A Dialectical Homeopathy Website By Chandran Nambiar K C

Basic document of fundamental concepts to be considered when preparing a Project Report for DH2011 


 “At least, we have to understand that it will never be possible for us to convincingly present homoeopathy as a branch of scientific medicine with the help of such ‘supernatural’ and ‘dynamic’ explanations,  which is far from a rational and scientific world outlook.”

 “The biggest intellectual challenge homeopathy face today is to explain and demonstrate this process of potentization in such a rational and convincing way that modern science could understand and experiment it using their tools and methodology.”

 “We have no other go but to demonstrate and explain our fundamental principles scientifically, and answer the following questions: What really happens at ‘material’ level during the process of potentisation?”

 “What are the active principles in the potentized medicines?”

 “How these potentized medicines exactly influence the biochemical processes and relieve the pathological molecular inhibitions?”

  “Yet another class of ‘experts’ shock us with their ‘scientific’ explanation of homoeopathy, declaring that some mysterious sub atomic particles are released during the process of potentization. They confuse people by using all the complex vocabulary of “quantum physics” to establish the most unscientific concepts in the guise of homeopathy.”

 “It is really an absurdity not even a primary school student can tolerate, to hear that atomic division is possible through such a very simple mechanical process like potenlization.”

 “Further, it is very unlikely that those people who talk about atomic energy in homoeopathic medicines had ever thought about how the simple sub-atomic particles could preserve and exhibit the specific medicinal properties of highly complex drug molecules subjected to potentization.”

 “It is only a primary knowledge of any student of physics that an object loses its gross molecular level properties when it is divided into atoms, and loses even the atomic level properties when atoms are divided in to sub-atomic particles.”

 “It is beyond any comprehension and common sense how the individual medicinal properties of complex drug molecules can be preserved and exhibited by simple sub-atomic particles they contain, as our ‘scientific’ interpreters of homoeopathic potentization try to ‘prove’.  All the similar particles at sub-atomic level are same, whether they come from nux vomica or sulphur or gold.”

 “We   should always bear in mind the fact that such a simple mechanical process involved in homoeopathic  potentization can never effect any atomic division at all. Only division we can imagine is ionization of atoms and molecules during this mechanical process.”

 “If the drug substances contain large complex molecules with high molecular weight, the limits of Avogadro’s  number will be crossed  even before the process of potentization  reaches 10th dilution in the centesimal scale.  If the drug molecules are simple and small in size, this may happen above 20 th dilution or so. As hydrogen is the smallest molecule, with least molecular weight, it will be the last to cross the Avogadro limit during dilution process. It is evident from calculations that in a homeopathic potency above 23C, which is very much diluted than the Avogadro limit, not even a single molecule of the original drug is likely to remain. It will contain only the molecules of water and alcohol used as the medium of potentization, along with some probable contaminants.”

 “Even though we name those highly diluted preparations using labels such as sulphur, mercury etc, which were used to start the process of dilution, the undeniable truth remains that they contain not a single atom of those substances.”

 “Same time, the fact remains that we successfully utilize those ultra dilutions to cure diseases, according to our therapeutic law: ‘similia similibus curentur’. We are obliged to prove how it works, and provide a reasonable  explanation for this mysterious riddle, if we hope homeopathy has to be finally acceptable to the modern scientific world.”

 “Whatever the critics of  homeopathy may say, we are fully confident of the fact that these highly diluted homeopathic preparations exhibit specific medicinal properties. These preparations can be effectively used as therapeutic agents on the basis of the principle of ‘Similia Similibus Curentur’. These facts are regularly being proved beyond doubt in everyday experience by thousands of homeopaths all over the world. It has been also proved in various controlled in vitro tests in the laboratories.”

 “Even in such a case, we are bound to convince the scientific community, how these highly diluted preparations preserve and exhibit the ‘reverse’ therapeutic properties of original drugs, even in the complete absence  of  their molecules.  We should realize that it is of no particular use, trying to evade from this obligation by labeling this phenomenon with non-specific phrases such as ‘dynamic force’ or the like, which even the die-hard homeopaths fail to fully comprehend.”

