‘Alpha Molecular Imprints’- Issue Of Potencies Finally Resolved

Once similimum is selected for a case through a process of exhaustive case taking, repertorization and material medica study, the next issue that bothers a young homeopath the most is the selection of potency, dosage and repetitions. A lot of confusions, controversies and phobias exist regarding the selection of potencies. Each homeopath has his own ways, and believes that only he is right. Young homeopaths get confused due to totally contradicting advices they get from their different teachers.

I am trying to resolve the issue of potencies in the light of scientifically viable working hypothesis regarding homeopathic therapeutics and potentization.

The word ‘drug potency’ and ‘drug potentization’ is associated with the concept of ‘dynamic drug energy’. As per this view, every drug substance has its ‘inherent qualities’, which exist as specific ‘energy’ of dynamic in form, and act up on the ‘vital force’ of organism by a dynamic way. This dynamic drug energy can exist free from ‘material drug, substance and transferred into rectified spirit or sugar of milk through a process called ‘potentization’. By this process, the ‘dynamic drug energy’ gettin freed from the drug substance moves to the potentizing medium and ‘energizes’ it. By the process of serial dilution and succussion, this dynamic energy could be ‘raised’ to new energy levels, and as such, it is believed that ‘higher’ dilutions are more ‘potentized’ and more powerful. This ‘dynamic drug energy’ carried by the ‘potentized drugs’ act upon the vital force and induces a ‘healing process’.

According to the MIT concept I propose, I am explaining the process involved in potentization in terms of ‘molecular imprinting’. It is not the ‘dynamic drug energy’ that is transferred into the medium during so-called process of potentization, but the three dimensional configuration of constituent drug molecules getting imprinted into the supra-molecular matrix of potentizing medium in the form of nanocavities, through a process of forming hydration shells. These nanocavities act as artificial binding sites or artificial ‘key holes’ for pathogenic molecules having configurational similarity to imprinted molecules. This concept scientifically explains the molecular dynamics of homeopathic therapeutics involved in ‘similia similibus curentur’ in a way fitting to the concepts of modern biochemistry, molecular pathology and therapeutics.

Obviously, the term ‘potentization’ reflects the vitalistic philosophy behind it. It would be ideal to use the term ‘molecular imprinting’ to explain the exact process in scientific terms.

Once you understand and accept ‘molecular imprinting’ as the real process involved in potentization, and perceive ‘potentized’ drugs in terms of constituent molecular imprints, all confusions regarding selection of potencies will be scientifically resolved.

My inquiry for a more reliable and perfect way of preparing molecular imprinted drugs have finally resulted in presenting a new method called ‘Alpha Molecular Imprints’.

ALPHA MOLECULAR IMPRINTS will provide a most perfect method of preparing molecular imprints of drug substances, on the basis of MIT concepts

It is prepared by adding mother tincture of drug substance to equal quantity of rectified spirit, and serially diluting it in 1:1 ratio up to 80 steps, so as to cross the avogadro limit. During each step, 300 succussions are given at a rate of 1 succussion per second (5 minutes). During each step,the solution is given 10 minutes rest at a temperature of 5-10 celsius before succussion. That means, each step takes 15 minutes. Solution gets total 24000 succussion during 80 dilution steps. During succussion, bottles should not be filled more than half, to enable free movement of contents while shaking. If you are using 50 ml bottle, use only 10ml drug and 10ml diluent. If 100ml bottle is used, you can add 20ml drug and 20ml diluent. Whole process will take 20 working hours to get the finished product.

By this process, drug molecules get maximum exposure and interaction with vehicle molecules, enabling perfect molecular imprinting of all individual constituent molecules. By 80th step, all drug molecules will be removed from the medium, and only the molecular imprints representing diverse types of constituent molecules remain. Molecular imprints will be more saturated, perfect and stable than those we get from conventional ways of potentization. If used as similimum, this preparation will be acting as most effective therapeutic agent.

Since we use 1:1 dilution ratio, this product may be called ALPHA MOLECULAR IMPRINTS, to differentiate from other potency scales. May be labelled as Nux Vomica α. A drug will have only a ‘single’ potency in this scheme. If we use ALPHA MOLECULAR IMPRINTS, all confusions associated with selection of potencies will be resolved once and for all.

Exactly, I am not trying to find a new potency. I am searching for ways to get molecular imprinting done more perfectly and accurately, on the basis of MIT concepts. Better to say, I am trying to find a way of molecular imprinting, more perfect and scientific than ‘potentization’.

I am not introducing a new ‘potency scale’. In ALPHA MOLECULAR IMPRINTING, there is only one end product, not a series of potencies.

In ALPHA method, the procedure is stopped once avogadro limit is crossed. By that time, all constituent molecules will be removed, after imprinting into the medium as supramolecular clusters. We do not subscribe to the idea of ‘potency increasing’ by going to higher dilutions, which is an idea related with ‘dynamic energy’ concept.

In decimal scale of potentization, avogadro limit is crossed at 23x. In centecimal scale it happens by 12c. In ALPHA method I propose, avogadro limit is crossed by 80th step of dilution, which gives maximum exposure of drug molecules, enabling them to interact with imprinting medium very long time. Dilution is done through 80 steps, subjecting them to 24000 succussions by that time. That ensures a much higher perfection and accuracy of of molecular imprinting.

