In 2018, I, Reginald B. Little (RBL), wrote a book wherein I proposed multiple stable isotopes of nonzero nuclear magnetic moments (NMMs) play essential roles in living organisms. Prior scientists had reasoned nuclei with spin angular momentum could in some instances be involved in life and affect biomolecules and organisms thereby, but RBL first in 2002 proposed an nuclear orbital angular momentum with such nuclear spin angular momentum as expressed by NMMs and the import of parity of NMMs by positive and negative NMMs by bare protons and bare neutrons. On the basis of such, RBL later in 2013 proposed unusual isotopic distributions in molecules can causes diseases. In 2018, in his book RBL proposed that HIV and some other viruses fractionate stable isotopes for the origin of the virus and infectivity and advancement of the HIV and some other viruses. In 2023 a group of scientists led by Dr. Vincent Balters in France proved RBL theory of HIV fractionating stable isotopes correct as they measured HIV infecting cells fractionates zinc isotopes with HIV infected cells enriching in 64Zn and the HIV virus in the infected cell expressing similar 64Zn enrichment. These scientists measured the surrounding media and cells enriching in heavier zinc isotope 66Zn, 67Zn and 68Zn. In 2024, I developed more my theory from March 2020 of using static magnetic fields, electric fields and electromagnetic waves to stimulate the virus in this case HIV in presence of feeding particular stable isotope to induce mutating the virus, in this case HIV virus. I thereby proposed in 2024 using gamma rays to irradiate HIV host for selective inducing resonance in the 64Zn to selectively stimulate 64Zn enriched HIV infected cells and 64Zn enriched zinc fingers in the HIV virus and capsid in such infected cells for altering the biochemistry by the gamma stimulating of 64Zn in the HIV infected cells and HIV therein for killing the infected cells and mutating the HIV in the cells and even in hard to reach resevoirs. But I have not done much research on nuclear gamma spectroscopy. I read that there is a history of the uniqueness of 64Zn and a few other metals (four or five other metals) for giant dipole resonance (GDR) and such research on GDR dates back to the 1950s. I open this discussion to inquire about the feasibility of selectively using gamma dipole resonance on 64Zn in living organisms to kill HIV infected cells and inactivate HIV. Can the gamma rays be tuned only to 64Zn? Is there any general affect of the gamma rays on other biomolecules, cells and tissues and organs? Thanks Sincerely Reginald B. Little (Stillman College, Tuscaloosa, Alabama)
High levels of gamma rays of course can lead to cancer. But can low levels of gamma rays of specific wavelength only affect specific nuclei like 64Zn? Does the 64Zn have a specific frequency of gamma photon that only it will absorb and other atoms are not affected? As the 64Zn seems to have a natural giant dipole resonance of its nucleus can such resonance give sensitivity to low intensity gamma ray of such characteristic frequency so negligible effects on other nuclei of other elements and isotopes occur? Based on the answers to these questions and more it gives feasibility of a cure and the risk of side effects or creating other problems like cancer. This is a theory for a cure and the possibilities are interrogated . - Reginald B. Little (Stillman College ; Tuscaloosa Alabama)
On today Jan 23, 2025, I , Reginald B. Little invented a better process of feeding the patient 62Zn and intrinsic electron capture by 62Zn converts it to 62Cu and intrinsic electron capture by 62Cu converts 62Cu to 62Ni. On atomic scale, I (Reginald B. Little, RBL) thereby invent way to selectively kill HIV infected cells by the internal cellular Bremsstrahlung radiation internal to the HIV infected cell so such X-Rays, Gamma Rays are absorbed within the HIV infected cells selectively killing the HIV infected cells. The surrounding normal cells are not likely harmed. Furthermore in my invention , I (RBL) determine that the transmutations to from 62Zn to 62Cu alters the zinc finger and binding of the zinc finger by Zn as it transmutes to 62Cu for further sickening only HIV infected cells and mutating the HIV virus itself. Moreover by this technique as invented by me (RBL), the hidden HIV reservoirs are internally found by the nuclei of 62Zn and the HIV reservoirs are mutated and destroyed. My invention as described here is a powerful new theoretical cure for HIV! - Reginald B. Little (Stillman College, Tuscaloosa, Alabama)
Hi, I, Reginald B. Little (RBL), would like to note that this is a theoretical cure that I propose to better treat and possibly cure hiv. It is meant to inspire test on lab animals and not humans for fine tuning and testing it's treatment and safety. This theory is foundation to inspire more research but this is not intended to inspire application. Application should not be done without authorization by established authority. I hope to experiment also on mice to see if heavier isotopes enriched 65Zn, 67Zn,66Zn, 68Zn, 69Zn , 70Zn with no 64Zn to mice with stimulating by neutrinos, antineutrinos, neutrons and/or gamma or rays and rotating their photons for agitating these heavier isotopes with possible mutating and destroying zinc fingers in hiv infected cells in the mice and hiv in those infected cells to demonstrate new approach for inactivating hiv in hidden reservoirs fir possibly curing hiv. These type lab animals test and experiments are proposed to give initial test of this theory. Reginald B. Little
