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N-Acetyl
Carnosine eyedrops
an
interview with Mark Babizhayev Ph.D.
Dr. Mark Babizhayev is one
of the principal Russian researchers behind the development and use of
N-Acetyl Carnosine or NAC eye-drops, which are being heralded as a
breakthrough in the treatment and prevention of senile cataract. In
this interview, Dr. Babizhayev discusses with Phil from International
Anti-Aging Systems (IAS) some of the results of his research.
Phil:
“Dr. Babizhayev thank you for being kind enough to undertake this
interview for the IAS Anti-Aging Bulletin.
Dr.
Babizhayev: “You’re welcome.”
Phil:
“Perhaps I could start by asking you to please tell our readers how
many years you have been involved in the research with N-Acetyl
Carnosine (NAC)?.
Dr.
Babizhayev: “We
started our work on N-Acetyl Carnosine as a potent ophthalmic
drug in 1991, after we concluded the contract relations with the
executives Dr. Edoardo Bozzo Costa and Mr. Ovidio Caveri
of Bruschettini S.r.l., Genoa, Italy.”
Phil:
“In all that time, when did you first realize that NAC was something
special for the treatment of cataract?”
Dr.
Babizhayev: “We
initially realized that NAC was promising for the treatment of human
cataracts when the first pharmacokinetic studies were completed. They
showed that NAC can act in-vivo as a pro-drug of L-carnosine in
ophthalmic application, as an antioxidant.” [Ed.- Clin. Chim. Acta
1996, 254, 1-21].
Phil:
“Presumably, your first experiments were undertaken with
animals? Would you like to elaborate on some of the results you
obtained?”
Dr.
Babizhayev: “The NAC anti-cataract eye drops have been carefully
tested in animals. We have processed the treatment of age-related
cataracts in canines and experimental models of cataract in rabbits.
The most striking results have been obtained using a 1% NAC
instillation in canines with age-related cataracts. We have determined
the efficacy of cataract treatment, and we have revealed a new
phenomenon of melting snow upon the instillation of NAC, for
the chronic treatment of cataract within only 1-month.
The cortical appearance of cataract reversal starts from the
periphery and then the lens becomes more transparent. This is then
accompanied by the improved visual behavior of the animal. Rigorous
computerized image analysis have been supplied to support the evidence
of the cataract treatment in rabbits. The striking results of reversing cataract and the
prevention of the lens opacities are clear, and have been
revealed in traumatic and liposome-induced types of modeling
cataract.”
Phil:
“Later of course, you were also involved with NAC eye-drops in
human trials, what kind of results did you get there?”
Dr.
Babizhayev: “First we developed sensitive measurements for the
lens opacities in humans. These were original techniques of glare
tests they are very sensitive to even tiny changes
of the lens opacities and we also tested the macular function, which
is the vision behind the cataract. We have also utilized
stereocinematographic slit-image and retro-illumination
photography, with subsequent interactive digital image analysis and 3D
computer graphics for the lens light scattering, or absorption.
The
intra-reader reproducibility of the measuring techniques for
cataractous changes were good. One group of patients were the control
reference group, they demonstrated the variability in densitometric
readings of lens clouding and they had negative advance in glare
sensitivity at 6 months, and a gradual deterioration of visual acuity
and gross transmissivity of lenses at 24 months, these results
were compared at baseline and 6-month follow-up examinations. However,
when compared with baseline examination at 6 months, 41.5% of the eyes
treated with NAC eye drops presented a significant improvement in
visual acuity of 7-100% and 88.9% of the eyes ranged a 27-100%
improvement in glare sensitivity.
Topographic study demonstrated less
density and corresponding areas of opacification in posterior subcapsular
and cortical morphological regions of the lens. That is
consistent with visual acuity up to 0.3. The total study period was
over 24 months and it revealed that the beneficial effect of NAC is sustainable.
Image analytical readings of lenses indicated that no cases resulted
in a worsening of visual acuity for the NAC-treated group of patients,
and in most of the patients drug tolerance was good.
Statistical
analysis revealed significant differences between 6 and 24 months as
an overall cumulative and positive change of the characteristics of
cataracts in the NAC-treated group, when compared to the control
group. The synthesized N-acetylated carnosine eye drops are therefore proposed as
an effective and physiologically acceptable drug for non-surgical
treatment of age-related and senile cataracts.”
Phil:
“Were there any side-effects noted in the human trials?”
Dr.
Babizhayev: “For most of the patients treated, drug tolerance
was good and no side effects were specifically associated with the
application of 1% NAC. What is more, no recurrence of cataract development occurred during the
period of NAC application.”
