A Remarkable Study That May Support The Concept Of ‘Molecular Imprints’ As Active Principles Of Potentized Drugs

Here is a remarkable study regarding the variation in Fourier Transform Infrared Spectra of some homeopathic potencies and their diluent media, conducted by N.C.SUKUL, Ph.D., SUDESHNA GHOSH, M.Sc., A. SUKUL, Ph.D., and S.P. SINHABABU, Ph.D. It is published in THE JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE, Volume 11,  Number 5, 2005, pp. 807–812. The report is available at this link: http://www.homeopathy.org/research/basic/acm-2005-11_11.pdf

Published report reads as follows: “The aim of this study was to determine whether potentized homeopathic drugs and their diluent media differ from each other with respect to their Fourier transform infrared (FTIR) spectra. FTIR spectra of Nux  vomica 30C,  Lycopodium 30C,  Santonin 30C,  Cina 30C,  Cina 206C,  Cina 1006C, and their diluent media (90% ethanol and Ethanol) 30C were obtained in the wave number range of  2000–1000 cm_1 at 20°C. Potassium bromide powder soaked with the potencies, pressed into pellets, and air dried were used to measure the spectra. Because water structures in homeopathic potencies are thought to carry specific information on drug molecules and because O-H bending vibrational band (v2) exclusively belongs to water, the study was restricted to the bands in that wave number region. Alcohol has no absorption in the O-H bending region.

 The potencies were found to differ from each other and their diluent media in the number of v2 bands, their wave number (cm_1), shape, and half-width (cm_1) of the bands.

The number and other characteristics of the v2 band represent the number of hydrogen-bonded water species and their hydrogen-bonding strength, respectively. The potencies and their diluent media therefore differ from each other in the number of hydrogen-bonded water species and their hydrogen-bonding strength. The observation that KBr pellets soaked with a potentized drug retains its specific spectral absorption properties simply confirms that medicated sucrose globules, used in homeopathic dispensing, are capable of retaining the therapeutic properties of the drug.

Drugs are prepared and stored in aqueous ethanol. Sucrose globules soaked with liquid potencies retain therapeutic properties of the drugs for a long time. Water also serves as a good medium but it does not keep the properties of a potency for long. It has been suggested that water structures in a potentized drug are responsible for carrying the information of drug molecules or particles present in the mother tincture. Ethanol molecules are thought to promote or to preserve water structures characteristic of a potentized drug.1A basic quality of a hydrogen-bonded solvent such as water is the hydrogen bond strength.

Physicochemical properties of the water in aqueous alcohol mixtures have been studied widely by such techniques as X-ray or light scattering, dielectric relaxation, nuclear magnetic resonance imaging et cetera. Among these methods, infrared (IR) spectroscopy is one of the most promising for the study of the distribution of hydrogen- bonding strengths of the water molecules in the mixtures because of the short time scale of measurements. There are two kinds of fundamental vibrations for molecules: (1) stretching, in which the distance between two atoms increase or decrease but the atom remains in the same bond axis; and (2) bending, in which the position of the atom changes relative to the original bond axis. Infrared radiation causes vibrational excitation of the molecular framework of a compound. In aqueous alcohol O-H stretching vibrational bands of water (v1 and v3) overlap the alcoholic O-H band. For this the IR spectra in the stretching region are of no use for studying hydrogen bonds of the water molecules in water/alcohol mixtures. In the region of bending vibrational band of water (v2), alcohols have no absorption bands. The purpose of the present work is to study v2 bands through Fourier transform infrared (FTIR) spectroscopy in 90% ethanol, Ethanol 30C, and some potentized drugs such as Nux vomica 30C, Lycopodium 30C, Santonin 30C, Cina 30C, Cina 206C, and Cina 1006C prepared in 90% ethanol. Conventionally vibrations are labeled in decreasing frequency within their symmetry type. The symmetric vibrations of H2O are labeled v1 for the highest fully symmetric frequency (3651.7 cm_1) and v2 for the next highest (1595.0 cm_1).7 FTIR spectroscopy provides simultaneous and almost instantaneous recording of the whole spectrum in the infrared region while minimizing background noise.

