique for the treatment of numerous chronic diseases and conditions, primarily arthritis, chronic pain from injuries, and wound healing, such as bed sores, decubitus, and diabetic ulcers.
2. Description of the Prior Art
The present invention specifically describes the mode of biophysical mechanisms of action, which has not been accomplished in any prior art or device.
Current U.S. standard and FDA approved treatments for the above mentioned chronic diseases and conditions include medication, surgery and physical therapy. Other existing therapies and therapy devices that are known in the world market attempt to treat described conditions with non-invasive electromagnetic radiation applications, but lack an accurate explanation of a mechanism of action. Therefore, they are unable to maximize their efficiency.
SUMMARY OF THE INVENTION
The general purpose of the present invention is to provide a non-invasive treatment of disease conditions such as arthritis; healing of wounds, and soft tissue injuries, i.e. sports injuries; and relief from chronic conditions, such as Carpal Tunnel Syndrome and chronic ulcers.
The present invention is intended for use in general medical practice. The use of the present invention will, in many cases, eliminate the need for medication, physical therapy, surgery, and ongoing patient care.
The present invention also provides a treatment system for chronic disease conditions. The present invention is based upon application of the theoretical concepts of Quantum Biology to a variety of disease and chronic conditions. The principles of operation are based on stimulating the production of a Bose-Einstein condensate in living tissue The wavenumbers necessary for this excitation are derived from the solution to the equations for optical phonon scattering in living tissue generated by optical photon excitation. The establishment of this degeneracy condition induces a superconducting state in the tissue providing the appropriate instruction set for correct DNA replication, transcription and translation. Thus, allowing the proper formation or regeneration of healthy tissue.
Electromagnetic frequencies excite ordered water around proteins at about 10
-
Hz. The present invention is based upon excitation of the Frohlich resonant frequencies in human tissue. Resonant energy transfer, generated by photon excitation at specific wavelengths of 655 nm and 1060 nm generate Brillouin scattered phonons at 0.424×10
11
Hz and 0.262×10
11
Hz, respectively. These frequencies establish a Bose-Einstein condensate within the living tissue. The ratio of 1060 nm/655 nm=1.618 which is the golden mean ratio and known to be biologically active. 655 nm is the solution to the Balmer series equation for the first line of hydrogen emission. Biological tissue involves extensive hydrogen bonding. The dimensional resonance of DNA is also known to be 34 Å/21 Å≈1.618 for efficient energy transfer from the golden mean ratio. 655 nm is also the main absorption band of Heat Shock Protein 47 (HSP47), which is the chaperon for collagen synthesis. The use of multiple wavelengths at the golden mean ratio provide a synergistic effectiveness.
If we start with the first line of the Balmer Series for hydrogen:
&lgr;(
B
)=3646(
N
2
/N
2
−4) for
N=
3
&lgr;(
B
)=656.28 nm
&lgr;(
B
)≈655 nm
Therefore, this 655 nm becomes the primary absorption wavelength in this invention. The Frohlich resonance of ordered water around proteins is ≈10
14
Hz. The optical excitations at 655 nm and 1060 nm both provide excitation in this band.
Electromagnetic radiation coherently excites the ordered water molecules, which in turn excite tunneling through the creation of evanescent photons in the nucleotide bonds. The Frohlich resonance is a non-local effect occurring in the water surrounding and in the core of the microtubules connecting all cellular structure. Excitations at a frequency of 10
14
Hz, excites the water surrounding the protein structure and a frequency of 10
14
Hz, excites water in the core of the protein structure of the microtubules. This in turn generates a collective and cooperative behavior of a great number of the constituents, known in Quantum Mechanics as the degeneracy state, or multiples of identical quantum numbers. This can then be associated with a non-local long range order, in which information is transmitted in the superconducting state. This long range transfer is established through longitudinal electric modes in the microtubules and generates a single quantum state. If energy is fed into these modes and transferred to other degrees of freedom, then a stationary state will be reached where the energy content of the electric mode is larger than thermal equilibrium. A coherent electric wave is then channeled into a single mode. The local vibrations of the cell membrane then create a positive and negative part of particular sections of the membrane that vibrate against each other leading to an oscillating electric dipole frequency of the order of 10
11
Hz.
The hydrogen bonds have distinctive dipolar properties. The alpha helix is expected to exhibit collective dipole oscillations in the same frequency region, and also from non-localized electrons in this region of the cell.
The dielectric systems have a certain range of macroscopic wavelengths capable of longitudinal electric oscillations over the whole material. Processes involving cell membrane or H-bonds are expected to feed energy locally to particular dipole oscillators. Long range coulomb interactions can cause energy to be shared with other dipoles that will oscillate coherently provided energy supply is sufficient and a single longitudinal mode can exhibit long range phase correlations. Since biological tissue exhibits very wide absorption bands, optical excitation ranging from the UVA to the near IR can stimulate biological activity.
The purpose of the present invention is to maximize this biological activity, even though a broad spectral range can still exhibit stimulatory effects. The free energy associated with vibration can be decreased if the system is permitted to undergo deformations or interactive decoherence. Therefore, coherence must be re-established. Relevant components can be connected with certain regions in the cell membrane by H-bonds. If energy is supplied locally (in regions containing non-localized electrons), then energy is shared by all components which establish a branch of electric modes. When cells are closely packed, deformations in the cell membrane will no longer influence the di-electric response, this is known as contact inhibition.
Coherent electromagnetic excitation presents a reservoir of energy and when the absorption of light is
w>>kT it can lead to energy storage in a single state. This coherently excites the ordered water molecules, which in turn excite the tunneling in the nucleotide bonds. When the conformational grooves of a protein are filled with water, the entire protein is in coherent vibration. This also applies to the B form of DNA, which is the hydrated form found in living organisms. Non-local effects such as remote triggering are expected whenever a very fast coupling (i.e., optical) occurs in a system with slow local dynamics (i.e., conformational changes in biological systems). Examples include biochemical processes coupled by electric field effects, such as are present in tissue. The force constant for dangling N—H bonds, such as that seen in nucleotide base pairs, is 8.955×10
13
;≈10
14

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