 “It is obvious that during the initial process of ‘trituration’, the complex molecules contained in the drug substances probably get liberated themselves from their inter-molecular bonds and get ionized, when they are mixed with crystals of ‘sugar of milk’ and subjected to strong molecular friction. These ionized drug molecules thus attains a full expression of their chemical and biological properties, and become more virulent than the tightly packed original molecules. The secret of even those substances which seem to be chemically inert,  turning into potent  medicinal agents through the process of  homeopathic trituration may be  due to the liberation and ionization of individual molecules contained in those drugs.”

 “But, apart from low potencies, we cannot explain the medicinal properties of the highly diluted homeopathic potencies even on the  basis of ionization,  or liberation of individual drug molecules.”

 “There is least chances of even a single molecule of the drug substance  still  remaining in those preparations.”

 “More over, the medicinal properties exhibited by these high potency dilutions are exactly reverse to the medicinal properties of  the same drug substances in crude forms. Homeopathic potencies are capable of removing disease symptoms that are ‘similar’ to those produced by the original drugs  substance during drug proving. It means that homeopathic potenices act not exactly as original drugs, but in an exactly reverse direction. Any theory we put forward regarding potentization should also be capable of explaining this peculiar phenomenon.”

 “The fact that the higher potencies behave somewhat like antidotes towards their original drug substances obviously indicates that properties of drug substances are somehow transferred into the medium in a some what reverse order during the process of potentization. This important observation gives us certain vital clues in solving the whole mystery.”

 “The wonder is that, it has been proven through minute chemical analysis, that even after the process of potentisation is completed, the mixture still remained simply water and alcohol in the same initial proportion. In other words, The medium used for potentization, and the product of potentization are similar in chemical structure.”

 “The hardest challenge we face is, how to explain the diverse specific medicinal properties and therapeutic effects exhibited by these potentized preparations, having only a chemical structure of simple alcohol-water mixture. It is imperative that a satisfactory answer to this question should given at least to the people who do not have any doubts regarding the therapeutic capabilities of homeopathic potencies.”

 “Another important factor we have to note is that the therapeutic properties of potentized homeopathic preparations are found to be lost by the influence of certain physical forces such as violent motion, strong magnetic fields, powerful light, excessive heat, electricity, and other electro-magnetic radiations. Every homeopath would have observed this phenomenon during his clinical experience. It means that the medicinal properties of homeopathic potencies are preserved in such a particular form that can be adversely affected by above said physical influences.”

 “It is evident from this observation that through the process of potentization, the water-alcohol mixture attains some sort of  physical transformations that can be reversed by certain physical influences described above.”

 “Obviously, it is through this transformation of purely physical nature, without any chemical changes happening, that the therapeutic properties of the original drug substance are transferred into the alcohol-water mixture in a reverse order. With the help of modern material sciences, we have to inquire into the exact mechanism of this physical transformation, so that we can solve the riddle of homeopathic potentization once and for ever.”

 “It should be especially noted that the therapeutic properties of homeopathic potencies are exactly reverse to the medicinal properties of original drug molecules used for potentization. Diseases with symptoms similar to those produced by a drug substance during proving are cured by the potentized form of the same drug.”

 “Since no chemical changes take place in the alcohol-water mixture during potentization, we can conjecture that changes happens only at the level of the physical formations.”

 “More over, these physical transformations occurring in the nanoscopic level  are liable to be reversed by the influence of above-said physical forces.”

 “As a result of this nanoscopic physical transformations happened  through potentization, the alcohol-water mixture attains the capacity to interfere in the biochemical processes in the living organism, resulting in desired therapeutic effects.”

 “It can be proven by simple experiments that the rate of evaporation, solubility, surface tension, spectrosopic analysis  etc, of alcohol-water mixture before and after potentization are different. It indicates that, though the chemical structure of water-alcohol mixture remains the same, some changes have occurred in the supra-molecular level as a result of potentization. Key to the mystery of homeopathy may be available by pursuing these primary observations in scientific directions.”

