Mr.X said:
Oral IGF is just bull, it's not bioavailable orally - yes, there are petri dishishes for everything, but I wont believe that it will be orally effective...probably the same as "oral GH spray" LOL
Nothing against the poster or the company, I just don't like to feed members bullshit
no bullshit is being feed here from me bro
and you are missing the point here bro...this form of igf doesnt even reach the stomach
heres some info:
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Introduction
********* has been working in partnership with a research and development company that focuses on the most effective formulations for drug delivery and drug delivery discovery. They would like to focus primarily on Pharmaceutical drugs and delivery technologies and have chosen not to currently focus on the expansion of manufacturing dietary supplements except for the few they are currently developing such as our Oral IGF-1-LR3, Anatropin. They develop new technologies to deliver drugs more effectively, conveniently, safely and with fewer side effects. This company works solely with pharmaceutical development with exception to *********. This allows them focus on our company’s needs, such as, future product development and bulk production as well as their pharmaceutical direction without distraction. Out of respect for their privacy the company name will not be disclosed.
It is customary for companies during preliminary study release of products, to use discretion for the sources revealed and the extent of formulation, pharmacological, and composition data openly published. We are using every caution to protect from false duplication and/or right infringement while we initiate open marketing of such a valuable product.
What is Anatropin
AnaTropin™ is a patent pending composition that delivers IGF-1-LR3, including other similar large peptides, to the blood. Signaling occurs from specific Insulin and Insulin-Like Growth Factor (IGF-1) receptors that regulate and transcribe the message allowing for site-specific receptor binding. Anatropin utilizes oral absorption to deliver into the portal blood allowing a sustained, pulsatile delivery resulting in a better utilization and potentially safer form of IGF administration in comparison to injection.
Pre clinical trials show that this particular form of oral absorption of Human Recombinant Insulin delivers the insulin, orally, for greater than 24 hours as well as absorbing orally at a rate of greater than 61%. Because of this pusatile motion and slow absorption into the blood, IGF can have a longer half-life per dose. The rate Anatropin mediates through the cell replicates the natural IGF secretion. This is also true with the Insulin study relative to the rate of natural, pancreatic secretion of Insulin from beta cells. This allows Anatropin to deliver at a constant equilibrium and sustained longer half-life.
Also, Anatropin will not be overdosed in the blood because it will effectively replicate natural cell mediation and the rate of diffusion into the blood will not “spike” blood plasma IGF levels where IGF is active (IGF is only active in circulatory blood).
Ground-Breaking Technology
******** utilizes a technology that is clinically proven to mimic injection yielding high bioavailability and non-degradation of the IGF-1-LR3. Current clinical trials have shown this technology to achieve near 100% bioavailability of Insulin through oral absorption. Studies show that greater than 61% Insulin is absorbed in blood plasma utilizing this technology. Currently, this Oral Insulin is beginning Phase 3 Clinical Trials.
Oral Bioavailability Study on Insulin
Our partner has completed several bioavailability studies for its Insulin drug. An independent 3rd Party Laboratory with over 30 years of clinical, toxicological and pharmacological experience has performed all studies referenced in this release. The pharmacologists’ involved have experience with such companies as; Bristol Meyer, Squibb and Dupont. We are having relevant studies conducted on Anatropin.
Their studies have revealed a minimum of 61% absorption in a 24 hour to 48 hour time period and are reported to achieve near 100% bioavailability upon further study. Currently this Insulin is undergoing a diseased study (Diabetes Induced Study) that will determine higher bioavailability in 48 hours.
Why is insulin relevant?
Insulin and IGF (Insulin-Like Growth Factor) are almost identical and IGF and Insulin share the same binding receptors. The problem with IGF is that it has only a half-life in the blood for 15-20 minutes and is not biologically active in oral administration. IGF has poor to no absorption orally. IGF is very similar, almost identical to Human Recombinant Insulin. The pre-clinical studies (which we offer for your review) can be directly correlated between the Insulin and IGF with a minimum 61% oral absorption in the blood with 24-48 hour sustainability. They have similar amino acid sequence and pharmacology.