According to my view of potentization as a process of molecular imprinting, I wanted to do it in a way most appropriate to happen molecular imprinting. According to this view, dilution has to be done up to avogadro limit only, same time giving maximum exposure of drug molecules to interact with vehicle. So I selected 1:1 ratio for dilution. As per calculations, dilution would cross avogadro limit by 80th dilution step. By that time, all drug molecules will be removed. Regarding succussions, I consider it a way to break hydration shells and make them free molecular imprints. I wanted to give alternate succussions and resting period to allow formation of new hydration shells and then break them open. So i decided to give a 10 minute rest after each dilution, followed by 5 minutes succussion. When succussion was done by hand, I could do it at a rate of 1 per second. Hence, 300 succussions could be dobne by 5 minutes. Actually, it would be better if we give maximimu number of succussions during each dilution steps. I decided 5 minutes succussion from a practical point of view. In this way, we can prepare a molecular imprinted drug by 20 working hours

1:1 is the most appropriate ratio we can practically do. Maximum dilution steps within avogadro limit-that was my objective

If dilution does not cross avogadro limit, the product will contain ‘drug molecules’ also, which would act on biological molecules. I want only ‘molecular imprints’ only, which act on pathogenic molecules only. Drug molecules act exactly similar to allopathic drug action. That is why I insist to cross avogadro limit.

If we continue diluting even after crossing avogadro limit, there will be no drug molecules in them for ‘imprinting’. Just crossing avogadro limit, the product will be saturated with molecular imprints, same time without any crude drug molecules. That will be the ideal product to be used as per similia similibus curentur

Since we stop potentization at 80th step, we can do it by hand itself. If we can use a machine acting exactly similar to our hands in actions, there will not be any harm

Number of succussions, intermediary rest period and number of dilutions are all very important. They should be maximum as possible, but all should be limited below avogadro limit. There is no meaning in diluting and succussing after all molecules are removed. Because, according to me, molecular imprinting is what we want to happen

Shaking helps in mixing the drug molecules with vehicle well. Rest period facilitates formation of hydration shells around drug molecules. By keeping in low temperatures above freezing point, movements of molecules are restricted, which help in formation of hydrogen bonded shells. Succussions facilitates breaking of hydration shells and freeing of drug molecules. Serial dilutions facilitates systematic removal of drug molecules. Hence, I think all three steps are very important in effective molecular imprinting. I limited succussions to 300 per step out of practical considerations. There is no harm if you do it a bit longer. But everything should be limited below avogadro limit

I would request all my scientific-minded friends to make ALPHA MOLECULAR IMPRINTS of one or two drugs commonly used, and verify their effectiveness. I hope, this may lead to a great revolution in homeopathy. Be a part of history by participating this experiment.


To start working, we should first decide the drug we intend to work up on. Before making this decision, discuss with the group and ensure other members are not doing it, so as to avoid duplication of work.

Procure a good sample of mother tincture of selected drug from a most reliable source. Only sealed bottles should be purchased. 30ml is enough.

Collect 10 high quality amber colored glass bottles of 100 ml capacity. Emplty bottles of german potentized drugs can be used, after rinsing and washing for long time in hot water, and drying well in sunlight. Well graduated stickers should be then affixed on the bottles. Keep them well corked in a dust free place.

Procure 4 pounds of high quality rectified spirit from trusted pharmacy.

Arrange a clean, dust and moisture free room. and work table.

Now we can start work:

Add 20ml mother tincture into one 100ml bottle. Then add 20ml rectified spirit into the bottle. Since bottles are graduated, no measuring utensils are required.

Cork the bottle well, Label the bottle as ALPHA 1,shake for 2-3 minutes. Keep the bottle still for 10 minutes. It will be good it it is kept at 5-10 celsius, in the lower part of refrigerator.

Then take the bottle out, and start succussing using hand using right hand, and hitting the bottle on left palm strongly, with right elbow fully abducted and making anti-clockwise motions. A rubber padding on right palm will be useful. One succussion per second (approximate), do it for 5 minutes without stopping(300 succussions approximate).

Stop succussing and immediately pour away 20 ml from the bottle.

(You can discard it or keep it for later use, in a seperate bottle labeling the dilution step on the bottle)

Add 20ml rectified spirit into the original bottle, cork well, label as ALPHA 2, shake well for 2-3 minutes and keep 10 minutes at 5-10 celsius. Then take the bottle out and give 300 succussions (5 minutes). Immediately pour away 20ml from the bottle, add 20ml rectified spirit to the bottle, cork it, label ALPHA 3, shake for 2-3 minutes, rest for 10 minutes, give 300 succussions, immediately pour away 20 ml.

Repeat this process continuously up to 80 steps of dilution and succussion. Final product is now ready. Affix the label a s ‘DRUG NAME.ALPHA’, and keep for use.

Be careful to save the discarded portion of final 10 or 20 steps, labeling well in separate bottles, for future use as back potencies below avogadro limit

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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