Nux vomica 30C, Lycopodium 30C, Santonin 30C, and Cina 30C were prepared by successive dilution (1:100 v/v) with 90% ethanol followed by succussion in 30 steps from the respective mother tinctures in this laboratory.8 Cina 200C and Cina 1000C, purchased from M. Bhattacharyya and Co. (Calcutta, India), were further diluted (1:100) and succussed with 90% ethanol in 6 more steps to prepare Cina206C and Cina 1006C. All of these potencies have the same absorbance (3.135) at 255 nm, showing similar concentrations of ethanol (90%). The purpose was to replace the manufacturer’s aqueous ethanol in Cina 200C and Cina 1000C with the ethanol in this laboratory so that the diluent medium (90% ethanol) of all the test potencies would be of the same quality. Ethanol was obtained from Bengal Chemical and Pharmaceuticals Ltd. (Calcutta, India). Sterile deionized and double-distilled water was added to absolute ethanol to prepare 90% ethanol, which served as the diluent medium of all potenties as well as the control.

 FTIR spectra were measured at 20°C by a Jasco FTIR spectrometer (Jasco, model 420, Japan). The wave number resolution was 4 cm_1. Spectra  were obtained in the wave number range of 2000–1000 cm_1. Potassium bromide powder (_150 mg) was soaked with 90% ethanol (_0.15 mL) or any of the six potencies tested. The drug-soaked powder was mixed thoroughly with a mortar and pestle, spread in thin film (1 mm deep) in a petri dish, and allowed to dry at 30°C (50% humidity). The powder was then pressed into small equal-sized pellets. The KBr pellets, which simulate sucrose globules soaked with a potency, were exposed to IR radiation in the spectrometer. Five pellets were prepared for each drug or the diluent medium, and the IR spectra measured.

Data were analyzed by one way analysis of variance. Different potencies and their diluent media (90% ethanol, Ethanol  30C) differ significantly (_ 0.01) from each other with respect to the positions of bands in the wave number regions, their half-widths, and their absorption intensities except the wave numbers.  ……..

 Because all KBr pellets were prepared under similar conditions, it is quite unlikely that they have different amounts of water in them. In earlier work the present authors observed a marked variation in O-H bending vibration among 90% ethanol, Nux vom 30C (unsuccussed), and Nux vom 30C succussed.5 The results of the present study show that potentized drugs differ from each other and also from their diluent medium, 90% ethanol, in the number of v2 bands. The number of observed v2 bands should provide the number of water species with different hydrogen-bonding strengths.6 There may be a few more water species than those actually observed by v2 bands in the spectra. According to Mizuno (personal communication, June 2003), IR spectroscopy has superior power in that different water species are distinctive from each other, but it is very difficult to resolve the curve into components. Mizuno further observed that there was no linearity in the absorption intensities of different bands. Thus different potentized drugs have different water species with different hydrogen-bonding strengths. The v2 bands have different half-widths in different potencies. The broadening of v2 bands has been attributed to the distribution of hydrogen-bonding strengths and vibrational coupling.6 The v2 band of pure water has an unusually broad width of 82 cm_1 at half-maximum. The v2 band is found to be narrower with an increase in the alcohol concentration. The narrowing of the v2 band is considered to be caused by the weakening of the vibrational coupling as a result of dilution by the alcohol. The concentration of ethanol was the same (90%) in all the potencies tested. The variation in the half-width of the v2 band may thus be caused by influence of original molecules at the start of the dilution process and also by succussion. Previously the present authors observed that succussion caused blue shift of the v2 in Nux vomica 30C.In each column of Table 1 the band of different drugs showed either a blue or red shift. Blue shifts represent the formation of stronger hydrogen bonds among water molecules. This has also been confirmed by 1H-NMR studies. It has long been known in clinical practice that sucrose globules soaked with a liquid potentized drug retain all the therapeutic properties of the drugs. FTIR spectra of KBr pellets soaked with potentized drugs simply confirm the long-standing clinical observation.

