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Dr. Babizhayev Interview 2003

Q: Dr. Babizhayev, why does Can-C work so much better than the less expensive NAC eye drops on the internet?

news06A. Please allow me to address this question. Interestingly during our research we found that the antioxidant activities of the released carnosine molecule were dependent upon a highly specific purity factor of the raw material itself or rather, the precise content of the transition metal ion traces. There were vast differences in the cataract reversal results achieved in the trials due to the varying levels of ionic trace mineral levels within the n-acetylcarnosine raw material. This patent protected refinement of our specific grade of N-acetylcarnosine, with the Japanese, is what ultimately resulted in the anti-cataract successes achieved in our clinical trials. It is only this proprietary form and grade of N-acetylcarnosine raw material that will ever be used in Can-C. Equally significant is the extended “half life” of this particular formulation which greatly increases the anti-cataract activity. I am most concerned that when consumers purchase the random n-acetylcarnosine eye drop formulations available in the market place that their poor results will reflect on my research.. Amazingly these companies often reference my research in their marketing efforts even though they have no affiliation with me and are definitely not offering my proprietary N-acetylcarnosine (Can-C™) formulation which the research was based upon. Additionally there is the real disappointment for the individuals who have unknowingly purchased one of these inferior formulations, who were seeking to improve the health of their eyes and who have been given hope as a result of our research. Fortunately there is a simple way for consumers to verify if they have purchased our clinically proven formula as we have placed a hologram on the front of our box to protect against these copy cats.


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February 2003 – 
Pharmacist Phil Micans interviews Dr. Babizhayev further, about the precise role of 1% N-acetylcarnosine in the treatment and prevention of Ocular Disease  
 

Q:  “Dr. Babizhayev, thank you very much for joining me here today, to discuss your important breakthrough of an eye-drop to treat, and possibly to prevent senile cataract. I know by the response that the readers of the IAS Anti-Aging Bulletin enjoyed our previous discussion.”     

A:  “It’s a pleasure to be here in Paris with you Phil.                      

Q:  “As you know, we have already covered a lot in our previous article and interview, (Ed.- IAS Anti-Aging Bulletin, Winter 2001), about the development of N-acetylcarnosine and its role in combating the common aging-disease of senile cataract. We were made very aware in those, that there are significant differences between L-carnosine and n-acetylcarnosine, and we warned everyone then that they shouldn’t use L-carnosine for eye-use. But tell us, are there any differences  in N-acetylcarnosine itself?”

A: We have developed a very precise product with N-acetylcarnosine, both from the point of view of purification, and its content of transition metal ions traces.  This is because, rather uniquely, only certain types and levels of impurities enable the maintenance of the peculiar antioxidant activities of the released molecule, including those scavenging the hydroxyl-radical, singlet oxygen, lipid peroxidase-like and ferroxidase-like activities. This very particular active product is responsible for the anti-cataract efficacy, and for the protection of the lens proteins from the singlet oxygen-induced oxidation of the lens protein, specifically the amino acid tryptophan residues, which have been measured using chemiluminescenece technique and L-Gly-Tryptophan peptide. Some details of this  were published in one of our papers. (Ed.- see reference 1 below).

Q:  “So, when you were experimenting with different N-acetylcarnosines, was there a difference in their efficacy, or side effects?

A: “Oh yes, sure! With either too much or too little metals, side-effects were caused, or we saw less efficacy. The manifested lipid hydroperoxides scavenging,and the ferroxidase activities of the final released product in the eye are all very important.”

Q: “Thus, I imagine, you must have decided upon a specific N-acetylcarnosine with a narrow range of purity, that was, in terms of its impurities, not-too-much, not-too-little. Is that form commonly available?

A: “No, that form is not commonly available, and the information is kept proprietary. The specific grade of N-acetylcarnosine raw material used in Can-C™ is manufactured by our Japanese partner under a cGMP specific know-how process. Therefore, this material is currently only available from one source.

Q: “So how can people tell if they are using the correct material in their purchased eye-drop product?”

A: “We have provided a hologram on the front of the packaging to assure consumers that they have purchased the correct formula and to prevent copycats.

Q: “Now we understand the importance of the type of N-acetylcarnosine and its purity factor, what could happen if one were to try to change the formula by adding additional ingredients?                

