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1.
Article | IMSEAR | ID: sea-219366

ABSTRACT

To create life, the first step should logically be the formation of the condensed system that defines a cell. If the original contents were dispersed widely, then those components would require condensation. Absent the needed condensation forces, those prime substances would have remained scattered, with no particular proclivity to form a cell. Energy is needed for the above-described process. Without energy for the splitting of water molecules, EZ cannot build. The required energy comes from light. Particularly effective, we found, is infrared light. The impacted water is presumably its EZ fraction, whose crystal-like structure allows for information-storage capability. Ordinary liquid water has no such capability: its randomly oriented, rapidly fluctuating molecules would be expected to show no capacity for retention of information. EZ water, on the other hand, seems practically 揹esigned� to carry information.

2.
Int. j. high dilution res ; 15(2): 10-21, 2016. tab, ilus
Article in English | LILACS | ID: biblio-972907

ABSTRACT

INTRODUCTION: Conventional homeopathy advocates giving 10 strokes (agitation/succussions) to a prescription bottle containing liquid dilution, before taking it. To scientifically support such activity, it must be based on studies on the physicochemical aspects of the memory of water and agitated water chains, supplemented with spectrometry. OBJECTIVE: To analyze spectrometric profiles of homeopathic high dilutions, comparing additionally agitated and non-agitated dilutions, and to define differences according to each dilution´s kingdom. METHODOLOGY: Homeopathic dilutions were prepared using a ratio of 1:100 obtaining dilutions from 1cH to 15cH. Measurements of absorbance of 15cH dilutions were performed at 340 nm and 200 nm, with and without additional agitation. RESULTS: Statistically significant differences were found between agitated and non-agitated dilutions (p <0.05) for Apis mellifica, Bufo rana, and Calcium iodatum, with a decrease in the mean value of absorbance (340 nm) in agitated solutions. For A nica montana, Matricaria chamomilla, Coffea arabica, Pulsatilla nigricans, Calcium iodatum and Natrum muriaticum, the absorbance values increased; these values decreased for Apis and Bufo. In addition, measurements were performed with a shorter wavelength (200 nm); it was observed that there are significant differences for all homeopathic dilutions studied. Additionally, when comparing the mean values of the absorbance for each kingdom, and observing the agitation factor, a statistically significant difference was found in the animal kingdom (p<0.05), having lower absorbance for agitated dilutions. CONCLUSION: Comparisons of the spectrometric profiles of agitated and non-agitated solutions allow to observe that there is a difference of the absorbance when comparing a previously agitated solution and a solution with no agitation before taking it.


Subject(s)
Homeopathy , Spectrum Analysis , Dynamization , High Potencies , Water/chemistry
3.
Int. j. high dilution res ; 14(4): 8-15, 2015. tab, graf
Article in English | LILACS | ID: lil-783318

ABSTRACT

Using Fourier Transform Infrared spectroscopy (FTIR) we have demonstrated that homeopathic potencies of Natrum mur, Cantharis, Nux vomica and Sulphur show differences with respect to the number of free water molecules and strength of hydrogen bonding. The purpose of the present study is to confirm this phenomenon in three potencies of two more drugs Calcarea carb and Silicea. Design: The potencies used for each of the two drugs were 30cH, 200cH and 1000cH. The control was 90% ethanol as also the potentized drugs. The control, as well as the potencies, were diluted with distilled water to reduce the level of ethanol to 0.03 molar fraction in each of them. FTIR spectra of all the potentized drugs, control and sterile distilled water (reference water) were taken in the wave number region of 4000-2800 cm-1. The full width at half maximum (fwhm) of OH band was measured for each spectrum. The width was divided into two in the middle. The difference spectrum (absorbance of drug solution - absorbance of reference water) for each potency and the control was obtained after normalization of the spectrum at 3410 cm-1. One difference spectrum so obtained for a potency was subtracted from another to find out if there is a difference between two different potencies. Results: The half width half maximum (hwhm) in both the high and low-frequency sides of the OH band is far less narrow in potencies than in the control as compared to that in water. The difference spectra for different potencies show different levels of fall in intensity at the wave number region of dip at 3630 cm-1...


Subject(s)
High Potencies , Calcarea Carbonica/pharmacology , Hydrogen Bonding , Mechanisms of Action of Homeopathic Remedies , Silicea Terra/pharmacology
4.
J Biosci ; 1992 Dec; 17(4): 431-439
Article in English | IMSEAR | ID: sea-160872

ABSTRACT

Hydrogen bonding pattern of nucleotides and carbohydrates has been analysed using Cambridge database. An analysis on ribonucleotides shows the 3' ···5' hydrogen bond mediated aggregation to be the most common alignment. The 2' ···5' alignment, which occurs under special circumstances in nature, is found to be the second choice. An analysis on carbohydrates suggests that self assembly of these molecules is not conducive to the formation of polysaccharides of the type which are found in present day living organisms. Further, the role of water molecules in the polymerization of three important biomolecules, namely nucleotides, carbohydrates and amino acids, has been analysed. Implication of these results to prebiotic polymerization is discussed.

5.
Article in English | IMSEAR | ID: sea-160875

ABSTRACT

Hydrogen bonding pattern of nucleotides and carbohydrates has been analysed using Cambridge database. An analysis on ribonucleotides shows the 3' ···5' hydrogen bond mediated aggregation to be the most common alignment. The 2' ···5' alignment, which occurs under special circumstances in nature, is found to be the second choice. An analysis on carbohydrates suggests that self assembly of these molecules is not conducive to the formation of polysaccharides of the type which are found in present day living organisms. Further, the role of water molecules in the polymerization of three important biomolecules, namely nucleotides, carbohydrates and amino acids, has been analysed. Implication of these results to prebiotic polymerization is discussed.

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