Cowan et al. demonstrated that the three-dimensional structure of liquid water loses its memory of molecular arrangement through the H-bond network in about 50 fs. The work was based on O-H stretching vibrations of pure H2O. Pure water is not comparable to a homeopathic potency that is prepared by successive dilution and succession from a mother tincture and preserved in 90% ethanol. Ethanol molecules with large nonpolar parts can preserve or promote water structures specific to a homeopathic potency. The efficacy of a homeopathic potency prepared in pure water is very short-lived. An electrostatic component is usually the dominant force contributing to H-bonding. Succussion or any mechanical agitation would therefore make the H-bonding stronger in a homeopathic potency. In ethanol solution the sequential H-bond dissociation and reassociation occur between the same OH groups. In water the broken bonds probably reform to give the same H-bond. Dissociation is a rare event occurring only twice a day, that is, once for every 1016 times the H-bond breaks. Thus clusters can persist for much longer times. The relative proportions of different polymers of water preserved by ethanol are at dynamic equilibria of specific geometric configurations. It is assumed that this dynamic geometric configuration of water clusters in a collective way confers specificity on a potentized homeopathic drug. The homeopathic potencies used in the present study were prepared in 90% ethanol and soaked in KBr pellets. Here water structures were preserved by ethanol and their random.

Based on the study findings several conclusions can be drawn. First, in the FTIR spectra of aqueous alcohol mixtures O-H bending vibrational bands (v2) exclusively belong to water. Nux vomica 30C, Lycopodium 30C,  Santonin 30C,  Cina 30C, Cina 206C, and Cina 1006C differ from each other and also from their diluent medium, 90% ethanol, in the number of v2 bands, their wave-number (cm_1), their shape, and half-width (cm_1) in the FTIR spectra. Second, the number of v2 bands and other parameters of the same represent, respectively, the number of hydrogen-bonded species of water and their hydrogen bonding strengths. Thus the potencies and their diluent medium differ from each other with respect to the number of H-bonded water species and their H-bonding strengths. Third, KBr pellets soaked with potentized drug, such as medicated sucrose globules used in homeopathic dispensing, retain specific spectral properties of the drugs concerned. Finally, homeopathic potencies can be differentiated from each other by FTIR spectra with respect to the O-H bending vibrational band.”

This elaborate study rightly observes that the homeopathic potencies and their original diluent medium differ from each other with respect to the number of H-bonded water species and their H-bonding strengths.

Even though the authors could not understand the real process of “MOLECULAR IMPRINTING” involved in this phenomenon, their observation amply proves that the supra-molecular structure of potentized medicines differs from ethyl alcohol/water mixture, even though their chemical composition remained the same. That means, through the process of potentization, supra-molecular structure of ethyl alcohol/water mixture has undergone fundamental changes. Obviously, it is through these structural changes that the medicinal properties of drug molecules are transferred to the diluent medium.  

This difference in the structure of potentized medicines from their original medium, the specificity of medicinal properties exhibited by potentized medicines, and the fact that potentized medicines exhibit medicinal properties just opposite to that of parent drugs can be satisfactorily explained only on the basis of “molecular imprinting’ as proposed by DIALECTICAL HOMEOPATHY.