 “What is the exact character and dynamics of this physical transformations occurring in the alcohol-water mixture during potentization?  How is the information regarding the medicinal properties of drug molecules encoded into these physical formations, and preserved even without the presence of a single original drug molecule?  What is the exact molecular dynamics of therapeutic action of these highly diluted preparations? How they interfere in the bio-chemic interactions of an organism, thereby removing the specific pathologic molecular inhibitions? The future of homeopathy and medical sciences at large, depends on the answers we provide for these fundamental questions.”

 “The presence of ethyl alcohol in water is considered as a factor reducing the rate of protonation/deprotonation processes, thereby enhancing the stability of hydration shells. Importance of using water-ethanol mixture for homeopathic potentization is self-explained here.”

 “It has been already stated that hydrogen bond strength can also be affected by electromagnetic and magnetic effects. Any factors, such as polarization, that reduces the hydrogen bond length, is expected to increase its covalency. There is still some dispute over the size of this co-valency, however any co-valency will increase the network stability relative to purely electrostatic effects. As hydrogen bond strength depends almost linearly on its length (shorter length giving stronger hydrogen bonding), it also depends almost linearly (outside extreme values) on the temperature and pressure.”

 “It has to be verified whether the violent succussion and rotatory motion done during potentization procedure any how plays a role in polarization of molecules, thereby reducing the hydrogen bond lengths, and  increasing the stability of hydration shells formed.”

“Hydrogen bonded chains (that is, O-H····O-H····O) are cooperative; the breakage of the first bond is the hardest, then the next one is weakened, and so on (see the cyclic water pentamer). Thus unzipping may occur with complex macromolecules held together by hydrogen bonding, for example, nucleic acids. Such co-operativity is a fundamental property of liquid water where hydrogen bonds are up to 250% stronger than the single hydrogen bond in the dimer. A strong base at the end of a chain may strengthen the bonding further.”

 “The molecules of alcohol also have the dipole structure as water molecules. It is possible for them to establish mutual connection through hydrogen bonding.”

 “The molecular weight of alcohol molecule is 46. The molecular weight of water(H2O) is 18. That means that the number of water molecules contained in 18 gram of water and the number of alcohol molecules contained in 46 gram of ethyl alcohol are equal.”

 “When alcohol and water are thoroughly mixed alcohol molecules forms a network with water molecules through hydrogen bonds, The mobility of water molecules is restricted by the bonds established with alcohol molecules. Hence, hydration shells formed in alcohol–water mixture are comparatively more stable. The count of alcohol molecules and the count of water molecules contained in their mixture in 73:27 ratio will be equal. (73% w/w. alcohol and 27% w/w water) This mixture is known as (40 power   spirit).”

 “Medium used for homoeopathic potentization contains 87% w/w of alcohol and 13% w/w of water. In this ratio, the number of alcohol molecules will be about more than that of of water molecules. Such a ratio will be very suitable for the production of stable hydration shells. More over, the presence of ethyl alcohol in water is considered as a factor reducing the rate of protonation/deprotonation processes, thereby enhancing the stability of hydration shells. This may further explain the importance of water-ethyl alcohol mixture being used as the medium of homoeopathic potentization.”

 “It should be specially noted that the vessels and utensils used for potentization are made of high quality glass or porcelain, which contains large quantities of Silica (Silicon Dioxide). Chances of silica particles liberated into the medium during the process of trituration, succussion and potentization of drugs have to be seriously considered. Studies have proved that potentized homeopathic preparations contain trace quantities of silica. Silica is hence considered to be an unavoidable contaminant we have to cope with.”

 “Chances of silica particles playing a role in the molecular imprinting process during potentization cannot be ruled out at present. The peculiar molecular structure and physico chemical properties of silica proposes such a role. It has been noted that homeopathic potencies prepared using utensils made of material other than silica glass are of low quality. Anyhow, more research is required on these lines.”

 “‘Molecular memory of water’ is a rarely understood phenomenon, and is a subject of much controversies and speculations in the world of science. Even now, scientists differ much in their opinion regarding this phenomenon. Final outcome of these controversies will have great concern and significance in the realm of homoeopathy. Let us examine some details of  the nature and essence of this controversial phenomenon.”

 “If we carefully examine the history of Benevenite’s failure, we would  understand that it was not his basic propositions that failed, but the experiments he was subjected to in order to to prove his arguments. Firstly, his argument that the drugs so diluted to the extend of making it impossible to contain a single molecule, can interfere in biological processes exactly mimicking the basic drug substance was a little inaccurate interpretation of results of his original experiments.”

