sytenhance systemic rate

  1. sytenhance systemic rate

    after searching and finding very little i wanted to ask those who have some info on this have we come to a consenses on if the stuff actually goes systemic or not? i know some say negligible ammounts do, but others say they still see side effects etc. i was wondering if anyone actually had work done or was able to conclusively and scientifically see if the stuff went to the blood stream. as we already know, if it doesnt go to blood stream then we technically may be able to use this for longer or as a bridge between cycles. also, the amount of 1test in it may be a little low, so how many grams might u suggest to add to each 4 ounce bottle?

  2. I've used the 1-test beta version, I think it has 6g in 4oz. I'm convinced a good amount gets into the bloodstream. I was taking m1t & 4ad at the time. After adding the sytenhance, the lethargy from the m1t greatly increased (from the 1-test going systemic). Sytenhance was all the rage about a year ago, you never hear about it anymore. I assume it never took off because it really doesnt only work locally. If it did, everybody would be bridging with it. I've never heard of anybody getting proper tests either. The ultimate test would be to use it unilaterally, like just 1 arm.

    I can see how an active compound lile 1t maybe could work locally. But how is 4ad going to convert to test in your muscle bellies? The conversion is done in the liver. Most sytenhance versions have 4ad in them.

    I have an old bottle left I plan to run with M4ohn in a few months. I should be able to notice the systemic 1-test effects better with that cycle.

  3. Unhappy

    good point bout the 4ad conversion. makes sense. i was just wondering the reason sytenhance never caught on, i guess because it didnt work as hoped. longdog, i dont mean to discredit ur info on this at all, but ive actually seen ur input in other threads about sytenhance. seems u may be 1 out of a slim handful that have tried it to bring light on the subject. anybody new with anymore info, positive or negative. or has nobody even tried to see its systemic rate due to its lack of potency, so to speak. great idea on paper, at least

  4. i've used it. Only applied to biceps and tricep, it was quite obvious it didn't stay localized, as i gained size all over, and gained a lot of water weight and was bloated all over. (i used the 1-test/4-ad version)

    I think the thing w/ the sytenhance is that at best LESS gets systemic released and more stays local, but to say it wont shut down natural test, or that it'll stay even 90% localized, is not a true statement.

  5. From Big Cat:


    The current wave of local delivery topicals is based on the work of Marcel Nimni (Nimni, 1989, Nimni et al, 1997 & 1998) who developed and patented the trans-phase delivery system in 1989. The local delivery of products was reviewed by Guy and Maibach in 1982, and clearly demonstrated a number of products substantially increased localized subcutaneous concentrations of topically applied products. The products that best succeeded in doing this were those that were amphiphillic, that means they are soluble in both water and organic solvents (alcohols and oils for example).

    Nimni's idea was simple : make the compound that needs to be delivered stable and amphiphillic and you can get substantial local delivery, with very minimal systemic delivery. This gives a predominantly localized effect, with minimum systemic (side-)effects. As research has previously demonstrated, benzyl alcohol can form micelles with organic ingredients, like most drugs used, in an aqueous environment. That means if you dissolve the products in benzyl alcohol you form an amphiphillic complex that can pass the skin and is taken up locally in the subcutaneous tissue to a great extent. Simply using benzyl alcohol and your product would already allow for local delivery, especially since benzyl is also a good penetrant of the skin due to its amphiphillic properties. But Nimni's system consisted of two phases. The second phase being a mixture of acetone and isopropanol. Both these solvents are very volatile and have both been shown to enhance skin permeation (Onken and Moyer, 1963). The idea is that the acetone and isopropanol make the skin more permeable and then evaporate, creating a sort of funneling effect that leaves the product entirely dissolved in the less volatile benzyl alcohol, which forms the amphiphillic micelles and carries the product across the skin. It transfers as it were, from one phase to another, and hence was dubbed the trans-phase delivery system by Nimni and his associates (Nimni et al, 1997).

    Here are some good tips for people wanting to try this :

    - All the ingredients, contrary to the current line of products using this technology are very cheap and very easy to get at any drugstore.

    - The current line of products does not use acetone, even though research shows it to be the better product. they only use isopropanol. Using both however will create a much better and more stable effect. Nimni's idea was to use the two products with different evaporation rates to create more of a funneling effect whereby the acetone evaporates, leaving product funneled in a mixture of isopropanol and benzyl and then shortly after the isopropanol evaporates leaving it all in the benzyl.

    How to make your own TPDS :

    Take the product you wish to deliver, then add benzyl alcohol until it is entirely dissolved, even a few drops more (adequate benzyl for product). Then add a mixture of 4 parts acetone and 5 parts isopropanol, until you get the volume that gives you the desired concentration of drug per ml, and then apply as many ml as necessary to the site of application, twice daily.