Today, Jan 27, 2025, I, Reginald B. Little (RBL), have another idea regarding zinc isotopes and hiv zinc fingers. It seems that intrinsically hiv takes zinc from the normal cells and with progression of the disease zinc is depleted in the rest of the body with progression of the diease. And moreover, it has been predicted by RBL of isotopic fractionation by hiv during its infection onset and latent period in Jan 2018; and measured by Balter and coworkers observed that 64Zn in particular is enriched in hiv virus and hiv infected cells in Jan 2025. On such basis, here RBL on Jan 27, 2025 suggests another possibility of treating and possibly curing HIV by feeding the patient pure 67Zn and the hiv virus and hiv infected cells have no choice but enrich in the 67Zn due to its abundant presence in the food. RBL here notes that such 67Zn is not normal for the hiv and hiv infected cells; as the hiv and hiv infected cells prefer 64Zn. So the 67Zn may slowly progressively accumulate in hiv or possibly sicken and cure the hiv by inactivating the hiv virus and killing hiv cells. The 64Zn may induce altered properties of the zinc finger fpr hiv by lowering the activity of the zinc finger by 64Zn relative to heavier Zn isotopes which by RBL's theory (such heavier Zn isotopes) are more active due to their proximity to midway half filled magnetic number nuclear shells. RBL here notes that the 64Zn inherently in the hiv virus may be the cause of the virus as RBL notes here with 67Zn the possibility of loading 67Zn in hidden reservoirs of hiv for curing hiv. RBL here notes that he has no knowledge of how the 67Zn may affect normal cells, in magnetic field the 67Zn is thought to slow RNA replication by Anatoly Buchachenko (2024). The 67Zn in normal and hiv infected cells may shorten the RNA replication in both type cells. But finding a way to restrict the 67Zn to the zinc fingers in hiv virus would lower side effects. But such effect on RNA of the infected hiv patient is reasoned to be shorter during this proposed treatment. But test on lab animals like rats and monkeys can determine the inactivating power of 67Zn on hiv in lab animals and possible side effects on normal cells. With the 67Zn, today on Jan 27, 2025, RBL proposes more possibilities of using rotating x-rays to selectively stimulate the 67Zn in hidden hiv reservoirs to inactivate the zinc (Zn) fingers of the hiv and kill hiv infected cells for possibly curing hiv. Although alluded to in published document by RBL in Jan 2025 (RBL) of using external gamma rays to selectively excite Zn isotopes to inactivate hiv virus for curing hiv, RBL further speculates the possibility of using Mossbauer Effect by 67Zn (which is Mossbauer active) but in the zinc finger the 67Zn is speculated to be in nonrigid matrix for not meeting requirement of Mossbauer Resonance. But the liquid like zinc finger protein having 67Zn can subject 67Zn in the zinc finger to Mossbauer Effect whereby the 67Zn in the zinc finger of hiv virus is selectively excited by 93.5 keV gamma rays and the nonresonance due to liquid like zinc finger would cause the 67Zn to recoil from the gamma absorption. RBL here on Jan 27, 2025 predicts the recoil from gamma absorption by Mossbauer Effect would damage the zinc finger proteins in the hiv virus selectively to inactivate the zinc fingers in hiv virus. RBL notes that restricting the 67Zn to the hiv zinc fingers would spare zinc fingers in normal cells from gamma ray induced recoil and Mossbauer Effect for theoretically curing hiv! - Reginald B. Little (Stillman College; Tuscaloosa, Alabama)
On Jan 30, 2025, I, Reginald B. Little (RBL), notes that his theoretical cure involves using laboratory animals (mice and monkeys) to study the effects of altering isotopes of zinc in zinc fingers of hiv virus and hiv cells for inactivating the hiv and hiv genes in hidden reservoirs for determining cure for hiv. The author (RBL) further determines and concludes that 64Zn enriches in HIV virus (zinc fingers) and HIV infected cells can be either: external stimulated by neutrinos/antineutrinos; replaced by lighter radio nuclides 63Zn, 62Zn, and/or 61Zn for spontaneous electron capture forming corresponding Cu and Ni isotopes to alter/inactivate HIV zinc fingers; or replaced by 67Zn and stimulated gamma rays of 93.3 keV by Mossbauer Effect to selectively inactivate the HIV zinc fingers; and/ or replaced by the heavier 66Zn, 67Zn, 68Zn and 70Zn isotopes for external, intrinsic neutrino/antineutrino stimulations for altering HIV Zn fingers and Zn Finger genes for treating and/or curing HIV. Such hiv treatments and cures should be tested first in laboratory animals and such treatments should be authorized by health authorities before attempts on humans. - Reginald B. Little (Stillman College ; Tuscaloosa, Alabama)
In addition to my theory reasoning hidden previously unknown elastic neutrino and antineutrino interactions by their wave natures causing (and vice versa they neutrino and antineutrinos themselves are affected by) hydrogen bonding, resonance and tautomerism for organic and biochemical phenomena, I also reason such hidden neutrino and antineutrino elastic interactions by their wave natures causing the dispersive interactions, London forces and Pomeranchuk Effect. - Reginald B. Little
On today, I , Reginald B. Little (RBL), reasoned that 15N in lysine and isotopes of Zn may be a new treatment for hiv. The heavy isotopes (66Zn, 68Zn and 70Zn) by RBL's theory have induced negative nuclear magnetic moments (NMMs) and 67Zn has permanent negative NMM relative to zero NMM of 64Zn. 64Zn is enriched in hiv and hiv enriched cells during infection. RBL thinks the 64Zn and its zero NMM more strongly binds 14N. But the negative NMM in 15N will causes stronger binding to heavier Zn isotopes due to their induced negative NMM and -NMM of 67Zn. The 15N in urea treatment can have more 15N in lysine and the interaction of 15N enriched lysine with 66Zn, 67Zn and 68Zn and 70Zn by negative NMMs interaction with negative NMMs for stronger binding for limiting replication of hiv virus. Urine is known to have certain inhibitor molecules, and I think such is due to 15N in these urines. Lysine is known to accelerate hiv replication. Thereby this isotopic enriched treatment will interact in new ways with these molecules of lysine and urine which are already known to affect hiv , but the 15N will alter their effects for anti-hiv outcomes. - Reginald B. Little (March 26, 2025)
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