 “This inaccurate interpretation of the phenomenon he observed, led him to agree to subject himself to inappropriate and hostile experiments, that were obviously designed to defeat him. He failed to realize  that the molecular memory of the drug substances is imprinted into water not as exact ‘mimics’, but in a ‘reverse’ direction, in a complementary configuration. Put in another way, drug molecules will be imprinted in water not as exact configurational duplicates, but as negative complements, and hence, they cannot ‘mimic’ the original drug molecules in biological processes. Failure to understand this phenomenon correctly was a grave mistake, that cost heavy to him.”

 “His conclusion that the molecular imprinted water interferes in biochemical processes exactly like the original drug molecules proved to be immature, and obviously he failed. He failed to comprehend the exact mechanism of molecular imprinting in water, and plan the experiments accordingly. Had he understood the real mechanism of molecular imprinting in its correct perspective, he would have been aware of the unsteady behavior of hydration shells in water, and taken necessary precautions, before subjecting himself to a controlled experiment.  He could have devised some techniques to ensure the stability of hydration shells, such as using alcohol-water mixture instead of pure water, as done in homeopathic potentization.”

 “We know that water is a good solvent. Let us see what happens when foreign molecules are made to dissolve in water. If a foreign molecule, ion,  or colloidal particle happens to enter the matrix of 3-dimensional dynamic network of water molecules, they are entrapped inside this network. Water molecules arrange themselves around the intruder or ‘guest’ in a peculiar way by the formation hydrogen bonds. These formations of water molecules around the ‘guest’ molecules are known as hydration shells. These hydration shells exist in a dynamic state, and are more or less unstable. The foreign molecules dissolved in water exist in a state of being entrapped inside these hydration shells as ‘guests’. This phenomenon can be seen both in ionic solutions and colloidal solutions. Obviously, hydration shells assume an internal spacial arrangement exactly fitting to the 3-dimensional spacial configuration of the foreign molecule entrapped in them. If we could devise some technique to remove the entrapped ‘guest’ molecules from these hydration shells, without disturbing the hydrogen bonds between the constituent water molecules, these hydration shells can still retain the molecular memory of the molecular configurations of the removed ‘guest’ molecules. This rarely studied phenomenon is known as ‘molecular memory of water’.”

 “Actual mechanism and forces underlying this phenomenon has to be investigated minutely by physical scientists. Minute changes occurring in the electron clouds of atoms of water molecules during the formation of hydration shells may be one factor responsible for this phenomenon.”

 “It has been well proven that these hydration shells later show a peculiar capability to differentially recognize the original ‘guest’ molecules which were responsible for their formation. This may be due to the existence of some imprinted memory of those ‘guest’ molecules retained in the hydration shells. This imprinting of memory may be compared to formation of finger prints. As in the case of finger prints, configuration of these molecular imprints also will be a complementary negative of ‘guest’ molecules.  These empty hydration shells, or supra-molecular formations of water subjected to molecular imprinting, may be called ‘hydrosomes’, which means, minute ‘nano-cavities of water’. Homeopathic process of potentization is essentially a crude method of preparing hydrosomes, prepared by using various drug molecules as ‘guests’.”

 “It should be specifically noted that the medium used for homeopathic potentisation is not pure water, but it is mixed with ethyl alcohol in a particular ratio. It may be  inferred that the presence of comparatively heavy ethyl alcohol molecules in this mixture may be contributing to stabilization of ‘hydrosomes’, preventing their easy dissociation.”

 “The convergent forces of rotational movements to which the mixture is subjected as part of potentization, may also be a contributing factor in stabilizing the empty hydration shells by polarization and subsequent reduction of hydrogen bond lengths.”

 “This peculiar configuration of hydrosomes are destroyed only when their energy level of water molecules are disturbed by the effect of heat,  electricity, magnetism and other electro magnetic radiations. As stated earlier the hydration shells formed in pure water are comparatively unstable. Here lies the importance of the fact that homeopathic potencies are made using alcohol- water mixture.”