    Penetration enhancement

    The rate limiting step, believe it or not, is still the permeation through the skin. The rate limiting step for that is permeation through the outer most layer, the stratum corneum. The stratum corneum can be depicted, for functional purposes, as a brick wall. The cells, called corneocytes, are the bricks, and in between is a continuous lipid layer that represents the mortar. Whether you traverse the stratum corneum through or between the cells, your penetration enhancers shoudl always exert an effect on the lipid layer. Almost all known permeation enhancers, with the exception of DMSO, work solely on the lipid layer. So that should not be a problem.

    Here comes the tricky part, and another were manufacturers of existing products have fumbled a great deal. Penetration enhancers that do not evaporate (like acetone and isopropanol) also traverse the skin. They also dissolve organic compounds very well. That means if you volume of penetration enhancers is to great, a great deal of your product will traverse the skin dissolved in your permeation enhancer instead of in the benzyl micelles, and will be taken up systemic. Making all your efforts fruitless and rendering your product nothing more than a more expensive transdermal product. So when selecting permeation enhancers, select those that have the most effect in the smallest known volume. That is one area where most current products drop the ball.

    Occlusion : the contradiction

    Occlusion is often used with percutaneous absorption, whether it be local or transdermal, and has been shown to increase penetration of the skin. At first it was believed that this occured through the increase of water in the skin, but increased water was shown to have a minimal effect on lipid disorder in the lipid layers of the stratum corneum (Suhonen et al, 1999), so most likely it is a combination of both increased hydration and increased heat together, with either factor being relatively irrelevant alone.

    The contradiction however is that occlusion is not an option with TPDS, since it would prevent evaporation of the first phase, resulting in part of the first phase traversing the skin, with product dissolved, resulting in systemic and not local delivery

    This is yet another reason for an extremely small volume of penetration enhancers. If you cannot accomodate this, then it is best not to use PE's at all, as Nimni himself did, rather than risk affecting your primary delivery system.

    Why Skulpt didn't work, but how you can make it work in your favour

    Skulpt was an analog that was released for a while and then pulled again, that attempted to compete with aforementioned products, but despite all the obvious flaws in said products, failed at doing so.

    The idea behind it was to use DMSO as a carrier instead of benzyl alcohol. DMSO is an incredibly potent penetration enhancer that affects both the lipid layers and the structure of the cells in between. It is also amphiphillic and easily builds up in subcutaneous tissues in high concentrations, and a good solvent for most organic compounds. So what was the problem ? Well, apparently DMSO does not function as a carrier. Instead it traverses the skin first and then pulls the product through, so to speak (kurihara-Bergstromm et al, 1987). Which is why skulpt failed.

    Using a smaller dose of DMSO with the TPDS would also fail. First of all, when using DMSO as a solvent you need at least 50% for it to work adequately, while even 5% would already be enough to prevent TPDS from working properly. It traverses the skin and is a good solvent, so most of the product would dissolve in the DMSO and be lost systemically, rather than delivered locally through funneling to the benzyl phase.

    Using DMSO however would benefit us greatly. Repeated application of percutaneous products results in less and less uptake with each use, and this occurs mostly through resistance in the lipid layers (Barry et all, 1972). So using a product that also works on the cells would definitely attenuate this decrease much much longer.

    So how can we use DMSO ? Well the same researchers that found DMSO did not function as a carrier also tested an assymetrical model where they applied the DMSO first, and then the product. This resulted in a notably enhanced uptake of the compound WITH LESS DMSO THAN WHEN USING IT AS A SOLVENT. That means if you pretreat the skin with DMSO, and then apply your TPDS 5-10 minutes later, you have effectively created a product that blows any existing product out of the water.

    But because you need less DMSO, and still have better and longer working penetration because of it, and don't require any of the large volume penetration enhancers often used, that screw up TPDS delivery, you save even more money (less DMSO, no other PE's and cheap TPDS in drug store) and get a much greater effect (DMSO stronger PE, TPDS works better).

    Considering it was the PE's (and possibly greed) that made these initial formula's so extremely expensive, and that skulpt was also extremely expensive because of the high dose and high quality DMSO (you can choose for yourself now what quality DMSO you like) and both delivered relatively poor results, its basically a win-win situation.


    You can no effectively make a local delivery formula in your kitchen that is ten times more effective, and ten times cheaper than any existing formula, and on top of that it allows you to look for cheaper ingredients, ingredients or combinations thereof that you deem more fit, or ingredients that couldn't be legally used by supplement companies.

    And trust me, the inquisitive mind can easily improve on even this formula 5-10 times
    Has anyone tried this?

  6. There were quite a few threads on sysenhance, I remembered BDC and others here were quite unconvinced. But if you hop over to avant, everyone affiliated to Avant and some regulars seem to think its good science that there is enough anecdotal evidence that it works. I'm still skeptical.

  7. true. the theory and explanation behind it is good, but i guess the real world evidence and feedback shows its not as localized as we would have hoped anyone design there own homebrew and get more localized results?

  8. The ultimate test would be to use it unilaterally, like just 1 arm.
    Here's your feedback as requested:


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