A: (Innovative Vision Products (IVP) has conducted serious pharmacokinetic studies utilizing precise chromatographic techniques of analysis, and using the final formulated patented product and other various possible formulations. The ratio of NAC concentrations upon the topical application of to the eye, is equal to 9 in the aqueous humor. This means that virtually all N-acetylcarnosine (Can-C™)is converted to the more powerful antioxidant L-carnosine in the aqueous humor. This can then enter the lens tissue and epithelial cells and act as the anti-cataract remedy.

The de-acetylation of N-acetylcarnosine by N-acetylesterases and N-acetyltransferases, at the level of the cornea and the conjunctiva, can be inhibited with the addition of other substances to the ophthalmic formulation, substances such as vitamin E and vitamin A. This is because they are endowed with a branched hydrophobic hydrocarbon skeleton. Such formulas, which do not originate from the validated source of 1% N-acetylcarnosine, when applied, can be readily hydrolyzed at the peptide bond site and then allergenic histamine is released because of the peptide hydrolysis with acid hydrolases in the tear fluid.

N-acetylcarnosine is a delicate molecule. The biotransformation of N-acetylcarnosine into L-carnosine in unsolicited external topical formulations can be promptly inhibited. Active L-carnosine can not be detected in the aqueous humor after the topical installation of hydrophobic vitamin-loaded remedies after 15 minutes, at any significant doses. It is not apparent that when chemicals are mixed together, chemicals which, by themselves may have efficacy, that the sum is greater than the single parts. These chemicals interact with one another, and in the eye, these additional interactions could cause side effects or lose the efficacy of the original product.”

Q: “As I understand it, now we know that the amount of transformation of N-acetylcarnosine into L-carnosine, and the length of life/ activity of that L-carnosine in the aqueous humor are all essential elements in the efficacy of N-acetylcarnosine eye-drops. I therefore suspect that you must be concerned about copy-cat products that claim your research, but actually contain inferior N-acetylcarnosine and formulas that have little value?”

A: “Yes, I fear that such inferior products will mar the research and maybe people will think that all N-acetylcarnosine is the same. However, we are addressing this issue, and in those countries where such products are currently being used, our patents there will be in force later this year and we shall pursue them.”

Q: “I guess it’s actually part of that old adage, when we say, the devil is in the detail.”

A: “Indeed it is Phil.”

Q: “I appreciate that it is still early days, but do you feel, or do you have any scientific reasoning, if N-acetylcarnosine (Can-C™) will
be useful in other eye-disorders?”

A:  “Yes, we believe that our ocular release N-acetylcarnosine will have a  role for glaucoma, especially when combined with some other substances that we are currently working on. In particular, we know that N-acetylcarnosine is  efficacious for its anti-glare effect and improvement for color vision. So, for example, we envisage that this could lead to safer driving, especially night  driving.

Another  interesting, recent development is the fact that we have shown Can-C™  to prevent and reverse the acidosis in the corneal stroma due to the actions of accumulated lactic acid. This means that individuals can wear contact lenses, particularly soft contact lenses, which are not gas permeable, for longer and with more comfort.”

Q: “Have you enjoyed yourself here in Paris? I mean, professionally of course! What kind of response are you getting to your trials that show your N-acetylcarnosine  (Can-C™) to be highly efficacious in the prevention and treatment of senile cataract?”

A: “Yes, the response wherever I go is very favorable and I think that eventually the word about this breakthrough is going to spread worldwide. We are close to some arrangements that would probably mean the general media would know and report about this, when that happens I expect much will change quickly.”

Q: “I’m sure there will continue to be some resistance to this breakthrough, after-all, it always takes some time to accept new ideas, and especially for the mainstream media to start reporting on it. But then, that’s why people read the IAS Anti-Aging Bulletin, to be ahead of the crowd, and keep up-to-date on the cutting-edge.”

A:  “Yes, I believe it is a most worthy enterprise.”

Q: “Dr. Babizhayev, Thank you for your time with us here today and enjoy the  rest of your stay in Paris.

A:  “Thank you Phil, I will.”    

References:

  1. Babizhayev
    MA, Lozovskaya EL, Makareyeva EN, Lulkin YA, Sapezhinskii II, “Photoprotector
    and antioxidant properties of histamine containing peptidomimetics
    in the photooxidation of glycyltryptophan.”
    Biochemistry
    (Moscow), 1998 May;63(5):523-8.

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