Author: Chandran Nambiar K C

I started practicing homeopathy in 1970, when I was 20 years old and studying for final year of BSc (Zoology) course. My interest in homeopathy happened very accidentally, through a constant relationship with a local practitioner who happened to be father of my classmate. I was a regular visitor in his clinic, where from I started reading BOERICKE MATERIA MEDICA and other homeopathic books, which helped me to cure myself my troublesome asthma that have been haunting me since my childhood days. I became a voracious reader of homeopathy. I was also deeply involved in studying marxism and dialectical materialism during my college days, which attracted me to political activities. MARXISM and HOMEOPATHY became two essential parts of my intellectual and practical life, which still continues so. Even though I joined DHMS course in a karnataka homeopathic college, I could not continue it due to my intense involvement in revolutionary political activities that resulted in jail life and a lot of criminal cases. Once that phase was over, I took a diploma in veterinary science and became a livestock inspector in animal husbandry department under govt of kerala. I have been continuing my study and practice of homeopathy all through these years. Since CCH act came into force only in 1976, and it contained provisions allowing existing practitioners to continue, my homeopathic practice went smoothly in parallel with my government job. In 1987, co-operating with some local homeopaths and social activists, I started Kannur District Homeopathic Hospital Sociey, which established a chain of hospitals and homeopathic clinics in different parts of Kannur district. After a few years I had to leave the society for some political reasons, and I established a 100 bedded well equipped homeopathic hospital in Taliparamba, employing a number of prominent homeopaths. That was ended up as a financial disaster for me due to many reasons, including my lack of skills as a money manager, and I was compelled to close down my dream project with in a short period. I lost huge money I invested, lost my reputation, and it pulled me into a debt trap. I learned a lot of valuabl lessons from this failure- about life, human psychology, relationships, and above all, about myself. I realized failure is the greatest teacher, if you are prepared learn from it. I learned how will power and determination to win will help us come back into life as a phoenix from our own ashes. I learned, one does not fail unless he stops fighting and accepts failure. My failure and the hardships that followed has moulded my personality in such a way that I can now withstand any disaster and fight back. I tell you, you will not know what life really is, unless you miserably fail at least once in your life. By this time, I left my government job also, and settled as a full time homeopathic practitioner. By this practice, I could repair my earlier financial losses, and establish well in life. It was during this period that I felt the need of developing a simple and user-friendly homeopathic software, that resulted in the evolution of SIMILIMUM, which was later upgraded into SIMILIMUM ULTRA. Similimum Ultra was well accepted by the profession, and it collected good revenues which continues even today. I stopped my practice a few years back , and concentrated in the study and research activities to evolve scientifically viable explanations to the so-called riddles of homeopathy. This unrelenting study resulted in MIT or Molecular Imprints Therapeutics, which provides a scientific and rational explanation for homeopathy. I started a homeopathic discussion group on facebook called HOMEOPATHY FOR TOTAL CURE, which has more than 35000 homeopaths as members. By this work on facebook, I could establish close relationship with many homeopaths around the world. It goes on. I could successfully convert facebook as my office and work place, from where I propagate my MIT ideas, co-ordinate my works for homeopathic community, and sell my Similimum Ultra Software. My years of hardwork in search of HOW HOMEOPATHY WORKS ultimately resulted in the publication of a book titled REDEFINING HOMEOPATHY (3000 pages, 3 volumes, hard bound, Rs 6000), in which I have compiled my articles regarding my scientific explanations of basic principles of homeopathy. These ideas are called MIT or MOLECULAR IMPRINTS THERAPEUTICS. MIT is now included in the syllabus of MD (HOM) course of prestigious DY PATIL DEEMED UNIVERSITY, PUNE, INDIA. Research department of SARADA KRISHNA HOMEOPATHIC COLLEGE, Kulashekharam, Tamilnadu, India, the only NAC accredited homeopathy college in India, has recently taken up certain reserch projects for proving the scientific explanations proposed by MIT. Based on MIT perspective of homeopathy, I had developed an MIT PROTOCOL for scientific homeopathy, and initiated a project for establishing a chain of MIT NETWORK CLINICS all over India, where MIT PROTOCOL will be practiced. More over, I have developed a whole range of 351 MIT FORMULATIONS, which are disease-specific combinations of post-avogadro diluted homeopathy drugs. NOW I AM IN 71st YEAR OF MY LIFE, AND STILL LOOKING FOR NEW HORRIZONS!

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