 “Information we recently receive from various research institutions, regarding the wonderful  supra-molecular  structures of materials and their hitherto unknown peculiar properties, may greatly contribute in our  efforts to unravel the secrets of homeopathic potentization. Studies on  ‘water clusters’, ‘crystalline structure of water’, ‘shape memory property’, ‘molecular imprinting’,  ‘nano-technology’,  ‘clathrate formations’ and other diverse phenomena are offering promising indications in this direction. We have to utilize all these new revelations in our scientific study of homeopathy. Generally speaking, we have to deal with homeopathic potentization as a branch of modern nano-technology.”

 “Homeopathy is much interested in this area of researches pertaining to this peculiar crystalline nature of water. It is believed that in the process of molecular imprinting of water using drug molecules,  this crystalline structure of water plays a crucial role. It is likely that more advanced studies about dynamics of crystallization of water may help us help us to correctly explain the phenomenon of duplication of molecular imprints during homeopathic potentization.”

 “The studies about Clathrate Compounds or ‘host-guest’ compounds in supra-molecular chemistry is an area in which homeopathy has sincere interest. Clathrates are the molecular networks which are formed when gases dissolve  in water under high pressure. They exist in a peculiar ‘host–guest’ relationships. Studies about this phenomenon are still in their infancy. Clathrates have a crystalline nature,  existing as molecular networks,  formed by a process of water molecules arranging around the ‘guest’ molecules. Understanding the dynamics of clathrate formation are also likely to help in explaining  the phenomenon of homeopathic potentization. Even if  the ‘host’ molecules are removed from clathrates, the network of water molecules have been found to remain intact. More over, the existing clathrates can induce the formation of similar clathrates. It will be very useful to consider these above discoveries connecting them with the phenomenon of homeopathic  potentization.”

 “A lot of studies has been published regarding ‘shape memory materials’.  Several alloys having  crystalline structure have been observed to possess shape memory property. Such materials are known as SMART materials. This phenomenon also has to be understood well while trying to explain homeopathic potentization in a scientific language. Perhaps, water may also would have to be a considered as a ‘smart’ material.”

 “It is in the phenomenon of ‘molecular memory of water’ itself that we naturally land on when we attempt to scientifically explain the homeopathic potentisation of drugs. We have already seen that the alcohol–water molecules contained in the medium used for potentization,  arrange themselves around the drug molecules, and form hydration shells. The drug molecules entrapped in the hydration shells are systematically removed as a result of serial dilutions and shaking, done as part of potentization. Empty   hydration shells or ‘hydrosomes’ remain. These ‘hydrosomes’ are nano-cavities, imprinted with the three-dimensional ‘finger print’ of drug molecules used as ‘guest’ molecules.  This phenomenon may be called as ‘molecular imprinting in water’. These ‘hydrosomes’ are the real active principles of homeopathic medicines, potentized above 30C.”

 “First stage of potentization involves division of complex drug molecules into simpler constituents. When a medicinal substance is subjected to homeopathic potentization, if it is not soluble in water or alcohol, it is first mixed with sugar of milk and subjected to repeated trituration. Then the substance is  potentized using alcohol–water mixture as medium. If the medicinal substance is by itself soluble in water or alcohol, potentisation is done directly in that medium. During the initial stages of  this process individual molecules contained in the medicinal substance are liberated from their inter-molecular bonds, or ionized. Crude drug substance undergoes this division into individual molecules and ions, due to the mechanism of violent trituration and shaking. Inter-molecular bonds are broken, and the constituent molecules and ions are liberated. As a result, these ions and molecules become more virulent, capable of exhibiting their interaction potentials to their full extent, and become ready to undergo hydration in water-alcohol medium. Since the individual properties of drug molecules come out in their totality, it is observed that even seemingly inert substances become powerful drugs due to the division during first phase of potentization. Insoluble substances thus become soluble in water. The difference between crude Lyco and Lyco 6x, crude Silica and silicea 6x, crude table salt and Natrum Mur 6x etc are examples for this phenomenon. This first phase may be called ‘liberation phase’.”

 “Second stage of potentization involves actual hydration and molecular imprinting of individual drug molecules and ions. This phase may be called ‘imprinting phase’.