Phil:
“Have you drawn any conclusions on why NAC is able to treat
cataract so successfully? Is NAC breaking existing cross-links of
proteins as well as inhibiting them? Or are there other forces at work
here too?”
Dr.
Babizhayev: “The therapeutical indication for NAC to treat
senile cataract can lead to diminishing of light-scattering units in
the lens, probably by prevention of the oxidative modification of crystallins
and utilization of lipid peroxides, that promote lens opacities.
Most known biological antioxidants that can prevent oxidative damage
to biological molecules show some specificity in their mechanism of
action, and so they can provide only one type of protection. N-Acetyl Carnosine and its bioactivated analog L-carnosine may exert
their antioxidant properties by removing high reactive peroxide
compounds from the lipid phase of the lens, i.e. the fiber cellular
membranes.
We assume the advantage of NAC is as a universal
antioxidant, which relates to its ability to give efficient protection
against lipid peroxidation, both in the lipid phase of biological
membranes and in the aqueous environment. We maintain the hypothesis
that NAC assists the proprietary lens antioxidant systems including
glutathione, and the enzymatic antioxidant systems of the lens, to
provide their operation most effectively. Glutathione in conjunction
with glutathione-related systems, like glutathione reductase, can
partially reduce the S-S bonds in the cross-linked lens proteins.
Besides, we agree that NAC can prevent and reverse the cross-linking
of the lens proteins, including crystallins induced by lipid hydroperoxides
and their secondary breakdown molecular products, like aldehydes. This
mechanism can be prominent to reverse and prevent lens opacification
that is related to the glycation reactions of the lens proteins, and
as you know they are also associated with complications of
diabetes.”
Phil:
“To-date what is the longest period that anyone has been continuing
to receive NAC eye-drops?”
Dr.
Babizhayev: “Usually, we only provide well-controlled randomized
trials. Accordingly, we have no personal experience of clinical
evaluations lasting more than 2 years of therapy. We have always
avoided any substance materials that have originated from uncertain
sources, so recently we developed the precise cGMP manufacturing
process for NAC.”
Phil:
“So are the benefits of NAC eye-drops being preserved in these
long-term patient trials?”
Dr.
Babizhayev: “Again, the total study period over 24 months
revealed that the beneficial effect of NAC is sustainable.”
Phil:
“I appreciate that your work has focused on the treatment of
patients with cataract, but do you envisage that NAC may also have a
role to help prevent cataract?”
Dr.
Babizhayev: “Oh yes! We usually pursue the following
therapeutical strategy for the treatment of human cataracts with NAC.
Firstly, we expect to obtain the maximal effect of improvement of
visual acuity within the first 3-5 months of therapy, then the
clinical strategy is to maintain the received visual outcome for a
lasting period. In this connection, NAC
does indeed help to prevent human cataracts.”
Phil:
“It has also been documented that
L-carnosine, the sister to NAC, is able to help prevent
cross-linking from occurring, yet you do not advocate
L-carnosine as an eye-drop. Could you please explain to our readers
why not?”
Dr.
Babizhayev: “Topical administration of pure L-carnosine to the
eye does not lead to accumulation of this compound in the
aqueous humor within a reasonable amount of time, or in a
concentration exceeding that of the placebo-treated eye. Exogenous
L-carnosine entering the organism topically to the eye, intravenously,
intraperitoneally, or with food is not accumulated by the
tissues, but is excreted or destroyed by carnosinase, a dipeptidase
enzyme that is present in blood plasma and in the aqueous humor of the
anterior chamber of the eye.
With a topical eye application,
L-carnosine releases the toxic compound, histamine, which can
severely promote oxidation reactions.
Compared to L-carnosine and due
to its relative hydrophobicity, NAC appears to penetrate
through the cornea gradually, thus maintaining a longer active
therapeutic concentration of L-carnosine in the aqueous humor and the
lens of the treated eye. Importantly, NAC is highly resistant to
hydrolysis by carnosinases. Different techniques of ocular
administration with NAC prove its efficacy for the treatment of
cataracts, combined with excellent tolerability to the eye, safety,
and the lack of possible side effects.”
Phil:
“Please allow me to recap. Your results indicate that
L-carnosine when used as an eye-drop could be dangerous. However, some
NAC breaks down into L-carnosine, but presumably NAC is not causing
any side effects because it only breaks down into L-carnosine at a
later stage; which is then not dangerous to the eye. Is that basically
correct?”
Dr.