IGF also mimics insulin in the human body. It makes muscles more sensitive to the effects of insulin, therefore allowing a person currently using insulin to effectively lower their dosages and still achieve the same response as well as the ability of IGF to keep the insulin from increasing fat.
Because of the recent pro-hormone/steroid ban, there is a need for a muscle-building supplement that is as good as 4-AD, 1-AD and 1-Testosterone. IGF at 61% absorption and 24-48 hour sustainability orally, will be better than any pro-hormone/steroid and even will be better than IGF injection because the sustainability is much longer. This remarkable technology is protected with an internationally filed patent to ensure protection against possible infringement from competitors.
Oral vs. Injectible
Current methods of delivery rely on injection to maximize dosage and to ensure no degradation of the compound occurs. Current injections of IGF can only bind a quantitative amount of IGF dependent on the receptor availability and half-life of the IGF per injected dose. Because a needle penetrating the cell surface bypasses cell-mediated endocytosis, there’s no natural cell diffusion to control the IGF’s absorption into portal blood.
Currently, the only effective forms of IGF injections include IGF-1-LR3 Media and Receptor grades. As a matter of fact, there have been recent findings proving that unregulated levels of IGF in the bloodstream can put an individual at risk of dysphasia and stomach enlargement due to IGF overdose. The Anatropin formulation eliminates this risk with its unique and precise systematic release of IGF-1-LR3 into the bloodstream during the 24-48 hour time frame of absorption. When blood levels reach a point of saturation of IGF-1-LR3 administration stops and resumes when levels reach safer concentrations.
In layman’s terms, injection administration results in an unregulated release of IGF-1-LR3 into the bloodstream, which leaves a higher risk of resultant dysphasia and stomach enlargement causing significant safety concerns. Anatropin safely administers IGF-1-LR3 into the bloodstream throughout a 24-48 hour time frame. With better utilization, Anatropin proves to be more effective and holds a significantly less chance of overdose in the blood. This fact along with completely eliminating the painful daily injections required are only a few of the advantages Anatropin holds over current IGF injections.
Benefits of IGF-1-LR3 Supplementation
Long R3 IGF-1 is an amino acid analog of IGF-1. This analog of IGF-1-LR3 has been produced with the purpose of increasing the biological activity of the IGF peptide and remains as the only feasibly effective injectable form of IGF available on the market. Long R3 IGF-1 is significantly more potent than IGF-1 and its enhanced potency is result of the decreased binding of IGF-1-LR3 to all known IGF binding proteins. These binding proteins normally inhibit the biological actions of IGF.
In early human developmental phases, IGF is responsible for the natural muscle growth that occurs. There are many functionalities of IGF in the human body including increased amino acid transport to cells, increased glucose transport, increased protein synthesis, decreased protein degradation and increased RNA synthesis. Active IGF responds differently in different types of tissues. For example, muscle cell proteins and associated cell components are effectively stimulated. Protein synthesis is increased along with amino acid absorption. Acting as a source of energy, IGF will mobilize fat for use as energy in adipose tissue. In response within lean tissue, IGF will prevent insulin from transporting glucose across cell membranes. The result of this activity will be a switch within the cells to burning fat as a source of energy.
One of the most remarkable effects of IGF supplementation is its ability to cause hyperplasia, which is the actual splitting of cells. Hypertrophy is the result of weight training, which is the increase of the size of a muscle cell, but hyperplasia signifies actual muscle cell replication. In adulthood, we reach a plateau in muscle cell count. Weight training will effectively increase the size of these pre-existing cells but still will have its limitations in effective muscle gain. IGF supplementation will actually increase the number of muscle cells present in the tissue and throughout muscle training will create the added benefit of larger, increased muscle cell counts. So in a way you are able to manipulate your genetic capabilities in relation to muscle tissue and cell generation. IGF will uniquely define the number of various types of cells present in the body. At a genetic level it has the potential to alter your capacity to build superior muscle density and design.
Although we have concentrated our focus on muscle cell development benefits, there are many more cell growth and regeneration benefits IGF has to offer including vital organ repair and growth, immune system strengthening, anti-aging benefits, fat cell decrease and overall body repair with a new found vitality.
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