 Molecules, ions and colloidal  particles, liberated through the first phase undergoes process of hydration and molecular imprinting in water- ethyl alcohol mixture during second phase. Each individual molecule or ion is naturally subjected to hydration and molecular imprinting, independently of others. Individual drug molecules act as ‘guest’ molecules in this imprinting process. Obviously, potentized homeopathic medicines consist of a mixture of independent molecular imprints of constituent molecules contained in the drug substance. This is an important point to be specifically noted. When Nux Vomica is potentized, it is not Nux Vomica as such getting imprinted, but its individual constituent molecules, independently of one another. During the peculiar process of serial dilution and shaking done as part of potentization, concentration of drug molecules gradually decrease in the medium, while concentration of empty hydration shells or ‘molecular imprints’ increase. The memory of the three dimensional structure of each individual drug molecule  will remain imprinted into these empty hydration shells, in a complementary negative configuration. These complementary factors are called ‘hydrosomes’, which means ‘nano-cavities of water’. Hydrosomes are capable of acting as ‘counteractive complementary factors’ (CCF) towards pathological molecules during therapeutic process, if the pathologic molecules are similar in configuration to the drug molecules used as ‘guest’ molecules. We can conceive these hydrosomes as the 3-D finger-prints of drug molecules used as ‘guest’ molecules, and hence capable of fitting exactly to the three dimensional configuration of any similar molecules. We should remember that these hydration shells or molecular imprints of each constituent drug molecules act as therapeutic agents, independently of one another. Here we also understand that what we consider as a ‘single medicine’ in homeopathy is in reality only a mixture of hydrosomes which bear molecular imprints of different types of constituent molecules which are independent.”

 “Potentization can now be explained as a process in which molecular imprints of drug molecules are formed and stabilized. At a particular stage of potentization all the drug molecules are completely removed from the potentizing medium. This stage depends up on the exact size of individual drug molecules subjected to imprinting. Large molecules disappear much earlier, and smaller ones at higher stage. Anyhow, when the potentization crosses 23C, even the smallest drug molecules will be completely removed. We can understand this stage by calculating on the basis of Avagado’s number and molecular weight. At potentazation some where above 23C, we may reach a state in which all the original drug  molecules become totally absent. If  the potentization is carried still higher, there will be no drug molecules for imprinting. Advisability of potentization after this stage have to be considered on the basis of studies regarding the possibility of duplication of existing molecular imprints, as in the case of duplicating of crystals and clathrates. More research studies are required in this matter.”

 “As of now, there are no ample scientific data available, helpful to explain the admissibility of homeopathic medicines being potentized above 30C. May be that, even after the removal of all drug molecules from the medium, copies of existing molecular imprints are serially generated in higher and higher potencies, thereby saturating the medium with more and more molecular imprints. Until that could be proved, I would suggest 23-30c as the most appropriate homeopathic potency for therapeutic purpose.”

 “If it is finally accepted that molecular imprinting is the real mechanism of potentization,  we may reach a consensus that there is no likelihood of any special benefit by higher and higher potentisations above 23C. Logically, potentization need be continued only just beyond the limit of Avagadro number. By that stage the molecular imprinted water–alcohol mixture will have  attained sufficient medicinal properties, to be used on the basis of ‘similia similibus curentur’. The three-dimensional structure of drug molecules used as ‘guests’ will have already got sufficiently imprinted into the hydration shells or hydrosomes by that time. I find no point in continuing potentization even after that stage.”

 “As per my observation, the medicinal property of any homeopathic drug beyond 23c will be the same. It is only a very rare possibility that there could be any significant difference between various higher potencies used by us,  with regard to their content or medicinal qualities.  Many master prescribers  have already put on record that if the selection of similimum is correct,  any potency would render the expected therapeutic result.”

 “More over, instead of the existing primitive method of potentization in homeopathy, modern science and nano-technology may definitely develop a more perfect and scientific way of molecular imprinted drug designing in water. Homeopaths should whole heartedly welcome such a positive development when it happens. Until such a perfect scientific technology of molecular imprinting  in water evolves, the existing system of homeopathic potentization is bound to prevail with all its limitations.’