Babizhayev: “Yes that is correct. Specifically, L-carnosine is
first hydrolyzed with carnosinase and histamine and is released
postponed from its histidine moiety via the activity of histidine
decarboxylases in tissues. As the aqueous humor of the eye is a flow
system, L-carnosine can be released from the NAC ophthalmic vehicle in
the eye and becomes active as an ophthalmic antioxidant. L-Carnosine
released in situ from its ophthalmic pro-drug NAC enters the lens,
which is not equipped with carnosinase activity and concurrently
L-carnosine is washed out with the aqueous humor flow, this then
allows the chronical application of NAC for the treatment of human
cataracts over years.”
Phil:
“I also understand that you have acquired the proprietary process of
producing a high-purity NAC for eye-drop use. Did you find that normal
production of NAC was in some way inferior?”
Dr.
Babizhayev: “Thank you for this important question. The
application of NAC for the treatment of cataracts has been protected
by the PCT patents by our group.”
[Ed.-
They are as follows: Babizhayev MA, Bozzo Costa E. Composizioni
farmaceutiche contenenti N-acetilcarnosina per il trattamento della
cataratta. Italian Patent A61K gruppo37/00 20122 MI, Priority
15.10.1993 and Babizhayev MA, Bozzo Costa, E. Pharmaceutical
compositions containing N-Acetyl Carnosine for the treatment of
cataract. Patent PCT/EP 94/03340 SCB 238 PCT, 10.10.1994].
“However,
we advise competitors not to rush forward. There are many carnosines
with little or abandoned biological activities. This strongly varies
with the content of transition metals in the peptide moiety,
admixtures of hydrazine and other impurities dependent to the type of
obtention and/or synthesis. We have developed the important cGMP
manufacturing process for NAC which demonstrates its extraordinary
biological anti-cataract activity in humans. We have provided the
chemical-functional correlation of the NAC properties and ensured the
clinical anti-cataract efficacy of the product for human lenses. But
if NAC is extremely pure this also abandons the antioxidant and
biological activities of the peptide product. Innovative Vision
Products, Inc., of Delaware, keeps secret their know how on
the processing and permanent biological and analytical controls, in
order to manufacture the effective anti-cataract NAC bulk material.
This technology has been envisaged by cooperation and extensive
studies with a Japanese manufacturing facility.”
Phil:
“This is obviously an important breakthrough in anti-aging
medicine and I can foresee numerous attempts to copy your innovation.
How can patients be sure that they are getting your particularly
pure NAC eye-drops when purchasing such material?”
Dr.
Babizhayev: “They should ensure that the label tells them that
the product was formulated by Innovative Vision Products [Ed.-
IVP]. If it does not state that, it isn’t our
high-purity NAC and will either be ineffective or possibly even
dangerous for eye-use.”
Phil:
“I congratulate you Dr. Babizhayev on your incredibly important
work. It certainly appears that NAC eye-drops are a major contribution
to the control and indeed the eradication of cataract, which by itself
is clearly an age-related disorder. Do you believe that NAC may be
useful for any other eye disorders?”
Dr.
Babizhayev: “We think that further attention should be directed
to ophthalmic application of NAC to treat cataract, ophthalmic
manifestations of diabetes, ocular inflammation, primary open-angle
glaucoma, and retinal disorders which involve the pathological
mechanisms associated with oxidative stress.
Phil:
“I think this is one of the most exciting anti-aging products to
emerge in recent years and I believe it is a clear example of anti-aging
medicine at its best. I wish you all success with this project and
your future projects.
Dr.
Babizhayev: “Thank you.”
Phil:
“Will you come back and tell the readers of the IAS Anti-Aging
Bulletin about any further developments and breakthroughs you
have?”
Dr.
Babizhayev: “Of course, my pleasure.”
1.
2nd interview with Dr.
Babizhayev
click
2.
additional eyedrop article
click
ALL INFORMATION IS EDUCATIONAL
AND PROVIDED UNDER IAS TERMS AND CONDITIONS AND SHOULD NOT
REPLACE THE ADVICE OF YOUR PHYSICIAN.
The above
article is copyrighted and may not be copied without the written permission of
International Antiaging Systems, Les Autelets Suite A, Sark GY9 0SF, Channel Islands, UK.
ingredients
Active ingredients Glycerin (lubricant) 1.0%
Hydroxypropylmethylcellulose (lubricant) 0.15%
Inactive Ingredients Sterile water (ophthalmic grade isotonic solution, pH 6.4 to
6.5); antioxidants N-Acetyl-Carnosine (NAC) 1.0%, buffered with boric acid,
citric acid, and
potassium bicarbonate and as a preservative, purified benzyl alcohol.
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