 “We should remember that low potency and high potency medicines contain different class of active principles, and hence, their mode of actions are also entirely different.”

 “In my opinion, the phenomenon of ‘hormesis’ could have been better explained on the basis of ‘hydrosomes’ or ‘molecular imprints’ of drug molecules, which are likely to be formed in the highly diluted solution of a toxic substance.”

 “Obviously, molecular tracking employed in modern medical research protocols are not at all applicable in the study of transportation and targeting of potentized drugs inside the organism, since there is no single drug molecule present in our medicinal preparations. As for now, there is no scientific technology available to help us track the ‘molecular imprints’ inside the organism. Until such a sophisticated technology is evolved, rational analysis and logical deductions based on available scientific information alone are possible in this respect.”

 “Some homeopathic theoreticians argue that potentezed medicines act through nervous system, being transported through nervous system as nerve impulses, and the mind and “vital force” in turn induces the curative process. The fact that we can demonstrate the medicinal properties of potentized drugs through ‘in vitro’ experiments, such as clotting of blood, or antibody-antigen interactions, where nervous system or ‘vital force’ is not present, clearly negates this theory of drug action.”

 “Potentized homeopathic medicine, when introduced into the organism by any route, is carried by the body fluids, and transported to different parts of body by internal transport system. When the nanocavities of ‘molecular imprints’ contained these preparations come in the vicinity of active groups of pathological foreign molecules, having similarity to the original ‘guest’ molecules used for imprinting, these ‘molecular imprints’ selectively bind to the pathological molecules due to configurational affinity. By this process, pathological foreign molecules are prevented from binding to biological molecules, thereby relieving the biological molecules from pathological molecular blocks. This can be concieved as some sort of ‘molecular scavenging’ or ‘entrapping’ of pathological molecules, by ‘hydrosomes’ or molecular imprints contained in the potentized medicines.”

 “The concept of ‘similimum’ can now be investigated here with a new scientific perspective. We have seen during our earlier discussions, how the individual constituent molecules of a drug substance introduced into the organism during drug proving creates molecular blocks, leading to inhibitions of certain bio-chemic pathways, expressed by a specific train of subjective and objective symptoms. These symptoms are called ‘drug symptoms’, and compiled in the materia medica of that particular drug substance. When similar train of symptoms appears in an organism during a disease condition, it means that, the pathological foreign molecules responsible for the disease has been attacking same biological molecules, causing similar molecular blocks and bio-chemic inhibitions, expressing similar subjective and objective symptoms. The fact that both drug molecules and pathologic molecules could attack same biological molecules in an identical way, shows that the drug molecules and pathologic molecules were having some factors(chemical groups) with similar spacial configurations. Due to such a configurational similarity to the pathological molecules, the ‘molecular imprints’ of drug molecules contained in the potentized preparations will be having a counteractive configurational affinity towards the pathologic molecules. Due to the configurational affinity, these molecular imprints or ‘hydrosomes’ can selectively bind to the active groups of pathologic molecules, when coming in their vicinity. This is the exact molecular kinetics of homeopathic therapeutics, underlying the fundamental principle of ‘similia similibus curentur’.”

  “When we apply a highly potentized homeopathic drug as a therapeutic agent on the basis of similarity of symptoms, we are actually using the ‘molecular imprints’ or ‘hydrosomes’ of individual constituent drug molecules, having complementary configurational affinity towards the pathologic molecules, so that they can bind and inactivate the pathological molecules by capping their active groups.”

 “We should also be aware of the difference between crude drugs and low potencies or triturations. Even though both preparations contain same drug molecules, their therapeutic properties are found to be different. In crude form, drug molecules are packed tightly, with their chemical bonds remaining saturated by  interacting with various other molecules or ions. Hence, they are not at all free to exhibit all their individual interactive potentials. Whereas in triturations and low potencies, the drug molecules are free or ionized, they can exhibit all their properties. Hence, pathologic and therapeutic capability of triturations and low potencies are much higher to crude forms of same drug. We already know that various drugs which appear  comparatively inert in their crude forms become very potent medicinal agents in triturated forms. Differences between crude Siliciea and Silice 3x, crude Lyco and Lyco 3x etc. are examples for this phenomenon.”